Comparative study on toxic effects induced by oral or intravascular administration of commonly used disinfectants and surfactants in rats

ABSTRACT Accidental ingestion or injection of household products sometimes occurs due to their accessibility, but the toxic manifestations have not been well characterized when they are internally administered. The aim of this study was to investigate the toxic effects induced by ingestion or inject...

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Veröffentlicht in:Journal of applied toxicology 2012-07, Vol.32 (7), p.480-487
Hauptverfasser: Xue, Yuying, Zhang, Shanshan, Tang, Meng, Zhang, Ting, Wang, Yiqing, Hieda, Yoko, Takeshita, Haruo
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container_issue 7
container_start_page 480
container_title Journal of applied toxicology
container_volume 32
creator Xue, Yuying
Zhang, Shanshan
Tang, Meng
Zhang, Ting
Wang, Yiqing
Hieda, Yoko
Takeshita, Haruo
description ABSTRACT Accidental ingestion or injection of household products sometimes occurs due to their accessibility, but the toxic manifestations have not been well characterized when they are internally administered. The aim of this study was to investigate the toxic effects induced by ingestion or injection of different ionic surfactants and disinfectants in rats. The test drugs involved benzalkonium and benzethonium (BZK and BZT, both cationic surfactants used as disinfectants), alkyldiaminoethylglycine (AEG, an amphoteric surfactant used as a disinfectant), linear alkylbenzenesulfonate (LAS, an anionic surfactant), polyoxyethylene cetylether (PEC, a nonionic surfactant), chlorhexidine (CHX, not a surfactant but a disinfectant) and saline (control). Male Sprague–Dawley rats were administered one of the test drugs orally (p.o.), intravenously (i.v.) or intraarterially (i.a.). The fatal effects appeared rapidly (5 h) in i.a./p.o.‐administered rats after a dose of around LD50, although the progress and degree of toxic effects varied among the drugs tested. In intravascular administration, BZK and BZT were fatal at doses of 15–20 mg kg−1. Higher concentrations in lung and kidney than in blood were determined. CHX showed a high toxic effect compared with cationic surfactants. The rats administered anionic (LAS) or amphoteric (AEG) surfactant died in less than 24 h at doses over 100 mg kg−1. In p.o. administration, the toxic effects were concentration/dose‐dependent, and all rats administered high doses of surfactants except for PEC died at 5–20 h. The overall toxic ranks could be: cationic surfactant/CHX> anionic/amphoteric surfactant > nonionic surfactant. Copyright © 2011 John Wiley & Sons, Ltd. Acute toxic effects induced by ingestion or injection of different ionic (cationic, amphoteric, anionic and nonionic) surfactants and disinfectants (chlorhexidine, CHX) in rats were investigated comparatively. The results revealed that the toxic effects varied from one type of surfactant or disinfectant to another, and with the route of administration. Different kinetic properties between benzalkonium chloride, cationic surfactant used as disinfectant, and CHX were observed. The overall toxic ranks could be: cationic surfactant/ CHX> anionic/ amphoteric surfactant> nonionic surfactant.
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The aim of this study was to investigate the toxic effects induced by ingestion or injection of different ionic surfactants and disinfectants in rats. The test drugs involved benzalkonium and benzethonium (BZK and BZT, both cationic surfactants used as disinfectants), alkyldiaminoethylglycine (AEG, an amphoteric surfactant used as a disinfectant), linear alkylbenzenesulfonate (LAS, an anionic surfactant), polyoxyethylene cetylether (PEC, a nonionic surfactant), chlorhexidine (CHX, not a surfactant but a disinfectant) and saline (control). Male Sprague–Dawley rats were administered one of the test drugs orally (p.o.), intravenously (i.v.) or intraarterially (i.a.). The fatal effects appeared rapidly (&lt;30 min) in i.v.‐administered rats, while taking hours (&gt;5 h) in i.a./p.o.