口腔给药
口腔粘膜下纤维性变
没食子酸表没食子酸酯
体内
渗透
化学
离体
Zeta电位
药理学
纤维化
黏膜黏附
纳米颗粒
药物输送
体外
毒品携带者
医学
材料科学
膜
纳米技术
病理
生物化学
有机化学
多酚
抗氧化剂
生物技术
生物
作者
Chetan Hasmukh Mehta,Varalakshmi Velagacherla,Suman Manandhar,Yogendra Nayak,K. Sreedhara Ranganath Pai,Shruthi Acharya,Usha Y. Nayak
出处
期刊:Aaps Pharmscitech
[Springer Science+Business Media]
日期:2024-03-22
卷期号:25 (4): 66-66
被引量:6
标识
DOI:10.1208/s12249-024-02787-w
摘要
Oral submucous fibrosis (OSF) is a chronic progressive disease associated with increased collagen deposition and TGF-β1 release. The current therapy and management have been a limited success due to low efficacy and adverse drug reactions. This study aimed to evaluate epigallocatechin 3-gallate (EGCG) encapsulated nanoparticles loaded mucoadhesive hydrogel nanocomposite (HNC) for OSF. Developed HNC formulations were evaluated for their permeation behaviour using in vitro as well as ex vivo studies, followed by evaluation of efficacy and safety by in vivo studies using areca nut extract-induced OSF in rats. The disease condition in OSF-induced rats was assessed by mouth-opening and biochemical markers. The optimized polymeric nanoparticles exhibited the required particle size (162.93 ± 13.81 nm), positive zeta potential (22.50 ± 2.94 mV) with better mucoadhesive strength (0.40 ± 0.002 N), and faster permeation due to interactions of the positively charged surface with the negatively charged buccal mucosal membrane. HNC significantly improved disease conditions by reducing TGF-β1 and collagen concentration without showing toxicity and reverting the fibroid buccal mucosa to normal. Hence, the optimized formulation can be further tested to develop a clinically alternate therapeutic strategy for OSF.
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