Porphyrin-phospholipid liposomes with tunable leakiness

被引:47
作者
Luo, Dandan [1 ]
Carter, Kevin A. [1 ]
Razi, Aida [2 ,3 ]
Geng, Jumin [1 ]
Shao, Shuai [1 ]
Lin, Cuiyan [1 ]
Ortega, Joaquin [2 ,3 ]
Lovell, Jonathan F. [1 ]
机构
[1] SUNY Buffalo, Dept Biomed Engn, Buffalo, NY 14260 USA
[2] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON L8S 4L8, Canada
[3] McMaster Univ, MG DeGroote Inst Infect Dis Res, Hamilton, ON L8S 4L8, Canada
基金
美国国家卫生研究院;
关键词
Liposomes; Photodynamic therapy; Porphyrin; Doxorubicin; Vasculature; Cancer; DRUG-DELIVERY SYSTEM; TO-LIPID RATIO; PHOTODYNAMIC THERAPY; PHOSPHATIDYLCHOLINE LIPOSOMES; DOXORUBICIN; TUMOR; EFFICACY; RELEASE; CHEMOTHERAPY; COMBINATION;
D O I
10.1016/j.jconrel.2015.11.011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Drug bioavailability is a key consideration for drug delivery systems. When loaded with doxorubicin, liposomes containing 5 molar % porphyrin-phospholipid (HPPH liposomes) exhibited in vitro and in vivo serumstability that could be fine-tuned by varying the drug-to-lipid ratio. A higher drug loading ratio destabilized the liposomes, in contrast to standard liposomes which displayed an opposite and less pronounced trend. Following systemic administration of HPPH liposomes, near infrared laser irradiation induced vascular photodynamic damage, resulting in enhanced liposomal doxorubicin accumulation in tumors. In laser-irradiated tumors, the use of leaky HPPH liposomes resulted in improved doxorubicin bioavailability compared to stable standard liposomes. Using this approach, a single photo-treatment with 10 mg/kg doxorubicin rapidly eradicated tumors in athymic nude mice bearing KB or MIA Paca-2 xenografts. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:484 / 494
页数:11
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