Therapeutic efficacy of a polymeric micellar doxorubicin infused by convection-enhanced delivery against intracranial 9L brain tumor models

被引:56
作者
Inoue, Tomoo [1 ]
Yamashita, Yoji [1 ]
Nishihara, Masamichi [2 ]
Sugiyama, Shinichiro [1 ]
Sonoda, Yukihiko [1 ]
Kumabe, Toshihiro [1 ]
Yokoyama, Masayuki [2 ]
Tominaga, Teiji [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Neurosurg, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Kanagawa Acad Sci & Technol, Yokoyama Nanomed Polymers Project, Kawasaki, Kanagawa, Japan
关键词
brain tumors; convection-enhanced delivery; doxorubicin; drug delivery system; polymeric micelle; PEGYLATED LIPOSOMAL DOXORUBICIN; ANTITUMOR-ACTIVITY; INTRACEREBRAL CLYSIS; MALIGNANT GLIOMA; ANTICANCER DRUG; SOLID TUMORS; IN-VIVO; ADRIAMYCIN; TOPOTECAN;
D O I
10.1215/15228517-2008-068
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Convection-enhanced delivery (CED) with various drug carrier systems has recently emerged as a novel chemotherapeutic method to overcome the problems of current chemotherapies against brain tumors. Polymeric micelle systems have exhibited dramatically higher in vivo antitumor activity in systemic administration. This study investigated the effectiveness of CED with polymeric micellar doxorubicin (DOX) in a 9L syngeneic rat model. Distribution, toxicity, and efficacy of free, liposomal, and micellar DOX infused by CED were evaluated. Micellar DOX achieved much wider distribution in brain tumor tissue and surrounding normal brain tissue than free DOX. Tissue toxicity increased at higher doses, but rats treated with micellar DOX showed no abnormal neurological symptoms at any dose tested (0.1-1.0 mg/ml). Micellar DOX infused by CED resulted in prolonged median survival (36 days) compared with free DOX (19.6 days; p = 0.0173) and liposomal DOX (16.6 days; p = 0.0007) at the same dose (0.2 mg/ml). This study indicates the potential of CED with the polymeric micelle drug carrier system for the treatment of brain tumors. Neuro-Oncology 11, 151-157, 2009 (Posted to Neuro-Oncology [serial online], Doc. D08-00039, August 28, 2008. URL http://neuro-oncology.dukejournals.org; DOI: 10.1215/15228517-2008-068)
引用
收藏
页码:151 / 157
页数:7
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