hplc instrumentation and trends - mohsin al-saleh...mar 03, 2017 · hplc detectors ‐criteria. z....
TRANSCRIPT
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HPLC instrumentation and Trends
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Content
Composition of the HPLC systemPumpsInjectorsDetectorsData handling system
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The Chromatographic SystemBasic
Solvent
Pump
Injection
HPLC Column
Detector
Waste
Data System
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The Chromatographic SystemAdvanced
Solvent Can be more then 1
PumpCan be more then 1
InjectionManual or Automatic
HPLC Column
Detector
Waste
Data System
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Criteria for HPLC Solvent Delivery System (Pumps)
Constructed of materials that are chemically resistant to themobile phaseProvide precise and pulse‐free delivery of solvents at typical flowratesRange for flow rate 0.1–10 mL/min and pressure up to 6,000 psi(42MPa)Flow reproducibility << 1% R.S.DDesirable to have small holdup volume for rapid solventchanges/gradient elutionCompatible with common organic solvents, buffers, and saltsReliable operation with long pump seal life
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Pressure Units and Conversion
BarPounds per Square Inch (PSI)PascalAtm
1 Bar = 14.5 PsiI Bar = 0.9869 AtmI Bar = 100000 Pascal
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Pump Head
Outlet check valve
Plunger seal
Ball and seat
Plunger
Inlet check valve
Filter cup
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Pumps in Gradient System
Gradient proportioning valve
2 pump gradient systemMixing on high pressure side
1 pump gradient systemMixing on low pressure side
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Gradient Systems
“High-pressure mixing”Advantages
Usually lower system volumeDegassing not as critical
DisadvantagesOne pump per solvent Only practical with up to 3 solvents (usually only 2)
“Low-pressure mixing”Advantages
Only one pumpUsually more solvents (normally 4)
DisadvantagesUsually higher system volumeDegassing more critical
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INJECTORS
An HPLC injector is used to introduce the sample to the column under high pressure. A commoninjector is the Rheodyne model 7125 or 7725 injector,
from Pump
to Column
from Pump
to ColumnINJECT
LOAD
from Pump
from Pump
to Column
to Column
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Loading of sample loop
The sample loop can be loaded in two ways :
• Complete Filling : The loop is flushed with an excessamount of sample. For best results the sample volumeshould be more then twice of the volume of loop. Themaximum injection volume can be changed by replacing thesample volume.
• Partial filling : The loop can be partially filled with aspecially calibrated syringe or pump. Any volume between0.1 uL and the volume of the loop itself can be injected.
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Fixed loop Injection Valve
Initial fluid element Fluid element after flow
Tube wallSample loop
Laminar flow
pump
column
Position 1 (load) Position 2 (inject)
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Characteristics of a Fixed Loop Injector
As a consequence of laminar flow each 1ul loaded in the loop occupies 2ul.Full loop injections means that 2-3 times the loop size should be loaded.Partial loop injections this means that only up to 50% of loop size should be loaded.Using pre- and post- sample air gaps (2-3ul) the laminar flow can be eliminated
SampleAir gaps
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Auto samplers,Sample Formats, Vials
Crimp capCheapest solutionNeeds a crimping tool
Snap capEasy to use - no toolsTraditional or New LectraBondTM versions
Screw capThe universal versionTraditional or New LectraBondTM versions
Limited volume vialsInsertsWith internal taper
Needle opening
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Auto samplers,Sample Formats, Plates
Plate formatsFor traditional vials96- or 384-well plates
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An HPLC detector measures the concentration (or mass) of eluting analytes by monitoring oneof their inherent properties, such as UV absorbance. A detector can be “universal” to allanalytes or “specific” to particular classes of analytes.
HPLC Detectors ‐ Criteria
Operates by registering an output in response to sample detection.
A linear relationship is expected between response of the detector and concentration of thesample, and calibration techniques are designed to promote this relationship.
Not all detectors are linear and effects from other components of the HPLC system maycause the detector to deviate from a linear relationship between response andconcentration.
High sensitivity
Negligible baseline noise
Large linear dynamic range
Response independent of variations in operating parameters (pressures, temperature, flow‐rate…etc.)
