Towards new boron carriers for boron neutron capture therapy:: metallacarboranes and their nucleoside conjugates

被引:80
作者
Lesnikowski, ZJ
Paradowska, E
Olejniczak, AB
Studzinska, M
Seekamp, P
Schüssler, U
Gabel, D
Schinazi, RF
Plesek, J
机构
[1] Polish Acad Sci, Lab Mol Virol & Biol Chem, Ctr Med Biol, PL-93232 Lodz, Poland
[2] Univ Bremen, Dept Chem, D-28334 Bremen, Germany
[3] Vet Affairs Med Ctr, Decatur, GA 30033 USA
[4] Emory Univ, Sch Med, Dept Pediat, Biochem Pharmacol Lab, Atlanta, GA 30322 USA
[5] Acad Sci Czech Republic, Inst Inorgan Chem, Rez 25068, Czech Republic
关键词
D O I
10.1016/j.bmc.2005.04.042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thymidine conjugates containing metallacarborane, {8-[5-(N-3-thymidine)-3-oxa-pentoxy]-3-cobalt bis(1,2-dicarbollide)}(-) (5) and {8-[5-(O-4-thymidine)-3-oxa-pentoxy]-3-cobalt bis(1,2-dicarbollide)}(-) (6) ions and several simple [3-cobalt bis(1,2-dicarbollide)]- ion (1) derivatives have been studied as potential boron carriers for BNCT. Compound 6 and some nonnucleoside derivatives of 1 were not toxic above 100 mu M. The partition coefficient for both metallacarborane bearing thymidine conjugates 5 and 6 was more than 500 times higher than that of unmodified nucleoside. The cellular uptake studies showed accumulation of compounds 6 in V79 Chinese hamster cells but not of compound 5. The low toxicity of conjugate type of 6 together with its high partition coefficient suggest that judicially designed derivatives of metallacarboranes can be considered as potential boron carriers for BNCT. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4168 / 4175
页数:8
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