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纳米颗粒载药对抗癌药物药代动力学的影响。

The effects of nanoparticle drug loading on the pharmacokinetics of anticancer agents.

作者信息

Petschauer Jennifer S, Madden Andrew J, Kirschbrown Whitney P, Song Gina, Zamboni William C

机构信息

Division of Pharmacotherapy & Experimental Therapeutics, University of North Carolina at Chapel Hill (UNC) Eshelman School of Pharmacy, Chapel Hill, NC 27599, USA.

出版信息

Nanomedicine (Lond). 2015 Feb;10(3):447-63. doi: 10.2217/nnm.14.179.


DOI:10.2217/nnm.14.179
PMID:25707978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4594874/
Abstract

Major advances in carrier-mediated agents, which include nanoparticles, nanosomes and conjugates, have revolutionized drug delivery capabilities over the past decade. While providing numerous advantages, such as greater solubility, duration of exposure and delivery to the site of action over their small-molecule counterparts, there is substantial variability in systemic clearance and distribution, tumor delivery and pharmacologic effects (efficacy and toxicity) of these agents. This review provides an overview of factors that affect the pharmacokinetics and pharmacodynamics of carrier-mediated agents in preclinical models and patients.

摘要

在过去十年中,包括纳米颗粒、纳米脂质体和偶联物在内的载体介导药物取得了重大进展,彻底改变了药物递送能力。虽然这些药物具有诸多优势,比如相较于小分子药物具有更高的溶解度、更长的暴露时间以及能将药物递送至作用部位,但这些药物在全身清除率和分布、肿瘤递送以及药理作用(疗效和毒性)方面存在很大差异。本综述概述了在临床前模型和患者中影响载体介导药物药代动力学和药效学的因素。

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本文引用的文献

[1]
Age affects pegylated liposomal doxorubicin elimination and tolerability in patients over 70 years old.

Cancer Chemother Pharmacol. 2014-1-18

[2]
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PLoS One. 2014-1-8

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PLoS One. 2013-5-1

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Cancer Res. 2013-2-19

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