<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(10)</volume><submitter>Gonzalo X</submitter><pubmed_abstract>We evaluated a novel physiological 3-D bioelectrospray model of the tuberculosis (TB) granuloma to test the activity of a known anti-TB drug, clofazimine; three carbapenems with potential activity, including one currently used in therapy; and nitazoxanide, an anti-parasitic compound with possible TB activity (all chosen as conventional drug susceptibility was problematical). PBMCs collected from healthy donors were isolated and infected with &lt;i>M. tuberculosis&lt;/i> H37Rv lux (i.e., luciferase). Microspheres were generated with the infected cells; the anti-microbial compounds were added and bacterial luminescence was monitored for at least 21 days. Clavulanate was added to each carbapenem to inhibit beta-lactamases. &lt;i>M. tuberculosis&lt;/i> (MTB) killing efficacy was dose dependent. Clofazimin</pubmed_abstract><journal>Antibiotics (Basel, Switzerland)</journal><pagination>1274</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9598577</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Anti-Tuberculosis Activity of Three Carbapenems, Clofazimine and Nitazoxanide Using a Novel Ex Vivo Phenotypic Drug Susceptibility Model of Human Tuberculosis.</pubmed_title><pmcid>PMC9598577</pmcid><pubmed_authors>Bielecka MK</pubmed_authors><pubmed_authors>Elkington P</pubmed_authors><pubmed_authors>Drobniewski F</pubmed_authors><pubmed_authors>Gonzalo X</pubmed_authors><pubmed_authors>Tezera L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Anti-Tuberculosis Activity of Three Carbapenems, Clofazimine and Nitazoxanide Using a Novel Ex Vivo Phenotypic Drug Susceptibility Model of Human Tuberculosis.</name><description>We evaluated a novel physiological 3-D bioelectrospray model of the tuberculosis (TB) granuloma to test the activity of a known anti-TB drug, clofazimine; three carbapenems with potential activity, including one currently used in therapy; and nitazoxanide, an anti-parasitic compound with possible TB activity (all chosen as conventional drug susceptibility was problematical). PBMCs collected from healthy donors were isolated and infected with &lt;i>M. tuberculosis&lt;/i> H37Rv lux (i.e., luciferase). Microspheres were generated with the infected cells; the anti-microbial compounds were added and bacterial luminescence was monitored for at least 21 days. Clavulanate was added to each carbapenem to inhibit beta-lactamases. &lt;i>M. tuberculosis&lt;/i> (MTB) killing efficacy was dose dependent. Clofazimin</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-04T11:29:26.49Z</modification><creation>2025-04-04T11:29:26.49Z</creation></dates><accession>S-EPMC9598577</accession><cross_references><pubmed>36289932</pubmed><doi>10.3390/antibiotics11101274</doi></cross_references></HashMap>