Using Quality by Design Tools to Study Gel Formulation from Brassica juncea Leaves and Conducting its In vitro, In vivo, Molecular Docking, and ADMET Analyses.

Mahibub Mahamadsa Kanakal, Syed Atif Abbas, Abdullah Khan, Saleha Sultana, Humaira Fatima, Ruheena Tabasssum, Mohammed Gulzar Ahmed, Rokeya Sultana, Jaffer Sadik Mohammed, Roshan Salfi
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Abstract

Introduction: This research aims to create a gel formulation of Brassica juncea leaf extract and assess its anti-inflammatory properties using an in silico study. The anti-inflammatory activity has been compared with Diclofenac molecules in PDB id: 4Z69. Further, the Absorption, Distribution, Metabolism, Excretion, and Toxicity analysis has been performed to ensure the therapeutic potential and safety of the drug development process. The Quality by Design tool has been applied to optimize formulation development.

Methods: The extracted gel is characterized by performing Fourier transformer infrared, zeta potential, particle size, Scanning Electron Microscope, and entrapment efficiency. Further, the formulation is evaluated by examining its viscosity, spreadability, and pH measurement. An In vitro study of all nine extract suspensions was conducted to determine the drug contents at 276 nm.

Results: The optimized suspension has shown the maximum percentage of drug release (82%) in 10 hours of study. Animal study for anti-inflammatory activity was performed, and results of all five groups of animals compared the % inhibition of paw edema at three hours; gel (56.70%), standard (47.86%), and (39.72%) were found.

Conclusion: The research could conclude that the anti-inflammatory activity of gel formulation is high compared to extract, and a molecular docking study validates the anti-inflammatory therapeutic effects. ADMET analysis ensures the therapeutic effects and their safety.

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利用设计质量工具研究甘蓝叶凝胶配方,并进行体外、体内、分子对接和 ADMET 分析。
简介:本研究旨在创建芸苔属植物叶提取物的凝胶配方,并通过硅学研究评估其抗炎特性。其抗炎活性与 PDB id: 4Z69 中的双氯芬酸分子进行了比较。此外,还进行了吸收、分布、代谢、排泄和毒性分析,以确保药物开发过程的治疗潜力和安全性。此外,还采用了 "质量指标"(Quality by De-sign)工具来优化制剂开发:方法:通过傅立叶变换红外光谱、ZETA 电位、粒度、扫描电子显微镜和夹带效率对提取的凝胶进行表征。此外,还通过粘度、铺展性和 pH 值测量对配方进行评估。对所有九种提取物悬浮液进行了体外研究,以确定在 276 纳米波长下的药物含量:结果:经过优化的悬浮液在 10 小时的研究中显示出最大的药物释放率(82%)。对动物进行了抗炎活性研究,比较了五组动物在三小时后爪水肿的抑制率,结果发现凝胶(56.70%)、标准(47.86%)和(39.72%):研究得出的结论是,与提取物相比,凝胶制剂的抗炎活性较高,分子对接研究验证了其抗炎治疗效果。ADMET 分析确保了治疗效果及其安全性。
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