前药靶向给药的治疗潜力。

Q2 Pharmacology, Toxicology and Pharmaceutics
Open Medicinal Chemistry Journal Pub Date : 2018-10-23 eCollection Date: 2018-01-01 DOI:10.2174/1874104501812010111
Abhinav P Mishra, Suresh Chandra, Ruchi Tiwari, Ashish Srivastava, Gaurav Tiwari
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引用次数: 27

摘要

在Prodrugs的设计中,靶向可以通过两种方式实现:定点给药和定点药物生物活化。通过考虑酶-底物特异性或载体-底物特异性,可以设计针对特定酶或载体的前药,以克服各种不良药物性质。目前用于肿瘤靶向治疗的技术有抗体定向酶前药物治疗(Antibody Directed Enzyme Prodrug Therapy, ADEPT)、基因定向酶前药物治疗(Gene-Directed Enzyme Prodrug Therapy, GDEPT)、病毒定向酶前药物治疗(Virus -Directed Enzyme Prodrug Therapy, VDEPT)和基因前药物激活治疗(Gene Prodrug Activation Therapy, GPAT)。本文综述了前药在肿瘤靶向给药系统中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Therapeutic Potential of Prodrugs Towards Targeted Drug Delivery.

Therapeutic Potential of Prodrugs Towards Targeted Drug Delivery.

Therapeutic Potential of Prodrugs Towards Targeted Drug Delivery.

Therapeutic Potential of Prodrugs Towards Targeted Drug Delivery.

In designing of Prodrugs, targeting can be achieved in two ways: site-specified drug delivery and site-specific drug bioactivation. Prodrugs can be designed to target specific enzymes or carriers by considering enzyme-substrate specificity or carrier-substrate specificity in order to overcome various undesirable drug properties. There are certain techniques which are used for tumor targeting such as Antibody Directed Enzyme Prodrug Therapy [ADEPT] Gene-Directed Enzyme Prodrug Therapy [GDEPT], Virus Directed Enzyme Prodrug Therapy [VDEPT] and Gene Prodrug Activation Therapy [GPAT]. Our review focuses on the Prodrugs used in site-specific drug delivery system specially on tumor targeting.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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