文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

近年来前药作为药物传递系统的进展。

Recent advances in prodrugs as drug delivery systems.

机构信息

Department of Pharmacology, Rush University Medical Center, Chicago, IL, USA.

出版信息

Am J Ther. 2012 Jan;19(1):33-43. doi: 10.1097/MJT.0b013e3181f47f3f.


DOI:10.1097/MJT.0b013e3181f47f3f
PMID:21150770
Abstract

Prodrugs are a class of drug derivatives with little or no pharmacological activity that are converted in vivo to therapeutically active compounds. The primary utility of a prodrug approach is to improve pharmaceutical properties. Because it does not alter the primary structure of the parent drug, the synthesis of prodrugs is usually much less difficult than the synthesis of analogs. The derived physicochemical properties of the resulting derivatives can be carefully tailored by means of structural modification of the promoiety. However, sufficient levels of intrinsic activity of the parent drug need to be assured through in vivo cleavage of the prodrug. The prodrug approach has been successfully applied to a wide variety of drugs. This article briefly discusses advances in strategies for development of prodrugs and their mechanisms of drug release.

摘要

前药是一类药理活性很小或没有的药物衍生物,在体内可转化为治疗活性化合物。前药方法的主要用途是改善药物性质。由于前药不改变母体药物的基本结构,因此前药的合成通常比类似物的合成容易得多。通过对前药部分的结构修饰,可以仔细调整所得衍生物的衍生物理化学性质。然而,需要通过体内切割前药来确保母体药物具有足够的固有活性水平。前药方法已成功应用于多种药物。本文简要讨论了前药的发展策略及其药物释放机制方面的进展。

相似文献

[1]
Recent advances in prodrugs as drug delivery systems.

Am J Ther. 2012-1

[2]
Synthesis of dendrimers and drug-dendrimer conjugates for drug delivery.

Curr Opin Drug Discov Devel. 2007-11

[3]
Prodrugs: design and clinical applications.

Nat Rev Drug Discov. 2008-3

[4]
Prodrugs--from serendipity to rational design.

Pharmacol Rev. 2011-7-7

[5]
Recent advances in retrometabolic drug design and targeting approaches.

Pharmazie. 2000-3

[6]
Polymeric prodrugs.

Crit Rev Ther Drug Carrier Syst. 1987

[7]
[Research of oral prodrugs: opportunities and challenges].

Yao Xue Xue Bao. 2008-4

[8]
Amino acids as promoieties in prodrug design and development.

Adv Drug Deliv Rev. 2012-10-22

[9]
Prodrug approaches for CNS delivery.

AAPS J. 2008

[10]
Remarkable drug-release enhancement with an elimination-based AB3 self-immolative dendritic amplifier.

Bioorg Med Chem. 2007-6-1

引用本文的文献

[1]
Drug Delivery Across the Blood-Brain Barrier: A New Strategy for the Treatment of Neurological Diseases.

Pharmaceutics. 2024-12-19

[2]
Comprehensive evaluation of ibuprofenate amino acid isopropyl esters: insights into antioxidant activity, cytocompatibility, and cyclooxygenase inhibitory potential.

Pharmacol Rep. 2024-12

[3]
Conjugation of Methotrexate-Amino Derivatives to Macromolecules through Carboxylate Moieties Is Superior Over Conventional Linkage to Amino Residues: Chemical, Cell-Free and In Vitro Characterizations.

PLoS One. 2016-7-12

[4]
Clinical pharmacokinetics of antibacterials in cerebrospinal fluid.

Clin Pharmacokinet. 2013-7

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索