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Hyphenated
Techniques
(GC-MS/MS, LC-
MS/MS, HPTLC-
MS)
Presented By
Prof.(Dr.) Dinesh Kr. Mehta
MM College of Pharmacy,
MM(DU), Mullana
Hyphenated techniques
• Hyphenated technique is a combination or coupling of two analytical
techniques with the help of proper interface.
• The hyphenated technique is developed from the coupling of a separation
technique and detection technique. The term “hyphenation” was first adapted
by Hirschfeld in 1980 to refer to the on-line combination of a separation
technique and one or more spectroscopic detection techniques.
• The aim of the coupling is to obtain an information-rich detection for both
identification and quantification compared to that with a single analytical
technique.
Advantages
For fast and accurate analysis
 A Higher degree of automation.
 Higher sample throughput.
 Better reproducibility.
 Reduction of contamination due to its closed system.
 Separation of quantification at the same time.
Types of hyphenated techniques
Double hyphenated techniques.
Triple hyphenated techniques.
Double hyphenated techniques
• LC-MS
• LC-NMR
• LC-IR
• CE-MS
• GC-IR
• GC-MS
• HPLC-DAD
• GC-FTIR
Hyphenated Technique(GC-MS/MS)
CONTENTS
 General Introduction
 Principle
 Instrumentation
 GC-MS Setup
 Types of Mass Spectrometer detector
 Application
General Introduction
• Gas Chromatography – Mass Spectrometry (GC-MS) is an analytical method
that combines the features of gas chromatography and mass spectrometry to
identify different substances with in a test sample.
• GC-MS separates chemical mixtures into individual components (using a gas
chromatograph) and identifies / quantifies the components at a molecular
level (using a MS detector).
• It is one of the most accurate and efficient tools for analyzing volatile
organic samples.
• Mass spectrometer (MS) is an instrument that serves for establishment of the
molecular weight and structure of both inorganic and organic compounds,
and the identification and determination of analytes in complex mixtures.
Principle
GC-MS instrument separates chemical mixtures (the GC component) and
identifies the components at a molecular level (the MS component). GC
works on the principle that a mixture will separate into individual substances
when heated. The heated gases are carried through a column with an inert
gas.
As the separated substances emerge from the column opening, they flow
into MS.
Mass spectrometry identifies compounds by the mass of the analyte
molecule.
Instrumentation
The GC-MS is
composed of two major
building blocks:
• Gas chromatograph
• Mass spectrometer
 The molecules are retained by the
capillary column and elute from the
column at different times.
 The Mass spectrometer capture, ionize,
accelerate, deflect and detect the
ionized molecules separately by
breaking each molecule into ionize
fragments and detecting these
fragments using their mass to charge
ratio.
Types of Mass spectrometer Detectors
1. Quadrupole Mass Spectrometer- most common
2. Ion Trap Mass Spectrometer
3. Magnetic Mass Spectrometer
Advantages of GC-MS
• Accurate identification of a particular molecule is possible.
• Differentiate between multiple molecules in the same amount of time.
• Identification carried out at a molecular level.
• Easy to Operate.
Application
 Quantitation of pollutants in drinking and waste water.
 Identification of unknown organic compounds in hazardous waste dumps
and reaction products by synthetic organic chemistry
 Quantitation of drug in metabolites and urine is done for the
pharmacological and forensic use.
 Used for drug analysis, pesticide and herbicide detection
 Characterization of odour and flavor component of food
 Law enforcement
 Sports Anti- doping analysis
 Medical Diagnosis
 Security of Airports
 Criminal Forensics
Liquid Chromatography-Mass Spectrometry (LC/MS)
General Introduction
• The coupling of MS with LC (LC-MS) was an obvious extension but
progress in this area was limited for many years due to the relative
incompatibility of existing MS ion sources with a continuous liquid stream.
• The reasons for choosing LC-MS over LC with conventional detectors are
essentially the same as with GC-MS, namely high specificity and the ability
to handle complex mixtures.