Response independent of mobile phase
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HPLC Detectors ‐ Types
UV/VisibleVariable wavelengthPhoto diode array (PDA/DAD)
FluorescenceRefractive IndexConductivityElectrochemicalMass SpectrometryEvaporative Light ScatteringNuclear Magnetic Resonance (NMR)
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HPLC Detectors
HPLC detectors can be classified as:Solute property detectors -respond to physical or chemical properties of the solute that are generally not exhibited by the mobile phase.
Bulk property detectors -respond to an overall change in the physical property of mobile phase with and without solute.
There is no single detector that can be employed for all HPLC separations “the magic box”!
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Classification of Different Detector Types
Solute PropertyFluorescence
Electrochemical
Fixed WavelengthVariable WavelengthPhotodiode array
UV/Visible
Mass spectrometry
Bulk Property
Conductivity
Refractive Index
Evaporative light scattering
NMR
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UV/Visible Detectors
Most frequently used detector in HPLC analysisCompounds must contain a UV absorbing chromophoreMust work in the linear range of Beer’s Law
A = ε b c
Molar extinction coefficient cell path length (cm)
Sample concentration (moles/l)Absorbance
The UV/Vis absorbance detector monitors the absorption of UV or visible light in the HPLC eluent.
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Schematics of a Variable Wavelength UV/Vis Detector
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Flow Cell Design
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The Photodiode Array (PDA) Detector
AdvantagesCan provide UV spectra across peaksCan be used to assess peak “purity”/ spectral homogeneityCan be used to track peaks via their UV spectra (library search)
A photodiode array detector (PDA), also known as a diode array detector (DAD),provides UV spectra of eluting peaks while functioning as a multi wavelength UV/Visabsorbance detector. It facilitates peak identification and is the preferred detector formethod development.
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Schematic of a PDA Detector
Lamp
MirrorMirror
50 mm slit
Taper Beam cell
Grating
PDA
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Optical ResolutionInfluence on Linearity
1 nm10 nm #210 nm #1
AU
Concentration
Narrow spectral peak #1 with a wide bandpass (10 nm) is non-linear
230 240 250 260 Wavelength, nm
Abs
orba
nce
1 nm
10 nm
1
2
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Example of UV Spectra
“Spectrum index plot”
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Example of Library Search
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U.V. Cutoffs for Some Common Solvents
SolventSolvent UV CutoffUV Cutoff SolventSolvent UV CutoffUV CutoffWaterWater 180180 N-HeptaneN-Heptane 197197MethanolMethanol 205205 CyclohexaneCyclohexane 200200N-PropanolN-Propanol 205205 Carbon tetrachlorideCarbon tetrachloride 265265AcetonitrileAcetonitrile 190190 ChloroformChloroform 245245THFTHF 225225 BenzeneBenzene 280280AcetoneAcetone 330330 TolueneToluene 285285Methyl acetateMethyl acetate 260260 Methylene chlorideMethylene chloride 232232Ethyl AcetateEthyl Acetate 260260 TetrachloroethyleneTetrachloroethylene 280280NitromethaneNitromethane 380380 1,2-Dichloroethane1,2-Dichloroethane 225225
All wavelengths reported in nm.
Remember that Solvents chosen can affect detection!!
UV cutoff = Wavelength at which solvent absorb 1 AU
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Fluorescence
Increased selectivityAnalytes not only absorb UV/Vis radiation but also release the energy in the form of light of longer wavelength.This property is typically associated with non-ionic molecules which are strongly conjugated and have rigid structures.Sensitivity is in the femto gram regionDetector is sensitive to the presence of dissolved gasses and other “quenchers”
A fluorescence detector monitors the emitted fluorescent light of the HPLC eluent in the flow cell
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Fundamentals of Fluorescence
Some ApplicationsEnvironmental
Polyaromatic HydrocarbonsPhenols, carbamates
Food and BeverageAlfatoxins in Food ProductsDyes
Biotech and PharmaceuticalsDerivatized amino acids (AccQ-Tag or OPA)
Conjugated and aromatic systems are most likely to exhibit fluorescence
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Refractive Index Detectors
First HPLC detector developed
Typically referred to as Universal detectorsDetects all dissolved solutes- “non-specific”
RI response depends on the difference in RI between mobile phase and solute(s).
Sensitivity reaches maximum when RI differences are greatest.
