Tumor Eradication by Boron Neutron Capture Therapy with 10B‐enriched Hexagonal Boron Nitride Nanoparticles Grafted with Poly(Glycerol)

Author:

Zhang Yucai1,Kang Heon Gyu2,Xu Hua‐zhen3,Luo Honghui1,Suzuki Minoru4,Lan Qing5,Chen Xiao3,Komatsu Naoki2,Zhao Li1ORCID

Affiliation:

1. State Key Laboratory of Radiation Medicine and Protection School of Radiation Medicine and Protection & School for Radiological and Interdisciplinary Sciences (RAD‐X) Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions Soochow University Suzhou Jiangsu 215123 China

2. Graduate School of Human and Environmental Studies Kyoto University Sakyo‐ku Kyoto 606–8501 Japan

3. Department of Pharmacology School of Basic Medical Sciences Hubei Provincial Key Laboratory of Developmentally Originated Disease Wuhan University Donghu Avenue No.185 Wuhan 430072 China

4. Institute for Integrated Radiation and Nuclear Science Kyoto University 2–1010 Asashiro‐nishi, Kumatori‐cho Sennan‐gun Osaka 590‐0494 Japan

5. Department of Neurosurgery The Second Affiliated Hospital of Soochow University Suzhou 215004 China

Abstract

AbstractBoron neutron capture therapy (BNCT) has emerged as a treatment modality with high precision and efficacy of intractable tumors. At the core of effective tumor BNCT are 10B carriers with facile preparation as well as advantageous pharmacokinetic and therapeutic profiles. Herein, the design and preparation of sub‐10 nm 10B‐enriched hexagonal boron nitride nanoparticles grafted with poly(glycerol) (h‐10BN‐PG), and their application to cancer treatment by BNCT are reported. By virtue of their small particle size and outstanding stealth property, h‐10BN‐PG nanoparticles accumulate efficiently in murine CT26 colon tumors with a high intratumor 10B concentration of 8.8%ID g−1 or 102.1 µg g−1 at 12 h post‐injection. Moreover, h‐10BN‐PG nanoparticles penetrate into the inside of the tumor parenchyma and then are taken up by the tumor cells. BNCT comprising a single bolus injection of h‐10BN‐PG nanoparticles and subsequent one‐time neutron irradiation results in significant shrinkage of subcutaneous CT26 tumors. h‐10BN‐PG‐mediated BNCT not only causes direct DNA damage to the tumor cells, but also triggers pronounced inflammatory immune response in the tumor tissues, which contributes to long‐lasting tumor suppression after the neutron irradiation. Thus, the h‐10BN‐PG nanoparticles are promising BNCT agents to eradicate tumor through highly efficient 10B accumulation.

Funder

Science and Technology Program of Suzhou

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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