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Calcium Oxalate Crystallization: Influence of pH, Energy Input, and Supersaturation Ratio on the Synthesis of Artificial Kidney Stones
[Image: see text] The removal of kidney stones can lead to small residual fragments remaining in the human body. Residual stone fragments can act as seeds for kidney stone crystallization and may necessitate another intervention. Therefore, it is important to create a consistent model with a particl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515601/ https://www.ncbi.nlm.nih.gov/pubmed/34661011 http://dx.doi.org/10.1021/acsomega.1c03938 |
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author | Werner, Helen Bapat, Shalmali Schobesberger, Michael Segets, Doris Schwaminger, Sebastian P. |
author_facet | Werner, Helen Bapat, Shalmali Schobesberger, Michael Segets, Doris Schwaminger, Sebastian P. |
author_sort | Werner, Helen |
collection | PubMed |
description | [Image: see text] The removal of kidney stones can lead to small residual fragments remaining in the human body. Residual stone fragments can act as seeds for kidney stone crystallization and may necessitate another intervention. Therefore, it is important to create a consistent model with a particle size comparable to the range of kidney stone fragments. Thus, the size-determining parameters such as supersaturation ratio, energy input, and pH value are examined. The batch crystallizations were performed with supersaturation ratios between 5.07 and 6.12. The compositions of the dried samples were analyzed with Raman spectroscopy, infrared spectroscopy, and X-ray diffraction (XRD). The samples were identified as calcium oxalate monohydrate with spectroscopic analysis, while calcium oxalate dihydrate being the most prominent crystalline species at all supersaturation ratios for the investigated conditions. The aggregate size, obtained with analytical centrifugation, varied between 2.9 and 4.3 μm, while the crystallite domain size, obtained from XRD, varied from 40 to 61 nm. Our results indicate that particle sizes increase with increasing supersaturation, energy input, and pH. All syntheses yield a high particle heterogeneity and represent an ideal basis for reference materials of small kidney stone fragments. These results will help better understand and control the crystallization of calcium oxalate and the aggregation of such pseudopolymorphs. |
format | Online Article Text |
id | pubmed-8515601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85156012021-10-15 Calcium Oxalate Crystallization: Influence of pH, Energy Input, and Supersaturation Ratio on the Synthesis of Artificial Kidney Stones Werner, Helen Bapat, Shalmali Schobesberger, Michael Segets, Doris Schwaminger, Sebastian P. ACS Omega [Image: see text] The removal of kidney stones can lead to small residual fragments remaining in the human body. Residual stone fragments can act as seeds for kidney stone crystallization and may necessitate another intervention. Therefore, it is important to create a consistent model with a particle size comparable to the range of kidney stone fragments. Thus, the size-determining parameters such as supersaturation ratio, energy input, and pH value are examined. The batch crystallizations were performed with supersaturation ratios between 5.07 and 6.12. The compositions of the dried samples were analyzed with Raman spectroscopy, infrared spectroscopy, and X-ray diffraction (XRD). The samples were identified as calcium oxalate monohydrate with spectroscopic analysis, while calcium oxalate dihydrate being the most prominent crystalline species at all supersaturation ratios for the investigated conditions. The aggregate size, obtained with analytical centrifugation, varied between 2.9 and 4.3 μm, while the crystallite domain size, obtained from XRD, varied from 40 to 61 nm. Our results indicate that particle sizes increase with increasing supersaturation, energy input, and pH. All syntheses yield a high particle heterogeneity and represent an ideal basis for reference materials of small kidney stone fragments. These results will help better understand and control the crystallization of calcium oxalate and the aggregation of such pseudopolymorphs. American Chemical Society 2021-10-01 /pmc/articles/PMC8515601/ /pubmed/34661011 http://dx.doi.org/10.1021/acsomega.1c03938 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Werner, Helen Bapat, Shalmali Schobesberger, Michael Segets, Doris Schwaminger, Sebastian P. Calcium Oxalate Crystallization: Influence of pH, Energy Input, and Supersaturation Ratio on the Synthesis of Artificial Kidney Stones |
title | Calcium Oxalate Crystallization: Influence of pH,
Energy Input, and Supersaturation Ratio on the Synthesis of Artificial
Kidney Stones |
title_full | Calcium Oxalate Crystallization: Influence of pH,
Energy Input, and Supersaturation Ratio on the Synthesis of Artificial
Kidney Stones |
title_fullStr | Calcium Oxalate Crystallization: Influence of pH,
Energy Input, and Supersaturation Ratio on the Synthesis of Artificial
Kidney Stones |
title_full_unstemmed | Calcium Oxalate Crystallization: Influence of pH,
Energy Input, and Supersaturation Ratio on the Synthesis of Artificial
Kidney Stones |
title_short | Calcium Oxalate Crystallization: Influence of pH,
Energy Input, and Supersaturation Ratio on the Synthesis of Artificial
Kidney Stones |
title_sort | calcium oxalate crystallization: influence of ph,
energy input, and supersaturation ratio on the synthesis of artificial
kidney stones |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515601/ https://www.ncbi.nlm.nih.gov/pubmed/34661011 http://dx.doi.org/10.1021/acsomega.1c03938 |
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