Utilizes Snell’s Law Principlesμg sensitivity but only for isocratic runs
Commonly used for:
Sugars, Polymers and Fatty Acids
A refractive index detector measures the refractive index change between the sample cell containing the eluting analyte and the reference cell purged with pure eluent
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Schematic of an RI Detector
LAMPLED or
Incandescent R
S
To Amplifier
No sample
With sample
R
S
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Conductivity Detectors
Generally used for ion ChromatographyDetects the ability of analyte to carry a charge
solutes are ionic (that is, acid and bases)Inorganic anions and cations
Sensitivity is at the low ppb (ng/L) levelTypically used with isocratic systems but can utilize isoconductive gradients
A conductivity detector measures the electrical conductivity of the HPLC eluent stream
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Schematics of Conductivity Detector
Mobile phase
Mobile phase and solute(s)
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Electrochemical Detector (ECD)
“Destructive”-detection modeSample is electrochemically modified in the cell with the concomitant generation of current detected as response.High sensitivity with picogram (10-12 grams) to high femtogram (10-15 grams) range.Proper selection of buffer, electrode and voltage is critical to success as well as conditioning the mobile phase.
An electrochemical detector (ECD) measures the electrical current generated by electroactive analytes in the HPLC eluent between electrodes in the flow cell
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Schematics of Electrochemical Cell
Reference Electrode
Working Electrode
Electrolyte (mobile phase)
AuxiliaryElectrode
Analyte is oxidized or reduced
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Some Compound Types Sensed by ECD
Oxidation ReductionPhenolic Ketones
Oximes Aldehydes
Dihydroxy Oximes
Mercaptans Conjugated acids
Peroxides Conjugated esters
Hydroperoxides Conjugated unsaturation
Aromatic Amines, diamines Activated halogens
Purines Aromatic halogens
Heterocyclic Rings Nitro compounds
Heterocyclic rings
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Benefits of MS DetectionAdditional information
Molecular weight Structure
Better SelectivityPossible Quantification of “UV co-eluted compounds”Shorter analysis
SensitivityIn Sir mode, MS detection can be much more sensitive than UV detection (100 times)
Cross check UV and MS library searchImproved compounds characterization and differentiation
Speed up method developmentImprove impurities identificationImprove impurities characterization
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Additional Information
277 278 279 280 281 2820
2,000
4,000
6,000
8,000
10,000
12,000
Parent Ion RegionMW 278
100 150 200 250 3000
2,000
4,000
6,000
8,000
10,000
12,000
m/z
Intensity
[M+H]+
m/z
Positive ion mode, ESI, 2 ul/min, 50% MeOH:49% H2O:1% HOAc
0.3 mg/ml
100 150 200 250 3000
2,000
4,000
6,000
8,000
10,000
m/z
Intensity
[M+H]+
Fragment Ion Region
183 184 185 186 187 188 1890
2,000
4,000
6,000
8,000
10,000
m/z
C H N O S6 8 3 2
m/z = 186
NHN
NCH3
CH3
NH2 S
O
O
Sulfamethazine
92
156
186
At High Cone Voltage (fragmentation occurs)
At Low Cone Voltage (typically a Protonated Molecule is
observed)
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Need for Selectivity.Matrix interferencevery similar structures, impossible separation
Better Selectivity
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The molecules are difficult to detect.Zero or poor UV absorbance or FluorescenceMatrix interference
2.00 4.00 6.00 8.00 10.00 12.00 14.00 16.00 18.00 20.00 22.00 24.00 26.00 28.00 30.00 32.00 34.00Time9
100
%
-149
100
%
3: Diode Array TIC
3.45e6
TIC8.96e5
Sensitivity
UV
MS
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Need for better Qualitative InformationComponent Confirmation
Mass Spectrum (next to UV-Spectrum)Library
Valuable information on Unknowns
UV and MS Libraries
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Choosing a Detector for HPLC
RI UV/VIS Fluor. ECD Cond. MS
Response Universal Selective (Chromaphor)
Selective(Fluorophor)
Selective(Redox)
Selective(Ions)
Selective (Ionizable)
Sensitivity μgram nanogram picogram picogram picogram picogram
Linear Range
104 105 103 106 105 103
Flow Sensitive
Yes No No Yes Yes Yes
Temp. Sensitive
Yes No No Yes Yes No