the use of evaporative light scattering detection in pharmaceutical analysis 1

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The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

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Page 1: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

The Use of Evaporative Light Scattering Detection in

Pharmaceutical Analysis

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Page 2: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Introduction

Traditional HPLC detectors such as UV and RI have limited capabilities

• RI detection is not gradient compatible• RI detection is susceptible to thermal instability and long

equilibration times• Different analytes produce different UV responses

depending on their extinction coefficient• UV and RI are not compatible with all solvents• Important information can be missed with an RI and a UV

detector• ELSD better alternative than UV detection at low

wavelengths

Page 3: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Advantages of Evaporative Light Scattering Detection

Universal detection : responds to all compounds in the mobile phase

• Detects compounds that do not possess a UV chromophore

e.g. polymers, sugars

Not dependent on the spectroscopic properties of an analyte

Produces more uniform detection sensitivity for analytes

Not susceptible to baseline drift during gradient elution, temperature or solvent pump fluctuations

ELSD compatible with a much wider range of solvents compared to refractive index

Page 4: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Column: PL Hi-Plex Ca, 250x4.0mmEluent: WaterFlow Rate: 0.6ml/minInj Vol: 10µlTemp: 85°CDetector: PL-ELS 2100 (neb=30°C, evap=90°C, gas=1.6 L/min) Samples: 1. Fructose, 2. Glucose, 3. Sucrose I, 4. Lactose, 5. Stachyose

300 min

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Advantages of Evaporative Light Scattering Detection: Compounds With No Chromophore

Page 5: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Samples : 1. α-cyclodextrin 2. ß-cyclodextrin

3. Ibuprofen

Column: Aquasil C18 5µm, 150x4.6mm

Eluent A: Water

Eluent B: Acetonitrile

Gradient: 50-95% B in 5 mins

Flow Rate: 1.0 ml/min

Inj Vol: 20µl

Detector: PL-ELS 2100

(neb=30°C ,

evap=50°C,

gas=1.0 L/min)

Detects all components in a single run

ELSD

UV @ 220nm

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Advantages of Evaporative Light Scattering Detection: Pharmaceutical Mixture

Page 6: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Column: PLRP-S 100Å 5µm, 150x4.6mm

Eluent A: 50% 0.1% TFA in Water : 50% 0.1% TFA in ACN

Flow Rate: 1.0ml/min

Inj Vol: 10µl

Detector: PL-ELS 2100 (neb=30°C, evap=30°C, gas=1.4 L/min)

UV-VIS @ 280nm

ELSD allows for a more uniform response than UV detection

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Advantages of Evaporative Light Scattering Detection: Uniform Response

Page 7: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

• Ideal for High Throughput Screening

• Removal of mobile phase eluent allows rapid HPLC gradients

• Fast setup and equilibration

• Flow rates up to 5ml/min can be achieved with no effect on baseline stability

• No interference from solvent front peaks

• Removes the need for derivatization steps

(e.g. for amino acids, toxins)

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Advantages of Evaporative Light Scattering Detection

Page 8: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

0 30min

1. Serine, 2. Glutamic Acid, 3. Arginine, 4. Proline, 5. Valine, 6. Methionine, 7. Isoleucine, 8.Leucine, 9. Phenylanine, 10. Tryptophan

ELSD removes the need for derivatization for applications such as amino acids

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Underivatized Amino Acids

Page 9: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Advantages of Evaporative Light Scattering Detection: Ideal Complement to LC-MS

Similar operating principles to LC-MS • Volatile buffers• Favors lower flow rates (i.e. 0.2-0.5ml/min)

Can develop LC methods on ELSD then transfer to LC-MS

ELSD can provide supporting information when used in tandem with LC-MS

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Page 10: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Sample mixture of known 1:1 ratio

LC-MS results show ratio to be3:1

UV-Vis result show ratio to be10:1

PL-ELS 2100 results show ratio to be1:1

(Response independent of optical properties)

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Ideal Complement to LC-MS

Page 11: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Analytical Techniques• HPLC analytical,

microbore, preparative• SFC• LC-MS• High Throughput

Screening• GPC/SEC• High temperature GPC• GPEC• 2D Chromatography

Application Areas• Pharmaceuticals• Nutraceuticals• Combinatorial libraries• Carbohydrates• Lipids• Phospholipids• Triglycerides• Fatty acids• Amino acids• Polymers• Surfactants11

ELSD application areas

Page 12: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

ELSD capable of handling supercritical CO2

Properties of supercritical CO2 are complementary to the nebulization step in ELSD

Low baseline noise & improved S/N with SFC–ELSD

Nebulizer must be heated to counter the Joule-Thompson cooling effect; prevents blockage of the nebulizer

ELSD provides an alternative detection method to FID and UV for SFC separations

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Supercritical Fluid Chromatography: Steroid Separation

Page 13: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Sample: PEG 1000

Column: Berger SFC Diol Column 60Å 6µm, 250x4.6mm

Eluent: Carbon Dioxide with 5% Methanol

Flow Rate: 2ml/min,

Pressure: Carbon Dioxide was pressure programmed from 100bar to 250bar at 10bar/min.

