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在批准的给药方案期间和之后,阿奇霉素和莫西沙星在人眼结合膜和房水中的药代动力学。

Pharmacokinetics of azithromycin and moxifloxacin in human conjunctiva and aqueous humor during and after the approved dosing regimens.

机构信息

PRN Pharmaceutical Research Network, LLC, Charleston, South Carolina, USA.

出版信息

Am J Ophthalmol. 2010 Nov;150(5):744-751.e2. doi: 10.1016/j.ajo.2010.05.039. Epub 2010 Sep 1.

Abstract

PURPOSE

To evaluate the ocular pharmacokinetics of azithromycin and moxifloxacin in human conjunctiva and aqueous humor in subjects undergoing cataract surgery.

DESIGN

Multicenter, open-label, randomized study.

METHODS

Subjects scheduled for routine cataract surgery and with normal-appearing conjunctiva were eligible. One conjunctival biopsy sample and 1 aqueous humor sample were obtained from subjects randomly assigned to 1 of 10 prespecified time points (1 to 312 hours) after treatment initiation of azithromycin ophthalmic solution 1% or moxifloxacin ophthalmic solution 0.5%. Samples were assayed using liquid chromatography tandem mass spectrometry.

RESULTS

Azithromycin 1% provided high concentrations (peak level, 559.7 μg/g) in human conjunctiva that were sustained at levels 1 to 2 orders of magnitude higher than those of moxifloxacin 0.5% throughout the 7-day dosing period and for at least 7 days thereafter. Azithromycin also showed an extended half-life (65.7 hours) in conjunctiva relative to that of moxifloxacin (28.6 hours). Accordingly, the concentration of azithromycin was maintained well above the minimum inhibitory concentration required for inhibition of growth of 90% of tested bacterial isolates for at least 7 days, whereas moxifloxacin conjunctival levels fell to levels at or less than the minimum inhibitory concentration required for inhibition of growth of 90% of tested bacterial isolates approximately 24 hours after the last dose. Peak aqueous humor concentration of moxifloxacin was higher (0.77 μg/mL) than that of azithromycin (0.053 μg/mL). No clinically relevant safety findings were observed.

CONCLUSIONS

Azithromycin 1% demonstrated high, therapeutic levels in the conjunctiva that were maintained up to 7 days after completion of a 1-week dosing regimen. Aqueous humor levels, however, were subtherapeutic with this dosing regimen. In comparison, moxifloxacin achieved lower conjunctival tissue levels, but higher aqueous humor levels.

摘要

目的

评估在接受白内障手术的患者中,阿奇霉素和莫西沙星在人结膜和房水中的眼部药代动力学。

设计

多中心、开放标签、随机研究。

方法

符合条件的受试者为计划接受常规白内障手术且结膜外观正常的患者。将受试者随机分配至阿奇霉素滴眼液 1%或莫西沙星滴眼液 0.5%治疗起始后 10 个预设时间点(1 至 312 小时)中的 1 个时间点,从每个受试者中获得 1 个结膜活检样本和 1 个房水样本。使用液相色谱-串联质谱法对样本进行检测。

结果

阿奇霉素 1%在人结膜中提供了高浓度(峰水平为 559.7μg/g),在整个 7 天给药期间,其浓度始终比莫西沙星 0.5%高 1 至 2 个数量级,并且至少在 7 天后仍维持在高浓度。阿奇霉素在结膜中的半衰期(65.7 小时)也比莫西沙星(28.6 小时)长。因此,阿奇霉素的浓度至少在 7 天内维持在抑制 90%测试细菌分离物生长所需的最低抑菌浓度之上,而莫西沙星结膜水平在最后一次给药后约 24 小时降至抑制 90%测试细菌分离物生长所需的最低抑菌浓度或以下。莫西沙星的房水峰浓度较高(0.77μg/mL),而阿奇霉素的房水峰浓度较低(0.053μg/mL)。未观察到与临床相关的安全性发现。

结论

阿奇霉素 1%在完成 1 周给药方案后,在结膜中保持高达 7 天的高治疗浓度。然而,该剂量方案下房水水平低于治疗浓度。相比之下,莫西沙星在结膜组织中达到较低的浓度,但在房水中达到较高的浓度。

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