Sustainability Journal (MDPI)
2009 | 1,010,498,008 words
Sustainability is an international, open-access, peer-reviewed journal focused on all aspects of sustainability—environmental, social, economic, technical, and cultural. Publishing semimonthly, it welcomes research from natural and applied sciences, engineering, social sciences, and humanities, encouraging detailed experimental and methodological r...
Sustainable Processes and Chemical Characterization of Natural Food Additives
Dung Huynh Thi Le
College of Biotechnology and Bioresources, Da-Yeh University, No. 168 University Rd, Dacun, Changhua 51591, Taiwan
Wen-Chien Lu
Department of Food and Beverage Management, Chung-Jen Junior College of Nursing, Health Sciences and Management, No. 217, Hung-Mao-Pi, Chia-Yi City 60077, Taiwan
Po-Hsien Li
Department of Medicinal Botanical and Health Applications, Da-Yeh University, No.168, University Rd, Dacun, Changhua 51591, Taiwan
Year: 2020 | Doi: 10.3390/su12072650
Copyright (license): Creative Commons Attribution 4.0 International (CC BY 4.0) license.
[Full title: Sustainable Processes and Chemical Characterization of Natural Food Additives: Palmyra Palm (Borassus Flabellifer Linn.) Granulated Sugar]
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[Summary: This page introduces a study on palmyra palm granulated sugar, examining nutritional changes, antioxidant properties, and biological activity across different drying processes. It highlights the sugar's vitamin content, volatile compounds, and phenolic content. The study aims to determine optimal preparation conditions for enhanced quality and reduced HMF content.]
sustainability Article Sustainable Processes and Chemical Characterization of Natural Food Additives: Palmyra Palm ( Borassus Flabellifer Linn.) Granulated Sugar Dung Huynh Thi Le 1,2 , Wen-Chien Lu 3, * and Po-Hsien Li 4, * 1 College of Biotechnology and Bioresources, Da-Yeh University, No. 168 University Rd, Dacun, Changhua 51591, Taiwan; huynhkate 2018@gmail.com 2 Faculty of Food Science and Technology, Ho-Chi-Minh City University of Food Industry, No.140, Le Trong Tan Street, Tay Thanh Ward, Tan Phu District, Ho-Chi-Minh City 700000, Vietnam 3 Department of Food and Beverage Management, Chung-Jen Junior College of Nursing, Health Sciences and Management, No. 217, Hung-Mao-Pi, Chia-Yi City 60077, Taiwan 4 Department of Medicinal Botanical and Health Applications, Da-Yeh University, No.168, University Rd, Dacun, Changhua 51591, Taiwan * Correspondence: m 104046@cjc.edu.tw (W.-C.L.); pohsien 0105@gmail.com (P.-H.L.); Tel.: + 886-5-277-2932#860 (W.-C.L.); + 886-9-2876-7532 (P.-H.L.) Received: 20 February 2020; Accepted: 18 March 2020; Published: 27 March 2020 Abstract: Palmyra palm ( Borassus flabellifer Linn.) is an important sugar-producing plant that is widely distributed in tropical Asian countries. Its jaggery and sweet sap are prevalent in Cambodia as a substitute for table sugar. They contain essential minerals, vitamins, and biological compounds We investigated the changes in the nutritional composition, antioxidant properties, and biological activity of palm granulated sugar prepared by using three di ff erent drying–solidification processes under vacuum conditions: the drying temperature was controlled at 80 ◦ C, 90 ◦ C, and 100 ◦ C, and the drying time was 60, 75, and 90 min, respectively. Palm granulated sugar contains 10 kinds of vitamins (mainly vitamin E 52.15–55.12 mg / 100 g), 5-hydroxymethylfurfural (2.18 to 41.92 mg / 100 g), and 38 volatile compounds that belong to the alcohol, ketones, pyrazines, acids, and phenols groups, and an aldehyde group. Moreover, palm granulated sugar exhibits a high total phenolic content (2.77–8.94 mg gallic acid equivalent / 100 g), 2,2-diphenyl-1-1 picrylhydrazyl (DPPH) radical scavenging activity (20.15%–37.88%), and ferric reducing antioxidant power (FRAP) value (322.68–378.23 µ mol Fe 2 + / mL) Furthermore, palm granulated sugar-treated NIH 3 T 3 cells showed a higher cell viability of 18.10% to 23.68%. This study confirmed that palm granulated sugar prepared at 90 ◦ C for 75 min can have a better product quality with increased vitamin and mineral contents, antioxidant properties, and biological activity, while also being low in 5-hydroxymethylfurfural (HMF) content Keywords: palmyra palm; granulated sugar; antioxidant properties; biological activity 1. Introduction Borassus Flabellifer , also called palmyra palm, is a popular material used to produce palm sugar in Asian countries [ 1 ]. Palm trees play an important role in agriculture in Cambodia B. flabellifer sap is used for wine, palm jaggery, and palm sugar, which are all rich in vitamins and minerals [ 2 ]. Many pharmacological advantages of B. flabellifer have also been reported [ 3 , 4 ]. B. flabellifer sap extract reduced the growth of serum glucose levels in sucrose-loaded rats [ 5 ] and has anti-inflammatory activity [ 6 ] and analgesic e ff ects [ 7 ]. In addition, 2,3,4-trihydroxy-5-methylacetophenone extract from palm syrup exhibited 2,2-diphenyl-1-1 picrylhydrazyl (DPPH) radical scavenging activity [ 8 ]. Sustainability 2020 , 12 , 2650; doi:10.3390 / su 12072650 www.mdpi.com / journal / sustainability
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[Summary: This page discusses palmyra palm sugar's various names and its unique flavor. It notes the palm sugar industry's unorganized nature and traditional production methods, which lead to quality inconsistencies. The page also mentions the global palm sugar market's growth and the need for improved production techniques like vacuum-drying to enhance product features.]
Sustainability 2020 , 12 , 2650 2 of 21 Palmyra palm sugar in Cambodia is known by other names such as palm jaggery, palmyra jaggery, Neera (India), and Gur (South Asia). It has a unique flavor and produces less energy than cane sugar [ 9 ]. The palm sugar industry is an unorganized rural industry in Asian countries. The clean sap of Borassus flabellifer is heated to 110 ◦ C to 120 ◦ C and blended until it is brown and thickened [ 10 ]. This process is mainly based on the traditional practices of village producers and was transferred down from older generations without accompanying scientific data. The disadvantages of palm sugar developed using this method are its unstable product quality with low dry matter content (under 80%) [ 11 ], dark color [ 12 ], and uncontrollable bacteria According to the report titled “Palm Sugar Market: Global Industry Analysis (2012–2016) and Forecast (2017–2025)”, the value of the worldwide palm sugar market was US$ 1684.2 million in 2017 and was estimated to reach US$ 2205.8 million in 2025. Income from trade is anticipated to gain at a compounded annual growth rate of 3.4% in the prediction time (2017–2025) [ 13 ]. Recently, the commercialization potential of palm sugar as an important alternate sweetener has become an attractive prospect. However, these products are not currently popular. The price of palm sugar is often decided by its quality, as well as by its color, flavor, and texture. The amount of palm sugar available depends on the genetic and metabolite characteristics of the plant, environmental factors, soil, harvest, and production process. Moreover, the aroma, texture, color, and taste of palm sugar are a ff ected by the dominance of assorted physical and chemical changes occurring during the method of concentration [ 12 ]. The palmyra jaggery industry faces the problem of determining the correct quantification of lime to be used to prevent the fermentation of palm sugar as well as the tapping, heating temperature, and heating time variables required for maintaining proper quality, yield, and nutritional properties [ 14 ]. Vacuum-drying allows materials dried in a reduced-pressure atmosphere to counter any undesirable e ff ects and enhances a product’s quality and nutritional value [ 15 ]. Therefore, the vacuum-drying method could improve palm sugar’s features [ 16 , 17 ]. Some published studies on B. flabellifer sugar only focused on palm sugar cake made from palm trees grown in Thailand [ 16 ], India [ 18 ], and Indonesia [ 19 ]. Several studies have also concentrated on the physicochemical, thermo-physical, and antioxidant properties of cake palm sugar [ 12 , 16 , 17 ]. However, no report is currently available regarding the changes in vitamin content, 5-hydroxymethylfurfural (HMF) content, volatile compounds, and biological activity of palm granulated sugar produced using a vacuum-drying process Consequently, we evaluated the chemical composition (physicochemical properties, nutritional components, vitamin, HMF content, and volatile compounds) and biological activities (total phenolic content, DPPH, ferric reducing antioxidant power, and cytoprotective activity) of palm granulated sugar produced using concentrated palm syrup of B. flabellifer flower sap from Cambodia under di ff erent drying–solidification conditions 2. Materials and Methods 2.1. Preparation of Palmyra Palm Granulated Sugar Concentrated palmyra palm syrup (86 ± 2 ◦ Brix) was provided by LU SHU Health Co., Phnom Penh, Cambodia (collected during November 2018, from many palmyra palm trees in the Kampot countryside). The syrup was heated to 40 ◦ C to 50 ◦ C and poured into an evaporating flask Drying–solidification was carried out using a vacuum pan (1 MPa, rotary speed 80 rpm) with di ff erent drying temperature (80 ◦ C, 90 ◦ C, and 100 ◦ C) and time (60 min, 75 min, and 90 min) conditions. The samples prepared at 80 ◦ C, 90 ◦ C, and 100 ◦ C for 60, 75, and 90 min were respectively represented by EPS 1, EPS 2, and EPS 3, NPS 1, NPS 2, and NPS 3, and OPS 1, OPS 2, and OPS 3, individually (Figure A 1 ). Then, the granulated sugar was milled and separated by using a laboratory sieve with a diameter of 6.3 mm. All samples (Figure A 2 ) were stored at − 20 ◦ C for two months.
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[Summary: This page details the methods used to analyze palmyra palm granulated sugar. These include measuring color, pH, moisture, water activity, total sugar, reducing sugar, and mineral content using various spectrophotometric and chromatographic techniques. It also describes methods for determining total phenolic content, DPPH radical scavenging activity, and ferric reducing antioxidant power.]
