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Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii

OBJECTIVE: The main objective of this study is to isolate, identify, and quantify the active antimicrobial compounds present in the crude aqueous stem bark extract of B. dalzielii using some common pathogenic microorganisms as well as toxicological profile. MATERIAL AND METHODS: Crude aqueous stem b...

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Autores principales: Dandashire, Bahauddeen Salisu, Magashi, Abdulkadir Magaji, Abdulkadir, Bashir, Abbas, Muhammad Adamu, Goni, Mohammed Dauda, Yakubu, Abdulmalik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: A periodical of the Network for the Veterinarians of Bangladesh (BDvetNET) 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702886/
https://www.ncbi.nlm.nih.gov/pubmed/31453189
http://dx.doi.org/10.5455/javar.2019.f330
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author Dandashire, Bahauddeen Salisu
Magashi, Abdulkadir Magaji
Abdulkadir, Bashir
Abbas, Muhammad Adamu
Goni, Mohammed Dauda
Yakubu, Abdulmalik
author_facet Dandashire, Bahauddeen Salisu
Magashi, Abdulkadir Magaji
Abdulkadir, Bashir
Abbas, Muhammad Adamu
Goni, Mohammed Dauda
Yakubu, Abdulmalik
author_sort Dandashire, Bahauddeen Salisu
collection PubMed
description OBJECTIVE: The main objective of this study is to isolate, identify, and quantify the active antimicrobial compounds present in the crude aqueous stem bark extract of B. dalzielii using some common pathogenic microorganisms as well as toxicological profile. MATERIAL AND METHODS: Crude aqueous stem bark extract of Boswellia dalzielii (CASEB) was partitioned by preparative thin layer chromatography (PTLC) using chloroform–methanol–water, 8:2:1 (v/v). The resulting bands were extracted using chloroform–methanol (50:50). The extract of each band was evaluated for antimicrobial activity on Streptococcus pyogenes, Staphylococcus aureus, Escherichia coli, Enterococcus faecalis, Klebsiella pneumonia, Pseudomonas aeruginosa, Proteus mirabilis, Salmonella typhi, and Candida albicans by disc diffusion. Compounds in the most antimicrobially bioactive fraction (MAAF) were identified by high performance liquid chromatography (HPLC), Fourier transform infrared spectrophotometry (FT-IR), and gas chromatography-mass spectrometry (GC-MS). Toxicological profile of the CASEB was evaluated by studying its effect in albino Wister rats. RESULTS: PTLC produced five bands/fractions of which the MAAF was identified as RF(2)-fraction being active against all the isolates except E. coli and K. pneumoniae. HPLC of the MAAF revealed seven components; FT-IR revealed 17 functional groups; GC-MS revealed five compounds of which 93.18% are Oleic acid (44.88%), Squalene (34.16%), and n-Hexadecanoic acid (14.14%). The acute toxicity showed LD(50) > 3,000 mg/kg. Sub-chronic toxicity showed that higher doses of the CASEB caused significant changes in liver function indices and a fatty change with lymphocytic infiltration (sign of acute hepatitis) in the liver tissues, but none of these changes were observed in the kidneys. CONCLUSION: The antimicrobially active compounds in CASEB were Oleic acid, Squalene, and n-Hexadecanoic acid. These can be further purified and used as precursors of new antimicrobial agents for treating infections especially those due to fungi and Pseudomonas spp. that are known to resist wide array of antimicrobial agents. The LD(50) of CASEB is >3,000 mg/kg in rats. However, long-term consumption of CASEB is associated with significant liver damage.
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spelling pubmed-67028862019-08-26 Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii Dandashire, Bahauddeen Salisu Magashi, Abdulkadir Magaji Abdulkadir, Bashir Abbas, Muhammad Adamu Goni, Mohammed Dauda Yakubu, Abdulmalik J Adv Vet Anim Res Original Article OBJECTIVE: The main objective of this study is to isolate, identify, and quantify the active antimicrobial compounds present in the crude aqueous stem bark extract of B. dalzielii using some common pathogenic microorganisms as well as toxicological profile. MATERIAL AND METHODS: Crude aqueous stem bark extract of Boswellia dalzielii (CASEB) was partitioned by preparative thin layer chromatography (PTLC) using chloroform–methanol–water, 8:2:1 (v/v). The resulting bands were extracted using chloroform–methanol (50:50). The extract of each band was evaluated for antimicrobial activity on Streptococcus pyogenes, Staphylococcus aureus, Escherichia coli, Enterococcus faecalis, Klebsiella pneumonia, Pseudomonas aeruginosa, Proteus mirabilis, Salmonella typhi, and Candida albicans by disc diffusion. Compounds in the most antimicrobially bioactive fraction (MAAF) were identified by high performance liquid chromatography (HPLC), Fourier transform infrared spectrophotometry (FT-IR), and gas chromatography-mass spectrometry (GC-MS). Toxicological profile of the CASEB was evaluated by studying its effect in albino Wister rats. RESULTS: PTLC produced five bands/fractions of which the MAAF was identified as RF(2)-fraction being active against all the isolates except E. coli and K. pneumoniae. HPLC of the MAAF revealed seven components; FT-IR revealed 17 functional groups; GC-MS revealed five compounds of which 93.18% are Oleic acid (44.88%), Squalene (34.16%), and n-Hexadecanoic acid (14.14%). The acute toxicity showed LD(50) > 3,000 mg/kg. Sub-chronic toxicity showed that higher doses of the CASEB caused significant changes in liver function indices and a fatty change with lymphocytic infiltration (sign of acute hepatitis) in the liver tissues, but none of these changes were observed in the kidneys. CONCLUSION: The antimicrobially active compounds in CASEB were Oleic acid, Squalene, and n-Hexadecanoic acid. These can be further purified and used as precursors of new antimicrobial agents for treating infections especially those due to fungi and Pseudomonas spp. that are known to resist wide array of antimicrobial agents. The LD(50) of CASEB is >3,000 mg/kg in rats. However, long-term consumption of CASEB is associated with significant liver damage. A periodical of the Network for the Veterinarians of Bangladesh (BDvetNET) 2019-04-14 /pmc/articles/PMC6702886/ /pubmed/31453189 http://dx.doi.org/10.5455/javar.2019.f330 Text en Copyright: © Journal of Advanced Veterinary and Animal Research http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 4.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Dandashire, Bahauddeen Salisu
Magashi, Abdulkadir Magaji
Abdulkadir, Bashir
Abbas, Muhammad Adamu
Goni, Mohammed Dauda
Yakubu, Abdulmalik
Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii
title Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii
title_full Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii
title_fullStr Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii
title_full_unstemmed Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii
title_short Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii
title_sort toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of boswellia dalzielii
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702886/
https://www.ncbi.nlm.nih.gov/pubmed/31453189
http://dx.doi.org/10.5455/javar.2019.f330
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