纳米凝胶
普鲁兰
硼
纳米颗粒
化学
中子俘获
材料科学
药物输送
放射化学
核化学
纳米技术
有机化学
多糖
作者
Riku Kawasaki,H. Hirano,Keita Yamana,Hinata Isozaki,Shogo Kawamura,Yu Sanada,Kaori Bando,Anri Tabata,Kouhei Yoshikawa,Hideki Azuma,Takushi Takata,Hiroki Tanaka,Yoshinori Sakurai,Minoru Suzuki,Naoki Tarutani,Kiyofumi Katagiri,Shin‐ichi Sawada,Yoshihiro Sasaki,Kazunari Akiyoshi,Takeshi Nagasaki
标识
DOI:10.1016/j.nano.2023.102659
摘要
Boron neutron capture therapy shows is a promising approach to cancer therapy, but the delivery of effective boron agents is challenging. To address the requirements for efficient boron delivery, we used a hybrid nanoparticle comprising a carborane = bearing pullulan nanogel and hydrophobized boron oxide nanoparticle (HBNGs) enabling the preparation of highly concentrated boron agents for efficient delivery. The HBNGs showed better anti-cancer effects on Colon26 cells than a clinically boron agent, L-BPA/fructose complex, by enhancing the accumulation and retention amount of the boron agent within cells in vitro. The accumulation of HBNGs in tumors, due to the enhanced permeation and retention effect, enabled the delivery of boron agents with high tumor selectivity, meeting clinical demands. Intravenous injection of boron neutron capture therapy (BNCT) using HBNGs decreased tumor volume without significant body weight loss, and no regrowth of tumor was observed three months after complete regression. The therapeutic efficacy of HBNGs was better than that of L-BPA/fructose complex. BNCT with HBNGs is a promising approach to cancer therapeutics.
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