‐administered rats after a dose of around LD50, although the progress and degree of toxic effects varied among the drugs tested. In intravascular administration, BZK and BZT were fatal at doses of 15–20 mg kg−1. Higher concentrations in lung and kidney than in blood were determined. CHX showed a high toxic effect compared with cationic surfactants. The rats administered anionic (LAS) or amphoteric (AEG) surfactant died in less than 24 h at doses over 100 mg kg−1. In p.o. administration, the toxic effects were concentration/dose‐dependent, and all rats administered high doses of surfactants except for PEC died at 5–20 h. The overall toxic ranks could be: cationic surfactant/CHX&gt; anionic/amphoteric surfactant &gt; nonionic surfactant. Copyright © 2011 John Wiley &amp; Sons, Ltd. Acute toxic effects induced by ingestion or injection of different ionic (cationic, amphoteric, anionic and nonionic) surfactants and disinfectants (chlorhexidine, CHX) in rats were investigated comparatively. The results revealed that the toxic effects varied from one type of surfactant or disinfectant to another, and with the route of administration. Different kinetic properties between benzalkonium chloride, cationic surfactant used as disinfectant, and CHX were observed. 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Appl. Toxicol</addtitle><description>ABSTRACT Accidental ingestion or injection of household products sometimes occurs due to their accessibility, but the toxic manifestations have not been well characterized when they are internally administered. The aim of this study was to investigate the toxic effects induced by ingestion or injection of different ionic surfactants and disinfectants in rats. The test drugs involved benzalkonium and benzethonium (BZK and BZT, both cationic surfactants used as disinfectants), alkyldiaminoethylglycine (AEG, an amphoteric surfactant used as a disinfectant), linear alkylbenzenesulfonate (LAS, an anionic surfactant), polyoxyethylene cetylether (PEC, a nonionic surfactant), chlorhexidine (CHX, not a surfactant but a disinfectant) and saline (control). Male Sprague–Dawley rats were administered one of the test drugs orally (p.o.), intravenously (i.v.) or intraarterially (i.a.). The fatal effects appeared rapidly (&lt;30 min) in i.v.‐administered rats, while taking hours (&gt;5 h) in i.a./p.o.‐administered rats after a dose of around LD50, although the progress and degree of toxic effects varied among the drugs tested. In intravascular administration, BZK and BZT were fatal at doses of 15–20 mg kg−1. Higher concentrations in lung and kidney than in blood were determined. CHX showed a high toxic effect compared with cationic surfactants. The rats administered anionic (LAS) or amphoteric (AEG) surfactant died in less than 24 h at doses over 100 mg kg−1. In p.o. administration, the toxic effects were concentration/dose‐dependent, and all rats administered high doses of surfactants except for PEC died at 5–20 h. The overall toxic ranks could be: cationic surfactant/CHX&gt; anionic/amphoteric surfactant &gt; nonionic surfactant. Copyright © 2011 John Wiley &amp; Sons, Ltd. Acute toxic effects induced by ingestion or injection of different ionic (cationic, amphoteric, anionic and nonionic) surfactants and disinfectants (chlorhexidine, CHX) in rats were investigated comparatively. The results revealed that the toxic effects varied from one type of surfactant or disinfectant to another, and with the route of administration. Different kinetic properties between benzalkonium chloride, cationic surfactant used as disinfectant, and CHX were observed. 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dosage</subject><subject>Surface-Active Agents - toxicity</subject><subject>surfactant</subject><subject>Surfactants</subject><subject>Toxic</subject><subject>toxic effects</subject><subject>Toxicology</subject><issn>0260-437X</issn><issn>1099-1263</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd9qFDEUh4Modq2CTyABEbyZmj-TTHJZFt0qpV5YtXgTziQZyDqTWZOZ2n0E39osHVsQxJuE5HznOwk_hJ5TckIJYW-2MJ1QKdkDtKJE64oyyR-iFWGSVDVvro7Qk5y3hJQaU4_REaNcNbxWK_RrPQ47SDCFa4_zNLs9HiOexptgse86b6eMQ3Sz9Q63pZagL0u5mhJcQ7ZzDwmDG0IMeTpoSvfYYTsOwxj7PZ5zaXQhh3hwQSw6iA7nOXWwnEPEpTE_RY866LN_tuzH6PO7t5frs-r84-b9-vS8sqLWrFLSCdsIRVqlwQnlaOs776kUToH2SghPa6-Y19Y5IAqUbkHx2taUCSYdP0avb727NP6YfZ7MELL1fQ_Rj3M2tBG81g3j6v-okIRSTTgv6Mu_0O04p1g-UqhaEKmo4PdCm8ack-_MLoUB0t5QYg5JmpKkOSRZ0BeLcG4H7-7AP9EV4NUClBig7xJEG_I9V57GCCOFq265n6H3-38ONB9OL5fBC18C9Td3PKTvRja8EebrxcZ8O9tcXH3RwnzivwHuEcWZ</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Xue, Yuying</creator><creator>Zhang, Shanshan</creator><creator>Tang, Meng</creator><creator>Zhang, Ting</creator><creator>Wang, Yiqing</creator><creator>Hieda, Yoko</creator><creator>Takeshita, Haruo</creator><general>John Wiley &amp; 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dosage</topic><topic>Benzalkonium Compounds - toxicity</topic><topic>Benzethonium - administration &amp; dosage</topic><topic>Benzethonium - toxicity</topic><topic>Biological and medical sciences</topic><topic>Cationic</topic><topic>Cetomacrogol - administration &amp; dosage</topic><topic>Chlorhexidine - administration &amp; dosage</topic><topic>Chlorhexidine - toxicity</topic><topic>disinfectant</topic><topic>Disinfectants - administration &amp; dosage</topic><topic>Disinfectants - toxicity</topic><topic>Domestic and cosmetic products toxicology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Ingestion</topic><topic>Injections, Intravenous</topic><topic>intravascular administration</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>kinetics</topic><topic>Lethal Dose 50</topic><topic>Lung - drug effects</topic><topic>Lung - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nonionic</topic><topic>oral administration</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Surface-Active Agents - administration &amp; 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Appl. Toxicol</addtitle><date>2012-07</date><risdate>2012</risdate><volume>32</volume><issue>7</issue><spage>480</spage><epage>487</epage><pages>480-487</pages><issn>0260-437X</issn><eissn>1099-1263</eissn><coden>JJATDK</coden><abstract>ABSTRACT Accidental ingestion or injection of household products sometimes occurs due to their accessibility, but the toxic manifestations have not been well characterized when they are internally administered. The aim of this study was to investigate the toxic effects induced by ingestion or injection of different ionic surfactants and disinfectants in rats. The test drugs involved benzalkonium and benzethonium (BZK and BZT, both cationic surfactants used as disinfectants), alkyldiaminoethylglycine (AEG, an amphoteric surfactant used as a disinfectant), linear alkylbenzenesulfonate (LAS, an anionic surfactant), polyoxyethylene cetylether (PEC, a nonionic surfactant), chlorhexidine (CHX, not a surfactant but a disinfectant) and saline (control). Male Sprague–Dawley rats were administered one of the test drugs orally (p.o.), intravenously (i.v.) or intraarterially (i.a.). The fatal effects appeared rapidly (&lt;30 min) in i.v.‐administered rats, while taking hours (&gt;5 h) in i.a./p.o.‐administered rats after a dose of around LD50, although the progress and degree of toxic effects varied among the drugs tested. In intravascular administration, BZK and BZT were fatal at doses of 15–20 mg kg−1. Higher concentrations in lung and kidney than in blood were determined. CHX showed a high toxic effect compared with cationic surfactants. The rats administered anionic (LAS) or amphoteric (AEG) surfactant died in less than 24 h at doses over 100 mg kg−1. In p.o. administration, the toxic effects were concentration/dose‐dependent, and all rats administered high doses of surfactants except for PEC died at 5–20 h. The overall toxic ranks could be: cationic surfactant/CHX&gt; anionic/amphoteric surfactant &gt; nonionic surfactant. Copyright © 2011 John Wiley &amp; Sons, Ltd. Acute toxic effects induced by ingestion or injection of different ionic (cationic, amphoteric, anionic and nonionic) surfactants and disinfectants (chlorhexidine, CHX) in rats were investigated comparatively. The results revealed that the toxic effects varied from one type of surfactant or disinfectant to another, and with the route of administration. Different kinetic properties between benzalkonium chloride, cationic surfactant used as disinfectant, and CHX were observed. The overall toxic ranks could be: cationic surfactant/ CHX&gt; anionic/ amphoteric surfactant&gt; nonionic surfactant.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>21387348</pmid><doi>10.1002/jat.1662</doi><tpages>8</tpages></addata></record>
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subjects Administration, Oral
Amphoterics
Animals
Benzalkonium Compounds - administration & dosage
Benzalkonium Compounds - toxicity
Benzethonium - administration & dosage
Benzethonium - toxicity
Biological and medical sciences
Cationic
Cetomacrogol - administration & dosage
Chlorhexidine - administration & dosage
Chlorhexidine - toxicity
disinfectant
Disinfectants - administration & dosage
Disinfectants - toxicity
Domestic and cosmetic products toxicology
Dose-Response Relationship, Drug
Ingestion
Injections, Intravenous
intravascular administration
Kidney - drug effects
Kidney - metabolism
kinetics
Lethal Dose 50
Lung - drug effects
Lung - metabolism
Male
Medical sciences
Nonionic
oral administration
Rats
Rats, Sprague-Dawley
Surface-Active Agents - administration & dosage
Surface-Active Agents - toxicity
surfactant
Surfactants
Toxic
toxic effects
Toxicology
title Comparative study on toxic effects induced by oral or intravascular administration of commonly used disinfectants and surfactants in rats
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