Division of Chemistry and Biological Chemistry, School of Physical & Mathematical Sciences, Nanyang Technological University, Singapore, 637371 (Singapore).
Angew Chem Int Ed Engl. 2014 Jan 20;53(4):1012-6. doi: 10.1002/anie.201308834. Epub 2013 Dec 6.
Platinum-based drugs are among the most active antitumor reagents in clinical practice; their application is limited by side effects and drug resistance. A novel and personalized near-infrared (NIR) light-activated nanoplatform is obtained by combining a photoactivatable platinum(IV) prodrug and a caspase imaging peptide conjugated with silica-coated upconversion-luminescent nanoparticles (UCNPs) for the remote control of antitumor platinum prodrug activation, and simultaneously for real-time imaging of apoptosis induced by activated cytotoxicity. Upon NIR light illumination, the Pt(IV) prodrug complex is activated at the surface of the nanoparticle and active components are selectively released which display cytotoxicity against human ovarian carcinoma A2780 cells and its cisplatin-resistant variant A2780cis cells. More importantly, the caspases enzymes triggered by cytotoxicity would effectively cleave the probe peptide, thereby allowing the direct imaging of apoptosis in living cells.
基于铂的药物是临床实践中最有效的抗肿瘤试剂之一;但其应用受到副作用和耐药性的限制。本研究通过将光活化的顺铂前药与与二氧化硅包覆的上转换发光纳米颗粒(UCNPs)偶联的半胱天冬酶成像肽相结合,得到了一种新型的、个性化的近红外(NIR)光激活纳米平台,用于远程控制抗肿瘤铂前药的激活,并同时实时成像由激活的细胞毒性诱导的细胞凋亡。在近红外光照射下,纳米颗粒表面的 Pt(IV) 前药复合物被激活,活性成分被选择性释放,对人卵巢癌 A2780 细胞及其顺铂耐药变体 A2780cis 细胞表现出细胞毒性。更重要的是,细胞毒性引发的半胱天冬酶可有效切割探针肽,从而可以直接在活细胞中成像细胞凋亡。