Solid Self-Nano Emulsifying Drug Delivery Systems: Advances and Applications
novel solid self nano emulsifying drug delivery system
Journal name: World Journal of Pharmaceutical Research
Original article title: Review on
The WJPR includes peer-reviewed publications such as scientific research papers, reports, review articles, company news, thesis reports and case studies in areas of Biology, Pharmaceutical industries and Chemical technology while incorporating ancient fields of knowledge such combining Ayurveda with scientific data.
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Subtitle: lyophilization process of pharmaceuticals
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Siddhi Pandhare, Mallinath Harwalkar, N.B Mahale, S.R. Chaudhari
World Journal of Pharmaceutical Research:
(An ISO 9001:2015 Certified International Journal)
Full text available for: Review on
Source type: An International Peer Reviewed Journal for Pharmaceutical and Medical and Scientific Research
Summary of article contents:
Introduction
The study presented in this article focuses on the development of a new solid self-nano emulsifying drug delivery system (S-SNEDDS) designed to enhance the oral bioavailability of poorly water-soluble drugs. Approximately 40% of new drug candidates exhibit low solubility in water, which can lead to inadequate oral bioavailability and related complications. Traditional self-emulsifying drug delivery systems (SEDDS) have proven effective in addressing these solubility issues; however, they often exist in liquid forms, potentially limiting their stability and usability. By converting liquid SEDDS into solid forms, S-SNEDDS can enhance production efficiency, stability, and patient compliance.
Advantages of S-SNEDDS
One of the primary advantages of S-SNEDDS is their ability to improve the oral bioavailability of drugs. The solid self-nanoemulsifying formulations facilitate a more stable drug delivery mechanism upon contact with gastrointestinal fluids. This allows for the formation of nano-emulsions, which have a smaller globule size (less than 100nm) than conventional formulations. The creation of this finer emulsion increases the surface area available for drug absorption, thus accelerating the dissolution rate and potentially reducing the required dosage while minimizing side effects. Additionally, S-SNEDDS formulations are easier and more cost-effective to manufacture compared to their liquid counterparts, which require complex emulsification processes.
Mechanism of Self-Emulsification
The self-emulsification process involves minimal energy input, primarily relying on the entropy changes that favor dispersion when the formulated ingredients are introduced to the gastrointestinal tract. The process is defined by the free energy relationships that describe the conditions under which oil and water can form a stable emulsion. Emulsifying agents play a crucial role in stabilizing the resulting emulsion by reducing interfacial energy. By enhancing the spontaneous formation of emulsions upon contact with aqueous media, the self-emulsifying systems leverage the natural motility of the gastrointestinal tract, ultimately leading to improved drug absorption and bioavailability.
Formulation Components and Techniques
The formulation of S-SNEDDS involves several critical components, including the drug, oil phase, surfactants, co-surfactants, and adsorbents for solidifying the liquid formulation. Various solidification techniques are available for transitioning liquid SNEDDS into solid forms, including adsorption to solid carriers, spray-drying, and melt granulation. The careful selection and combination of these components play a key role in optimizing the performance of the final formulation. The article identifies notable natural and synthetic oils, surfactants, and co-surfactants known for their effective incorporation within S-SNEDDS, as well as the importance of pseudo ternary phase diagrams for attaining optimal excipient concentrations.
Conclusion
In summary, solid self-nano-emulsifying drug delivery systems (S-SNEDDS) present a promising solution for improving the solubility and bioavailability of poorly water-soluble drugs. By transitioning liquid formulations into stable solid forms, S-SNEDDS provide a range of advantages, including reduced production costs, improved stability, and better patient compliance. Future research in this area should focus on further enhancing the performance of S-SNEDDS, targeting sustained or controlled drug releases, and exploring the potential for reducing gastrointestinal irritation. Overall, S-SNEDDS can play a crucial role in the pharmaceutical field by addressing the challenges posed by low-solubility drugs.
FAQ section (important questions/answers):
What is the main purpose of S-SNEDDS?
The primary goal of S-SNEDDS is to improve the oral bioavailability of poorly water-soluble drugs, providing a stable and cost-effective alternative to liquid formulations.
How do S-SNEDDS improve drug solubility and absorption?
S-SNEDDS facilitate the formation of nano-emulsions in the gastrointestinal tract, enhancing dissolution rates and providing a larger surface area for better absorption of lipophilic drugs.
What techniques are used to convert SEDDS to S-SNEDDS?
Common solidification techniques for converting SEDDS to S-SNEDDS include spray drying, adsorption on solid carriers, and melt granulation, which lead to more stable solid formulations.
What are the advantages of using solid forms over liquid SEDDS?
Solid S-SNEDDS offer improved stability, lower production costs, easier handling, and better patient compliance compared to traditional liquid self-emulsifying drug delivery systems.
What are the typical components of a S-SNEDDS formulation?
A typical S-SNEDDS formulation consists of a drug, oil, surfactants, co-surfactants, and solidifying agents that work together to enhance drug solubility and absorption.
How is the self-emulsification efficiency of S-SNEDDS evaluated?
Self-emulsification efficiency is assessed through visual observation of emulsion clarity, time taken to form the emulsion, and stability under various dilution conditions in a laboratory setting.
Glossary definitions and references:
Scientific and Ayurvedic Glossary list for “Solid Self-Nano Emulsifying Drug Delivery Systems: Advances and Applications”. This list explains important keywords that occur in this article and links it to the glossary for a better understanding of that concept in the context of Ayurveda and other topics.
1) Drug:
Drug refers to any active chemical substance that is used to diagnose, treat, or prevent diseases or conditions. In the context of Self-Nano Emulsifying Drug Delivery Systems (S-SNEDDS), it is essential for formulating effective treatments targeting poorly soluble compounds to enhance their bioavailability and therapeutic efficacy. Thus, understanding drug properties is vital for successful formulation.
2) Water:
Water is a crucial solvent in pharmaceutical formulations and plays a significant role in the self-emulsification process of S-SNEDDS. It serves as the medium where emulsions form, affecting the stability, solubility, and bioavailability of drugs. Water’s properties can impact the interaction with surfactants and oils, influencing the performance of the emulsion.
3) Powder:
Powder refers to the solid form of a drug or formulation created through various processes, such as spray drying, that enables easier transport and increased shelf life. In S-SNEDDS, transforming liquids into powders facilitates encapsulation and improves stability, which is essential for enhancing drug formulation’s performance when administered orally.
4) Castor:
Castor oil is a natural oil commonly used in pharmaceutical formulations for its surfactant properties. It plays a crucial role in S-SNEDDS by solubilizing lipophilic drugs, thus enhancing their bioavailability. Castor oil's high hydrophilic-lipophilic balance (HLB) value positions it as a vital excipient in formulating effective self-emulsifying systems.
5) Medium:
Medium refers to the environment in which the drug interacts with other components, such as the gastrointestinal tract. In the context of S-SNEDDS, the medium is often aqueous, which is essential for the emulsification process. Understanding the interactions within this medium is key to optimizing drug absorption and release.
6) Study (Studying):
Study denotes a systematic investigation into the properties, mechanisms, and efficacy of S-SNEDDS. Such research is crucial for developing better drug delivery systems by analyzing self-emulsification processes, formulation stability, and bioavailability enhancements for poorly soluble drugs, ultimately leading to improved therapeutic outcomes.
7) Gelatin:
Gelatin is a natural polymer used in pharmaceutical formulations, especially for capsule manufacturing. It plays a significant role in the development of both hard and soft capsules used to deliver liquid formulations like S-SNEDDS. Gelatin's properties ensure the stability and bioavailability of the encapsulated drugs within the gastrointestinal tract.
8) Surface:
Surface refers to the outermost layer of the emulsion droplets formed during the self-emulsification process. The surface properties impact the stability, interaction with gastrointestinal fluids, and the overall performance of S-SNEDDS. The choice of surfactants affects the interfacial tension and the ability to form stable emulsions.
9) Filling (Filled):
Filling describes the method of introducing drug formulations into dosage forms, like capsules. This step is crucial for the administration of S-SNEDDS, as the filling process ensures proper dosing and impacts the pharmacokinetics of the drug. It directly influences the bioavailability upon ingestion.
