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1
Supervised by :
Dr. Noel Rahul Shaw
Assistant Professor
Department of Quality Assurance
Presented by :
Lakshay Tayal
B.Pharm VII Sem
B.Pharm VII Sem (2020-2021)
HPLC
Affiliated to
Jai Narain Vyas University, jodhpur
Presentation Plan
• Introduction
• Types of HPLC
• Flow Scheme of HPLC
• Instrumentation
• Advantages and Disadvantages
• Applications
2
Introduction
• Chromatography is a laboratory technique used for separation of mixture.
• HPLC is a type of Chromatography which shows high Performance
• HPLC is a process of separation of mixture containing two or more
components under high pressure by passing sample through a column
containing stationary solid bed by means of pressurized flow of liquid mobile
phase.
• The pressure used is 1000- 5000 psi.
• The Principle of separation of component of mixture depends upon their
relative affinity towards St. phase and m.phase or depends upon adsorption/
partition coefficient or depend upon charge or molecular size of mixture. 3
Types of HPLC
According to Phases:
• Liquid-solid chromatography or adsorption Chromatography
• Liquid-liquid chromatography or Partition Chromatography
• Ion exchange chromatography or Separation base on charge
• Size exclusion chromatography or Separation base on molecular size
of particle.
4
Types of HPLC
On the basis of modes:
1. Normal phase HPLC
• Stationary phase: High polar rigid silica, or silica based
compositions.( Hydrophilic, Polar)
• Mobile phase: Relatively non polar solvent, hexane, heptane etc.
2. Reverse phase HPLC ( Often used )
• Stationary phase: Bonded hydrocarbons (C18, C8 etc.)
• Mobile phase: Polar solvents or mixtures such as methanol-water or
acetonitrile -water.
• The most polar component is eluted first.
• It is useful for polar sample analysis (organic compounds)
5
6
A flow scheme of HPLC showing operation mode of
its parts 7
Instrumentation of HPLC
• Degasser
• Reservoir
• Pump
• Injector
• Column
• Detector
• Waste collector
• Display unit
8
Parts of HPLC
• Degasser: It is used to remove the air from solvent.
• Reservoir: These are glass or stainless steel containers capable of holding mobile
phase.
Pump: The pump provide a steady high pressure to the sample solution/mobile
phase flowing inside the column. Eg . Reciprocating pump/ constant flow pump
. Displacement pump/ syringe pump
Ideal pump property:
- Ability to generate high pressure
-Accurate control of flow
- Corrosion resistant
9
Injector: It is used to inject the sample into the continuously flowing mobile phase stream that carries the
sample into the HPLC column.
Column: They are constructed of stainless steel for highest pressure resistance.
• - Length (10-30 cm)
• - Internal diameter (4-10 mm)
• - Particles size (3-10 µm);
Detector: It is used to detect the separated compound bands as they elute from the HPLC column.
Generally UV detector is used in it.
• Characteristics of an ideal detector:
- Adequate sensitivity
- Good stability and reproducibility
- Gives linear response to analysts
- Short response time
Waste collector: The mobile phase/ sample solution exits from the detector and is collected in the waste
chamber where it is either collected or thrown, as desired.
Display unit: A device that records the electrical response of a detector on a computer screen in the form of
a chromatogram.
10
Applications
• Widely applicable to numerous fields of study; both academic and
industrial work.
• Separate, identify and quantify the active compounds.
• Qualitative and quantitative determination of sample.
• Separation of non-volatiles:
Amino acids, proteins, carbohydrates, pharmaceuticals, pesticides,
pigments, antibiotics, steroids, vitamins, and various other organic and
inorganic substances.
11
Applications
Food and Flavor Analysis:
• Ensuring the quality of drinking water.
• Sugar analysis in fruit juices
• Analysis of compounds in vegetables.
• Trace analysis of agricultural crops
Application in Clinical Tests :
1.Urine Analysis
2.Antibiotic analysis in blood
3.Identification of Steroids in blood and urine
12
Applications
In drug manufacturing stage:
• Identification tests of the drug product or its ingredients
• Assay/ Content Uniformity test
• Dissolution test
• Drug Impurity testing
• Drug Stability
• Cleaning Validation/testing of the manufacturing equipments such as blender, tablet
press, etc.
