RESUMO
Phospholipid derivatives of anticancer nucleosides cladribine and fludarabine (F-ara-A) bearing 1,2- and 1,3-diacylglycerol moieties have been prepared by the H-phosphonate approach using 1,1,3,3-tetraisopropyldisiloxane-1,3-diyl protecting group for cladribine and a combination of tert-butyldimethylsilyl and levulinyl protecting groups for 2-fluoroadenine nucleosides. The synthesized conjugates exhibited lower in vitro antiproliferative activity against human tumor cell lines in comparison with the same concentrations of the parent cladribine and fludarabine phosphate. In the course of biokinetic study, it was found that intragastric administration of phospholipid F-ara-A derivatives to Wistar rats and ICR outbred male mice led to a slow release of F-ara-A into the bloodstream, a smooth increase in nucleoside concentration, and prolonged serum circulation of liberated nucleoside. The oral bioavailability of F-ara-A from 1,2-dimyristoylglycerophosphate derivative 29 was similar to its oral bioavailability from fludarabine phosphate.
Assuntos
Antimetabólitos Antineoplásicos/farmacocinética , Cladribina/farmacocinética , Diglicerídeos/química , Fosfolipídeos/química , Pró-Fármacos , Vidarabina/análogos & derivados , Animais , Antimetabólitos Antineoplásicos/sangue , Antimetabólitos Antineoplásicos/síntese química , Disponibilidade Biológica , Biotransformação , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Cladribina/análogos & derivados , Cladribina/sangue , Cladribina/síntese química , Diglicerídeos/metabolismo , Humanos , Masculino , Camundongos , Camundongos Endogâmicos ICR , Estrutura Molecular , Organofosfonatos/química , Fosfolipídeos/metabolismo , Ratos , Ratos Wistar , Vidarabina/sangue , Vidarabina/síntese química , Vidarabina/farmacocinéticaRESUMO
The conjugates of anticancer nucleoside clofarabine [2-chloro-9-(2-deoxy-2-fluoro-ß-d-arabinofuranosyl)adenine] with 1,2- and 1,3-diacylglycerophosphates have been prepared by the phosphoramidite method using a combination of 1,1,3,3-tetraisopropyldisiloxane-1,3-diyl protecting group for the sugar moiety of the nucleoside and 2-cyanoethyl protection for the phosphate fragment. Some of the synthesized conjugates exhibited cytostatic activity against HL-60, A-549, MCF-7, and HeLa tumor cell lines.