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MYCOLOGICAL ANALYSIS AND AFLATOXIN B(1) CONTAMINANT ESTIMATION OF HERBAL DRUG RAW MATERIALS
BACKGROUND: The present study explores the fungal contamination of important herbal drug raw materials (HDRM), which are widely used in the preparation of many herbal drugs. Understanding of the microbial contamination status of HDRM is one of the important steps to ensure the safety and efficacy of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
African Traditional Herbal Medicine Supporters Initiative (ATHMSI)
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416630/ https://www.ncbi.nlm.nih.gov/pubmed/28487902 http://dx.doi.org/10.21010/ajtcam.v13i5.16 |
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author | Rajeshwari, Puttaswamy Raveesha, KoteshwarAnandrao |
author_facet | Rajeshwari, Puttaswamy Raveesha, KoteshwarAnandrao |
author_sort | Rajeshwari, Puttaswamy |
collection | PubMed |
description | BACKGROUND: The present study explores the fungal contamination of important herbal drug raw materials (HDRM), which are widely used in the preparation of many herbal drugs. Understanding of the microbial contamination status of HDRM is one of the important steps to ensure the safety and efficacy of herbal drugs. MATERIALS AND METHODS: Eighteen samples of six herbal drug raw materials (HDRM) viz., Acorus calamus Linn., Cassia angustifolia Vahl., Centella asiatica (Linn.) Urban, Myristica fragrans Houtt., Tinospora cardifolia (Wild) Miers and Withania somnifera (Linn.) Dunal, were screened for fungal contamination, by employing serial dilution method. All the isolates of Aspergillus flavus were screened for their ability to produce aflatoxin B(1) (AB(1)) and highly contaminated samples were subjected to AB(1) estimation by using Thin Layer Chromatography (TLC), spectrophotometric method and occurrence of Aflatoxin B(1) was confirmed by Liquid Chromatography-Mass Spectrometry analysis (LCMS). RESULTS: A total of 302 isolates of 42 fungal species belonging to 17 genera were found in association with test the samples. More than 61% of A. flavus isolates tested positive for production of AB(1) and highest yield recorded was 5008.20 ppb from the isolates of T. cordifolia. Amongthesix highly contaminated samples three samples tested positive for AB(1). Highest AB(1) was recorded from T. cordifolia (104.19 μg/kg), followed by A. calamus (13.73 μg/kg) and M. fragrans (12.02 μg/kg). CONCLUSION: Assessment of fungal and mycotoxin contamination should be a part of the quality check while selecting HDRM for manufacture of herbal products. Safe processing and storage practices are necessary. |
format | Online Article Text |
id | pubmed-5416630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | African Traditional Herbal Medicine Supporters Initiative (ATHMSI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-54166302017-08-12 MYCOLOGICAL ANALYSIS AND AFLATOXIN B(1) CONTAMINANT ESTIMATION OF HERBAL DRUG RAW MATERIALS Rajeshwari, Puttaswamy Raveesha, KoteshwarAnandrao Afr J Tradit Complement Altern Med Article BACKGROUND: The present study explores the fungal contamination of important herbal drug raw materials (HDRM), which are widely used in the preparation of many herbal drugs. Understanding of the microbial contamination status of HDRM is one of the important steps to ensure the safety and efficacy of herbal drugs. MATERIALS AND METHODS: Eighteen samples of six herbal drug raw materials (HDRM) viz., Acorus calamus Linn., Cassia angustifolia Vahl., Centella asiatica (Linn.) Urban, Myristica fragrans Houtt., Tinospora cardifolia (Wild) Miers and Withania somnifera (Linn.) Dunal, were screened for fungal contamination, by employing serial dilution method. All the isolates of Aspergillus flavus were screened for their ability to produce aflatoxin B(1) (AB(1)) and highly contaminated samples were subjected to AB(1) estimation by using Thin Layer Chromatography (TLC), spectrophotometric method and occurrence of Aflatoxin B(1) was confirmed by Liquid Chromatography-Mass Spectrometry analysis (LCMS). RESULTS: A total of 302 isolates of 42 fungal species belonging to 17 genera were found in association with test the samples. More than 61% of A. flavus isolates tested positive for production of AB(1) and highest yield recorded was 5008.20 ppb from the isolates of T. cordifolia. Amongthesix highly contaminated samples three samples tested positive for AB(1). Highest AB(1) was recorded from T. cordifolia (104.19 μg/kg), followed by A. calamus (13.73 μg/kg) and M. fragrans (12.02 μg/kg). CONCLUSION: Assessment of fungal and mycotoxin contamination should be a part of the quality check while selecting HDRM for manufacture of herbal products. Safe processing and storage practices are necessary. African Traditional Herbal Medicine Supporters Initiative (ATHMSI) 2016-08-12 /pmc/articles/PMC5416630/ /pubmed/28487902 http://dx.doi.org/10.21010/ajtcam.v13i5.16 Text en Copyright: © 2016 Afr. J. Traditional Complementary and Alternative Medicines http://creativecommons.org/licenses/CC-BY/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License |
spellingShingle | Article Rajeshwari, Puttaswamy Raveesha, KoteshwarAnandrao MYCOLOGICAL ANALYSIS AND AFLATOXIN B(1) CONTAMINANT ESTIMATION OF HERBAL DRUG RAW MATERIALS |
title | MYCOLOGICAL ANALYSIS AND AFLATOXIN B(1) CONTAMINANT ESTIMATION OF HERBAL DRUG RAW MATERIALS |
title_full | MYCOLOGICAL ANALYSIS AND AFLATOXIN B(1) CONTAMINANT ESTIMATION OF HERBAL DRUG RAW MATERIALS |
title_fullStr | MYCOLOGICAL ANALYSIS AND AFLATOXIN B(1) CONTAMINANT ESTIMATION OF HERBAL DRUG RAW MATERIALS |
title_full_unstemmed | MYCOLOGICAL ANALYSIS AND AFLATOXIN B(1) CONTAMINANT ESTIMATION OF HERBAL DRUG RAW MATERIALS |
title_short | MYCOLOGICAL ANALYSIS AND AFLATOXIN B(1) CONTAMINANT ESTIMATION OF HERBAL DRUG RAW MATERIALS |
title_sort | mycological analysis and aflatoxin b(1) contaminant estimation of herbal drug raw materials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416630/ https://www.ncbi.nlm.nih.gov/pubmed/28487902 http://dx.doi.org/10.21010/ajtcam.v13i5.16 |
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