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在增生性玻璃体视网膜病变中,从可生物降解聚合物微球持续释放视黄酸。

Sustained delivery of retinoic acid from microspheres of biodegradable polymer in PVR.

作者信息

Giordano G G, Refojo M F, Arroyo M H

机构信息

Schepens Eye Research Institute, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts 02114.

出版信息

Invest Ophthalmol Vis Sci. 1993 Aug;34(9):2743-51.

PMID:8344796
Abstract

PURPOSE

The aims were to obtain a controlled intravitreous release of retinoic acid (RA) by injecting drug loaded microspheres of biodegradable polymers and to study the potential use of this RA delivery system in a rabbit model of proliferative vitreoretinopathy (PVR).

METHODS

The release of RA in vitro from 15 mg of 50-50 poly(DL-lactide-co-glycolide) (PLGA) in 1 ml of water at room temperature was measured with a spectrophotometer. In a rabbit model of PVR, 11 eyes were injected with 5 mg of microspheres containing 22 micrograms of RA/mg of PLGA, and seven control eyes were injected with microspheres of the same polymer that did not contain RA. In a third group, six rabbits were injected with 5 mg (n = 3) and 10 mg (n = 3) of microspheres containing RA.

RESULTS

The initial concentration of RA was 20.8 micrograms/mg of PLGA. The release curve showed a fairly constant daily release of 7 micrograms/d for about 30 days. At 40 days, the release rate decreased to about 6 micrograms/d. After 40 days, 82.8% of the RA was released. Four of 11 treated rabbits (36%) and 7/7 (100%) controls showed tractional retinal detachment (TRD) (P < 0.01) after 2 months. Histopathologically, a mild, localized, foreign body reaction was observed.

CONCLUSIONS

The authors obtained a sustained release of RA from PLGA microspheres in vitro for 40 days. A single injection of RA-loaded microspheres in suspension in BSS was effective in reducing the incidence of TRD after 2 months in a rabbit model of PVR.

摘要

目的

通过注射载有药物的可生物降解聚合物微球来实现视黄酸(RA)在玻璃体内的可控释放,并研究这种RA递送系统在增殖性玻璃体视网膜病变(PVR)兔模型中的潜在用途。

方法

用分光光度计测量15mg 50-50聚(DL-丙交酯-共-乙交酯)(PLGA)在室温下于1ml水中的RA体外释放情况。在PVR兔模型中,11只眼注射含22μg RA/mg PLGA的5mg微球,7只对照眼注射不含RA的相同聚合物微球。在第三组中,6只兔子分别注射5mg(n = 3)和10mg(n = 3)含RA的微球。

结果

RA的初始浓度为20.8μg/mg PLGA。释放曲线显示约30天内每日释放量相当恒定,为7μg/d。40天时,释放速率降至约6μg/d。40天后,82.8%的RA被释放。2个月后,11只治疗兔中有4只(36%)和7只对照兔中的7只(100%)出现牵拉性视网膜脱离(TRD)(P < 0.01)。组织病理学检查发现有轻度、局限性的异物反应。

结论

作者在体外实现了RA从PLGA微球中的持续释放达40天。在PVR兔模型中,单次注射悬浮于平衡盐溶液(BSS)中的载RA微球可有效降低2个月后TRD的发生率。

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