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Do organic substances act as a degradable binding matrix in calcium oxalate kidney stones?

BACKGROUND: Calcium oxalate (CaOx) stones are considered to be highly resistant to chemolysis. While significant organic matter has been identified within these stones, which is presumed to bind (inorganic) CaOx particles and aggregates, most chemolysis efforts have focused on methods to attack the...

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Autores principales: Adelman, Adi, Shilo, Yaniv, Modai, Jonathan, Leibovici, Dan, Dror, Ishai, Berkowitz, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995742/
https://www.ncbi.nlm.nih.gov/pubmed/33765979
http://dx.doi.org/10.1186/s12894-021-00818-3
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author Adelman, Adi
Shilo, Yaniv
Modai, Jonathan
Leibovici, Dan
Dror, Ishai
Berkowitz, Brian
author_facet Adelman, Adi
Shilo, Yaniv
Modai, Jonathan
Leibovici, Dan
Dror, Ishai
Berkowitz, Brian
author_sort Adelman, Adi
collection PubMed
description BACKGROUND: Calcium oxalate (CaOx) stones are considered to be highly resistant to chemolysis. While significant organic matter has been identified within these stones, which is presumed to bind (inorganic) CaOx particles and aggregates, most chemolysis efforts have focused on methods to attack the CaOx components of a stone. We examine the feasibility of inducing chemolysis of CaOx kidney stones, within hours, by specifically attacking the organic matrix present in these stones. METHODS: In contrast to previous studies, we focused on the possible “brick and mortar” stone configuration. We systematically tested, via in vitro experiments, the ability of an extensive range of 26 potential chemolysis agents to induce relatively fast disintegration (and/or dissolution) of a large set of natural CaOx stone fragments, extracted during endourological procedures, without regard to immediate clinical application. Each stone fragment was monitored for reduction in weight and other changes over 72 h. RESULTS: We find that agents known to attack organic material have little, if any, effect on stone chemolysis. Similarly, protein and enzymatic agents, and oral additive medical treatments, have little immediate effect. CONCLUSIONS: These findings suggest that the organic and inorganic constituents present in CaOx stones are not structured as “brick and mortar” configurations in terms of inorganic and organic components.
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spelling pubmed-79957422021-03-30 Do organic substances act as a degradable binding matrix in calcium oxalate kidney stones? Adelman, Adi Shilo, Yaniv Modai, Jonathan Leibovici, Dan Dror, Ishai Berkowitz, Brian BMC Urol Research Article BACKGROUND: Calcium oxalate (CaOx) stones are considered to be highly resistant to chemolysis. While significant organic matter has been identified within these stones, which is presumed to bind (inorganic) CaOx particles and aggregates, most chemolysis efforts have focused on methods to attack the CaOx components of a stone. We examine the feasibility of inducing chemolysis of CaOx kidney stones, within hours, by specifically attacking the organic matrix present in these stones. METHODS: In contrast to previous studies, we focused on the possible “brick and mortar” stone configuration. We systematically tested, via in vitro experiments, the ability of an extensive range of 26 potential chemolysis agents to induce relatively fast disintegration (and/or dissolution) of a large set of natural CaOx stone fragments, extracted during endourological procedures, without regard to immediate clinical application. Each stone fragment was monitored for reduction in weight and other changes over 72 h. RESULTS: We find that agents known to attack organic material have little, if any, effect on stone chemolysis. Similarly, protein and enzymatic agents, and oral additive medical treatments, have little immediate effect. CONCLUSIONS: These findings suggest that the organic and inorganic constituents present in CaOx stones are not structured as “brick and mortar” configurations in terms of inorganic and organic components. BioMed Central 2021-03-26 /pmc/articles/PMC7995742/ /pubmed/33765979 http://dx.doi.org/10.1186/s12894-021-00818-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Adelman, Adi
Shilo, Yaniv
Modai, Jonathan
Leibovici, Dan
Dror, Ishai
Berkowitz, Brian
Do organic substances act as a degradable binding matrix in calcium oxalate kidney stones?
title Do organic substances act as a degradable binding matrix in calcium oxalate kidney stones?
title_full Do organic substances act as a degradable binding matrix in calcium oxalate kidney stones?
title_fullStr Do organic substances act as a degradable binding matrix in calcium oxalate kidney stones?
title_full_unstemmed Do organic substances act as a degradable binding matrix in calcium oxalate kidney stones?
title_short Do organic substances act as a degradable binding matrix in calcium oxalate kidney stones?
title_sort do organic substances act as a degradable binding matrix in calcium oxalate kidney stones?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995742/
https://www.ncbi.nlm.nih.gov/pubmed/33765979
http://dx.doi.org/10.1186/s12894-021-00818-3
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