Direct Analysis of Multicomponent Adjuvants by HPLC with Charged Aerosol Detection

Similar documents
Direct Determination of Native N-linked Glycans by UHPLC with Charged Aerosol Detection

Analysis of Emulsifiers in Foods by High Pressure Liquid Chromatography and Corona Charged Aerosol Detection

Analysis of Phospholipids in Natural Samples by Normal Phase HPLC and Corona Charged Aerosol Detection

Marc Plante, Bruce Bailey, and Ian N. Acworth Thermo Fisher Scientific, Chelmsford, MA, USA

Rapid and Direct Analysis of Free Phytosterols by Reversed Phase HPLC with Electrochemical Detection

Impurity Profiling of Carbamazepine by HPLC/UV

Determination of Clinically Relevant Compounds using HPLC and Electrochemical Detection with a Boron-Doped Diamond Electrode

Determination of Polymerized Triglycerides by High Pressure Liquid Chromatography and Corona Veo Charged Aerosol Detector

Novel, Universal Approach for the Measurement of Natural Products in a Variety of Botanicals and Supplements, Part 2

Detection and Quantification of Inorganic Arsenic in Fruit Juices by Capillary Ion Chromatography with Suppressed Conductivity Detection

Measuring Phytosterols in Health Supplements by LC/MS. Marcus Miller and William Schnute Thermo Fisher Scientific, San Jose, CA, USA

Characterization of Used Cooking Oils by High Performance Liquid Chromatography and Corona Charged Aerosol Detection

Mercury Speciation Determinations in Asian Dietary Supplements

High-Throughput, Cost-Efficient LC-MS/MS Forensic Method for Measuring Buprenorphine and Norbuprenorphine in Urine

Determination of Olive Oil Adulteration by Principal Component Analysis with HPLC Charged Aerosol Detector Data

A Rapid UHPLC Method for the Analysis of Biogenic Amines and Metabolites in Microdialysis Samples

LC-MS/MS Method for the Determination of Tenofovir from Plasma

Rapid and sensitive UHPLC screening of additives in carbonated beverages with a robust organic acid column

Improved Extraction and Analysis of Hexavalent Chromium from Soil and Water

Enhanced LC-MS Sensitivity of Vitamin D Assay by Selection of Appropriate Mobile Phase

Rapid and sensitive UHPLC screening for water soluble vitamins in sports beverages

MS/MS as an LC Detector for the Screening of Drugs and Their Metabolites in Race Horse Urine

High-Throughput Quantitative LC-MS/MS Analysis of 6 Opiates and 14 Benzodiazepines in Urine

Fast UHPLC Methods for Analysis of Amino Acids

The Investigation of Factors Contributing to Immunosuppressant Drugs Response Variability in LC-MS/MS Analysis

LC-MS/MS Method for the Determination of 21 Opiates and Opiate Derivatives in Urine

SPE-LC-MS/MS Method for the Determination of Nicotine, Cotinine, and Trans-3-hydroxycotinine in Urine

Development and Validation of a Polysorbate 20 Assay in a Therapeutic Antibody Formulation by RP-HPLC and Charged Aerosol Detector (CAD)

Bioanalytical Quantitation of Biotherapeutics Using Intact Protein vs. Proteolytic Peptides by LC-HR/AM on a Q Exactive MS

Carl Fisher, Terri Christison, Hua Yang, Monika Verma, and Linda Lopez Thermo Fisher Scientific, Sunnyvale, CA, USA

A New HILIC/RP Mixed-Mode Column and Its Applications in Surfactant Analysis

GC-MS/MS Analysis of Benzodiazepines Using Analyte Protectants

Quantitative Analysis of THC and Main Metabolites in Whole Blood Using Tandem Mass Spectrometry and Automated Online Sample Preparation

Comparison of Full Scan MS2 and MS3 Linear Ion Trap Approaches for Quantitation of Vitamin D

Dayana Argoti, Kerry Hassell, Sarah J. Fair, and Joseph Herman Thermo Fisher Scientific, Franklin, MA, USA

Determination of Clinically Relevant Compounds using HPLC and Electrochemical Detection with Boron-Doped Diamond Electrode

Mass-Based Purification of Natural Product Impurities Using an Agilent 1260 Infinity II Preparative LC/MSD System

Sialic Acid Determination in Glycoproteins: Comparison of Two Liquid Chromatography Methods. Experimental. Introduction. Method 1.

Application Note. Agilent Application Solution Analysis of ascorbic acid, citric acid and benzoic acid in orange juice. Author. Abstract.