10) Measurement:
Measurement refers to the evaluation of specific physical properties of the S-SNEDDS formulations, such as droplet size, zeta potential, and bioavailability. Accurate measurement ensures that formulations meet required specifications for stability, efficacy, and safety, thereby guiding the optimization processes needed for effective drug delivery.
11) Transformation (Transform, Transforming):
Transform refers to the process of converting liquid formulations into solid ones. In the context of S-SNEDDS, transforming liquid self-emulsifying formulations into solid forms is essential for improving stability, enhancing manufacturing efficiency, and ensuring better patient compliance through easier handling and storage.
12) Pur:
Poor refers to the suboptimal bioavailability and solubility of certain drug candidates. Many drugs demonstrate poor aqueous solubility, which limits their therapeutic effectiveness. Developing S-SNEDDS aims to overcome this challenge by enhancing the solubility and absorption profiles of poorly soluble drugs, thus improving treatment outcomes.
13) Performance:
Performance relates to the efficiency and effectiveness of the S-SNEDDS formulations in delivering the active drug. Evaluations include self-emulsification efficiency, stability during storage, and bioavailability upon administration. Optimal performance ensures that the formulation achieves therapeutic concentrations quickly and maintains activity within the body.
14) Irritation:
Irritation pertains to the adverse effects that can occur in the gastrointestinal tract as a result of certain excipients or surfactants used in S-SNEDDS. Minimizing irritation is crucial for patient compliance and comfort; hence, formulations must be carefully designed to mitigate gastrointestinal side effects while enhancing absorption.
15) Nature:
Nature refers to the inherent characteristics of the ingredients and the resulting emulsions in S-SNEDDS. Understanding the nature of the oils, surfactants, and co-surfactants used is crucial in determining how they interact during emulsification, stability of the formulation, and ultimately the drug's bioavailability.
16) Ahmednagar:
Ahmednagar is referenced as the location of the Amrutvahini College of Pharmacy, where research on S-SNEDDS is conducted. This geographical identifier signifies the institution's connection to ongoing pharmaceutical studies, including the development of novel drug delivery systems aimed at enhancing oral bioavailability.
17) Patil:
Patil signifies an individual contributing to the research on S-SNEDDS, reflecting the collaborative nature of scientific studies. Such researchers are instrumental in uncovering insights into formulation development, methodology, and potential therapeutic applications, driving innovation in drug delivery systems for improved patient outcomes.
18) Glass:
Glass in this context likely refers to the dry emulsions that resemble glass-like properties due to their solid-state formation. The incorporation of glassy states can enhance the stability and shelf-life of emulsion formulations, making them suitable for further processing into solid dosage forms.
19) Trade:
Trade may refer to the commercial aspect involving the exchange and business of pharmaceutical products, including S-SNEDDS. Understanding trade dynamics is essential for the successful marketing and distribution of these advanced drug delivery systems, ensuring they reach the appropriate clinical settings effectively.
20) Cloud:
Cloud relates to the observation of turbidity in emulsified systems, which can indicate the onset of phase separation. Monitoring cloud points during stability testing of S-SNEDDS is essential to predict how formulations perform under gastrointestinal conditions, impacting their efficiency and bioavailability once administered.
21) Pharmacological:
Pharmacological pertains to the study of how drugs impact biological systems. In the context of S-SNEDDS, understanding pharmacological properties is essential for ensuring that poorly soluble drugs can achieve therapeutic concentrations, thus evaluating their effectiveness and optimizing formulations for better treatment outcomes.
22) Antibiotic (Antibacterial):
Antibacterial describes the ability of a substance to inhibit the growth of bacteria. Developing formulations in S-SNEDDS that have antibacterial properties can enhance the therapeutic action against infections, making them important for medical formulations that require efficient delivery of active antimicrobial agents.
23) Observation:
Observation refers to the systematic monitoring of formulation characteristics and performance metrics during the research and development of S-SNEDDS. Careful observation of properties like droplet size, stability, and bioavailability is vital for adapting formulations to enhance their efficacy and therapeutic application.
