Speciation and supersaturation of urine
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13520%2F18%3A43893831" target="_blank" >RIV/44555601:13520/18:43893831 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1007/s00706-017-2115-5" target="_blank" >http://dx.doi.org/10.1007/s00706-017-2115-5</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00706-017-2115-5" target="_blank" >10.1007/s00706-017-2115-5</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Speciation and supersaturation of urine
Popis výsledku v původním jazyce
Thermodynamic equilibria in urine at 37 oC showed that the inorganic urinary constituents, citrate and oxalate are present as 76 different species. Complexes formed by uric acid and various organic compounds, such as creatinine, proteins, hormones and metabolites, for which the relevant thermodynamic data are not available in the library of the computer program MINTEQA2 Version 3 were not considered. The actual thermodynamic supersaturation of urine with respect to calcium oxalate monohydrate and dihydrate was calculated. The effects of varying composition of urine at the same pH and the violation of the condition of electroneutrality on the calculated supersaturation were shown. The supersaturation of urine should never be computed from incomplete data of urine composition. Incomplete urine composition should always be supplemented with data for the other urinary components. Guidelines for extension of urine composition were suggested. A requisite condition for formation of solid calcium oxalate in urine is the presence of active heterogeneous nuclei. Supersaturation of urine with respect to calcium oxalates per se cannot be regarded as a diagnostic measure of the risk of calcium oxalate stone formation. Graphical abstract Open image in new window COM formation through heterogenous nucleation on hydroxyapatite
Název v anglickém jazyce
Speciation and supersaturation of urine
Popis výsledku anglicky
Thermodynamic equilibria in urine at 37 oC showed that the inorganic urinary constituents, citrate and oxalate are present as 76 different species. Complexes formed by uric acid and various organic compounds, such as creatinine, proteins, hormones and metabolites, for which the relevant thermodynamic data are not available in the library of the computer program MINTEQA2 Version 3 were not considered. The actual thermodynamic supersaturation of urine with respect to calcium oxalate monohydrate and dihydrate was calculated. The effects of varying composition of urine at the same pH and the violation of the condition of electroneutrality on the calculated supersaturation were shown. The supersaturation of urine should never be computed from incomplete data of urine composition. Incomplete urine composition should always be supplemented with data for the other urinary components. Guidelines for extension of urine composition were suggested. A requisite condition for formation of solid calcium oxalate in urine is the presence of active heterogeneous nuclei. Supersaturation of urine with respect to calcium oxalates per se cannot be regarded as a diagnostic measure of the risk of calcium oxalate stone formation. Graphical abstract Open image in new window COM formation through heterogenous nucleation on hydroxyapatite
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
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OECD FORD obor
30217 - Urology and nephrology
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Monatshefte fur Chemie
ISSN
0026-9247
e-ISSN
—
Svazek periodika
2018
Číslo periodika v rámci svazku
149
Stát vydavatele periodika
AT - Rakouská republika
Počet stran výsledku
7
Strana od-do
333-339
Kód UT WoS článku
000425536700015
EID výsledku v databázi Scopus
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