Spectrophotometric evaluation of hemolysis in plasma by quantification of free oxyhemoglobin, methemoglobin, and methemalbumin in presence of bilirubin.
derivative spectrophotometry
free hemoglobin
hemolysis
methemalbumin
methemoglobin
oxyhemoglobin
Journal
Journal of biophotonics
ISSN: 1864-0648
Titre abrégé: J Biophotonics
Pays: Germany
ID NLM: 101318567
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
revised:
28
01
2021
received:
17
11
2020
accepted:
28
01
2021
pubmed:
3
2
2021
medline:
13
7
2021
entrez:
2
2
2021
Statut:
ppublish
Résumé
Severe intravascular hemolysis leads to the simultaneous presence of free heme pigments (oxyhemoglobin, methemoglobin, and methemalbumin) and bilirubin in human plasma. Standard spectrophotometric methods used to assess in vivo hemolysis inadequately address this complex analytical situation. Thus, we propose a novel quantification algorithm to ensure the highest analytical specificity. A corresponding second-derivative fitting algorithm was validated according to the guideline of bioanalytical method validation from the European Medicines Agency using plasma specimens (n = 1759) spiked with different concentrations of oxyhemoglobin and methemoglobin. The results were compared to standard spectrophotometric quantification methods described by Harboe, Noe, and Fairbanks. Based on the second-derivative method, simultaneous quantification of oxyhemoglobin and methemoglobin/methemalbumin in samples with total bilirubin concentrations ≤4.9 mg/dL (83.8 μmol/L) provided robust results (inaccuracy ≤20%, imprecision ≤16%). Analyzing UV/VIS spectra of plasma from patients with confirmed severe intravascular hemolysis evidenced an underestimation of up to 33% for the combined free heme pigment content. The employed second-derivative algorithm allows for automated and highly specific quantification of the free heme pigment content in diluted human plasma, which cannot be realized with standard spectrophotometric evaluation methods. An Excel-based tool readily applicable to clinical datasets accompanies this manuscript.
Identifiants
pubmed: 33527705
doi: 10.1002/jbio.202000461
doi:
Substances chimiques
Hemoglobins
0
Methemalbumin
0
Oxyhemoglobins
0
Methemoglobin
9008-37-1
Bilirubin
RFM9X3LJ49
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202000461Informations de copyright
© 2021 The Authors. Journal of Biophotonics published by Wiley-VCH GmbH.
Références
D. J. Schaer, P. W. Buehler, A. I. Alayash, J. D. Belcher, G. M. Vercellotti, Blood 2013, 121, 1276.
B. Faivre, P. Menu, P. Labrude, C. Vigneron, Artif. Cells Blood Substit. Immobil. Biotechnol. 1998, 26, 17.
T. R. Kelly, R. L. Klein, J. M. Porquez, G. M. Homer, Ann. Surg. 1972, 175, 15.
M. T. Gladwin, T. Kanias, D. B. Kim-Shapiro, J. Clin. Invest. 2012, 122, 1205.
D. R. Janz, L. B. Ware, J. Intensive Care 2015, 3, 20.
M. Frimat, I. Boudhabhay, L. T. Roumenina, Toxins (Basel) 2019, 11, 660.
M. Adamzik, T. Hamburger, F. Petrat, J. Peters, H. de Groot, M. Hartmann, Crit. Care 2012, 16, R125.
J. R. Neal, E. Quintana, R. B. Pike, J. D. Hoyer, L. D. Joyce, G. Schears, J. Extra Corpor. Technol. 2015, 47, 103.
S. O. Sowemimo-Coker, Transfus. Med. Rev. 2002, 16, 46.
Instand: Gesellschaft zur Förderung der Qualitätssicherung in medizinischen Laboratorien e.V. Ringversuch: Hämatologie 16 - Freies Hämoglobin (236), 2020.
M. Harboe, Scand. J. Clin. Lab. Invest. 1959, 11, 66.
D. A. Noe, V. Weedn, W. R. Bell, Clin. Chem. 1984, 30, 627.
V. F. Fairbanks, S. C. Ziesmer, P. C. O'Brien, Clin. Chem. 1992, 38, 132.
S. E. Kahn, B. F. Watkins, E. W. Bermes Jr., Ann. Clin. Lab. Sci. 1981, 11, 126.
M. Matthiae, X. Zhu, R. Marie, A. Kristensen, Analyst 2019, 144, 602.
D. K. R. Medipally, D. Cullen, V. Untereiner, J. Bryant, G. D. Sockalingum, T. N. Q. Nguyen, E. Noone, S. Bradshaw, M. Finn, M. Dunne, A. M. Shannon, J. Armstrong, A. D. Meade, F. M. Lyng, J. Biophotonics 2020, 13, e201960173.
M. Paal, A. Lang, G. Hennig, M. L. Buchholtz, R. Sroka, M. Vogeser, Clin. Biochem. 2018, 56, 62.
A. Taulier, P. Levillain, A. Lemonnier, Clin. Chem. 1987, 33, 1767.
C. C. Winterbourn, Methods Enzymol. 1990, 186, 265.
F. Meng, A. I. Alayash, Anal. Biochem. 2017, 521, 11.
M. Rosenfeld, D. M. Surgenor, J. Biol. Chem. 1950, 183, 663.
C. A. Daniels, C. Wagner, R. C. Hartmann, D. E. Jenkins Jr., Am. J. Clin. Pathol. 1967, 47, 631.
A. Savitzky, M. J. E. Golay, Anal. Chem. 1964, 36, 1627.
European Medicines Agency.Guideline on Bioanalytical Method Validation. London, UK: Committee for Medicinal Product for Human Use (CHMP), 2011.
R. B. Bednar, Laboratoriumsmedizin 1994, 18, 196.
A. Lang, C. Heckl, M. Vogeser, T. Stauch, C. Homann, G. Hennig, R. Sroka, H. Stepp, J. Biomed. Opt. 2018, 23, 1.
J. P. Acker, I. M. Croteau, Q. L. Yi, Clin. Chem. Acta 2012, 413, 1746.
K. Nagy, I. Skagervik, H. Tumani, A. Petzold, M. Wick, H. J. Kuhn, M. Uhr, A. Regeniter, J. Brettschneider, M. Otto, J. Kraus, F. Deisenhammer, R. Lautner, K. Blennow, L. Shaw, H. Zetterberg, N. Mattsson, Clin. Chem. Lab. Med. 2013, 51, 2073.