化学
谷氨酸羧肽酶Ⅱ
连接器
结合
内化
有效载荷(计算)
小分子
前列腺癌
生物物理学
组合化学
药品
内体
癌症研究
药理学
生物化学
癌症
受体
生物
医学
数学分析
计算机网络
数学
网络数据包
计算机科学
内科学
操作系统
作者
Emily A. Savoy,Feyisola P. Olatunji,Nooshin Mesbahi,Ryanne Ballard,Christine L. Lovingier,Aaron T. Hendricksen,Melody D. Fulton,Clifford E. Berkman
标识
DOI:10.1016/j.bmcl.2024.129657
摘要
Herein, we report the modular synthesis and evaluation of a prostate-specific membrane antigen (PSMA) targeted small molecule drug conjugate (SMDC) carrying the chemotherapeutic agent, SN38. Due to the fluorogenic properties of SN38, payload release kinetics from the platform was observed in buffers representing the pH conditions of systemic circulation and cellular internalization. It was found that this platform is stable with minimal payload release at physiological pH with most rapid payload release observed at pH values representing the endosome complex. We confirmed selective payload release and chemotherapeutic efficacy for PSMA(+) prostate cancer cells over PSMA(−) cells. These results demonstrate that chemotherapeutic agents with limited solubility can be conjugated to a water-soluble targeting and linker platform without attenuating efficacy.
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