Evaluation and standarisation of Shatavaryadi Churna

Srishti Vyas; Ashwini A. Patil; Kavita A. Jadhav; Mugdha Sawle; Akash P. Gaikwad; Vaishnavi D. Patil

doi:10.53730/ijhs.v8nS1.14752

Authors

Srishti Vyas Final year MS Scholar at Deepartment of Shalakya Tantra, D. Y. Patil, Deemed to be University, School of Ayurveda Nerul, Navi-Mumbai
Ashwini A. Patil HOD & Professor at Deepartment of Shalakya Tantra, D. Y. Patil, Deemed to be University, School of Ayurveda Nerul, Navi-Mumbai
Kavita A. Jadhav Associated Professor at Deepartment of Shalakya Tantra, D. Y. Patil, Deemed to be University, School of Ayurveda Nerul, Navi-Mumbai
Mugdha Sawle Associated Professor at Deepartment of Shalakya Tantra, D. Y. Patil, Deemed to be University, School of Ayurveda Nerul, Navi-Mumbai
Akash P. Gaikwad Final year MS Scholar at Deepartment of Shalakya Tantra, D. Y. Patil, Deemed to be University, School of Ayurveda Nerul, Navi-Mumbai
Vaishnavi D. Patil Final year MS Scholar at Deepartment of Shalakya Tantra, D. Y. Patil, Deemed to be University, School of Ayurveda Nerul, Navi-Mumbai

Keywords:

evaluation, standarisation, Shatavaryadi Churna

Abstract

Introduction-The Ayurvedic medical system has recently got a lot of medical and healthcare services in India. To evaluate the quality, safety, and effectiveness of the medicine, standards and purity of herbal formulation are crucial. However, pharmacopoeia testing is the protocol that all medicines must follow in order to be accepted globally. A compound herbal formulation called Shatvaryadi Churna is suggested for the treatment of a number of diseases. For the treatment of Timira Vyadhi, patal vyadhi, kancha vyadhi and many other raktaj vikara the formulation was documented in the Ayurvedic classic Yoga Ratnakar. Materials & methods- Shatavaryadi Churna was made by using the standard procedure with all aseptic precautions and as described in the Ayurvedic Pharmacopoeia for Churna Kalpana (Powder Preparation). The manufactured medication has been standardised by adhering to the approved pharmacopeial protocol for quality control procedures. Results- Organoleptic parameters, physiochemical evaluation, and microbiological load test was done these analytical values were within the expected limits.

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