Analytes are separated by Liquid Chromatography (LC) prior to analysis
by Mass Spectrometry (MS)
• Provides enhanced specificity, based on retention times
• Reduces the number of molecules entering the MS ionization source at a
given time
• reduces the competition for charge
Principle
Liquid chromatography-mass spectrometry is the technique which performs
separation by liquid chromatography and mass analysis with the help of the
mass spectrometry.
Liquid chromatography tandem mass spectrometry (LC–MS/MS)
• Liquid Chromatography
• Separates mixture components
• Based on polarity
Tandem Mass Spectrometry
• Detector
• Identification & Quantification of components
• Based on compound mass
• It is now generally accepted as the preferred technique for quantitation of
small molecule drugs, metabolites in biological matrices (plasma, blood,
serum, urine, and tissue)
• • Electrospray needle is used as bridge to connect the liquid chromatography
with that of the mass.
• LC-MS is mainly separated into the three parts-
• Chromatography – In liquid chromatography separation is performed which
is detected with the help of Photo diode Array.
• These separated components then transferred to the interface.
• 2. Interface – In interface the liquid is volatilized and transferred to the MS.
• 3. Spectrometry – With the help of various ionization techniques the
compound is ionized and then it is analyzed by mass analyzer.
Instrumentation
Various mass analyzers are used viz. Quadrupoles, quadrupole ion traps, time-
to-flight (TOF), time-to-flight reflection (TOFR), and ion cyclotron resonance
(ICR) mass analyzers.
It is a method that combines separation power of HPLC with detection
power of Mass spectrometry.
• In LC-MS we remove the detector from the column of LC and fit the column
to interface of MS.
• In most of the cases the interface used in LC-MS are ionization source
• A liquid sample is introduced into the ionization source of the mass
spectrometer.
Example: Extracts from plasma, serum, whole blood, Urine, CSF, etc.
The liquid sample is usually delivered by an Liquid Chromatography (LC) system.
LC-MS System Components
• Mass spectrometers work by ionizing molecules and then sorting and identifying
the ions according to their mass- to-charge (m/z) ratios.
The mobile phase is the solvent that moves the solute throughout column.
Solvent strength and selectivity: - It is the ability of solvent to elute solutes from
a column.
COLUMN
The use of di-functional or tri-functional silanes to create bonded groups
with two or three attachment points leading to phases with higher stability in
low or higher pH and lower bleed for LC-MS
• Most widely used columns for LC-MS are: -
(1) fast LC column :- the use of short column.(15-50mm)
(2) Micro LC column :- the use of large column. (20-150mm)
Advantages of LC-MS/MS Accuracy and Precision
• Robustness
• Sensitivity
• Allows multi-analyte panels
• Requires less sample prep
• Compatible with generic sample prep
• Versatility, can easily add new compounds
• Lower cost-per-sample
• Speed
Applications
• LC-MS used to detect compounds from polyaromatic (non-polar) to peptide
and proteins.
• LC-MS used for compounds identification and purity.
• Used for determination of pesticides, herbicides & organic pollutant for
environmental monitoring.
• Proteome analysis is done by this technique.
HPTLC-MS
General Introduction
The direct coupling of TLC/HPTLC with mass spectrometry (MS) is of
particular interest because of the later’s high sensitivity, rapid analysis, and
ability to aid structural characterization.
• TLC-MS is a versatile technique for separation as well as identification of
Pharmaceuticals and Phytopharmaceuticals. Traditionally the separation was
carried out by TLC/HPTLC then the separated materials was removed and
then identified by Mass spectrometry.
• This technique provides efficient, quick and simple method for identification
and separation of Narcotic drugs and psychotropic substances.
Key features
• HPTLC–MS is cost-effective because the chromatographic run is decoupled
with the detection step.
• Rapid and contamination-free elution of selected zones.
• Online transfer into the mass spectrometer.
• Advantages of HPTLC include that the technique is simple to learn, operate,
several analysis works could be done on same time, is a fast and economic
technique.
• Thin layer chromatography/high-performance thin-layer chromatography
can be used interchangeably for methods developed in the twenty-first
century.
HPTLC-MS Principle
• The versatile instrument is used to isolate unknown compounds from a
HPTLC/TLC plate and transfer them into a mass spectrometer for
identification or structure elucidation.
