紧身衣
喹诺酮类
抗菌剂
化学
光化学
可见光谱
组合化学
光解
溶剂
选择性
抗生素
有机化学
荧光
生物化学
材料科学
催化作用
光电子学
物理
量子力学
作者
Elena Contreras-García,Carmen Lozano,Cristina García‐Iriepa,Marco Marazzi,Arthur H. Winter,Carmén Torres,Diego Sampedro
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2022-05-17
卷期号:14 (5): 1070-1070
被引量:14
标识
DOI:10.3390/pharmaceutics14051070
摘要
Controlling the activity of a pharmaceutical agent using light offers improved selectivity, reduction of adverse effects, and decreased environmental build-up. These benefits are especially attractive for antibiotics. Herein, we report a series of photoreleasable quinolones, which can be activated using visible/NIR light (520-800 nm). We have used BODIPY photocages with strong absorption in the visible to protect two different quinolone-based compounds and deactivate their antimicrobial properties. This activity could be recovered upon green or red light irradiation. A comprehensive computational study provides new insight into the reaction mechanism, revealing the relevance of considering explicit solvent molecules. The triplet excited state is populated and the photodissociation is assisted by the solvent. The light-controlled activity of these compounds has been assessed on a quinolone-susceptible E. coli strain. Up to a 32-fold change in the antimicrobial activity was measured.
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