Download - Chromatography hplc iii-anu
Presenter: Dr.ANURAG YADAVModerator: Dr.AVINASH.S.S
Chromatography-III
HPLC
Contents
• HPLC:– Definition – Basic principle– Instrumentation– Practical consideration – Applications – Advantages & disadvantages of HPLC
HPLC (High-performance liquid chromatography)
• Type of liquid chromatography
• Conducted in a column
• Characterized by the use of high pressure & small particle
size to push a mobile phase solution through a column of
stationary phase allowing separation of complex mixtures
with high resolution.
Basic principle
• Based on distribution of solute between a liquid mobile phase
and a stationary phase.
• The small diameter particles are used as stationary phase
support.
• The table shows relation between various parameters of HPLC.
• Trendline:
• Stationary phase have small particulate size and high surface areas.
• Columns: 20 cm or less• Mobile phase pumped at high pressures of
400Bar, 6000 psi. • Flow rates: 1-3 cm3 per min
Column length No. of theoretical plates per unit area
Resolving power Column length
Particle size Surface area
Basic principle
Components of HPLC
1. Solvent Reservoir
2. Pumps
3. Sample Injection System
4. Columns
5. Detectors
6. Computer
7. Waste collector
Solvent Reservoir (mobile phase)
• Inert container → mobile phase • Must be free of contaminants & bubble forming gases that get
trapped in column or detector.• Measures: microfilter, degasser• Degassing : - Vacuum filtration - Warming - Stirring vigorously with magnetic stirrer
- Sparge with inert gas (N2 or He)
- Ultrasonication
HPLC Pump
• To produce an appropriate pressure to push solvent & sample into
the column.
• Ideal pump
Deliver high pressure (upto 50MPa)
Deliver pulse free flow
Constant volume delivery
Deliver high volumes (flow rates) of solvent (to 10 mL/min)
Solvent replacement is easy
Types of HPLC Pump
Constant Pressure
• A steady pump pressure
• (usually about 1000–2000 psi) is needed to ensure
reproducibility & accuracy.
Constant displacement Pump
Reciprocating pump: constant flow rate through the column
Slight cyclical variation in pressure→pulse dampeners.
Pumps in HPLC
HPLC Pump operating mode
Isocratic elution: A separation that employs a single solvent or solvent mixture of constant composition with single pump throughout the run.
Uses: Simple separation & compound with similar structures & retention time
Gradient elution: Here two or more solvent systems that differ significantly in polarity with separate pumps.
the ratio of the solvents is varied in a programmed way, sometimes continuously and sometimes in a series of steps. Separation efficiency is greatly enhanced by gradient elution.
Uses : complex separations
Sample Injector
1) Manual Injector:• Manually load sample into the injector using a syringe• and then injected sample → into the flowing mobile phase
→which transports the sample into the beginning (head) of the column, which is at high pressure
Sample Injector
2) Autosampler injector:
• User loads vials filled with sample
solution into the autosampler tray
(100 samples)
• Autosampler automatically
Takes appropriate sample volume,
injects the sample,
then flushes the injector to be
ready for the next sample, until all
sample vials are processed.
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Manual Injectors
Front View
Inject
Rear View
Load - Inject
Sample Loop
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Automatic Injectors
Step 1 Step 2
Step 3
• Control of column temperature as constant temp is required.
• Achieved by:– Column chambers– Water jackets– Temperature controlled blankets– Heating/cooling blooks
• Stable column temperature is required to generate reproducible retention time.
Column Heater/Chillers
Guard column
• Repeated application of impure samples (sera, urine) →
↓column resolving power.
• Installed between injector & analyte column
• Column characterstics: short(1-2cm), same ID & packed with
similar particles to that present in analytical column.
• Retains contaminating particles, can be replaced at regular
intervals.
Column:
• Considered the “heart of the chromatograph” the column’s stationary
phase separates the sample components of interest using various physical
and chemical parameters.
•The small particles inside the column are what cause the high
back pressure at normal flow rates.
•The pump must push hard to move the mobile phase through the
column and this resistance causes a high pressure within the
chromatograph.
Analyte Columns in HPLC
Analyte Columns in HPLC
• Standard Column : 3-25cm long, ID(4.6 mm) ;optimum flow volume = 1 ml/min.
