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9th International Conference and Exhibition on Spectroscopy and Analytical Techniques, will be organized around the theme “Advancements and Scope of Spectroscopy in Modern Chemistry”

Global Spectroscopy 2019 is comprised of 22 tracks and 126 sessions designed to offer comprehensive sessions that address current issues in Global Spectroscopy 2019.

Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.

Register now for the conference by choosing an appropriate package suitable to you.

Mass spectrometry (MS) is one of the major analytical techniques which ionizes chemical species and sorts out based on their mass-to-charge ratio of the ions. In general, it can be expressed as, a mass spectrum which measures the masses within a sample. This spectrometry is used in many other different fields which are applied to pure samples along with complex mixtures. Some of the new approaches in Mass Spectrometry are:


  • Track 1-1Materializing separation Technologies
  • Track 1-2Hybrid Mass Spectrometry
  • Track 1-3Paths in glycoproteins and glycans
  • Track 1-4Tom Probe Tomography
  • Track 1-5Protein Phosphorylation and Non-Covalent interaction
  • Track 1-6Overture in isolation, enrichment and separation
  • Track 1-7Structural proteomics and genomics
  • Track 1-8Lipidomic, metabolomics and ultra-trace analysis
  • Track 1-9Complementary Multi technique Acces
  • Track 1-10Mass spectrometry in the field of food science
  • Track 1-11New MS technologies in Metabolomics/Lipidomics
  • Track 1-12Biomolecular, Carbohydrates, and microbe analysis
  • Track 1-13Nano scale and microfluidic separations
  • Track 1-14High temperature Mass Spectrometry
  • Track 1-15Advances in laboratory medicine

Experimentation Tools in Mass Spectrometry consists of Diagnostic and Cancer Biomarker Discovery Tool, Potential of metabolomics as a functional genomics tool, the age of the proteome in proteomics. Mass spectrometric analysis of biological samples has increasingly entailed direct analysis of complex protein mixtures, often with the objective of detailed characterization of the various components. This trend toward ever greater sample complexity has been enabled and in turn driven by the rapid development of powerful mass spectrometric tools. A general characteristic of recent mass spectrometers is that most are composed of a sequence of multiple mass analysers with different strengths and properties, resulting in tandem instruments that possess capabilities unattainable by the individual components can combine high mass accuracy with high-speed measurement, greatly facilitating the analysis of complex mixtures. This option is advantageous when speed and accuracy are crucial for the success of analysis, as it is, for example, when the mass spectrometer is coupled on-line to an HPLC system


  • Track 2-1Andromeda (part of MaxQuant)
  • Track 2-2Andromeda (part of MaxQuant)
  • Track 2-3Mascot
  • Track 2-4Mascot
  • Track 2-5CycloBranch
  • Track 2-6MassChroQ
  • Track 2-7Mass++
  • Track 2-8XCMS Online (Cloud-Based)
  • Track 2-9MassMatrix

Computed tomography (CT) is an imaging procedure that uses special x-ray equipment to create detailed pictures, or scans, of areas inside the body. It is also called computerized tomography and computerized axial tomography (CAT).


  • Track 3-1CT Angiography
  • Track 3-2CT Colonography
  • Track 3-3CT Enterography

Analytical testing capabilities for these disciplines of Veterinary drug analysis have evolved significantly. So the scope of Analytical Techniques is playing a major role in the current Veterinary Medicine analysis. It majorly utilizes Chromatography and Mass Spectrometry to provide an array of toxicology and drug tests. The instrumentation majorly involved in drug testing are Gas Chromatography–Mass Spectrometry (GC/MS), Tandem Liquid Chromatography–Mass Spectrometry (LC/MS/MS), High-Resolution Accurate Mass Spectrometry (HRAMS), High Performance Liquid Chromatography (HPLC), Inductively Coupled Plasma – Mass Spectrometry (ICP-MS), Atomic Absorption (AA).


  • Track 4-1Various equipment’s used
  • Track 4-2Various analysis methods
  • Track 4-3Quality assurance of drugs

Nanoscale liquid chromatography coupled to tandem mass spectrometry has become an indispensable tool in the field of proteomics now-a-days. The advantages are grabbed with the sensitivity of nanotechnology over conventional LC-MS that allow the analysis of various  peptide mixtures in limited situations. This approach gives a strong cation-exchange, sample enrichment, reversed-phase chromatography and nanospray ion trap mass spectroscopy with data dependent tandem mass spectrometry spectra acquisition. Nanocolumn liquid chromatography and largely synonymous capillary liquid chromatography (capillary LC) are the most recent results of this process where miniaturization of column dimensions and sorbent particle size play crucial role along with the advances in mass spectrometry that has really brought a breakthrough. Configuration of Nano LC-electrospray ionization mass spectrometry (LC-ESI-MS) has become a essential tool in bioanalytical chemistry that basically indulges in proteomics. This particular session includes the brief account on pharmaceutical and biomedical research, Nano-proteomic analysis and Nano-proteomic analysis.


  • Track 5-1Pharmaceutical and Biomedical Research
  • Track 5-2Pharmaceutical and Biomedical Research
  • Track 5-3Nano-Proteomic Analysis
  • Track 5-4Amendments of Nanomaterials in LC-MS
  • Track 5-5Ultraviolet-Visible spectroscopy (UV-Vis)
  • Track 5-6Furrier transformed infrared spectroscopy (FT-IR)

HPLC/UHPLC chromatography is a commonly used separation mode in Reversed phase. Its retention of compounds possessing hydrophobic and organic functionality are provided dynamically. Combination of both hydrophobic and van der Waals type interactions between all the target compounds including both the stationary and mobile phases enables by reversed phase retention of these compounds.


  • Track 6-1Ultra high performance liquid chromatography
  • Track 6-2Fast protein liquid chromatography
  • Track 6-3HPLC-mass spectrometry
  • Track 6-4Characterization of HPLC stationary phases

Secondary Ion Mass Spectrometry (SIMS) is a mature surface analysis technique with a broad range of applications in Materials Science. In this article the SIMS process is described, the fundamental SIMS equations are derived, and the main terminology is explained. The issue of quantification is addressed. The various modes of SIMS analysis including static SIMS, imaging SIMS, depth profiling SIMS and three-dimensional (3D) SIMS are discussed as are specialized analysis strategies such as the imaging of shallow and cross-sections and reverse side analysis.


  • Track 7-1Semiconductors
  • Track 7-2Glass and stainless steel
  • Track 7-3Solid oxide fuel cell components
  • Track 7-4Aerospace alloys and biomaterials
  • Track 7-5Aerospace alloys and biomaterials

Luminescence spectroscopy is a technique which studies the of chemical systems. Luminescence is the emission of light by a substance. It occurs when an electron returns to the electronic ground state from an excited state and loses its excess energy as a photon. Luminescence spectroscopy is a collective name given to three related spectroscopic techniques. 


  • Track 8-1Fluorescence
  • Track 8-2Fluorescence
  • Track 8-3Internal and External Conversion
  • Track 8-4Intersystem Crossing
  • Track 8-5Phosphorescence
  • Track 8-6Chemiluminescence

Chromatography Mass Spectrometry, different method for identifying and separating the components, or solutes, of a mixture on the basis of the relative amounts of each solute distributed between a moving fluid streams, called the mobile phase, and a contiguous stationary phase. Liquid-chromatography is one of the mostly employed and useful techniques in pharmaceutical industry for sample preparation. Another one is electrophoretic separation technique designed for rapid and selective sample analysis. Immuno affinity chromatography (IAC) is a different method of Liquid Chromatography in which the stationary phase consists of an antibody or it might include antibody-related reagent. This technique involves a unique sub type of affinity chromatography, in which a biologically related binding agent is taken for the selective separation or analysis of a target compound. Capillary electrophoresis is other method which identifies and distributes ions depending on their electrophoretic mobility with the use of an applied voltage. Compact mass spectrometer is widely used in the food safety, water purity and clinical diagnosis. Gas chromatography mass spectrometry (GC/MS) is an instrumental technique, comprising a gas chromatograph (GC) coupled to a mass spectrometer (MS), by which complex mixtures of chemicals may be separated, identfied and quantified. 


  • Track 9-1Liquid chromatography
  • Track 9-2Gas chromatography
  • Track 9-3Column chromatography
  • Track 9-4Planar chromatography
  • Track 9-5Thin layer chromatography
  • Track 9-6Ion exchange chromatography
  • Track 9-7Latest techniques in Chromatography

Terahertz spectroscopy is a rapidly evolving field with interesting applications in medical imaging, security, scientific imaging (chemistry, biochemistry and astronomy), communications, and manufacturing. Many molecules, especially biomolecules, provide fingerprint spectroscopic lines in the Terahertz region


  • Track 10-1Terahertz Spectrum
  • Track 10-2Terahertz Sources
  • Track 10-3Ultrafast laser spectroscopy
  • Track 10-4Frequency-Domain terahertz
  • Track 10-5Pulsed Terahertz Techniques
  • Track 10-6Applications

EPR (Electron Paramagnetic Resonance) is a spectroscopic technique that detects species that have unpaired electrons. It is also called as ESR (Electron Spin Resonance). A large number of materials have unpaired electrons which include free radicals, many transition metal ions, and defects. Free electrons are often short-lived, but still play vital roles in many processes such as photosynthesis, oxidation, catalysis, and polymerization reactions. As a result EPR crosses several disciplines like chemistry, physics, biology, materials science, medical science and many more.


  • Track 11-1ERI - Electron Resonance Imaging
  • Track 11-2Hyperfine Splitting
  • Track 11-3EPR spin-trapping technique
  • Track 11-4EPR spin-labelling
  • Track 11-5Analytical Applications
  • Track 11-6Biological Applications

Nuclear Magnetic Resonance (NMR) is a spectroscopy technique which is based on the absorption of electromagnetic radiation by nuclei of the atoms. Proton Nuclear magnetic resonance spectroscopy is one of the most powerful tools for elucidating the number of hydrogen or proton in the compound. It is used to study a wide variety of nuclei.


  • Track 12-1Nuclear Spin
  • Track 12-2Detecting the Signal: Fourier Transform NMR Spectrometers
  • Track 12-3Shielding and Deshielding of Protons
  • Track 12-4Chemical Shift
  • Track 12-5Chemical Shift Equivalent and Non-equivalent Protons
  • Track 12-6Signal Splitting: Spin–Spin Coupling
  • Track 12-7Two-Dimensional (2D) NMR Techniques
  • Track 12-8Proton NMR Spectroscopy
  • Track 12-9Carbon NMR Spectroscopy

There are different ways in which X-rays can be employed. Absorption of X-rays is about absorbing material in other regions of the spectrum. Fluorescence emission of X-rays enables to identify and measure heavy elements in any medium. Diffraction of X-rays enables to analyse the specificity and accuracy of crystalline materials with a high degree. 

  • Track 13-1X-Ray Emission Spectroscopy
  • Track 13-2Auger Emission Spectroscopy
  • Track 13-3X-Ray Fluorescence Spectroscopy
  • Track 13-4Electron Spectroscopy – Chemical Analysis (ESCA)
  • Track 13-5X-Ray Absorption Spectroscopy
  • Track 13-6X-Ray Diffraction Spectroscopy

Time-resolved spectroscopy is the study of dynamic processes in materials or chemical compounds by means of spectroscopic techniques. Most often, processes are studied after the illumination of a material occurs, but in principle, the technique can be applied to any process that leads to a change in properties of a material.

  • Track 14-1Light sources for Ultrafast Spectroscopy
  • Track 14-2Time-resolved fluorescence
  • Track 14-3Time-resolved fluorescence - Biological applications
  • Track 14-4Pump-probe spectroscopy - Transient Absorption measurements
  • Track 14-5Application of Transient Absorption - Investigation of biological processes

Ultraviolet Spectroscopy is the measurement of the decrease in the beam of light after passing through a sample or after reflection from a sample surface. Absorption measurements can be at a single wavelength or over an extended spectral range.

  • Track 15-1Functional Groups
  • Track 15-2Qualitative Analysis
  • Track 15-3Instrumentation
  • Track 15-4Sample handling and Measurements
  • Track 15-5Method development & Validation

Tandem mass spectrometry involves multiple steps of mass selection or analysis, usually separated by some form of fragmentation. It is simply a matter of reading Mass Spectrometry value from the spectrum. A tandem mass spectrometer is one capable of multiple rounds of understanding mass spectrometry. For example, one mass analyzer can isolate one peptide from many entering a mass spectrometer. A second mass analyzer then stabilizes the peptide ions while they collide with a gas, causing them to fragment by collision-induced dissociation (CID). A third mass analyzer then catalogues the fragments produced from the peptides. Tandem MS can also be done in a single mass analyzer over time as in a quadrupole ion trap. There are various methods for fragmenting molecules for tandem MS, including collision-induced dissociation (CID), electron capture dissociation (ECD), infrared multiphoton dissociation (IRMPD) and blackbody infrared radiative dissociation (BIRD).


  • Track 16-1Isobaric tags for relative and absolute quantitation (iTRAQ)
  • Track 16-2Tandem mass tag (TMT)
  • Track 16-3Peptides
  • Track 16-4Fragmentation

It is noticed that LC/MS system during the past 2 years has been used to quantify natural small molecules biologically.Numerous developments have been made in LCMS analysis such as phospholipids and drugs with respect to pharmacokinetics and pharmacodynamics studies interfering with the metabolism of sphingolipids. Simultaneous measurements of drugs with the levels of natural metabolites are designed to modify. The processes incorporated inLC-MS method development for the pharmacological studies includes three anti-cancer drugs (i.e., methoxyamine, fludarabine, and 6-benzylthioinosine). Some others being specific are tetra-enzyme cocktail utilizing for release of DNA adducts All these methods are applied to study the drug effect and drug mechanism through other integrated prospects like therapeutics and detection & determination of impurities


  • Track 17-1Clinical Chemistry Instruments

Analytical chemistry is concerned with providing qualitative and quantitative information about the chemical and structural composition of a sample of matter. A huge variety of samples, from high concentrations of elements in alloy steels to part-per-billion levels of drugs in biological tissue, are handled by the analyst. The field is founded on the conversion of a measured physical property of the species being examined to a usable signal. It is generally divided into two categories, classical and instrumental, on the basis of its historical development. The overall strategy is to prepare a sample correctly, choose a particular method of analysis, and report the results in a meaningful format, which may include a statistical evaluation.


  • Track 18-1State-of-the-art instrumentation
  • Track 18-2Nanoscale sensors for the detection of disease biomarkers
  • Track 18-3Biological and medical importance of chemical tools
  • Track 18-4Analytical detection of biological events on surfaces
  • Track 18-5Biomaterials and nano-biomaterials

The use of LCMS has become a paramount in two dimensional hyphenated technology to be useful in a wide assortment of analytical and bioanalytical techniques of nucleic acids, amino acids, peptides, proteins, carbohydrates, lipids, and etcetera and in categorizing the field of genomics, proteomics, metabolomics, lipidomics. Current trends are may be gripped of  mass analyzers, ionization protocols, fast LC–MS, LC–MALDI-MS, ion mobility spectrometry used in LC–MS, quantitation issues specific to MS and emerging mass spectrometric approaches which are complementary base in LC–MS are also discussed to focus on the recent innovations in LC–MS especially from the last decade and then to enlist  mass spectrometers offered currently by main manufacturers for LC–MS and MALDI-MS configurations together with the technical specifications. The forthcoming supplements in LC-MS could be emphasized on Bioanalysis, Aspects in Clinical Chemistry, Qualitative and Quantitative Analysis of Compounds


  • Track 19-1UHPLC Systems
  • Track 19-2Flow Injection Analyzers
  • Track 19-3Viscometer/Rheometer
  • Track 19-4ICP/ICPMS
  • Track 19-5X-Ray Analytical (XRD, XRF)

Infrared Spectroscopy is the study of infrared light interacting with a molecule. This can be analysed by measuring absorption, emission and reflection. The technique is applied in organic and inorganic chemistry. It is used by chemists to determine functional groups in molecules. Infrared Spectroscopy measures the vibrations of atoms and based on this it is possible to define the functional group.


  • Track 20-1Experimental Methods
  • Track 20-2Spectral Analysis
  • Track 20-3Organic Molecules
  • Track 20-4Polymers
  • Track 20-5Advancements in Applications

It is one of the vibrational spectroscopic techniques used to provide information on molecular vibrations and crystal structures. This technique uses a laser light source to irradiate a sample, and generates an infinitesimal amount of Raman scattered light, which is detected as a Raman spectrum. The characteristic fingerprinting pattern in a Raman spectrum makes it possible to identify substances including polymorphs and evaluate local crystallinity, orientation and stress.

  • Track 21-1Raman scattering
  • Track 21-2Resonance-Enhanced Raman Scattering
  • Track 21-3Surface-Enhanced Raman Scattering
  • Track 21-4The Raman Spectrum
  • Track 21-5Qualitative vs. Quantitative Raman
  • Track 21-6Advantages - Raman Spectroscopy

The process of separation is integral unit operation in most of the Modern Pharmaceutical Techniques, chemical and other process plants. Among the separation processes, some are standard and conventional processes, like, distillation Process, absorption process, adsorption process, etc. These processes are quite common and the relevant technologies are well developed and well-studied. On the other hand, newer separation processes like membrane based techniques, supercritical fluid extraction, chromatographic separation, etc., are gaining importance in modern days plants as novel separation processes.


  • Track 22-1Hyphenated Separation Techniques
  • Track 22-2Hyphenated Separation Techniques
  • Track 22-3Chromatography as a Separation Technique
  • Track 22-4Spectroscopy as Separation Technique
  • Track 22-5Latest Innovations