Srikanth N, Singh A, Ota S, Sreedhar B, Dhiman K S
Central Council for Research in Ayurvedic Sciences, 61-65, Institutional Area, Opp. D-Block, Janakpuri, New Delhi, India.
Central Council for Research in Ayurvedic Sciences, 61-65, Institutional Area, Opp. D-Block, Janakpuri, New Delhi, India.
J Ayurveda Integr Med. 2019 Oct-Dec;10(4):262-268. doi: 10.1016/j.jaim.2018.01.002. Epub 2018 Nov 20.
To protect the massive trust of patient in Ayurveda, a need aroused for the researches to ascertain the quality, safety & efficacy of herbo-mineral preparations on scientific lines. The rasa-aushadhis are having qualities such as instant effectiveness, requirement in very small dosage and ample therapeutic utility. Mahalaxmi Vilas Rasa [AFI, 20:27] has been used for treatment of a variety of ailments since time immemorial.
To prepare Mahalaxmi Vilas Rasa as per standard operating procedures (SoPs) mentioned in classical text and to characterize it chemically using modern analytical techniques.
The drug (Mahalaxmi Vilas Rasa) in three batches was prepared in GMP certified pharmacy. Physico-chemical analysis, HPTLC, Assay of elements by AAS & ICP-AES were carried out as per Ayurvedic Pharmacopoeia of India. Powder X-ray diffraction (XRD) was conducted using Rigaku Ultima-IV X-ray diffractometer.
The elemental analysis shown the presence of Mercury, Sulphur, Calcium, Copper, Gold, Iron & Tin etc. and HPTLC revealed presence of organic constituents from plant material. The XRD had indicated that prepared drug contained free sulphur, cinnabar (mercury sulphide added as Kajjali), cassiterite (tin oxide, Vanga Bhasma), orpiment (Hartal, arsenic III sulphide) and mica (Leucite/ Zeolite, Abhrak Bhasma). The drug was also tested for residual pesticide and microbiological contamination which were found within permissible limits.
Classical pharmaceutical procedures of Mahalaxmi Vilas Rasa showed converting the macro elements into therapeutically effective medicines of micro form. Standards laid down in this study certainly utilized as an important tool for standardization and quality assurance of this herbo-mineral formulation.
为保护患者对阿育吠陀医学的高度信任,有必要开展研究,从科学角度确定草药-矿物制剂的质量、安全性和有效性。味药剂具有起效迅速、用量极小且治疗用途广泛等特点。自古以来,玛哈拉什米维拉什 rasa [AFI, 20:27] 就被用于治疗各种疾病。
按照经典文献中提及的标准操作规程 (SoP) 制备玛哈拉什米维拉什 rasa,并使用现代分析技术对其进行化学表征。
在获得 GMP 认证的药房中制备了三批该药物(玛哈拉什米维拉什 rasa)。按照《印度阿育吠陀药典》进行了理化分析、HPTLC、原子吸收光谱法 (AAS) 和电感耦合等离子体发射光谱法 (ICP-AES) 元素测定。使用理学 Ultima-IV X 射线衍射仪进行粉末 X 射线衍射 (XRD) 分析。
元素分析表明存在汞、硫、钙、铜、金、铁和锡等元素,HPTLC 显示存在来自植物材料的有机成分。XRD 表明所制备的药物含有游离硫、朱砂(作为 Kajjali 添加的硫化汞)、锡石(氧化锡,Vanga Bhasma)、雌黄(Hartal,三硫化二砷)和云母(白榴石/沸石,Abhrak Bhasma)。还对该药物进行了残留农药和微生物污染检测,结果均在允许范围内。
玛哈拉什米维拉什 rasa 的经典制药工艺显示可将宏观元素转化为具有治疗效果的微观形式药物。本研究制定的标准肯定可作为该草药-矿物制剂标准化和质量保证的重要工具。