• Narrow Bore : 3 mm(ID); flow volume 0.6 ml/min • Microbore /Open tubular : 25-50cm long, 1 mm(ID); 50
microliter/min.
Several Column Types ( can be classified as)
• Normal phase
• Reverse phase
• Size exclusion
• Ion exchange
Normal phase • In this column type, the retention is governed by
the interaction of the polar parts of the stationary phase and solute.
• For retention to occur in normal phase, the packing must be more polar than the mobile phase with respect to the sample
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HO Si
O
O
STATIONARY PHASES(NORMAL POLARITY)
Silica or alumina possess polar sites that interact with polar molecules.
Most polar…….Least polar
Components elute in increasing order of polarity.
Components elute in increasing order of polarity.
Polar Group
silica
Reverse phase• In this column the packing material is relatively nonpolar and the solvent is
polar with respect to the sample. Retention is the result of the interaction of the nonpolar components of the solutes and the nonpolar stationary phase.
• Typical stationary phases are nonpolar hydrocarbons, waxy liquids, or bonded hydrocarbons (such as C18, C8, etc.) and the solvents are polar aqueous-organic mixtures such as methanol-water or acetonitrile-water.
Common Reverse Phase Solvents –
Methanol
Acetonitrile
Tetrahydrofuran
Water
CH3OH
CH3CN
H2O
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STATIONARY PHASES(REVERSE POLARITY)
If the polar sites on silica or alumina are capped with non-polar groups, they interact strongly with non-polar molecules.
Most non-polar…….Least non-polar
Components elute in decreasing order of polarity.
Components elute in decreasing order of polarity.
C18 phasesilica
Si
Me
Me
O Si
O
O
Size exclusion
• In size exclusion the HPLC column is consisted of substances which have controlled pore sizes and is able to be filtered in an ordinarily phase according to its molecular size.
• Small molecules penetrate into the pores within the packing while larger molecules only partially penetrate the pores. The large molecules elute before the smaller molecules.
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STATIONARY PHASES(SIZE EXCLUSION)
Size exclusion gels separate on the basis of molecular size. Individual gel beads have pores of set size, that restrict entry to molecules of a minium size.
Larger molecules…….Smaller molecules
Large molecules elute fast (restricted path), while small molecules elute slowly (long path length)
Large molecules elute fast (restricted path), while small molecules elute slowly (long path length)
Ion exchange
• In this column type the sample components are separated based upon attractive ionic forces between molecules carrying charged groups of opposite charge to those charges on the stationary phase.
• Separations are made between a polar mobile liquid, usually water containing salts or small amounts of alcohols, and a stationary phase containing either acidic or basic fixed sites.
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STATIONARY PHASES(CATION EXCHANGE)
Silica is substituted with anionic residues that interact strongly with cationic species (+ve charged)
Most +ve…….Least +ve
+ve charged species adhere to the supportand are later eluted with acid (H+)
+ve charged species adhere to the supportand are later eluted with acid (H+)
Cations exchange Na+ silica
S
O
O
ONa
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STATIONARY PHASES(ANION EXCHANGE)
Silica is substituted with cationic residues that interact strongly with anionic species (-ve charged)
Most -ve…….Least -ve
-ve charged species adhere to the supportand are later eluted with acid (H+)
-ve charged species adhere to the supportand are later eluted with acid (H+)
Anions exchange Cl- silica
Me N
Me
MeCH2Cl
HPLC ColumnsWithin the Column is where separation occurs.
Key Point –Proper choice of column is critical for success in HPLC
Materials of construction for the tubing• Stainless steel (the most popular; gives high pressure capabilities)• Glass (mostly for biomolecules)• PEEK polymer (biocompatible and chemically inert to most solvents
Packing material:
The packing material is prepared from SILICA particle, ALUMINA particle and ion exchange RESIN.
Porous plug of stainless steel or Teflon are used in the end of the columns to retain the packing material.
According to the mode of HPLC , they are available in different size , diameters, pore size or they can have special materials attached ( such as antigen or antibody ) for immuno affinity chromatography.
