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醋氯芬酸黏膜黏附口腔片的制剂与评价

Formulation and evaluation of mucoadhesive buccal tablets of aceclofenac.

作者信息

Koirala Santosh, Nepal Prabin, Ghimire Govinda, Basnet Rojina, Rawat Ishwori, Dahal Aashma, Pandey Jitendra, Parajuli-Baral Kalpana

机构信息

Department of Pharmaceutical Sciences, School of Health and Allied Sciences, Pokhara University, Kaski, 33370, Nepal.

Department of Pharmacy, Nepal Medical College, Kohalpur Banke, Nepal.

出版信息

Heliyon. 2021 Mar 15;7(3):e06439. doi: 10.1016/j.heliyon.2021.e06439. eCollection 2021 Mar.

Abstract

This project was aimed to formulate and characterize mucoadhesive buccal tablets of aceclofenac, utilizing different proportions of three polymers carbopol 934, hydroxypropyl methylcellulose, and sodium carboxymethylcellulose. Twelve batches of buccoadhesive aceclofenac were prepared by the direct compression method. The compressed tablets were then evaluated for physicochemical parameters such as hardness, thickness, weight variation, drug content, friability, swelling index, surface pH, and ex vivo mucoadhesion. In vitro dissolution test was conducted for 12 h according to Indian Pharmacopeia 2018, using the rotating paddle method in phosphate buffer of pH 7.4. Physiochemical parameters like weight variation (231.25-268.75 mg), hardness (8.32-11.56 kg), friability (0.04-0.2%), diameter (9.00 mm), thickness (3.8-4.05 mm), and drug content ((97.67-102.25%) were within the acceptable limit as per Indian Pharmacopeia 2018. The swelling index was reported to be in the range of 112.93-450.19%, at 8 h. The surface pHs of all the batches were in between 6.72 to 6.96. The mucoadhesive strengths (40.5-50 g) varied with the change in polymer concentrations especially of carbopol 934. The dissolution profile of all the batches varied greatly, with a maximum release of 109.41% (in batch 12 at 6 h) to a minimum release of 44.82% (in batch 3 at 12 h). Among them, only batch 1 ensured sustained and effective drug release (88.34% at 12 h) with appropriate swelling index (112.93%) and mucoadhesive strength (40 g). Fourier Transform Infrared Spectroscopy analysis showed no evidence of drug excipients interaction. Hence, the results concluded that buccal mucoadhesive aceclofenac tablets can be formulated. Furthermore, the property of the tablet not only depends on the concentration but also the behavior of the polymers used.

摘要

本项目旨在利用卡波姆934、羟丙基甲基纤维素和羧甲基纤维素钠三种聚合物的不同比例,制备醋氯芬酸的粘膜粘附口腔片并对其进行表征。采用直接压片法制备了12批口腔粘附性醋氯芬酸片。然后对压制片进行物理化学参数评估,如硬度、厚度、重量差异、药物含量、脆碎度、溶胀指数、表面pH值和体外粘膜粘附性。根据《印度药典2018》,使用旋转桨法在pH 7.4的磷酸盐缓冲液中进行12小时的体外溶出试验。物理化学参数如重量差异(231.25 - 268.75毫克)、硬度(8.32 - 11.56千克)、脆碎度(0.04 - 0.2%)、直径(9.00毫米)、厚度(3.8 - 4.05毫米)和药物含量(97.67 - 102.25%)均在《印度药典2018》规定的可接受限度内。据报道,8小时时溶胀指数在112.93 - 450.19%范围内。所有批次的表面pH值在6.72至6.96之间。粘膜粘附强度(40.5 - 50克)随聚合物浓度的变化而变化,尤其是卡波姆934的浓度。所有批次的溶出曲线差异很大,最大释放率为109.41%(第12批在6小时),最小释放率为44.82%(第3批在12小时)。其中,只有第1批确保了持续有效的药物释放(12小时时为88.34%),具有适当的溶胀指数(112.93%)和粘膜粘附强度(40克)。傅里叶变换红外光谱分析表明没有药物辅料相互作用的证据。因此,结果表明可以制备口腔粘膜粘附性醋氯芬酸片。此外,片剂的性质不仅取决于浓度,还取决于所用聚合物的性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7677/7988282/f21566d1cdcf/gr1.jpg

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