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通过一种新的微囊化方法制备的 GDNF/Vit E-PLGA 微球对青光眼模型中海马神经节细胞的存活作用。

Retinal ganglion cells survival in a glaucoma model by GDNF/Vit E PLGA microspheres prepared according to a novel microencapsulation procedure.

机构信息

Dept. of Pharmacy and Pharmaceutical Technology, School of Pharmacy, Complutense University, Avda. Complutense s/n, Madrid, Spain.

出版信息

J Control Release. 2011 Nov 30;156(1):92-100. doi: 10.1016/j.jconrel.2011.06.023. Epub 2011 Jun 24.

Abstract

The present experimental work describes the use of a novel protein encapsulation method to achieve protection of the biological factor during the microencapsulation procedure. With this aim, the protein is included in poly(lactic-co-glycolic acid) (PLGA) microspheres without any preliminary manipulation, in contrast to the traditional S/O/W (solid-in-oil-in-water) method where the bioactive substance is first dissolved and then freeze-dried in the presence of lyoprotectors. Furthermore, the presented technique involves the use of an oily additive, vitamin E (Vit E), useful from a technological point of view, by promoting additional protein protection and also from a pharmacological point of view, because of its antioxidant and antiproliferative properties. Application of this microencapsulation technique has been performed for GDNF (glial cell line-derived neurotrophic factor) designed for the treatment of optic nerve degenerative diseases, such as glaucoma, the second leading cause of blindness in the western world. The protein was released in vitro in its bioactive form for more than three months, demonstrated by the survival of their potential target cells (photoreceptors and retinal ganglion cells (RGC)). Moreover, the intravitreal injection of GDNF/Vit E PLGA microspheres in an experimental animal model of glaucoma significantly increased RGC survival compared with GDNF, Vit E or blank microspheres (p<0.01). This effect was present for at least eleven weeks, which suggests that the formulation prepared may be clinically useful as a neuroprotective tool in the treatment of glaucomatous optic neuropathy.

摘要

本实验工作描述了一种新的蛋白质包封方法,用于在微囊化过程中保护生物因子。为此,目的蛋白被包含在聚(乳酸-共-乙醇酸)(PLGA)微球中,而无需进行任何初步操作,与传统的 S/O/W(固体在油中-在水中)方法形成对比,其中生物活性物质首先溶解,然后在冷冻保护剂存在下冻干。此外,所提出的技术涉及使用油溶性添加剂,维生素 E(Vit E),从技术角度来看是有用的,因为它可以促进额外的蛋白质保护,并且从药理学角度来看,因为它具有抗氧化和抗增殖特性。该微囊化技术已应用于 GDNF(胶质细胞系衍生的神经营养因子),用于治疗视神经退行性疾病,如青光眼,这是西方世界第二大致盲原因。体外实验证明,蛋白质以其生物活性形式释放了超过三个月,其潜在的靶细胞(光感受器和视网膜神经节细胞(RGC))得以存活。此外,在青光眼实验动物模型中玻璃体内注射 GDNF/Vit E PLGA 微球可显著增加 RGC 存活,与 GDNF、Vit E 或空白微球相比(p<0.01)。这种作用至少持续了 11 周,这表明所制备的制剂可能作为治疗青光眼视神经病变的神经保护工具在临床上是有用的。

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