Pharmacokinetics of disodium fosfomycin in broilers and dose strategies to comply with its pharmacodynamics versus Escherichia coli

The objective of this study was to determine, in broilers, which modality of disodium fosfomycin (DF) administration and at what dose the best pharmacokinetic (PK) profile could be obtained, taking as reference a 110 field bacterial strains of Escherichia coli minimum inhibitory concentration survey...

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Veröffentlicht in:Poultry science 2010-10, Vol.89 (10), p.2106-2115
Hauptverfasser: Gutierrez, L, Ocampo, L, Rosario, C, Sumano, H
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creator Gutierrez, L
Ocampo, L
Rosario, C
Sumano, H
description The objective of this study was to determine, in broilers, which modality of disodium fosfomycin (DF) administration and at what dose the best pharmacokinetic (PK) profile could be obtained, taking as reference a 110 field bacterial strains of Escherichia coli minimum inhibitory concentration survey. The DF was administered via drinking water either ad libitum or at a higher concentration having 1 h of water restriction to build up thirst in the birds (loading dose). Dosages tested were 10, 20, 40, and 80 mg/kg per administration, either once or twice daily. Birds included were 24-d-old Cornish broilers randomly assigned to 16 groups of 200 birds per group and 3 replicates per group. The PK of DF was determined after ad libitum administration of either a single- or double-loading dose or after an initial loading dose followed by ad libitum medication. Also, PK after i.v. administration was studied in separate groups. Serial blood samplings were performed in all groups. Serum obtained was analyzed for DF and a possible active metabolite by means of a microbiological agar diffusion assay. The DF showed a short elimination half-life (approximately 2 h after oral loading administration) with a rapid clearance (1.23 to 1.42 mL/kg per h). Apparent volume of distribution-area under the curve values were also low (10 and 80 mg/kg = 0.25 L/kg and 0.22 L/kg, respectively). Considering a minimum inhibitory concentration level that inhibited 90% of total strains of 8 μg/mL for E. coli, it is concluded that single-loading administration at 10, 20, 40, and 80 mg/kg complies poorly with sustained serum concentrations over a dosing interval of 24 h. Doses of 10 and 20 mg/kg twice a day also were insufficient to attain therapeutic concentrations. Useful serum concentrations of DF to treat outbreaks of susceptible E. coli require an initial loading dose of 40 mg/kg, followed by an ad libitum medication of 40 mg/kg 8 h later (80 mg/kg per d).
doi_str_mv 10.3382/ps.2010-00892
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The DF was administered via drinking water either ad libitum or at a higher concentration having 1 h of water restriction to build up thirst in the birds (loading dose). Dosages tested were 10, 20, 40, and 80 mg/kg per administration, either once or twice daily. Birds included were 24-d-old Cornish broilers randomly assigned to 16 groups of 200 birds per group and 3 replicates per group. The PK of DF was determined after ad libitum administration of either a single- or double-loading dose or after an initial loading dose followed by ad libitum medication. Also, PK after i.v. administration was studied in separate groups. Serial blood samplings were performed in all groups. Serum obtained was analyzed for DF and a possible active metabolite by means of a microbiological agar diffusion assay. The DF showed a short elimination half-life (approximately 2 h after oral loading administration) with a rapid clearance (1.23 to 1.42 mL/kg per h). Apparent volume of distribution-area under the curve values were also low (10 and 80 mg/kg = 0.25 L/kg and 0.22 L/kg, respectively). Considering a minimum inhibitory concentration level that inhibited 90% of total strains of 8 μg/mL for E. coli, it is concluded that single-loading administration at 10, 20, 40, and 80 mg/kg complies poorly with sustained serum concentrations over a dosing interval of 24 h. Doses of 10 and 20 mg/kg twice a day also were insufficient to attain therapeutic concentrations. Useful serum concentrations of DF to treat outbreaks of susceptible E. coli require an initial loading dose of 40 mg/kg, followed by an ad libitum medication of 40 mg/kg 8 h later (80 mg/kg per d).</description><identifier>ISSN: 0032-5791</identifier><identifier>EISSN: 1525-3171</identifier><identifier>DOI: 10.3382/ps.2010-00892</identifier><identifier>PMID: 20852101</identifier><language>eng</language><publisher>Oxford, UK: Poultry Science Association</publisher><subject>ad libitum feeding ; animal pathogenic bacteria ; Animals ; antibiotics ; Area Under Curve ; blood chemistry ; broiler chickens ; Chickens ; disodium fosfomycin ; dosage ; Dose-Response Relationship, Drug ; drinking water ; drug therapy ; Escherichia coli ; Escherichia coli - drug effects ; Escherichia coli Infections - prevention &amp; control ; Escherichia coli Infections - veterinary ; Fosfomycin - pharmacokinetics ; Fosfomycin - pharmacology ; Fosfomycin - therapeutic use ; Half-Life ; intravenous injection ; metabolites ; Microbial Sensitivity Tests ; minimum inhibitory concentration ; oral administration ; pharmacokinetics ; Poultry Diseases - prevention &amp; control ; Protein Binding ; Time Factors</subject><ispartof>Poultry science, 2010-10, Vol.89 (10), p.2106-2115</ispartof><rights>2010 Poultry Science Association Inc. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-e81ddc592e928a245be4f2b8d61a0bbf99e436772ba3e146482c49d8183bad603</citedby><cites>FETCH-LOGICAL-c420t-e81ddc592e928a245be4f2b8d61a0bbf99e436772ba3e146482c49d8183bad603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20852101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gutierrez, L</creatorcontrib><creatorcontrib>Ocampo, L</creatorcontrib><creatorcontrib>Rosario, C</creatorcontrib><creatorcontrib>Sumano, H</creatorcontrib><title>Pharmacokinetics of disodium fosfomycin in broilers and dose strategies to comply with its pharmacodynamics versus Escherichia coli</title><title>Poultry science</title><addtitle>Poult Sci</addtitle><description>The objective of this study was to determine, in broilers, which modality of disodium fosfomycin (DF) administration and at what dose the best pharmacokinetic (PK) profile could be obtained, taking as reference a 110 field bacterial strains of Escherichia coli minimum inhibitory concentration survey. The DF was administered via drinking water either ad libitum or at a higher concentration having 1 h of water restriction to build up thirst in the birds (loading dose). Dosages tested were 10, 20, 40, and 80 mg/kg per administration, either once or twice daily. Birds included were 24-d-old Cornish broilers randomly assigned to 16 groups of 200 birds per group and 3 replicates per group. The PK of DF was determined after ad libitum administration of either a single- or double-loading dose or after an initial loading dose followed by ad libitum medication. Also, PK after i.v. administration was studied in separate groups. Serial blood samplings were performed in all groups. Serum obtained was analyzed for DF and a possible active metabolite by means of a microbiological agar diffusion assay. The DF showed a short elimination half-life (approximately 2 h after oral loading administration) with a rapid clearance (1.23 to 1.42 mL/kg per h). Apparent volume of distribution-area under the curve values were also low (10 and 80 mg/kg = 0.25 L/kg and 0.22 L/kg, respectively). Considering a minimum inhibitory concentration level that inhibited 90% of total strains of 8 μg/mL for E. coli, it is concluded that single-loading administration at 10, 20, 40, and 80 mg/kg complies poorly with sustained serum concentrations over a dosing interval of 24 h. Doses of 10 and 20 mg/kg twice a day also were insufficient to attain therapeutic concentrations. Useful serum concentrations of DF to treat outbreaks of susceptible E. coli require an initial loading dose of 40 mg/kg, followed by an ad libitum medication of 40 mg/kg 8 h later (80 mg/kg per d).</description><subject>ad libitum feeding</subject><subject>animal pathogenic bacteria</subject><subject>Animals</subject><subject>antibiotics</subject><subject>Area Under Curve</subject><subject>blood chemistry</subject><subject>broiler chickens</subject><subject>Chickens</subject><subject>disodium fosfomycin</subject><subject>dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>drinking water</subject><subject>drug therapy</subject><subject>Escherichia coli</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli Infections - prevention &amp; control</subject><subject>Escherichia coli Infections - veterinary</subject><subject>Fosfomycin - pharmacokinetics</subject><subject>Fosfomycin - pharmacology</subject><subject>Fosfomycin - therapeutic use</subject><subject>Half-Life</subject><subject>intravenous injection</subject><subject>metabolites</subject><subject>Microbial Sensitivity Tests</subject><subject>minimum inhibitory concentration</subject><subject>oral administration</subject><subject>pharmacokinetics</subject><subject>Poultry Diseases - prevention &amp; control</subject><subject>Protein Binding</subject><subject>Time Factors</subject><issn>0032-5791</issn><issn>1525-3171</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQQC0EokvhyBV8g0uKZ5wP-4iq8iFVKhL0bDm20zUkcfAkVHvuH2-W3XJDlUaaw7x5l8fYaxBnUir8MNEZChCFEErjE7aBCqtCQgNP2UYIiUXVaDhhL4h-CoFQ181zdoJCVQgCNuzu29bmwbr0K45hjo546riPlHxcBt4l6tKwc3Hk67Q5xT5k4nb03CcKnOZs53ATA_E5cZeGqd_x2zhveZyJT0e134122Kv_rM8L8Qty25Cj20a7_vTxJXvW2Z7Cq-M-ZdefLn6cfykurz5_Pf94WbgSxVwEBd67SmPQqCyWVRvKDlvla7CibTutQynrpsHWygBlXSp0pfYKlGytr4U8Ze8O3imn30ug2QyRXOh7O4a0kFGiQYWAj5NNVYGWNaqVLA6ky4koh85MOQ427wwIsw9kJjL7QOZvoJV_czQv7RD8P_qhyAq8PwBpmf7nKh5cbw9oZ5OxNzmSuf6-3qUApXRZgrwH4vmjpA</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Gutierrez, L</creator><creator>Ocampo, L</creator><creator>Rosario, C</creator><creator>Sumano, H</creator><general>Poultry Science Association</general><general>Oxford University Press</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20101001</creationdate><title>Pharmacokinetics of disodium fosfomycin in broilers and dose strategies