Surface enhanced Raman scattering for robust, sensitive detection and confirmatory identification of dried bloodstains

被引:21
|
作者
Shaine, M. L. [1 ]
Premasiri, W. R. [2 ,3 ]
Ingraham, H. M. [2 ,3 ]
Andino, R. [2 ,3 ]
Lemler, P. [2 ]
Brodeur, A. N. [1 ]
Ziegler, L. D. [2 ,3 ]
机构
[1] Boston Univ, Sch Med, Program Biomed Forens Sci, Boston, MA 02118 USA
[2] Boston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
[3] Boston Univ, Photon Ctr, 15 St Marys St, Boston, MA 02215 USA
关键词
WHOLE HUMAN BLOOD; RESONANCE RAMAN; FORENSIC IDENTIFICATION; MOLECULAR-MECHANISM; CYTOCHROME-C; SERS SPECTRA; BASIS-SETS; SPECTROSCOPY; HEMOGLOBIN; HEME;
D O I
10.1039/d0an01132k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An optimized procedure is described for the acquisition of 785 nm excited SERS spectra of dried bloodstains and shown to offer great potential for rapid, portable, highly sensitive and specific, confirmatory identification for forensic applications. Following extraction in 1 mu L of 50% acetic acid, a robust, highly reproducible SERS spectrum is observed from dried bloodstains resulting from a hematin-like heme moiety (ferric, high spin). As anticipated, this blood signature can be classified with 100% specificity and sensitivity with respect to the SERS spectra of other body fluids. High quality SERS spectra can be observed from stains of blood diluted by as much as 10(5). Dried blood spectra acquired on Au and Ag SERS active substrates exhibit very different relative intensities at this electronically, non-resonant excitation wavelength (785 nm) indicating that a strong chemical effect contributes to the SERS enhancement of this body fluid. DFT calculations further confirm the vibrational band assignments of the features seen in these SERS spectra of dried blood.
引用
收藏
页码:6097 / 6110
页数:14
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