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      Toxicological assessment of polyhexamethylene biguanide for water treatment

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          Abstract

          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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          Effect of bee venom on some blood and biochemical parameters in formaldehyde induced arthritis male rats in comparison with prednisolone drug

          Background Bee venom(BV) has been used to treat and reduce chronic inflammatory diseases such as rheumatoid arthritis(RA), pain, skin diseases and to treat cancerous tumors. The aim of this study was to investigate the effects of bee venom on some blood and biochemical parameters in male albino rats with Arthritis and compare it with prednisolone drug. Materials & methods: (42) mature male albino rats (135-150) gm, divided into (7) groups, (6) male rats for each group. The experiment was continued for (14) days and included: the first group (negative control) was injected by (0.1ml/animal) from physiological normal saline (0.9% Nacl),the second group(Arthritis group) was injected by (0.1ml/animal) formaldehyde, the third group (normal group) was injected by bee venom(i.p) (1mg / kg of B.W), the fourth group (normal group) was treated orally with prednisolone (5mg / kg of B.W), the fifth group (Arthritis group) was injected by bee venom(i.p) (1mg / kg of B.W), the sixth group (Arthritis group) was treated orally by prednisolone (5 mg / kg of B.W) and seventh group (Arthritis group) was injected by bee venom (1 mg/ kg of B.W) and treated orally with prednisolone (5mg / kg of B.W). Results : Our results showed that 2 nd group (Arthritis) significantly increased (p≤ 0.05) in the number of WBCs and platelets compared with control group, while the 3 rd and 4 th groups showed a significant decrease in WBCs and PLT compared with 2 nd group. The 5 th , 6 th and 7 th groups showed a significant decrease (P≤0.05) in the number of WBCs and platelets compared with 2 nd group. On the other hand, the present study demonstrated a significant decrease (p≤ 0.05) in RBCs, hemoglobin (Hb) and hematocrit (HCT) in the 2 nd group (Arthritis group) compared with control group, while the 3 rd and 4 th groups showed a significant increase in RBCs, Hb and HCT compared with 2 nd group. The 5 th , 6 th and 7 th groups showed increase (p≤ 0.05) in RBCs, Hb and HCT compared with 2 nd group. The results showed also, a significant increase in levels of cholesterol, triglycerides, LDL and a significant decrease in HDL level in 2 nd group compared with control group, while 3 rd ,4 th , 5 th , 6 th and 7 th groups showed a significant decrease (P≤0.05) in cholesterol, triglycerides, LDL and a significant increase in HDL level compared with 2 nd group. Conclusion : We conclude from the present study that bee venom attenuates development of Arthritis by improving some Blood and Biochemical parameters.
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            Interaction of some polyhexamethylene biguanides and membrane phospholipids in Escherichia coli.

            The interaction between some polyhexamethylene biguanides and the cell envelope of Escherichia coli has been investigated. An amine-ended dimer, (AED, n = 2), a polydisperse mixture (ICI plc) available as the active ingredient of Vantocil IB, (PHMB, n = 5.5), and a high molecular weight fraction, (HMW, n = greater than or equal to 10) of PHMB were used. The sensitivity of batch cultures depleted of magnesium (M-dep), phosphorus (P-dep) or glycerol (C-dep) towards the biocides was assessed by monitoring the rate and extent of potassium ion leakage. P-dep suspensions were particularly resistant to all these agents and possessed less than half the quantity of phospholipid of other cell types. This was compensated for by a proportionate increase in fatty acid and neutral lipid content of the cells. The reduction in phospholipid content was accounted for by decreases in phosphatidylglycerol (PG) and phosphatidylethanolamine (PE). Diphosphatidylglycerol (DPG) and phosphatidylserine (PS) content of the cultures remained unaffected by the depleting nutrient. Fourier-transform n.m.r. spectroscopy was used to study proton nuclei during the interaction of HMW, AED and PHMB with various phospholipid-vesicle preparations. The results strongly suggest that the biocides acted preferentially on the acidic phospholipids PG and DPG, rather than towards PE or PS. Resistance of P-dep cultures therefore reflected reductions in PG content. A molecular basis for the interaction of these compounds and membranes is proposed.
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              Influence of the Antiseptic Agents Polyhexanide and Octenidine on FL Cells and on Healing of Experimental Superficial Aseptic Wounds in Piglets

              The main target of the combination of octenidine with phenoxyethanol (Octenisept ® ) is the antisepsis of acute wounds, whereas polyhexanide combined with polyethylene glycol in Ringer solution (Lavasept ® ) is the agent of choice for antisepsis of chronic wounds and burns. Because comparative data for both agents on the effects on wound healing are lacking, we investigated the influence of preparations based on polyhexanide and octenidine versus placebo (Ringer solution) in experimental superficial aseptic skin wounds (n = 108) of 20 mm diameter, using a double-blind, randomised, stratified, controlled, parallel-group design in piglets. Computerised planimetry and histopathological methods were used for the assessment of wound healing. Histologically, no significant differences could be verified at any time between the 3 groups. However, in the early phase (day 9 after wounding), the octenidine-based product retarded wound contraction to a significantly greater extent than placebo and polyhexanide, whereas in the later phase (days 18 and 28), polyhexanide promoted contraction significantly more than did placebo and octenidine. The consequence is complete wound closure after 22.9 days using polyhexanide, in comparison to the placebo after 24.1 days (p < 0.05) and octenidine after 28.3 days (no statistical difference to placebo). This may be explained by the better tolerance of polyhexanide in vitro, which was demonstrated with dose and time dependence in cytotoxicity tests on human amnion cells.
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                Author and article information

                Journal
                Interdiscip Toxicol
                Interdiscip Toxicol
                ITX
                Interdisciplinary Toxicology
                Slovak Toxicology Society SETOX
                1337-6853
                1337-9569
                December 2015
                December 2015
                : 8
                : 4
                : 193-202
                Affiliations
                [1 ]Department of Pharmacology and Toxicology, University of Ghana School of Pharmacy, College of Health Sciences, Legon, Ghana
                [2 ]Department of Pathology, School of Biomedical and Allied Health Sciences, College of Health Sciences, Korle-Bu, Ghana
                [3 ]Division of Pharmacology, Faculty of Health Sciences, University of Stellenbosch, Cape Town, South Africa
                Author notes
                Correspondence address: Dr. Isaac Julius Asiedu-Gyekye, MSc Pharm., PhD., University of Ghana School of Pharmacy, College of Health Sciences, University of Ghana, Legon, Ghana. TEL.: +233(0)208111590. E-MAIL: asiedugyekye@ 123456yahoo.co.uk , ijagyekye@ 123456ug.edu.gh
                Article
                ITX-8-193
                10.1515/intox-2015-0029
                4961918
                27486381
                220b8c78-36e4-4db1-98e5-b87775307844
                Copyright © 2015 SETOX & Institute of Experimental Pharmacology and Toxicology, SASc.

                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.

                History
                : 20 January 2014
                : 28 August 2015
                : 10 September 2015
                Categories
                Original Article

                Toxicology
                polyhexamethylene biguanide,toxicity,biochemical hematology,histopathology,ld50,therapeutic index

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