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部分视网膜破坏和胶质增生对HPMPC玻璃体内药代动力学的影响。

Effect of partial retinal destruction and gliosis on the intravitreal pharmacokinetics of HPMPC.

作者信息

Kim J W, el-Haig W, Capparelli E V, Besen G, Connor J D, Freeman W R

机构信息

Department of Ophthalmology, University of California-San Diego School of Medicine, USA.

出版信息

Retina. 1995;15(6):513-7. doi: 10.1097/00006982-199515060-00010.

DOI:10.1097/00006982-199515060-00010
PMID:8747447
Abstract

PURPOSE

Intravitreal HPMPC ([S]-1-[3-hydroxy-2 phosphonylmethoxypropyl cytosine) has a long antiviral effect in patients with cytomegalovirus retinitis. The authors evaluated the pharmacokinetics of intravitreal injections of HPMPC to understand major route of HPMPC elimination in a pigmented rabbit that had undergone scatter laser photocoagulation over half of the retinal surface.

METHODS

The authors treated the inferior half of the retina, receiving an average of 605 grade 3 or 4 (gray-white or white) diode laser burns in a scatter fashion in the left eyes of 13 rabbits. After 4 weeks, 13 rabbits received intravitreal injection of HPMPC (100 micrograms in 0.1 mL) in both eyes. Forty-eight hours after injection, unfixed vitreous samples were obtained for high-pressure liquid chromatography analysis. Two rabbits were used for light microscopic examination of diode laser photocoagulated retina with the perfusion fixation.

RESULTS

The HPMPC concentration in the vitreous was 5.93 +/- 1.75 micrograms/mL in the laser-treated group and 4.76 +/- 1.2 micrograms/mL in the control group 48 hours after intravitreal HPMPC injection. The difference was statistically different (P = 0.037).

CONCLUSIONS

Results showed a higher concentration of intravitreal HPMPC in the eye that had approximately 25% of the retina destroyed by the laser photocoagulation. The higher concentration is likely the result of reduced elimination and a concomitant increase in half-life. This suggests that HPMPC may be eliminated via the retinal route. Eyes with more extensive retinal involvement with human cytomegalovirus may have an even longer duration of action of intravitreal HPMPC. This may lead to modification of dosing regimens.

摘要

目的

玻璃体内注射HPMPC([S]-1-[3-羟基-2-膦酰甲氧基丙基]胞嘧啶)对巨细胞病毒性视网膜炎患者具有长效抗病毒作用。作者评估了玻璃体内注射HPMPC的药代动力学,以了解在视网膜表面一半接受了散射激光光凝的有色兔中HPMPC的主要消除途径。

方法

作者对13只兔的左眼视网膜下半部进行治疗,以散射方式平均接受605次3级或4级(灰白色或白色)二极管激光灼伤。4周后,13只兔双眼均接受玻璃体内注射HPMPC(0.1 mL中含100微克)。注射后48小时,获取未固定的玻璃体样本进行高压液相色谱分析。使用2只兔对二极管激光光凝的视网膜进行灌注固定后进行光镜检查。

结果

玻璃体内注射HPMPC后48小时,激光治疗组玻璃体中HPMPC浓度为5.93±1.75微克/毫升,对照组为4.76±1.2微克/毫升。差异有统计学意义(P = 0.037)。

结论

结果显示,在约25%的视网膜被激光光凝破坏的眼中,玻璃体内HPMPC浓度较高。较高的浓度可能是消除减少和半衰期相应延长的结果。这表明HPMPC可能通过视网膜途径消除。人类巨细胞病毒累及视网膜范围更广的眼睛,玻璃体内HPMPC的作用持续时间可能更长。这可能会导致给药方案的调整。

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