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Quality control evaluation of Keshamasi, Keshanjana and Keshamasi eye ointment

BACKGROUND: Keshanjana (collyrium) is a well known Ayurvedic preparation prepared out of Keshamasi (ash prepared by scalp hairs) mixed with Goghrita (cow's ghee). This medicine is indicated for the treatment of Shushkakshipaka (dry eye syndrome) in the classical literature of Ayurveda; hence, i...

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Autores principales: Dhiman, Kartar Singh, Shukla, Vinay J., Bhalodia, Nayan R., Sharma, Vinay R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213971/
https://www.ncbi.nlm.nih.gov/pubmed/25364202
http://dx.doi.org/10.4103/0974-8520.141938
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author Dhiman, Kartar Singh
Shukla, Vinay J.
Bhalodia, Nayan R.
Sharma, Vinay R.
author_facet Dhiman, Kartar Singh
Shukla, Vinay J.
Bhalodia, Nayan R.
Sharma, Vinay R.
author_sort Dhiman, Kartar Singh
collection PubMed
description BACKGROUND: Keshanjana (collyrium) is a well known Ayurvedic preparation prepared out of Keshamasi (ash prepared by scalp hairs) mixed with Goghrita (cow's ghee). This medicine is indicated for the treatment of Shushkakshipaka (dry eye syndrome) in the classical literature of Ayurveda; hence, it was under taken for standardization and clinical evaluation in an extra-mural research project from Central Council for Research in Ayurvedic Sciences, Department of AYUSH, New Delhi. AIM: To develop standard quality parameters for the Keshamasi, Keshanjana and Keshamasi ointment. MATERIALS AND METHODS: Scalp hairs of male and females collected from saloons were converted to classical Masi Kalpana and mixed with cow ghee and petrolatum in the ratio of 1:5 to prepare the Keshanjana and Keshamasi ointment respectively. Standard Operation Procedure (SOP) were adopted and recorded accordingly. The raw material, furnished products and plain Goghrita were subjected for quality control parameters i.e., physico-chemical evaluation, anti-microbial study, particle size analysis, heavy metal analysis through inductive couple plasma spectroscopy with high performance thin layer liquid chromatography fingerprints. RESULTS: Rancidity was negative in all the samples, indicating that the physico-chemical parameters are in acceptable range. Lead and zinc were present in most of the samples; while all samples are were free from microbial contamination. CONCLUSION: As no standards are available to compare the results of the current study, the observations cannot be compared. Thus the profile generated in the current study can be considered as standard to refer in future studies.
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spelling pubmed-42139712014-10-31 Quality control evaluation of Keshamasi, Keshanjana and Keshamasi eye ointment Dhiman, Kartar Singh Shukla, Vinay J. Bhalodia, Nayan R. Sharma, Vinay R. Ayu Pharmaceutical Standardization BACKGROUND: Keshanjana (collyrium) is a well known Ayurvedic preparation prepared out of Keshamasi (ash prepared by scalp hairs) mixed with Goghrita (cow's ghee). This medicine is indicated for the treatment of Shushkakshipaka (dry eye syndrome) in the classical literature of Ayurveda; hence, it was under taken for standardization and clinical evaluation in an extra-mural research project from Central Council for Research in Ayurvedic Sciences, Department of AYUSH, New Delhi. AIM: To develop standard quality parameters for the Keshamasi, Keshanjana and Keshamasi ointment. MATERIALS AND METHODS: Scalp hairs of male and females collected from saloons were converted to classical Masi Kalpana and mixed with cow ghee and petrolatum in the ratio of 1:5 to prepare the Keshanjana and Keshamasi ointment respectively. Standard Operation Procedure (SOP) were adopted and recorded accordingly. The raw material, furnished products and plain Goghrita were subjected for quality control parameters i.e., physico-chemical evaluation, anti-microbial study, particle size analysis, heavy metal analysis through inductive couple plasma spectroscopy with high performance thin layer liquid chromatography fingerprints. RESULTS: Rancidity was negative in all the samples, indicating that the physico-chemical parameters are in acceptable range. Lead and zinc were present in most of the samples; while all samples are were free from microbial contamination. CONCLUSION: As no standards are available to compare the results of the current study, the observations cannot be compared. Thus the profile generated in the current study can be considered as standard to refer in future studies. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4213971/ /pubmed/25364202 http://dx.doi.org/10.4103/0974-8520.141938 Text en Copyright: © AYU (An International Quarterly Journal of Research in Ayurveda) http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Pharmaceutical Standardization
Dhiman, Kartar Singh
Shukla, Vinay J.
Bhalodia, Nayan R.
Sharma, Vinay R.
Quality control evaluation of Keshamasi, Keshanjana and Keshamasi eye ointment
title Quality control evaluation of Keshamasi, Keshanjana and Keshamasi eye ointment
title_full Quality control evaluation of Keshamasi, Keshanjana and Keshamasi eye ointment
title_fullStr Quality control evaluation of Keshamasi, Keshanjana and Keshamasi eye ointment
title_full_unstemmed Quality control evaluation of Keshamasi, Keshanjana and Keshamasi eye ointment
title_short Quality control evaluation of Keshamasi, Keshanjana and Keshamasi eye ointment
title_sort quality control evaluation of keshamasi, keshanjana and keshamasi eye ointment
topic Pharmaceutical Standardization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213971/
https://www.ncbi.nlm.nih.gov/pubmed/25364202
http://dx.doi.org/10.4103/0974-8520.141938
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