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用于药物递送的脂质纳米颗粒及其水凝胶复合材料:综述

Lipid Nanoparticles and Their Hydrogel Composites for Drug Delivery: A Review.

作者信息

Desfrançois Claire, Auzély Rachel, Texier Isabelle

机构信息

CEA LETI MlNATEC Campus, University Grenoble Alpes, F-38000 Grenoble, France.

CERMAV-CNRS, University Grenoble Alpes, F-38000 Grenoble, France.

出版信息

Pharmaceuticals (Basel). 2018 Nov 1;11(4):118. doi: 10.3390/ph11040118.

Abstract

Several drug delivery systems already exist for the encapsulation and subsequent release of lipophilic drugs that are well described in the scientific literature. Among these, lipid nanoparticles (LNP) have specifically come up for dermal, transdermal, mucosal, intramuscular and ocular drug administration routes in the last twenty years. However, for some of them (especially dermal, transdermal, mucosal), the LNP aqueous dispersions display unsuitable rheological properties. They therefore need to be processed as semi-solid formulations such as LNP-hydrogel composites to turn into versatile drug delivery systems able to provide precise spatial and temporal control of active ingredient release. In the present review, recent developments in the formulation of lipid nanoparticle-hydrogel composites are highlighted, including examples of successful encapsulation and release of lipophilic drugs through the skin, the eyes and by intramuscular injections. In relation to lipid nanoparticles, a specific emphasis has been put on the LNP key properties and how they influence their inclusion in the hydrogel. Polymer matrices include synthetic polymers such as poly(acrylic acid)-based materials, environment responsive (especially thermo-sensitive) polymers, and innovative polysaccharide-based hydrogels. The composite materials constitute smart, tunable drug delivery systems with a wide range of features, suitable for dermal, transdermal, and intramuscular controlled drug release.

摘要

目前已经存在几种用于包裹亲脂性药物并随后释放的给药系统,科学文献中对这些系统已有详细描述。其中,脂质纳米颗粒(LNP)在过去二十年中特别适用于皮肤、透皮、粘膜、肌肉注射和眼部给药途径。然而,对于其中一些给药途径(尤其是皮肤、透皮、粘膜途径),LNP水分散体表现出不合适的流变学性质。因此,它们需要加工成半固体制剂,如LNP-水凝胶复合材料,以成为能够对活性成分释放提供精确时空控制的多功能给药系统。在本综述中,重点介绍了脂质纳米颗粒-水凝胶复合材料制剂的最新进展,包括通过皮肤、眼睛和肌肉注射成功包裹和释放亲脂性药物的实例。关于脂质纳米颗粒,特别强调了LNP的关键特性以及它们如何影响其在水凝胶中的包封。聚合物基质包括合成聚合物,如基于聚(丙烯酸)的材料、环境响应性(特别是热敏性)聚合物以及新型多糖基水凝胶。这些复合材料构成了具有多种特性的智能、可调给药系统,适用于皮肤、透皮和肌肉注射控释给药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7312/6315535/09f319b6f857/pharmaceuticals-11-00118-g001.jpg

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