Vibrational Spectroscopic Methods Research Articles

Stabilisation of a Strontium Hydride with a Monodentate Carbazolyl Ligand and its Reactivity.

The molecular strontium hydride 2[(dtbpCbz)SrH(L)]2 (L = benzene, toluene) was isolated and stabilized by employing a sterically demanding carbazole ligand (dtbpCbz = 1,8-bis(3,5-ditert-butyl-phenyl)-3,6-ditertbutylcarbazolyl). Compound 2 was synthesized via phenylsilane metathesis with the corresponding amide (dtbpCbz)SrN(SiMe3)2 and characterized by 1HNMR, XRD and vibrational spectroscopy methods. We further investigated the stoichiometric reactivity of 2 towards carbon monoxide, azobenzene and trimethylsilylacetylene, showing three distinct reactivity pathways: addition, reduction and deprotonation. The reaction of 2 with carbon monoxide yields the ethenediolate complex 4 via addition, while with azobenzene reduction of the N-N double bond and release of hydrogen were observed, affording a heteroleptic strontium complex with a radical azobenzenyl ligand (5). The terminal alkyne is deprotonated by the hydride moiety to give the acetylide complex 6.

Machine Learning Approaches for the Fusion of Near-Infrared, Mid-Infrared, and Raman Data to Identify Cartilage Degradation in Human Osteochondral Plugs.

Vibrational spectroscopy methods such as mid-infrared (MIR), near-infrared (NIR), and Raman spectroscopies have been shown to have great potential for in vivo biomedical applications, such as arthroscopic evaluation of joint injuries and degeneration. Considering that these techniques provide complementary chemical information, in this study, we hypothesized that combining the MIR, NIR, and Raman data from human osteochondral samples can improve the detection of cartilage degradation. This study evaluated 272 osteochondral samples from 18 human knee joins, comprising both healthy and damaged tissue according to the reference Osteoarthritis Research Society International grading system. We established the one-block and multi-block classification models using partial least squares discriminant analysis (PLSDA), random forest, and support vector machine (SVM) algorithms. Feature modeling by principal component analysis was tested for the SVM (PCA-SVM) models. The best one-block models were built using MIR and Raman data, discriminating healthy cartilage from damaged with an accuracy of 77.5% for MIR and 77.8% for Raman using the PCA-SVM algorithm, whereas the NIR data did not perform as well achieving only 68.5% accuracy for the best model using PCA-SVM. The multi-block approach allowed an improvement with an accuracy of 81.4% for the best model by PCA-SVM. Fusing three blocks using MIR, NIR, and Raman by multi-block PLSDA significantly improved the performance of the single-block models to 79.1% correct classification. The significance was proven by statistical testing using analysis of variance. Thus, the study suggests the potential and the complementary value of the fusion of different spectroscopic techniques and provides valuable data analysis tools for the diagnostics of cartilage health.

Radiobiological Applications of Vibrational Spectroscopy: A Review of Analyses of Ionising Radiation Effects in Biology and Medicine

Vibrational spectroscopic techniques, such as Fourier transform infrared (FTIR) absorption and Raman spectroscopy (RS), offer unique and detailed biochemical fingerprints by detecting specific molecular vibrations within samples. These techniques provide profound insights into the molecular alterations induced by ionising radiation, which are both complex and multifaceted. This paper reviews the application of rapid and label-free vibrational spectroscopic methods for assessing biological radiation responses. These assessments span from early compartmentalised models such as DNA, lipid membranes, and vesicles to comprehensive evaluations in various living biological models, including tissues, cells, and organisms of diverse origins. The review also discusses future perspectives, highlighting how the field is overcoming methodological limitations. RS and FTIR have demonstrated significant potential in detecting radiation-induced biomolecular alternations, which may facilitate the identification of radiation exposure spectral biomarkers/profiles.

Synthesis of anhydrous lanthanum acetate. Analysis of it’s structural, thermal and electronic properties

Acetate complexes of rare earth elements are extensively studied compounds known for their diverse properties and potential applications and lanthanum acetate hydrate is commercially available. In this work, a powdered anhydrous lanthanum acetate (La(CH3COO)3) sample was prepared by dissolving lanthanum oxide (La2O3) in an excess of acetic acid (CH3COOH) and distilled water (H2O), followed by direct evaporation at 150 °C. The decomposition of La(CH3COO)3 was studied, showing initiation around 300 °C and conclusion at ≥700 °C, with four distinct thermal events (I–IV) of mass loss. Gas phase identification revealed acetone and carbon dioxide as decomposition products, indicating pyrolytic decarboxylation. The final thermal effect (IV) is linked to the decomposition of La2O2CO3 to La2O3. The DFT refinement of atomic coordinates of hydrogen atoms, which were unavailable from experiment, was successfully performed. Obtained structural data was checked using vibrational spectroscopy method. The calculated electronic band structure of La(CH3COO)3 indicates it as an indirect wide band gap material with values of direct transition close to indirect. The optical bandgap is found to be 5.49 eV, suggesting that the charge transfer in La(CH3COO)3 can be optically activated with wavelengths shorter than 226 nm, which falls within the deep UV (DUV) region.

Vibrational spectroscopy data fusion for enhanced classification of different milk types

The aim of this study is to classify seven types of Irish milk (butter, fresh, heart active, lactose free, light, protein, and slimline), supplied by a specific company, using vibrational spectroscopy methods: Near infrared (NIR), mid infrared (MIR), and Raman spectroscopy. In this regard, chemometric methods were used, and the impact of spectral data fusion on prediction accuracy was evaluated. A total of 105 samples were tested, with 21 used in the test set. The study assessed principal component analysis (PCA), partial least square discriminant analysis (PLS-DA), and sequential and orthogonalized partial least squares linear discriminant analysis (SO-PLS-LDA) for classifying different milk types. The prediction accuracy, when applying PLS-DA on individual blocks of data and low-level fused data, did not exceed 85.71 %. However, implementing the SO-PLS-LDA strategy significantly improved the accuracy to 95 %, suggesting a promising method for the development of classification models for milk using data fusion strategies.

Spectral histology of hair and hair follicle using infrared microspectroscopy.

Today, there is only limited knowledge of the spatial organization of hair chemistry. Infrared microspectroscopy is a well-established tool to provide such information and has significantly contributed to this field. In this study, we present new results combining multiple infrared microspectroscopy methods at different length scales to create a better chemical histology of human hair, including the hair follicle, hair shaft, hair medulla and hair cuticle. We used hyperspectral IR imaging & spectroscopy (HIRIS) and synchrotron-radiation FTIR microspectroscopy (SR-μFTIR) to measure transversal hair sections and SR-μFTIR to obtain high-resolution maps of longitudinal sections from the hair shaft and from the hair follicle. We used optical photothermal IR microspectroscopy (OPTIR) to analyse the cuticle surface of intact hairs. By mapping longitudinal sections of the human hair follicle with confocal SR-μFTIR, we report the first demonstration of glycogen presence in the outer root sheath of the hair follicle by spectroscopy, and its quantification at the micron scale. Spectral maps, combined with machine learning-based analysis, enabled us to differentiate the various layers of the hair follicle and provided insights into the chemical changes that occur during hair formation in the follicle. Using HIRIS and SR-μFTIR to analyse the hair medulla in transversal sections of human hairs, we report here, for the first time by vibrational spectroscopy methods, the detection of unsaturated lipids at very low concentrations in the medulla. By analysing longitudinal sections of the hair shaft with SR-μFTIR, we found that calcium carboxylates are present in large regions of the hair cuticle, and not just in small focal areas as previously thought. We then use OPTIR to analyse the hair cuticle of intact hairs at submicron resolution without sectioning and report the distribution of calcium carboxylates at the surface of intact hair for the first time. These new findings illustrate the potential of infrared microspectroscopy for imaging the chemical composition of human hair and may have implications for biomedical research or cosmetology.

Current Perspectives in the Forensic Analysis of Timbers using Vibrational Spectroscopy: A Review

Wildlife crime has increased significantly with respect to timbers such as illegal timber trading, logging, harvesting, and counterfeiting. It has tremendously drained the economy of different countries since timber trafficking at the global level has an average annual net worth of US$ 50-150 billion. Moreover, timbers can act as important forensic evidence as they can be found at the crime scenes revealing the relationships between the crime scene and corpus delicti. Since ancient times, various traditional techniques have been used for timber identification such as anatomical investigation by visual method at the macroscopic and microscopic levels. However, morphological and anatomical techniques have some advantages, such as cost effectiveness, and limitations as they require experienced personnel. Vibrational spectroscopic tools such as infrared and Raman spectroscopy help in discriminating various species of timber as different timber species have unique phytochemicals. By examining the concentrations of cellulose, lignin, and hemicelluloses, the chemical composition can also be estimated. Herein, this review is carried out using vibrational spectroscopic methods for timber identification to combat criminal activities related to timbers for the dissemination of justice. Recent advancements and prospects are also emphasized in this review paper.

Renewed spectroscopic and theoretical research of hydrogen bonding in ascorbic acid

The studies of two isomers of ascorbic acid and their deuteroanalogues, presented in the paper, have been accomplished by vibrational spectroscopy methods and quantum-chemical simulations. The spectroscopic research of L-ascorbic and D-isoascorbic acids have been carried out by the infrared (IR) and Raman (R) techniques. On the basis of the obtained results the spectral interpretation of the hydrogen bonded groups of ascorbic acids has been performed. Car-Parrinello Molecular Dynamics (CPMD) and Density Functional Theory (DFT) have been employed to support spectroscopic experimental findings and shed light onto the bridged proton dynamics in the L- and D- isomers of ascorbic acids. The accurate assignments of the hydrogen bond modes have been accomplished with the application of deuterosubstitution, CPMD-solid state simulations and Potential Energy Distribution (PED) analysis. The spectral and structural results have shown that dependency ν(OH) = f(γ(OH)) is the most common for the OHO hydrogen bond, whereas dependency d(OO) = f(γ(OH)) differs as for the ionic and resonance assisted hydrogen bonds.

Vibrational spectroscopic detection of radiation-induced structural changes in Chironomus hemoglobin

PurposeChironomus hemoglobin is known to exhibit higher gamma radiation resistance compared to human hemoglobin. In the present study, we have introduced a sensitive method to analyze radiation-induced alterations in Chironomus hemoglobin using Vibrational spectroscopy and further highlighting its potential for monitoring radiotoxicity in aquatic environments. Materials and methodsVibrational spectroscopic methods such as Raman and FT-IR spectroscopy were used to capture the distinctive chemical signature of Chironomus hemoglobin (ChHb) under both in vitro and in vivo conditions. Any radiation dose-dependent shifts could be analyzed Human hemoglobin (HuHb) as standard reference. ResultsDistinctive Raman peak detected at 930 cm-1 in (ChHb) was attributed to C–N stretching in the heterocyclic ring surrounding the iron atom, preventing heme degradation even after exposure to 2400 Gy dose. In contrast, for (HuHb), the transition from deoxy-hemoglobin to met-hemoglobin at 1210 cm-1 indicated a disruption in oxygen binding after exposure to 1200 Gy dose. Furthermore, while ChHb exhibited a consistent peak at 1652 cm-1 in FT-IR analysis, HuHb on the other hand, suffered damage after gamma irradiation. ConclusionThe findings suggest that vibrational spectroscopic methods hold significant potential as a sensitive tool for detecting radiation-induced molecular alterations and damages. Chironomus hemoglobin, with its robust interaction of the pyrrole ring with Fe, serves as a reliable bioindicator molecule to detect radiation damage using vibrational spectroscopic method.

Non-Destructive and Non-Invasive Approaches for the Identification of Hydroxy Lead-Calcium Phosphate Solid Solutions ((PbxCa1-x)5(PO4)3OH) in Cultural Heritage Materials.

Lead-calcium phosphates are unusual compounds sometimes found in different kinds of cultural heritage objects. Structural and physicochemical properties of this family of materials, which fall into the hydroxypyromorphite-hydroxyapatite solid solution, or (PbxCa1-x)5(PO4)3OH, have received considerable attention during the last few decades for promising applications in different fields of environmental and material sciences, but their diagnostic implications in the cultural heritage context have been poorly explored. This paper aims to provide a clearer understanding of the relationship between compositional and structural properties of the peculiar series of (PbxCa1-x)5(PO4)3OH solid solutions and to determine key markers for their proper non-destructive and non-invasive identification in cultural heritage samples and objects. For this purpose, a systematic study of powders and paint mock-ups made up of commercial and in-house synthesized (PbxCa1-x)5(PO4)3OH compounds with a different Pb2+/Ca2+ ratio was carried out via a multi-technique approach based on scanning electron microscopy, synchrotron radiation-based X-ray techniques, i.e., X-ray powder diffraction and X-ray absorption near edge structure spectroscopy at the Ca K- and P K-edges, and vibrational spectroscopy methods, i.e., micro-Raman and Fourier transform infrared spectroscopy. The spectral modifications observed in the hydroxypyromorphite-hydroxyapatite solid solution series are discussed, by assessing the advantages and disadvantages of the proposed techniques and by providing reference data and optimized approaches for future non-destructive and non-invasive applications to study cultural heritage objects and samples.

Sixty years of electrochemical optical spectroscopy: a retrospective.

Sixty years ago, Reddy, Devanatan, and Bockris performed the first in situ electrochemical ellipsometry experiment, which ushered in a new era in the study of electrochemistry, using optical spectroscopy. After six decades of development, electrochemical optical spectroscopy, particularly electrochemical vibrational spectroscopy, has advanced from a phase of immaturity with few methods and limited applications to a phase of maturity with excellent substrate generality and significantly improved resolutions. Here, we divide the development of electrochemical optical spectroscopy into four phases, focusing on the proof-of-concept of different electrochemical optical spectroscopy studies, the emergence of plasmonic enhancement-based electrochemical optical spectroscopic (in particular vibrational spectroscopic) methods, the realization of electrochemical vibrational spectroscopy on well-defined surfaces, and the efforts to achieve operando spectroelectrochemical applications. Finally, we discuss the future development trend of electrochemical optical spectroscopy, as well as examples of new methodology and research paradigms for operando spectroelectrochemistry.

Advancing cerumen analysis: exploring innovative vibrational spectroscopy techniques with respect to their potential as new point-of-care diagnostic tools.

Cerumen, commonly known as earwax, is a complex mixture composed of secretions from ceruminous glands. These secretions are heterogeneous mixtures mainly composed of lipids and proteins. Despite its prevalence, the potential diagnostic value of cerumen remains largely unexplored. Here, we present an in-depth analysis of cerumen utilizing well-known vibrational approaches such as conventional Raman spectroscopy or surface-enhanced Raman spectroscopy (SERS) together with advanced vibrational spectroscopy techniques such as coherent Raman scattering (CRS), i.e. broadband coherent anti-Stokes Raman scattering (CARS) or stimulated Raman scattering (SRS), as well as optical photothermal infrared (OPTIR) spectroscopy. Through the integration of these vibrational spectroscopic methods, lipids and proteins can be identified as the main components of cerumen; however, they contribute to the final spectral information to various extents depending on the vibrational detection scheme applied. The inherently weak Raman signal could be enhanced by linear (SERS) and non-linear (CRS) processes, resulting in efficient acquisition of fingerprint information and allowing for the detection of marker modes, which cannot be addressed by conventional Raman spectroscopy. OPTIR spectroscopy provides complementary information to Raman spectroscopy, however, without the contribution of a fluorescence background. Our findings underscore the utility of these cutting-edge techniques in unveiling the intricate molecular landscape of cerumen, paving the way for novel point-of-care diagnostic methodologies and therapeutic interventions.

Phenolics and Spectroscopy: Challenges and Successful Stories in The Grape and Wine Industry.

Phenolic compounds are considered to have a major role in the quality of grapes and wine. These compounds contribute to the sensory perception of red wine as they are involved in astringency and bitterness as well as in determining the colour intensity of grapes and wine (e.g. anthocyanins content). Several techniques are used to characterise and quantify these compounds in grapes and wine samples such as UV-Visible spectroscopy or high-performance liquid chromatography (HPLC). More recently, different applications and reports have shown the value of vibrational spectroscopy techniques to monitor and measure phenolic compounds along the grape and wine value chain. This article summarises as well as discusses challenges and successful stories in relation to the utilization of vibrational spectroscopy techniques to measure phenolic compounds in grapes and wine. Specifically, content presented at the workshop "Outstanding sensors challenge beverage and food future" organised by Italian Society of Food Science and Technology and the University of Pisa (Pisa, Italy) is summarised. Although vibrational spectroscopy techniques have been proven to be of importance to measure composition across the grape and wine value chain, the adoption of these technologies has been compromised by the accessibility and price of instruments. Understanding the basic principles of the different vibrational spectroscopy methods (e.g. characteristics, limit of detection) as well as how to effectively use the data generated are still main barriers facing the incorporation of these techniques into the grape and wine industry. Furthermore, is still not clear for many users of these technologies how they will contribute to the sustainability of the wine industry as well as to preserve the identity of the wine making process. This article is protected by copyright. All rights reserved.

The Application of Handheld Near-Infrared Spectroscopy and Raman Spectroscopic Imaging for the Identification and Quality Control of Food Products.

The following investigations describe the potential of handheld NIR spectroscopy and Raman imaging measurements for the identification and authentication of food products. On the one hand, during the last decade, handheld NIR spectroscopy has made the greatest progress among vibrational spectroscopic methods in terms of miniaturization and price/performance ratio, and on the other hand, the Raman spectroscopic imaging method can achieve the best lateral resolution when examining the heterogeneous composition of samples. The utilization of both methods is further enhanced via the combination with chemometric evaluation methods with respect to the detection, identification, and discrimination of illegal counterfeiting of food products. To demonstrate the solution to practical problems with these two spectroscopic techniques, the results of our recent investigations obtained for various industrial processes and customer-relevant product examples have been discussed in this article. Specifically, the monitoring of food extraction processes (e.g., ethanol extraction of clove and water extraction of wolfberry) and the identification of food quality (e.g., differentiation of cocoa nibs and cocoa beans) via handheld NIR spectroscopy, and the detection and quantification of adulterations in powdered dairy products via Raman imaging were outlined in some detail. Although the present work only demonstrates exemplary product and process examples, the applications provide a balanced overview of materials with different physical properties and manufacturing processes in order to be able to derive modified applications for other products or production processes.

Soluble thiabendazolium salts with anthelminthic properties

Thiabendazole is an anthelmintic drug used to treat strongyloidiasis (threadworm), cutaneous and visceral larva migrans, trichinosis, and other parasites. The active pharmaceutical ingredient is typically administered orally as tablets that should be chewed before swallowing. Current formulations combine the active ingredient with excipients, including sodium saccharinate as a sweetener. Thiabendazole’s low aqueous solubility hinders fast dissolution and absorption through the mucous membranes. We sought to reformulate this medicine to improve both solubility and palatability. We utilized the possibility of protonation of the azole nitrogen atom and selected four different hydrogen donors: saccharin, fumaric, maleic, and oxalic acids. Solvothermal synthesis resulted in salts with each co-former, whereas neat and liquid-assisted grinding enabled the synthesis of additional formulations. Product formation was observed by powder X-ray diffraction. To better understand the structural basis of the proton transfer, we solved the crystal structures of the salts with saccharin, maleic acid, and oxalic acid using single-crystal X-ray diffraction. The structure of the salt with fumaric acid was solved by powder X-ray diffraction. We further characterized the salts with vibrational spectroscopic and thermoanalytical methods. We report a broad tunability of the aqueous solubility of thiabendazole by salt formation. Reformulation with maleic acid provided a 60-fold increase in solubility, while saccharin and oxalic acid gave a modest improvement. Fumaric acid resulted in a solid with only slightly higher solubility. Furthermore, saccharin is a sweetener, while the acids taste sour. Therefore, the salts formed also result in an intrinsic improvement of palatability. These results can inform new strategies for oral and chewable tablet formulations for treating helminthic infections.

Simple Disulfides: Studies of Some Exponents of a Family Involved in Prominent Processes

AbstractExploring the fundamental chemistry and intrinsic properties of disulfide‐containing species has become an increasingly popular means to understand their action in various scientific fields, applications, and systems. In this study several representatives of this extensive family with the general formula CCl3SSR, where R represents CH2CH3, CH2CF3, C(CH3)3, C6H5 and C(O)CH3,were prepared and characterized by vibrational spectroscopy methods (FTIR and Raman), NMR spectroscopy, mass spectrometry, X‐ray structure determinations and photo electron spectroscopy. When complemented with computational chemistry, this range of methods and techniques sheds new light on numerous different processes. It is worth noting that the importance in disulfides compounds is related to inherent properties of this chemical family, such as chirality, theories involving the origin of life and its evolution, and, lately, the mechanisms of S−S bond formation in processes concerning therapies based on the use of peptides and COVID‐19.

Influence of heteroatoms and substituents on structural and spectroscopic parameters of saturated six-member ring heterocycles: experimental and theoretical study of 1-methyl-1-germacyclohexane

The conformational analysis of newly synthesized compound, 1-methyl-1-germacyclohexane, is performed by means of a combined vibrational spectroscopy and theoretical methods. The liquid 1-methyl-1-germacyclohexane at room temperature is investigated using conventional ATR-FTIR, FT-IR (gas phase) and Raman methods. FT-IR spectra of the isolated in low-temperature neon and nitrogen matrices are registered. The further detailed vibrational conformational analysis is performed utilizing density functional theory and perturbation theory based methods. All possible 12 canonical ring conformations considering axial/equatorial CH3 group position are analyzed by utilizing DFT/B3LYP, DFT/M06-2X and MP2 at aug-cc-pVTZ theory level.The most stable conformer with the global energy minimum structure in the chair axial conformation is investigated in detail. Analysis of the potential energy surface reveals transition states (TS) and energy barriers. The conformational path is found to be as follows: chair (1C4)→ envelope/half-chair (TS)→ skew-boat (1S3 - C1 symmetry)→ boat (TS)→ skew-boat (1S5 - C2 symmetry). The energy barrier for 1C4 (chair) to 1S3 (skew-boat) conversion is 4.8 kcal/mol while for the reverse process equals to 0.5 kcal/mol.A similar conformational analysis is performed for different configurations of germacyclohexane, silacyclohexane and cyclohexane with mono- and disubstituents: CH2Cl, CH3, Cl and F. Such approach enables investigation of influence of the heteroatoms and substituents of various size and type on the structural parameters and conformational diversity.

Structural, electronic, intermolecular interaction, reactivity, vibrational spectroscopy, charge transfer, Hirshfeld surface analysis, pharmacological and hydropathy plot on 5-Bromo nicotinic acid – Antiviral study (Hepatitis A, B, and C)

The therapeutic properties of 5-Bromonicotinatic acid (5BNA) were studied for antiviral illnesses like Hepatitis A, Hepatitis B and Hepatitis C and the influence of electron-donating and electron-withdrawing properties of functional groups on the nicotinic acid was evaluated and represented in this study using the DFT approach. The molecular parameters were determined for both gases as well as for various solvent phases. The reactive areas in the compound are examined utilising Fukui analysis. The molecular interactions are accomplished by recognising the different types of bonding found in the compound using the AIM, ELF, LOL, RDG and IRI. Solvation investigations were demonstrated to have an influence on molecular orbital energy, ESP, UV–Vis and NLO analyses. Electron-hole, NBO and Hirshfeld investigations are used to investigate the transfer of charges and interactions inside the molecule. The method of vibrational spectroscopy (IR and Raman) is used to differentiate and identify the various types of vibrations displayed by the compound. The hydropathy plots for the proteins 2A4O, 6CWD and 2OC8 associated with Hepatitis A, Hepatitis B and Hepatitis C illustrate the disquiet and attraction of the amino acids towards the water.

Importance of solvent roles in molecular, electronic and dynamical properties, thermodynamic quantities, Mulliken charges, reactive analysis and molecular docking of 2-Bromo-1H-imidazole-4,5-dicarbonitrile

The 2-Bromo-1H-imidazole-4,5-dicarbonitrile (2B1HID) molecule is studied by quantum mechanical and vibrational spectroscopic methods. Atoms In Molecules (AIM) was carried out to find the topological studies and know the type of bonding present in it. The calculations of NBO studies are used to determine the solidity. By HOMO and LUMO analysis various chemical parameters and band gaps were determined. The TD-DFT approach is used with the help of simulated UV–Vis with various solvents to know the electronic transition. Explanation of the Fukui function and studies of Molecular Electrostatic Potential demonstrate the molecule's bioactive nature and reactive areas. NLO studies were carried out to find Non-linear applications of the molecule. Thermodynamic studies confirm that this molecule’s important parameters increase with an increase in temperature. By using drug-likeness, the drug characters of the molecule are obtained. By molecular docking, the target protein and the ligand reactions were examined.

Vibrational spectroscopy methods for investigation of the animal models of glioblastoma multiforme

Glioblastoma multiforme (GBM) is the most common and devastating primary brain tumor among adults. It is highly lethal disease, as only 25% of patients survive longer than 1 year and only 5% more than 5 years from the diagnosis. To search for the new, more effective methods of treatment, the understanding of mechanisms underlying the process of tumorigenesis is needed.The new light on this problem may be shed by the analysis of biochemical anomalies of tissues affected by tumor growth. Therefore, in the present work, we applied the Fourier transform infrared (FTIR) and Raman microspectroscopy to evaluate changes in the distribution and structure of biomolecules appearing in the rat brain as a result of glioblastoma development. In turn, synchrotron X-ray fluorescence microscopy was utilized to determine the elemental anomalies appearing in the nervous tissue. To achieve the assumed goals of the study animal models of GBM were used. The rats were subjected to the intracranial implantation of glioma cells with different degree of invasiveness. For spectroscopic investigation brain slices taken from the area of cancer cells administration were used.The obtained results revealed, among others, the decrease content of lipids and compounds containing carbonyl groups, compositional and structural changes of proteins as well as abnormalities in the distribution of low atomic number elements within the region of tumor.