Sustainability 2020 , 12 , 2650 3 of 21 2.2. Measurement of Color, pH, Moisture Content, and Water Activity The moisture content was determined by a drying method at 105 ◦ C. Water activity (A w ) was measured by a water activity meter (HygroPalm AW, Switzerland). The color was measured by using a color meter (ZE 6000, Japan). The results are expressed according to L*, a*, and b* values, showing black to white, green to red, and blue to yellow, respectively 2.3. Determination of Total Sugar and Reducing Sugar The phenol-sulfuric acid method was used to measure total sugar content [ 20 ]. The reducing sugar was determined by the dinitrosalicylic acid method [ 21 ]. 2.4. Determination of Mineral Content The levels of minerals (potassium, iron, sodium) were analyzed by using a flame atomic absorption spectrophotometer (PinAAcle 500, PerkinElmer, Waltham, MA, USA) [ 22 ]. 2.5. Determination of Vitamin Content Determination of water and fat-soluble vitamins (A, B 1 , B 2 , B 3 , B 5 , B 6 , C, D 2 , E) and folic acid was performed with high-performance liquid chromatography with UV-PDA (Photo diode array) detection [ 23 , 24 ]. 2.6. Determination of Total Phenolic Content The determination of total phenolic content involved the use of a Folin–Ciocalteu reagent method with the gallic acid standard [ 25 , 26 ]. Briefly, 20 µ L of 10% palm granulated sugar solution was mixed with 100 µ L Folin–Ciocalteu reagent. Then, 80 µ L of 10% sodium carbonate compound was added to the blend after 5 min. The mixture was set at room temperature for 1 h. Finally, the absorbance was measured at 765 nm 2.7. Determination of DPPH Radical Scavenging Activity The method of Payet and Asikin was used to estimate the DPPH free radical scavenging activity of palm granulated sugar with minor modification [ 27 , 28 ]. Briefly, 50 µ L of sugar solution (5 mg / mL concentration) was added to 50 µ L DPPH solution 0.1 mM and 100 µ L MES bu ff er (200 mM) (pH 6.0). Absorbance was measured at 517 nm by using an Epoch microplate spectrophotometer (BioTek Instruments, Winooski, VT, USA) after 15 min. The percentage of DPPH radical scavenging ability was determined using Equation (1): DPPH ( % ) = Absorbance of control − Absorbance of the sample Absorbance of control × 100 (1) 2.8. Determination of Ferric Reducing Antioxidant Power (FRAP) The method of Phillips was used to determine the FRAP value [ 29 ]. Briefly, 100 µ L sugar solution (5 mg / mL concentration) was blended with 100 µ L of 0.2 M sodium phosphate bu ff er and 100 µ L of 1% (w / v) K 3 [Fe(CN) 6 ] solution. The blend was incubated at 50 ◦ C for 20 min, mixed with 100 µ L of 10% (w / v) trichloroacetic acid and centrifuged at 5000 rpm for 10 min. Next, 200 µ L of the supernatant was combined with 200 µ L distilled water. An amount of 200 µ L of the above blend was transferred to a 96-well plate (Costar 3599, Corning Inc., Corning, NY, USA). Each well contained 10 µ L of 0.1% (w / v) iron (III) chloride. The absorbance was measured at 700 nm 2.9. Determination of 5-Hydroxymethylfurfural (HMF) Content HMF content was detected as described in [ 30 ] with some modifications. Firstly, 10 g sugar was dissolved and made up to 50 mL with deionized water. Then, the mixture was centrifuged at 5000 rpm
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[Summary: This page continues detailing the methods used to analyze the sugar, including determining 5-Hydroxymethylfurfural (HMF) content using a spectrophotometric method and volatile compositions using gas chromatography combined with mass spectrophotometry. It also describes odor detection analyses and the cytoprotective effect of the sugar against tert-Butyl Hydroperoxide (tBuOOH) in NIH 3T3 fibroblast cells.]
Sustainability 2020 , 12 , 2650 4 of 21 for 15 min. The supernatant was used to measure HMF content. Next, 2 mL supernatant was imported into a tube. An amount of 2 mL of 12% trichloroacetic acid and 2 mL of 0.025 M thiobarbituric acid was added and mixed completely. The tube was placed in a water bath at 40 ◦ C for 50 min. After incubating, the tube was immediately cooled with water to room temperature. The absorbance was measured at 445 nm. A standardization curve for HMF was used to quantify the HMF concentration 2.10. Determination of Volatile Compositions The analysis of volatile components proceeded according to Asikin [ 28 ] with some modifications Briefly, the volatile components of palm granulated sugar were extracted using an organic solvent The sample (50 g) was mixed with 200 mL diethyl ether and cyclohexanol 1% and put into a flask. The mixture was kept at 5 ◦ C for 24 h. Then, the solution was filtered by filter paper, and the volatile components were separated by solvent-assisted flavor evaporation using a vacuum at 40 ◦ C. Next, the extract was dried by 10 g anhydrous sodium sulfate for 12 h at 5 ◦ C and concentrated in a vacuum by a gentle nitrogen stream. The extract was stored at − 20 ◦ C All samples were analyzed by using gas chromatography (GC) combined with an aflame ionization detector (FID) and mass spectrophotometry. In the process, 1 mL sample was injected into a DB-Wax column (60 m × 0.25 mm i.d., film thickness 0.25 mm) at a split ratio of 1:10, and the linear velocity of the helium carrier gas was determined. The temperatures of the GC injector and FID were set at 250 ◦ C. The oven was set initially at 40 ◦ C for 2 min, increased up to 200 ◦ C at a rate of 2 ◦ C / min, and kept constant at 20 ◦ C for 38 min 2.11. Odor Description and Detection Analyses The odor of volatile components of palm granulated sugar was determined by using gas chromatography (GC)-olfactometry with an Agilent system connected to an FID and olfactory detection port [ 28 ]. 2.12. Cytoprotective E ff ect of Palm Granulated Sugar against tert-Butyl Hydroperoxide (tBuOOH) NIH 3 T 3 fibroblast cells were bought from BCRC (BCRC 60008, Hsinchu, Taiwan) and maintained in our laboratory (1 × 10 6 cells / mL, kept at 37 ◦ C under 5% CO 2 and 95% air in the RPMI 1640 medium) were used for the examination. The cells were subjected to oxidative stress as described in [ 31 , 32 ]. Briefly, cells were cultivated with or without sugar (20 µ L, 20 mg / mL) dissolved in phosphate-bu ff ered saline in a 96-well microplate for 30 min, then treated with 500 µ M tBuOOH and incubated for 3 h Cell viability was evaluated by the microculture tetrazolium assay [ 33 ]. Next, 25 mL of MTT solution (5 mg / mL) was added to wells and kept at 37 ◦ C for 4 h. Then, 100 µ L of lysis bu ff er was added to wells and incubated at 37 ◦ C for 16 h to dissolve dark blue formazan crystals. The absorption of formazan solution was measured at 570 nm and shown as cell viability by using a microplate spectrophotometer (BioTek Instruments, Winooski, VT, USA) 2.13. Data Analysis All analyses were repeated three times, and the data were expressed as mean ± standard deviation The data were analyzed by ANOVA followed by the Tukey test for comparing means. A value of p < 0.05 was considered statistically significant. Statistical analysis involved using Minitab 17 software 3. Results 3.1. Physicochemical Characteristics The physical parameters (water content, a w , pH, color) of palm granulated sugar are presented in Table 1 . The water content of tested palms ranged from 2.91% to 5.12%. The water content of drying samples at 100 ◦ C was higher than at 80 ◦ C and 90 ◦ C and was also similar to previous reports for
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[Summary: This page presents the physicochemical characteristics of the palm granulated sugar, including water content, water activity (Aw), and pH. It also discusses color changes observed with varying drying temperatures and times, attributing these changes to the Maillard reaction. The results indicate that the granulated sugars could extend storage time, with OPS 1 being the most stable.]
Sustainability 2020 , 12 , 2650 5 of 21 palm sugar (0.98%–2.47%) [ 17 ]. The water content variation of sugars is created by di ff erences in the manufacturing process [ 34 ]. The A w values of the palm granulated sugar ranged from 0.48 to 0.30. The lowest and highest A w values were for samples OPS 1 (100 ◦ C, 90 min) and EPS 1 (80 ◦ C, 60 min). The high A w values quickly promote microbial growth and biochemical degradation reactions, all of which shorten the storage of sugars [ 22 ]. These results showed that palm granulated sugars could extend the storage time, and the OPS 1 sample was the most stable. This result agreed with an earlier report on water activity [ 17 ]. The pH values were modified slightly, from 6.90 to 6.99. Our data were higher than the results of previous studies in which granulated jaggery had pH values of 5.26 and 6.60 [ 35 , 36 ]. The pH value change may be explained by chemical reactions occurring during the palm jaggery heating process [ 37 ] and by the appearance of Maillard reaction products (MRPs) [ 38 ]. The food product color is the most important factor a ff ecting acceptance by the customer and also expresses the natural transformation of the product (ripeness, processing, and storage) [ 16 ]. Table 1 shows the color change of palm granulated sugar with increasing drying temperature and time. All these samples displayed similar trends: the palm granulated sugar color changed from a green-yellow (low -a*, L and high + b*-values) to a red-golden yellow (high + a*, L and low + b*-values) [ 39 ]. The result showed a slight change of L-value (lightness–darkness) from 115.69 (NPS 1) to 122.57 (OPS 2). The a* values ranged from − 0.21 (EPS 1) to 0.39 (OPS 3). The b* values tended to decrease from 3.18 (EPS 1) to 1.57 (OPS 3). The a* and L values at 100 ◦ C were higher than at 80 ◦ C and 90 ◦ C. The di ff erent colors of all samples might have been due to the di ff erence in drying conditions used in our study. A previous study used the boiling and drying process to lead to the increased a* value that may result from non-enzymatic browning, including MRPs and caramelization products [ 16 ]. However, the caramelization could not occur here because this reaction e ff ectively takes place at temperatures > 120 ◦ C. Therefore, only the Maillard reaction can lead to the browning of palm granulated sugar [ 40 , 41 ].
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[Summary: This page shows a table displaying the color, moisture content, pH, and water activity (Aw) of palm granulated sugar samples (EPS 1-3, NPS 1-3, OPS 1-3). It presents the mean and standard deviation of triplicate measurements for each property, indicating significant differences between samples with different letters.]