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Modes of High Performance Liquid Chromatography
Types of Compounds Mode StationaryPhase
Mobile Phase
NeutralsWeak AcidsWeak Bases
ReversedPhase
C18, C8, C4cyano, amino
Water/Organic Modifiers
Ionics, Bases, Acids Ion Pair
C-18, C-8 Water/Organic Ion-Pair Reagent
Compounds notsoluble in water
NormalPhase
Silica, Amino,Cyano, Diol
Organics
Ionics Inorganic Ions Ion Exchange
Anion or CationExchange Resin
Aqueous/Buffer Counter Ion
High Molecular WeightCompoundsPolymers
Size Exclusion
Polystyrene Silica
Gel Filtration- AqueousGel Permeation-Organic
Types of columns in HPLC:
• Guard Column
• Fast Column
• Preparative(i.d. > 4.6 mm; lengths 50 –250 mm)
• Capillary(i.d. 0.1 -1.0 mm; various lengths)
• Nano(i.d. < 0.1 mm, or sometimes stated as < 100 μm)
• Analytical[internal diameter (i.d.) 1.0 -4.6-mm; lengths 15 –250 mm]
Fast Column
• One of the primary reasons for using these column is to obtain improved sample output ( amount of compound per unit time).
• Fast column are designed to decrease the time of chromatographic analysis
• Here internal diameter is same but length is short and packed with smaller particles , that are 3 μm diameter.
• Advantages-
Increased sensitivity
Decreased analysis time
Decreased mobile phase usage
Increase reproducibility
Capillary Column
• It is also known as micro columns
• It has a diameter much less than a millimeter and there 3 types:
Open tubular
Partially packed
Tightly packed
They allow the user to work with nanoliter sample volume , decreased flow rate and decreased solvent usage volume , led to cost effectiveness
Preparatory Column
• Used when objective is to prepare bulk ( milligrams) of sample for laboratory preparatory application.
• It has usually a large column diameter , which is designed to facilitate large volume injections into the HPLC system
Column packing
• Particulate packings : particle diameters 1.8 to 10 μm.
1) Bonded phase : stationary phase is bonded chemically to
surface of silica particles through a silica ester or silicone
polymeric linkage.
Eg. In reverse phase HPLC, ODS bound to silica particles
(C 18 column).
2) Polymeric : eg. Polystyrene-polyvinylbenzene, stable at PH
2-13
3) Chiral : separation of enantiomers.
• The detector can see (detect) the individual molecules that come
out (elute) from the column.
•A detector serves to measure the amount of those molecules
so that the chemist can quantitatively analyze the sample
components.
•The detector provides an output to a recorder or computer
that results in the liquid chromatogram(i.e., the graph of the
detector response).
Detectors in HPLC
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Common HPLC Detectors
•UV-VIS•Diode Array•Multiple Wavelength•Variable Wavelength
•Mass Spectrometers
•Refractive Index
•Fluorescence
•Light Scattering
•Electrochemical
•Radioactivity
•Conductivity
1. Variable wavelength (UV-VIS absorbance) detector
• UV-Visible spectrometry
• Measures absorbance of light as
down to 190nm.
• Detection limit < 1 ng
ADV:
• High sensitive
• Small amount of sample.
Uses: amides, carboxylic acid,
cholesterol.,
2. Scanning wavelength detector
• Records complete absorption spectrum of analyte
• By using photodiode array technique
• Scans complete spectrum of analyte within 0.01 sec
• Adv : could analyse sample simultaneously at diff wavelength.
• Disadv: less sensitive than UV-VIS detector.
3. Fluorescence detector
• Based on measurement of fluorescence
• Compared to UV-Vis detectors fluorescence detectors offer a higher
sensitivity and selectivity that allows to quantify and identify
compounds in complex matrices at extremely low concentration levels
(trace level analysis).
• Detection limit: pg to ng
• Uses: amino acids and amines.
• Limitation: only fluorescent
• analytes measured.
4 .Electrochemical detector
• Electroactive analytes
• Electrochemically measures
Oxidation reaction: hydrocarbon,
amines, phenols, catecholamines
Reduction reaction: alkenes,
esters, ketones
• Detection limit: pg to ng.
5. Refractive Index (RI) Detection
• The refractive index (RI) detector uses a monochromator and is one of the least sensitive LC detectors.
