硼
中子俘获
碳硼烷
脂质体
化学
放射化学
癌症治疗
癌细胞
癌症
癌症研究
医学
生物化学
立体化学
内科学
有机化学
作者
Riku Kawasaki,Ayano Oshige,Keita Yamana,H. Hirano,Kotaro Nishimura,Yamato Miura,Ryuji Yorioka,Yoshinori Sanada,Kaori Bando,Anri Tabata,Kazuma Yasuhara,Yusuke Miyazaki,Wataru Shinoda,Tomoki Nishimura,Hideki Azuma,Takushi Takata,Yoshinori Sakurai,Hiroki Tanaka,Minoru Suzuki,Takeshi Nagasaki,Atsushi Ikeda
标识
DOI:10.1002/chem.202302486
摘要
Boron neutron capture therapy (BNCT) is a promising modality for cancer treatment because of its minimal invasiveness. To maximize the therapeutic benefits of BNCT, the development of efficient platforms for the delivery of boron agents is indispensable. Here, carborane-integrated immunoliposomes were prepared via an exchanging reaction to achieve HER-2-targeted BNCT. The conjugation of an anti-HER-2 antibody to carborane-integrated liposomes successfully endowed these liposomes with targeting properties toward HER-2-overexpressing human ovarian cancer cells (SK-OV3); the resulting BNCT activity toward SK-OV3 cells obtained using the current immunoliposomal system was 14-fold that of the l-BPA/fructose complex, which is a clinically available boron agent. Moreover, the growth of spheroids treated with this system followed by thermal neutron irradiation was significantly suppressed compared with treatment with the l-BPA/fructose complex.
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