Pharmacokinetics and Tissue Penetration of Ceftolozane-Tazobactam in Diabetic Patients with Lower Limb Infections and Healthy Adult Volunteers

Ceftolozane-tazobactam displays potent activity against Gram-negative bacteria that can cause diabetic foot infections (DFI), making it an attractive treatment option when few alternatives exist. The pharmacokinetics and tissue penetration of ceftolozane-tazobactam at 1.5 g every 8 h (q8h) in patien...

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Veröffentlicht in:Antimicrobial agents and chemotherapy 2017-12, Vol.61 (12)
Hauptverfasser: Monogue, Marguerite L, Stainton, Sean M, Baummer-Carr, Arlinda, Shepard, Ashley K, Nugent, James F, Kuti, Joseph L, Nicolau, David P
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container_title Antimicrobial agents and chemotherapy
container_volume 61
creator Monogue, Marguerite L
Stainton, Sean M
Baummer-Carr, Arlinda
Shepard, Ashley K
Nugent, James F
Kuti, Joseph L
Nicolau, David P
description Ceftolozane-tazobactam displays potent activity against Gram-negative bacteria that can cause diabetic foot infections (DFI), making it an attractive treatment option when few alternatives exist. The pharmacokinetics and tissue penetration of ceftolozane-tazobactam at 1.5 g every 8 h (q8h) in patients ( = 10) with DFI were compared with those in healthy volunteers ( = 6) using microdialysis. In the patient participants, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: maximum concentration ( ), 55.2 μg/ml (range, 40.9 to 169.3 μg/ml); half-life ( ), 3.5 h (range, 2.3 to 4.7 h); and area under the concentration-time curve (AUC) from time zero to 8 h (AUC ), 191.6 μg · h/ml (range, 147.1 to 286.6 μg · h/ml). The median AUC for tissue (AUC ; where AUC was the AUC for tissue for ceftolozane)/AUC for plasma for each antibiotic corrected by the fraction of free drug ( AUC ) was 0.75 (range, 0.35 to 1.00), resulting in a mean free time above 4 μg/ml (the susceptibility breakpoint) in tissue of 99.8% (range, 87.5 to 100%). In the patient participants, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 14.2 μg/ml (range, 7.6 to 64.2 μg/ml); , 2.0 h (range, 0.7 to 2.4 h); and AUC , 27.1 μg · h/ml (range, 15.0 to 70.0 μg · h/ml). The AUC (where AUC was the AUC from time zero to the time of the last measureable concentration in tissue for tazobactam)/ AUC for tazobactam was 1.18 (range, 0.54 to 1.44). In the healthy volunteers, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: , 91.5 μg/ml (range, 65.7 to 110.7 μg/ml); , 1.9 h (range, 1.6 to 2.1 h); and AUC , 191.3 μg · h/ml (range, 118.1 to 274.3 μg · h/ml). The median AUC / AUC was 0.87 (range, 0.54 to 2.20), resulting in a mean free time above 4 μg/ml in tissue of 93.8% (range, 87.5 to 100%). In the healthy volunteers, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 17.5 μg/ml (range, 15.4 to 27.3 μg/ml); , 0.7 h (range, 0.6 to 0.8 h); and AUC , 22.2 μg · h/ml (range, 19.2 to 36.4 μg · h/ml). The AUC / AUC for tazobactam was 0.85 (range, 0.63 to 2.10). Both ceftolozane and tazobactam penetrated into subcutaneous tissue with exposures similar to those of free drug in plasma in both patients with DFI and healthy volunteers. These data suggest that ceftolozane-tazobactam at 1.5 g q8h can achieve the optimal exposu
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The pharmacokinetics and tissue penetration of ceftolozane-tazobactam at 1.5 g every 8 h (q8h) in patients ( = 10) with DFI were compared with those in healthy volunteers ( = 6) using microdialysis. In the patient participants, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: maximum concentration ( ), 55.2 μg/ml (range, 40.9 to 169.3 μg/ml); half-life ( ), 3.5 h (range, 2.3 to 4.7 h); and area under the concentration-time curve (AUC) from time zero to 8 h (AUC ), 191.6 μg · h/ml (range, 147.1 to 286.6 μg · h/ml). The median AUC for tissue (AUC ; where AUC was the AUC for tissue for