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The increasing number of terrorist attacks within the last decade has demonstrated that taking preventive protective measures is highly important. In addition to existing measures, automated detection systems for fast and reliable explosive detection are required. A sensitive spectroscopic system based on mid-infrared spectroscopy has been developed and applied to explosive samples on different types of fabric under various geometric conditions. Using this system, traces of TNT, RDX, PETN and ammonium nitrate can be detected in less than a second. Various approaches for data pretreatment (wavelength calibration) and subsequent analysis (normalization, removal of atmospheric water absorption lines) are presented and the remaining challenges on the road to a fully automated system, including a robust classification algorithm, are discussed.
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Sustancias Explosivas , Textiles , Análisis Espectral , Calibración , AguaRESUMEN
The variable configuration of Raman spectroscopic platforms is one of the major obstacles in establishing Raman spectroscopy as a valuable physicochemical method within real-world scenarios such as clinical diagnostics. For such real world applications like diagnostic classification, the models should ideally be usable to predict data from different setups. Whether it is done by training a rugged model with data from many setups or by a primary-replica strategy where models are developed on a 'primary' setup and the test data are generated on 'replicate' setups, this is only possible if the Raman spectra from different setups are consistent, reproducible, and comparable. However, Raman spectra can be highly sensitive to the measurement conditions, and they change from setup to setup even if the same samples are measured. Although increasingly recognized as an issue, the dependence of the Raman spectra on the instrumental configuration is far from being fully understood and great effort is needed to address the resulting spectral variations and to correct for them. To make the severity of the situation clear, we present a round robin experiment investigating the comparability of 35 Raman spectroscopic devices with different configurations in 15 institutes within seven European countries from the COST (European Cooperation in Science and Technology) action Raman4clinics. The experiment was developed in a fashion that allows various instrumental configurations ranging from highly confocal setups to fibre-optic based systems with different excitation wavelengths. We illustrate the spectral variations caused by the instrumental configurations from the perspectives of peak shifts, intensity variations, peak widths, and noise levels. We conclude this contribution with recommendations that may help to improve the inter-laboratory studies.
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Surface-enhanced Raman scattering (SERS) is a powerful and sensitive technique for the detection of fingerprint signals of molecules and for the investigation of a series of surface chemical reactions. Many studies introduced quantitative applications of SERS in various fields, and several SERS methods have been implemented for each specific application, ranging in performance characteristics, analytes used, instruments, and analytical matrices. In general, very few methods have been validated according to international guidelines. As a consequence, the application of SERS in highly regulated environments is still considered risky, and the perception of a poorly reproducible and insufficiently robust analytical technique has persistently retarded its routine implementation. Collaborative trials are a type of interlaboratory study (ILS) frequently performed to ascertain the quality of a single analytical method. The idea of an ILS of quantification with SERS arose within the framework of Working Group 1 (WG1) of the EU COST Action BM1401 Raman4Clinics in an effort to overcome the problematic perception of quantitative SERS methods. Here, we report the first interlaboratory SERS study ever conducted, involving 15 laboratories and 44 researchers. In this study, we tried to define a methodology to assess the reproducibility and trueness of a quantitative SERS method and to compare different methods. In our opinion, this is a first important step toward a "standardization" process of SERS protocols, not proposed by a single laboratory but by a larger community.
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Data fusion of different imaging techniques allows a comprehensive description of chemical and biological systems. Yet, joining images acquired with different spectroscopic platforms is complex because of the different sample orientation and image spatial resolution. Whereas matching sample orientation is often solved by performing suitable affine transformations of rotation, translation, and scaling among images, the main difficulty in image fusion is preserving the spatial detail of the highest spatial resolution image during multitechnique image analysis. In this work, a special variant of the unmixing algorithm Multivariate Curve Resolution Alternating Least Squares (MCR-ALS) for incomplete multisets is proposed to provide a solution for this kind of problem. This algorithm allows analyzing simultaneously images collected with different spectroscopic platforms without losing spatial resolution and ensuring spatial coherence among the images treated. The incomplete multiset structure concatenates images of the two platforms at the lowest spatial resolution with the image acquired with the highest spatial resolution. As a result, the constituents of the sample analyzed are defined by a single set of distribution maps, common to all platforms used and with the highest spatial resolution, and their related extended spectral signatures, covering the signals provided by each of the fused techniques. We demonstrate the potential of the new variant of MCR-ALS for multitechnique analysis on three case studies: (i) a model example of MIR and Raman images of pharmaceutical mixture, (ii) FT-IR and Raman images of palatine tonsil tissue, and (iii) mass spectrometry and Raman images of bean tissue.
