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Synthesis and evaluation of the antibiotic and adjuvant antibiotic potential of organotin(IV) derivatives.
Barbosa, Ana Soraya Lima; Guedes, Jéssica de Siqueira; da Silva, Douglas Rozendo; Meneghetti, Simoni Margareti Plentz; Meneghetti, Mario Roberto; da Silva, Amanda Evelyn; de Araujo, Morgana Vital; Alexandre-Moreira, Magna Suzana; de Aquino, Thiago Mendonça; de Siqueira Junior, José Pinto; de Araújo, Rodrigo Santos Aquino; da Cruz, Ryldene Marques Duarte; Mendonça-Junior, Francisco Jaime Bezerra.
Afiliación
  • Barbosa ASL; Group of Catalysis and Chemical Reactivity, Institute of Chemistry and Biotechnology, Federal University of Alagoas, 57072-970 Maceió, AL, Brazil.
  • Guedes JS; Group of Catalysis and Chemical Reactivity, Institute of Chemistry and Biotechnology, Federal University of Alagoas, 57072-970 Maceió, AL, Brazil.
  • da Silva DR; Group of Catalysis and Chemical Reactivity, Institute of Chemistry and Biotechnology, Federal University of Alagoas, 57072-970 Maceió, AL, Brazil.
  • Meneghetti SMP; Group of Catalysis and Chemical Reactivity, Institute of Chemistry and Biotechnology, Federal University of Alagoas, 57072-970 Maceió, AL, Brazil.
  • Meneghetti MR; Group of Catalysis and Chemical Reactivity, Institute of Chemistry and Biotechnology, Federal University of Alagoas, 57072-970 Maceió, AL, Brazil. Electronic address: mrm@qui.ufal.br.
  • da Silva AE; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720 Maceió, AL, Brazil.
  • de Araujo MV; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720 Maceió, AL, Brazil.
  • Alexandre-Moreira MS; Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, 57020-720 Maceió, AL, Brazil.
  • de Aquino TM; Group of Catalysis and Chemical Reactivity, Institute of Chemistry and Biotechnology, Federal University of Alagoas, 57072-970 Maceió, AL, Brazil; Nucleus of Analysis and Research in Nuclear Magnetic Resonance - NAPRMN, Institute of Chemistry and Biotechnology, Federal University of Alagoas, 57020-7
  • de Siqueira Junior JP; Laboratory of Genetics of Microorganism, Federal University of Paraiba, 58051-900 João Pessoa, PB, Brazil.
  • de Araújo RSA; Laboratory of Synthesis and Drug Delivery, Biological Science Department, State University of Paraiba, 58071-160 João Pessoa, PB, Brazil.
  • da Cruz RMD; Graduate Program in Natural and Synthetic Bioactive Products, Federal University of Paraiba, 58071-160 João Pessoa, PB, Brazil.
  • Mendonça-Junior FJB; Laboratory of Synthesis and Drug Delivery, Biological Science Department, State University of Paraiba, 58071-160 João Pessoa, PB, Brazil; Graduate Program in Natural and Synthetic Bioactive Products, Federal University of Paraiba, 58071-160 João Pessoa, PB, Brazil. Electronic address: franciscojaime
J Inorg Biochem ; 180: 80-88, 2018 03.
Article en En | MEDLINE | ID: mdl-29247870
A series of organotin(IV) derivatives was investigated in vitro for their antibiotic and adjuvant antibiotic properties (efflux pump inhibitors) against Staphylococcus aureus strains that overexpress efflux pump proteins for norfloxacin (SA-1199B), erythromycin (RN-4220) and tetracycline (IS-58). Most organotin(IV) compounds showed significant antibacterial activity with small Minimum Inhibitory Concentration (MIC) values, some of which were close to 1.0µg/mL (3.1µM), but this feature was also associated with substantial cytotoxicity. Nevertheless, the cytotoxicity of these organotin(IV) compounds can be overcome when they are used as antibiotic adjuvants. Their remarkable adjuvant antibiotic properties allow potentiation of the action of tetracycline (against IS-58 strain) by up to 128-fold. This likely indicates that they can act as putative inhibitors of bacterial efflux pumps. These results reinforce organotin(IV) complexes as promising antibacterial agents, and many of these complexes, if associated with antibiotics, can act as potential adjuvant antibiotic candidates.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Compuestos Orgánicos de Estaño / Antibacterianos Límite: Animals Idioma: En Revista: J Inorg Biochem Año: 2018 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Compuestos Orgánicos de Estaño / Antibacterianos Límite: Animals Idioma: En Revista: J Inorg Biochem Año: 2018 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Estados Unidos