Intestinal Absorption and First-Pass Elimination of 2',3'-Dideoxynucleosides Following Oral Administration in Rats.

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Intestinal absorption and first-pass elimination of 2', 3'-dideoxynucleosides (ddNs), including 3'-azido-3'-deoxythymidine (AZT), 2', 3'-dideoxyinosine (DDI) and 2', 3'-didehydro-3'-deoxythymidine (D4T), following oral administration was investigated in rats. Enzymatic degradation of ddNs in rat intestinal washing and in the intestinal homogenate showed them to be stable in the washing with half lives of more than 140 h, whereas degradation of DDI in the intestinal homogenate was more than ten times as rapid as those of AZT and D4T. Intestinal absorption was studied in three segments of the rat intestine (duodenum, jejunum and colon) using an in situ closed-loop method. The area under plasma ddN concentration curve (AUC) and the residual percent of dose 1 h after dosing indicated a greater absorption of AZT and D4T in the upper intestinal tract than in the colon, very poor absorption of DDI in all segments, and considerable absorption of AZT in the colon. The AUC and the mean residence time (MRT) of ddNs following four different routes (intracenous : i.v., intra portal vein : i.p.v., intra duodenal : i.d. and intra gastric : i.g.) were measured using the in vivo multiple sites of input method in rats. AZT and D4T were rapidly absorbed from the gastrointestinal tract and their bioavabilaility was more than 90%. DDI was less absorbed (33.02%) following i.d. administration compared with AZT and D4T. This poor absorption of DDI was partly attributable to its metabolism in the intestine.

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