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Determination of Methemoglobin in Hemoglobin Submicron Particles Using NMR Relaxometry

Methemoglobin (MetHb) is a hemoglobin (Hb) derivative with the heme iron in ferric state (Fe(3+)), unable to deliver oxygen. Quantification of methemoglobin is a very important diagnostic parameter in hypoxia. Recently, novel hemoglobin microparticles (Hb-MP) with a narrow size distribution around 7...

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Detalles Bibliográficos
Autores principales: Kaewprayoon, Waraporn, Suwannasom, Nittiya, Kloypan, Chiraphat, Steffen, Axel, Xiong, Yu, Schellenberger, Eyk, Pruß, Axel, Georgieva, Radostina, Bäumler, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730817/
https://www.ncbi.nlm.nih.gov/pubmed/33256027
http://dx.doi.org/10.3390/ijms21238978
Descripción
Sumario:Methemoglobin (MetHb) is a hemoglobin (Hb) derivative with the heme iron in ferric state (Fe(3+)), unable to deliver oxygen. Quantification of methemoglobin is a very important diagnostic parameter in hypoxia. Recently, novel hemoglobin microparticles (Hb-MP) with a narrow size distribution around 700 nm, consisting of cross-linked Hb were proposed as artificial oxygen carriers. The cross-linking of Hb by glutaraldehyde (GA) generates a certain amount of MetHb. Due to the strong light scattering, quantitative determination of MetHb in Hb-MP suspensions by common spectrophotometry is not possible. Here, we demonstrate that (1)H(2)O NMR relaxometry is a perfect tool for direct measurement of total Hb and MetHb concentrations in Hb-MP samples. The longitudinal relaxation rate 1/T(1) shows a linear increase with increasing MetHb concentration, whereas the transverse relaxation rate 1/T(2) linearly increases with the total Hb concentration. In both linear regressions the determination coefficient (R(2)) is higher than 0.99. The method does not require time-consuming pretreatment or digestion of the particles and is not impaired by light scattering. Therefore, it can be established as the method of choice for the quality control of Hb-MP and similar hemoglobin-based oxygen carriers in the future.