Raman Spectroscopy Coupled with Advanced Chemometrics for Forensic Analysis of Semen and Blood Mixtures - - Spectroscopy
 Home   Mass Spectrometry   ICP-MS   Infrared   FT-IR   UV-Vis   Raman   NMR   X-Ray   Fluorescence  
Home
Magazine
Issue Archive
Subscribe/Renew
Special Issues
Reprints
The Application Notebook
Current Issue
Archive
Submission Guidelines
Training
SpecAcademy
E-solutions
Digital Edition
Subscribe to the Digital Edition
The Wavelength
Subcribe to The Wavelength
Subscribe to the MS E-news
Resources
Market Profiles
Information for Authors
SpecTube
Webcasts
Advertiser services
Contact Us
Columns
Atomic Perspectives
Chemometrics in Spectroscopy
Focus on Quality
Laser and Optics Interface
Mass Spectrometry Forum
The Baseline
Molecular Spectroscopy Workbench

Raman Spectroscopy Coupled with Advanced Chemometrics for Forensic Analysis of Semen and Blood Mixtures


Spectroscopy
Volume 28, Issue 12, pp. 25-29

Near-infrared (NIR) Raman spectroscopy has become widespread in different areas of the analytical study of materials, including forensic science. The nondestructive character, high selectivity, and possibility to explore a variety of materials make NIR Raman a valuable tool for the identification of body-fluid traces. In this study, we combined regression and classification chemometrical algorithms to achieve effective discrimination of pure body fluids from their binary mixtures. Raman spectra of dried blood, semen, and their mixtures in different ratios, collected in an automatic mapping manner, were used as a model system. The established detection limit for minor contributors is as low as a few percent. The proposed methodology takes into account the intrinsic heterogeneity of blood and semen and their variations between donors, and it potentially can be applied on other mixtures, including those which are of interest to forensic specialists.

In this article, we outline a recently published study on differentiating semen and blood mixtures from individual body fluids (1). The ultimate goal of this project is to develop a nondestructive, confirmatory method for the identification of trace amounts of body fluids for forensic purposes (2,3). Modern forensic tools, such as DNA- and RNA-based methods, provide confirmation of body-fluid type, race, and gender. Even a person involved in a crime can be unambiguously identified by genetic analysis of biological evidence. However, in real life, forensic laboratories equipped with such labor-intensive and expensive techniques are significantly outnumbered by the quantity of biological "footprints" associated with crimes. As a result, there are thousands of body-fluid samples waiting to be analyzed. This type of analysis can be difficult or impossible to perform when the amount of evidence is diminutive or is presented as a complex mixture.

Raman spectroscopy is a nondestructive, time-efficient, and easy-to-use technique suitable for the simultaneous characterization of multiple fluids. Our earliest studies demonstrated the exceptional potential of near-infrared (NIR) Raman spectroscopy for identifying pure body-fluid stains and encouraged us to address more complicated problems, such as differentiating pure body fluids from their mixtures (1,3–11). This practical task required a simplified formulation of the common statistical problem of spectroscopic signal demixing. A forensic expert is much more interested in determining the presence or absence of particular body fluids within a stain than their exact contributions (percentages), which are perfectly accidental.

This scientific problem has been studied using mixtures of blood and semen as model systems because they are highly practical. Blood and semen mixtures are often found at crime scenes related to sexual assaults. The detection of even minor remnants of these types of forensic evidence could be crucial for investigating a crime. Several methods for body-fluid identification were recently proposed and have been used efficiently in forensic laboratories. It is possible to characterize such biological evidence by fluorescence (12–14), immunological tests (15), electrophoretic separation (16), RNA and DNA profiling (17), and several other methods (18–22).

Despite the undeniable advantages of the methods listed above, a uniform approach that can save sample for further analysis and provide fast and accurate results is still a necessity. The Raman effect occurs due to the interaction of an incident photon with a vibrating molecule. The energies of the scattered photons with shifted frequencies can be graphically represented as Raman spectra that provide unique information about the biochemical composition of the analyzed samples (23). The volume of the analyzed matter can be as small as a few femtoliters or picograms of sample.

Recent developments in analytical instrumentation have allowed for the comprehensive manipulation of samples using techniques such as automatic imaging and mapping. This technique automatically collects spectra when a sample under the laser beam moves by a specified amount until all of the areas are scanned. This approach yields large data sets that can be preprocessed and treated with a variety of statistical software packages. Combining Raman spectroscopy with multivariate statistics helps avoid the problem of heterogeneity of body-fluid stains; their composition can vary between donors and within the sample. The method we propose can process samples with various fluorescent profiles and overlapping spectral bands, which are common features for biological objects.

Our method is based on the effective combination of regression and classification analyses that require a multistep discrimination procedure. Support vector machine (SVM) regression was selected to separate the mixture's spectra that can be easily distinguished from those of pure fluids. The final classification model was built on selected data using support vector machine discriminant analysis (SVMDA). Then, the entire data set was subjected to the analysis. As a result, we were able to distinguish spectra with minor contributions of blood or semen. The lowest concentrations that we were able to detect were 5% of blood in semen and approximately 1% of semen in blood stains. Lower concentrations could be detected, but the accuracy of detection decreased significantly. The proposed approach potentially can be plugged into portable instruments as a discriminative algorithm, which would be beneficial for forensic laboratories as a valuable tool for investigation directly at a crime scene.


Rate This Article
Your original vote has been tallied and is included in the ratings results.
View our top pages
Average rating for this page is: 6
Headlines from LCGC North America and Chromatography Online
Tosoh NA - Analysis of Monoclonal Antibody Aggregates by SEC using MS-Friendly Mobile Phases
Developing Successful UHPLC Methods
UCT - Extraction and Analysis of Nicotine, Cotinine, and Anabasine from Urine using SPE and GC?MS
Wyatt EU - UHPLC with Light Scattering
Wyatt NA - UHPLC with Light Scattering
Source: Spectroscopy,
Click here