Study of erythrocyte sedimentation in human blood through the photoacoustic signals analysis.

Aggregation Anemia Erythrocyte sedimentation Pulsed photoacoustic Speed of sound Whole human blood

Journal

Photoacoustics
ISSN: 2213-5979
Titre abrégé: Photoacoustics
Pays: Germany
ID NLM: 101622604

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 03 10 2023
revised: 22 12 2023
accepted: 26 02 2024
medline: 18 3 2024
pubmed: 18 3 2024
entrez: 18 3 2024
Statut: epublish

Résumé

In this study, we utilized the pulsed photoacoustic (PA) technique to analyze globular sedimentation in whole human blood, with a focus on distinguishing between healthy individuals and those with hemolytic anemia. Blood samples were collected from both healthy individuals (women and men) and those with hemolytic anemia, and temporal and spectral parameters of PA signals were employed for analysis. Significant differences (p < 0.05) were observed in PA metrics between the two groups. The proposed spectral analysis allowed significant differentiation within a 25-minute measurement window. Anemic blood samples exhibited higher erythrocyte sedimentation rate (ESR) values, indicating increased erythrocyte aggregation. This study underscores the potential of PA signal analysis in ESR assessment as an efficient method for distinguishing between healthy and anemic blood, surpassing traditional approaches. It represents a promising contribution to the development of precise and sensitive techniques for analyzing human blood samples in clinical settings.

Identifiants

pubmed: 38495950
doi: 10.1016/j.pacs.2024.100599
pii: S2213-5979(24)00016-8
pmc: PMC10940783
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100599

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Argelia Pérez-Pacheco (A)

Unidad de Investigación y Desarrollo Tecnológico (UIDT), Hospital General de México, Dr. Eduardo Liceaga, Ciudad de México 06726, Mexico.

Roberto G Ramírez-Chavarría (RG)

Instituto de Ingeniería, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico.

Marco Polo Colín-García (MP)

Instituto de Ciencias Aplicadas y Tecnología (ICAT), Universidad Nacional Autónoma de México, Apartado Postal 70‑186, Ciudad de México 04510, Mexico.

Flor Del Carmen Cortés-Ortegón (FDC)

Instituto de Ciencias Aplicadas y Tecnología (ICAT), Universidad Nacional Autónoma de México, Apartado Postal 70‑186, Ciudad de México 04510, Mexico.

Rosa María Quispe-Siccha (RM)

Unidad de Investigación y Desarrollo Tecnológico (UIDT), Hospital General de México, Dr. Eduardo Liceaga, Ciudad de México 06726, Mexico.

Adolfo Martínez-Tovar (A)

Laboratorio de Biología Molecular, Servicio de Hematología, Hospital General de México, Dr. Eduardo Liceaga, Ciudad de México 06726, Mexico.

Irma Olarte-Carrillo (I)

Laboratorio de Biología Molecular, Servicio de Hematología, Hospital General de México, Dr. Eduardo Liceaga, Ciudad de México 06726, Mexico.

Luis Polo-Parada (L)

Department of Medical Pharmacology and Physiology and Dalton Cardiovascular Research Center, University of Missouri, Columbia, MO 65211, USA.

Gerardo Gutiérrez-Juárez (G)

Departamento de Ingeniería Física, División de Ciencias e Ingenierías, Universidad de Guanajuato-Campus León, León, Guanajuato C.P. 37150, Mexico.

Classifications MeSH