Universidade da Coruña, Grupo de Polímeros, Departamento de Física y Ciencias de la Tierra, Escuela Universitaria Politécnica, Serantes, Avda. 19 de Febrero s/n, 15471 Ferrol, Spain; Cellular and Molecular Cardiology Research Unit, Institute of Biomedical Research (IDIS-SERGAS), University Clinical Hospital, Santiago de Compostela, Spain.
Universidade da Coruña, Grupo de Polímeros, Departamento de Física y Ciencias de la Tierra, Escuela Universitaria Politécnica, Serantes, Avda. 19 de Febrero s/n, 15471 Ferrol, Spain.
Int J Pharm. 2019 Sep 10;568:118519. doi: 10.1016/j.ijpharm.2019.118519. Epub 2019 Jul 13.
Poly-(3-hydroxybutyrate-co-3-hydroxyvalerate) nanoparticles (PHBV-NPs) to encapsulate hydrocortisone (HC) for topical ophthalmic administration were prepared and characterized. The technique used to prepare the nanoparticles (NPs) was emulsification/solvent evaporation. The obtained size was 237.3 ± 2.7 nm, suitable for topical ocular administration. The obtained results for the entrapment efficiency were between 1 and 2.5% and for the drug loading were around 0.5%. The release behaviour of HC from the PHBV-NPs was also analyzed, adjusting this to a Higuchi kinetic model. For the new drug delivery system developed the ocular toxicity profile was determined by viability studies carried out on bovine keratocytes, by a Hen's Egg Test - Chorioallantoic Membrane (HET-CAM) and by a Bovine Corneal Opacity and Permeability assay (BCOP). The obtained results concluded that the new system is no cytotoxic on bovine keratocytes and is neither irritating nor produces any alteration in the transparency and in the permeability of the cornea. Confocal studies were also performed and confirmed that PHBV-NPs are able to penetrate efficiently into the corneal tissue. This novel PHBV-based drug delivery system could be a good option for topical ophthalmic administration of drugs.
聚(3-羟基丁酸酯-共-3-羟基戊酸酯)纳米粒(PHBV-NPs)被用于包封氢化可的松(HC)以用于局部眼科给药,并对其进行了制备和特性研究。所采用的制备纳米粒(NPs)的技术为乳化/溶剂蒸发法。所获得的 NPs 粒径为 237.3±2.7nm,适用于局部眼部给药。所获得的包封效率结果在 1%至 2.5%之间,载药量约为 0.5%。还分析了 HC 从 PHBV-NPs 中的释放行为,并将其调整到 Higuchi 动力学模型。对于所开发的新药物递送系统,通过在牛角膜细胞上进行的活力研究、通过鸡胚绒毛尿囊膜(HET-CAM)和牛角膜混浊和通透性测定(BCOP)来确定其眼部毒性概况。所得结果表明,新系统对牛角膜细胞无细胞毒性,既不刺激也不改变角膜的透明度和通透性。还进行了共聚焦研究,证实 PHBV-NPs 能够有效地穿透角膜组织。这种新型基于 PHBV 的药物递送系统可能是局部眼科递药的一个很好的选择。