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脂质体和微/纳米颗粒作为用于鼻腔给药的胶体载体

Liposomes and micro/nanoparticles as colloidal carriers for nasal drug delivery.

作者信息

Mainardes Rubiana Mara, Urban Maria Cristina Cocenza, Cinto Priscila Oliveira, Chaud Marco Vinícius, Evangelista Raul Cesar, Gremião Maria Palmira Daflon

机构信息

Pós-graduação em Ciências Farmacêuticas, UNESP-Araraquara, Brasil.

出版信息

Curr Drug Deliv. 2006 Jul;3(3):275-85. doi: 10.2174/156720106777731019.

Abstract

The use of the nasal route for drug delivery has attracted much interest in recent years in the pharmaceutical field. Local and principally systemic drug delivery can be achieved by this route of administration. But the nasal route of delivery is not applicable to all drugs. Polar drugs and some macromolecules are not absorbed in sufficient concentration due to poor membrane permeability, rapid clearance and enzymatic degradation into the nasal cavity. Thus, alternative means that help overcome these nasal barriers are currently in development. Absorption enhancers such as phospholipids and surfactants are constantly used, but care must be taken in relation to their concentration. Drug delivery systems including liposomes, cyclodextrins, micro- and nanoparticles are being investigated to increase the bioavailability of drugs delivered intranasally. This review article discusses recent progress and specific development issues relating to colloidal drug delivery systems in nasal drug delivery.

摘要

近年来,鼻腔给药途径在制药领域备受关注。通过这种给药途径可以实现局部给药,主要是全身给药。但并非所有药物都适用于鼻腔给药途径。由于膜通透性差、清除迅速以及鼻腔内的酶降解作用,极性药物和一些大分子药物无法以足够的浓度被吸收。因此,目前正在开发有助于克服这些鼻腔屏障的替代方法。诸如磷脂和表面活性剂等吸收促进剂一直在使用,但必须注意其浓度。包括脂质体、环糊精、微米和纳米颗粒在内的药物递送系统正在进行研究,以提高鼻腔给药药物的生物利用度。这篇综述文章讨论了鼻腔给药中胶体药物递送系统的最新进展和具体开发问题。

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