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一种新型抗青光眼药物拉坦前列素在兔体内的药代动力学。

The pharmacokinetics of a new antiglaucoma drug, latanoprost, in the rabbit.

作者信息

Sjöquist B, Basu S, Byding P, Bergh K, Stjernschantz J

机构信息

Glaucoma Research Laboratories, Pharmacia & Upjohn, Stockholm, Sweden.

出版信息

Drug Metab Dispos. 1998 Aug;26(8):745-54.

PMID:9698288
Abstract

Latanoprost (13,14-dihydro-17-phenyl-18,19,20-trinor-prostaglandin F2alpha-1-isopropyl ester) is a unique prostaglandin analogue developed for the treatment of glaucoma. To investigate the pharmacokinetics, tritium-labeled latanoprost was administered topically on the eyes of rabbits and intravenously. About 7.7% of the applied dose was found in the cornea at 15 min after the drug administration. The following Cmax and elimination half-life (interval 1-6 hr) values of the total radioactivity in the eye tissues were found: aqueous humor, 0.09 ng eq/ml and 3.0 hr; anterior sclera, 1.49 ng eq/mg and 1.8 hr; cornea, 1.59 ng eq/mg and 1.8 hr; ciliary body, 0.39 ng eq/mg and 2.8 hr; conjunctiva, 1.41 ng eq/mg and 1.4 hr; and iris, 0.39 ng eq/mg and 2.1 hr. Latanoprost was rapidly hydrolyzed, and most of the radioactivity found in the aqueous humor, anterior eye tissues, and plasma corresponded to the pharmacologically active acid of latanoprost. The initial plasma elimination half-life of the acid of latanoprost was 9.2 +/- 3.2 min after iv and 2.3 +/- 1.9 min after topical administration on the eyes. The plasma clearance of the acid of latanoprost was 1.8 +/- 0.3 liters/hr.kg, and the volume of distribution was 0.4 +/- 0.1 liter/kg after iv administration. Based on the retention times on HPLC and GC-MS, the main metabolite in urine and feces was identified as the 1,2,3,4-tetranor metabolite of acid of latanoprost. This acid existed in equilibration with the corresponding delta-lactone. The AUC of radioactivity in the eye tissues was approximately 1000 times higher than in plasma AUC. The recovery of radioactivity was complete.

摘要

拉坦前列素(13,14-二氢-17-苯基-18,19,20-三降-前列腺素F2α-1-异丙酯)是一种开发用于治疗青光眼的独特前列腺素类似物。为研究其药代动力学,将氚标记的拉坦前列素经眼部局部和静脉给药于兔眼。给药后15分钟,约7.7%的给药剂量存在于角膜中。眼部组织中总放射性的以下Cmax和消除半衰期(1 - 6小时时间段)值如下:房水,0.09 ng当量/毫升和3.0小时;前巩膜,1.49 ng当量/毫克和1.8小时;角膜,1.59 ng当量/毫克和1.8小时;睫状体,0.39 ng当量/毫克和2.8小时;结膜,1.41 ng当量/毫克和1.4小时;虹膜,0.39 ng当量/毫克和2.1小时。拉坦前列素迅速水解,房水、眼前部组织和血浆中发现的大部分放射性与拉坦前列素的药理活性酸相对应。拉坦前列素酸的初始血浆消除半衰期静脉注射后为9.2±3.2分钟,眼部局部给药后为2.3±1.9分钟。拉坦前列素酸的血浆清除率为1.8±0.3升/小时·千克,静脉给药后分布容积为0.4±0.1升/千克。根据高效液相色谱(HPLC)和气相色谱 - 质谱联用(GC - MS)的保留时间,尿液和粪便中的主要代谢物被鉴定为拉坦前列素酸的1,2,3,4-四降代谢物。该酸与相应的δ-内酯处于平衡状态。眼部组织中放射性的AUC比血浆AUC高约1000倍。放射性回收完全。

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