Li Cheng-Hsuan, Huang Rui, Makabenta Jessa Marie, Schmidt-Malan Suzannah, Patel Robin, Rotello Vincent M
Department of Chemistry, University of Massachusetts Amherst, Amherst, MA, USA.
Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Microbiol Insights. 2021 Feb 24;14:1178636121997121. doi: 10.1177/1178636121997121. eCollection 2021.
Prodrug strategies use chemical modifications to improve the pharmacokinetic properties and therefore therapeutic effects of parent drugs. Traditional prodrug approaches use endogenous enzymes for activation. Bioorthogonal catalysis uses processes that endogenous enzymes cannot access, providing a complementary strategy for prodrug uncaging. Site-selective activation of prodrugs to drugs (uncaging) using synthetic catalysts is a promising strategy for localized drug activation. We discuss here recent studies that incorporate metal catalysts into polymers and nanoparticle scaffolds to provide biocompatible "enzyme-like" catalysts that can penetrate bacterial biofilms and activate prodrug antibiotics , affording a new strategy to treat bacterial biofilm infections with the potential for reduced off-target effects.
前药策略利用化学修饰来改善母体药物的药代动力学性质,从而提高其治疗效果。传统的前药方法利用内源性酶进行激活。生物正交催化利用内源性酶无法参与的过程,为前药解笼提供了一种补充策略。使用合成催化剂将前药位点选择性激活为药物(解笼)是一种有前景的局部药物激活策略。我们在此讨论最近的研究,这些研究将金属催化剂整合到聚合物和纳米颗粒支架中,以提供可穿透细菌生物膜并激活前药抗生素的生物相容性“类酶”催化剂,从而提供一种治疗细菌生物膜感染的新策略,有可能减少脱靶效应。