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基于二氢卟吩p6的水溶性氨基酸衍生物作为光动力疗法的强效光敏剂

Chlorin p6-Based Water-Soluble Amino Acid Derivatives as Potent Photosensitizers for Photodynamic Therapy.

作者信息

Meng Zhi, Yu Bin, Han Guiyan, Liu Minghui, Shan Bin, Dong Guoqiang, Miao Zhenyuan, Jia Ningyang, Tan Zou, Li Buhong, Zhang Wannian, Zhu Haiying, Sheng Chunquan, Yao Jianzhong

机构信息

Department of Medicinal Chemistry, School of Pharmacy, Second Military Medical University , 325 Guohe Road, Shanghai 200433, China.

Department of Cell Biology, Second Military Medical University , 800 Xiangyin Road, Shanghai 200433, China.

出版信息

J Med Chem. 2016 May 26;59(10):4999-5010. doi: 10.1021/acs.jmedchem.6b00352. Epub 2016 May 6.

Abstract

The development of novel photosensitizer with high phototoxicity, low dark toxicity, and good water solubility is a challenging task for photodynamic therapy (PDT). A series of chlorin p6-based water-soluble amino acid conjugates were synthesized and investigated for antitumor activity. Among them, aspartylchlorin p6 dimethylester (7b) showed highest phototoxicity against melanoma cells with weakest dark toxicity, which was more phototoxic than verteporfin while with less dark toxicity. It also exhibited better in vivo PDT antitumor efficacy on mice bearing B16-F10 tumor than verteporfin. The biological assays revealed that 7b was localized in multiple subcellular organelles and could cause both cell necrosis and apoptosis after PDT in a dose-dependent manner, resulting in more effective cell destruction. As a result, 7b represents a promising photosensitizer for PDT applications because of its strong absorption in the phototherapeutic window, relatively high singlet oxygen quantum yield, highest dark toxicity/phototoxicity ratio, good water solubility, and excellent in vivo PDT antitumor efficacy.

摘要

开发具有高光毒性、低暗毒性和良好水溶性的新型光敏剂是光动力疗法(PDT)面临的一项具有挑战性的任务。合成了一系列基于二氢卟吩p6的水溶性氨基酸共轭物,并对其抗肿瘤活性进行了研究。其中,天冬氨酰二氢卟吩p6二甲酯(7b)对黑色素瘤细胞显示出最高的光毒性,暗毒性最弱,其光毒性比维替泊芬更强,而暗毒性更小。它在携带B16-F10肿瘤的小鼠体内的PDT抗肿瘤疗效也比维替泊芬更好。生物学分析表明,7b定位于多个亚细胞器,PDT后可剂量依赖性地导致细胞坏死和凋亡,从而更有效地破坏细胞。因此,7b因其在光治疗窗口的强吸收、相对较高的单线态氧量子产率、最高的暗毒性/光毒性比、良好的水溶性以及优异的体内PDT抗肿瘤疗效,是一种有前景的用于PDT应用的光敏剂。

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