Atorvastatin and clopidogrel interfere with photosensitization in vitro

被引:8
|
作者
Lee, Dong Kun [1 ,2 ]
Choi, Yongdoo [3 ]
Shon, Soo-Min [1 ]
Schellingerhout, Dawid [4 ]
Park, Jin Eok [1 ]
Kim, Dong-Eog [1 ,2 ]
机构
[1] Dongguk Univ, Ilsan Hosp, Mol Imaging & Neurovasc Res MINER Lab, Dept Neurol,Coll Med, Goyang, South Korea
[2] Dongguk Univ, Coll Med, Dept Neurol, Seoul, South Korea
[3] Natl Canc Ctr, Mol Imaging & Therapy Branch, Div Convergence Technol, Goyang, South Korea
[4] Univ Texas MD Anderson Canc Ctr, Dept Radiol & Expt Diagnost Imaging, Houston, TX 77030 USA
关键词
PHOTODYNAMIC THERAPY; ATHEROSCLEROTIC PLAQUES; PHARMACOKINETICS;
D O I
10.1039/c0pp00363h
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Photodynamic therapy (PDT) has been used to eliminate undesired cells by using a combination of photosensitizers and light illumination to generate reactive oxygen species. There is great interest in applying PDT to atherosclerosis; preferential destruction of pro-inflammatory macrophages in atheromata might attenuate plaque growth or rupture-prone vulnerability. Here, we report on a previously unknown interaction between cardiovascular drugs that are commonly prescribed for atherosclerosis patients and the cytolytic effects of photodynamic therapy using Cathepsin B activatable photosensitizer L-SR15 on murine macrophage Raw 264.7 cells in culture. Atorvastatin and clopidogrel significantly interfered with in vitro photosensitization effect while aspirin did this to a lesser extent; these drugs did not change the efficiency of cellular uptake of L-SR15 after in vitro photosensitization. A photosensitization interference effect of atorvastatin and clopidogrel was also observed when using a conventional photosensitizer free Ce6 or NCI-H1299 cancer cells. Considering the clinical implications of PDT, our study merits further investigation in clinical settings as well as in animal models.
引用
收藏
页码:1587 / 1592
页数:6
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