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聚酰胺(PEA)和聚酯(PLGA)微球作为眼内药物传递系统在白化大鼠中的评价。

Evaluation of polyesteramide (PEA) and polyester (PLGA) microspheres as intravitreal drug delivery systems in albino rats.

机构信息

Institute for Ophthalmic Research at the Centre for Ophthalmology, University of Tübingen, Germany.

Department of Ophthalmology, Korea University College of Medicine, Seoul, South Korea.

出版信息

Biomaterials. 2017 Apr;124:157-168. doi: 10.1016/j.biomaterials.2017.02.006. Epub 2017 Feb 7.

Abstract

PURPOSE

To study the suitability of injectable microspheres based on poly(ester amide) (PEA) or poly lactic-co-glycolic acid (PLGA) as potential vehicles for intravitreal drug delivery in rat eyes. Dexamethasone-loaded PEA microspheres (PEA + DEX) were also evaluated.

METHODS

Forty male Sprague Dawley rats were divided into four groups that received different intravitreally injected microspheres: PEA group (n = 12); PLGA group (n = 12); PEA + DEX group (n = 8); and control group (no injection, n = 8). Electroretinography (ERG), fundus autofluorescence (FAF), and spectral domain optical coherence tomography (sdOCT) were performed at baseline, weeks 1 and 2, and months 1, 2, and 3 after intravitreal injection. Eyes were histologically examined using light microscopy and transmission electron microscopy at the end of the in vivo study.

RESULTS

There were no statistically significant changes in ERG among the groups. Abnormal FAF pattern and abnormal deposits in OCT were observed after injection but almost completely disappeared between week 2 and month 3 in all injected groups. GFAP staining showed that Müller glia cell activation was most pronounced in PLGA-injected eyes. Increased cell death was not observed by TUNEL staining at month 1. In electron microscopy at month 3, the remnants of microparticles were found in the retinal cells of all injected groups, and loss of plasma membrane was seen in the PLGA group.

CONCLUSIONS

Although morphological changes such as mild glial activation and material remnants were observed histologically 1 month and 3 months after injection in all injected groups, minor cell damage was noted only in the PLGA group at 3 months after injection. No evidence of functional abnormality relative to untreated eyes could be detected by ERG 3 months after injection in all groups. Changes observed in in vivo imaging such as OCT and FAF disappeared after 3 months in almost all cases.

摘要

目的

研究基于聚酯酰胺(PEA)或聚乳酸-共-羟基乙酸(PLGA)的可注射微球作为潜在的眼内药物输送载体在大鼠眼中的适用性。还评估了负载地塞米松的 PEA 微球(PEA+DEX)。

方法

将 40 只雄性 Sprague Dawley 大鼠分为四组,分别接受不同的眼内注射微球:PEA 组(n=12);PLGA 组(n=12);PEA+DEX 组(n=8);对照组(未注射,n=8)。在眼内注射后基线、第 1 周和第 2 周、第 1、2 和 3 个月进行视网膜电图(ERG)、眼底自发荧光(FAF)和光谱域光相干断层扫描(sdOCT)检查。在体内研究结束时,使用光镜和透射电镜对眼睛进行组织学检查。

结果

各组之间的 ERG 没有统计学上的显著变化。注射后观察到 FAF 模式异常和 OCT 异常沉积,但在所有注射组中,在第 2 周和第 3 月之间几乎完全消失。GFAP 染色显示,PLGA 注射眼的 Müller 胶质细胞激活最为明显。TUNEL 染色在第 1 个月未观察到细胞死亡增加。在第 3 个月的电子显微镜下,在所有注射组的视网膜细胞中都发现了微颗粒的残留物,并且在 PLGA 组中观察到质膜丢失。

结论

尽管在注射后 1 个月和 3 个月所有注射组的组织学观察到形态学变化,如轻度胶质细胞激活和物质残留,但仅在注射后 3 个月的 PLGA 组中观察到轻微的细胞损伤。在所有组中,在注射后 3 个月,通过 ERG 未检测到与未处理眼相比的功能异常。在几乎所有情况下,在 3 个月后,OCT 和 FAF 等体内成像观察到的变化几乎完全消失。

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