Aqueous humour concentration of topically applied 2.0% ganciclovir eye drops in eyes with cytomegalovirus anterior uveitis and endotheliitis.

IF 4.9 2区 医学 Q1 OPHTHALMOLOGY
Samanthila Waduthantri, Lei Zhou, Soon Phaik Chee
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Abstract

Background: To investigate the level of ganciclovir in the aqueous humour (AH) following topical application of 2.0% ganciclovir eye drop in eyes with cytomegalovirus (CMV) anterior segment infection.

Methods: This is a prospective, non-randomised, interventional clinical study. We enrolled patients with active CMV anterior segment infection. Patients were treated with 2.0% ganciclovir eye drop, which was administered one drop every 3 h for 6 weeks. At the end of week 6, the CMV viral load in the AH was measured using real time polymerase chain reaction and the ganciclovir concentration in the AH was measured using high-performance liquid chromatography-mass spectrometry. The clinical activity and central corneal thickness (CCT) were recorded at baseline and post-treatment.

Results: Of the 25 eyes of 25 patients studied, 21 had anterior uveitis and 4 had endotheliitis. After 6 weeks of treatment, 22 eyes did not have any inflammation in the anterior chamber (AC) and CMV was undetectable on real time PCR. Three eyes of non-compliant patients responded partially with reduced AC inflammation and decreased CMV viral load in the AH. The mean ganciclovir concentration in the AH was 1252.88 ± 2408.82 ng/mL. There was no significant correlation between the ganciclovir concentration in the AH and the CCT (Spearmen's r = +0.19, p = 0.36).

Conclusions: Three-hourly application of 2.0% ganciclovir eye drops resulted in effective intra-cameral penetration with drug concentrations in the AH exceeding the 50% inhibitory dose for CMV replication. The ocular penetration of the ganciclovir eye drop was not dependent on corneal thickness.

巨细胞病毒前葡萄膜炎和内皮细胞炎患者眼部局部使用 2.0% 更昔洛韦滴眼液的水液浓度。
背景:研究巨细胞病毒(CMV)前节感染患者局部使用 2.0% 更昔洛韦滴眼液后,水样液(AH)中更昔洛韦的含量:这是一项前瞻性、非随机、干预性临床研究。我们招募了活动性巨细胞病毒前节感染患者。患者接受 2.0% 更昔洛韦滴眼液治疗,每 3 小时滴一滴,连续 6 周。第 6 周结束时,使用实时聚合酶链式反应检测角膜前组织中的 CMV 病毒载量,并使用高效液相色谱-质谱法检测角膜前组织中的更昔洛韦浓度。记录基线和治疗后的临床活动和中央角膜厚度(CCT):在研究的 25 位患者的 25 只眼睛中,21 只患有前葡萄膜炎,4 只患有内皮炎。治疗 6 周后,22 只眼睛的前房(AC)没有任何炎症,实时 PCR 检测不到 CMV。三只未遵医嘱患者的眼睛出现了部分反应,前房炎症减轻,AH 中的 CMV 病毒载量减少。AH 中的平均更昔洛韦浓度为 1252.88 ± 2408.82 ng/mL。AH中的更昔洛韦浓度与CCT之间无明显相关性(Spearmen's r = +0.19,p = 0.36):结论:每三小时滴用一次 2.0% 更昔洛韦滴眼液可有效地渗透到巩膜内,AH 中的药物浓度超过了 CMV 复制抑制剂量的 50%。更昔洛韦滴眼液的眼部渗透与角膜厚度无关。
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来源期刊
CiteScore
7.60
自引率
12.50%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Clinical & Experimental Ophthalmology is the official journal of The Royal Australian and New Zealand College of Ophthalmologists. The journal publishes peer-reviewed original research and reviews dealing with all aspects of clinical practice and research which are international in scope and application. CEO recognises the importance of collaborative research and welcomes papers that have a direct influence on ophthalmic practice but are not unique to ophthalmology.
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