Suppr超能文献

用于递送疏水性药物的微凝胶和纳凝胶。

Microgels and Nanogels for the Delivery of Poorly Water-Soluble Drugs.

机构信息

Department of Chemical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4L8, Canada.

出版信息

Mol Pharm. 2022 Jun 6;19(6):1704-1721. doi: 10.1021/acs.molpharmaceut.1c00967. Epub 2022 Mar 23.

Abstract

While microgels and nanogels are most commonly used for the delivery of hydrophilic therapeutics, the water-swollen structure, size, deformability, colloidal stability, functionality, and physicochemical tunability of microgels can also offer benefits for addressing many of the barriers of conventional vehicles for the delivery of hydrophobic therapeutics. In this review, we describe approaches for designing microgels with the potential to load and subsequently deliver hydrophobic drugs by creating compartmentalized microgels (e.g., core-shell structures), introducing hydrophobic domains in microgels, leveraging host-guest interactions, and/or applying "smart" environmentally responsive materials with switchable hydrophobicity. In particular, the challenge of promoting hydrophobic drug loading without compromising the inherent advantages of microgels as delivery vehicles and ensuring practically relevant release kinetics from such structures is highlighted, with an eye toward the practical translation of such vehicles to the clinic.

摘要

虽然微凝胶和纳米凝胶最常用于传递亲水性治疗剂,但微凝胶的水膨胀结构、尺寸、变形性、胶体稳定性、功能性和物理化学可调性也可为解决传统疏水性治疗剂传递载体的许多障碍提供益处。在这篇综述中,我们描述了设计微凝胶的方法,这些微凝胶具有通过创建分隔微凝胶(例如核壳结构)、在微凝胶中引入疏水区、利用主体-客体相互作用和/或应用具有可切换疏水性的“智能”环境响应材料来负载和随后传递疏水性药物的潜力。特别强调了在不损害微凝胶作为载体的固有优势的情况下促进疏水性药物负载的挑战,并确保从这些结构中获得实际相关的释放动力学,着眼于将这些载体实际转化为临床应用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验