贝西沙星对兔、猴和人进行局部给药后的眼药代动力学。

Ocular pharmacokinetics of besifloxacin following topical administration to rabbits, monkeys, and humans.

作者信息

Proksch Joel W, Granvil Camille P, Siou-Mermet Raphaële, Comstock Timothy L, Paterno Michael R, Ward Keith W

机构信息

Global Research and Development, Bausch & Lomb, 1400 N. Goodman Street, Rochester, NY 14609, USA.

出版信息

J Ocul Pharmacol Ther. 2009 Aug;25(4):335-44. doi: 10.1089/jop.2008.0116.

Abstract

PURPOSE

Studies were conducted to evaluate the ocular penetration and systemic exposure to besifloxacin, a fluoroquinolone antibiotic, following topical ocular administration to animals and humans.

METHODS

Besifloxacin ophthalmic suspension (0.6%) was administered as a topical ocular instillation to pigmented rabbits, cynomolgus monkeys, and human subjects. At predetermined intervals after dosing, samples of ocular tissues and plasma were collected and analyzed for besifloxacin levels using HPLC/MS/MS methods.

RESULTS

Besifloxacin demonstrated good ocular penetration in rabbits and monkeys, with rapid absorption and sustained concentrations observed in anterior ocular tissues through 24 h after a single administration. Maximum besifloxacin concentrations in conjunctiva, cornea, and aqueous humor of monkeys were 6.43 microg/g, 2.10 microg/g, and 0.796 microg/mL, respectively, after a single topical dose, and concentrations declined in these tissues with an apparent half-life of 5-14 h. Following a single topical ocular administration to humans, the maximum besifloxacin concentration in tears was 610 microg/g with concentrations decreasing to approximately 1.6 microg/g at 24 h. The resulting pharmacokinetic parameters for besifloxacin in human tears were evaluated relative to the MIC(90) values (microg/mL) for besifloxacin against Streptococcus pneumoniae (0.125), Staphylococcus aureus (0.25), Staphylococcus epidermidis (0.5), and Haemophilus influenzae (0.06). Following a single topical administration, the C(max)/MIC(90) ratios for besifloxacin in human tears were > or =1,220, and the AUC((0-24))/MIC(90) ratios were > or =2,500 for these relevant ocular pathogens. Following repeated 3-times daily (TID) topical ocular administration to human subjects with clinically diagnosed bacterial conjunctivitis, maximum besifloxacin concentrations in plasma were less than 0.5 ng/mL, on average.

CONCLUSIONS

Taken together, the results of the current investigation provide a PK/PD-based rationale that supports the use of besifloxacin for the safe and effective treatment of ocular infections.

摘要

目的

开展研究以评估氟喹诺酮类抗生素贝西沙星经眼部局部给药后在动物和人体中的眼内渗透及全身暴露情况。

方法

将贝西沙星眼用混悬液(0.6%)作为眼部局部滴注剂给予有色家兔、食蟹猴和人类受试者。给药后在预定时间间隔采集眼组织和血浆样本,采用HPLC/MS/MS方法分析贝西沙星水平。

结果

贝西沙星在兔和猴中显示出良好的眼内渗透性,单次给药后在前眼部组织中观察到快速吸收和持续的浓度,持续24小时。单次局部给药后,猴结膜、角膜和房水中贝西沙星的最大浓度分别为6.43微克/克、2.10微克/克和0.796微克/毫升,这些组织中的浓度下降,表观半衰期为5 - 14小时。对人类进行单次眼部局部给药后,泪液中贝西沙星的最大浓度为610微克/克,24小时时浓度降至约1.6微克/克。相对于贝西沙星对肺炎链球菌(0.125)、金黄色葡萄球菌(0.25)、表皮葡萄球菌(0.5)和流感嗜血杆菌(0.06)的MIC(90)值(微克/毫升),评估了贝西沙星在人泪液中的药代动力学参数。单次局部给药后,贝西沙星在人泪液中的C(max)/MIC(90)比值≥1220,对于这些相关眼部病原体,AUC((0 - 24))/MIC(90)比值≥2500。对临床诊断为细菌性结膜炎的人类受试者每日重复3次(TID)眼部局部给药后,血浆中贝西沙星的最大浓度平均低于0.5纳克/毫升。

结论

总体而言,当前研究结果提供了基于药代动力学/药效学的理论依据,支持使用贝西沙星安全有效地治疗眼部感染。

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