Neil G L, Moxley T E, Kuentzel S L, Manak R C, Hanka L J
Cancer Chemother Rep. 1975 May-Jun;59(3):459-65.
5-Azacytidine is more active when administered parenterally than orally in the treatment of L1210 leukemic mice. Oral coadministration of tetrahydrouridine, a pyrimidine nucleoside deaminase inhibitor with no intrinsic antitumor activity, greatly increases the oral activity of 5-azacytidine. 5-azacytidine (or cytotoxic equivalent) blood levels in BDF mice are much higher after oral administration of the 5-azacytidine-tetrahydrouridine combination than when 5-azacytidine is administered alone by the same route. The therapeutic results (L1210 leukemia) achieved with the oral combination are similar to those observed with parenteral 5-azacytidine alone.
在治疗L1210白血病小鼠时,5-氮杂胞苷经肠胃外给药比口服更具活性。口服给予四氢尿苷(一种无内在抗肿瘤活性的嘧啶核苷脱氨酶抑制剂)与5-氮杂胞苷共同给药,可大大提高5-氮杂胞苷的口服活性。BDF小鼠口服5-氮杂胞苷与四氢尿苷的组合后,其血液中5-氮杂胞苷(或细胞毒性等效物)水平比通过相同途径单独给予5-氮杂胞苷时要高得多。口服该组合所取得的治疗效果(L1210白血病)与单独肠胃外给予5-氮杂胞苷所观察到的效果相似。