• This detector is extremely useful for detecting those compounds that are non-ionic, do not absorb ultraviolet light and do not fluoresce.
• e.g. sugar, alcohol, fatty acid and polymers.
LC-MS• HPLC column eluted solutes
introduced into a ion source of a MS, blasted with electrons, which cause them to turn into positively charged molecular ions and fragmented ions (ion source).
• When these charged particles passed through filter → separated according to m/e ratio → ions collected.
• TIC the current generated by all such ions from analytes is measured, which would be proportional to the concentration of analyte.
HPLC Detectors
Computer
• Electronic signals generated by detectors are recorded in the
form of chromatograghic peak at varied function of time
• Peak Area, height, retention time, base width of
chromatograghic peak is measured to compute analyte
concentration of each peak.
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How can We Analyze the Sample?
For example:Carbohydrates1. fructose2. Glucose3. Saccharose4. Palatinose5. Trehalulose6. isomaltose
1
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4
5
mAU
time
6
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SeparationsSeparation in based upon differential migration between the stationary and mobile phases.
Stationary Phase - the phase which remains fixed in the column, e.g. C18, Silica
Mobile Phase - carries the sample through the stationary phase as it moves through the column.
Injector
Detector
Column
Solvents
Mixer
Pumps
High Performance Liquid Chromatograph
Waste
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SeparationsInjector
Detector
Column
Solvents
Mixer
Pumps
Chromatogram
Start Injection
mAU
time
High Performance Liquid Chromatograph
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SeparationsInjector
Detector
Column
Solvents
Mixer
Pumps
Chromatogram
Start Injection
mAU
time
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SeparationsInjector
Detector
Column
Solvents
Pumps
Mixer
Chromatogram
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mAU
time
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SeparationsInjector
Detector
Column
Solvents
Pumps
Mixer
Chromatogram
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mAU
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SeparationsInjector
Detector
Column
Solvents
Pumps
Mixer
Chromatogram
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mAU
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SeparationsInjector
Detector
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Solvents
Pumps
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mAU
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SeparationsInjector
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SeparationsInjector
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Solvents
Pumps
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SeparationsInjector
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SeparationsInjector
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SeparationsInjector
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Mixer
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mAU
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SeparationsInjector
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SeparationsInjector
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Pumps
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SeparationsInjector
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Solvents
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SeparationsInjector
Detector
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Solvents
Pumps
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Start Injection
mAU
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SeparationsInjector
Detector
Column
Solvents
Pumps
Mixer
Chromatogram
Start Injection
mAU
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The Chromatogram
Injection
to
tR
mAU
time
tR
to - elution time of unretained peak
tR- retention time - determines sample identity
Area or height is proportionalto the quantity of analyte.
Preparation for HPLCSample preparation :
• Sample purification and Sample Derivatization.
• Before HPLC analysis , solutes are chemically derivatized
before or after chromatographic separation to increase their
ability to be detected .
• Eg. Derivatization of amino acids with O-Phthalaldehyde OR
Dansyl chloride.
• Degassing
Factors which influence the HPLC performance
1. Internal diameter of column
- the smaller in diameter, the higher in sensitivity
2. Pump pressure
- the higher in pressure, the higher in separation
3. Sample size
4. The polarity of sample, solvent.
5. Temperature
- the higher in temperature, the higher in separation
CALIBRATION
Calibration of HPLC is done to check the performance of its instrument.
1.flowrate(pump calibration)
2. Detector and injector linearity
3.System precision
4.Column oven temperature
5.Detector wavelength accuracy
1.Pump calibration
• Disconnect the column and connect the inlet and outlet tubing’s with a union.
• Prime all the lines at 5 ml/min flow rate with water and ensure that flow line is free from air bubbles.
• Set the flow rate at 1ml / min and collect the mobile phase (water) in a dry preweighed beaker and collect the mobile phase for 10 min. weigh the beaker to get the weight of mobile phase.
• Calculate the flow rate by dividing the weight obtained with weight per ml and 10 (run time).
• Calculate the corresponding flow rate. Carry out the experiment in duplicate.