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Cellular senescence is a terminal cell cycle arrested state, assumed to be involved in tumor suppression. We studied four human fibroblast cell strains (BJ, MRC-5, IMR-90, and WI-38) from proliferation into senescence. Cells were investigated by label-free vibrational Raman and infrared spectroscopy, following their transition into replicative senescence. During the transition into senescence, we observed rather similar biomolecular abundances in all four cell strains and between proliferating and senescent cells; however, in the four aging cell strains, we found common molecular differences dominated by protein and lipid modifications. Hence, aging induces a change in the appearance of biomolecules (including degradation and storage of waste) rather than in their amount present in the cells. For all fibroblast strains combined, the partial least squares-linear discriminant analysis (PLS-LDA) model resulted in 75% and 81% accuracy for the Raman and infrared (IR) data, respectively. Within this validation, senescent cells were recognized with 93% sensitivity and 90% specificity for the Raman and 84% sensitivity and 97% specificity for the IR data. Thus, Raman and infrared spectroscopy can identify replicative senescence on the single cell level, suggesting that vibrational spectroscopy may be suitable for identifying and distinguishing different cellular states in vivo, e.g., in skin.
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Proliferación Celular , Senescencia Celular , Espectroscopía Infrarroja por Transformada de Fourier , Espectrometría Raman , Puntos de Control del Ciclo Celular , Células Cultivadas , Análisis Discriminante , Fibroblastos/citología , Fibroblastos/metabolismo , Humanos , Análisis de los Mínimos CuadradosRESUMEN
Hierarchical cluster analysis (HCA) is extensively used for the analysis of hyperspectral data. In this work, hyperspectral data sets obtained from Raman maps were analyzed using an alternative mode of cluster analysis, clustering "images" instead of spectra, under the assumption that images showing similar spatial distributions are related to the same chemical species. Such an approach was tested with two Raman maps: one simple "test map" of micro-crystals of four different compounds for a proof of principle and a map of a biological tissue (i.e., cartilage) as an example of chemically complex sample. In both cases, the "image-clustering" approach gave similar results as the traditional HCA, but at lower computational effort. The alternative approach proved to be particularly helpful in cases, as for the cartilage tissue, where concentration gradients of chemical composition are present. Moreover, with this approach, yielded information about correlation between bands in the average spectrum makes band assignment and spectral interpretation easier.
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Vancomycin is an important glycopeptide antibiotic which is used to treat serious infections caused by Gram-positive bacteria. However, during the last years, a tremendous rise in vancomycin resistances, especially among Enterococci, was reported, making fast diagnostic methods inevitable. In this contribution, we apply Raman spectroscopy to systematically characterize vancomycin-enterococci interactions over a time span of 90 min using a sensitive Enterococcus faecalis strain and two different vancomycin concentrations above the minimal inhibitory concentration (MIC). Successful action of the drug on the pathogen could be observed already after 30 min of interaction time. Characteristic spectral changes are visualized with the help of multivariate statistical analysis (linear discriminant analysis and partial least squares regressions). Those changes were employed to train a statistical model to predict vancomycin treatment based on the Raman spectra. The robustness of the model was tested using data recorded by an independent operator. Classification accuracies of >90 % were obtained for vancomycin concentrations in the lower range of a typical trough serum concentration recommended for most patients during appropriate vancomycin therapy. Characterization of drug-pathogen interactions by means of label-free spectroscopic methods, such as Raman spectroscopy, can provide the knowledge base for innovative and fast susceptibility tests which could speed up microbiological analysis as well as finding applications in novel antibiotic screenings assays. Graphical Abstract E. faecalis is incubated with vancomycin and characterized by means of Raman spectroscopy after different time points. Characteristic spectral changes reveal efficient vancomycin-enterococci-interaction.
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Antibacterianos/farmacología , Enterococcus faecalis/efectos de los fármacos , Infecciones por Bacterias Grampositivas/tratamiento farmacológico , Pruebas de Sensibilidad Microbiana/métodos , Espectrometría Raman/métodos , Vancomicina/farmacología , HumanosRESUMEN
Three important technical innovations are reported here towards Raman-activated cell sorting. Firstly, a microfluidic chip made of quartz is introduced which integrates injection of single cells, trapping by laser fibres and sorting of cells. Secondly, a chip holder was designed to provide simple, accurate and stable adjustment of chips, microfluidic connections and the trapping laser fibres. The new setup enables to the collection of Raman spectra of single cells at 785 nm excitation with 10 s exposure time. Lastly, a new type of modelling the various background contributions is described, improving Raman-based cell identification by the classification algorithm linear discriminant analysis. Mean sensitivity and specificity determined by iterated 10-fold cross validation were 96 and 99 %, respectively, for the distinction of leucocytes extracted from blood, breast cancer cells BT-20 and MCF-7, and leukaemia cells OCI-AML3.
