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用于靶向药物递送的适配体-药物偶联物的自动化模块化合成。

Automated modular synthesis of aptamer-drug conjugates for targeted drug delivery.

作者信息

Wang RuoWen, Zhu Guizhi, Mei Lei, Xie Yan, Ma Haibin, Ye Mao, Qing Feng-Ling, Tan Weihong

机构信息

Molecular Sciences and Biomedicine Laboratory, State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering and College of Biology, Collaborative Innovation Center for Chemistry and Molecular Medicine, Hunan University , Changsha 410082, China.

出版信息

J Am Chem Soc. 2014 Feb 19;136(7):2731-4. doi: 10.1021/ja4117395. Epub 2014 Feb 7.

Abstract

Aptamer-drug conjugates (ApDCs) are promising targeted drug delivery systems for reducing toxicity while increasing the efficacy of chemotherapy. However, current ApDC technologies suffer from problems caused by the complicated preparation and low controllability of drug-aptamer conjugation. To solve such problems, we have designed and synthesized a therapeutic module for solid phase synthesis, which is a phosphoramdite containing an anticancer drug moiety and a photocleavable linker. Using this module, we have realized automated and modular synthesis of ApDCs, and multiple drugs were efficiently incorporated into ApDCs at predesigned positions. The ApDCs not only recognize target cancer cells specifically, but also release drugs in a photocontrollable manner. We demonstrated the potential of automated and modular ApDC technology for applications in targeted cancer therapy.

摘要

适体-药物偶联物(ApDCs)是一种很有前景的靶向给药系统,可在提高化疗疗效的同时降低毒性。然而,目前的ApDC技术存在药物-适体偶联制备复杂且可控性低所导致的问题。为解决此类问题,我们设计并合成了一种用于固相合成的治疗模块,它是一种含有抗癌药物部分和光可裂解连接子的亚磷酰胺。利用该模块,我们实现了ApDCs的自动化和模块化合成,多种药物能够在预先设计的位置高效地掺入到ApDCs中。这些ApDCs不仅能特异性识别靶癌细胞,还能以光控方式释放药物。我们展示了自动化和模块化ApDC技术在靶向癌症治疗中的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe77/3985443/1dcce3ff91b5/ja-2013-117395_0002.jpg

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