Pharmacokinetic/pharmacodynamic profile for tigecycline—a new glycylcycline antimicrobial agent
Tigecycline is a new first-in-class glycylcycline antimicrobial agent with expanded broad-spectrum activity against both Gram-negative and Gram-positive aerobes and anaerobes, as well as atypical bacterial species. The spectrum of activity extends to clinically relevant susceptible and multidrug-res...
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Veröffentlicht in: | Diagnostic microbiology and infectious disease 2005-07, Vol.52 (3), p.165-171 |
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creator | Meagher, Alison K. Ambrose, Paul G. Grasela, Thaddeus H. Ellis-Grosse, Evelyn J. |
description | Tigecycline is a new first-in-class glycylcycline antimicrobial agent with expanded broad-spectrum activity against both Gram-negative and Gram-positive aerobes and anaerobes, as well as atypical bacterial species. The spectrum of activity extends to clinically relevant susceptible and multidrug-resistant strains of
Staphylococcus aureus, Streptococcus pneumoniae, vancomycin-resistant enterococci, and Enterobacteriaceae, including extended-spectrum β-lactamase–producing strains. Tigecycline is administered as an intravenous formulation and has been studied in the treatment of serious polymicrobial infections, including complicated skin and skin-structure infections and intra-abdominal infections. Pharmacokinetic analysis of data from phase 1 trials of healthy subjects indicate that tigecycline has a large volume of distribution, signifying extensive tissue penetration, and a long terminal elimination half-life (approximately 40 h), easily allowing for twice-daily dose administration. Tigecycline penetrates well into blister fluid, which supports the positive findings of phase 2 and 3 studies of the efficacy of tigecycline in the treatment of serious skin and skin-structure infections. Metabolic studies in humans have revealed that tigecycline undergoes very limited metabolism and the primary route of elimination of unchanged drug is through the feces, with glucuronidation and renal elimination as secondary routes. A preliminary pharmacokinetic (PK)/pharmacodynamic analysis in experimental animal models of infection indicates that the efficacy of tigecycline is probably best predicted by the ratio of the area under the concentration–time curve to the minimum inhibitory concentration. The expanded in vitro activity against a broad range of bacteria, including resistant pathogens, and favorable PK profile of tigecycline suggest that this novel antimicrobial agent should offer clinicians an option for the treatment of patients with serious bacterial infections. |
doi_str_mv | 10.1016/j.diagmicrobio.2005.05.006 |
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Staphylococcus aureus, Streptococcus pneumoniae, vancomycin-resistant enterococci, and Enterobacteriaceae, including extended-spectrum β-lactamase–producing strains. Tigecycline is administered as an intravenous formulation and has been studied in the treatment of serious polymicrobial infections, including complicated skin and skin-structure infections and intra-abdominal infections. Pharmacokinetic analysis of data from phase 1 trials of healthy subjects indicate that tigecycline has a large volume of distribution, signifying extensive tissue penetration, and a long terminal elimination half-life (approximately 40 h), easily allowing for twice-daily dose administration. Tigecycline penetrates well into blister fluid, which supports the positive findings of phase 2 and 3 studies of the efficacy of tigecycline in the treatment of serious skin and skin-structure infections. Metabolic studies in humans have revealed that tigecycline undergoes very limited metabolism and the primary route of elimination of unchanged drug is through the feces, with glucuronidation and renal elimination as secondary routes. A preliminary pharmacokinetic (PK)/pharmacodynamic analysis in experimental animal models of infection indicates that the efficacy of tigecycline is probably best predicted by the ratio of the area under the concentration–time curve to the minimum inhibitory concentration. The expanded in vitro activity against a broad range of bacteria, including resistant pathogens, and favorable PK profile of tigecycline suggest that this novel antimicrobial agent should offer clinicians an option for the treatment of patients with serious bacterial infections.