Contemporary Nanoemulsion Research: Extensive Examination of Self-Nanoemulsifying Drug Delivery Systems

Q3 Medicine
Aakriti Patel, Astha Singh, Neha Minocha
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引用次数: 0

Abstract

The administration of new pharmaceutical compounds orally can pose certain challenges in terms of drug absorption, bioavailability, and pharmacokinetic profile. However, a widely recognized method for enhancing bioavailability involves lipid-based drug delivery systems. Lipid-based drug delivery systems (LBDDS) are the most favourable method for formulating medicines that have low solubility in water. Nanotechnology exerts a significant impact on the therapeutic efficacy of hydrophobic medicines and has emerged as a crucial method in the field of drug delivery research. Self-nanoemulsifying drug delivery systems (SNEDDs) are an important approach that combines the advantages of lipid-based drug delivery systems (LBDDS) and nanotechnology. SNEDDs are currently the favoured method for enhancing the formulation of pharmaceuticals that have low solubility in water. SNEDDs are homogenous mixtures that can self-emulsify spontaneously with gentle stirring, forming an oil-in-water emulsion that conveniently protects and creates a pathway for the lipophilic drug. The small particle size of <200nm increases the solubilisation capacity of the drug by increasing its surface area. SNEDDs have demonstrated the ability to enhance the bioavailability of medicines that are not easily soluble in water. SNEDDs stand apart from other solubility enhancement approaches due to their inclusion of biodegradable components, their ease of large-scale manufacture, and their numerous potential for drug targeting. The aim of the present review was to provide basic knowledge about formulation, applications, and benefits of using SNEDDs. A detailed manuscript has been prepared by doing a literature survey on databases like Google Scholar, SCOPUS, and Pubmed to review the current state of nanotechnology applications, industrial developments, and challenges for using SNEDDS as a novel delivery system is provided in this manuscript.
当代纳米乳液研究:自纳米乳化给药系统的广泛研究
口服给药新化合物会在药物吸收、生物利用度和药代动力学特征方面带来一定的挑战。脂质给药系统(LBDDS)是配制在水中溶解度低的药物的最有利方法。纳米技术对疏水性药物的疗效有重大影响,已成为给药研究领域的重要方法。自纳米乳化给药系统(SNEDDs)是一种结合了脂基给药系统(LBDDS)和纳米技术优点的重要方法。SNEDD 是一种均匀的混合物,轻轻搅拌就能自乳化,形成水包油型乳液,为亲脂性药物提供保护和途径。小于 200nm 的小粒径增加了药物的表面积,从而提高了药物的溶解能力。SNEDDs 由于含有可生物降解的成分、易于大规模生产以及在药物靶向方面具有众多潜力,因此有别于其他提高溶解度的方法。本综述旨在提供有关 SNEDD 的配方、应用和益处的基本知识。通过对 Google Scholar、SCOPUS 和 Pubmed 等数据库进行文献调查,对纳米技术的应用现状、工业发展以及使用 SNEDDS 作为新型递送系统所面临的挑战进行了综述,并撰写了一份详细的手稿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Nanomedicine
Current Nanomedicine Medicine-Medicine (miscellaneous)
CiteScore
2.00
自引率
0.00%
发文量
15
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