ceftolozane)/AUC for plasma for each antibiotic corrected by the fraction of free drug ( AUC ) was 0.75 (range, 0.35 to 1.00), resulting in a mean free time above 4 μg/ml (the susceptibility breakpoint) in tissue of 99.8% (range, 87.5 to 100%). In the patient participants, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 14.2 μg/ml (range, 7.6 to 64.2 μg/ml); , 2.0 h (range, 0.7 to 2.4 h); and AUC , 27.1 μg · h/ml (range, 15.0 to 70.0 μg · h/ml). The AUC (where AUC was the AUC from time zero to the time of the last measureable concentration in tissue for tazobactam)/ AUC for tazobactam was 1.18 (range, 0.54 to 1.44). In the healthy volunteers, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: , 91.5 μg/ml (range, 65.7 to 110.7 μg/ml); , 1.9 h (range, 1.6 to 2.1 h); and AUC , 191.3 μg · h/ml (range, 118.1 to 274.3 μg · h/ml). The median AUC / AUC was 0.87 (range, 0.54 to 2.20), resulting in a mean free time above 4 μg/ml in tissue of 93.8% (range, 87.5 to 100%). In the healthy volunteers, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 17.5 μg/ml (range, 15.4 to 27.3 μg/ml); , 0.7 h (range, 0.6 to 0.8 h); and AUC , 22.2 μg · h/ml (range, 19.2 to 36.4 μg · h/ml). The AUC / AUC for tazobactam was 0.85 (range, 0.63 to 2.10). Both ceftolozane and tazobactam penetrated into subcutaneous tissue with exposures similar to those of free drug in plasma in both patients with DFI and healthy volunteers. These data suggest that ceftolozane-tazobactam at 1.5 g q8h can achieve the optimal exposure with activity against susceptible Gram-negative pathogens in the tissue of patients with DFI. (This study has been registered at ClinicalTrials.gov under identifier NCT02620774.).</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AAC.01449-17</identifier><identifier>PMID: 28893779</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Anti-Bacterial Agents ; Cephalosporins ; Clinical Therapeutics ; Diabetes Mellitus, Type 1 ; Diabetes Mellitus, Type 2 ; Diabetic Foot ; Gram-Negative Bacterial Infections ; Penicillanic Acid</subject><ispartof>Antimicrobial agents and chemotherapy, 2017-12, Vol.61 (12)</ispartof><rights>Copyright © 2017 American Society for Microbiology.</rights><rights>Copyright © 2017 American Society for Microbiology. 2017 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a461t-40e677b2166d1085ef042cd791a5c7c0352c5114dc7f1e36ca8935e6897bf0373</citedby><cites>FETCH-LOGICAL-a461t-40e677b2166d1085ef042cd791a5c7c0352c5114dc7f1e36ca8935e6897bf0373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700352/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700352/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28893779$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Monogue, Marguerite L</creatorcontrib><creatorcontrib>Stainton, Sean M</creatorcontrib><creatorcontrib>Baummer-Carr, Arlinda</creatorcontrib><creatorcontrib>Shepard, Ashley K</creatorcontrib><creatorcontrib>Nugent, James F</creatorcontrib><creatorcontrib>Kuti, Joseph L</creatorcontrib><creatorcontrib>Nicolau, David P</creatorcontrib><title>Pharmacokinetics and Tissue Penetration of Ceftolozane-Tazobactam in Diabetic Patients with Lower Limb Infections and Healthy Adult Volunteers</title><title>Antimicrobial agents and chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>Ceftolozane-tazobactam displays potent activity against Gram-negative bacteria that can cause diabetic foot infections (DFI), making it an attractive treatment option when few alternatives exist. The pharmacokinetics and tissue penetration of ceftolozane-tazobactam at 1.5 g every 8 h (q8h) in patients ( = 10) with DFI were compared with those in healthy volunteers ( = 6) using microdialysis. In the patient participants, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: maximum concentration ( ), 55.2 μg/ml (range, 40.9 to 169.3 μg/ml); half-life ( ), 3.5 h (range, 2.3 to 4.7 h); and area under the concentration-time curve (AUC) from time