</description><identifier>ISSN: 0732-8893</identifier><identifier>EISSN: 1879-0070</identifier><identifier>DOI: 10.1016/j.diagmicrobio.2005.05.006</identifier><identifier>PMID: 16105560</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Age Factors ; Animals ; Anti-Bacterial Agents - administration & dosage ; Anti-Bacterial Agents - pharmacokinetics ; Anti-Bacterial Agents - pharmacology ; Enterobacteriaceae ; Humans ; Infusions, Intravenous ; Microbial Sensitivity Tests ; Minocycline - administration & dosage ; Minocycline - analogs & derivatives ; Minocycline - pharmacokinetics ; Minocycline - pharmacology ; Pharmacokinetics ; Pharmacology ; Sex Factors ; Staphylococcus aureus ; Statistics, Nonparametric ; Streptococcus pneumoniae ; Tigecycline</subject><ispartof>Diagnostic microbiology and infectious disease, 2005-07, Vol.52 (3), p.165-171</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-8df1d60f0dcc33e7eaefa2f4341d8e2a234f30704a4e952e29b1fad8152292683</citedby><cites>FETCH-LOGICAL-c409t-8df1d60f0dcc33e7eaefa2f4341d8e2a234f30704a4e952e29b1fad8152292683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.diagmicrobio.2005.05.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3552,27931,27932,46002</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16105560$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meagher, Alison K.</creatorcontrib><creatorcontrib>Ambrose, Paul G.</creatorcontrib><creatorcontrib>Grasela, Thaddeus H.</creatorcontrib><creatorcontrib>Ellis-Grosse, Evelyn J.</creatorcontrib><title>Pharmacokinetic/pharmacodynamic profile for tigecycline—a new glycylcycline antimicrobial agent</title><title>Diagnostic microbiology and infectious disease</title><addtitle>Diagn Microbiol Infect Dis</addtitle><description>Tigecycline is a new first-in-class glycylcycline antimicrobial agent with expanded broad-spectrum activity against both Gram-negative and Gram-positive aerobes and anaerobes, as well as atypical bacterial species. The spectrum of activity extends to clinically relevant susceptible and multidrug-resistant strains of
Staphylococcus aureus, Streptococcus pneumoniae, vancomycin-resistant enterococci, and Enterobacteriaceae, including extended-spectrum β-lactamase–producing strains. Tigecycline is administered as an intravenous formulation and has been studied in the treatment of serious polymicrobial infections, including complicated skin and skin-structure infections and intra-abdominal infections. Pharmacokinetic analysis of data from phase 1 trials of healthy subjects indicate that tigecycline has a large volume of distribution, signifying extensive tissue penetration, and a long terminal elimination half-life (approximately 40 h), easily allowing for twice-daily dose administration. Tigecycline penetrates well into blister fluid, which supports the positive findings of phase 2 and 3 studies of the efficacy of tigecycline in the treatment of serious skin and skin-structure infections. Metabolic studies in humans have revealed that tigecycline undergoes very limited metabolism and the primary route of elimination of unchanged drug is through the feces, with glucuronidation and renal elimination as secondary routes. A preliminary pharmacokinetic (PK)/pharmacodynamic analysis in experimental animal models of infection indicates that the efficacy of tigecycline is probably best predicted by the ratio of the area under the concentration–time curve to the minimum inhibitory concentration. The expanded in vitro activity against a broad range of bacteria, including resistant pathogens, and favorable PK profile of tigecycline suggest that this novel antimicrobial agent should offer clinicians an option for the treatment of patients with serious bacterial infections.</description><subject>Age Factors</subject><subject>Animals</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Anti-Bacterial Agents - pharmacokinetics</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Enterobacteriaceae</subject><subject>Humans</subject><subject>Infusions, Intravenous</subject><subject>Microbial Sensitivity Tests</subject><subject>Minocycline - administration & dosage</subject><subject>Minocycline - analogs & derivatives</subject><subject>Minocycline - pharmacokinetics</subject><subject>Minocycline - pharmacology</subject><subject>Pharmacokinetics</subject><subject>Pharmacology</subject><subject>Sex Factors</subject><subject>Staphylococcus aureus</subject><subject>Statistics, Nonparametric</subject><subject>Streptococcus pneumoniae</subject><subject>Tigecycline</subject><issn>0732-8893</issn><issn>1879-0070</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1qHDEQhUWIiSe2r2CaLLLrcUnqVkvZBTtxAoZ4Ya-FRiqNNemfidTj0DsfwifMSaJhGpKdDQVC4iu9qvcI-UBhSYGKi83SBbPugo3DKgxLBlAv9wXiDVlQ2agSoIG3ZAENZ6WUih-T9yltAChTFbwjx1RQqGsBC2JuH0zsjB1-hh7HYC-2891NvckSxTYOPrRY-CEWY1ijnWyb0T9Pz6bo8Xexbic7tfNrYfoxzIOZtjBr7MdTcuRNm_BsPk_I_dcvd5ffypsf198vP9-UtgI1ltJ56gR4cNZyjg0a9Ib5ilfUSWSG8crzvFZlKlQ1Q6ZW1Bsnac2YYkLyE_Lx8G-e-NcO06i7kCy2relx2CUtZCWFapoXQZY9lkzxDH46gHmflCJ6vY2hM3HSFPQ-Cb3R_yeh90nofYHIzeezym7VofvXOlufgasDgNmUx4BRJxuwt-hCRDtqN4TX6PwFjaykSA</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Meagher, Alison K.</creator><creator>Ambrose, Paul G.</creator><creator>Grasela, Thaddeus H.</creator><creator>Ellis-Grosse, Evelyn J.