Quality by Design (QbD) Enabled and Central-Composite Design Assisted Approach for Formulation of Oral Herbal Gastro-retentive In-situ Gel

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Rishabh P Malge, V. S. Mannur, Rahul Koli
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引用次数: 0

Abstract

Purpose

The delivery of herbal medications is currently a growing area in pharmacy. One of the areas of interest for the scientists conducting pharmaceutical research is the use of floating drug delivery system (FDDS) for herbal medicine. In this study, we developed an oral herbal gastro-retentive in-situ gel using extracts from Azadirachta indica and Piper longum Linn, employing the quality by design (QbD) approach.

Methods

For the formulation and optimization of an oral herbal in-situ gel, a central composite design (CCD) was used. This design is based on 2-level factorial designs that have been supplemented with center and axial points to match quadratic models. The amounts of two independent variables, gellan gum (X1) and calcium carbonate (X2), were altered at five distinct levels. For the current investigation, the response variables viscosity (Y1), floating lag time (Y2), and gelling time (Y3) were used. According to DoE software, a total of 13 formulations were prepared by changing the gellan gum and calcium carbonate concentrations.

Results

The optimized formulation (OF2), which contains gellan gum 0.293% & calcium carbonate 0.706, satisfies the requirements of quality target product profile (QTPP) and critical quality attributes (CQA) for oral herbal in-situ gel with 75% and 73% drug content. OF2 had a 35.5 s gelling time, a 53 s floating lag time, and a viscosity of 53 cps. The formulated oral herbal in-situ gel exhibited stability for over 2 months under both freezing (-4 °C) and 40 °C with 60% relative humidity (RH) storage conditions.

Conclusion

The developed formulation presents a promising and innovative approach to enhance the gastric retention of herbal extracts, ultimately amplifying their therapeutic efficacy. This paper establishes the foundation for future preclinical and clinical studies on an oral herbal in-situ gel containing long pepper and neem leaf extracts for the treatment of peptic ulcer disease (PUD).

Abstract Image

采用质量源于设计(QbD)和中央复合设计辅助方法配制口服中药保胃原位凝胶
目的 目前,中草药的给药是一个不断发展的制药领域。将浮动给药系统(FDDS)用于中草药是从事制药研究的科学家们感兴趣的领域之一。在这项研究中,我们采用质量源于设计(QbD)的方法,利用 Azadirachta indica 和 Piper longum Linn 的提取物开发了一种口服中草药保胃原位凝胶。该设计基于 2 级阶乘设计,并辅以中心点和轴心点以匹配二次方程模型。两个自变量,即结冷胶(X1)和碳酸钙(X2)的量在五个不同的水平上发生变化。本次研究使用了粘度(Y1)、浮动滞后时间(Y2)和胶凝时间(Y3)这三个响应变量。结果含有结冷胶 0.293% & 碳酸钙 0.706 的优化配方(OF2)满足药物含量分别为 75% 和 73% 的口服中药原位凝胶的质量目标曲线(QTPP)和关键质量属性(CQA)的要求。OF2 的胶凝时间为 35.5 秒,漂浮滞后时间为 53 秒,粘度为 53 cps。所配制的口服中草药原位凝胶在冷冻(-4 °C)和 40 °C、相对湿度(RH)为 60% 的贮藏条件下均表现出 2 个月以上的稳定性。本文为今后对含有长胡椒和楝树叶提取物的口服中草药原位凝胶治疗消化性溃疡病(PUD)进行临床前和临床研究奠定了基础。
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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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