机构地区:[1]中山大学附属第一医院器官移植中心,广州510080 [2]中山大学附属第一医院药学部实验室,广州510080
出 处:《中华移植杂志(电子版)》2009年第3期150-153,共4页Chinese Journal of Transplantation(Electronic Edition)
摘 要:目的比较吗替麦考酚酯分散片(商品名顺友)与片剂(商品名骁悉)在肾移植术后早期麦考酚酸(mycophenolic acid,MPA)浓度随时间的变化及疗效。方法30例首次肾移植受者随机分为顺友组和骁悉组,于术后24 h内开始口服顺友或骁悉,均为1.5 g/d,一日两次。术后第7、14天分别于服药前(0 h)及服药后0.5、1、1.5、2、3、4、6、8、10、12 h采集外周静脉血,用高效液相色谱分析法测定MPA血药浓度,比较两组MPA的达峰时间(MPA-Tmax)、峰浓度(MPA-Cmax)及浓度-时间曲线下面积(MPA-AUC0-12 h),同时比较两组术后早期移植肾功能及3个月内的急性排斥反应和不良反应发生率。结果顺友组和骁悉组MPA-Tmax第7天[(1.27±0.88)h比(1.27±0.68)h,P>0.05)]、第14天[(0.73±0.32)h比(0.80±0.46)h,P>0.05)差异均无统计学意义,两组第14天MPA-Tmax均比各组内第7天提前(均P<0.05)。两组MPA-Cmax第7天[(12.10±5.00)ng/mL比(12.20±5.60)ng/mL,P>0.05)、第14天[(15.40±6.36)ng/mL比(12.80±6.36)ng/mL,P>0.05)无差异,组内比较均无差异(P>0.05)。两组MPA-AUC0-12 h第7天[(31.90±15.62)mg.h.L-1比(31.50±12.88)mg.h.L-1,P>0.05)、第14天[(33.30±8.68)mg.h.L-1比(34.30±7.31)mg.h.L-1,P>0.05]差异无统计学意义,第14天均高于各组内第7天值,但差异无统计学意义(P>0.05)。两组术后早期血肌酐浓度差异无统计学意义。顺友组和骁悉组均无急性排斥反应发生,两组分别有4例、3例受者发生不良反应。结论顺友和骁悉在肾移植受者术后早期MPA血药浓度变化和疗效无明显差异。顺友用于肾移植后早期的联合免疫抑制治疗安全有效,其远期效果有待进一步研究。Objective To compare the basic pharmacokinetic features of mycophenolic acid (MPA) in renal transplant recipients at the early postoperative stage when mycophenolate mofetil dispersible tablets (MMF-DT) or mycophenloate mofetil tablets (MMF-T) were administered, and to observe both therapeutic effects. Methods Thirty de novo renal transplant recipients were randomly divided into the MMF-DT group and MMF-T group. Both drugs were administered twice daily, 1.5 g per day, initiating within 24 h posttransplantation. Peripheral vein blood samples were harvested at right before drug administration and 0.5, 1, 1.5, 2, 3,4, 6, 8, 10, 12 h after administration on day 7 and 14 posttransplant. The MPA concentration was monitored by high performance liquid chromatography. Maximum concentration ( MPA-Cmax ), time to Cmax ( MPA-Tmax ), and area under curve ( MPA- AUC0.12 h) were compared, as well as renal graft function, acute rejection, and side effect rates.Results In the MMF-DT and MMF-T groups, MPA-Tmax were ( 1.27 ±0.88) and ( 1.27 ±0.68) h on day7 (P〉0.05), and (0.73±0.32) and (0.80±0.46) honday 14 (P〉0.05). MPA-Tmax was shorter on day 14 than that on day 7 in both groups (P 〈 0.05 ). MPA-Cmax were (12.10 ±5.00) and (12.20±5.60) ng/mL on day 7, and (15.40±6.36) and (12.80±6.36) ng/mL on day 14, with no in-group statistical difference in both groups ( P 〉 0.05). MPA-AUC0-12 h were (31. 90 ± 15.62) and (31.50±12.88) mg·h·L^-1 on day 7, (33.30 ±8.68) and (34.30 ±7.31) mg·h·L^-1 on day 14. MPA-AUC0.12h increased on day 14, but no statistical difference was found (P 〉 0.05 ). No significant difference was noted as compared serum creatinine levels in both groups. No acute rejection happened in both groups. Four patients in the MMF-DT group and 3 in the MMF-T group had side effects. Conclusions The basic pharmacokinetic features of MMF-DT and MMF-T and their therapeutic effects are not significantly different at
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