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Diethylentriaminepenta acetic acid glucose conjugates as a cell permeable iron chelator

OBJECTIVE: To find out whether DTPA-DG complex can enhance clearance of intracellular free iron. MATERIALS AND METHODS: Diethylenetriaminepentaacetic acid-D-deoxy-glucosamine (DTPA-DG) was synthesized and examined for its activity as a cell-permeable iron chelator in human hepatocellular carcinoma (...

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Detalles Bibliográficos
Autores principales: Mosayebnia, Mona, Shafiee-Ardestani, Mehdi, Pasalar, Parvin, Mashayekhi, Mojgan, Amanlou, Massoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917162/
https://www.ncbi.nlm.nih.gov/pubmed/24554907
http://dx.doi.org/10.4103/0976-500X.124416
Descripción
Sumario:OBJECTIVE: To find out whether DTPA-DG complex can enhance clearance of intracellular free iron. MATERIALS AND METHODS: Diethylenetriaminepentaacetic acid-D-deoxy-glucosamine (DTPA-DG) was synthesized and examined for its activity as a cell-permeable iron chelator in human hepatocellular carcinoma (HEPG2) cell line exposed to high concentration of iron sulfate and compared with deferoxamine (DFO), a prototype iron chelator. The effect of DTPA-DG on cell viability was monitored using the 3-(4,5-dimethythiazol-2-yl)-2,5-diphenyl tetrazolium bromide MTT assay as well. RESULTS: There was a significant increase of iron level after iron overload induction in HEPG2 cell culture. DTPA-DG presented a remarkable capacity to iron burden reducing with estimated 50% inhibitory concentration value of 65.77 nM. In fact, glycosyl moiety was gained access of DTPA to intracellular iron deposits through glucose transporter systems. CONCLUSION: DTPA-DG, more potent than DFO to sequester deposits of free iron with no profound toxic effect. The results suggest the potential of DTPA-DG in chelating iron and permitting its excretion from primary organ storage.