zero to 8 h (AUC ), 191.6 μg · h/ml (range, 147.1 to 286.6 μg · h/ml). The median AUC for tissue (AUC ; where AUC was the AUC for tissue for ceftolozane)/AUC for plasma for each antibiotic corrected by the fraction of free drug ( AUC ) was 0.75 (range, 0.35 to 1.00), resulting in a mean free time above 4 μg/ml (the susceptibility breakpoint) in tissue of 99.8% (range, 87.5 to 100%). In the patient participants, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 14.2 μg/ml (range, 7.6 to 64.2 μg/ml); , 2.0 h (range, 0.7 to 2.4 h); and AUC , 27.1 μg · h/ml (range, 15.0 to 70.0 μg · h/ml). The AUC (where AUC was the AUC from time zero to the time of the last measureable concentration in tissue for tazobactam)/ AUC for tazobactam was 1.18 (range, 0.54 to 1.44). In the healthy volunteers, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: , 91.5 μg/ml (range, 65.7 to 110.7 μg/ml); , 1.9 h (range, 1.6 to 2.1 h); and AUC , 191.3 μg · h/ml (range, 118.1 to 274.3 μg · h/ml). The median AUC / AUC was 0.87 (range, 0.54 to 2.20), resulting in a mean free time above 4 μg/ml in tissue of 93.8% (range, 87.5 to 100%). In the healthy volunteers, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 17.5 μg/ml (range, 15.4 to 27.3 μg/ml); , 0.7 h (range, 0.6 to 0.8 h); and AUC , 22.2 μg · h/ml (range, 19.2 to 36.4 μg · h/ml). The AUC / AUC for tazobactam was 0.85 (range, 0.63 to 2.10). Both ceftolozane and tazobactam penetrated into subcutaneous tissue with exposures similar to those of free drug in plasma in both patients with DFI and healthy volunteers. These data suggest that ceftolozane-tazobactam at 1.5 g q8h can achieve the optimal exposure with activity against susceptible Gram-negative pathogens in the tissue of patients with DFI. (This study has been registered at ClinicalTrials.gov under identifier NCT02620774.).</description><subject>Anti-Bacterial Agents</subject><subject>Cephalosporins</subject><subject>Clinical Therapeutics</subject><subject>Diabetes Mellitus, Type 1</subject><subject>Diabetes Mellitus, Type 2</subject><subject>Diabetic Foot</subject><subject>Gram-Negative Bacterial Infections</subject><subject>Penicillanic Acid</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kU9v1DAQxS0Eokvhxhn5CBIpdhLbyQVptfxppZXYw8LVmjgT1iWxi-1QtR-Cz4zDlgoOnCx7nn9vZh4hzzk747xs3qzXmzPG67otuHpAVpy1TSFFKx-SFWNSFnXD6hPyJMZLlu-iZY_JSdk0baVUuyI_dwcIExj_zTpM1kQKrqd7G-OMdIf5LUCy3lE_0A0OyY_-FhwWe7j1HZgEE7WOvrPQLb_pLovRpUivbTrQrb_GQLd26uiFG9AsoKPBOcKYDjd03c9jol_8OLuEGOJT8miAMeKzu_OUfP7wfr85L7afPl5s1tsCaslTUTOUSnUll7LnrBE4sLo0vWo5CKMMq0RpBOd1b9TAsZIG8rwCZdOqbmCVqk7J2yP3au4m7E3uOcCor4KdINxoD1b_W3H2oL_6H1oottAz4OUdIPjvM8akJxsNjmNejp-j5m3VlNlJyCx9fZSa4GMMONzbcKaXCHWOUP-OUPOltVdHOcSp1Jd-Di5v4n_aF3-PcQ_-k2_1C3Gtplo</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Monogue, Marguerite L</creator><creator>Stainton, Sean M</creator><creator>Baummer-Carr, Arlinda</creator><creator>Shepard, Ashley K</creator><creator>Nugent, James F</creator><creator>Kuti, Joseph L</creator><creator>Nicolau, David P</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171201</creationdate><title>Pharmacokinetics and Tissue Penetration of Ceftolozane-Tazobactam in Diabetic Patients with Lower Limb Infections and Healthy Adult Volunteers</title><author>Monogue, Marguerite L ; Stainton, Sean M ; Baummer-Carr, Arlinda ; Shepard, Ashley K ; Nugent, James F ; Kuti, Joseph L ; Nicolau, David P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a461t-40e677b2166d1085ef042cd791a5c7c0352c5114dc7f1e36ca8935e6897bf0373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Anti-Bacterial Agents</topic><topic>Cephalosporins</topic><topic>Clinical Therapeutics</topic><topic>Diabetes Mellitus, Type 1</topic><topic>Diabetes Mellitus, Type 2</topic><topic>Diabetic Foot</topic><topic>Gram-Negative Bacterial Infections</topic><topic>Penicillanic Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Monogue, Marguerite L</creatorcontrib><creatorcontrib>Stainton, Sean