Electrochemical Investigations of L-Cysteine Interactions with Bismuth Ions

被引:5
作者
Cheek, G. T. [1 ]
Pena, D. [1 ]
机构
[1] US Naval Acad, Dept Chem, Annapolis, MD 21402 USA
关键词
Bismuth; L-Cysteine; Pharmaceutical; Voltammetry; Complexation; Organic Electrochemistry; Bioelectrochemistry; GLUTATHIONE;
D O I
10.1149/1945-7111/abbea6
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The interaction of L-cysteine with bismuth compounds bismuth(III) salicylate, bismuth(III) citrate, and bismuth(III) nitrate, was studied at pH 1.0 (0.100 M HNO(3)and 0.100 M HCl) and pH 7.4 MOPS buffer by cyclic voltammetry at glassy carbon and boron-doped diamond electrodes. pH 1.0, at which bismuth (III) exists as the simple Bi(3+)ion, was chosen to approximate the acid strength of stomach contents. pH 7.4, at which bismuth(III) exists as BiO, was used for its similarity to general physiological conditions. The amino acid L-cysteine was chosen because its sulfhydryl group undergoes intense interaction with many metal cations, serving as a model for cysteine-containing proteins in the digestive system. It was determined that Bi(III) and L-cysteine (Cys) form soluble complexes at both pH 1.0 and pH 7.4. UV-vis spectroscopic investigations support interaction of Bi(III) and L-cysteine to form a 1:2 Bi(III): Cys complex in pH 7.4 MOPS buffer. L-cysteine addition to solutions of the pharmaceutical bismuth(III) salicylate was found to alter the voltammetric behavior of the salicylate complex. These results, especially at pH 1.0, are relevant to understanding the interaction of various cysteine-containing proteins in the human digestive system with bismuth pharmaceuticals and may help guide future explorations of bismuth formulations.
引用
收藏
页数:4
相关论文
共 21 条
[1]  
Bard A. J., 2001, ELECTROCHEMICAL METH, P36
[2]  
Bard A. J., 1985, STANDARD POTENTIALS
[3]   THE ACID STRENGTH OF THE -SH GROUP IN CYSTEINE AND RELATED COMPOUNDS [J].
BENESCH, RE ;
BENESCH, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (22) :5877-5881
[4]   Bismuth(III) complexes derived from α-amino acids: the impact of hydrolysis and oxido-cluster formation on their activity against Helicobacter pylori [J].
Busse, Madleen ;
Border, Emily ;
Junk, Peter C. ;
Ferrero, Richard L. ;
Andrews, Philip C. .
DALTON TRANSACTIONS, 2014, 43 (48) :17980-17990
[5]   Electrochemical Studies of Zinc/L-Cysteine Interactions in Aqueous Buffers [J].
Cheek, G. T. ;
Worosz, M. A. ;
Doan, M. Y. ;
Clark, D. C. .
SELECTED PROCEEDINGS FROM THE 232ND ECS MEETING, 2017, 80 (10) :1159-1166
[6]  
Cheek G. T., 2016, ECS T, V72, P1, DOI 10.1149/07227.0001ecst
[7]   Electrochemical Studies of Zinc/Cysteine Interactions [J].
Doan, M. Y. ;
Worosz, M. A. ;
Cheek, G. T. .
SELECTED PROCEEDINGS FROM THE 231ST ECS MEETING, 2017, 77 (11) :1537-1544
[8]   (Un)suitability of the use of pH buffers in biological, biochemical and environmental studies and their interaction with metal ions - a review [J].
Ferreira, Carlos M. H. ;
Pinto, Isabel S. S. ;
Soares, Eduardo V. ;
Soares, Helena M. V. M. .
RSC ADVANCES, 2015, 5 (39) :30989-31003
[9]   Bioinorganic chemistry of bismuth and antimony: Target sites of metallodrugs [J].
Ge, Ruiguang ;
Sun, Hongzhe .
ACCOUNTS OF CHEMICAL RESEARCH, 2007, 40 (04) :267-274
[10]  
Harris D. C., 2016, QUANTITATIVE CHEM AN, pAP27