• In process quality control testing
•Data manipulation can be prevented 13
Advantages and Disadvantages
• Speed (analysis can be accomplished in 20 min. or less)
• Greater sensitivity (various detectors can be employed)
• Improved resolution (wide variety of stationary phases)
• Reusable columns (expensive columns but can be used for many analysis)
• Used for sepration of sample which tend to decompose at higher Temp
• Disadvantages:
1. It is Costly
2. It is complex
3. Low sensitivity for some compounds
14
Reference
• https://lab-training.com/hplc/
• https://microbenotes.com/high-performance-liquid-chromatography-
hplc/Accessed on 15/01/21
• https://lab-training.com/wp-content/uploads/2014/11/HPLC-E-Book.pdf
• https://laboratoryinfo.com/hplc/ Accessed on 18/01/21
• Introduction to HPLC by Lab Training.com (Saurabh Arora )
• Handbook of HPLC New York: M. Dekker, ©1998 by Elena Katz
15
16

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Hplc

  • 1. 1 Supervised by : Dr. Noel Rahul Shaw Assistant Professor Department of Quality Assurance Presented by : Lakshay Tayal B.Pharm VII Sem B.Pharm VII Sem (2020-2021) HPLC Affiliated to Jai Narain Vyas University, jodhpur
  • 2. Presentation Plan • Introduction • Types of HPLC • Flow Scheme of HPLC • Instrumentation • Advantages and Disadvantages • Applications 2
  • 3. Introduction • Chromatography is a laboratory technique used for separation of mixture. • HPLC is a type of Chromatography which shows high Performance • HPLC is a process of separation of mixture containing two or more components under high pressure by passing sample through a column containing stationary solid bed by means of pressurized flow of liquid mobile phase. • The pressure used is 1000- 5000 psi. • The Principle of separation of component of mixture depends upon their relative affinity towards St. phase and m.phase or depends upon adsorption/ partition coefficient or depend upon charge or molecular size of mixture. 3
  • 4. Types of HPLC According to Phases: • Liquid-solid chromatography or adsorption Chromatography • Liquid-liquid chromatography or Partition Chromatography • Ion exchange chromatography or Separation base on charge • Size exclusion chromatography or Separation base on molecular size of particle. 4
  • 5. Types of HPLC On the basis of modes: 1. Normal phase HPLC • Stationary phase: High polar rigid silica, or silica based compositions.( Hydrophilic, Polar) • Mobile phase: Relatively non polar solvent, hexane, heptane etc. 2. Reverse phase HPLC ( Often used ) • Stationary phase: Bonded hydrocarbons (C18, C8 etc.) • Mobile phase: Polar solvents or mixtures such as methanol-water or acetonitrile -water. • The most polar component is eluted first. • It is useful for polar sample analysis (organic compounds) 5
  • 6. 6
  • 7. A flow scheme of HPLC showing operation mode of its parts 7
  • 8. Instrumentation of HPLC • Degasser • Reservoir • Pump • Injector • Column • Detector • Waste collector • Display unit 8
  • 9. Parts of HPLC • Degasser: It is used to remove the air from solvent. • Reservoir: These are glass or stainless steel containers capable of holding mobile phase. Pump: The pump provide a steady high pressure to the sample solution/mobile phase flowing inside the column. Eg . Reciprocating pump/ constant flow pump . Displacement pump/ syringe pump Ideal pump property: - Ability to generate high pressure -Accurate control of flow - Corrosion resistant 9
  • 10. Injector: It is used to inject the sample into the continuously flowing mobile phase stream that carries the sample into the HPLC column. Column: They are constructed of stainless steel for highest pressure resistance. • - Length (10-30 cm) • - Internal diameter (4-10 mm) • - Particles size (3-10 µm); Detector: It is used to detect the separated compound bands as they elute from the HPLC column. Generally UV detector is used in it. • Characteristics of an ideal detector: - Adequate sensitivity - Good stability and reproducibility - Gives linear response to analysts - Short response time Waste collector: The mobile phase/ sample solution exits from the detector and is collected in the waste chamber where it is either collected or thrown, as desired. Display unit: A device that records the electrical response of a detector on a computer screen in the form of a chromatogram. 10
  • 11. Applications • Widely applicable to numerous fields of study; both academic and industrial work. • Separate, identify and quantify the active compounds. • Qualitative and quantitative determination of sample. • Separation of non-volatiles: Amino acids, proteins, carbohydrates, pharmaceuticals, pesticides, pigments, antibiotics, steroids, vitamins, and various other organic and inorganic substances. 11
  • 12. Applications Food and Flavor Analysis: • Ensuring the quality of drinking water. • Sugar analysis in fruit juices • Analysis of compounds in vegetables. • Trace analysis of agricultural crops Application in Clinical Tests : 1.Urine Analysis 2.Antibiotic analysis in blood 3.Identification of Steroids in blood and urine 12
  • 13. Applications In drug manufacturing stage: • Identification tests of the drug product or its ingredients • Assay/ Content Uniformity test • Dissolution test • Drug Impurity testing • Drug Stability • Cleaning Validation/testing of the manufacturing equipments such as blender, tablet press, etc. • In process quality control testing •Data manipulation can be prevented 13
  • 14. Advantages and Disadvantages • Speed (analysis can be accomplished in 20 min. or less) • Greater sensitivity (various detectors can be employed) • Improved resolution (wide variety of stationary phases) • Reusable columns (expensive columns but can be used for many analysis) • Used for sepration of sample which tend to decompose at higher Temp • Disadvantages: 1. It is Costly 2. It is complex 3. Low sensitivity for some compounds 14
  • 15. Reference • https://lab-training.com/hplc/ • https://microbenotes.com/high-performance-liquid-chromatography- hplc/Accessed on 15/01/21 • https://lab-training.com/wp-content/uploads/2014/11/HPLC-E-Book.pdf • https://laboratoryinfo.com/hplc/ Accessed on 18/01/21 • Introduction to HPLC by Lab Training.com (Saurabh Arora ) • Handbook of HPLC New York: M. Dekker, ©1998 by Elena Katz 15
  • 16. 16