24) Substance:
Substance denotes any material or compound involved in the formulation of S-SNEDDS, including drugs, oils, and excipients. Understanding the interactions between these substances is critical for optimizing formulations to achieve desired bioavailability and drug release profiles, ultimately ensuring effective treatment strategies.
25) Toxicity:
Toxicity denotes the degree to which a substance can cause harmful effects to biological systems. Assessing the toxicity of ingredients within S-SNEDDS is essential to ensure patient safety and compliance, as well as the overall acceptance of the formulations in clinical applications.
26) Turmeric:
Turmeric is highlighted for its potential pharmacological properties, particularly the active compound curcumin known for its anti-inflammatory and antioxidant effects. This natural ingredient may be explored within S-SNEDDS formulations to enhance delivery and efficacy of therapeutic agents, showcasing the versatility of additive components.
27) Activity:
Activity refers to the effectiveness of a drug in producing a desired therapeutic effect. In the context of S-SNEDDS, maintaining and optimizing the biological activity of poorly water-soluble drugs is a key goal, ensuring that formulations achieve the intended pharmacological outcomes upon administration.
28) Relative:
Relative pertains to the relationship between various properties or formulations and their performance. In the context of S-SNEDDS, understanding the relative performance of different oils, surfactants, and co-surfactants can inform formulation decisions, enhancing drug delivery effectiveness and bioavailability.
29) Channel:
Channel may refer to the micro-environment within the delivery system through which encapsulated drugs permeate. Understanding the channels in which droplets interact with biological systems can shed light on the dynamics of drug release and absorption, influencing the overall efficacy of S-SNEDDS.
30) Heating:
Heating refers to the process of applying temperature to formulations, which can impact the physical state and stability of S-SNEDDS. Controlled heating may be used during various manufacturing processes to ensure optimal solubilization and proper solidification of self-emulsifying ingredients.
31) Falling:
Falling could refer to the behavior of droplets or emulsions over time, particularly in stability assessments during formulation evaluation. Monitoring any 'falling' or separation phenomena in S-SNEDDS helps predict the long-term stability and effectiveness of drug delivery systems.
32) Mineral:
Mineral may refer to minerals that serve as excipients or solidifying agents in the formulation of S-SNEDDS. The presence of certain minerals can influence the physical properties of the final product, impacting solubility, stability, and, ultimately, the therapeutic efficacy of the formulation.
33) Coconut (Cocoanut):
Coconut oil is a commonly used oil in SEDDS formulation because of its solubilizing properties for lipophilic drugs. Its ability to improve absorption through various mechanisms makes it a vital component for developing effective S-SNEDDS, enhancing bioavailability and therapeutic effectiveness of poorly soluble drugs.
34) Reason:
Reason signifies the rationale behind employing specific methodologies or components in developing S-SNEDDS. Understanding the reasons for selecting particular surfactants, oils, or solid carriers is crucial for optimizing formulations that achieve desired outcomes in drug delivery and patient compliance.
35) Field:
Field refers to the area of study or research concerning S-SNEDDS, encompassing diverse disciplines such as pharmaceuticals, biochemistry, and material science. Advancements in this field are critical for developing innovative drug delivery systems that address the challenges of drug solubility and bioavailability.
36) Blood:
Blood represents a primary system through which drugs circulate in the body. For S-SNEDDS, understanding how formulations affect drug absorption into the bloodstream is key; achieving the desired plasma levels is essential for ensuring therapeutic effectiveness and optimizing patient treatment outcomes.
37) Coca:
Coca may refer to the coca plant, the source of cocaine, but within the context of pharmaceuticals, it is not primarily relevant. Its mention may implicitly touch on the properties or potential explorations of plant-based compounds in drug delivery systems like S-SNEDDS that could enhance bioavailability.
38) Food:
Food indicates the interaction of drug formulations with dietary substances. When considering S-SNEDDS, assessing how these formulations behave in the presence of food is important, as lipid-based systems can be influenced by dietary components, affecting their effectiveness, bioavailability, and overall patient compliance.
39) Hand:
Hand may refer to the manipulation and processing involved in handling drug formulations. In the context of S-SNEDDS, proper handling during preparation, filling, and administration is crucial for ensuring consistency and maintaining the integrity of drug formulations, ultimately affecting therapeutic outcomes.
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