to comply with its pharmacodynamics versus Escherichia coli</title><author>Gutierrez, L ; Ocampo, L ; Rosario, C ; Sumano, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-e81ddc592e928a245be4f2b8d61a0bbf99e436772ba3e146482c49d8183bad603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>ad libitum feeding</topic><topic>animal pathogenic bacteria</topic><topic>Animals</topic><topic>antibiotics</topic><topic>Area Under Curve</topic><topic>blood chemistry</topic><topic>broiler chickens</topic><topic>Chickens</topic><topic>disodium fosfomycin</topic><topic>dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>drinking water</topic><topic>drug therapy</topic><topic>Escherichia coli</topic><topic>Escherichia coli - drug effects</topic><topic>Escherichia coli Infections - prevention &amp; control</topic><topic>Escherichia coli Infections - veterinary</topic><topic>Fosfomycin - pharmacokinetics</topic><topic>Fosfomycin - pharmacology</topic><topic>Fosfomycin - therapeutic use</topic><topic>Half-Life</topic><topic>intravenous injection</topic><topic>metabolites</topic><topic>Microbial Sensitivity Tests</topic><topic>minimum inhibitory concentration</topic><topic>oral administration</topic><topic>pharmacokinetics</topic><topic>Poultry Diseases - prevention &amp; control</topic><topic>Protein Binding</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gutierrez, L</creatorcontrib><creatorcontrib>Ocampo, L</creatorcontrib><creatorcontrib>Rosario, C</creatorcontrib><creatorcontrib>Sumano, H</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Poultry science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gutierrez, L</au><au>Ocampo, L</au><au>Rosario, C</au><au>Sumano, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics of disodium fosfomycin in broilers and dose strategies to comply with its pharmacodynamics versus Escherichia coli</atitle><jtitle>Poultry science</jtitle><addtitle>Poult Sci</addtitle><date>2010-10-01</date><risdate>2010</risdate><volume>89</volume><issue>10</issue><spage>2106</spage><epage>2115</epage><pages>2106-2115</pages><issn>0032-5791</issn><eissn>1525-3171</eissn><abstract>The objective of this study was to determine, in broilers, which modality of disodium fosfomycin (DF) administration and at what dose the best pharmacokinetic (PK) profile could be obtained, taking as reference a 110 field bacterial strains of Escherichia coli minimum inhibitory concentration survey. The DF was administered via drinking water either ad libitum or at a higher concentration having 1 h of water restriction to build up thirst in the birds (loading dose). Dosages tested were 10, 20, 40, and 80 mg/kg per administration, either once or twice daily. Birds included were 24-d-old Cornish broilers randomly assigned to 16 groups of 200 birds per group and 3 replicates per group. The PK of DF was determined after ad libitum administration of either a single- or double-loading dose or after an initial loading dose followed by ad libitum medication. Also, PK after i.v. administration was studied in separate groups. Serial blood samplings were performed in all groups. Serum obtained was analyzed for DF and a possible active metabolite by means of a microbiological agar diffusion assay. The DF showed a short elimination half-life (approximately 2 h after oral loading administration) with a rapid clearance (1.23 to 1.42 mL/kg per h). Apparent volume of distribution-area under the curve values were also low (10 and 80 mg/kg = 0.25 L/kg and 0.22 L/kg, respectively). Considering a minimum inhibitory concentration level that inhibited 90% of total strains of 8 μg/mL for E. coli, it is concluded that single-loading administration at 10, 20, 40, and 80 mg/kg complies poorly with sustained serum concentrations over a dosing interval of 24 h. Doses of 10 and 20 mg/kg twice a day also were insufficient to attain therapeutic concentrations. Useful serum concentrations of DF to treat outbreaks of susceptible E. coli require an initial loading dose of 40 mg/kg, followed by an ad libitum medication of 40 mg/kg 8 h later (80 mg/kg per d).</abstract><cop>Oxford, UK</cop><pub>Poultry Science Association</pub><pmid>20852101</pmid><doi>10.3382/ps.2010-00892</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Alma/SFX Local Collection; EZB Electronic Journals Library
subjects ad libitum feeding
animal pathogenic bacteria
Animals
antibiotics
Area Under Curve
blood chemistry
broiler chickens
Chickens
disodium fosfomycin
dosage
Dose-Response Relationship, Drug
drinking water
drug therapy
Escherichia coli
Escherichia coli - drug effects
Escherichia coli Infections - prevention & control
Escherichia coli Infections - veterinary
Fosfomycin - pharmacokinetics
Fosfomycin - pharmacology
Fosfomycin - therapeutic use
Half-Life
intravenous injection
metabolites
Microbial Sensitivity Tests
minimum inhibitory concentration
oral administration
pharmacokinetics
Poultry Diseases - prevention & control
Protein Binding
Time Factors
title Pharmacokinetics of disodium fosfomycin in broilers and dose strategies to comply with its pharmacodynamics versus Escherichia coli
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