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Coordination Dynamics and Coordination Mechanism of a New Type of Anticoagulant Diethyl Citrate with Ca2+ Ions

DOI: 10.1155/2013/354736

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Abstract:

Diethyl citrate (Et2Cit) is a new potential anticoagulant. The coordination dynamics and coordination mechanism of Et2Cit with Ca2+ ions and the effect of pH on the complex were examined. The result was compared with that for the conventional anticoagulant sodium citrate (Na3Cit). The reaction order (n) of Et2Cit and Na3Cit with Ca2+ was 2.46 and 2.44, respectively. The reaction rate constant (k) was 120 and 289?L·mol?1·s?1. The reverse reaction rate constant ( ) was 0.52 and 0.15?L·mol?1·s?1, respectively. It is indicated that the coordination ability of Et2Cit with Ca2+ was weaker than that of Na3Cit. However, the dissociation rate of the calcium complex of Et2Cit was faster than that of Na3Cit. Increased pH accelerated the dissociation rate of the complex and improved its anticoagulant effect. The Et2Cit complex with calcium was synthesized and characterized by elemental analysis, XRD, FT-IR, 1H NMR, and ICP. These characteristics indicated that O in –COOH and C–O–C of Et2Cit was coordinated with Ca2+ in a bidentate manner with 1?:?1 coordination proportion; that is, complex CaEt2Cit was formed. Given that CaEt2Cit released Ca2+ more easily than Na3Cit, a calcium solution was not needed in intravenous infusions using Et2Cit as anticoagulant unlike using Na3Cit. Consequently, hypocalcemia and hypercalcemia were avoided. 1. Introduction An anticoagulant must be added to dialysates to prevent blood solidification in vitro (in a dialysis machine). Sodium citrate (Na3Cit) is an important anticoagulant used in clinical settings [1–3]. However, using Na3Cit as an anticoagulant easily causes hypocalcemia and hypercalcemia [4, 5] because of the strong chelating ability of Na3Cit with Ca2+ ions. Given this ability, the dissociation metabolism of the formed chelate CaCit in vivo takes 30?min. Using Na3Cit also negatively affects the maintenance of coagulation stability of high-risk hemorrhage patients in vivo, which easily causes complications such as hypocalcemia during or after dialysis. Our group has previously synthesized a new anticoagulant [6], namely, diethyl citrate (Et2Cit). The anticoagulant mechanism of Et2Cit is based on the formation of Ca2+ with Et2Cit. This formation decreases the Ca2+ concentration in blood and inhibits prothrombin conversion into thrombin, thereby influencing the anticoagulant effect. The large steric effect of Et2Cit weakens the coordination of Ca2+ ion compared with that of Na3Cit. Therefore, hypocalcemia and hypercalcemia can be avoided using Et2Cit as anticoagulant [7]. The frequency of blood gas analyses can also be

