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Formulation and evaluation of mucoadhesive buccal tablets of aceclofenac

机译:丙伯芬酸粘膜粘附性口腔片的配制与评价

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摘要

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.
机译:该项目旨在配制和表征含有嘧素的粘膜粘附性口腔片,利用不同比例的三种聚合物Carbopol 934,羟丙基甲基纤维素和羧甲基纤维素钠。通过直接压缩方法制备12批BucoCoadghersive aceClofenac。然后评估压缩片剂,用于物理化学参数,如硬度,厚度,重量变异,药物含量,脆性,溶胀指数,表面pH和离体粘膜。在PH 7.4的磷酸盐缓冲液中使用旋转桨叶方法,在印度药典2018下进行体外溶解试验12小时。物理化学参数,如体重变化(231.25-268.75mg),硬度(8.32-11.56千克),脆性(0.04-0.2%),直径(9.00 mm),厚度(3.8-4.05 mm)和药物含量(97.67-102.25 %)在2018年的印度药典中的可接受限度内。据报道,肿胀指数在8小时的范围内为112.93-450.19%。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)随着聚合物浓度的变化而变化,特别是Carbopol 934.所有批次的溶出曲线大大变化,最大释放为109.41%(在6小时的批量12)至最低释放44.82% (在12小时的批次3)。其中,只有批次1确保持续和有效的药物释放(12小时,88.34%),具有适当的溶胀指数(112.93%)和粘膜粘附强度(40g)。傅里叶变换红外光谱分析显示没有药物赋形剂相互作用的证据。因此,结果得出结论,颊米卡可以配制ESIVE醋氯芬酸片剂。此外,平板电脑的性质不仅取决于浓度,还取决于所用聚合物的行为。

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