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Can Drug Repurposing be Effective Against Carbapenem-Resistant Acinetobacter baumannii?
Aline Vidal Lacerda Gontijo1, Sharlene Lopes Pereira2, Herval de Lacerda Bonfante2,3,4
1Department of Pharmacology, Institute of Biological Sciences, Federal University of Juiz de Fora (UFJF), Rua José Lourenço Kelmer, s/n, São Pedro, Juiz de Fora, Minas Gerais, 36036-900, Brazil. aline.gontijo@gmail.com.
Drug repurposing offers a promising strategy against carbapenem-resistant Acinetobacter baumannii infections. Fusidic acid and colistin show potential as well-tolerated treatments, possibly in combination therapy.
Area of Science:
- Microbiology
- Infectious Diseases
- Pharmacology
Background:
- Carbapenem-resistant Acinetobacter baumannii (CRAB) is a critical pathogen with limited treatment options.
- Antibiotic resistance in CRAB necessitates novel therapeutic strategies.
- Drug repurposing presents a viable approach for developing new CRAB treatments.
Purpose of the Study:
- To critically evaluate repurposed drugs for CRAB infections.
- To correlate antimicrobial activity with toxicity and side effect data.
- To identify promising drug candidates for CRAB treatment.
Main Methods:
- Literature review of repurposed drugs against CRAB.
- Analysis of antimicrobial efficacy data.
- Assessment of drug toxicity and plasma concentration data.
Main Results:
- Several repurposed drugs show potential but face challenges with toxicity and low plasma concentrations.
- Fusidic acid and colistin demonstrate favorable applicability for CRAB treatment.
- Combination therapy with fusidic acid and colistin may offer improved outcomes.
Conclusions:
- Fusidic acid and colistin are promising candidates for repurposing against CRAB infections.
- Optimizing drug combinations and formulations is crucial for clinical success.
- Further research is needed to fully establish the safety and efficacy of repurposed drugs.
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