Literature DB >> 15458722

Kinetic characteristics and toxic effects of benzalkonium chloride following intravascular and oral administration in rats.

Yuying Xue1, Yoko Hieda, Kojiro Kimura, Koji Takayama, Junko Fujihara, Yoshio Tsujino.   

Abstract

Kinetic characteristics and toxic effects of benzalkonium chloride (BZK) following injection via jugular vein (JV), femoral artery (FA) and oral administration (PO) were experimentally investigated using rats. The BZK concentrations in blood and tissues (lung, liver and kidney) were determined by high-performance liquid chromatography with solid phase extraction. Toxic doses of 15 and 250 mg/kg of BZK were used for intravascular (JV and FA) and PO administration, respectively. The fatal effects appeared soon after the dose in JV-rats, while delayed in FA- or PO-rats. The blood BZK concentrations and the elimination half-lives were similar between JV- and FA-rats, while the distribution of BZK in tissues was slightly different. In PO administration, the rats that aspirated BZK into their lungs had some symptoms, while the rats that did not aspirate BZK appeared to be normal. The BZK concentrations in blood and tissues were significantly higher in the aspirated PO-rats. The toxic degree of BZK was correlated with the BZK concentration in orally dosed rats. Lung and kidney had higher BZK concentrations compared to blood or liver, and they could be the target organs of BZK.Keyword: Benzalkonium chloride

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Year:  2004        PMID: 15458722     DOI: 10.1016/j.jchromb.2004.03.075

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  6 in total

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5.  Assessment of respiratory and systemic toxicity of Benzalkonium chloride following a 14-day inhalation study in rats.

Authors:  Hye-Yeon Choi; Yong-Hoon Lee; Cheol-Hong Lim; Yong-Soon Kim; In-Seop Lee; Ji-Min Jo; Ha-Young Lee; Hyo-Geun Cha; Hee Jong Woo; Dong-Seok Seo
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6.  Effects of toxic cellular stresses and divalent cations on the human P2X7 cell death receptor.

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Journal:  Mol Vis       Date:  2008-05-19       Impact factor: 2.367

  6 in total

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