苯佐卡因口腔溃疡膜的设计与表征

J. Jose, M. V. Sisira, M. Prasanth, C. Prasanth, P. Pradeep
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引用次数: 0

摘要

口腔溃疡是近年来非常常见的疾病,它是由于上皮组织和/或固有层的损伤而最终导致组织坏死。苯佐卡因具有良好的局部麻醉效果,可减轻口腔溃疡引起的疼痛,已被用于治疗口腔溃疡。因此,本研究试图研制苯佐卡因治疗口腔溃疡的口腔膜,并对其进行表征,以期延长药物释放时间,提高患者使用的方便性。采用壳聚糖黏附聚合物和hpmc溶剂铸造法制备膜,研究膜的物理力学特性、体外药物释放特性和体外口腔粘膜渗透特性。制备的薄膜配方光滑,几乎不透明,柔韧性好。所有配方的重量和厚度都是均匀的。膜中药物含量在97 ~ 99%之间,具有良好的载药量和均匀性。HPMC包合显著降低壳聚糖膜的生物黏附强度和体外黏附时间,但肿胀程度增加。体外药物释放和在模拟唾液中的渗透研究表明,所有制剂的释放时间都延长了6小时。以壳聚糖:HPMC比例为1:1、10% w/w聚山梨酯80和10% w/w丙二醇为增塑剂的配方效果最佳,6 h的累积释药率为87.9%,累计释药量为7.62mg/ cm2。采用DSC和FT-IR技术对药物与辅料的相互作用进行了研究;薄膜显示药物和聚合物之间没有化学相互作用。
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Design and Characterization of Buccal Films of Benzocaine for Mouth Ulcer
Mouth ulcer is very common in recent years, which occurs due to the damage of epithelial tissue and/or lamina propria that finally leads to tissue necrosis. Benzocaine has been used to treat the mouth ulcers due to its excellent local anaesthetic effect that relieves the pain associated with mouth ulcer. Hence an attempt was made to develop and characterize the buccal films of Benzocaine to treat mouth ulcers with an aim of prolonging the drug release and improving the patient convenience. The films were fabricated using the mucoadhesivepolymerblendofchitosanandHPMCbysolventcastingmethodandthephysico-mechanical, in vitro drug release and ex vivo buccal mucosal permeation characteristics of the films were studied. All fabricated film formulations prepared were smooth and almost opaque, with good flexibility. The weight and thickness of all the formulations were found to be uniform. Drug content in the films ranged from 97–99%, indicating favorable drug loading and uniformity. The inclusion of HPMC, significantly reduced the bioadhesive strength and in vitro mucoadhesion time of chitosan films, although the degree of swelling increased. In vitro drug release and permeation studies in simulated saliva showed a prolonged release for a period of 6 h for all formulations. The formulation with Chitosan: HPMC ratio 1:1, 10% w/w polysorbate 80 and 10% w/w propylene glycol as plasticizers showed the best results which exhibited the cumulative percentagedrugreleaseof87.9%andthecumulativeamountofdrugpermeationof7.62mg/cm 2 acrossgoat buccal mucosa in 6 h. Drug-excipient interaction studies were carried out using DSC and FT-IR technique; films indicated no chemical interaction between drug and polymers used.
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