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Evaluation of the Toxicity of Intravitreally Injected PLGA Microspheres and Rods in Monkeys and Rabbits: Effects of Depot Size on Inflammatory Response

机译:猴子和兔子玻璃体内注射PLGA微球和棒的毒性评估:储库大小对炎症反应的影响

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Purpose: Poly(lactic-co-glycolic) acid (PLGA) inserts have been successfully developed for the treatment of posterior eye disease as a means of reducing injection frequency of intravitreally administered therapeutics. PLGA microspheres are also of interest for the delivery of intravitreal drugs, since they offer the advantage of being easily injected without surgical procedures or large injectors. Methods: In the current study, the toxicity of PLGA microspheres and rods was investigated in nonhuman primates (NHPs) and rabbits. An in vitro assessment of cytokine responses to PLGA in peripheral blood mononuclear cells (PBMCs) and macrophages was also performed. Results: Intravitreal administration of 3, 10, or 12.5 mg/eye of PLGA microspheres in NHPs resulted in a severe immune response characterized by a foreign body response. Follow-up studies in the rabbit confirmed this finding for PLGA microspheres ranging in size from 20 to 100 ??m. In contrast, administration of PLGA rod implants with a similar PLGA mass did not elicit a significant immune response. In vitro assays in PBMCs and macrophages confirmed proinflammatory cytokine release upon treatment with PLGA microspheres but not PLGA rods. Conclusions: These data demonstrate a lack of tolerability of PLGA microspheres upon intravitreal injection, and suggest that the size, shape, and/or surface area of PLGA depots are critical attributes in determining ocular toxicity.
机译:目的:聚乳酸-乙醇酸(PLGA)插件已成功开发用于治疗眼后部疾病,作为减少玻璃体内给药治疗剂注射频率的手段。 PLGA微球对于玻璃体内药物的输送也很感兴趣,因为它们具有无需手术程序或大型注射器即可轻松注射的优势。方法:在本研究中,研究了PLGA微球和棒对非人类灵长类动物(NHP)和兔子的毒性。还进行了外周血单核细胞(PBMC)和巨噬细胞对PLGA的细胞因子反应的体外评估。结果:在NHP中玻璃体内施用3、10或12.5 mg /眼的PLGA微球会导致严重的免疫反应,其特征是异物反应。在兔子中的后续研究证实了这一发现,适用于大小为20至100μm的PLGA微球。相反,给予具有相似PLGA质量的PLGA杆植入物并没有引起明显的免疫反应。 PBMC和巨噬细胞的体外测定证实,用PLGA微球而非PLGA棒处理后促炎性细胞因子释放。结论:这些数据表明玻璃体内注射后PLGA微球缺乏耐受性,并且表明PLGA贮库的大小,形状和/或表面积是确定眼毒性的关键属性。

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