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已发表论文
对兔子玻璃体内注射聚（乳酸 -乙醇酸）共聚物/聚（乳酸）微球的安全性评估
Authors Rong XF, Yuan WE, Lu Y, Mo XF
Published Date June 2014 Volume 2014:9(1) Pages 3057—3068
DOI http://dx.doi.org/10.2147/IJN.S64100
Received 14 March 2014, Accepted 9 April 2014, Published 24 June 2014
Abstract: Poly(lactic-co-glycolic acid) (PLGA) and/or poly(lactic-acid) (PLA) microspheres are important drug delivery systems. This study investigated eye biocompatibility and safety of PLGA/PLA microspheres through intravitreal injection in rabbits. Normal New Zealand rabbits were randomly selected and received intravitreal administration of different doses (low, medium, or high) of PLGA/PLA microspheres and erythropoietin-loaded PLGA/PLA microspheres. The animals were clinically examined and sacrificed at 1, 2, 4, 8, and 12 weeks postadministration, and retinal tissues were prepared for analysis. Retinal reactions to the microspheres were evaluated by terminal deoxynucleotidyl transferase-mediated dUTP nick end staining and glial fibrillary acidic protein immunohistochemistry. Retinal structure changes were assessed by hematoxylin and eosin staining and transmission electron microscopy. Finally, retinal function influences were explored by the electroretinography test. Terminal deoxynucleotidyl transferase-mediated dUTP nick end staining revealed no apoptotic cells in the injected retinas; immunohistochemistry did not detect any increased glial fibrillary acidic protein expression. Hematoxylin and eosin staining and transmission electron microscopy revealed no micro- or ultrastructure changes in the retinas at different time points postintravitreal injection. The electroretinography test showed no significant influence of scotopic or photopic amplitudes. The results demonstrated that PLGA/PLA microspheres did not cause retinal histological changes or functional damage and were biocompatible and safe enough for intravitreal injection in rabbits for controlled drug delivery.
Keywords: PLGA/PLA microspheres, intravitreal injection, posterior segment diseases, biocompatibility
Keywords: PLGA/PLA microspheres, intravitreal injection, posterior segment diseases, biocompatibility
