MIDTERM LEC 2.2
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Principle: It determines the components of a sample where the xaxis represents the mass-to-charge (m/z) ratio and the y-axis is their relative abundance within the sample.
Mass Spectrometry
It is based on the fragmentation and ionization of molecules using a suitable source of energy.
Mass Spectrometry
It separates diverse molecules from one another in the gas phase (gas-liquid chromatography) utilizing the so-called mass spectroscopy-mass spectroscopy (MS-MS) methodology
Mass Spectrometry
It is vital in structural identification and determination of molecular weight.
Mass Spectrometry
Uses: Detection and quantification of analytes in human fluids and tissues; utilized in proteomics, metabolomics, and toxicology: differentiates normal tissues from malignant tissues; quanti-assay of both therapeutic and illicit drugs; and drug development
Mass Spectrometry
Requirement: Before a compound can be detected and quantified by MS, it must be separated by GC
Mass Spectrometry
Advantage: Qualitative and quantitative analysis of complicated samples; in biomedical research
Mass Spectrometry
Basic components: Sample inlet, ion source, mass analyzer, and ion detector
Mass Spectrometry
Mass Spectrometry Samples:
Blood (serum and plasma), urine, tissues, and other body fluids
It involves doing mass analysis twice while performing a dissociation process or a chemical reaction to change an ion’s mass or charge.
Tandem Mass Spectrometry (MS/MS or MS2)
Determines two physical properties of the analytes: Precursor (parent source) and Product ion mass
Tandem Mass Spectrometry (MS/MS or MS2)
It enhances specificity beyond molecular weight separation, gives clarification on complex structures, and assists in the identification of basic composition of the sample.
Tandem Mass Spectrometry (MS/MS or MS2)
It is a procedure utilized in mass spectrometry (MS) for direct detection of the analytes in biofluid samples such as blood.
Paper Spray Ionization
It is both applied in therapeutic drug monitoring and testing of illicit drugs.
Paper Spray Ionization
It is also applied in cancer study and analysis of immunosuppressants.
Paper Spray Ionization
Paper Spray Ionization Sample volume:
0.4 uL (may vary depending on the procedure)
Paper Spray Ionization Substrate used:
Chromatographic paper
Paper Spray Ionization Solvent:
Methanol (water solution may be added)
It can be used in POCT especially in the analysis of drugs of abuse by utilizing “dried blood spot” sample.
Paper Spray Ionization
Utilizes a charged solvent stream instead of a laser
Desorption Electrospray Ionization (DESI)
It is a rapid analysis of drugs in biofluids even in dried blood spots.
Desorption Electrospray Ionization (DESI)
It is also used in cancer biology specifically in the study of brain cancer markers.
Desorption Electrospray Ionization (DESI)
The charged sample ions that is formed between the sample (blood or urine) and the charged solvent are determined by MS
Desorption Electrospray Ionization (DESI)
Principle: It is basically the study of proteins in aid of disease diagnosis.
Proteomics