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与缺氧诱导因子-1抑制剂的主链聚缩醛共轭物:温度响应性、pH可降解药物递送载体。

Main-chain polyacetal conjugates with HIF-1 inhibitors: temperature-responsive, pH-degradable drug delivery vehicles.

作者信息

Samanta Sanjoy, De Silva Chathuranga C, Leophairatana Porakrit, Koberstein Jeffrey T

机构信息

Department of Chemical Engineering, Columbia University, 500 West 120th Street, New York, New York 10027, USA.

出版信息

J Mater Chem B. 2018 Jan 28;6(4):666-674. doi: 10.1039/c7tb01417a. Epub 2018 Jan 15.

Abstract

Main-chain polymer-drug conjugates are prepared from polyacetals (PA) and three hydrophobic diol-based HIF-1 inhibitors. The new conjugates are temperature-responsive with lower critical solution temperature (LCST) behavior and are intrinsically pH-degradable. While soluble in plasma at room temperature, they lose solubility above a target temperature that can be adjusted to virtually any temperature of physicological interest, providing mechanisms for site-specific delivery by active thermal targeting or temperature-induced gelation. The reverse phase transition temperature can be precisely tuned by proper choice of four structural variables that characterize the amphiphilic diol and divinyl ether monomers used in the synthesis, or by adjusting the content of drug incorporated within the polymer. These main-chain PA-drug conjugates also allow for site-specific controlled release as they degrade in acidic microenvironments such as tumors. The degradation rates increase with decreasing pH, degradation products are neutral, and pristine drug is released, without any remnants of the conjugation chemistry.

摘要

主链聚合物-药物缀合物由聚缩醛(PA)和三种基于二醇的疏水性缺氧诱导因子-1(HIF-1)抑制剂制备而成。这些新型缀合物具有温度响应性,呈现出较低临界溶液温度(LCST)行为,并且本质上可在pH作用下降解。它们在室温下可溶于血浆,但在高于目标温度时会失去溶解性,该目标温度可被调节至几乎任何具有生理意义的温度,从而通过主动热靶向或温度诱导凝胶化提供位点特异性递送机制。通过适当选择用于合成的两亲性二醇和二乙烯基醚单体的四个结构变量,或者通过调整聚合物中掺入的药物含量,可以精确调节反相转变温度。这些主链PA-药物缀合物在诸如肿瘤等酸性微环境中降解时,还能够实现位点特异性控释。降解速率随pH降低而增加,降解产物呈中性,并且原始药物得以释放,不会留下任何缀合化学的残余物。

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