期刊
CELLS
卷 10, 期 12, 页码 -出版社
MDPI
DOI: 10.3390/cells10123421
关键词
boron neutron capture therapy; boron lipid; liposomes; boron drug
类别
资金
- JSPS KAKENHI [JP19K18409, 18H02909, JP15K21327]
- Grants-in-Aid for Scientific Research [18H02909] Funding Source: KAKEN
The study focuses on improving the accumulation and retention of boron in tumor tissues by designing novel PBL liposomes, providing promising candidates for BNCT treatment.
Boron neutron capture therapy (BNCT) is a cancer treatment with clinically demonstrated efficacy using boronophenylalanine (BPA) and sodium mercaptododecaborate (BSH). However, tumor tissue selectivity of BSH and retention of BPA in tumor cells is a constant problem. To ensure boron accumulation and retention in tumor tissues, we designed a novel polyethylene glycol (PEG)-based boron-containing lipid (PBL) and examined the potency of delivery of boron using novel PBL-containing liposomes, facilitated by the enhanced permeability and retention (EPR) effect. PBL was synthesized by the reaction of distearoylphosphoethanolamine and BSH linked by PEG with Michael addition while liposomes modified using PBL were prepared from the mixed lipid at a constant molar ratio. In this manner, novel boron liposomes featuring BSH in the liposomal surfaces, instead of being encapsulated in the inner aqueous phase or incorporated in the lipid bilayer membrane, were prepared. These PBL liposomes also carry additional payload capacity for more boron compounds (or anticancer agents) in their inner aqueous phase. The findings demonstrated that PBL liposomes are promising candidates to effect suitable boron accumulation for BNCT.
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