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眼内给予含环孢素 A 的纳米脂质体的安全性评价。

Safety evaluation of nanoliposomes containing cyclosporine a after ocular administration.

机构信息

Department of Pharmaceutics, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Curr Eye Res. 2012 Jun;37(6):453-6. doi: 10.3109/02713683.2012.660595.

Abstract

AIM

Cyclosporine A (CyA) is an anti inflammatory drug which modulates immune system. We prepared two liposomal formulations of CyA for ophthalmic administration. In the present study, the safety of these formulations was tested in rabbits.

MATERIALS AND METHODS

Fusogenic and positively charged liposomes were prepared by solvent evaporation method. CyA concentration in ophthalmic preparations was 0.2% w/v. Twenty New Zealand albino rabbits (40 eyes) were divided into two groups. Right eyes were treated and left eyes served as control. Eyes were examined clinically in 1, 3, 7, 14 and 28th days of the study. Eleven eyes were enucleated for pathological evaluation at the end of the study.

RESULTS

Mean size and charge of positively charged and fusogenic liposomes were 110.7 ± 1.5 and 114.9 ± 15.2 nm; 19.0 ± 2.2 and 2.5 ± 0.5 mV, respectively. Clinically, there were transient conjunctival injections and corneal epithelial defects in a few cases which were not limited to the treated eyes. Positively charged liposomes caused conjunctival injection in two cases, while this complication occurred in only one eye after administration of fusogenic liposomes. Histopathological examination revealed the presence of follicular conjunctivitis in two eyes with conjunctival injection. Inflammation in cases received the fusogenic form of the drug was mild and non-specific.

CONCLUSIONS

The results of this study suggest that fusogenic liposomal preparation of CyA is safe and can be useful for future studies.

摘要

目的

环孢素 A(CyA)是一种具有免疫调节作用的抗炎药物。我们制备了两种用于眼部给药的 CyA 脂质体制剂。本研究旨在测试这些制剂在兔子体内的安全性。

材料和方法

采用溶剂蒸发法制备融合性和正电荷脂质体。眼部制剂中 CyA 的浓度为 0.2%(w/v)。将 20 只新西兰白兔(40 只眼)分为两组。右眼治疗,左眼作为对照。在研究的第 1、3、7、14 和 28 天对眼睛进行临床检查。研究结束时,11 只眼睛被摘除进行病理评估。

结果

正电荷和融合性脂质体的平均粒径和电荷分别为 110.7±1.5nm 和 114.9±15.2nm;19.0±2.2mV 和 2.5±0.5mV。临床上,少数情况下会出现短暂的结膜充血和角膜上皮缺损,但不限于治疗眼。正电荷脂质体在 2 例中引起结膜充血,而融合性脂质体给药后仅 1 只眼出现此并发症。组织病理学检查显示,结膜注射的 2 只眼中存在滤泡性结膜炎。接受融合性药物制剂的病例炎症较轻且非特异性。

结论

本研究结果表明,CyA 的融合性脂质体制剂安全且可用于进一步研究。

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