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Células/química , Microfluídica/métodos , Espectrometría Raman/métodos , Línea Celular Tumoral , Humanos , Microfluídica/instrumentación , Pinzas Ópticas , Cuarzo , Espectrometría Raman/instrumentaciónRESUMEN
Positively charged nanoparticles to be used as substrates for surface-enhanced Raman scattering (SERS) were prepared by coating citrate-reduced silver nanoparticles with the cationic polymer poly-l-lysine. The average diameter of the coated nanoparticles is 75 nm, and their zeta potential is +62.3 ± 1.7 mV. UV-vis spectrophotometry and dynamic light scattering measurements show that no aggregation occurs during the coating process. As an example of their application, the so-obtained positively charged coated particles were employed to detect nanomolar concentrations of the anionic chromophore bilirubin using SERS. Because of their opposite charge, bilirubin molecules interact with the coated nanoparticles, allowing SERS detection. The SERS intensity increases linearly with concentration in a range from 10 to 200 nM, allowing quantitative analysis of bilirubin aqueous solutions.
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Nanopartículas del Metal/química , Polilisina/química , Plata/química , Espectrometría Raman/métodos , Tamaño de la Partícula , Electricidad Estática , Propiedades de SuperficieRESUMEN
Gliomas are the most frequent primary brain tumours. During neurosurgical treatment, locating the exact tumour border is often difficult. This study assesses grading of astrocytomas based on Raman spectroscopy for a future application in intra-surgical guidance. Our predictive classification models distinguish the surgically relevant classes "normal tissue" and "low" and "high grade astrocytoma" in Raman maps of moist bulk samples (80 patients) acquired with a fibre-optic probe. We introduce partial class memberships as a strategy to utilize borderline cases for classification. Borderline cases supply the most valuable training and test data for our application. They are (a) examples of the sought boundary and (b) the cases for which new diagnostics are needed. Besides, the number of suitable training samples increases considerably: soft logistic regression (LR) utilizes 85% more spectra and 50% more patients than linear discriminant analysis (LDA). The predictive soft LR models achieve ca. 85, 67 and 84% (normal, low and high grade) sensitivity and specificity. We discuss the different heuristics of LR and LDA in the light of borderline samples. While we focus on prediction, the spectroscopic interpretation of the predictive models agrees with previous descriptive studies. Unsaturated lipids are used to differentiate between normal and tumour tissues, while the total lipid content prominently contributes to the determination of the tumour grade. The high-wavenumber region above 2,800 cm(-1) alone did not allow successful grading. We give a proof of concept for Raman spectroscopic grading of moist astrocytoma tissues and propose to include borderline samples into classifier training and testing.
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Astrocitoma/patología , Encéfalo/patología , Espectrometría Raman/métodos , Análisis Discriminante , HumanosRESUMEN
Raman mapping in combination with uni- and multi-variate methods of data analysis is applied to articular cartilage samples. Main differences in biochemical composition and collagen fibers orientation between superficial, middle and deep zone of the tissue are readily observed in the samples. Collagen, non-collagenous proteins, proteoglycans and nucleic acids can be distinguished on the basis of their different spectral characteristics, and their relative abundance can be mapped in the label-free tissue samples, at so high a resolution as to permit the analysis at the level of single cells. Differences between territorial and inter-territorial matrix, as well as inhomogeneities in the inter-territorial matrix, are properly identified. Multivariate methods of data analysis prove to be complementary to the univariate approach. In particular, our partial least squares regression model gives a semiquantitative mapping of the biochemical constituents in agreement with average composition found in the literature. The combination of hierarchical and fuzzy cluster analysis succeeds in detecting variations between different regions of the extra-cellular matrix. Because of its characteristics as an imaging technique, Raman mapping could be a promising tool for studying biochemical changes in cartilage occurring during aging or osteoarthritis.
