Assessment of in vitro interactions between delafloxacin and other antimicrobials against multi-drug resistant Pseudomonas aeruginosa strains.

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES
Emel Mataracı Kara, Selin Melis Çakmak, Sevda Er
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引用次数: 0

Abstract

Novel therapeutic interventions are required to address the critical antimicrobial resistance caused by multidrug-resistant Pseudomonas aeruginosa (MDR-PA) infections. This study examines the impact of combining delafloxacin with antibiotics on MDR-PA isolated from various samples. The minimum inhibitory concentrations (MICs) of delafloxacin, alone and in combination with other antibiotics, were determined against forty distinct MDR-PA isolates using the broth microdilution method. Time-kill curve assays were used to determine the bactericidal and synergistic effects of delafloxacin alone and in combination with other antibiotics in vitro against the selected five strains. Our studies showed delafloxacin exhibited four times greater in-vitro activity against MDR-PA strains than levofloxacin compared with both MIC50 and MIC90 results. Delafloxacin + tobramycin and delafloxacin + ceftazidime/avibactam showed synergy in two out of five strains tested at concentrations equal to the MIC. The outcomes of this research also suggest that these combinations may replace therapy for MDR-PA strains.

德拉沙星与其他抗多重耐药铜绿假单胞菌菌株的体外相互作用评价。
需要新的治疗干预措施来解决由耐多药铜绿假单胞菌(MDR-PA)感染引起的关键抗微生物药物耐药性。本研究考察了德拉沙星联合抗生素对从各种样品中分离出的耐多药pa的影响。采用微量肉汤稀释法测定了德拉沙星单用及联用其他抗生素对40株不同耐多药菌株的最低抑菌浓度(mic)。采用时间杀伤曲线法测定了德拉沙星单用及与其他抗生素联用对所选5株菌株的体外抑菌增效作用。我们的研究表明,与MIC50和MIC90结果相比,德拉沙星对耐多药pa菌株的体外活性是左氧氟沙星的四倍。德拉沙星+妥布霉素和德拉沙星+头孢他啶/阿维巴坦在与MIC浓度相等的5个菌株中有2个显示协同作用。这项研究的结果还表明,这些组合可能取代耐多药pa菌株的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chemotherapy
Journal of Chemotherapy 医学-药学
CiteScore
3.70
自引率
0.00%
发文量
144
审稿时长
6-12 weeks
期刊介绍: The Journal of Chemotherapy is an international multidisciplinary journal committed to the rapid publication of high quality, peer-reviewed, original research on all aspects of antimicrobial and antitumor chemotherapy. The Journal publishes original experimental and clinical research articles, state-of-the-art reviews, brief communications and letters on all aspects of chemotherapy, providing coverage of the pathogenesis, diagnosis, treatment, and control of infection, as well as the use of anticancer and immunomodulating drugs. Specific areas of focus include, but are not limited to: · Antibacterial, antiviral, antifungal, antiparasitic, and antiprotozoal agents; · Anticancer classical and targeted chemotherapeutic agents, biological agents, hormonal drugs, immunomodulatory drugs, cell therapy and gene therapy; · Pharmacokinetic and pharmacodynamic properties of antimicrobial and anticancer agents; · The efficacy, safety and toxicology profiles of antimicrobial and anticancer drugs; · Drug interactions in single or combined applications; · Drug resistance to antimicrobial and anticancer drugs; · Research and development of novel antimicrobial and anticancer drugs, including preclinical, translational and clinical research; · Biomarkers of sensitivity and/or resistance for antimicrobial and anticancer drugs; · Pharmacogenetics and pharmacogenomics; · Precision medicine in infectious disease therapy and in cancer therapy; · Pharmacoeconomics of antimicrobial and anticancer therapies and the implications to patients, health services, and the pharmaceutical industry.
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