-
Something wrong with this record ?
Rapid method for screening of both calcium and magnesium chelation with comparison of 21 known metal chelators
L. Konečný, Z. Lomozová, G. Karabanovich, J. Roh, K. Vávrová, P. Mladěnka
Language English Country Germany
Document type Journal Article, Comparative Study
Grant support
CZ.02.01.01/00/22_008/0004607
NETPHARM
SVV 260 663
Charles University
- MeSH
- Platelet Aggregation drug effects MeSH
- Chelating Agents * chemistry MeSH
- Magnesium * chemistry MeSH
- Humans MeSH
- Drug Evaluation, Preclinical methods MeSH
- Blood Platelets drug effects metabolism MeSH
- Calcium * analysis metabolism MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
Chelation is the rational treatment modality in metal overload conditions, but chelators are often non-selective and can, hence, cause an imbalance in the homeostasis of physiological metals including calcium and magnesium. The aim of this study was to develop an affordable, rapid but sensitive and precise method for determining the degree of chelation of calcium and magnesium ions and to employ this method for comparison on a panel of known metal chelators. Spectrophotometric method using o-cresolphthalein complexone (o-CC) was developed and its biological relevance was confirmed in human platelets by impedance aggregometry. The lowest detectable concentration of calcium and magnesium ions by o-CC was 2.5 μM and 2 μM, respectively. The indicator was stable for at least 110 days. Four and seven out of twenty-one chelators strongly chelated calcium and magnesium ions, respectively. Importantly, the chelation effect of clinically used chelators was not negligible. Structure-activity relationships for eight quinolin-8-ols showed improvements in chelation particularly in the cases of dihalogen substitution, and a negative linear relationship between pKa and magnesium chelation was observed. Calcium chelation led to inhibition of platelet aggregation in concentrations corresponding to the complex formation. A novel method for screening of efficacy and safety of calcium and magnesium ion chelation was developed and validated.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25003211
- 003
- CZ-PrNML
- 005
- 20250206104152.0
- 007
- ta
- 008
- 250121s2024 gw f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s00775-024-02078-6 $2 doi
- 035 __
- $a (PubMed)39422739
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Konečný, Lukáš $u Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, 50003, Hradec Králové, Czechia
- 245 10
- $a Rapid method for screening of both calcium and magnesium chelation with comparison of 21 known metal chelators / $c L. Konečný, Z. Lomozová, G. Karabanovich, J. Roh, K. Vávrová, P. Mladěnka
- 520 9_
- $a Chelation is the rational treatment modality in metal overload conditions, but chelators are often non-selective and can, hence, cause an imbalance in the homeostasis of physiological metals including calcium and magnesium. The aim of this study was to develop an affordable, rapid but sensitive and precise method for determining the degree of chelation of calcium and magnesium ions and to employ this method for comparison on a panel of known metal chelators. Spectrophotometric method using o-cresolphthalein complexone (o-CC) was developed and its biological relevance was confirmed in human platelets by impedance aggregometry. The lowest detectable concentration of calcium and magnesium ions by o-CC was 2.5 μM and 2 μM, respectively. The indicator was stable for at least 110 days. Four and seven out of twenty-one chelators strongly chelated calcium and magnesium ions, respectively. Importantly, the chelation effect of clinically used chelators was not negligible. Structure-activity relationships for eight quinolin-8-ols showed improvements in chelation particularly in the cases of dihalogen substitution, and a negative linear relationship between pKa and magnesium chelation was observed. Calcium chelation led to inhibition of platelet aggregation in concentrations corresponding to the complex formation. A novel method for screening of efficacy and safety of calcium and magnesium ion chelation was developed and validated.
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a hořčík $x chemie $7 D008274
- 650 12
- $a vápník $x analýza $x metabolismus $7 D002118
- 650 12
- $a chelátory $x chemie $7 D002614
- 650 _2
- $a agregace trombocytů $x účinky léků $7 D010974
- 650 _2
- $a trombocyty $x účinky léků $x metabolismus $7 D001792
- 650 _2
- $a vztahy mezi strukturou a aktivitou $7 D013329
- 650 _2
- $a preklinické hodnocení léčiv $x metody $7 D004353
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a srovnávací studie $7 D003160
- 700 1_
- $a Lomozová, Zuzana $u Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmacy in Hradec Králové, Charles University, 50003, Hradec Králové, Czechia
- 700 1_
- $a Karabanovich, Galina $u Department of Organic and Bioorganic Chemistry, Faculty of Pharmacy in Hradec Králové, Charles University, 50003, Hradec Králové, Czechia
- 700 1_
- $a Roh, Jaroslav $u Department of Organic and Bioorganic Chemistry, Faculty of Pharmacy in Hradec Králové, Charles University, 50003, Hradec Králové, Czechia
- 700 1_
- $a Vávrová, Kateřina $u Department of Organic and Bioorganic Chemistry, Faculty of Pharmacy in Hradec Králové, Charles University, 50003, Hradec Králové, Czechia
- 700 1_
- $a Mladěnka, Přemysl $u Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, 50003, Hradec Králové, Czechia. mladenkap@faf.cuni.cz $1 https://orcid.org/0000000260766900 $7 xx0233006
- 773 0_
- $w MED00005752 $t JBIC, Journal of biological inorganic chemistry $x 1432-1327 $g Roč. 29, č. 7-8 (2024), s. 785-800
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39422739 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250121 $b ABA008
- 991 __
- $a 20250206104148 $b ABA008
- 999 __
- $a ok $b bmc $g 2263139 $s 1239218
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 29 $c 7-8 $d 785-800 $e 20241018 $i 1432-1327 $m JBIC, Journal of biological inorganic chemistry $n J Biol Inorg Chem $x MED00005752
- GRA __
- $a CZ.02.01.01/00/22_008/0004607 $p NETPHARM
- GRA __
- $a SVV 260 663 $p Charles University
- LZP __
- $a Pubmed-20250121