Surface enhanced Raman scattering specificity for detection and identification of dried bloodstains.


Journal

Forensic science international
ISSN: 1872-6283
Titre abrégé: Forensic Sci Int
Pays: Ireland
ID NLM: 7902034

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 25 04 2021
revised: 16 08 2021
accepted: 10 09 2021
pubmed: 27 9 2021
medline: 9 2 2022
entrez: 26 9 2021
Statut: ppublish

Résumé

Surface enhanced Raman spectroscopy (SERS) provides highly specific vibrational signatures identifying dried blood for a variety of forensic applications. SERS spectra on Au nanoparticle substrates excited at 785 nm are found to identify dried stains of human and nonhuman blood from seven animals, and distinguish stains due to menstrual and peripheral blood. In addition, the unique SERS bloodstain spectrum is distinct from the SERS spectra of thirty red-brown stains of potential household substances that could be visually mistaken for bloodstains and from food stains that have been shown to give positive results with presumptive colorimetric blood tests. Finally, a SERS swab procedure has been developed and demonstrates that the substrates that a blood sample dried on does not offer any Raman or fluorescence interference for the SERS identification of dried blood. Such bloodstains on porous and nonporous materials are all identical and exclusively due to the heme moiety of hemoglobin. Optimized selection of the extraction solvent is found to control the chemical composition of molecular components appearing in the SERS spectrum of complex, multicomponent biological mixtures, such as body fluids.

Identifiants

pubmed: 34564021
pii: S0379-0738(21)00320-0
doi: 10.1016/j.forsciint.2021.111000
pii:
doi:

Substances chimiques

Gold 7440-57-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111000

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

T Reese (T)

Program in Biomedical Forensic Sciences, Boston University School of Medicine, Boston, MA 02118, USA.

C Suarez (C)

Department of Chemistry, Boston University, 590 Commonwealth Ave., Boston, MA 02215, USA.

W R Premasiri (WR)

Department of Chemistry, Boston University, 590 Commonwealth Ave., Boston, MA 02215, USA; Photonics Center, Boston University, 15 Saint Mary's St., Boston, MA 02215, USA.

M L Shaine (ML)

Program in Biomedical Forensic Sciences, Boston University School of Medicine, Boston, MA 02118, USA.

H Ingraham (H)

Department of Chemistry, Boston University, 590 Commonwealth Ave., Boston, MA 02215, USA; Photonics Center, Boston University, 15 Saint Mary's St., Boston, MA 02215, USA.

A N Brodeur (AN)

Program in Biomedical Forensic Sciences, Boston University School of Medicine, Boston, MA 02118, USA.

L D Ziegler (LD)

Department of Chemistry, Boston University, 590 Commonwealth Ave., Boston, MA 02215, USA; Photonics Center, Boston University, 15 Saint Mary's St., Boston, MA 02215, USA. Electronic address: lziegler@bu.edu.

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Classifications MeSH