Acceptance criteria
0.05ml for small quantities0.1ml for larger quantities
2.Detector and Injector linearity
Column : ODS or C18
Mobile phase : milli Q water and acetonitrile (80:20)
Flow rate: 1ml/min
Temperature: 40°Centigrade
Detector wavelength:272 nm
Runtime:10min
Preparation of stock solution:
•Take 50mg of caffeine and transfer into 50ml of flask and make it up to the mark with the diluent
•Caffeine is used a it gives a multiwavelength response and is stable
•Prepare solutions of different PPM (100-600)
•Inject them and calculate the area
•Correlation coefficient r is used to check the detector linearity and cannot be less than .999
• r = NƩXY-ƩXƩY/√ [NƩX²-(Ʃx) ²][NƩY²-(ƩY)²]
•The graph obtained between concentration and area is linear
3.System precision
•From the stock solution pipette out 1ml of stock solution and transfer into 10ml flask and make it upto the mark with diluent for 100PPM conc.
•Calculate the percentage of RSD of areas of 5 different injections
•% RSD = standard deviation/average value of above 5 injection areas × 100
•Where SD = √ Ʃ(X-M) ²/n-1
N= # of injectionsM=average areaX=area
For system precision % of RSD is not more than 1
4.Column oven temperature
1. Set the column oven temperature to 30° and leave it for 30 minutes
2. Open the door of the column oven and keep the thermometer and leave it for 30 min
3. now note down the reading in the thermometer
4. Similarly change the column oven temperature to 40°C and 50°C and repeat the above procedure
Acceptance criteria
±2°c
5.Detector wavelength accuracy
Column : C18
Mobile phase: HPLC grade methanalFlow rate:1ml/minRetention time:5 minutesWavelength:272nm
1. Inject the methanol and record blank
2. Inject 20 ml of standard solution at 268nm
3. Similarly inject the standard solution by increasing the nm upto 278nm(increasing it 1 at a time)
Acceptance criteria
273nm ± 1
MAINTAINANCE
1.RESERVOIR
Possible Cause Preventive Maintenance
1. Blocked inlet frit 1. a. Replace (3–6 months)
b. Filter mobile phase with 0.4 - 0.5 µm filter
2. Gas bubbles 2. Degas mobile phase, sonification
2. PUMPPossible Cause Preventive Maintenance
1. Air bubbles 1. Degas mobile phase , do not change mobile phase during run
2. Pump seal failure 2. Replace (3 months),clean with 1 N acid
3. Check valve failure 3. Filter mobile phase; use inlet-line frit ; keep spare
4.Improper cleaning 4.Clean with Isopropyl alcohol , mobile phase container must be cleaned with mobile phase and other sections with solvent
3.INJECTOR
Possible Cause Preventive Maintenance
1.Washing 1.wash before and after use
2. Rotor seal wear 2. a. Do not overtighten
3.Syringe
b. Filter samples3.Sterilize when fresh sample is used
C. Injector
4.Column
Possible Cause Preventive Maintenance
1. Number of injections 1. 2000 or less
2. Blocked frit 2.. a. Filter mobile phase
b. Filter samples
c. Use in-line filter and/or guard column
3. Void at head of column 3.. a. Avoid mobile phase pH >8
b. Use guard column
c. Use precolumn (saturator column
D. Column
5.Detector
Possible Cause Preventive Maintenance
1. Lamp failure; decreased detector
1. Replace (6 months) or keep spare lamp
response; increased detector noise
2. Bubbles in cell 2. a. Keep cell clean
b. Use restrictor after cell
c. Degas mobile phase
6.Software
Update frequently , around 6-12 months
TROUBLESHOOTING
Identifying problem using a chromatogram
1.The above pattern occurs when the mobile phase is not suitable
2.Baseline noise
I. Blank base(normal)
II. Noisy : •occurs when there is contamination of mobile phase• improper cleaning
3.Drift
•Temperature is unstable•Contamination of column
4.Peak tailing
•Improper mixing of mobile phase(90% of the time)
•Problems with column(30% of the time)
After adjusting PH with buffer
Good resolution
5.Peak fronting
•Low temperature•Overloading of sample•Flow rate•Overfilling of column•Insufficient mixing of mobile phase
6.High concentration of sample
RT=4.0
7.Retention time variation
Occurs due to problems with mobile phase
RT=3.0
RT=3.5
8.Communication error
Due to problem in communication between detector and the software
9.Peak splitting
Occurs when column lifetime is diminished
10.Power fluctuation
11.Variation in area
•Problem with injector•Fluctuation in flow rate•Error in detection
A=3010
A=3215
A=3516
12. Ghost peaks
•Contamination of mobile phase•Upset equilibrium•Production not finished
13.Detector lifetime diminished
Applications of HPLCTherapeutic & diagnostic uses
In clinical diagnosis : detection and
estimation of amino acids,
metabolites, sugars in physiological
samples,
Mucopolysaccharides in urine and
blood –useful for screening and
diagnosis of inborn metabolic
disorders
Clinical diagnosis of Aminoacidurias,
hemoglobinopathies,
mucopolysaccharidoses, etc.
