口服给药纳米乳技术:提高溶解度和生物利用度的途径。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Akash Vikal, Rashmi Maurya, Preeti Patel, Balak Das Kurmi
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引用次数: 0

摘要

纳米乳液(NEs)是亚微米大小的胶体分散体(20-500 nm),由油和水相组成,经表面活性剂和助表面活性剂稳定。尽管它们的热力学不稳定,但它们保持了动力学稳定性,防止了分离和聚集。这种稳定性将它们与微乳液区分开来,微乳液是热力学稳定的,是自发形成的。乳化过程涉及到吉布斯表面自由能的降低,乳化剂可以降低界面张力,这对于补偿与小液滴尺寸相关的高表面积至关重要。吉布斯自由能还原是至关重要的,因为它有助于稳定纳米乳,而由液滴曲率产生的拉普拉斯压力则影响系统的稳定性和均匀性。小液滴中的高拉普拉斯压力会导致聚结,但适当的表面活性剂配方可以帮助减轻这种影响。本文研究了NEs通过优化其配方和稳定性来显著提高疏水药物的溶解度和生物利用度的假设。我们关注乳化技术在制备稳定纳米乳液中的作用,特别关注亲水-亲脂平衡(HLB)和关键填料参数(CPP)对液滴尺寸和稳定性的影响。此外,我们还详细比较了各种制备方法,包括超声和高压均质,强调了它们对液滴大小、稳定性和可扩展性的影响。体外和体内研究的实验数据说明了NEs在口服给药方面的优势,研究结果显示,在优化的配方条件下,紫杉醇和姜黄素等难溶性药物的生物利用度显著提高。这篇综述强调了NEs克服传统给药系统局限性的潜力,并为未来的研究提供了路线图,以提高其商业可行性和治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanoemulsion Technology in Oral Drug Delivery: A Path to Enhanced Solubility and Bioavailability.

Nanoemulsions (NEs) are submicron-sized colloidal dispersions (20-500 nm) consisting of oil and aqueous phases stabilized by surfactants and cosurfactants. Despite their thermodynamic instability, NEs maintain kinetic stability, preventing separation and aggregation. This stability distinguishes them from microemulsions, which are thermodynamically stable and formed spontaneously. The emulsification process involves a reduction in Gibbs surface free energy facilitated by emulsifiers that lower interfacial tension, crucial for compensating for the high surface area associated with small droplet sizes. The Gibbs free energy reduction is vital as it helps in stabilizing nanoemulsions, while Laplace pressure, resulting from the curvature of the droplets, affects the stability and uniformity of the system. High Laplace pressures in smaller droplets can lead to coalescence, but the proper formulation with suitable surfactants can help mitigate this effect. This review investigates the hypothesis that NEs can significantly enhance the solubility and bioavailability of hydrophobic drugs by optimizing their formulation and stability. We focus on the role of emulsification techniques in creating stable nanoemulsions, with particular attention to the impact of hydrophilic-lipophilic balance (HLB) and critical packing parameters (CPP) on droplet size and stability. Furthermore, we provide a detailed comparison of various preparation methods, including ultrasonication and high-pressure homogenization, emphasizing their influence on droplet size, stability, and scalability. Experimental data from in vitro and in vivo studies illustrate the advantages of NEs for oral drug delivery, with findings showing significant improvements in bioavailability for poorly soluble drugs, such as paclitaxel and curcumin, under optimized formulation conditions. This review highlights the potential of NEs to overcome the limitations of traditional drug delivery systems and provides a roadmap for future research to improve their commercial viability and therapeutic outcomes.

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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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