• TLC/MS Interface can be bring together to any brand of LC-coupled mass
spectrometer.
• Plug and play installation by two HPLC fittings at a given HPLC-MS
system.
• Semi-automatic instrument involving automatic piston movement for
pressure seal the HPTLC/TLC zone on both glass plates and aluminum foils
take out directly from the plate using a suitable solvent delivered by the
HPLC/HPTLC pump Online transfer into the mass spectrometer.
• Automatic cleaning of the piston between the extractions.
INSTRUMENTATION
A typical automated LC-MS system consists of :
• Double three-way diverter in-line with an autosampler
• LC system
• mass spectrometer.
The diverter generally operates as an automatic switching valve to divert
undesired portions of the eluate from the LC system to waste before the
sample enters the MS.
Fig: LC-MS (electrospray ionization interface) system
Application:
It can be used about the fragmentation patterns of degraded products
References
• Kanak Lata Verma, et al. HPTLC-MS as a Neoteric Hyphenated Technique for Separation and Forensic
Identification of Drugs, Journal of Analytical Sciences, Methods and Instrumentation, 2018, 8, 1-15
• S. Nagajyothi, et al. Hyphenated Techniques- A Comprehensive Review, International Journal of Advance Research
and Development,2017.
• Ashwini B. Sambherao, et al.TLC- MS HYPHENATED TECHNIQUE IN ANALYTICAL CHEMISTRY,
World Journal of Pharmacy and Pharmaceutical Sciences, Vol 6, Issue 10, 2017
• HYPHENATED TECHNIQUE- A BOON TO ANALYTICAL WORLD | INTERNATIONAL JOURNAL OF
PHARMACEUTICAL SCIENCES AND RESEARCH (ijpsr.com)
• Hyphenated Technique - an overview | ScienceDirect Topics
• (PDF) Introduction to hyphenated techniques and their applications in pharmacy (researchgate.net)
• GC × GC-MS HYPHENATED TECHNIQUES FOR THE ANALYSIS OF VOLATILE ORGANIC COMPOUNDS IN AIR: Journal of
Liquid Chromatography & Related Technologies: Vol 34, No 13 (tandfonline.com)
Thank You

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Hyphenated techniques(GC-MS/MS, LC-MS/MS, HPTLC-MS)

  • 1. Hyphenated Techniques (GC-MS/MS, LC- MS/MS, HPTLC- MS) Presented By Prof.(Dr.) Dinesh Kr. Mehta MM College of Pharmacy, MM(DU), Mullana
  • 2. Hyphenated techniques • Hyphenated technique is a combination or coupling of two analytical techniques with the help of proper interface. • The hyphenated technique is developed from the coupling of a separation technique and detection technique. The term “hyphenation” was first adapted by Hirschfeld in 1980 to refer to the on-line combination of a separation technique and one or more spectroscopic detection techniques. • The aim of the coupling is to obtain an information-rich detection for both identification and quantification compared to that with a single analytical technique.
  • 3. Advantages For fast and accurate analysis  A Higher degree of automation.  Higher sample throughput.  Better reproducibility.  Reduction of contamination due to its closed system.  Separation of quantification at the same time.
  • 4. Types of hyphenated techniques Double hyphenated techniques. Triple hyphenated techniques. Double hyphenated techniques • LC-MS • LC-NMR • LC-IR • CE-MS • GC-IR • GC-MS • HPLC-DAD • GC-FTIR
  • 5. Hyphenated Technique(GC-MS/MS) CONTENTS  General Introduction  Principle  Instrumentation  GC-MS Setup  Types of Mass Spectrometer detector  Application
  • 6. General Introduction • Gas Chromatography – Mass Spectrometry (GC-MS) is an analytical method that combines the features of gas chromatography and mass spectrometry to identify different substances with in a test sample. • GC-MS separates chemical mixtures into individual components (using a gas chromatograph) and identifies / quantifies the components at a molecular level (using a MS detector). • It is one of the most accurate and efficient tools for analyzing volatile organic samples. • Mass spectrometer (MS) is an instrument that serves for establishment of the molecular weight and structure of both inorganic and organic compounds, and the identification and determination of analytes in complex mixtures.
