Formulation, Development and Evaluation of Effervescent Tablet of Green Tea (Camellia sinensis).

Prabhjot Kaur, Geeta Deswal, Bhawna Chopra, Priyanka Kriplani, Ajmer Singh Grewal, Ashwani K Dhingra
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Abstract

Background: Camellia sinensis has an extensive variety of pharmacological properties, including neuroprotection, photo-aging resistance, stress resistance, antioxidant, anti-tumour, hypoglycemic, antibacterial, and antiviral effects tracing a good potential in addressing illness and preventing disease. Challenges with conventional dosage forms include patient incompatibility, improper dosing, the inclusion of microplastics, etc. Objective: The present work aims to deliver a novel formulation devoid of microplastics and with improved consumer compliance.

Methods: Wet granulation was used to formulate 500 mg Camellia sinensis effervescent tablets, with improved effervescent time and rapid release. Citric acid and sodium bicarbonate's impacts on disintegration time and pH were examined using a factorial design. Pre-compression variables were assessed for the granule mixture. Post-compression criteria were employed to assess effervescent tablets. The optimum formulation was selected using a central composite response surface and assessment criteria.

Results: The physicochemical characteristics of the developed formulations were significantly influenced by the independent factors. Low concentrations of sodium bicarbonate have positive impact on pH whereas high concentrations of sodium bicarbonate as well as citric acid enhance disintegration time. The design outcomes showed that the optimized effervescent tablets (F10) prepared with 697.5 mg and 448.38 mg of citric acid and sodium bicarbonate respectively had good physicochemical properties.

Conclusion: In compliance with present quality standards, factorial design was efficiently utilized for the development of Camellia sinensis effervescent tablets. It was concluded that green tea effervescent tablet (F10) would function as a substitute for conventional green tea powder along with green tea bags as a means of administration.

绿茶泡腾片的研制与评价。
背景:山茶具有广泛的药理作用,包括神经保护、抗光老化、抗应激、抗氧化、抗肿瘤、降血糖、抗菌和抗病毒作用,在治疗疾病和预防疾病方面具有良好的潜力。传统剂型的挑战包括患者不相容、给药不当、微塑料夹杂等。目的:目前的工作旨在提供一种新的配方缺乏微塑料和提高消费者的合规性。方法:采用湿造粒法制备500 mg山茶泡腾片,改善泡腾片泡腾片泡腾片泡腾片的泡腾片时间,提高泡腾片的释放速度。采用析因设计考察了柠檬酸和碳酸氢钠对崩解时间和pH的影响。评估颗粒混合物的预压缩变量。采用压缩后标准对泡腾片进行评价。采用中心复合响应面法和评价标准优选出最佳配方。结果:各独立因素对制剂的理化特性有显著影响。低浓度的碳酸氢钠对pH值有正向影响,而高浓度的碳酸氢钠和柠檬酸会延长崩解时间。设计结果表明,以柠檬酸697.5 mg和碳酸氢钠448.38 mg分别制备的最佳泡腾片F10具有良好的理化性能。结论:采用析因设计方法研制山茶泡腾片符合现行质量标准。结果表明,绿茶泡腾片(F10)可以替代传统的绿茶粉,同时绿茶包也可以作为给药手段。
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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