Sustainability 2020 , 12 , 2650 6 of 21 Table 1. Color, moisture content, pH, and water activity (Aw) of palm granulated sugar Properties EPS 1 EPS 2 EPS 3 NPS 1 NPS 2 NPS 3 OPS 1 OPS 2 OPS 3 Moisture content (%) 5.12 ± 0.18 a 4.24 ± 0.25 b 3.88 ± 0.09 c 5.08 ± 0.06 a 3.31 ± 0.18 d 3.26 ± 0.08 d 4.97 ± 0.07 a 3.00 ± 0.06 de 2.91 ± 0.02 e Water activity (A w ) 0.48 ± 0.01 a 0.45 ± 0.02 b 0.35 ± 0.03 de 0.40 ± 0.01 c 0.33 ± 0.01 def 0.31 ± 0.01 f 0.35 ± 0.00 d 0.32 ± 0.01 ef 0.30 ± 0.02 f pH 6.90 ± 0.04 a 6.96 ± 0.03 a 6.99 ± 0.01 a 6.92 ± 0.04 a 6.95 ± 0.18 a 6.99 ± 0.08 a 6.86 ± 0.11 a 6.98 ± 0.05 a 6.99 ± 0.03 a L* value 116.24 ± 0.28 cd 117.13 ± 0.84 cd 119.14 ± 0.72 b 115.69 ± 0.39 d 116.25 ± 2.02 cd 121.04 ± 0.22 a 117.83 ± 0.39 bc 122.57 ± 0.62 a 121.54 ± 1.05 a a* value − 0.21 ± 0.02 e − 0.17 ± 0.03 e − 0.21 ± 0.02 e − 0.11 ± 0.02 e 0.05 ± 0.02 d 0.15 ± 0.02 cd 0.26 ± 0.04 bc 0.31 ± 0.02 ab 0.39 ± 0.09 a b* value 3.18 ± 0.24 ab 2.85 ± 0.21 abc 2.38 ± 0.20 cd 2.86 ± 0.35 abc 1.84 ± 0.42 de 1.83 ± 0.31 de 3.27 ± 0.18 a 2.39 ± 0.24 bcd 1.57 ± 0.27 e Values are mean ± standard deviation of triplicates. The same letters within a row are not significantly di ff erent ( p < 0.05).
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[Summary: This page discusses the chemical composition of palm granulated sugar, noting sugar as the major component. It details the total sugar and reducing sugar content, and the mineral composition (potassium, sodium, iron). Potassium content was the highest. The mineral content varied, but the differences were not statistically significant.]
Sustainability 2020 , 12 , 2650 7 of 21 3.2. Chemical Composition One of the standard characteristics of palm granulated sugar compared to white sugar and refined sugar is its nutritional rate and mineral load. The chemical composition of palm granulated sugar is shown in Table 2 . According to the composition, sugar was a major component of palm granulated sugar, at 91.04% to 93.28%. The total sugar content of palm granulated sugar at 100 ◦ C (0.35%–2.24%) was higher than at 80 ◦ C and 90 ◦ C. This was also higher than in a previous study of palm sugar powder [ 11 ]. The reducing sugar content was 5.55% to 6.61%, and this decreased slightly with increasing drying temperature and time. The reason for this could be that reducing sugars participate in the Maillard reaction and increase the browning of palm granulated sugar (increasing the HMF content). Besides, previous studies have demonstrated the slow degradation over time of reducing sugar (fructose, glucose) into various intermediates and advanced MRPs, including α -dicarbonyl compounds, organic acids, and melanoidins [ 42 ]. Additionally, some authors noted that the di ff erence between total sugar and reducing sugar content may explain the contamination of lactic acid bacteria in sugar. Microorganisms can convert sucrose to glucose and fructose and to organic acids or alcohols [ 11 ]. The mineral composition of fresh inflorescence sap has a high concentration of potassium, sodium, iron, and phosphorus [ 43 ]. We also detected all components at high levels in palm granulated sugar Potassium had the highest content among all other minerals (688.45–705.27 mg / 100 g). This result was consistent with granulated panelas [ 22 ] but higher than brown sugar (10.30 mg / L) [ 44 ]. Potassium is a vital mineral to balance fluids, di ff erent minerals within the body and maintain blood pressure [ 45 ]. The other elements found were sodium and iron. The sodium content ranged from 23.10 to 24.50 mg / 100 g, which was much higher than that of the granulated non-centrifugal sugars (1.94–5.60 mg / 100 g) [ 46 ]. Moreover, the iron content in palm granulated sugar was also higher than that of brown sugar (1.88–2.05 mg / kg vs. 2.3 mg / kg) [ 44 ]. In general, the mineral content varied in samples, but these di ff erences were not statistically significant.
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[Summary: This page presents a table showing the chemical composition of palm granulated sugar samples (EPS 1-3, NPS 1-3, OPS 1-3). The table lists the total sugar, reducing sugars, sodium, potassium, and iron content. Values are expressed as mean ± standard deviation of triplicates, with significant differences indicated by different letters within each row.]
Sustainability 2020 , 12 , 2650 8 of 21 Table 2. Chemical composition of palm granulated sugar Compositions EPS 1 EPS 2 EPS 3 NPS 1 NPS 2 NPS 3 OPS 1 OPS 2 OPS 3 Total sugar (%) 91.04 ± 0.75 d 91.65 ± 0.72 abcd 92.01 ± 0.16 abcd 91.23 ± 0.78 cd 92.87 ± 0.64 abcd 92.93 ± 0.93 abc 91.36 ± 0.44 bcd 93.11 ± 0.13 ab 93.28 ± 0.71 a Reducing sugars (%) 6.61 ± 0.30 a 5.87 ± 0.22 bcd 5.81 ± 0.21 bcd 6.48 ± 0.22 ab 5.73 ± 0.36 cd 5.63 ± 0.16 d 6.34 ± 0.17 abc 5.62 ± 0.27 d 5.55 ± 0.13 d Sodium (mg) 24.12 ± 4.85 a 24.39 ± 1.62 a 23.52 ± 3.93 a 24.16 ± 3.84 a 23.73 ± .59 a 24.50 ± .21 a 23.32 ± .87 a 23.07 ± .89 a 22.72 ± .13 a Potassium (mg) 688.45 ± 8.43 a 689.63 ± 5.07 a 690.76 ± 3.14 a 702.13 ± 10.47 a 699.93 ± 7.48 a 698.45 ± 4.67 a 701.49 ± 3.65 a 705.27 ± 5.85 a 699.73 ± 6.95 a Iron (mg) 1.99 ± 0.14 a 2.02 ± 0.07 a 2.03 ± 0.08 a 1.88 ± 0.08 a 1.92 ± 0.04 a 1.98 ± 0.03 a 2.05 ± 0.07 a 2.04 ± 0.05 a 2.01 ± 0.04 a Values are mean ± standard deviation of triplicates. The same letters within a row are not significantly di ff erent ( p < 0.05).
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[Summary: This page discusses the vitamin content of palm granulated sugar, highlighting the presence of ten vitamins including A, B1, B2, B3, B5, B6, C, D2, E, and folic acid. Vitamin E content was the highest. The results suggest that the sugar is a good source of these essential nutrients.]
Sustainability 2020 , 12 , 2650 9 of 21 3.3. Vitamin Content Vitamins are essential for maintaining the physiological state of humans, and the lack of a su ffi cient intake will result in severe diseases. Water-soluble vitamins act mainly as coenzymes, whereas fat-soluble ones act in numerous and more advanced ways [ 47 ]. The palm sap collected from the inflorescence of palmyra palm is a good source of vitamins such as vitamin A, niacin, thiamin and riboflavin [ 48 , 49 ]. Our study is the first to present the vitamin content of palm granulated sugar. The results of the vitamin composition are in Table 3 . The 10 vitamins found included vitamins A, B 1 , B 2 , B 3 , B 5 , B 6 , C, D 2 , E, and folic acid. Vitamin E content was the highest, from 52.15 to 55.12 mg / 100 g, and vitamin B 2 content was the lowest, from 0.04 to 0.07 mg / 100 g. Moreover, palm granulated sugar contained vitamin C, with a value from 2.78 to 4.01 mg / 100 g, and vitamin D 2 , with a value from 2.11 to 2.23 mg / 100 g. Palm granulated sugar also contained vitamin B groups including B 1 , B 2 , B 3 , B 5 , and B 6 with values that ranged from 0.04 to 2.15 mg / 100 g. The result was similar to a previous examination which showed that fresh sap of B. flabellifer was a good source of vitamin B complex and ascorbic acid [ 50 ]. Moreover, the levels of folic acid ranged from 2.51 to 3.33 µ g / 100 g in this study.
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[Summary: This page contains a table presenting the vitamin content of palm granulated sugar samples (EPS 1-3, NPS 1-3, OPS 1-3). It shows the levels of various vitamins per 100g. Values are mean ± standard deviation of triplicates. The same letters indicate no significant difference (p < 0.05).]
Sustainability 2020 , 12 , 2650 10 of 21 Table 3. Vitamin content of palm granulated sugar Vitamin (Per 100 g) EPS 1 EPS 2 EPS 3 NPS 1 NPS 2 NPS 3 OPS 1 OPS 2 OPS 3 Vit A (mg) 1.86 ± 0.09 a 1.84 ± 0.06 a 1.74 ± 0.06 ab 1.84 ± 1.11 a 1.76 ± 0.04 ab 1.65 ± 0.05 b 1.76 ± 0.04 ab 1.72 ± 0.04 ab 1.60 ± 0.04 ab B 1 (mg) 0.97 ± 0.09 a 0.92 ± 0.05 ab 0.91 ± 0.09 ab 0.90 ± 0.02 abc 0.83 ± 0.05 abcd 0.72 ± 0.04 cd 0.83 ± 0.10 abcd 0.77 ± 0.05 bcd 0.70 ± 0.04 d B 2 (mg) 0.07 ± 0.01 a 0.06 ± 0.01 abc 0.06 ± 0.01 ab 0.06 ± 0.01 ab 0.05 ± 0.01 abc 0.05 ± 0.00 abc 0.05 ± 0.01 bc 0.05 ± 0.01 abc 0.04 ± 0.01 c B 3 (mg) 2.15 ± 0.04 a 2.15 ± 0.02 a 2.14 ± 0.07 a 2.1 ± 0.12 a 2.09 ± 0.11 a 2.08 ± 0.07 a 2.01 ± 0.04 a 1.98 ± 0.12 a 1.95 ± 0.07 a B 5 (mg) 0.66 ± 0.08 ab 0.58 ± 0.05 abc 0.50 ± 0.02 cd 0.67 ± 0.02 a 0.56 ± 0.03 bc 0.5 ± 0.02 cd 0.61 ± 0.04 abc 0.56 ± 0.02 bc 0.44 ± 0.04 d B 6 (mg) 0.19 ± 0.02 a 0.14 ± 0.02 bc 0.11 ± 0.02 cd 0.16 ± 0.01 ab 0.13 ± 0.02 bc 0.12 ± 0.01 cd 0.15 ± 0.02 abc 0.12 ± 0.03 bcd 0.09 ± 0.01 d Folic acid ( µ g) 3.12 ± 0.15 a 3.08 ± 0.04 ab 2.95 ± 0.11 abc 3.01 ± 0.06 abc 2.85 ± 0.10 abc 2.72 ± 0.11 bc 2.89 ± 0.09 abc 2.72 ± 0.17 bc 2.64 ± 0.24 c Vit C (mg) 4.01 ± 0.14 a 3.45 ± 0.17 bcd 3.15 ± 0.16 de 3.85 ± 0.07 ab 3.41 ± 0.21 bcd 3.07 ± 0.14 de 3.66 ± 0.23 abc 3.21 ± 0.16 cde 2.78 ± 0.09 e Vit D 2 (mg) 2.15 ± 0.04 abc 2.23 ± 0.02 a 2.11 ± 0.05 c 2.17 ± 0.03 abc 2.21 ± 0.03 ab 2.14 ± 0.02 bc 2.17 ± 0.02 abc 2.11 ± 0.05 c 2.15 ± 0.02 abc Vit E (mg) 55.12 ± 0.88 a 54.68 ± 1.11 a 54.34 ± 0.69 ab 55.01 ± 0.18 a 54.98 ± 1.07 a 54.23 ± 1.06 ab 54.23 ± 0.75 ab 54.12 ± 1.10 ab 52.15 ± 0.60 b Values are mean ± standard deviation of triplicates. The same letters within a row are not significantly di ff erent ( p < 0.05).
