Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Int J Phytoremediation ; 22(13): 1440-1447, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32619359

RESUMO

In this study, zinc ferrite nanoparticles (ZF-NPs) were synthesized using aqueous seed extract of Piper nigrum as a bio-reducing and stabilizing agent. FTIR, SEM, FE-SEM, XRD, and TGA have been used for characterizing ZF-NPs. The results showed that Piper nigrum stabilized ZF-NPs have high purity and size range of 60-80 nm. The performance of the ZF-NPs has been investigated by photocatalytic reduction of methylene blue (MB) in the presence of sunlight. The factors responsible for affecting the degradation values of the reaction were also explored for developing a better understanding of the phenomenon.


Assuntos
Nanopartículas Metálicas , Nanopartículas , Antibacterianos , Biodegradação Ambiental , Compostos Férricos , Azul de Metileno , Zinco
2.
J Enzyme Inhib Med Chem ; 25(3): 383-90, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19857049

RESUMO

The mechanochemical synthesis and characterization of a zinc complex with famotidine is described. The complex was characterized by microanalysis and a number of spectroscopic techniques. The complex was of M:L dihydrate type. Derivatization of famotidine with zinc appears to enhance the activity of the drug by inhibiting the growth of Helicobacter pylori (two reference and 34 clinical isolates). The complex inhibited the growth of H. pylori in an MIC range of 1-8 microg mL(-1). The anti-H. pylori activity of the zinc-famotidine complex against antibiotic-resistant strains was nearly comparable to that of antibiotic-susceptible strains. The complex was found to be far less toxic than the parent drug, as demonstrated by its higher LD(50) value. In the human urease enzyme inhibition assay the complex exhibited significant inhibition. The new complex appears to be more useful in eradicating both the antibiotic-susceptible and antibiotic-resistant strains of H. pylori.


Assuntos
Antibacterianos/síntese química , Famotidina/química , Helicobacter pylori/efeitos dos fármacos , Urease/antagonistas & inibidores , Zinco/química , Antibacterianos/farmacologia , Antiulcerosos , Resistência Microbiana a Medicamentos , Famotidina/farmacologia , Humanos , Testes de Sensibilidade Microbiana
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa