前药
药品
药理学
药物输送
化学
纳米技术
医学
材料科学
作者
Rupa Bargakshatriya,Sumit Kumar Pramanik
出处
期刊:ChemBioChem
[Wiley]
日期:2023-06-21
卷期号:24 (18)
被引量:13
标识
DOI:10.1002/cbic.202300155
摘要
Abstract Prodrugs are pharmacologically inactive, chemically modified derivatives of active drugs, which, following in vivo administration, are converted to the parent drugs through chemical or enzymatic cleavage. The prodrug approach holds tremendous potential to create the enhanced version of an existing pharmacological agent and leverage those improvements to augment the drug molecules′ bioavailability, targeting ability, therapeutic efficacy, safety, and marketability. Especially in cancer therapy, prodrug application has received substantial attention. A prodrug can effectively broaden the therapeutic window of its parent drug by enhancing its release at targeted tumor sites while reducing its access to healthy cells. The spatiotemporally controlled release can be achieved by manipulating the chemical, physical, or biological stimuli present at the targeted tumor site. The critical strategy comprises drug‐carrier linkages that respond to physiological or biochemical stimuli in the tumor milieu to yield the active drug form. This review will focus on the recent advancements in the development of various fluorophore‐drug conjugates that are widely used for real‐time monitoring of drug delivery. The use of different stimuli‐cleavable linkers and the mechanisms of linker cleavage will be discussed. Finally, the review will conclude with a critical discussion of the prospects and challenges that might impede the future development of such prodrugs.
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