Separation & identificaton of lipids,
carbohydrates & proteins.
Applications of HPLC
Therapeutic & diagnostic uses
• Measurement of drugs & other
metabolites in biological fluids
• Monitoring of cirrhosis pt through
aquaporin-2 in urine
Applications of HPLC
Forensic analysis• Forensic analysis of blood and
urine alcohol levels• Forensic analysis of blood and
urine levels of drug abuse and steroids.
• Used for toxiclogical analysis of biological fluid – op poisoning
Applications of HPLC
Pharmaceuticals industry uses• Quantity of drug determination from pharmaceutical dosage
forms, ex. Paracetamol determination in panadol tablet• Quantity of drug determination from biological fluids.
Analysis of natural contamination
- Phenol & Mercury from sea water
Food and essence manufacture
- sweetener analysis in the fruit juice
- preservative analysis in sausage.
Advantages of HPLC
1. Needs a small sample with a high accuracy and precision
2. Non-destruction of sample
Disadvantages
• Need a skill to run the instruments
• Solvents consuming
• Maintenance .
Advantages & disadvantages
HPLC
• Both volatile & non-volitile
analytes can be measured
without degradation.
• Time of separation is very less
bec high pressure pump is used.
• Length of column is small
• Non-explosive
• Non-expensive
GC
• Only volatile analytes can be
measured.
• More time
• Bigger coloumn than HPLC
• Explosive
• Expensive
Ultra-performance liquid chromatography (UPLC)
• As pointed earlier, the resolution of a mixture of analytes
increases as the particle size of stationary phase decreased.
• But such a decrease leads to a high back-pressure from the
eluent flow.
• Solution to this is represented by HPLC with new sationary
phase less than 2μm diameter by the waters corporation (1.7 μm
diameter)- made of Bridged Ethylsiloxane silica Hybrid (BEH)TM
• This can sustain of back-pressure of 150MPa.
• The instrument available under the trade name of
ACQUITYTM & the term UPLC is registered under
Waters.
• this operates upto 10 times faster than the conventional
HPLC, & can complete in less than 5mins
• The peaks may last for only 1s, so the detectors should
respond ultra fast to respond to the peaks.
Perfusion chromatography
• The high resolution achieved by the HPLC si based on use of
small diameter particles.
• However, same can be achieved at low cost by generating high
flow rate without high pressure.
• Perfusion chromatography comes with this, with particle size
around 10-50μm diameter, that have channels of around 1μm
diameter running through them.
• The high flow rate result in small plate heights & hence high
resolution in very short separation times.
• The particles are made of polystyrene-divinylbenzene &
are available under the name of POROS.
References
• Keith wilson-technique text book.
• Tietz –clinical chemistry text book.
• Kaplan-technique text book.
• Upadhyay- biophysical chemistry.
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UV-Vis Detectors
b
c
Detector Flow Cell
I0 I
Log I0 = A = abcI
Principles: The fraction of light transmitted through the detector cell is related to the solute concentration according to Beer’s Law.
Characteristics: Specific, Concentration Sensitive, good stability, gradient capability.
Special: UV-Vis Spectral capability (Diode Array Technology ).
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Fluorescence Detection
Emission Monochromatorsignal & spectra mode
PMT detector
Reference Diode
8 µl Flow Cell, auto-recognition
Trigger pack
Exitation Monochromator,signal & spectra mode
Mirror
Lens(condensor EX)
Lens (condensor EM)
Slit EM Slit PMTSlit EX
Diffuser
Xenonflash Lamp,15 W