</creator><general>Elsevier Inc</general><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>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20050701</creationdate><title>Pharmacokinetic/pharmacodynamic profile for tigecycline—a new glycylcycline antimicrobial agent</title><author>Meagher, Alison K. ; Ambrose, Paul G. ; Grasela, Thaddeus H. ; Ellis-Grosse, Evelyn J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-8df1d60f0dcc33e7eaefa2f4341d8e2a234f30704a4e952e29b1fad8152292683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Age Factors</topic><topic>Animals</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Anti-Bacterial Agents - pharmacokinetics</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Enterobacteriaceae</topic><topic>Humans</topic><topic>Infusions, Intravenous</topic><topic>Microbial Sensitivity Tests</topic><topic>Minocycline - administration & dosage</topic><topic>Minocycline - analogs & derivatives</topic><topic>Minocycline - pharmacokinetics</topic><topic>Minocycline - pharmacology</topic><topic>Pharmacokinetics</topic><topic>Pharmacology</topic><topic>Sex Factors</topic><topic>Staphylococcus aureus</topic><topic>Statistics, Nonparametric</topic><topic>Streptococcus pneumoniae</topic><topic>Tigecycline</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meagher, Alison K.</creatorcontrib><creatorcontrib>Ambrose, Paul G.</creatorcontrib><creatorcontrib>Grasela, Thaddeus H.</creatorcontrib><creatorcontrib>Ellis-Grosse, Evelyn J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Diagnostic microbiology and infectious disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meagher, Alison K.</au><au>Ambrose, Paul G.</au><au>Grasela, Thaddeus H.</au><au>Ellis-Grosse, Evelyn J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetic/pharmacodynamic profile for tigecycline—a new glycylcycline antimicrobial agent</atitle><jtitle>Diagnostic microbiology and infectious disease</jtitle><addtitle>Diagn Microbiol Infect Dis</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>52</volume><issue>3</issue><spage>165</spage><epage>171</epage><pages>165-171</pages><issn>0732-8893</issn><eissn>1879-0070</eissn><abstract>Tigecycline is a new first-in-class glycylcycline antimicrobial agent with expanded broad-spectrum activity against both Gram-negative and Gram-positive aerobes and anaerobes, as well as atypical bacterial species. The spectrum of activity extends to clinically relevant susceptible and multidrug-resistant strains of
Staphylococcus aureus, Streptococcus pneumoniae, vancomycin-resistant enterococci, and Enterobacteriaceae, including extended-spectrum β-lactamase–producing strains. Tigecycline is administered as an intravenous formulation and has been studied in the treatment of serious polymicrobial infections, including complicated skin and skin-structure infections and intra-abdominal infections. Pharmacokinetic analysis of data from phase 1 trials of healthy subjects indicate that tigecycline has a large volume of distribution, signifying extensive tissue penetration, and a long terminal elimination half-life (approximately 40 h), easily allowing for twice-daily dose administration. Tigecycline penetrates well into blister fluid, which supports the positive findings of phase 2 and 3 studies of the efficacy of tigecycline in the treatment of serious skin and skin-structure infections. Metabolic studies in humans have revealed that tigecycline undergoes very limited metabolism and the primary route of elimination of unchanged drug is through the feces, with glucuronidation and renal elimination as secondary routes. A preliminary pharmacokinetic (PK)/pharmacodynamic analysis in experimental animal models of infection indicates that the efficacy of tigecycline is probably best predicted by the ratio of the area under the concentration–time curve to the minimum inhibitory concentration. The expanded in vitro activity against a broad range of bacteria, including resistant pathogens, and favorable PK profile of tigecycline suggest that this novel antimicrobial agent should offer clinicians an option for the treatment of patients with serious bacterial infections.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16105560</pmid><doi>10.1016/j.diagmicrobio.2005.05.006</doi><tpages>7</tpages></addata></record> |
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subjects | Age Factors Animals Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - pharmacokinetics Anti-Bacterial Agents - pharmacology Enterobacteriaceae Humans Infusions, Intravenous Microbial Sensitivity Tests Minocycline - administration & dosage Minocycline - analogs & derivatives Minocycline - pharmacokinetics Minocycline - pharmacology Pharmacokinetics Pharmacology Sex Factors Staphylococcus aureus Statistics, Nonparametric Streptococcus pneumoniae Tigecycline |
title | Pharmacokinetic/pharmacodynamic profile for tigecycline—a new glycylcycline antimicrobial agent |
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