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[Summary: This page discusses the HMF content in palm granulated sugar, noting its formation through the Maillard reaction and caramelization. It highlights HMF's potential toxicity and the varying levels found in the samples. The HMF content was much lower at 80 and 90 °C than at 100 °C. The page also compares these findings to other studies.]
Sustainability 2020 , 12 , 2650 11 of 21 3.4. HMF content HMF is a heterocyclic compound and forms from reducing sugars through the Maillard reaction and caramelization [ 51 ]. HMF is formed as products or intermediates in heat-induced reactions and significantly adds to the sensory properties of heated foods [ 52 ]. HMF used to be a top-quality indicator of thermally processed foods until its toxic properties were discovered. HMF was purported to induce genotoxic and mutagenic e ff ects in microorganisms and human cells and promote carcinoma in rats [ 53 ]. The HMF content in palm granulated sugar ranged from 2.18 to 41.92 mg / 100 g (Figure 1 ). The HMF contents of EPS 1, EPS 2, and EPS 3 were rather low, at 2.18, 3.39, and 3.77 mg / 100 g, respectively However, this increased quickly and was highest at 100 ◦ C (10.09–41.92 mg / 100 g). The HMF content of palm granulated sugars at 80 ◦ C and 90 ◦ C was much lower than at 100 ◦ C. The HMF content is based greatly on the processing technique, heating level, pH, total acidity and storage condition [ 54 , 55 ]. With increasing drying temperature, the reaction speed between sugar and amino acid groups increased, leading to an exponentially increasing Maillard reaction rate [ 56 ]. The same research has not yet shown HMF contents; however, Naknean’s study showed that the HMF content of palm sugar cake samples in Songkhla province ranged from 21.81 to 341.80 mg / kg [ 16 ]. Moreover, a palm sugar syrup study reported that HMF content varied from 20.13 to 185.39 mg / kg [ 57 ]. For the Codex Alimentarius on sugars, the HMF content of honey should not be more than 40 mg / kg. However, the HMF content can be up to 80 mg / kg in honey from regions with tropical ambient temperatures. The HMF content of samples dried at 100 ◦ C was higher than the maximum limit recommended by Codex Alimentarius Sustainability 2020 , 12 , x FOR PEER REVIEW 8 of 21 Figure 1. 5-hydroxymethylfurfural ( HMF) content in palm granulated sugar under different drying– solidification conditions. 3.5. Composition of volatiles The best-known character of palm granulated sugar is its unique flavor, which is achieved by the Maillard reaction. The volatile compositions of palm granulated sugar are displayed in Table 4. A total of seven volatile groups was analyzed, including alcohol, ketones, pyrazines, acids, phenols, and aldehyde groups. The maximum and minimum values of volatile compounds were found in NPS 1 (1.45 mg/100 g) and OPS 3 (1.17 mg/100 g). The dried palm granulated sugar at 80 °C and 90 °C presented a higher number of volatile components than at 100 °C (3.98 and 4.01 vs 3.87 mg/100 g). This result agreed with other studies [58,59]. Flavor compound formation in the Maillard reaction involves the reaction temperature and time, pH, and water content, together with the types of sugar and amino acids. Both the quantity and quality of volatile compounds affect the precursors, thermal process parameters, pH, and ratio of amino nitrogen to reducing sugar [60]. Palm granulated sugar extract contains mainly volatile fractions such as alcohols (0.48–0.56 mg/100 g, six compounds), ketones (0.34–0.39 mg/100 g, 12 compounds) and acids (0.49–0.64 mg/100 g, nine compounds). Moreover, palm granulated sugars included two sulfurs, two phenols, six pyrazines, and one aldehyde. The rate and quantity of those compounds represent the volatile profile with different forms of odors [28]. Our results showed the major compounds of ketones to be 2,3- dihydro-3,5-dihydroxy-6-methyl-4-pyran-4-one, 1-hydroxy-2-propanone, 2,5-pyrrolidinedione and pantolactone, which could create a pleasantly sweet, cotton candy-like, caramel, and coffee-like characteristic [28]. MRPs can range from a pleasant, flowery, and fragrant aroma to a burnt, pungent, nutty, and caramel-like odor [61], based on the amino acid and sugar composition in foods and also their reaction pathways [62]. Likewise, the pyrazines are Maillard reaction-derived flavor compounds that display associated flavors of cooked, roasted, toasted, and baked cereals [61]. The number of pyrazines of palm granulated sugar was reduced (from 0.06 to 0.08 mg/100 g) as the production of pyrazines was encouraged at pH values from 8.00 to 9.55 [59]. The presence of 2,5- dimethyl-pyrazine, 2,6-dimethyl-pyrazine, and 2,3,5-trimethyl-pyrazine provides a nutty, roasted, coffee-like and earthy odor for palm granulated sugar [63]. However, aldehyde and phenol groups such as 2-methoxy-phenol, 2,6-dimethoxy-phenol, and vanillin may provide sweet, herbaceous, maple-like, caramel, and cotton candy-like odors. The alcohol groups contained six compounds that EPS 1 EPS 2 EPS 3 NPS 1 NPS 2 NPS 3 OPS 1 OPS 2 OPS 3 H M F c ont ent ( m g/ 100 g) 0 10 20 30 40 50 a b c d d ef f e e Figure 1. 5-hydroxymethylfurfural (HMF) content in palm granulated sugar under di ff erent drying–solidification conditions 3.5. Composition of Volatiles The best-known character of palm granulated sugar is its unique flavor, which is achieved by the Maillard reaction. The volatile compositions of palm granulated sugar are displayed in Table 4 . A total of seven volatile groups was analyzed, including alcohol, ketones, pyrazines, acids, phenols, and aldehyde groups. The maximum and minimum values of volatile compounds were found in NPS 1 (1.45 mg / 100 g) and OPS 3 (1.17 mg / 100 g). The dried palm granulated sugar at 80 ◦ C and 90 ◦ C presented a higher number of volatile components than at 100 ◦ C (3.98 and 4.01 vs. 3.87 mg / 100 g).
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[Summary: This page details the volatile compositions of palm granulated sugar, emphasizing the unique flavor achieved through the Maillard reaction. It identifies seven volatile groups, including alcohols, ketones, pyrazines, acids, phenols, and aldehydes. The page notes that lower drying temperatures result in a higher number of volatile components and describes specific compounds contributing to the sugar's aroma.]
Sustainability 2020 , 12 , 2650 12 of 21 This result agreed with other studies [ 58 , 59 ]. Flavor compound formation in the Maillard reaction involves the reaction temperature and time, pH, and water content, together with the types of sugar and amino acids. Both the quantity and quality of volatile compounds a ff ect the precursors, thermal process parameters, pH, and ratio of amino nitrogen to reducing sugar [ 60 ]. Palm granulated sugar extract contains mainly volatile fractions such as alcohols (0.48–0.56 mg / 100 g, six compounds), ketones (0.34–0.39 mg / 100 g, 12 compounds) and acids (0.49–0.64 mg / 100 g, nine compounds). Moreover, palm granulated sugars included two sulfurs, two phenols, six pyrazines, and one aldehyde. The rate and quantity of those compounds represent the volatile profile with di ff erent forms of odors [ 28 ]. Our results showed the major compounds of ketones to be 2,3-dihydro-3,5-dihydroxy-6-methyl-4-pyran-4-one, 1-hydroxy-2-propanone, 2,5-pyrrolidinedione and pantolactone, which could create a pleasantly sweet, cotton candy-like, caramel, and co ff ee-like characteristic [ 28 ]. MRPs can range from a pleasant, flowery, and fragrant aroma to a burnt, pungent, nutty, and caramel-like odor [ 61 ], based on the amino acid and sugar composition in foods and also their reaction pathways [ 62 ]. Likewise, the pyrazines are Maillard reaction-derived flavor compounds that display associated flavors of cooked, roasted, toasted, and baked cereals [ 61 ]. The number of pyrazines of palm granulated sugar was reduced (from 0.06 to 0.08 mg / 100 g) as the production of pyrazines was encouraged at pH values from 8.00 to 9.55 [ 59 ]. The presence of 2,5-dimethyl-pyrazine, 2,6-dimethyl-pyrazine, and 2,3,5-trimethyl-pyrazine provides a nutty, roasted, co ff ee-like and earthy odor for palm granulated sugar [ 63 ]. However, aldehyde and phenol groups such as 2-methoxy-phenol, 2,6-dimethoxy-phenol, and vanillin may provide sweet, herbaceous, maple-like, caramel, and cotton candy-like odors. The alcohol groups contained six compounds that were reported to have volatile aroma components in non-centrifugal cane brown sugar [ 28 ]. Amounts of S-(R’,R’)-2,3-butanediol (0.24 mg / 100 g), R-(R’,R’)-2,3-butanediol (0.09 mg / 100 g), and ethanol (0.21 mg / 100 g) in EPS 1 were higher than OPS 3, at 0.03, 0.02, and 0.03 mg / 100 g, respectively. Additionally, 2-propenoic acid, 2-hydroxy-propanoic acid, and benzoic acid showed high quantities in the acid group. Besides originating from tissue, the acid compounds arise in the sap collection process [ 18 , 64 ] and the clear levels of sulfur compounds were identified as dimethyl sulfoxide (0.10–0.15 mg / 100 g) and dimethyl sulfone (0.01–0.02 mg / 100 g). Altogether, sulfur-containing Maillard odorants represent the most dominant aroma compounds and provide the flavor of cooked meats. These volatile compounds are stable and present the flavor and aroma of stewed beef juice, bread crust, roasted chicken, cocoa powder, peanuts, roasted beef, popcorn, and co ff ee [ 65 ].
