Kiesel L, Sandow J, Bertges K, Jerabek-Sandow G, Trabant H, Runnebaum B
Division of Gynecological Endocrinology, University of Heidelberg, West Germany.
J Clin Endocrinol Metab. 1989 Jun;68(6):1167-73. doi: 10.1210/jcem-68-6-1167.
We studied the pharmacokinetics of iv and intranasally administered buserelin, a LHRH agonist peptide, in 14 women with endometriosis. Serum and urinary buserelin concentrations were determined by specific RIA (buserelin antiserum AS-639). Intact buserelin and the metabolites in urine were separated by reverse phase high performance liquid chromatography and measured by RIA. The mean serum buserelin concentrations were 101 +/- 33 (+/- SD) ng/mL 20 min and 1.12 +/- 0.12 ng/mL 360 min after its iv injection in 6 women, and the mean elimination half-life between 20 and 360 min was 51 min. In serum, intact buserelin was the main constituent (10 min, 90%; 120 min, 74%; 360 min, 52%), and the major metabolite was the buserelin-(5-9) pentapeptide (10 min, 0.6%; 120 min, 19%; 360 min, 12%). In the urine collected 0-1 h after buserelin administration, intact buserelin was 66% and the 5-9 pentapeptide was 28% of the total excretion. In the urine collected between 6-24 h after buserelin administration, intact buserelin accounted for 67% and the 5-9 pentapeptide for 32% of the total excretion. The urinary buserelin concentration was 1345 +/- 156 micrograms/g creatinine 1 h and 25 +/- 5 micrograms/g creatinine 6-24 h after buserelin administration. Serum LH, FSH, and estradiol concentrations increased acutely up to 10-fold above basal values; the mean peak LH, FSH, and estradiol values occurred at 180-240 min, 240 min, and 24 h, respectively. In therapeutic studies with buserelin nasal spray in 5 women, serum concentrations of 0.9-1.4 ng/mL were found 15 min after a single dose of 300 micrograms, intranasally, and the urinary excretion was 2.52-3.68 micrograms/24 h during daily administration of 3 doses of 300 micrograms at intervals of 8 h. These results confirm that buserelin is slowly inactivated and remains available to pituitary receptors for a prolonged period after its iv or intranasal administration.
我们研究了14名子宫内膜异位症女性静脉注射和鼻内给药的促性腺激素释放激素(LHRH)激动剂肽布舍瑞林的药代动力学。通过特异性放射免疫分析(布舍瑞林抗血清AS - 639)测定血清和尿液中的布舍瑞林浓度。尿液中的完整布舍瑞林及其代谢产物通过反相高效液相色谱分离,并用放射免疫分析测定。6名女性静脉注射布舍瑞林后20分钟时血清布舍瑞林平均浓度为101±33(±标准差)ng/mL,360分钟时为1.12±0.12 ng/mL,20至360分钟之间的平均消除半衰期为51分钟。血清中,完整布舍瑞林是主要成分(10分钟时为90%;120分钟时为74%;360分钟时为52%),主要代谢产物是布舍瑞林 -(5 - 9)五肽(10分钟时为0.6%;120分钟时为19%;360分钟时为12%)。布舍瑞林给药后0 - 1小时收集的尿液中,完整布舍瑞林占总排泄量的66%,5 - 9五肽占28%。布舍瑞林给药后6 - 24小时收集的尿液中,完整布舍瑞林占总排泄量的67%,5 - 9五肽占32%。布舍瑞林给药后1小时尿液中布舍瑞林浓度为1345±156微克/克肌酐,6 - 24小时为25±5微克/克肌酐。血清促黄体生成素(LH)、促卵泡生成素(FSH)和雌二醇浓度急剧升高至基础值的10倍以上;LH、FSH和雌二醇的平均峰值分别出现在180 - 240分钟、240分钟和24小时。在5名女性使用布舍瑞林鼻喷雾剂的治疗研究中,单次鼻内给予300微克后15分钟血清浓度为0.9 - 1.4 ng/mL,每日间隔8小时给予3剂300微克期间,尿排泄量为2.52 - 3.68微克/24小时。这些结果证实,布舍瑞林静脉注射或鼻内给药后灭活缓慢,可在较长时间内作用于垂体受体。