Manna Soumyarwit, Donnell Anna M, Faraj Rafaela Q Caixeta, Riemann Blanca I, Riemann Christopher D, Augsburger James J, Correa Zelia M, Banerjee Rupak K
Department of Mechanical and Materials Engineering, University of Cincinnati, Cincinnati, OH 45221, USA.
Department of Chemistry, University of Cincinnati, Cincinnati, OH 45221, USA.
Pharmaceutics. 2021 Aug 9;13(8):1227. doi: 10.3390/pharmaceutics13081227.
The present research investigates the pharmacokinetics and toxicity of a chitosan (CS) and poly(lactic-co-glycolic) acid (PLGA)-based methotrexate (MTX) intravitreal micro-implant in normal rabbit eyes. PLGA and CS-based micro-implants containing 400 µg of MTX were surgically inserted in the vitreous of twenty-four New Zealand rabbits using minimally invasive procedures. The PLGA-coated CS-MTX micro-implant and the placebo micro-implant were inserted in the right eye and in the left eye, respectively, of each rabbit. The intravitreal MTX concentration was evaluated on Days 1, 3, 7, 14, 28 and 56. A therapeutic concentration of MTX (0.1-1.0 µM) in the rabbit vitreous was observed for 56 days. The release of MTX in the therapeutic release phase followed first-order kinetics. Histopathologic evaluation on Days 14, 28 and 56 of the enucleated eyes demonstrated no signs of toxicity or any anatomical irregularity in the vitreoretinal domain. Additionally, the micro-implants were stationary at the position of their implantation throughout the duration of the study. The PLGA-coated CS-MTX micro-implant can serve as a potential alternative to the current treatment modality of intravitreal MTX injections based on its performance, thereby avoiding associated complications and the treatment burden of multiple injections.
本研究调查了一种基于壳聚糖(CS)和聚乳酸-羟基乙酸共聚物(PLGA)的甲氨蝶呤(MTX)玻璃体内微植入物在正常兔眼中的药代动力学和毒性。采用微创方法,将含有400μg MTX的PLGA和CS基微植入物手术植入24只新西兰兔的玻璃体中。将PLGA包被的CS-MTX微植入物和安慰剂微植入物分别植入每只兔子的右眼和左眼。在第1、3、7、14、28和56天评估玻璃体内MTX浓度。在兔玻璃体中观察到MTX的治疗浓度(0.1 - 1.0μM)持续56天。MTX在治疗释放阶段的释放遵循一级动力学。对摘除眼球在第14、28和56天进行的组织病理学评估表明,在玻璃体视网膜区域没有毒性迹象或任何解剖学异常。此外,在整个研究期间,微植入物在其植入位置保持固定。基于其性能,PLGA包被的CS-MTX微植入物可作为目前玻璃体内注射MTX治疗方式的潜在替代方法,从而避免相关并发症和多次注射的治疗负担。