journal article·2017-08-23Open access

Quartz Crystal Microbalance Assay of Clinical Calcinosis Samples and Their Synthetic Models Differentiates the Efficacy of Chelation-Based Treatments

Fan Fei, Andrzej Gallas, Yun-Chuan Chang, Yikun Rao, Alan Christy Hunter, Richard E. P. Winpenny, Ariane L. Herrick, Nicholas P. Lockyer, Christopher F. Blanford

Abstract

This paper sets out in vitro protocols for studying the relative effectiveness of chelators used in the dissolution-based treatment of hard calcinosis. Pulverized hard calcinosis samples from human donors or synthetic hydroxyapatite nanoparticles were deposited by electrophoretic deposition on the surface of a quartz crystal microbalance sensor. Over 150 deposits of <20 μg were dissolved over the course of 1 h by aliquots of buffered, aqueous solutions of two calcium chelators, EDTA and citrate, with the surface-limited dissolution kinetics monitored with <1 s time resolution. There was no statistically significant difference in dissolution rate between the four synthetic hydroxyapatite materials in EDTA, but the dissolution rates in citrate were lower for hydroxyapatite produced by acetate or nitrate metathesis. Hard calcinosis and synthetic hydroxyapatites showed statistically identical dissolution behavior, meaning that readily available synthetic mimics can replace the rarer samples of biological origin in the development of calcinosis treatments. EDTA dissolved the hydroxyapatite deposits more than twice as fast as citrate at pH 7.4 and 37 °C, based on a first-order kinetic analysis of the initial frequency response. EDTA chelated 6.5 times more calcium than an equivalent number of moles of citrate. Negative controls using nonchelating N,N,N',N'-tetraethylethylenediamine (TEEDA) showed no dissolution effect. Pharmaceutical dissolution testing of synthetic hydroxyapatite tablets over 6 h showed that EDTA dissolved the tablets four to nine times more quickly than citrate.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Bone Tissue Engineering Materials · Medical Imaging and Pathology Studies · MXene and MAX Phase Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Manchester Institute of Biotechnology, University of Manchester, 131 Princess Street, Manchester, M1 7DN, U.K.

Funding

Scleroderma and Raynaud's UK · School of Materials, University of Manchester

References (55)

Show source-provided references
1. 10.1097/BOR.0b013e32834ff5cd10.1097/BOR.0b013e32834ff5cd ↗
2. 10.1093/rheumatology/28.4.28110.1093/rheumatology/28.4.281 ↗
3. Salazar, G. A.; Mayes, M. D.InA Visual Guide to Scleroderma and Approach to Treatment;Springer: 2014; p89–96.10.1007/978-1-4939-0980-3_8 ↗
4. 10.1016/j.jaad.2010.08.03810.1016/j.jaad.2010.08.038 ↗
5. 10.5301/jsrd.500021110.5301/jsrd.5000211 ↗
6. 10.1016/j.jaad.2010.08.03910.1016/j.jaad.2010.08.039 ↗
7. 10.1097/BOR.000000000000022010.1097/BOR.0000000000000220 ↗
8. Lanigan R. S. · Int. J. Toxicol. · 2001 · 21 · 95
9. 10.1016/j.joen.2009.11.01110.1016/j.joen.2009.11.011 ↗
10. 10.2174/09298670577446298710.2174/092986705774462987 ↗
11. 10.1016/S0002-9343(55)80025-310.1016/S0002-9343(55)80025-3 ↗
12. Davis H. · Pediatrics · 1959 · 24 · 78010.1542/peds.24.5.780 ↗
13. 10.1001/archderm.1960.0158005007400910.1001/archderm.1960.01580050074009 ↗
14. 10.1001/archpedi.1963.0208004039201210.1001/archpedi.1963.02080040392012 ↗
15. 10.1002/art.178007030810.1002/art.1780070308 ↗
16. 10.1093/rheumatology/keu117.00810.1093/rheumatology/keu117.008 ↗
17. 10.1016/0022-0248(91)90630-N10.1016/0022-0248(91)90630-N ↗
18. Leroux J. L. · J. Rheumatol. · 1983 · 10 · 242
19. 10.1017/erm.2014.610.1017/erm.2014.6 ↗
20. 10.1177/0022034576055003320110.1177/00220345760550033201 ↗
21. 10.1002/jps.260073020310.1002/jps.2600730203 ↗
22. 10.1016/0142-9612(96)88714-X10.1016/0142-9612(96)88714-X ↗
23. 10.1109/JSEN.2005.85925710.1109/JSEN.2005.859257 ↗
24. 10.1007/BF0133793710.1007/BF01337937 ↗
25. 10.1002/cctc.20130090010.1002/cctc.201300900 ↗
26. 10.1016/j.desal.2014.08.00410.1016/j.desal.2014.08.004 ↗
27. 10.1016/j.bios.2006.01.01310.1016/j.bios.2006.01.013 ↗
28. 10.1016/j.jcis.2012.06.07410.1016/j.jcis.2012.06.074 ↗
29. 10.1021/acsami.5b0711810.1021/acsami.5b07118 ↗
30. 10.2320/matertrans.43.301010.2320/matertrans.43.3010 ↗
31. 10.1039/b109684m10.1039/b109684m ↗
32. 10.1016/j.surfcoat.2015.05.02610.1016/j.surfcoat.2015.05.026 ↗
33. 10.1016/j.msec.2015.12.07510.1016/j.msec.2015.12.075 ↗
34. 10.1016/j.biomaterials.2006.07.02910.1016/j.biomaterials.2006.07.029 ↗
35. 10.4028/0-87849-457-x.111910.4028/0-87849-457-x.1119 ↗
36. 10.1111/j.1151-2916.1996.tb08929.x10.1111/j.1151-2916.1996.tb08929.x ↗
37. 10.1016/j.jeurceramsoc.2007.12.01110.1016/j.jeurceramsoc.2007.12.011 ↗
38. 10.1007/s10856-005-0630-010.1007/s10856-005-0630-0 ↗
39. 10.1016/j.ejpb.2015.08.00210.1016/j.ejpb.2015.08.002 ↗
40. 10.1039/c3ee00043e10.1039/c3ee00043e ↗
41. British Pharmacopoeia Commission · 2004 · 4
42. 10.1007/BF0030552910.1007/BF00305529 ↗
43. 10.1097/00003086-198309000-0003610.1097/00003086-198309000-00036 ↗
44. 10.1007/s00216-013-7414-z10.1007/s00216-013-7414-z ↗
45. 10.1073/pnas.141334711210.1073/pnas.1413347112 ↗
46. Lydon C. · Clin. Exp. Rheumatol. · 2014 · 32 · S43
47. 10.1238/Physica.Regular.059a0039110.1238/Physica.Regular.059a00391 ↗
48. 10.1016/0040-6031(83)80309-810.1016/0040-6031(83)80309-8 ↗
49. 10.1021/j100819a04510.1021/j100819a045 ↗
50. 10.6028/jres.074A.03610.6028/jres.074A.036 ↗
51. 10.1111/j.1365-2591.2007.01371.x10.1111/j.1365-2591.2007.01371.x ↗
52. 10.1016/j.chemgeo.2007.05.01510.1016/j.chemgeo.2007.05.015 ↗
53. 10.1021/ac901381z10.1021/ac901381z ↗
54. Chow, L. C.InOctacalcium Phosphate;Chow, L. C.; Eanes, E. D., Eds.Karger:Basel, 2001; Vol.18, pp94–111.10.1159/isbn.978-3-318-00704-6 ↗
55. 10.1016/j.actbio.2011.11.01710.1016/j.actbio.2011.11.017 ↗