Atorvastatin and clopidogrel interfere with photosensitization in vitro

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作者
Dong Kun Lee
Yongdoo Choi
Soo-Min Shon
Dawid Schellingerhout
Jin Eok Park
Dong-Eog Kim
机构
[1] Dongguk University Ilsan Hospital,Molecular Imaging and Neurovascular Research (MINER) Laboratory, Department of Neurology
[2] Dongguk University College of Medicine,Department of Neurology
[3] 814 Siksa-dong,Molecular Imaging and Therapy Branch, Division of Convergence Technology
[4] Dongguk University College of Medicine,Department of Radiology and Experimental Diagnostic Imaging
[5] National Cancer Center,Laboratory of Genome to Drug Medicine
[6] The University of Texas M.D. Anderson Cancer Center,undefined
[7] Joint Center for Biosciences,undefined
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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.
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页码:1587 / 1592
页数:5
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