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[Summary: This page presents a table of volatile compositions in palm granulated sugar. It includes compound names, retention indices (RI), content in mg/100g for each sample (EPS 1-3, NPS 1-3, OPS 1-3), and odor descriptions. Values are mean ± standard deviation of triplicates, with significant differences indicated by different letters.]
Sustainability 2020 , 12 , 2650 13 of 21 Table 4. Volatile compositions of palm granulated sugar No. RI Compound Content (mg / 100 g) Odor Description EPS 1 EPS 2 EPS 3 NPS 1 NPS 2 NPS 3 OPS 1 OPS 2 OPS 3 Total alcohols 0.560 0.518 0.498 0.545 0.513 0.504 0.544 0.498 0.477 1 931 Ethanol 0.211 ± 0.010 a 0.208 ± 0.009 ab 0.201 ± 0.004 ab 0.213 ± 0.014 a 0.206 ± 0.013 ab 0.198 ± 0.010 ab 0.208 ± 0.009 ab 0.200 ± 0.008 ab 0.184 ± 0.007 b Alcoholic, solvent 2 1540 R-(R’,R’)-2,3-butanediol 0.088 ± 0.003 a 0.078 ± 0.004 abc 0.072 ± 0.004 cd 0.084 ± 0.005 ab 0.077 ± 0.005 bc 0.070 ± 0.003 cd 0.085 ± 0.005 ab 0.068 ± 0.002 cd 0.066 ± 0.003 d Sweet, grassy, fruity 3 1579 S-(R’,R’)-2,3-butanediol 0.239 ± 0.011 a 0.213 ± 0.006 cd 0.207 ± 0.005 d 0.227 ± 0.006 abc 0.21 ± 0.005 cd 0.219 ± 0.006 bcd 0.232 ± 0.005 ab 0.211 ± 0.006 cd 0.210 ± 0.004 cd Sweet, flowery, rancid 4 1656 2-Furanmethanol 0.019 ± 0.001 a 0.015 ± 0.002 b 0.015 ± 0.001 b 0.018 ± 0.02 ab 0.017 ± 0.001 a 0.014 ± 0.001 b 0.016 ± 0.001 b 0.016 ± 0.002 ab 0.014 ± 0.001 ab Roasted, nutty, fruity 5 1720 5-Methyl-2-furanmethanol 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a Sweet, fruity, minty 6 2069 5-Methyl-2-pyrazinylmethanol 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a Acidic, sweat-like, sweet Total ketones 0.351 0.341 0.338 0.348 0.385 0.383 0.368 0.378 0.388 7 1256 4,5-Dihydro-2-methyl-3(2 H)-furanone 0.003 ± 0.000 a 0.002 ± 0.000 b 0.002 ± 0.000 b 0.002 ± 0.000 b 0.003 ± 0.000 b 0.002 ± 0.000 a 0.002 ± 0.000 b 0.003 ± 0.000 a 0.001 ± 0.000 c Toasted, buttery 8 1278 3-Hydroxy-2-butanone 0.004 ± 0.000 a 0.004 ± 0.000 a 0.004 ± 0.000 a 0.004 ± 0.000 a 0.004 ± 0.000 a 0.004 ± 0.000 a 0.004 ± 0.000 a 0.004 ± 0.000 a 0.004 ± 0.000 a Sweet, nutty, dairy-like 9 1292 1-Hydroxy-2-propanone 0.048 ± 0.003 a 0.044 ± 0.003 ab 0.042 ± 0.003 abc 0.04 ± 0.002 bc 0.036 ± 0.003 cd 0.032 ± 0.003 d 0.041 ± 0.002 bc 0.033 ± 0.002 d 0.032 ± 0.002 d Sweet, grassy, co ff ee-like 10 1614 Butyrolactone 0.009 ± 0.000 a 0.006 ± 0.000 d 0.005 ± 0.000 e 0.007 ± 0.000 c 0.006 ± 0.000 d 0.007 ± 00.000 c 0.008 ± 0.000 b 0.006 ± 0.001 d 0.007 ± 0.000 c Cooked, sweet 11 1746 2(5 H)-Furanone 0.008 ± 0.000 ab 0.006 ± 0.001 c 0.006 ± 0.001 c 0.009 ± 0.001 a 0.006 ± 0.001 c 0.006 ± 0.000 c 0.007 ± 0.000 bc 0.004 ± 0.000 d 0.004 ± 0.000 d Pungent, cheesy 12 1826 3-Methyl-1,2-cyclopentanedione 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a 0.001 ± 0.000 a Sweet, maple-like, medicinal 13 1966 2-Acetyl pyrrole 0.014 ± 0.004 a 0.012 ± 0.003 a 0.008 ± 0.001 ab 0.012 ± 0.003 a 0.008 ± 0.001 ab 0.006 ± 0.001 b 0.010 ± 0.002 ab 0.008 ± 0.001 ab 0.006 ± 0.001 b Herbaceous, metallic, sweet 14 2027 Pantolactone 0.029 ± 0.002 ab 0.026 ± 0.003 bc 0.022 ± 0.002 c 0.031 ± 0.002 ab 0.030 ± 0.003 ab 0.028 ± 0.002 a 0.033 ± 0.003 a 0.029 ± 0.002 ab 0.026 ± 0.003 bc Sweet, caramel 15 2035 2,5-Dimethyl-4-hydroxy-3(2 H)-furanone 0.001 ± 0.000 c 0.003 ± 0.003 a 0.002 ± 0.000 b 0.001 ± 0.000 c 0.002 ± 0.000 b 0.001 ± 0.000 c 0.002 ± 0.000 b 0.002 ± 0.000 b 0.002 ± 0.000 b Sweet, cotton candy-like, caramel 16 2044 2-Pyrrolidinone 0.002 ± 0.00 a 0.002 ± 0.00 a 0.002 ± 0.00 a 0.002 ± 0.00 a 0.002 ± 0.00 a 0.002 ± 0.00 a 0.002 ± 0.00 a 0.002 ± 0.00 a 0.002 ± 0.00 a Sweet, cotton candy-like, caramel 17 2268 2,3-Dihydro-3,5-dihydroxy-6-methyl-4 H-pyran-4-one 0.188 ± 0.012 c 0.192 ± 0.009 c 0.202 ± 0.009 c 0.198 ± 0.009 c 0.242 ± 0.010 ab 0.247 ± 0.013 a 0.217 ± 0.006 bc 0.243 ± 0.013 ab 0.254 ± 0.011 a Sweet, maple-like, caramel 18 2467 2,5-Pyrrolidinedione 0.044 ± 0.002 ab 0.043 ± 0.002 ab 0.042 ± 0.002 b 0.041 ± 0.003 b 0.045 ± 0.003 ab 0.047 ± 0.002 ab 0.041 ± 0.002 b 0.043 ± 0.003 ab 0.049 ± 0.002 a Sweet, cotton candy-like, caramel Total pyrazines 0.081 0.069 0.064 0.078 0.07 0.064 0.073 0.065 0.065 19 1262 2-Methyl-pyrazine 0.006 ± 0.000 a 0.005 ± 0.000 a 0.005 ± 0.000 a 0.005 ± 0.000 a 0.006 ± 0.000 a 0.006 ± 0.000 a 0.005 ± 0.000 a 0.006 ± 0.000 a 0.005 ± 0.000 a Sweet, grassy, acidic 20 1321 2,5-Dimethyl-pyrazine 0.047 ± 0.003 ab 0.041 ± 0.002 bc 0.043 ± 0.002 abc 0.049 ± 0.003 a 0.046 ± 0.001 abc 0.042 ± 0.002 bc 0.041 ± 0.001 bc 0.040 ± 0.003 c 0.046 ± 0.002 abc Nutty, earthy, roasted 21 1327 2,6-Dimethyl-pyrazine 0.016 ± 0.002 ab 0.013 ± 0.001 bc 0.007 ± 0.007 e 0.017 ± 0.002 a 0.008 ± 0.001 de 0.006 ± 0.001 e 0.015 ± 0.015 ab 0.011 ± 0.011 cd 0.005 ± 0.001 e Nutty, sweet 22 1345 2,3-Dimethyl-pyrazine 0.002 ± 0.000 a 0.001 ± 0.000 b 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.001 ± 0.000 b 0.001 ± 0.000 b 0.002 ± 0.000 a 0.001 ± 0.000 b Nutty, roasted, co ff ee-like 23 1407 2,3,5-Trimethyl-pyrazine 0.009 ± 0.001 a 0.006 ± 0.001 bc 0.005 ± 0.001 cd 0.004 ± 0.000 d 0.006 ± 0.001 bc 0.007 ± 0.000 ab 0.008 ± 0.001 a 0.005 ± 0.000 cd 0.006 ± 0.001 bc Nutty, earthy, roasted 24 1458 2-Ethyl-3,6-dimethyl-pyrazine 0.001 ± 0.000 a 0.003 ± 0.000 c 0.002 ± 0.000 ab 0.001 ± 0.000 a 0.002 ± 0.000 ab 0.002 ± 0.000 ab 0.003 ± 0.00 c 0.001 ± 0.000 a 0.002 ± 0.000 ab Nutty, earthy, co ff ee-like Total acids 0.637 0.545 0.500 0.633 0.581 0.522 0.624 0.554 0.495 25 1528 Propanoic acid 0.047 ± 0.002 a 0.042 ± 0.001 ab 0.037 ± 0.003 bc 0.042 ± 0.002 ab 0.038 ± 0.002 bc 0.036 ± 0.002 cd 0.039 ± 0.003 bc 0.031 ± 0.002 de 0.029 ± 0.002 e Rancid, acidic 26 1560 2-Methyl-propanoic acid 0.013 ± 0.002 ab 0.007 ± 0.001 cd 0.01 ± 0.000 bc 0.012 ± 0.003 ab 0.011 ± 0.000 e 0.007 ± 0.001 cd 0.014 ± 0.002 a 0.006 ± 0.001 d 0.004 ± 0.001 de —- 27 1618 Butanoic acid 0.015 ± 0.002 bc 0.012 ± 0.002 c 0.011 ± 0.002 c 0.019 ± 0.002 ab 0.016 ± 0.001 abc 0.012 ± 0.002 c 0.021 ± 0.002 a 0.015 ± 0.002 bc 0.012 ± 0.003 c Cheesy, yogurt-like, acidic 28 1622 2-Propenoic acid 0.241 ± 0.005 abc 0.227 ± 0.010 bc 0.213 ± 0.017 c 0.266 ± 0.012 a 0.245 ± 0.009 abc 0.223 ± 0.012 bc 0.275 ± 0.018 a 0.256 ± 0.012 ab 0.227 ± 0.014 bc Baked, vinegar-like 29 1664 3-Methyl-butanoic acid 0.029 ± 0.003 a 0.021 ± 0.003 bc 0.019 ± 0.003 bc 0.018 ± 0.002 c 0.026 + 0.003 ab 0.024 ± 0.002 abc 0.023 ± 0.003 abc 0.021 ± 0.002 bc 0.019 ± 0003 bc Cheesy, foul smell, acidic 30 1735 Pentanoic acid 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a 0.002 ± 0.000 a Rancid, buttery 31 2176 2-Hydroxy-propanoic acid 0.088 ± 0.005 a 0.073 ± 0.004 bc 0.062 ± 0.004 d 0.089 ± 0.004 a 0.082 ± 0.003 ab 0.071 ± 0.003 bcd 0.084 ± 0.005 a 0.080 ± 0.004 ab 0.068 ± 0.003 cd Grassy, sweat-like 32 2417 Benzoic acid 0.158 ± 0.030 a 0.121 ± 0.002 bc 0.108 ± 0.006 cde 0.143 ± 0.004 a 0.117 ± 0.009 bcd 0.109 ± 0.001 cde 0.127 ± 0.003 b 0.103 ± 0.004 de 0.094 ± 0.003 e Sweet, caramel 33 2482 Dodecanoic acid 0.044 ± 0.002 a 0.040 ± 0.002 ab 0.038 ± 0.001 b 0.042 ± 0.002 ab 0.044 ± 0.002 a 0.038 ± 0.002 b 0.039 ± 0.002 b 0.040 ± 0002 ab 0.041 ± 0.002 ab Dairy-like, caramel Total sulfurs 0.163 0.137 0.133 0.169 0.148 0.12 0.163 0.139 0.114 34 1581 Dimethyl sulfoxide 0.144 ± 0.003 ab 0.121 ± 0.004 c 0.117 ± 0.006 cd 0.154 ± 0.005 a 0.132 ± 0.010 bc 0.105 ± 0.004 de 0.149 ± 0.003 a 0.125 ± 0.008 c 0.101 ± 0.004 e Rancid, pungent, metallic 35 1895 Dimethyl sulfone 0.019 ± 0.002 a 0.016 ± 0.001 ab 0.016 ± 0.001 ab 0.015 ± 0.001 b 0.016 ± 0.001 ab 0.015 ± 0.002 b 0.014 ± 0.001 b 0.014 ± 0.001 b 0.013 ± 0.001 b Sweet, waxy, sulfuric Total phenols and aldehyde 0.026 0.023 0.024 0.023 0.019 0.017 0.026 0.021 0.016 36 1852 2-Methoxy-phenol 0.015 ± 0.001 ab 0.014 ± 0.001 ab 0.013 ± 0.001 abc 0.012 ± 0.001 bc 0.011 ± 0.002 cd 0.009 ± 0.001 d 0.016 ± 0.001 a 0.012 ± 0.002 bc 0.009 ± 0.001 d Sweet, medicinal, herbaceous 37 2263 2,6-Dimethoxy-phenol 0.009 ± 0.000 a 0.006 ± 0.000 d 0.008 ± 0.000 b 0.007 ± 0.000 c 0.006 ± 0.000 d 0.005 ± 0.000 e 0.007 ± 0.000 c 0.006 ± 0.000 d 0.005 ± 0.000 e Sweet, maple-like, caramel 38 2549 Vanillin 0.002 ± 0.000 c 0.003 ± 0.000 b 0.003 ± 0.000 b 0.004 ± 0.000 a 0.002 ± 0.000 c 0.003 ± 0.000 b 0.003 ± 0.000 b 0.003 ± 0.000 b 0.002 ± 0.000 c Sweet, cotton candy-like Values are mean ± standard deviation of triplicates. The same letters within a row are not significantly di ff erent ( p < 0.05).
