纳米混悬液的创新:拓展给药技术的视野。

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Shery Jacob, Fathima Sheik Kather, Sai H S Boddu, Mahesh Attimarad, Anroop B Nair
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引用次数: 0

摘要

纳米悬浮液(NS),以其亚微米粒度和独特的物理化学性质,为增强不溶于水或脂质的药物的给药提供了一种通用的解决方案。这篇综述强调了nss给药的最新进展、未来前景和挑战,特别是口服、眼、透皮、肺和肠外给药途径。将口服NS转化为粉末、颗粒、颗粒、片剂和胶囊,并将其掺入薄膜剂型以解决稳定性问题。本文总结了主要的稳定剂、聚合物、表面活性剂和赋形剂,以及正在进行的临床试验和最近的专利。此外,还对NS的各种制备方法进行了综合分析。本文还探讨了各种体外和体内表征技术,以及按比例缩小的技术和自下而上的制备方法。选定的商业NS药品的例子进行了讨论。NS领域的快速发展可以解决与渗透性限制吸收和肝脏首过代谢相关的问题,为基于蛋白质和肽的药物提供了希望。新型稳定剂的发展对于克服目前NS制剂的局限性,提高其稳定性、生物利用度、靶向性和安全性至关重要,最终加速其临床应用和商业化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nanosuspension Innovations: Expanding Horizons in Drug Delivery Techniques.

Nanosuspension Innovations: Expanding Horizons in Drug Delivery Techniques.

Nanosuspension Innovations: Expanding Horizons in Drug Delivery Techniques.

Nanosuspension Innovations: Expanding Horizons in Drug Delivery Techniques.

Nanosuspensions (NS), with their submicron particle sizes and unique physicochemical properties, provide a versatile solution for enhancing the administration of medications that are not highly soluble in water or lipids. This review highlights recent advancements, future prospects, and challenges in NS-based drug delivery, particularly for oral, ocular, transdermal, pulmonary, and parenteral routes. The conversion of oral NS into powders, pellets, granules, tablets, and capsules, and their incorporation into film dosage forms to address stability concerns is thoroughly reviewed. This article summarizes key stabilizers, polymers, surfactants, and excipients used in NS formulations, along with ongoing clinical trials and recent patents. Furthermore, a comprehensive analysis of various methods for NS preparation is provided. This article also explores various in vitro and in vivo characterization techniques, as well as scale-down technologies and bottom-up methods for NS preparation. Selected examples of commercial NS drug products are discussed. Rapid advances in the field of NS could resolve issues related to permeability-limited absorption and hepatic first-pass metabolism, offering promise for medications based on proteins and peptides. The evolution of novel stabilizers is essential to overcome the current limitations in NS formulations, enhancing their stability, bioavailability, targeting ability, and safety profile, which ultimately accelerates their clinical application and commercialization.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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