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纳米载体药物递送系统中使用的生物材料的吸收、分布、代谢和排泄。

Absorption, distribution, metabolism and excretion of the biomaterials used in Nanocarrier drug delivery systems.

机构信息

Research Center for Drug Metabolism, School of Life Sciences, Jilin University, Changchun, 130012, PR China; Beijing Institute of Drug Metabolism, Beijing 102209, PR China.

Research Center for Drug Metabolism, School of Life Sciences, Jilin University, Changchun, 130012, PR China; Beijing Institute of Drug Metabolism, Beijing 102209, PR China; School of Pharmaceutical Sciences, Jilin University, Changchun 130012, PR China.

出版信息

Adv Drug Deliv Rev. 2019 Mar 15;143:97-114. doi: 10.1016/j.addr.2019.06.008. Epub 2019 Jun 28.

Abstract

Nanocarriers (NCs) are a type of drug delivery system commonly used to regulate the pharmacokinetic and pharmacodynamic properties of drugs. Although a wide variety of NCs has been developed, relatively few have been registered for clinical trials and even fewer are clinically approved. Overt or potential toxicity, indistinct mechanisms of drug release and unsatisfactory pharmacokinetic behavior all contribute to their high failure rate during preclinical and clinical testing. These negative characteristics are not only due to the NCs themselves but also to the materials of the drug nanocarrier system (MDNS) that are released in vivo. In this article, we review the main analytical techniques used for bioassay of NCs and MDNS and their pharmacokinetics after administration by various routes. We anticipate our review will serve to improve the understanding of MDNS pharmacokinetics and facilitate the development of NC drug delivery systems.

摘要

纳米载体(NCs)是一种药物传递系统,常用于调节药物的药代动力学和药效学特性。尽管已经开发出了多种 NCs,但只有相对较少的 NCs被注册用于临床试验,甚至更少的 NCs被临床批准。明显或潜在的毒性、药物释放机制不明确以及不理想的药代动力学行为都导致它们在临床前和临床试验中失败率很高。这些负面特征不仅归因于 NCs 本身,还归因于体内释放的药物纳米载体系统(MDNS)的材料。本文综述了用于 NCs 和 MDNS 的生物测定以及通过各种途径给药后的药代动力学的主要分析技术。我们预计,我们的综述将有助于提高对 MDNS 药代动力学的理解,并促进 NC 药物传递系统的发展。

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