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[Summary: This page discusses the total phenolic content and antioxidant properties of palm granulated sugar. It explains how phenolic compounds act as antioxidants and presents results on total phenolic content, DPPH radical scavenging activity, and FRAP. The highest total phenolic content was at 80 °C. The antioxidant activity is affected by phenolic content.]
Sustainability 2020 , 12 , 2650 14 of 21 3.6. Total Phenolic Content and Antioxidant Properties Phenolic compounds contain the hydroxylated aromatic ring and have redox properties—properties that allow them to be antioxidants [ 66 ]. Antioxidants are exogenous or endogenous molecules that mitigate any form of oxidative / nitrosative stress or its consequences [ 67 ]. Figure 2 shows the results of the determination of total phenolic content and the antioxidant capacity of palm granulated sugar Sustainability 2020 , 12 , x FOR PEER REVIEW 1 of 21 3.6. Total phenolic content and antioxidant properties Phenolic compounds contain the hydroxylated aromatic ring and have redox properties— properties that allow them to be antioxidants [66]. Antioxidants are exogenous or endogenous molecules that mitigate any form of oxidative/nitrosative stress or its consequences [67]. Figure 2 shows the results of the determination of total phenolic content and the antioxidant capacity of palm granulated sugar. 100 °C (a) (b) (c) 90 °C (d) (e) (f) 80 °C (g) (h) (i) Figure 2. The total phenolic content and antioxidant activity of palm granulated sugar under different drying–solidification conditions. ( a , d , g ) Total phenolic content, ( b , e , h ) DPPH, and ( c , f , i ) FRAP The amount of total phenolic contents differed among samples from 2.77 to 8.94 mg/100 g. At 80 °C, the total phenolic content was the highest from 7.55 to 8.94 mg/100 g. When the temperature OPS 1 OPS 2 OPS 3 T ot al phenol ic c ont ent ( m g G A E / 100 g) 0 2 4 6 8 OPS 1 OPS 2 OPS 3 D P P H (% ) 0 5 10 15 20 25 30 35 40 OPS 1 OPS 2 OPS 3 F R AP ( µ mo l F e 2+ /m L ) 0 50 100 150 200 250 300 350 Tot a l phe nol ic c ont e nt ( m g GA E / 1 0 0 g) NPS 1 NPS 2 NPS 3 0 2 4 6 8 NPS 1 NPS 2 NPS 3 D PPH ( % ) 0 5 10 15 20 25 30 35 40 NPS 1 NPS 2 NPS 3 F RA P ( µ m ol Fe 2+ / mL ) 0 50 100 150 200 250 300 350 EPS 1 EPS 2 EPS 3 T ot al phenol ic c ont ent ( m g G A E /100 g) 0 2 4 6 8 EPS 1 EPS 2 EPS 3 D P P H (% ) 0 5 10 15 20 25 30 35 40 EPS 1 EPS 2 EPS 3 F R AP ( µ mo l F e 2+ /m L ) 0 50 100 150 200 250 300 350 Figure 2. The total phenolic content and antioxidant activity of palm granulated sugar under di ff erent drying–solidification conditions. ( a , d , g ) Total phenolic content, ( b , e , h ) DPPH, and ( c , f , i ) FRAP The amount of total phenolic contents di ff ered among samples from 2.77 to 8.94 mg / 100 g. At 80 ◦ C, the total phenolic content was the highest from 7.55 to 8.94 mg / 100 g. When the temperature increased to 90 ◦ C and 100 ◦ C, the total phenolic contents were significantly reduced from 4.64 to 7.62 mg / 100 g and from 2.77 to 3.13 mg / 100 g, respectively. Phenolic content is easily destroyed during the heating
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[Summary: This page continues the discussion of antioxidant properties, detailing DPPH content and FRAP values for the sugar. It suggests that increasing DPPH radical scavenging activity results from MRPs and caramelization products. The reducing power of samples is also presented. It also discusses the cytoprotective effect of the sugar on NIH 3T3 fibroblast cells.]
Sustainability 2020 , 12 , 2650 15 of 21 process. Similar findings reported that the total phenolic content of palm sugar ranged from 2.14 to 16.29 mg / 100 g [ 17 ] and 0.48 µ g of GAE / mg [ 26 ]. The relationship between phenolic content and antioxidant activities was reported in several studies [ 68 , 69 ]. Phenolic content a ff ects antioxidant potential by various mechanisms related to the scavenging of free radicals [ 68 , 70 ]. The DPPH content was about 20.15% to 37.88%. The highest and the lowest DPPH percentages were for NPS 3 (100 ◦ C, 90 min) and EPS 1 (80 ◦ C, 60 min). The scavenging e ff ect of studied samples with the DPPH radical was in the following order: NPS 3 > OPS 3 > EPS 3 > OPS 2 > NPS 2 > NPS 1 > OPS 1 > EPS 2 > EPS 1. A similar trend was observed in a study of the DPPH radical scavenging activity of cane brown sugar, from 14.5% to 26.90% [ 27 ], and granulated non-centrifugal sugars, from 38.04% to 71.08% [ 46 ]. The increasing DPPH radical scavenging activity could be a result of grown MRPs and caramelization products. Previous studies have reported that MRPs possessed the ability to donate hydrogen and had the potential for free radical reaction [ 71 , 72 ]. The possible antioxidant property of palm granulated sugar was predicted by its ability to reduce the TPTZ-Fe(III) complex to the TPTZ-Fe(II) complex [ 67 , 73 ]. All samples displayed reducing power to various degrees. The reducing power of all samples was in the order of OPS 1 > OPS 2 > EPS 3 > NPS 3 > OPS 1 > NPS 2 > NPS 1 > EPS 2 > EPS 1. Samples prepared at high temperatures, long periods or both showed higher FRAP values, such as OPS 3 (100 ◦ C, 90 min), OPS 2 (100 ◦ C, 75 min), EPS 3 (80 ◦ C, 90 min), and NPS 3 (90 ◦ C, 90 min), corresponding to 378.23, 356.71, 355.29, and 351.16 µ mol Fe 2 + / mL Similar results were found previously: the FRAP value of raw cane sugar was 0.17 to 0.33 mmol / 100 g, that of dark brown sugar was 0.69 mmol / 100 g and that of granulated white sugar was 0.01–0.02 mmol / 100 g, which were lower values than the present results [ 29 ]. The alterations in the antioxidant potential of unrefined sugars were determined by factors such as the methods used for preventing antioxidant e ff ectiveness [ 74 ]; the ratio of inverted sugars; the amount of phenolics, flavonoids [ 35 ] and MRPs [ 27 ]; and processing methods [ 28 ]. Another element is the concomitant production of Fe(II), which is a known pro-oxidant and can bring about the production of additional radicals in the reaction medium (such as OH • from the Fenton reaction). Then, the absorbance of these compounds was measured, leading to falsely high results for the FRAP value [ 52 ]. 3.7. Cytoprotective E ff ect NIH 3 T 3 fibroblast cells were treated with tBuOOH, and the cytoprotective ability of palm granulated sugar was investigated. However, to confirm the safety of palm granulated sugar with NIH 3 T 3 fibroblast cells, the sugar solution (20 mg / mL) was investigated for its toxicity for 24 h under 37 ◦ C and 5% CO 2 . The result showed that the sugar concentration of 20 mg / mL was not the cause of NIH 3 T 3 cell death (data not shown) tBuOOH is an organic hydroperoxide which is widely used to induce oxidative stress. The impact of palm granulated sugar on cell viability was estimated by microculture tetrazolium assay. NIH 3 T 3 cells incubated with tBuOOH and palm granulated sugar showed high cell viability as compared with tBuOOH individually (Figure 3 ). EPS 1 and OPS 3 showed the highest and lowest cell viability. The cell viability of palm granulated sugar-treated cells ranged from 63.23% to 68.81%, and this value was 45.13% for the sample without sugar. Palm granulated sugar -reated cells showed higher cell viability, from 18.10% to 23.684%. Although the cell viability for palm granulated sugar-treated cells varied, this change was not significantly di ff erent. A similar study reported the potential for inhibiting cellular reactive oxygen species of unrefined sugar by reduced DCFDA fluorescence signal intensity [ 26 ]. Variations in in vivo cell-based antioxidant potentials of unrefined sugars result from many elements, such as the availability of biological compounds, limitations on the take-up of the cells, and the method of activity and metabolism [ 26 ]. The cell viability of sugar-treated cells in this study was higher than that of white sugar and brown sugar and lower than that of jaggery sugar [ 32 ].
