1993
DOI: 10.1016/s0277-5387(00)80037-6
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Solubilities of calcium salts of dicarboxylic acids in methanol-water mixtures; transfer chemical potentials of dicarboxylate anions

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Cited by 14 publications
(4 citation statements)
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“…37 This observation is consistent with the severely reduced solubility of vicinal dicarboxylate species with Ca 2+ , as compared with other dicarboxylate chelators. 38,39 Lipid Dependency on Protein-Free Nanodisc Formation Previous studies of SMA copolymers report no solubilization preference toward specific types of lipids. [40][41][42] To determine whether the lipid composition has an effect on the solubilization efficiency of AASTY copolymers, we formed protein-free AASTYstabilized nanodiscs incorporating 2% of the fluorescent Lissamine Rhodamine B (Liss Rhod) phosphatidylethanolamine (PE) lipid with three different lipid mixtures:…”
Section: Articlementioning
confidence: 99%
“…37 This observation is consistent with the severely reduced solubility of vicinal dicarboxylate species with Ca 2+ , as compared with other dicarboxylate chelators. 38,39 Lipid Dependency on Protein-Free Nanodisc Formation Previous studies of SMA copolymers report no solubilization preference toward specific types of lipids. [40][41][42] To determine whether the lipid composition has an effect on the solubilization efficiency of AASTY copolymers, we formed protein-free AASTYstabilized nanodiscs incorporating 2% of the fluorescent Lissamine Rhodamine B (Liss Rhod) phosphatidylethanolamine (PE) lipid with three different lipid mixtures:…”
Section: Articlementioning
confidence: 99%
“…Oxalate ions are generated in the liver by glyoxalate metabolism, but due to low solubility they are carried at low concentrations in the plasma membrane [38]. Previous studies have shown that oxalate is quickly taken up by proximal tubule cells and high concentration of oxalate can be excreted in urine by the secretary pathway [39, 40].…”
Section: Oxalate and Calcium Oxalate Induced Injurymentioning
confidence: 99%
“…It seems that cisplatin, carboplatin and iproplatin do not show such potentially advantageous solvation characteristics, but rather show solubility behavior approximating to the linear dependence of log(solubility) on volume % organic cosolvent often used as a rule-of-thumb guide for estimating solubilities of lipophilic organic drugs (Hardaway & Yalkowsky 1991). Interestingly, the CBDC (cyclobutane-1,1-dicarboxylate) ligand of carboplatin is markedly hydrophilic, with a transfer chemical potential curve (Burgess & Drasdo 1993) rather close to that shown in Figure 1 for [PtCI6] 2-. It may be that third generation platinum anticancer drugs containing rather more lipophilic ligands may prove to have better membrane-crossing properties and thus prove more effective.…”
Section: Resultsmentioning
confidence: 99%