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Cartílago Articular/química , Análisis Multivariante , Espectrometría Raman/métodos , Animales , Cartílago Articular/citología , Análisis por Conglomerados , Matriz Extracelular/química , Análisis de Componente Principal , PorcinosRESUMEN
A Raman-based, strain-independent, semi-automated method is presented that allows the rapid (<3 hours) determination of antibiotic susceptibility of bacterial pathogens isolated from clinical samples. Applying a priori knowledge about the mode of action of the respective antibiotic, we identified characteristic Raman marker bands in the spectrum and calculated batch-wise weighted sum scores from standardized Raman intensity differences between spectra of antibiotic exposed and nonexposed samples of the same strains. The lead substances for three relevant antibiotic classes (fluoroquinolone ciprofloxacin, third-generation cephalosporin cefotaxime, ureidopenicillin piperacillin) against multidrug-resistant Gram-negative bacteria (MRGN) revealed a high sensitivity and specificity for the susceptibility testing of two Escherichia coli laboratory strains and 12 clinical isolates. The method benefits from the parallel incubation of control and treated samples, which reduces the variance due to alterations in cultivation conditions and the standardization of differences between batches leading to long-term comparability of Raman measurements.
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Cefalosporinas , Preparaciones Farmacéuticas , Antibacterianos/farmacología , Antibacterianos/uso terapéutico , Cefalosporinas/farmacología , Farmacorresistencia Bacteriana Múltiple , Escherichia coli , Fluoroquinolonas/farmacología , Pruebas de Sensibilidad MicrobianaRESUMEN
Small sample sizes are very common in multivariate analysis. Sample sizes of 10-100 statistically independent objects (rejects from processes or loading dock analysis, or patients with a rare disease), each with hundreds of data points, cause unstable models with poor predictive quality. Model stability is assessed by comparing models that were built using slightly varying training data. Iterated k-fold cross-validation is used for this purpose. Aggregation stabilizes models. It is possible to assess the quality of the aggregated model without calculating further models. The validation and aggregation methods investigated in this study apply to regression as well as to classification. These techniques are useful for analyzing data with large numbers of variates, e.g., any spectral data like FT-IR, Raman, UV/VIS, fluorescence, AAS, and MS. FT-IR images of tumor tissue were used in this study. Some tissue types occur frequently, while some are very rare. They are classified using LDA. Initial models were severely unstable. Aggregation stabilizes the predictions. The hit rate increased from 67% to 82%.
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Modelos Biológicos , Análisis Multivariante , Neoplasias/química , Neoplasias/clasificación , Probabilidad , Reproducibilidad de los Resultados , Tamaño de la MuestraRESUMEN
In biospectroscopy, suitably annotated and statistically independent samples (e.g. patients, batches, etc.) for classifier training and testing are scarce and costly. Learning curves show the model performance as function of the training sample size and can help to determine the sample size needed to train good classifiers. However, building a good model is actually not enough: the performance must also be proven. We discuss learning curves for typical small sample size situations with 5-25 independent samples per class. Although the classification models achieve acceptable performance, the learning curve can be completely masked by the random testing uncertainty due to the equally limited test sample size. In consequence, we determine test sample sizes necessary to achieve reasonable precision in the validation and find that 75-100 samples will usually be needed to test a good but not perfect classifier. Such a data set will then allow refined sample size planning on the basis of the achieved performance. We also demonstrate how to calculate necessary sample sizes in order to show the superiority of one classifier over another: this often requires hundreds of statistically independent test samples or is even theoretically impossible. We demonstrate our findings with a data set of ca. 2550 Raman spectra of single cells (five classes: erythrocytes, leukocytes and three tumour cell lines BT-20, MCF-7 and OCI-AML3) as well as by an extensive simulation that allows precise determination of the actual performance of the models in question.
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Modelos Teóricos , Células Cultivadas , Eritrocitos/química , Eritrocitos/clasificación , Eritrocitos/citología , Humanos , Leucocitos/química , Leucocitos/clasificación , Leucocitos/citología , Células MCF-7 , Tamaño de la Muestra , Espectrometría RamanRESUMEN
Spectroscopy-based imaging techniques can provide useful biochemical information about tissue samples. Here, we employ Raman and Fourier transform infrared (IR) imaging to characterize composition and constitution of atherosclerotic plaques of rabbits, fed with a high cholesterol diet. The results were compared with conventional light microscopy after staining with hematoxylin eosin, and elastica van Gieson. The spectral unmixing algorithm vertex component analysis was applied for data analysis and image reconstruction. IR microscopy allowed for differentiation between lipids and proteins in plaques of full aortic cross sections. Raman microscopy further discriminated cholesterol esters, cholesterol and triglycerides. FTIR and Raman images were recorded at a resolution near 20 micrometer per pixel for a large field of view. High resolution Raman images at 1 micrometer per pixel revealed structural details at selected regions of interest. The intima-media and the lipid-protein ratio were determined in five specimens for quantitation. These results correlate well with histopathology. The described method is a promising tool for easy and fast molecular imaging of atherosclerosis.
