Towards mitochondria-specific delivery of apoptosis-inducing agents: DQAsomal incorporated paclitaxel

被引:17
作者
Cheng, SM
Pabba, S
Torchilin, VP
Fowle, W
Kimpfler, A
Schubert, R
Weissig, V [1 ]
机构
[1] Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USA
[2] Northeastern Univ, Ctr Electron Microscopy, Boston, MA 02115 USA
[3] Univ Freiburg, Inst Pharmazeut Technol, D-79104 Freiburg, Germany
关键词
dequalinium; DQAsomes; paclitaxel; mitochondria; mitochondrial drug delivery; apoptosis;
D O I
10.1016/S1773-2247(05)50010-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
DQAsomes have been developed by us as the first mitochondria-specific colloidal drug carrier system. Previously we have shown that DQAsomes meet all criteria for a mitochondria-targeted DNA delivery system. Here we describe for the first time the use of DQA somes for encapsulating low-molecular weight compounds. As a model drug we have used paclitaxel, which has recently been shown to trigger apoptosis in tumor cells by acting directly on mitochondria. We demonstrate that paclitaxel can be incorporated into DQAsomes at an approximate ratio of 0.5 mol paclitaxel per mol dequalinium. Following an extensive physicochemical characterization of paclitaxel-loaded DQAsomes using three different electron microscopic techniques we tested in a preliminary study the ability of paclitaxel-loaded DQAsomes to inhibit the growth of human colon cancer cells in nude mice.
引用
收藏
页码:81 / 86
页数:6
相关论文
共 39 条
[11]   The taxoids - Comparative clinical pharmacology and therapeutic potential [J].
Eisenhauer, EA ;
Vermorken, JB .
DRUGS, 1998, 55 (01) :5-30
[12]  
Ferreira CG, 2002, CLIN CANCER RES, V8, P2024
[13]  
Fulda S, 1998, CANCER RES, V58, P4453
[14]   Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312
[15]   Role of mitochondria in apoptosis [J].
Gulbins, E ;
Dreschers, S ;
Bock, J .
EXPERIMENTAL PHYSIOLOGY, 2003, 88 (01) :85-90
[16]   Paclitaxel affects cytosolic calcium signals by opening the mitochondrial permeability transition pore [J].
Kidd, JF ;
Pilkington, MF ;
Schell, MJ ;
Fogarty, KE ;
Skepper, JN ;
Taylor, CW ;
Thorn, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (08) :6504-6510
[17]   The mitochondrial permeability transition pore complex as a pharmacological target. An introduction [J].
Kroemer, G .
CURRENT MEDICINAL CHEMISTRY, 2003, 10 (16) :1469-1472
[18]   Dequalinium™ vesicles form stable complexes with plasmid DNA which are protected from DNase attack [J].
Lasch, J ;
Meye, A ;
Taubert, H ;
Koelsch, R ;
Mansa-ard, J ;
Weissig, V .
BIOLOGICAL CHEMISTRY, 1999, 380 (06) :647-652
[19]   FAILURE TO ENHANCE THE IN-VIVO KILLING OF HUMAN OVARIAN-CARCINOMA BY SEQUENTIAL TREATMENT WITH DEQUALINIUM CHLORIDE AND TUMOR-NECROSIS-FACTOR [J].
MANETTA, A ;
EMMA, D ;
GAMBOA, G ;
LIAO, S ;
BERMAN, M ;
DISAIA, P .
GYNECOLOGIC ONCOLOGY, 1993, 50 (01) :38-44
[20]   Delocalized lipophilic cations selectively target the mitochondria of carcinoma cells [J].
Modica-Napolitano, JS ;
Aprille, JR .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 49 (1-2) :63-70