  • 7. Principle GC-MS instrument separates chemical mixtures (the GC component) and identifies the components at a molecular level (the MS component). GC works on the principle that a mixture will separate into individual substances when heated. The heated gases are carried through a column with an inert gas. As the separated substances emerge from the column opening, they flow into MS. Mass spectrometry identifies compounds by the mass of the analyte molecule.
  • 9. The GC-MS is composed of two major building blocks: • Gas chromatograph • Mass spectrometer
  • 10.  The molecules are retained by the capillary column and elute from the column at different times.  The Mass spectrometer capture, ionize, accelerate, deflect and detect the ionized molecules separately by breaking each molecule into ionize fragments and detecting these fragments using their mass to charge ratio.
  • 11. Types of Mass spectrometer Detectors 1. Quadrupole Mass Spectrometer- most common 2. Ion Trap Mass Spectrometer 3. Magnetic Mass Spectrometer Advantages of GC-MS • Accurate identification of a particular molecule is possible. • Differentiate between multiple molecules in the same amount of time. • Identification carried out at a molecular level. • Easy to Operate.
  • 12. Application  Quantitation of pollutants in drinking and waste water.  Identification of unknown organic compounds in hazardous waste dumps and reaction products by synthetic organic chemistry  Quantitation of drug in metabolites and urine is done for the pharmacological and forensic use.  Used for drug analysis, pesticide and herbicide detection  Characterization of odour and flavor component of food  Law enforcement  Sports Anti- doping analysis  Medical Diagnosis  Security of Airports  Criminal Forensics
  • 13. Liquid Chromatography-Mass Spectrometry (LC/MS) General Introduction • The coupling of MS with LC (LC-MS) was an obvious extension but progress in this area was limited for many years due to the relative incompatibility of existing MS ion sources with a continuous liquid stream. • The reasons for choosing LC-MS over LC with conventional detectors are essentially the same as with GC-MS, namely high specificity and the ability to handle complex mixtures. Analytes are separated by Liquid Chromatography (LC) prior to analysis by Mass Spectrometry (MS) • Provides enhanced specificity, based on retention times • Reduces the number of molecules entering the MS ionization source at a given time • reduces the competition for charge
  • 14. Principle Liquid chromatography-mass spectrometry is the technique which performs separation by liquid chromatography and mass analysis with the help of the mass spectrometry. Liquid chromatography tandem mass spectrometry (LC–MS/MS) • Liquid Chromatography • Separates mixture components • Based on polarity Tandem Mass Spectrometry • Detector • Identification & Quantification of components • Based on compound mass
  • 15. • It is now generally accepted as the preferred technique for quantitation of small molecule drugs, metabolites in biological matrices (plasma, blood, serum, urine, and tissue) • • Electrospray needle is used as bridge to connect the liquid chromatography with that of the mass. • LC-MS is mainly separated into the three parts- • Chromatography – In liquid chromatography separation is performed which is detected with the help of Photo diode Array. • These separated components then transferred to the interface. • 2. Interface – In interface the liquid is volatilized and transferred to the MS. • 3. Spectrometry – With the help of various ionization techniques the compound is ionized and then it is analyzed by mass analyzer.
  • 16. Instrumentation Various mass analyzers are used viz. Quadrupoles, quadrupole ion traps, time- to-flight (TOF), time-to-flight reflection (TOFR), and ion cyclotron resonance (ICR) mass analyzers. It is a method that combines separation power of HPLC with detection power of Mass spectrometry. • In LC-MS we remove the detector from the column of LC and fit the column to interface of MS. • In most of the cases the interface used in LC-MS are ionization source • A liquid sample is introduced into the ionization source of the mass spectrometer. Example: Extracts from plasma, serum, whole blood, Urine, CSF, etc.
  • 17. The liquid sample is usually delivered by an Liquid Chromatography (LC) system.