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Placa Aterosclerótica/patología , Espectroscopía Infrarroja por Transformada de Fourier/métodos , Espectrometría Raman/métodos , Algoritmos , Animales , Aorta Torácica/patología , Aterosclerosis/metabolismo , Grosor Intima-Media Carotídeo , Diagnóstico por Imagen/métodos , Humanos , Procesamiento de Imagen Asistido por Computador , Lípidos/química , Masculino , Modelos Estadísticos , Placa Aterosclerótica/diagnóstico , Conejos , Triglicéridos/químicaRESUMEN
An all-fibre based Raman-on-chip setup is introduced which enables analysis of solutions and trapped particles without microscopes or objectives. Beside the novel quartz microfluidic chip, innovative multi-core single-mode fibres with integrated fibre Bragg gratings are used for detection. The limit of quantitation is 7.5 mM for urea and 2.5 mM for nicotine with linear Raman spectroscopy. This is an improvement of more than two orders of magnitude compared with previous fibre-based microfluidic Raman detection schemes. Furthermore, our device was combined with optical traps to collect Raman-on-chip spectra of spherical polymer beads.
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Técnicas Analíticas Microfluídicas/métodos , Nicotina/análisis , Espectrometría Raman , Urea/análisis , Calibración , Técnicas Analíticas Microfluídicas/instrumentación , Técnicas Analíticas Microfluídicas/normas , Nicotina/normas , Soluciones/química , Urea/normasRESUMEN
Infrared (IR) and Raman spectroscopy are emerging biophotonic tools to recognize various diseases. The current review gives an overview of the experimental techniques, data-classification algorithms and applications to assess soft tissues, hard tissues and body fluids. The methodology section presents the principles to combine vibrational spectroscopy with microscopy, lateral information and fiber-optic probes. A crucial step is the classification of spectral data by a variety of algorithms. We discuss unsupervised algorithms such as cluster analysis or principal component analysis and supervised algorithms such as linear discriminant analysis, soft independent modeling of class analogies, artificial neural networks support vector machines, Bayesian classification, partial least-squares regression and ensemble methods. The selected topics include tumors of epithelial tissue, brain tumors, prion diseases, bone diseases, atherosclerosis, kidney stones and gallstones, skin tumors, diabetes and osteoarthritis.
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Técnicas y Procedimientos Diagnósticos , Espectroscopía Infrarroja por Transformada de Fourier/métodos , Espectrometría Raman/métodos , Algoritmos , Animales , Aterosclerosis/diagnóstico , Enfermedades Óseas/diagnóstico , Neoplasias Encefálicas/diagnóstico , Cálculos/diagnóstico , Diabetes Mellitus/diagnóstico , Femenino , Humanos , Masculino , Neoplasias Glandulares y Epiteliales/diagnóstico , Enfermedades Neurodegenerativas/diagnóstico , Osteoartritis/diagnóstico , Neoplasias Cutáneas/diagnóstico , Espectroscopía Infrarroja por Transformada de Fourier/estadística & datos numéricosRESUMEN
The objectives of this study were to optimize the preparation of pristine brain tissue to obtain reference information, to optimize the conditions for introducing a fiber-optic probe to acquire Raman maps, and to transfer previous results obtained from human brain tumors to an animal model. Brain metastases of malignant melanomas were induced by injecting tumor cells into the carotid artery of mice. The procedure mimicked hematogenous tumor spread in one brain hemisphere while the other hemisphere remained tumor free. Three series of sections were prepared consecutively from whole mouse brains: dried, thin sections for FTIR imaging, hematoxylin and eosin-stained thin sections for histopathological assessment, and pristine, 2-mm thick sections for Raman mapping. FTIR images were recorded using a spectrometer with a multi-channel detector. Raman maps were collected serially using a spectrometer coupled to a fiber-optic probe. The FTIR images and the Raman maps were segmented by cluster analysis. The color-coded cluster memberships coincided well with the morphology of mouse brains in stained tissue sections. More details in less time were resolved in FTIR images with a nominal resolution of 25 microm than in Raman maps collected with a laser focus 60 microm in diameter. The spectral contributions of melanin in tumor cells were resonance enhanced in Raman spectra on excitation at 785 nm which enabled their sensitive detection in Raman maps. Possible reasons why metastatic cells of malignant melanomas were not identified in FTIR images are discussed.