Inj Vol: 10µl

Detector: PL-ELS 2100 (neb=40°C, evap=30°C, gas=0.9 L/min)

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Supercritical Fluid Chromatography: Steroid Separation

Page 14: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Minimal band broadening allows high resolution SFC separations to be performed

PEG 1000

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Supercritical Fluid Chromatography: Steroid Separation

Page 15: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Column: Lichrospher DIOL 5µm,150x2.1mm

Eluent A: IPA/Hexane/Water/Ammonia Hydroxide 57.8/40/2/0.2Eluent B: IPA/Hexane/Water/Ammonia Hydroxide 51.8/40/8/0.2 Gradient: 0-100% B in 7 min, 8 min hold; 100-0% B in 5 min, 10 min holdFlow Rate: 0.3ml/minDetector: PL-ELS 2100: (neb=30°C, evap=80°C, gas=1.0 L/min)Samples: 1: Cholesterol, 2: Phosphatidylethanolamine, 3: Phosphatidylcholine, 4: Sphingomyelin, 5: Lysophosphatidylcholine

Stable baseline for complex mobile phase systems

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Complex Eluent Systems: Phospholipid Separation

Page 16: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

• Combinatorial libraries are commonly stored in DMSO

• DMSO peak can mask fast eluting compounds

• DMSO peak can be removed at elevated evaporator temperatures (e.g. >50°C)

• Loss of volatile species occurs at higher evaporator temperatures

• Eliminates DMSO removal step in sample preparation

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PL-ELS 2100: DMSO Transparency

Page 17: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Sample: Pharmaceutical mixture in DMSO

Column: C8 5µm, 50x4.6mm

Eluent A: Water

Eluent B: Acetonitrile

Gradient: 5-100% B in 5 mins

Flow Rate: 1.0ml/min

Inj Vol: 20µl

Detector: PL-ELS 2100 (neb=25°C evap & gas flow varied)

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PL-ELS 2100: DMSO Transparency

Page 18: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Loss of volatile species occurs as temperature is increased

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PL-ELS 2100 DMSO Transparency:Ideal for High Throughput Screening

Page 19: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

The unique use of evaporation gas in the PL-ELS 2100 makes it transparent to DMSO at 25-30°C

PL-ELS 2100: neb=25°C, evap=30°C

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PL-ELS 2100 DMSO Transparency:Ideal for High Throughput Screening

Page 20: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Column: Aquasil C18 5µm, 150 x 4.6mmEluent A: Water + 0.1% TFAEluent B: ACN + 0.1% TFAGradient: 50-95% B in 10 mins, hold 5 minsFlow Rate: 1.0mL/minDetector: PL-ELS 2100 (neb=30°C, gas=1.6 L/min)Samples : Commercial Tablet

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Nutraceutical Application: St John’s Wort

Page 21: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Fast Centrifugal Partition Chromatography: St John’s Wort

PL-ELS 2100 is compatible with Centrifugal Partition Chromatography, for prep scale fractionation of compounds

• The LED intensity can be reduced for the high loading levels

• The evaporator gas can be used to control baseline noise, which can be a problem with this technique

• UV detection is noisy with this technique, because the mobile phase can form cloudy emulsions

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Page 22: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Fast Centrifugal Partition Chromatography: St John’s Wort

FCPC-ELSD was used to isolate Hypericin from a 3g sample of raw plant product

• Flow Rate 20ml/min

• Rotation speed 1000rpm

• Solvent: Heptane/MeOH/ Water/Ethyl Acetate

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Page 23: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

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Fast Centrifugal Partition Chromatography: St John’s Wort

Page 24: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

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Nutraceutical Application: Black Cohosh

Page 25: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Combichem Application: DMSO Stability

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Page 26: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

Nutraceutical : Vitamins

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Page 27: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

The PL-ELS 2100 offers the general benefits of evaporative light scattering detection which are well documented:

• Universal detector, does not rely on the optical properties of the solute

• Excellent baseline stability, compatible with gradient elution

• High sensitivity

• Removes the need for derivatization

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Features of the PL-ELS 2100

Page 28: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

•Low temperature operation, even for 100% water

•Improved detection of volatile compounds

•Extremely low dispersion for high resolution separations

•High eluent flow rates, up to 5ml/min

•Wide application range

•Extremely small footprint, stackable

•Ergonomic design

•Easy to use

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Additional Benefits of the PL-ELS 2100

Page 29: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1

PL-ELS 2100 Specification

Light source: LED 480nm

Detector: Photomultiplier tube

Nebulizer temperature: Ambient to 90°C in 1°C increments

Evaporator temperature: Ambient to 120°C in 1°C increments

Gas flow rate: Up to 3.25 L/min

Gas pressure: Typically 60-100psi, maximum 100psi

Eluent flow rate: Up to 5ml/min

Analog output: 0-1V FSD

Communications: Serial I/O (RS232), contact closure, TTL

Power requirements: 90/120V AC or 220/250V AC 50/60 Hz

Dimensions: 200x450x415mm (wxdxh)

Weight: 11kg

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Page 30: The Use of Evaporative Light Scattering Detection in Pharmaceutical Analysis 1