4.7 Review

Imaging the pharmacology of nanomaterials by intravital microscopy: Toward understanding their biological behavior

期刊

ADVANCED DRUG DELIVERY REVIEWS
卷 113, 期 -, 页码 61-86

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.addr.2016.05.023

关键词

Tumor-associated macrophage; Phagocyte; Extravasation; Microvascular perfusion; Orthotopic window; Drug efflux; Liposome; Quantum dot

向作者/读者索取更多资源

Therapeutic nanoparticles (NPs) can deliver cytotoxic chemotherapeutics and other drugs more safely and efficiently to patients; furthermore, selective delivery to target tissues can theoretically be accomplished actively through coating NPs with molecular ligands, and passively through exploiting physiological enhanced permeability and retention features. However, clinical trial results have been mixed in showing improved efficacy with drug nanoencapsulation, largely due to heterogeneous NP accumulation at target sites across patients. Thus, a clear need exists to better understand why many NP strategies fail in vivo and not result in significantly improved tumor uptake or therapeutic response. Multicolor in vivo confocal fluorescence imaging (intravital microscopy; IVM) enables integrated pharmacokinetic and pharmacodynamic (PK/PD) measurement at the single-cell level, and has helped answer key questions regarding the biological mechanisms of in vivo NP behavior. This review summarizes progress to date and also describes useful technical strategies for successful IVM experimentation. (C) 2016 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据