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[Summary: This page summarizes the study's findings, noting that low-temperature drying produced less reducing sugar and HMF while increasing vitamin and phenolic content. High-temperature drying resulted in darker color and lower water content, but slightly increased antioxidant activity. The study concludes that vacuum drying at 90 °C for 75 min is optimal.]
Sustainability 2020 , 12 , 2650 16 of 21 Sustainability 2020 , 12 , x FOR PEER REVIEW 3 of 21 Figure 3. Cytoprotective effect of palm granulated sugar with t-butyl hydroperoxide-induced cell damage in NIH 3 T 3 cells. Control, cells without sugar/tert-butyl hydroperoxide (tBuOOH) treatment; tBuOOH, cells treated with 500 μM tBuOOH. 4. Conclusion The current study is the first to investigate the changes in chemical composition, HMF content, volatile compounds and biological activity of palm granulated sugar from B. flabellifer L flower sap (Cambodia) under different drying–solidification conditions. The drying–solidification of palm granulated sugars at low temperatures produced less reducing sugar and HMF content but increased the vitamin and total phenolic content. Meanwhile, dried products at high temperatures formed a darker color, lower water content, and water activity, but the antioxidant activity was slightly increased by the functional properties of MRPs Within these experimental conditions, the pH value, mineral content, and cell viability of palm granulated sugars were not affected. In conclusion, the vacuum drying process at 90 °C for 75 min showed the potential of new industrial methods to shorten the production time and increase the bioactive phytochemical content of palm granulated sugar Author Contributions: Conceptualization, methodology, W.-C. L; data curation, writing—original draft, D.H.T.L; writing—review and editing, P.- H. L. Funding: This work was financially supported by LU SHU HEALTH (CAMBODIA) Co. Acknowledgments: This study was supported by Sam Su for their support in the present study. Conflicts of Interest: The authors declare no conflict of interest. Control tBuOOH EPS 1 EPS 2 EPS 3 NPS 1 NPS 2 NPS 3 OPS 1 OPS 2 OPS 3 C e ll v ia b il it y ( % ) 0 20 40 60 80 100 120 c a b c c c c c c c c Figure 3. Cytoprotective e ff ect of palm granulated sugar with t-butyl hydroperoxide-induced cell damage in NIH 3 T 3 cells. Control, cells without sugar / tert-butyl hydroperoxide (tBuOOH) treatment; tBuOOH, cells treated with 500 µ M tBuOOH 4. Conclusions The current study is the first to investigate the changes in chemical composition, HMF content, volatile compounds and biological activity of palm granulated sugar from B. flabellifer L flower sap (Cambodia) under di ff erent drying–solidification conditions. The drying–solidification of palm granulated sugars at low temperatures produced less reducing sugar and HMF content but increased the vitamin and total phenolic content. Meanwhile, dried products at high temperatures formed a darker color, lower water content, and water activity, but the antioxidant activity was slightly increased by the functional properties of MRPs. Within these experimental conditions, the pH value, mineral content, and cell viability of palm granulated sugars were not a ff ected. In conclusion, the vacuum drying process at 90 ◦ C for 75 min showed the potential of new industrial methods to shorten the production time and increase the bioactive phytochemical content of palm granulated sugar Author Contributions: Conceptualization, methodology, W.-C.L.; data curation, writing—original draft, D.H.T.L.; writing—review and editing, P.-H.L. All authors have read and agreed to the published version of the manuscript Funding: This work was financially supported by LU SHU HEALTH (CAMBODIA) Co Acknowledgments: This study was supported by Sam Su for their support in the present study Conflicts of Interest: The authors declare no conflict of interest.
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[Summary: This page presents the appendix of the study, including diagrams illustrating the process of palm granulated sugar production at different drying temperatures and times. It also includes a figure showing the appearance of palm granulated sugar under various drying-solidification conditions and begins the list of references.]
Sustainability 2020 , 12 , 2650 17 of 21 Appendix A Sustainability 2020 , 12 , x FOR PEER REVIEW 4 of 21 Appendix A Figure A 1. Diagram palm granulated sugar from concentrated palm syrup dried at 80 °C, 90 °C, and 100 °C and at time 60, 75 and 90 min. Figure A 2. Palm granulated sugar under different drying-solidification conditions . References 1 Lim, T.K. Edible Medicinal and Medicinal Plants , 1 st ed.; Springer: Dordrecht, The Netherlands, 2012; pp. 293–300, doi:10.1007/978-90-481-8661-7 Concentrated palm syrup Heat to 40 °C to 50 °C Vacuum drying at 80 °C Vacuum drying at 90 °C Vacuum drying at 100 °C 60 min 75 min 90 min EPS 1 EPS 2 EPS 3 60 min 75 min 90 min NPS 1 NPS 2 NPS 3 60 min 75 min 90 min OPS 1 OPS 2 OPS 3 Different drying-solidification conditions Figure A 1. Diagram palm granulated sugar from concentrated palm syrup dried at 80 ◦ C, 90 ◦ C, and 100 ◦ C and at time 60, 75 and 90 min Sustainability 2020 , 12 , x FOR PEER REVIEW 4 of 21 Appendix A Figure A 1. Diagram palm granulated sugar from concentrated palm syrup dried at 80 °C, 90 °C, and 100 °C and at time 60, 75 and 90 min. Figure A 2. Palm granulated sugar under different drying-solidification conditions . References 1 Lim, T.K. Edible Medicinal and Medicinal Plants , 1 st ed.; Springer: Dordrecht, The Netherlands, 2012; pp. 293–300, doi:10.1007/978-90-481-8661-7 Concentrated palm syrup Heat to 40 °C to 50 °C Vacuum drying at 80 °C Vacuum drying at 90 °C Vacuum drying at 100 °C 60 min 75 min 90 min EPS 1 EPS 2 EPS 3 60 min 75 min 90 min NPS 1 NPS 2 NPS 3 60 min 75 min 90 min OPS 1 OPS 2 OPS 3 Different drying-solidification conditions Figure A 2. Palm granulated sugar under di ff erent drying-solidification conditions.
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[Summary: This page provides a list of references cited in the study. These references include research articles and publications related to palmyra palm, its properties, and processing techniques. They cover topics such as medicinal uses, chemical compounds, and optimization of production parameters.]
