Standardization of Gandhaga Thailam: A Traditional Siddha Formulation for Skin Disorders

R. Adithya, E. M. Manikgantan, N. Kabilan, S. Kanimozhi
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Abstract

Standardization is a part of Drug development process. Identifying the quality of a Siddha formulation is essential before it taken up for In vivo, In vitro studies and Clinical trials. Gandhaga thailam a Mineral based Siddha medicine to treat various ailments like Eczema, Ulcer, Peptic ulcer diseases etc. Test samples were extracted with acetone and briefly homogenized. Further filtration followed by addition of acetone to the test mixture. The test samples were heated using a rotary evaporator at a temperature not exceeding 40°C until almost complete evaporation of the solvent. HPTLC analysis reveals the presence of thirteen prominent peaks corresponds to the presence of thirteen versatile phytocomponents present within it. Rf value of the peaks ranges from 0.02 to 0.80. Study indicates that the Gandhaga Thailam is in standard quality, hence the preparation and purification processes of ingredients were done as per the literature.  With these results Gandhaga thailam may be subjected to invitro and invivo toxicity studies in future. Results reveal the quality of the Medicine Gandhaga Thailam and may be the fingerprint for the future analysis on Gandhaga Thailam.
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Gandhaga Thailam 的标准化:治疗皮肤病的传统悉达配方
标准化是药物开发过程的一部分。在进行体内、体外研究和临床试验之前,确定 Siddha 配方的质量至关重要。Gandhaga thailam 是一种基于矿物质的 Siddha 药物,用于治疗湿疹、溃疡、消化性溃疡等各种疾病。试验样品用丙酮提取并简单均质。进一步过滤后向测试混合物中加入丙酮。使用旋转蒸发仪在不超过 40°C 的温度下加热测试样品,直到溶剂几乎完全蒸发为止。HPTLC 分析显示,样品中出现了 13 个明显的峰值,这表明样品中含有 13 种多功能植物成分。峰的 Rf 值在 0.02 到 0.80 之间。研究表明,Gandhaga Thailam 的质量符合标准,因此其成分的制备和提纯过程都是根据文献进行的。 有了这些结果,今后可以对甘达加泰兰进行体外和体内毒性研究。研究结果揭示了药物 Gandhaga Thailam 的质量,并可能成为今后分析 Gandhaga Thailam 的指纹图谱。
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