Chitosan-coated bovine serum albumin nanoparticles for topical tetrandrine delivery in glaucoma: in vitro and in vivo assessment.

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Salma El-Sayed Radwan, Riham M El-Moslemany, Radwa A Mehanna, Eman H Thabet, Elsayeda-Zeinab A Abdelfattah, Amal El-Kamel
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Abstract

Glaucoma is one of the leading causes of blindness. Therapies available suffer from several drawbacks including low bioavailability, repeated administration and poor patient compliance with adverse effects thereafter. In this study, bovine serum albumin nanoparticles (BSA-NPs) coated with chitosan(CS) were developed for the topical delivery of tetrandrine (TET) for glaucoma management. Optimized nanoparticles were prepared by desolvation. pH, BSA, CS and cross-linking agent concentrations effects on BSA-NPs colloidal properties were investigated. CS-BSA-NPs with particle size 237.9 nm and zeta potential 24 mV was selected for further evaluation. EE% exceeded 95% with sustained release profile. In vitro mucoadhesion was evaluated based on changes in viscosity and zeta potential upon incubation with mucin. Ex vivo transcorneal permeation was significantly enhanced for CS coated formulation. In vitro cell culture studies on corneal stromal fibroblasts revealed NPs biocompatibility with enhanced cellular uptake and improved antioxidant and anti-proliferative properties for the CS-coated formulation. Moreover, BSA-NPs were nonirritant as shown by HET-CAM test. Also, bioavailability in rabbit aqueous humor showed 2-fold increase for CS-TET-BSA-NPs compared to TET with a sustained reduction in intraocular pressure in a rabbit glaucoma model. Overall, results suggest CS-BSA-NPs as a promising platform for topical ocular TET delivery in the management of glaucoma.

壳聚糖包被的牛血清白蛋白纳米粒子用于青光眼局部给药粉防己碱的体内外评价
摘要青光眼是导致失明的主要原因之一。现有的治疗方法有几个缺点,包括生物利用度低、重复给药以及患者对不良反应的依从性差。在本研究中,开发了用壳聚糖(CS)包裹的牛血清白蛋白纳米颗粒(BSA-NPs),用于局部递送粉防己碱(TET)治疗青光眼。通过去溶剂化制备了优化的纳米颗粒。研究了pH、BSA、CS和交联剂浓度对BSA纳米粒子胶体性质的影响。CS BSA NPs,粒径237.9 nm和ζ电位24 选择mV进行进一步评估。持续释放的EE%超过95%。基于与粘蛋白孵育时粘度和ζ电位的变化来评估体外粘膜粘附。CS涂层制剂的离体经角膜渗透显著增强。对角膜基质成纤维细胞的体外细胞培养研究显示,CS涂层制剂具有增强的细胞摄取和改善的抗氧化和抗增殖特性的NPs生物相容性。此外,如HET-CAM测试所示,BSA NP是无刺激性的。此外,在兔青光眼模型中,与TET相比,CS TET BSA NP在兔房水中的生物利用度增加了2倍,眼压持续降低。总之,研究结果表明CS BSA NPs是一种很有前途的青光眼局部眼部TET递送平台。
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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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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