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通过刺激触发的自焚寡聚物、树枝状聚合物和线性聚合物的放大释放。

Amplified release through the stimulus triggered degradation of self-immolative oligomers, dendrimers, and linear polymers.

机构信息

Department of Chemical and Biochemical Engineering, The University of Western Ontario, London, Ontario, Canada.

出版信息

Adv Drug Deliv Rev. 2012 Aug;64(11):1031-45. doi: 10.1016/j.addr.2011.09.012. Epub 2011 Sep 29.

Abstract

In recent years, numerous delivery systems based on polymers, dendrimers, and nano-scale assemblies have been developed to improve the properties of drug molecules. In general, for the drug molecules to be active, they must be released from these delivery systems, ideally in a selective manner at the therapeutic target. As the changes in physiological conditions are relatively subtle from one tissue to another and the concentrations of specific enzymes are often quite low, a release strategy involving the amplification of a biological signal is particularly attractive. This article describes the development of oligomers, dendrimers, and linear polymers based on self-immolative spacers. This new class of molecules is designed to undergo a cascade of intramolecular reactions in response to the cleavage of a trigger moiety, resulting in molecular fragmentation and the release of multiple reporter or drug molecules. Progress in the development of these materials as drug delivery vehicles and sensors will be highlighted.

摘要

近年来,已经开发出了许多基于聚合物、树状大分子和纳米级组装体的递药系统,以改善药物分子的性质。通常,为了使药物分子具有活性,必须将其从这些递药系统中释放出来,理想情况下是在治疗靶点以选择性的方式释放。由于生理条件的变化在不同组织之间相对较细微,并且特定酶的浓度通常相当低,因此涉及放大生物信号的释放策略特别有吸引力。本文描述了基于自耗性间隔基的低聚物、树状大分子和线性聚合物的开发。这种新的分子类设计为响应触发部分的切割而经历级联的分子内反应,导致分子碎片化和多个报告器或药物分子的释放。将重点介绍这些材料作为药物传递载体和传感器的开发进展。

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