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猫经眼部局部给药后环孢素的药代动力学

Cyclosporine pharmacokinetics in cats following topical ocular administration.

作者信息

Gregory C R, Hietala S K, Pedersen N C, Gregory T A, Floyd-Hawkins K A, Patz J D

机构信息

California Veterinary Diagnostic Laboratory, School of Veterinary Medicine, University of California 95616.

出版信息

Transplantation. 1989 Mar;47(3):516-9. doi: 10.1097/00007890-198903000-00023.

Abstract

Topical ocular administration of two forms of cyclosporine were studied in the cat. Both forms were able to produce measurable whole-blood levels capable of suppressing in vitro lymphocyte stimulation. The kinetics of cyclosporine following administration of either oral solution or cyclosporine in olive oil were variable, with peak concentrations ranging from 450 to 1033 ng/ml and 288 to 648 ng/ml, respectively. Absorption lag time ranged from 0 to 1.34 hr for oral solution, and 0.27 to 1.2 hr for cyclosporine in olive oil. The half-life of elimination ranged from 2.41 to 10.04 hr, and 3.09 to 15.75 hr, respectively. When compared with the commercially available oral solution, cyclosporine dissolved in olive oil was better tolerated during administration. Topical ocular administration of cyclosporine in cats offers a possible alternative method of treatment for individuals intolerant of oral administration. Topical ocular administration might also replace the need for intravenous administration of cyclosporine during perioperative periods or during periods of vomiting and nausea associated with rejection or other illnesses. Due to individual variation in absorption and elimination of topically applied cyclosporine, dosages in each cat must be determined by monitoring blood, plasma, or serum levels.

摘要

在猫身上研究了两种形式的环孢素的局部眼部给药。两种形式都能够产生可测量的全血水平,能够抑制体外淋巴细胞刺激。口服溶液或橄榄油中环孢素给药后的动力学是可变的,峰值浓度分别为450至1033 ng/ml和288至648 ng/ml。口服溶液的吸收滞后时间为0至1.34小时,橄榄油中环孢素的吸收滞后时间为0.27至1.2小时。消除半衰期分别为2.41至10.04小时和3.09至15.75小时。与市售口服溶液相比,溶解在橄榄油中的环孢素在给药期间耐受性更好。猫局部眼部给予环孢素为不耐受口服给药的个体提供了一种可能的替代治疗方法。局部眼部给药也可能取代围手术期或与排斥反应或其他疾病相关的呕吐和恶心期间静脉给予环孢素的需求。由于局部应用环孢素的吸收和消除存在个体差异,每只猫的剂量必须通过监测血液、血浆或血清水平来确定。

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