| Literature DB >> 16260113 |
H Yanagie1, K Maruyama, T Takizawa, O Ishida, K Ogura, T Matsumoto, Y Sakurai, T Kobayashi, A Shinohara, J Rant, J Skvarc, R Ilic, G Kuhne, M Chiba, Y Furuya, H Sugiyama, T Hisa, K Ono, H Kobayashi, M Eriguchi.
Abstract
Tumour cell destruction in boron neutron-capture therapy (BNCT) is due to the nuclear reaction between (10)B and thermal neutrons. It is necessary for effective BNCT therapy to accumulate (10)B atoms in the tumour cells. The delivery system consisted of polyethylene-glycol (PEG) binding liposomes (DPPC/cholesterol/DSPC-PEG2000) with an entrapped (10)B-compound and we evaluated the cytotoxic effects of intravenously injected (10)B-PEG-liposomes on human pancreatic carcinoma xenografts in nude mice with thermal neutron irradiation. After thermal neutron irradiation of mice injected with (10)B-PEG-liposomes, growth of AsPC-1 tumours was suppressed relative to controls. Injection of (10)B-PEG-liposomes caused the greatest tumour suppression with thermal neutron irradiation in vivo. These results suggest that intravenous injection of (10)B-PEG-liposomes can increase the retention of (10)B atoms by tumour cells, causing suppression of tumour growth in vivo, after thermal neutron irradiation.Entities:
Mesh：
Substances：
Year: 2005 PMID： 16260113 DOI： 10.1016/j.biopha.2005.05.011
Source DB: PubMed Journal: Biomed Pharmacother ISSN： 0753-3322 Impact factor: 6.529