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Chelatingpolymers For Hereditary Hemochromatosis Treatment 12th Edition Ondřej Groborz

  • SKU: BELL-48603082
Chelatingpolymers For Hereditary Hemochromatosis Treatment 12th Edition Ondřej Groborz
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Chelatingpolymers For Hereditary Hemochromatosis Treatment 12th Edition Ondřej Groborz instant download after payment.

Publisher: Wiley
File Extension: PDF
File size: 2.87 MB
Pages: 16
Author: Ondřej Groborz, David Dunlop, Luděk Šefc, Jiří Beneš, Petr Štěpánek, Pavel Hobza, Martin Hrubý, et al
Language: English
Year: 2020
Edition: 12
Volume: 20

Product desciption

Chelatingpolymers For Hereditary Hemochromatosis Treatment 12th Edition Ondřej Groborz by Ondřej Groborz, David Dunlop, Luděk Šefc, Jiří Beneš, Petr Štěpánek, Pavel Hobza, Martin Hrubý, Et Al instant download after payment.

DOI 10.1002/mabi.202000254

Hemochromatosis (iron overload) encompasses a group of diseases that are characterized by a toxic hyperaccumulation of iron in parenchymal organs. Currently, only few treatments for this disease have been approved; however, all these treatments possess severe side effects. In this study, a paradigm for hemochromatosis maintenance/preventive therapy is investigated: polymers with negligible systemic biological availability form stable complexes with iron ions in the gastrointestinal tract, which reduces the biological availability of iron. Macroporous polymer beads are synthesized with three different ironchelating moieties (benzene-1,2-diol, benzene-1,2,3-triol, and 1,10-phenanthroline). The polymers rapidly chelate iron ions from aqueous solutions in vitro in the course of minutes, and are noncytotoxic and nonprooxidant. Moreover, the in vivo biodistribution and pharmacokinetics show a negligible uptake from the gastrointestinal tract (using 125I-labeled polymer and single photon emission computed tomography/computed tomography), which generally prevents them from having systemic side effects. The therapeutic efficacy of the prepared polymers is successfully tested in vivo, and exhibits a significant inhibition of iron uptake from the gastrointestinal tract without any noticeable signs of toxicity. Furthermore, an in silico method is developed for the prediction of chelator selectivity. Therefore, this paradigm can be applied to the next-generation maintenance/preventive treatment for hemochromatosis and/or other diseases of similar pathophysiology.

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