References

[1]  Z.-H. Zhang and H. Y. Ni, “Efficacy and safety of regional citrate anticoagulation in critically ill patients undergoing continuous renal replacement therapy,” Intensive Care Medicine, vol. 38, no. 1, pp. 20–28, 2012.
[2]  B. Szamosfalvi, S. Frinak, and J. Yee, “Automated regional citrate anticoagulation: technological barriers and possible solutions,” Blood Purification, vol. 29, no. 2, pp. 204–209, 2010.
[3]  N. Patnaik, R. K. Ratho, B. Mishra, A. Chakraborty, and V. K. Sakhuja, “Comparison of ethylenediaminetetraacetic acid and sodium citrate as anticoagulants in collection of samples for cytomegalovirus pp65 antigen detection in renal transplant recipients with suspected cytomegalovirus disease,” Journal of Virological Methods, vol. 147, no. 2, pp. 319–321, 2008.
[4]  Y.-J. Liao, L. Zhang, and P. Fu, “Simplified regional citrate anticoagulation using a calcium-containing replacement solution for continuous venovenous hemofiltration,” Nephrology Dialysis Transplantation, vol. 27, supplement 2, pp. 205–205, 2012.
[5]  J. Buturovi?-Ponikvar, J. Guben?ek, and R. Ponikvar, “Citrate anticoagulation for single-needle hemodialysis: safety and efficacy,” Therapeutic Apheresis and Dialysis, vol. 9, no. 3, pp. 237–240, 2005.
[6]  Y. Ou, J. Han, B. Chen et al., “Synthesis and characterization and anticoagulant properties of diethyl citrate,” Asian Journal of Chemistry, vol. 24, no. 11, pp. 4953–4960, 2012.
[7]  Z. Chen, B. Chen, X. Yao, B. Gui, Y. Ou, and J. Ouyang, “Anticoagulation of diethyl citrate and its comparison with sodium citrate in an animal model,” Blood Purification, vol. 33, no. 1–3, pp. 30–36, 2012.
[8]  Y. Ou, B. Chen, H. Peng, B.-S. Gui, X.-Q. Yao, and J.-M. Ouyang, “Thermodynamic features of diethyl citrate calcium complex and factors affecting the complex stability,” Asian Journal of Chemistry, vol. 24, no. 10, pp. 4717–4722, 2012.
[9]  Q. Tang, L.-M. Zhang, B.-B. Zou, H. Yu, and Y.-L. He, “Local citric acid in vitro anticoagulant, low molecular weight heparin and heparin in high-risk bleeding tendency of the efficacy and safety of the patients underwent hemodialysis,” Shanghai Medicine, vol. 30, no. 12, pp. 898–901, 2007.
[10]  M. Antoni?, J. Guben?ek, J. Buturovi?-Ponikvar, and R. Ponikvar, “Comparison of citrate anticoagulation during plasma exchange with different replacement solutions,” Therapeutic Apheresis and Dialysis, vol. 13, no. 4, pp. 322–326, 2009.
[11]  H. M. Oudemans-Van Straaten, R. J. Bosman, M. Koopmans et al., “Citrate anticoagulation for continuous venovenous hemofiltration,” Critical Care Medicine, vol. 37, no. 2, pp. 545–552, 2009.
[12]  J. A. Clark, G. Schulman, and T. A. Golper, “Safety and efficacy of regional citrate anticoagulation during 8-hour sustained low-efficiency dialysis,” Clinical Journal of the American Society of Nephrology, vol. 3, no. 3, pp. 736–742, 2008.
[13]  J. Kozik-Jaromin, V. Nier, U. Heemann, B. Kreymann, and J. B?hler, “Citrate pharmacokinetics and calcium levels during high-flux dialysis with regional citrate anticoagulation,” Nephrology Dialysis Transplantation, vol. 24, no. 7, pp. 2244–2251, 2009.
[14]  R. Palsson, K. A. Laliberte, and J. L. Niles, “Choice of replacement solution and anticoagulant in continuous venovenous hemofiltration,” Clinical Nephrology, vol. 65, no. 1, pp. 34–42, 2006.
[15]  S. Morgera, M. Haase, M. Ruckert et al., “Regional citrate anticoagulation in continuous hemodialysis-acid-base and electrolyte balance at an increased dose of dialysis,” Nephron, vol. 101, no. 4, pp. c211–c219, 2005.
[16]  H.-U. Meier-Kriesche, J. Gitomer, K. Finkel, and T. DuBose, “Increased total to ionized calcium ratio during continuous venovenous hemodialysis with regional citrate anticoagulation,” Critical Care Medicine, vol. 29, no. 4, pp. 748–752, 2001.
[17]  K.-N. Fan, Physical Chemistry, Higher Education Press, Beijing, China, 2005.
[18]  Y.-S. Yu, “The problems faced by today's peritoneal dialysis and its treatment,” Kidney Disease and Dialysis & Transplantation, vol. 6, no. 11, pp. 555–559, 2002.
[19]  A. Schwarzbeck, L. Wagner, H. U. Squarr, and M. Strauch, “Clotting in dialyzers due to low pH of dialysis fluid,” Clinical Nephrology, vol. 7, no. 3, pp. 125–127, 1977.
[20]  W.-Y. Sun, Coordination Chemistry, Chemical Industry Press, Beijing, China, 2004.

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