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SNF472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels

BACKGROUND: Cardiovascular calcification (CVC) is a major concern in hemodialysis (HD) and the loss of endogenous modulators of calcification seems involved in the process. Phytate is an endogenous crystallization inhibitor and its low molecular mass and high water solubility make it potentially dia...

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Autores principales: Perelló, Joan, Gómez, M., Ferrer, M. D., Rodríguez, N. Y., Salcedo, C., Buades, J. M., Pérez, M. M., Torregrosa, J. V., Martín, E., Maduell, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829128/
https://www.ncbi.nlm.nih.gov/pubmed/29350348
http://dx.doi.org/10.1007/s40620-018-0471-9
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author Perelló, Joan
Gómez, M.
Ferrer, M. D.
Rodríguez, N. Y.
Salcedo, C.
Buades, J. M.
Pérez, M. M.
Torregrosa, J. V.
Martín, E.
Maduell, F.
author_facet Perelló, Joan
Gómez, M.
Ferrer, M. D.
Rodríguez, N. Y.
Salcedo, C.
Buades, J. M.
Pérez, M. M.
Torregrosa, J. V.
Martín, E.
Maduell, F.
author_sort Perelló, Joan
collection PubMed
description BACKGROUND: Cardiovascular calcification (CVC) is a major concern in hemodialysis (HD) and the loss of endogenous modulators of calcification seems involved in the process. Phytate is an endogenous crystallization inhibitor and its low molecular mass and high water solubility make it potentially dialyzable. SNF472 (the hexasodium salt of phytate) is being developed for the treatment of calciphylaxis and CVC in HD patients. We aimed to verify if phytate is lost during dialysis, and evaluate SNF472’s behaviour during dialysis. METHODS: Dialyzability was assessed in vitro using online-hemodiafiltration and high-flux HD systems in blood and saline. SNF472 was infused for 20 min and quantified at different time points. RESULTS: Phytate completely dialyzed in 1 h at low concentrations (10 mg/l) but not when added at 30 or 66.67 mg/l SNF472. In bypass conditions, calcium was slightly chelated during SNF472 infusion but when the system was switched to dialysis mode the calcium in the bath compensated this chelation. CONCLUSION: Phytate dialyses with a low clearance. The administration of SNF472 as an exogenous source of phytate allows to attain supra-physiological levels required for its potential therapeutic properties. As SNF472 is infused during the whole dialysis session, the low clearance would not affect the drug’s systemic exposure.
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spelling pubmed-58291282018-03-01 SNF472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels Perelló, Joan Gómez, M. Ferrer, M. D. Rodríguez, N. Y. Salcedo, C. Buades, J. M. Pérez, M. M. Torregrosa, J. V. Martín, E. Maduell, F. J Nephrol Original Article BACKGROUND: Cardiovascular calcification (CVC) is a major concern in hemodialysis (HD) and the loss of endogenous modulators of calcification seems involved in the process. Phytate is an endogenous crystallization inhibitor and its low molecular mass and high water solubility make it potentially dialyzable. SNF472 (the hexasodium salt of phytate) is being developed for the treatment of calciphylaxis and CVC in HD patients. We aimed to verify if phytate is lost during dialysis, and evaluate SNF472’s behaviour during dialysis. METHODS: Dialyzability was assessed in vitro using online-hemodiafiltration and high-flux HD systems in blood and saline. SNF472 was infused for 20 min and quantified at different time points. RESULTS: Phytate completely dialyzed in 1 h at low concentrations (10 mg/l) but not when added at 30 or 66.67 mg/l SNF472. In bypass conditions, calcium was slightly chelated during SNF472 infusion but when the system was switched to dialysis mode the calcium in the bath compensated this chelation. CONCLUSION: Phytate dialyses with a low clearance. The administration of SNF472 as an exogenous source of phytate allows to attain supra-physiological levels required for its potential therapeutic properties. As SNF472 is infused during the whole dialysis session, the low clearance would not affect the drug’s systemic exposure. Springer International Publishing 2018-01-19 2018 /pmc/articles/PMC5829128/ /pubmed/29350348 http://dx.doi.org/10.1007/s40620-018-0471-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Perelló, Joan
Gómez, M.
Ferrer, M. D.
Rodríguez, N. Y.
Salcedo, C.
Buades, J. M.
Pérez, M. M.
Torregrosa, J. V.
Martín, E.
Maduell, F.
SNF472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels
title SNF472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels
title_full SNF472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels
title_fullStr SNF472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels
title_full_unstemmed SNF472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels
title_short SNF472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels
title_sort snf472, a novel inhibitor of vascular calcification, could be administered during hemodialysis to attain potentially therapeutic phytate levels
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829128/
https://www.ncbi.nlm.nih.gov/pubmed/29350348
http://dx.doi.org/10.1007/s40620-018-0471-9
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