M</creatorcontrib><creatorcontrib>Baummer-Carr, Arlinda</creatorcontrib><creatorcontrib>Shepard, Ashley K</creatorcontrib><creatorcontrib>Nugent, James F</creatorcontrib><creatorcontrib>Kuti, Joseph L</creatorcontrib><creatorcontrib>Nicolau, David P</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antimicrobial agents and chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Monogue, Marguerite L</au><au>Stainton, Sean M</au><au>Baummer-Carr, Arlinda</au><au>Shepard, Ashley K</au><au>Nugent, James F</au><au>Kuti, Joseph L</au><au>Nicolau, David P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics and Tissue Penetration of Ceftolozane-Tazobactam in Diabetic Patients with Lower Limb Infections and Healthy Adult Volunteers</atitle><jtitle>Antimicrobial agents and chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>61</volume><issue>12</issue><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>Ceftolozane-tazobactam displays potent activity against Gram-negative bacteria that can cause diabetic foot infections (DFI), making it an attractive treatment option when few alternatives exist. The pharmacokinetics and tissue penetration of ceftolozane-tazobactam at 1.5 g every 8 h (q8h) in patients ( = 10) with DFI were compared with those in healthy volunteers ( = 6) using microdialysis. In the patient participants, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: maximum concentration ( ), 55.2 μg/ml (range, 40.9 to 169.3 μg/ml); half-life ( ), 3.5 h (range, 2.3 to 4.7 h); and area under the concentration-time curve (AUC) from time zero to 8 h (AUC ), 191.6 μg · h/ml (range, 147.1 to 286.6 μg · h/ml). The median AUC for tissue (AUC ; where AUC was the AUC for tissue for ceftolozane)/AUC for plasma for each antibiotic corrected by the fraction of free drug ( AUC ) was 0.75 (range, 0.35 to 1.00), resulting in a mean free time above 4 μg/ml (the susceptibility breakpoint) in tissue of 99.8% (range, 87.5 to 100%). In the patient participants, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 14.2 μg/ml (range, 7.6 to 64.2 μg/ml); , 2.0 h (range, 0.7 to 2.4 h); and AUC , 27.1 μg · h/ml (range, 15.0 to 70.0 μg · h/ml). The AUC (where AUC was the AUC from time zero to the time of the last measureable concentration in tissue for tazobactam)/ AUC for tazobactam was 1.18 (range, 0.54 to 1.44). In the healthy volunteers, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: , 91.5 μg/ml (range, 65.7 to 110.7 μg/ml); , 1.9 h (range, 1.6 to 2.1 h); and AUC , 191.3 μg · h/ml (range, 118.1 to 274.3 μg · h/ml). The median AUC / AUC was 0.87 (range, 0.54 to 2.20), resulting in a mean free time above 4 μg/ml in tissue of 93.8% (range, 87.5 to 100%). In the healthy volunteers, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 17.5 μg/ml (range, 15.4 to 27.3 μg/ml); , 0.7 h (range, 0.6 to 0.8 h); and AUC , 22.2 μg · h/ml (range, 19.2 to 36.4 μg · h/ml). The AUC / AUC for tazobactam was 0.85 (range, 0.63 to 2.10). Both ceftolozane and tazobactam penetrated into subcutaneous tissue with exposures similar to those of free drug in plasma in both patients with DFI and healthy volunteers. These data suggest that ceftolozane-tazobactam at 1.5 g q8h can achieve the optimal exposure with activity against susceptible Gram-negative pathogens in the tissue of patients with DFI. (This study has been registered at ClinicalTrials.gov under identifier NCT02620774.).</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>28893779</pmid><doi>10.1128/AAC.01449-17</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Anti-Bacterial Agents
Cephalosporins
Clinical Therapeutics
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Diabetic Foot
Gram-Negative Bacterial Infections
Penicillanic Acid
title Pharmacokinetics and Tissue Penetration of Ceftolozane-Tazobactam in Diabetic Patients with Lower Limb Infections and Healthy Adult Volunteers
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