Kanazawa Y, Kurogi S, Shinohara S, Noda Y, Masuda K
Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Chem Pharm Bull (Tokyo). 1994 Apr;42(4):774-8. doi: 10.1248/cpb.42.774.
The suppression of alpha-fluoro-beta-alanine (FBAL) formation from 5-fluorouracil (FU) is an important subject in relation to tumor chemotherapy. This is the first comparative study of FU, 1-(2-tetrahydrofuryl)-5-fluorouracil (FT, a prodrug of FU) and of FT+uracil as a coadministration system (UFT) under an oral dose using the in vivo 19F NMR method. The slow release of FU from FT and the suppression of the catabolism of FU to FBAL in mouse livers and tumors by the coadministration of uracil with FT were demonstrated using consecutive NMR measurements. The applicability of the in vivo 19F NMR method to the drug evaluation in tumors and livers of small animals was successfully tested.
5-氟尿嘧啶(FU)生成α-氟-β-丙氨酸(FBAL)的抑制作用是肿瘤化疗领域的一个重要课题。这是首次使用体内19F NMR方法,对口服剂量下的FU、1-(2-四氢呋喃基)-5-氟尿嘧啶(FT,FU的前体药物)以及FT与尿嘧啶联合给药系统(UFT)进行比较研究。通过连续的NMR测量,证实了FT中FU的缓慢释放以及尿嘧啶与FT联合给药对小鼠肝脏和肿瘤中FU分解代谢为FBAL的抑制作用。体内19F NMR方法在小动物肿瘤和肝脏药物评估中的适用性得到了成功验证。