<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>40(1)</volume><submitter>Amann LF</submitter><funding>Universität Hamburg</funding><pubmed_abstract>&lt;h4>Purpose&lt;/h4>This study aimed to examine the degradation of tigecycline in Mueller Hinton broth (ca-MHB), as knowledge about bacterial susceptibility is key for therapeutic decisions.&lt;h4>Methods&lt;/h4>Antioxidative stabilizers were evaluated on tigecycline stability in a quantitative chromatography assay and tigecycline induced kill against Staphylococcus aureus (ATCC29213) was determined in time kill studies.&lt;h4>Results&lt;/h4>Ascorbic acid caused rapid degradation of tigecycline and resulted in loss of antibacterial activity. Tigecycline was stabilized in aged broth by 2% pyruvate and bacterial growth, and tigecycline killing was similar to fresh broth without supplementation, but independent of age.&lt;h4>Conclusion&lt;/h4>Our results underline the importance of using freshly prepared ca-MHB or</pubmed_abstract><journal>European journal of clinical microbiology &amp; infectious diseases : official publication of the European Society of Clinical Microbiology</journal><pagination>215-218</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7782409</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Stability studies with tigecycline in bacterial growth medium and impact of stabilizing agents.</pubmed_title><pmcid>PMC7782409</pmcid><pubmed_authors>Rathke M</pubmed_authors><pubmed_authors>Wicha SG</pubmed_authors><pubmed_authors>Broeker A</pubmed_authors><pubmed_authors>Riedner M</pubmed_authors><pubmed_authors>Vicente ER</pubmed_authors><pubmed_authors>Amann LF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stability studies with tigecycline in bacterial growth medium and impact of stabilizing agents.</name><description>&lt;h4>Purpose&lt;/h4>This study aimed to examine the degradation of tigecycline in Mueller Hinton broth (ca-MHB), as knowledge about bacterial susceptibility is key for therapeutic decisions.&lt;h4>Methods&lt;/h4>Antioxidative stabilizers were evaluated on tigecycline stability in a quantitative chromatography assay and tigecycline induced kill against Staphylococcus aureus (ATCC29213) was determined in time kill studies.&lt;h4>Results&lt;/h4>Ascorbic acid caused rapid degradation of tigecycline and resulted in loss of antibacterial activity. Tigecycline was stabilized in aged broth by 2% pyruvate and bacterial growth, and tigecycline killing was similar to fresh broth without supplementation, but independent of age.&lt;h4>Conclusion&lt;/h4>Our results underline the importance of using freshly prepared ca-MHB or</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2025-05-31T22:41:20.38Z</modification><creation>2025-05-31T22:41:20.38Z</creation></dates><accession>S-EPMC7782409</accession><cross_references><pubmed>32720091</pubmed><doi>10.1007/s10096-020-03970-0</doi></cross_references></HashMap>