TY - JOUR
T1 - Therapeutic effcacy of a Polymeric micellar doxorubicin infused by Convection-enhanced delivery against intracranial 9L brain tumor models
AU - Inoue, Tomoo
AU - Yamashita, Yoji
AU - Nishihara, Masamichi
AU - Sugiyama, Shinichiro
AU - Sonoda, Yukihiko
AU - Kumabe, Toshihiro
AU - Yokoyama, Masayuki
AU - Tominaga, Teiji
PY - 2009/4
Y1 - 2009/4
N2 - 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 effcacy 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 5 0.0173) and liposomal DOX (16.6 days; p 5 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;
AB - 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 effcacy 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 5 0.0173) and liposomal DOX (16.6 days; p 5 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;
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U2 - 10.1215/15228517-2008-068
DO - 10.1215/15228517-2008-068
M3 - Article
C2 - 18755917
AN - SCOPUS:65949110136
SN - 1522-8517
VL - 11
SP - 151
EP - 157
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 2
ER -