Sustainability 2020 , 12 , 2650 18 of 21 References 1 Lim, T.K Edible Medicinal and Medicinal Plants , 1 st ed.; Springer: Dordrecht, The Netherlands, 2012; pp. 293–300. [ CrossRef ] 2 Vengaiah, P.C.; Murthy, G.N.; Sattiraju, M.; Maheswarappa, H.P. Value Added Food Products from Palmyrah Palm ( Borassus Flabellifer L.) JNHS 2017 , 4 , 1–3. [ CrossRef ] 3 Mohite, M.; Pramod, H.J.; Yadav, A.V.; Raje, V.N.; Wadkar, G.H. Evaluation of antiulcer activity of aqueous extract of Borassus flabellifer (Linn.) Fruits J. Pharm. Res 2012 , 5 , 3782–3786. Available online: http: // jprsolutions.info / newfiles / journal-file-56 bc 119 b 914 ed 0.51098376.pdf (accessed on 27 June 2012) 4 Singh, T.; Ravi Kumar, V.; Kumar, R.; Yashaswini, Y.; Pravalika, D.; Pravalika, V. Comparative study of in vitro anthelmintic activity of sap Borassus Flabellifer World J. Pharm Pharm Sci 2015 , 5 , 701–706 Available online: https: // www.researchgate.net / publication / 317715107_COMPARATIVE_STUDY_OF_IN_VITRO_ ANTHELMINTIC_ACTIVITY_OF_SAP_OF_BORASSUS_FLABELLIFER (accessed on 1 December 2015) 5 Yoshikawa, M.; Xu, F.; Morikawa, T.; Pongpiriyadacha, Y.; Nakamura, S.; Asao, Y.; Kumahara, A.; Matsuda, H. Medicinal flowers. XII. (1) New spirostane-type steroid saponins with antidiabetogenic activity from Borassus flabellifer Chem. Pharm. Bull 2007 , 55 , 308–316. [ CrossRef ] [ PubMed ] 6 Paschapur, M.S.; Patil, M.B.; Kumar, R.; Patil, S.R. Evaluation of anti-inflammatory activity of ethanolic extract of Borassus flabellifer L. male flowers (inflorescences) in experimental animals J. Med. Plant Res 2009 , 3 , 49–54 Available online: http: // citeseerx.ist.psu.edu / viewdoc / download?doi = 10.1.1.875.7726&rep = rep 1&type = pdf (accessed on 19 December 2008) 7 Paschapur, M.S.; Patil, S.; Patil, S.R.; Kumar, R.; Patil, M.B. Evaluation of the anagesic and antipyretic activities of ethanolic extract of male folwers (inflorescences) of Borassus Flabellifer L. (Arecaceae) Int. J. Pharm. Pharm. Sci 2009 , 2 , 98–106. Available online: https: // pdfs.semanticscholar.org / 8423 / 5 cac 7 f 7 bd 64 de 1 b 7 a 54 a 53159 a 7310 f 649 e 5.pdf (accessed on 24 July 2009) 8 Reshma, M.V.; Jacob, J.; Syamnath, V.L.; Habeeba, V.P.; Kumar, B.S.; Lankalapalli, R.S. First report on isolation of 2,3,4-trihydroxy-5-methylacetophenone from palmyra palm (Borassus flabellifer Linn.) syrup, its antioxidant and antimicrobial properties Food Chem 2017 , 228 , 491–496. [ CrossRef ] 9 Mahilrajan, S.; Balakumar, S.; Arasaratnam, V.; Kumanan, T.; Kailayalinkam, R. Glycemic Index and Insulin Index of Palmyrah Based Edible Products Commonly Consumed in Ja ff na IOSR-JBB 2017 , 3 , 37–42 [ CrossRef ] 10 Radam, R.R.; Sari, H.N.; Lusyani, H.L. Chemical Compounds Of Granulated Palm Sugar Made From Sap Of Nipa Palm (Nypa Fruticans Wurmb) Growing In Three Different Places J. Wetlands Environ. Manag 2014 , 2 , 108–114 Available online: https: // ijwem.ulm.ac.id / index.php / ijwem / article / view / 37 / 23 (accessed on 1 April 2014) 11 Khongsak, S.; Janya, S.; Wirot, L. Productions and Functional Properties of Palm Sugars WJST 2018 , 16 , 897–907 Available online: http: // wjst.wu.ac.th / index.php / wjst / article / view / 5323 (accessed on 28 August 2018) 12 Jagannadha Rao, P.V.K.; Das, M.; Das, S.K. Changes in physical and thermo-physical properties of sugarcane, palmyra-palm and date-palm juices at di ff erent concentration of sugar J. Food Eng 2009 , 90 , 559–566 [ CrossRef ] 13 Sanyang, M.L.; Sapuan, S.M.; Jawaid, M.; Ishak, M.R.; Sahari, J. Recent developments in sugar palm (Arenga pinnata) based biocomposites and their potential industrial applications: A review Renew. Sust. Energy Rev 2016 , 54 , 533–549. [ CrossRef ] 14 Madhava, M.; Ravindra Babu, D.; Vengaiah, P.C.; Hari Babu, B. Optimization of Process Parameters for Production of Palmyrah Palm Jaggery JAE 2015 , 52 , 14–19. Available online: https: // www.indianjournals. com / ijor.aspx?target = ijor:joae&volume = 52&issue = 1&article = 002 (accessed on 26 March 2020) 15 Inyang, U.; Oboh, I.; Etuk, B. Drying and the Different Techniques Int. J. Food Nutr. Saf 2017 , 8 , 45–72 Available online: http: // modernscientificpress.com / Journals / ViewArticle.aspx?6 ZIT 7 oAL 6 Lqarm 6 Ljqm 1 ABiu FTINYiNR 0 EKTnHl + ifbzl + 1 BOQ 8 iCs 1 yNd 6 FcqQb (accessed on 20 November 2017) 16 Naknean, P.; Meenune, M.; Roudaut, G. Changes in properties of palm sugar syrup produced by an open pan and a vacuum evaporator during storage IFRJ 2013 , 20 , 2323–2334. Available online: https: // pdfs.semanticscholar.org / 7673 / 13 f 5204742 cbe 963 f 10 a 5 ff a 5 ecb 9318 a 745.pdf (accessed on 26 March 2020) 17 Aeimsard, R.; Thumthanaruk, B.; Jumnongpon, R.; Lekhavat, S. E ff ect of drying on total phenolic compounds, antioxidant activities and physical properties of palm sugar JFAT 2015 , 1 , 126–130. Available online: http: // rs.mfu.ac.th / ojs / index.php / jfat / article / view / 39 / 36 (accessed on 28 January 2015).
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[Summary: This page continues listing the references cited in the study. The listed articles cover topics such as carbohydrate analysis, vitamin determination, antioxidant activity, and the effects of thermal processing on food quality. The references provide supporting evidence and context for the study's findings.]
Sustainability 2020 , 12 , 2650 19 of 21 18 Valder, R.; Nooralabettu, K.P. Physico-chemical changes in Palmyra Palm (Borassus flabellifer) sap at di ff erent temperature IJSER 2018 , 9 , 761–766. Available online: https: // www.ijser.org / onlineResearchPaperViewer. aspx?Physico-chemical-Changes-in-Palmyra-Palm-Borassus-flabellifer-sap-at-di ff erent-temperature.pdf (accessed on 1 January 2018) 19 Apriyantono, A.; Aristyani, A.; Nurhayati; Lidya, Y.; Budiyanto, S.; Soekarto, S.T. Rate of browning reaction during preparation of coconut and palm sugar Int. Congr. Ser 2002 , 1245 , 275–278. [ CrossRef ] 20 Nielsen, S.S. Total Carbohydrate by Phenol-Sulfuric Acid Method. In Food Analysis Laboratory Manual , 3 rd ed.; Nielsen, S.S., Ed.; Springer: Cham, Switzerland, 2017; pp. 137–141. [ CrossRef ] 21 Miller, G.L. Use of Dinitrosalicylic Acid Reagent for Determination of Reducing Sugar Anal. Chem 1959 , 31 , 426–428. [ CrossRef ] 22 Guerra, M.; Mujica, M. Physical and chemical properties of granulated cane sugar “panelas” Ci ê nc. Tecnol Aliment 2010 , 30 , 250–257. [ CrossRef ] 23 Rizzolo, A.; Polesello, S. Chromatographic determination of vitamins in foods J. Chromatogr. A 1992 , 103–152 [ CrossRef ] 24 Antakli, S.; Sarkees, N.; Sarraf, T. Determination of water-soluble Vitamins B 1, B 2, B 3, B 6, B 9, B 12 and C on C 18 column with particle size 3 µ M in some manufactured food products b HPLC with UV-DAD / FLD detection Int. J. Pharm. Pharm. Sci 2015 , 7 , 219–224 25 Zhang, Q.; Zhang, J.; Shen, J.; Silva, A.; Dennis, D.; Barrow, C. A Simple 96-Well Microplate Method for Estimation of Total Polyphenol Content in Seaweeds J. Appl. Phycol 2006 , 18 , 445–450. [ CrossRef ] 26 Lee, J.S.; Ramalingam, S.; Jo, I.G.; Kwon, Y.S.; Bahuguna, A.; Oh, Y.S.; Kwon, O.J.; Kim, M. Comparative study of the physicochemical, nutritional, and antioxidant properties of some commercial refined and non-centrifugal sugars Food Res. Int 2018 , 109 , 614–625. [ CrossRef ] [ PubMed ] 27 Payet, B.; Sing, A.S.; Smadja, J. Assessment of antioxidant activity of cane brown sugars by ABTS and DPPH radical scavenging assays: Determination of their polyphenolic and volatile constituents J. Agric. Food Chem 2005 , 53 , 10074–10079. [ CrossRef ] 28 Asikin, Y.; Hirose, N.; Tamaki, H.; Ito, S.; Oku, H.; Wada, K. E ff ects of di ff erent drying–solidification processes on physical properties, volatile fraction, and antioxidant activity of non-centrifugal cane brown sugar LWT Food Sci. Technol 2016 , 66 , 340–347. [ CrossRef ] 29 Phillips, K.M.; Carlsen, M.H.; Blomho ff , R. Total Antioxidant Content of Alternatives to Refined Sugar J. Am Diet. Assoc 2009 , 109 , 64–71. [ CrossRef ] 30 Rattanathanalerk, M.; Naphaporn, C.; Walaiporn, S. E ff ect of thermal processing on the quality loss of pineapple juice J. Food Eng 2005 , 66 , 259–265. [ CrossRef ] 31 Nardini, M.; Pisu, P.; Gentili, V.; Natella, F.; Felice, M.D.; Piccolella, E.; Scaccini, C. E ff ect of ca ff eic acid on tert-butyl hydroperoxide-induced oxidative stress in U 937 Free Radic. Biol. Med 1998 , 25 , 1098–1105 [ CrossRef ] 32 Nayaka, M.A.; Sathisha, U.V.; Manohar, M.P.; Chandrashekar, K.B.; Dharmesh, S.M. Cytoprotective and antioxidant activity studies of jaggery sugar Food Chem 2009 , 115 , 113–118. [ CrossRef ] 33 Hansen, M.J.; Nielsen, S.E.; Berg, K. Re-examination and further development of a precise and rapid dye method for measuring cell growth / cell kill J. Immunol. Methods 1989 , 119 , 203–210. [ CrossRef ] 34 Ja ff é , W.R. Nutritional and functional components of non-centrifugal cane sugar: A compilation of the data from the analytical literature J. Food Compos. Anal 2015 , 43 , 194–202. [ CrossRef ] 35 Segu í , L.; Calabuig-Jim é nez, L.; Betoret, N.; Fito, P. Physicochemical and antioxidant properties of non-refined sugarcane alternatives to white sugar IJFST 2015 , 50 , 2579–2588. [ CrossRef ] 36 Unde, P.A.; Adagale, P.V.; Hashmi, S.I.; Raheem, A.K.; Gandhi, R. E ff ect of Di ff erent Particle Sizes of Jaggery Powder on Storability WJAS 2010 , 7 , 157–160. Available online: http: // www.panelamonitor.org / media / docrepo / document / files / e ff ect-of-di ff erent-particle-sizes-of-jaggery-powder-on-storability.pdf (accessed on 26 March 2020) 37 Akochi-K, E.; Alli, I.; Kermasha, S. Characterization of the Pyrazines Formed during the Processing of Maple Syrup J. Agric. Food Chem 1997 , 45 , 3368–3373. [ CrossRef ] 38 Ho, C.W.; Aida, W.M.W.; Maskat, M.Y.; Osman, H. Changes in volatile compounds of palm sap (Arenga pinnata) during the heating process for production of palm sugar Food Chem 2007 , 102 , 1156–1162 [ CrossRef ]
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[Summary: This page continues the list of references, citing works on Maillard reactions, flavor compounds, and antioxidant properties of various foods. These references contribute to the understanding of the chemical processes and health benefits associated with palm granulated sugar.]
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[Summary: This page concludes the list of references and includes a copyright statement. It indicates that the article is an open access publication distributed under the Creative Commons Attribution license.]
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