Arabi Mahshid, Mortazavi Seyed Alireza, Jafariazar Zahra, Farhadnejad Hassan, Alipour Harisa Golnoosh, Fatahi Yousef
Department of Pharmaceutics, Faculty of Pharmacy, Islamic Azad University, Tehran, Iran.
Department of Pharmaceutics and Pharmaceutical Nanotechnology, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Iran J Pharm Res. 2020 Summer;19(3):63-76. doi: 10.22037/ijpr.2019.111820.13378.
In this study, buccal mucoadhesive tablets of meloxicam were formulated for drug delivery as an alternative route. Direct compression method was applied for the preparation of tablets. Also, different polymers, including hydroxypropyl methyl cellulose (HPMC) 1000, 4000, and 10000, as well as carbopol 934p and carbopol 971p were used as the mucoadhesive polymer and retardant polymer. Thirteen formulations were investigated with various concentrations of polymers. The physicochemical characteristics, drug release, swelling index, and taste modification of tablets were evaluated. Also, Carr's index and Hausner ratio were studied. In addition, zero-order, first-order, and Higuchi kinetics were investigated and the results showed that the highest correlation coefficient (R) is related to zero-order kinetic for formulations B and B. Furthermore, the highest R is related to Higuchi kinetic for formulation C. Formulation B showed the maximum release of 99% in 12 h. The results demonstrated that Formulation B can be considered as a proper buccal mucoadhesive tablet of meloxicam with desired property.
在本研究中,制备了美洛昔康口腔黏膜黏附片作为一种替代给药途径。采用直接压片法制备片剂。此外,不同的聚合物,包括羟丙基甲基纤维素(HPMC)1000、4000和10000,以及卡波姆934p和卡波姆971p被用作黏膜黏附聚合物和阻滞剂聚合物。研究了13种不同聚合物浓度的制剂。对片剂的理化特性、药物释放、溶胀指数和口感改良进行了评估。此外,还研究了卡尔指数和豪斯纳比。另外,对零级、一级和 Higuchi 动力学进行了研究,结果表明,制剂B和B的最高相关系数(R)与零级动力学相关。此外,制剂C的最高R与Higuchi动力学相关。制剂B在12小时内显示出99%的最大释放率。结果表明,制剂B可被认为是一种具有所需特性的合适的美洛昔康口腔黏膜黏附片。