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K562细胞摄取光敏剂ZnPcS2P2的测定及药代动力学
引用本文:谢宝刚,黄慧芳,黄剑东,陈耐生,黄金陵.K562细胞摄取光敏剂ZnPcS2P2的测定及药代动力学[J].光谱学与光谱分析,2004,24(11):1415-1418.
作者姓名:谢宝刚  黄慧芳  黄剑东  陈耐生  黄金陵
作者单位:1. 福州大学化学化工学院,福州大学功能材料研究所,福建,福州,350002
2. 福建医科大学附属协和医院血液病研究所,福建,福州,350001
基金项目:国家自然科学基金青年基金(20201005), 教育部高等学校骨干教师资助计划和福建省自然科学基金(C010005)资助项目
摘    要:通过荧光分析方法,比较了2.0%SDS(Wt%),1.5%Triton X-100(φ为体积百分比V/V)及DMF等不同溶剂对K562细胞内摄取的两亲性酞菁锌ZnPcS2P2提取效率,结果表明Triton X-100具有较高的一次提取率。以1.5%Triton X-100为提取剂,获得了K562细胞摄取ZnPcS2P2及ZnPcS2P2-低密度脂蛋白(LDL)复合物的动力学曲线。结果显示,K562细胞对ZnPcS2P2-LDL的最大摄取量是ZnPcS2P2的两倍,表明LDL是有效的靶向载体。

关 键 词:K562细胞  LDL  摄取量  药代动力学  光敏剂  低密度脂蛋白  SDS  X-100  两亲性  荧光分析
文章编号:1000-0593(2004)11-1415-04
修稿时间:2003年7月6日

Determination and Pharmacokinetics of Photosensitizer ZnPcS2P2 Uptaken by K562 Cells
XIE Bao gang ,HUANG Hui fang ,HUANG Jian dong ,CHEN Nai sheng ,HUANG Jin ling.Determination and Pharmacokinetics of Photosensitizer ZnPcS2P2 Uptaken by K562 Cells[J].Spectroscopy and Spectral Analysis,2004,24(11):1415-1418.
Authors:XIE Bao gang  HUANG Hui fang  HUANG Jian dong  CHEN Nai sheng  HUANG Jin ling
Institution:Department of Chemistry, Institute of Research on Functional Materials, Fuzhou University, Fuzhou 350002, China.
Abstract:The di-sulfonated di-phthalimidomethyl phthalocyanine zinc (ZnPcS2P2) was an amphiphilic photosensitizer for photodynamic therapy of cancer. According to fluorescence analytical method, extracting efficiencies of 2.0% SDS (Wt%), 1.5% Triton X-100 (phi) and DMF for ZnPcS2P2 in K562 cells were compared. The results showed that 1.5% Triton X-100 was the most efficient reagent for the first time extracting. Using 1.5% Triton X-100 as extracting reagent, the kinetic curves of cellular uptake of ZnPcS2P2 as well as LDL-ZnPcS2P2 complex by K562 cells were determined. Compared with ZnPcS2P2, the maximum cellular uptake of LDL-ZnPcS2P2 by K562 was doubled, which indicated that LDL was an effective targeting delivery vehicle for ZnPcS2P2.
Keywords:Phthalocyanine  Cells  Fluorescence spectra  Kinetics
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