  • 18. LC-MS System Components • Mass spectrometers work by ionizing molecules and then sorting and identifying the ions according to their mass- to-charge (m/z) ratios. The mobile phase is the solvent that moves the solute throughout column. Solvent strength and selectivity: - It is the ability of solvent to elute solutes from a column. COLUMN The use of di-functional or tri-functional silanes to create bonded groups with two or three attachment points leading to phases with higher stability in low or higher pH and lower bleed for LC-MS • Most widely used columns for LC-MS are: - (1) fast LC column :- the use of short column.(15-50mm) (2) Micro LC column :- the use of large column. (20-150mm)
  • 19.
  • 20. Advantages of LC-MS/MS Accuracy and Precision • Robustness • Sensitivity • Allows multi-analyte panels • Requires less sample prep • Compatible with generic sample prep • Versatility, can easily add new compounds • Lower cost-per-sample • Speed
  • 21. Applications • LC-MS used to detect compounds from polyaromatic (non-polar) to peptide and proteins. • LC-MS used for compounds identification and purity. • Used for determination of pesticides, herbicides & organic pollutant for environmental monitoring. • Proteome analysis is done by this technique.
  • 22. HPTLC-MS General Introduction The direct coupling of TLC/HPTLC with mass spectrometry (MS) is of particular interest because of the later’s high sensitivity, rapid analysis, and ability to aid structural characterization. • TLC-MS is a versatile technique for separation as well as identification of Pharmaceuticals and Phytopharmaceuticals. Traditionally the separation was carried out by TLC/HPTLC then the separated materials was removed and then identified by Mass spectrometry. • This technique provides efficient, quick and simple method for identification and separation of Narcotic drugs and psychotropic substances.
  • 23. Key features • HPTLC–MS is cost-effective because the chromatographic run is decoupled with the detection step. • Rapid and contamination-free elution of selected zones. • Online transfer into the mass spectrometer. • Advantages of HPTLC include that the technique is simple to learn, operate, several analysis works could be done on same time, is a fast and economic technique. • Thin layer chromatography/high-performance thin-layer chromatography can be used interchangeably for methods developed in the twenty-first century.
  • 24. HPTLC-MS Principle • The versatile instrument is used to isolate unknown compounds from a HPTLC/TLC plate and transfer them into a mass spectrometer for identification or structure elucidation. • TLC/MS Interface can be bring together to any brand of LC-coupled mass spectrometer. • Plug and play installation by two HPLC fittings at a given HPLC-MS system. • Semi-automatic instrument involving automatic piston movement for pressure seal the HPTLC/TLC zone on both glass plates and aluminum foils take out directly from the plate using a suitable solvent delivered by the HPLC/HPTLC pump Online transfer into the mass spectrometer. • Automatic cleaning of the piston between the extractions.
  • 25. INSTRUMENTATION A typical automated LC-MS system consists of : • Double three-way diverter in-line with an autosampler • LC system • mass spectrometer. The diverter generally operates as an automatic switching valve to divert undesired portions of the eluate from the LC system to waste before the sample enters the MS.
  • 26. Fig: LC-MS (electrospray ionization interface) system Application: It can be used about the fragmentation patterns of degraded products
  • 27. References • Kanak Lata Verma, et al. HPTLC-MS as a Neoteric Hyphenated Technique for Separation and Forensic Identification of Drugs, Journal of Analytical Sciences, Methods and Instrumentation, 2018, 8, 1-15 • S. Nagajyothi, et al. Hyphenated Techniques- A Comprehensive Review, International Journal of Advance Research and Development,2017. • Ashwini B. Sambherao, et al.TLC- MS HYPHENATED TECHNIQUE IN ANALYTICAL CHEMISTRY, World Journal of Pharmacy and Pharmaceutical Sciences, Vol 6, Issue 10, 2017 • HYPHENATED TECHNIQUE- A BOON TO ANALYTICAL WORLD | INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH (ijpsr.com) • Hyphenated Technique - an overview | ScienceDirect Topics • (PDF) Introduction to hyphenated techniques and their applications in pharmacy (researchgate.net) • GC × GC-MS HYPHENATED TECHNIQUES FOR THE ANALYSIS OF VOLATILE ORGANIC COMPOUNDS IN AIR: Journal of Liquid Chromatography & Related Technologies: Vol 34, No 13 (tandfonline.com)