姜黄素抗炎治疗口腔面牙痛的实验研究。

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Devika Tripathi, Ramiza Akram, Raghavendra Kumar, Pranay Wal, Awani Kumar Rai, Vinayak Rai, Tanya Gupta
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引用次数: 0

摘要

背景:口面部粘膜是一种很有吸引力的药物输送途径,可以改善全身和局部治疗。本研究的目的是开发一种载姜黄素亲水固体分散体的口腔牙膜,用于在口腔面部区域持续给药。与其他剂型相比,薄膜是最优雅、最可口、最适合全身粘膜给药的系统。方法:采用2 μ M水杨酸钠为原料,采用亲水固体分散技术提高姜黄素的溶解度,解决姜黄素水溶性差的问题。通过溶剂蒸发形成1:4比例的固体分散体,考察了姜黄素负载体系的体外理化性质。结果:水杨酸钠的分子分散利用显著提高了姜黄素的溶解度和生物利用度。随后,以HPMC和明胶为黏附聚合物,采用溶剂铸造法制备了一种负载亲水固体分散体的口腔牙膜。用HPMC和明胶共混制备了6种不同的膜,膜均匀,颜色偏黄,药物含量均匀度为98.56±3.24,膜厚为0.16 ~ 0.24 mm。薄膜表现出优异的折叠耐力和拉伸强度,提高了患者的适口性。体外研究表明,姜黄素的释放显著增强,在水杨酸钠存在的情况下,姜黄素的释放在7天内达到94.66%的最大值,遵循第一反应动力学。体外渗透cu - f3膜对粘膜粘附有显著影响。结论:在口腔膜制剂中应用滑水剂是一种新的、可持续的通过口腔黏膜给药具有临床意义的姜黄素的方法。因此,它被推荐用于设计其他牙科疾病的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental Investigation into the Anti-inflammatory Properties of Curcumin for Orofacial Dental Pain Management.

Background: The orofacial mucous membrane is an appealing route for drug delivery to improve both systemic and local treatments. The aim of the present study was to develop an oral dental film loaded with curcumin hydrotropic solid dispersion for sustained drug delivery in the orofacial region. Compared to other dosage forms, films are the most elegant, palatable, and suitable systems for systemic mucosal drug delivery.

Methods: A hydrotropic solid dispersion technique utilizing 2 M sodium salicylate was developed to enhance the solubility of curcumin, addressing its poor water solubility. By forming a solid dispersion with a 1:4 ratio through solvent evaporation, the in-vitro physicochemical properties of the curcumin-loaded system were evaluated.

Results: The utilization of sodium salicylate hydrotrope in a molecular dispersion significantly improved the solubility and bioavailability of curcumin. Subsequently, an oral dental film loaded with hydrotropic solid dispersion was developed using the solvent casting method with HPMC and gelatin as mucoadhesive polymers. Six different films were prepared using polymeric blends with HPMC and gelatin, which showed homogeneity, yellowish colour, and high drug content uniformity of 98.56 ± 3.24, with thickness ranging from 0.16 mm to 0.24 mm. The films exhibited excellent folding endurance and tensile strength for improved patient palatability. In-vitro studies demonstrated a significant enhancement in curcumin release, reaching a maximum of 94.66% over seven days in the presence of sodium salicylate hydrotrope, following firstorder kinetics. An ex vivo permeation of Cur-F3 film had a significant effect on mucoadhesion.

Conclusion: Using hydrotropes in oral film formulation is a new and sustainable method for delivering clinically significant curcumin through the oral mucosa. As a result, it is recommended for use in the design of treatments for other dental diseases.

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CiteScore
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