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体内利用亲电试剂:使用2-丙基戊酰氯的疏水性不透射线制剂在猪身上进行的一项初步研究。

Harnessing Electrophiles In Vivo: A Pilot Study in Swine Using a Hydrophobic Radiopaque Formulation of 2-Propylpentanoyl Chloride.

作者信息

Cressman Erik, Stolley Danielle, Fowlkes Natalie, Felix Edd, Priebe Waldemar, Parrish Steve, Fuentes David

机构信息

Department of Interventional Radiology, MD Anderson Cancer Center, Houston, Texas 77030, United States.

Flow Cytometry & Cellular Imaging Core Facility, MD Anderson Cancer Center, Houston, Texas 77030, United States.

出版信息

Mol Pharm. 2025 Jun 2;22(6):3010-3016. doi: 10.1021/acs.molpharmaceut.4c01456. Epub 2025 May 13.

DOI:10.1021/acs.molpharmaceut.4c01456
PMID:40359181
Abstract

Manipulating biology through chemistry is older than the discipline of chemistry itself. Traditionally, selectivity of oral or intravenous drugs relied on preferential drug-receptor binding. A novel approach exploiting image-guided techniques to impart spatial selectivity opens up a wide range of new possibilities for study and manipulation of biology. Motivated initially by the poor prognosis for solid tumors such as liver cancer, we demonstrate the use of an extreme form of in vivo chemistry for targeted delivery of 2-propylpentanoyl chloride in a swine model. The ensuing reaction in tissue devitalizes it by multiple mechanisms with lasting effects and, critically, demonstrates very low systemic exposure compared to controls. This work points toward a new, powerful strategy for investigating the interface between chemistry and biology in vivo.

摘要

通过化学手段操控生物学比化学学科本身还要古老。传统上,口服或静脉注射药物的选择性依赖于药物与受体的优先结合。一种利用图像引导技术赋予空间选择性的新方法为生物学的研究和操控开辟了广泛的新可能性。最初受肝癌等实体瘤预后不佳的驱动,我们在猪模型中展示了一种极端形式的体内化学方法,用于靶向递送2-丙基戊酰氯。组织中随后发生的反应通过多种机制使其失活,并具有持久的效果,关键的是,与对照组相比,全身暴露极低。这项工作为体内研究化学与生物学之间的界面指明了一种新的、强大的策略。

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