Ihara M, Tsuchiya Y, Sawasaki Y, Hisaka A, Takehana H, Tomimoto K, Yano M
Central Research Laboratories, Banyu Pharmaceutical Company, Ltd., Tokyo, Japan.
J Pharm Sci. 1989 Jul;78(7):525-9. doi: 10.1002/jps.2600780703.
L-3-(3-Hydroxy-4-pivaloyloxyphenyl)alanine (1, NB-355) is a novel L-dopa prodrug. After oral administration with carbidopa in rats, 1 demonstrated 2.3 times longer duration (MRT) and 1.4 times larger bioavailability (AUC) on plasma L-dopa concentrations than those of L-dopa itself. Similar results were obtained in dogs. The prolonged profile of L-dopa was parallel to that of carbidopa, and the intact ester was undetectable in rat plasma. After intravenous administration in rats, 1 was converted quickly and completely to L-dopa in the systemic circulation. It was also noted that the oral LD50 value of 1 was greater than 6 g/kg in mice. These data suggest that 1 will offer long-lasting L-dopa therapy for the treatment of Parkinson's disease with little concern about toxicity.
L-3-(3-羟基-4-新戊酰氧基苯基)丙氨酸(1,NB-355)是一种新型左旋多巴前体药物。在大鼠中与卡比多巴一起口服给药后,1在血浆左旋多巴浓度上的持续时间(平均驻留时间)比左旋多巴本身长2.3倍,生物利用度(曲线下面积)大1.4倍。在犬中也得到了类似结果。左旋多巴的延长曲线与卡比多巴的曲线平行,且在大鼠血浆中未检测到完整的酯。在大鼠中静脉给药后,1在体循环中迅速且完全地转化为左旋多巴。还注意到1在小鼠中的口服半数致死量值大于6 g/kg。这些数据表明,1将为帕金森病的治疗提供持久的左旋多巴治疗,且几乎无需担心毒性。