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1.
Int J Biol Macromol ; 93(Pt A): 57-65, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27543345

RESUMO

Polysaccharides containing sulfated L-fucose are often called fucans. The seaweed Spatoglossum schröederi synthesizes three fucans, among which fucan A is the most abundant. This polymer is not cytotoxic against various normal cell lines and is non-toxic to rats when administered at high doses. In addition, it exhibits low toxicity against tumor cells. With the aim of increasing the toxicity of fucan A, silver nanoparticles containing this polysaccharide were synthesized using a green chemistry method. The mean size of these nanoparticles was 210nm. They exhibited a spherical shape and negative surface charge and were stable for 14 months. When incubated with cells, these nanoparticles did not show any toxic effects against various normal cell lines; however, they decreased the viability of various tumor cells, especially renal adenocarcinoma cells 786-0. Flow cytometry analyses showed that the nanoparticles induced cell death responses of 786-0 cells through necrosis. Assays performed with several renal cell lines (HEK, VERO, MDCK) showed that these nanoparticles only induce death of 786-0 cells. The data obtained herein leads to the conclusion that fucan A nanoparticles are promising agents against renal adenocarcinoma.


Assuntos
Antineoplásicos/síntese química , Apoptose/efeitos dos fármacos , Células 3T3 , Adenocarcinoma/tratamento farmacológico , Animais , Antineoplásicos/farmacologia , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Ensaios de Seleção de Medicamentos Antitumorais , Fucose/química , Química Verde , Células HEK293 , Humanos , Neoplasias Renais/tratamento farmacológico , Nanopartículas Metálicas/química , Camundongos , Polissacarídeos/química , Prata/química
2.
J Trace Elem Med Biol ; 26(1): 7-12, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22365073

RESUMO

Berardinelli-Seip syndrome (BSS) is a very rare disorder characterized by near-complete absence of adipose tissue from birth or early infancy, hypoleptinemia, hypertriglyceridemia, insulin resistance, diabetes mellitus, and other clinical signals. It is caused by mutations in AGPAT2 or Gng3lg. We evaluated 10 BSS patients and 10 healthy subjects. A single dose of 382.43 µmol zinc was administered intravenously before and after 3 months of oral zinc supplementation. Blood samples were collected from the contralateral arm at 0, 30, 60, 90, and 120 min after zinc injection. Plasma and serum were obtained to measure hematological and biochemical parameters. Urine was collected to measure creatinine, protein, and zinc. Basal serum zinc levels were similar in controls and BSS patients. However, serum zinc profiles were significant reduced in BSS patients in comparison with controls. The change in total-body zinc clearance was more significant in BSS patients, indicating that these patients had suboptimum zinc deficiency.


Assuntos
Lipodistrofia Generalizada Congênita/metabolismo , Zinco/sangue , Zinco/deficiência , Adulto , Suplementos Nutricionais/análise , Feminino , Humanos , Cinética , Masculino , Zinco/administração & dosagem , Zinco/urina
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