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Mass Spectrometry Analytical Technique to Measure the Mass-to-Charge Ratio of Ions
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Journal of Bioanalysis & Biomedicine

ISSN: 1948-593X

Open Access

Editorial Note - (2021) Volume 13, Issue 4

Mass Spectrometry Analytical Technique to Measure the Mass-to-Charge Ratio of Ions

Ankhitachobe*
*Correspondence: Ankhitachobe, Professor of Pharmacy, Government College of Pharmacy (GCP), Bangalore, India, Tel: 912222782730, Email:
Professor of Pharmacy, Government College of Pharmacy (GCP), Bangalore, India

Received: 21-Apr-2021 Published: 03-Jun-2021 , DOI: 10.37421/1948-593X.2021.13.251
Citation: Ankhita chobe. "Mass Spectrometry Analytical Technique to Measure the Mass-to-Charge Ratio of Ions." J Bioanal Biomed 13 (2021): 251
Copyright: © 2021 Chobe A. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

                         

Editorial Note

Mass spectrometry (MS) is an analytical technique that's wont to measure the mass-to-charge ratio of ions. The results are typically presented as a spectrum, a plot of intensity as a function of the mass-to-charge ratio. Mass spectrometry is employed in many various fields and is applied to pure samples also as complex mixtures.A spectrum may be a plot of the ion signal as a function of the mass-to-charge ratio. These spectra are wont to determine the basic or isotopic signature of a sample, the masses of particles and of molecules, and to elucidate the chemical identity or structure of molecules and other chemical compounds.

In a typical MS procedure, a sample, which can be solid, liquid, or gaseous, is ionized, for instance by bombarding it with a beam of electrons. This might cause a number of the sample's molecules to interrupt up into charged fragments or just become charged without fragmenting. These ions (fragments) are then separated consistent with their mass-to-charge ratio, for instance by accelerating them and subjecting them to an electrical or magnetic field: ions of an equivalent mass-to-charge ratio will undergo an equivalent amount of deflection. The ions are detected by a mechanism capable of detecting charged particles, like an tube. Results are displayed as spectra of the signal intensity of detected ions as a function of the mass-to-charge ratio. The atoms or molecules within the sample are often identified by correlating known masses (eg: a whole molecule) to the identified masses or through a characteristic fragmentation pattern.

In mass spectrometry, ionization refers to the assembly of gas phase ions suitable for resolution within the mass analyzer or mass filter. Ionization occurs within the ion source. There are several ion sources available; each has advantages and drawbacks for particular applications. For instance, Electron ionization (EI) gives a high degree of fragmentation, yielding highly detailed mass spectra which when skilfully analyzed can provide important information for structural elucidation/characterization and facilitate identification of unknown compounds by comparison to mass spectral libraries obtained under identical operating conditions. However, EI isn't suitable for coupling to HPLC, i.e. LCMS, since at air pressure, the filaments won’t to generate electrons blow out rapidly. Thus EI is coupled predominantly with GC, i.e. GC-MS, where the whole system is under high vacuum.

Hard ionization techniques are processes which impart high quantities of residual energy within the subject molecule invoking large degrees of fragmentation (i.e. the systematic rupturing of bonds acts to get rid of the surplus energy, restoring stability to the resulting ion). Resultant ions tend to possess m/z less than the molecular mass (other than within the case of proton transfer and not including isotope peaks). The foremost common example of hard ionization is Electron Ionization (EI).

Soft ionization refers to the processes which impart little residual energy onto the topic molecule and intrinsically end in little fragmentation. Examples include Fast Atom Bombardment (FAB), Chemical Ionization (CI), AtmosphericPressure Chemical Ionization (APCI), Electrospray Ionization (ESI), Desorption Electrospray Ionization (DESI), and Matrix-Assisted laser Desorption/ionization (MALDI).

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