Thiolated gellan gum/polyethylene glycol diacrylate hydrogels containing timolol maleate-loaded chitosan nanoparticles for ophthalmic delivery.

Golnaz Shajari, Hamid Erfan-Niya, Marziyeh Fathi, Nazanin Amiryaghoubi
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Abstract

The combination of hydrogels with nanoformulations can significantly enhance the delivery and effectiveness of drugs in ophthalmic drug delivery systems. In the current study, the polyethylene glycol diacrylate (PEGDA)/thiolated gellan gum (GGSH) hydrogels based on GGSH and PEGDA were prepared via thiol-ene reaction using Irgacure 2959 as a photoinitiator. To this end, the modification of GG was achieved by esterification of the hydroxyl groups of GG with the carboxyl group of mercaptopropionic acid with a free thiol amount of 95.5 μmol g-1. To provide sustained release, chitosan nanoparticles (CSNPs) containing timolol maleate (TM) with 56.4% entrapment efficiency were synthesized by the desolvation method and encapsulated in the developed hydrogel. The values of zeta potential and particle size of CSNPs were +26.0 mV and 182.4 nm, respectively. The physico/chemical properties of the hydrogels were investigated via texture analyzer, FT-IR, XRD, and SEM. Thein vitrodegradation, swelling behavior, rheological assessments, cell viability testing, and porosity determination were evaluated. With the increase in PEGDA concentration, the mechanical properties were increased. While the rate of swelling, degradation, and drug release were decreased. Thein vitrobiocompatibility of hydrogels was confirmed using the MTT test. According to anex vivostudy, ocular drug delivery using the obtained transparent hydrogels is promising due to improved drug permeation and sustained release of TM via CSNPs.

含马来酸噻莫洛尔壳聚糖纳米颗粒的硫代结冷胶/聚乙二醇二丙烯酸酯水凝胶。
在眼科给药系统中,水凝胶与纳米制剂的结合可以显著提高药物的递送和有效性。本研究以Irgacure 2959为光引发剂,通过巯基反应制备了基于硫代结冷胶(GGSH)和聚乙二醇二丙烯酸酯(PEGDA)的PEGDA/GGSH水凝胶。为此,在游离硫醇量为95.5 μmol/g的条件下,将结冷胶(GG)的羟基与巯基丙酸的羧基酯化,实现了GG的改性。为获得缓释效果,采用脱溶法制备了具有56.4%包封率的马来酸噻洛尔壳聚糖纳米粒(csnp),并将其包封在水凝胶中。csnp的zeta电位和粒径分别为+26.0 mV和182.4 nm。采用织构仪、FT-IR、XRD、SEM等对水凝胶的理化性质进行了表征。体外降解、膨胀行为、流变学评估、细胞活力测试和孔隙率测定进行了评估。随着PEGDA浓度的增加,材料的力学性能有所提高。同时,溶胀、降解和药物释放速率均有所降低。采用MTT法确定水凝胶的体外生物相容性。根据一项离体研究,使用所获得的透明水凝胶进行眼部给药是有希望的,因为它可以改善药物渗透和通过csnp持续释放TM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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