Finding Use for Sorghum Bicolor Leaf Sheath in Coating Technology

J. Isaac, Kayode Ilesanmi Fasuba
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Abstract

Abstract This study aimed to investigate the potential use of aqueous extract of Sorghum bicolor leaf sheath (SBLS) as a coating agent for paracetamol tablets. The mechanical properties of the coated tablets were assessed using crushing strength and friability test, while the release properties of the tablet were evaluated using disintegration and dissolution tests. The physicochemical properties of the coated tablets did not show any striking differences when compared with the uncoated tablet as par compendium specifications, which formed the basis for performing further in vitro dissolution study. Our data showed that SBLS enhanced the hardness and friability of the tablets in a dose-dependent manner. Tablets coated with 3, 5, and 7.5% of SBLS disintegrated in 8.13, 6.25, and 4.13 minutes, respectively, while the uncoated tablet disintegrated in 0.7 minutes. Furthermore, 3, 5, and 7.5% of SBLS-coated tablets exhibited slower release of their active ingredient (releasing 21, 16, and 17%, respectively) than that of the uncoated tablet (releasing 40%) in 5 minutes. Besides, comparison between the dissolution profiles was successfully achieved using difference factor (f1) and similarity factor (f2). The apparent dissimilarity between our coated tablets and the uncoated one led to further study of convolution in vitro–in vivo correlation, with the aim to obtain data that converted into mathematical prediction of in vivo data. For all batches, the percent predictable errors of C max and T max were within the acceptable limit of no more than 10%. In summary, SBLS aqueous extract is a potential and protective coat agent for paracetamol tablets. The in vitro established dissolution of the coated tablets provided scientific information for the prediction of the in vivo plasma drug profile.
高粱双色叶鞘在包衣技术中的应用
摘要本研究旨在探讨高粱双色叶鞘水提物作为对乙酰氨基酚片包衣剂的可行性。采用压碎强度和脆性试验评价包衣片的力学性能,崩解度和溶出度试验评价包衣片的释放性能。按照药典标准,包衣片的理化性质与未包衣片无明显差异,为进一步进行体外溶出度研究奠定了基础。我们的数据显示,SBLS以剂量依赖的方式增强了片剂的硬度和脆度。包被3、5、7.5% SBLS的片剂崩解时间分别为8.13、6.25、4.13 min,未包被SBLS的片剂崩解时间为0.7 min。此外,3、5和7.5%的sbls包衣片在5分钟内释放活性成分(分别释放21、16和17%)比未包衣片(释放40%)慢。此外,利用差异因子(f1)和相似因子(f2)成功地对溶出曲线进行了比较。我们的包衣片与未包衣片之间的明显差异促使我们进一步研究卷积的体内外相关性,目的是获得数据,并将其转化为体内数据的数学预测。对于所有批次,cmax和tmax的可预测误差百分比都在不超过10%的可接受限度内。综上所述,SBLS水提物是一种潜在的对乙酰氨基酚片保护剂。体外溶出度的测定为体内血浆药物谱的预测提供了科学依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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15 weeks
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