前药
癌细胞
化学
阿霉素
明胶
催化作用
细胞毒性T细胞
介孔二氧化硅
控制释放
活力测定
组合化学
细胞凋亡
介孔材料
体外
生物化学
材料科学
纳米技术
癌症
化疗
生物
遗传学
作者
Mahboubeh Nabavinia,Baishali Kanjilal,Manoj K. Pandey,Subash C. Jonnalagadda,Robert Hesketh,Manuela Martins‐Green,Iman Noshadi
出处
期刊:Biomolecules
[MDPI AG]
日期:2022-12-01
卷期号:12 (12): 1796-1796
被引量:4
摘要
A heterogenous Palladium anchored Resorcinol-formaldehyde-hyperbranched PEI mesoporous catalyst, made by one-pot synthesis, was used successfully for in situ Suzuki-Miyaura cross coupling synthesis of anticancer prodrug PP-121 from iodoprazole and boronic ester precursors. The mesoporous catalyst with the non-cytotoxic precursors were tested in 2D in vitro model with excellent cytocompatibility and a strong suppression of PC3 cancer cell proliferation, underscored by 50% reduction in PC3 cells viability and 55% reduction in cell metabolism activity and an enhanced rate of early and late apoptosis in flow cytometry, that was induced only by successful in situ pro drug PP121 synthesis from the precursors. The 3D gelatin methacrylate hydrogel encapsulated in vitro cell models underscored the results with a 52% reduction in cell metabolism and underscored apoptosis of PC3 cells when the Pd anchored catalyst was combined with the precursors. In situ application of Suzuki-Miyaura cross coupling of non-cytotoxic precursors to cancer drug, along with their successful encapsulation in an injectable hydrogel could be applied for tumor point drug delivery strategies that can circumvent deleterious side effects and poor bioavailability chemotherapy routes with concomitant enhanced efficacy.
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