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Toxicological assessment of polyhexamethylene biguanide for water treatment

Polyhexamethylene biguanide (PHMB) is an antiseptic with antiviral and antibacterial properties used in a variety of products including wound care dressings, contact lens cleaning solutions, perioperative cleansing products, and swimming pool cleaners. There are regulatory concerns with regard to it...

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Autores principales: Asiedu-Gyekye, Isaac J., Mahmood, Abdulai Seidu, Awortwe, Charles, Nyarko, Alexander K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Slovak Toxicology Society SETOX 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961918/
https://www.ncbi.nlm.nih.gov/pubmed/27486381
http://dx.doi.org/10.1515/intox-2015-0029
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author Asiedu-Gyekye, Isaac J.
Mahmood, Abdulai Seidu
Awortwe, Charles
Nyarko, Alexander K.
author_facet Asiedu-Gyekye, Isaac J.
Mahmood, Abdulai Seidu
Awortwe, Charles
Nyarko, Alexander K.
author_sort Asiedu-Gyekye, Isaac J.
collection PubMed
description Polyhexamethylene biguanide (PHMB) is an antiseptic with antiviral and antibacterial properties used in a variety of products including wound care dressings, contact lens cleaning solutions, perioperative cleansing products, and swimming pool cleaners. There are regulatory concerns with regard to its safety in humans for water treatment. We decided to assess the safety of this chemical in Sprague-Dawley rats. PHMB was administered in a single dose by gavage via a stomach tube as per the manufacturer's instruction within a dose range of 2 mg/kg to 40 mg/kg. Subchronic toxicity studies were also conducted at doses of 2 mg/kg, 8 mg/kg and 32 mg/kg body weight and hematological, biochemical and histopathological findings of the major organs were assessed. Administration of a dose of 25.6 mg/kg, i.e. 1.6 mL of 0.4% PHMB solution (equivalent to 6.4x10(3) mg/L of 0.1% solution) resulted in 50% mortality. Histopathological analysis in the acute toxicity studies showed that no histopathological lesions were observed in the heart and kidney samples but 30% of the animals had mild hydropic changes in zone 1 of their liver samples, while at a dosage of 32 mg/kg in the subchronic toxicity studies, 50% of the animals showed either mild hepatocyte cytolysis with or without lymphocyte infiltration and feathery degeneration. Lymphocyte infiltration was, for the first time, observed in one heart sample, whereas one kidney sample showed mild tubular damage. The acute studies showed that the median lethal dose (LD(50)) is 25.6 mg/kg (LC(50) of 1.6 mL of 0.4% PHMB. Subchronic toxicological studies also revealed few deleterious effects on the internal organs examined, as seen from the results of the biochemical parameters evaluated. These results have implications for the use of PHMB to make water potable.
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spelling pubmed-49619182016-08-02 Toxicological assessment of polyhexamethylene biguanide for water treatment Asiedu-Gyekye, Isaac J. Mahmood, Abdulai Seidu Awortwe, Charles Nyarko, Alexander K. Interdiscip Toxicol Original Article Polyhexamethylene biguanide (PHMB) is an antiseptic with antiviral and antibacterial properties used in a variety of products including wound care dressings, contact lens cleaning solutions, perioperative cleansing products, and swimming pool cleaners. There are regulatory concerns with regard to its safety in humans for water treatment. We decided to assess the safety of this chemical in Sprague-Dawley rats. PHMB was administered in a single dose by gavage via a stomach tube as per the manufacturer's instruction within a dose range of 2 mg/kg to 40 mg/kg. Subchronic toxicity studies were also conducted at doses of 2 mg/kg, 8 mg/kg and 32 mg/kg body weight and hematological, biochemical and histopathological findings of the major organs were assessed. Administration of a dose of 25.6 mg/kg, i.e. 1.6 mL of 0.4% PHMB solution (equivalent to 6.4x10(3) mg/L of 0.1% solution) resulted in 50% mortality. Histopathological analysis in the acute toxicity studies showed that no histopathological lesions were observed in the heart and kidney samples but 30% of the animals had mild hydropic changes in zone 1 of their liver samples, while at a dosage of 32 mg/kg in the subchronic toxicity studies, 50% of the animals showed either mild hepatocyte cytolysis with or without lymphocyte infiltration and feathery degeneration. Lymphocyte infiltration was, for the first time, observed in one heart sample, whereas one kidney sample showed mild tubular damage. The acute studies showed that the median lethal dose (LD(50)) is 25.6 mg/kg (LC(50) of 1.6 mL of 0.4% PHMB. Subchronic toxicological studies also revealed few deleterious effects on the internal organs examined, as seen from the results of the biochemical parameters evaluated. These results have implications for the use of PHMB to make water potable. Slovak Toxicology Society SETOX 2015-12 2015-12 /pmc/articles/PMC4961918/ /pubmed/27486381 http://dx.doi.org/10.1515/intox-2015-0029 Text en Copyright © 2015 SETOX & Institute of Experimental Pharmacology and Toxicology, SASc. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Asiedu-Gyekye, Isaac J.
Mahmood, Abdulai Seidu
Awortwe, Charles
Nyarko, Alexander K.
Toxicological assessment of polyhexamethylene biguanide for water treatment
title Toxicological assessment of polyhexamethylene biguanide for water treatment
title_full Toxicological assessment of polyhexamethylene biguanide for water treatment
title_fullStr Toxicological assessment of polyhexamethylene biguanide for water treatment
title_full_unstemmed Toxicological assessment of polyhexamethylene biguanide for water treatment
title_short Toxicological assessment of polyhexamethylene biguanide for water treatment
title_sort toxicological assessment of polyhexamethylene biguanide for water treatment
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961918/
https://www.ncbi.nlm.nih.gov/pubmed/27486381
http://dx.doi.org/10.1515/intox-2015-0029
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