Characterization and evaluation of the fruit mucilage of Cordia africana as tablet binder in paracetamol tablet formulation: optimization study

对非洲紫菀果实粘液作为扑热息痛片剂粘合剂的特性进行表征和评价:优化研究

阅读:4

Abstract

Several studies have revealed that the fruit mucilage of different species of Cordia is found to be an excellent binder in tablet manufacturing. However, the binding ability of the mucilage of Cordia Africana (CM) is not yet established. Therefore, this study aimed to evaluate the tablet-binding ability of the CM using paracetamol as a model drug. The fruit of Cordia Africana was extracted with the maceration technique and characterized for different properties, such as its compatibility with the model drug (paracetamol) using the Fourier transform infrared spectroscopy (FTIR) and its crystallinity nature with X-ray Diffractometer (XRD). Granules were prepared using the wet granulation method and compressed into tablets. The prepared tablets were evaluated for their hardness, disintegration time, friability, and drug release profile. The effect of these independent variables was further studied and optimized using the central composite design (CCD). The yield of extracted CM powder was 29%. The FTIR study revealed that the CM is compatible with the model drug. The loss in drying and moisture sorption studies was 6 ± 0.02% and 1.3-6.7%, respectively. The granules exhibited good flowability (angle of repose < 30 °) and compressibility properties with Carr's and Hausner ratios of < 10 and < 1.11, respectively. All the prepared tablets have shown a hardness value of less than 100 N and a disintegration time in the range of 0.55 to 10.27 min. The ANOVA analysis for model adequacy testing confirmed the adequacy of the optimization model. Accordingly, the model provided an optimum formulation at 5.32% of CM concentration, 5% of disintegrant (Starch), and 76.71 N of compression force (CF). Under this condition, the software predicted 83.3% drug release at 30 min and 0.63 of friability. The validity of this optimum formulation was confirmed experimentally. The CM can be used as an alternative binder for tablets, and the optimization model was proven to be effective in identifying the optimum concentration of the CM along with CF and ST.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。