Determination of Water- and Fat-Soluble Vitamins in Nutritional Supplements by HPLC with UV Detection

F. Al-Rimawi* Faculty of Science and Technology, Al-Quds University, P.O. Box 20002, East Jerusalem. Abstract

Doubling the throughput of long chromatographic methods by using a novel Dual LC workflow

Robust extraction, separation, and quantitation of structural isomer steroids from human plasma by SPE-UHPLC-MS/MS

Thermo Fisher Scientific, Sunnyvale, CA, USA; 2 Thermo Fisher Scientific, San Jose, CA, USA

Integrated Targeted Quantitation Method for Insulin and its Therapeutic Analogs

Core-Shell Technology for Proteins and Peptides

Determination of Carbohydrates in Kombucha Using HPAE-PAD

Journal of Chemical and Pharmaceutical Research

Sensitive Analysis of Commonly Used Artificial and Natural Sweeteners Including Stevia and Their Impurities and Degradation Products

Ensuring High Sensitivity and Consistent Response in UHPLC-MS Analyses

GlycanPac AXR-1 Columns

Determination of Ethyl Sulfate Impurity in Indinavir Sulfate Drug Using Ion Chromatography

New Solvent Grade Targeted for Trace Analysis by UHPLC-MS

Analysis of Commercially Available Products Containing Stevia

A Versatile Detector for the Sensitive and Selective Measurement of Numerous Fat-Soluble Vitamins and Antioxidants in Human Plasma and Plant Extracts

Detection of oxygenated polycyclic aromatic hydrocarbons (oxy-pahs) in APCI mode with a single quadrupole mass spectrometer

Determination of Tigecycline in a Cell Lysate

Determination of Plant-Derived Neutral Oligo- and Polysaccharides Using the CarboPac PA200

ASSAY AND IMPURITY METHOD FOR DURACOR TABLETS BY HPLC

Sanjog Ramdharane 1, Dr. Vinay Gaitonde 2

Robust and Fast Analysis of Tobacco-Specific Nitrosamines by LC-MS/MS

Rapid determination of phosphate and citrate in carbonated soft drinks using ion chromatography

Solving One of Chromatography s Biggest Dilemmas Proper Sealing of Chromatography Autosampler Vials

High-Resolution Analysis of Intact Triglycerides by Reversed Phase HPLC Using the Agilent 1290 Infinity LC UHPLC System

Testing robustness: Immunosuppressant drugs in blood with a TSQ Quantis MS for clinical research

2D-LC as an Automated Desalting Tool for MSD Analysis

Evaluation of an LC-MS/MS Research Method for the Analysis of 33 Benzodiazepines and their Metabolites

Selectivity Comparison of Agilent Poroshell 120 Phases in the Separation of Butter Antioxidants

Determination of Inorganic Ions and Organic Acids in Non-Alcoholic Carbonated Beverages

Increased Identification Coverage and Throughput for Complex Lipidomes

Fast and easy separation of 23 drugs of abuse. including high, stable resolution of isobaric opioids from human urine by UHPLC-MS/MS

Determination of Amantadine Residues in Chicken by LCMS-8040

New Solvent Grade Targeted for Trace Analysis by UHPLC-MS

UPLC/MS Monitoring of Water-Soluble Vitamin Bs in Cell Culture Media in Minutes

Increasing resolution using longer columns while maintaining analysis time Advantages of the wide power range of the Agilent 1290 Infinity LC System

Simultaneous Analysis of Active Pharmaceutical Ingredients and Their Counter-Ions Using a Mixed-Mode Column

The Determination of Sugars in Molasses by High-Performance Anion Exchange with Pulsed Amperometric Detection

New Solvent Grade Targeted for Trace Analysis by UHPLC-MS

Effective use of Pharmacopeia guidelines to reduce cost of chromatographic analysis for Fluticasone propionate

Analysis of Isoflavones with the PerkinElmer Flexar FX-15 UHPLC System Equipped with a PDA Detector

Pelagia Research Library

APPLICATIONS TN µm Core-Shell Particle. (continued on page 2) Page 1 of 8. For additional technical notes, visit

Providing a Universal, One-step Alternative to Liquid-Liquid Extraction in Bioanalysis

Thermo Scientific LipidSearch Software for Lipidomics Workflows. Automated Identification and Relative. Quantitation of Lipids by LC/MS

ACQUITY UPLC WITH PDA DETECTION: DETERMINING THE SENSITIVITY LIMITS OF OXYBUTYNIN AND RELATED COMPOUNDS

SeQuant ZIC -HILIC For all who expect more...

SeQuant ZIC -HILIC For all who expect more...

Application Note. Agilent Application Solution Analysis of fat-soluble vitamins from food matrix for nutrition labeling. Abstract.

FT-Raman Surface Mapping of Remineralized Artificial Dental Caries

Improving Food Process Control Using the

Converting a CHP Method for Insulin to Agilent Poroshell 120 Columns

Determination of Steviol Glycosides by HPLC with UV and ELS Detections

Determination of Benzoate in Liquid Food Products by Reagent-Free Ion Chromatography

USP purity analysis of pravastatin sodium using the Agilent 1120 Compact LC

Increasing Extraction Efficiency of Wet Samples Using a Novel New Polymer During Accelerated Solvent Extraction

Analytical Method Development for USP Related Compounds in Paclitaxel Using an Agilent Poroshell 120 PFP

Small Scale Preparative Isolation of Corticosteroid Degradation Products Using Mass-Based Fraction Collection Application

vii LIST OF TABLES TABLE NO DESCRIPTION PAGE 1.1 System Suitability Parameters and Recommendations Acidic and Alkaline Hydrolysis 15

APPLICATIONS TN Overview of Kinetex 2.6 µm Core-Shell Technology

Transcription:

Direct Analysis of Multicomponent Adjuvants by HPLC with Charged Aerosol Detection David Thomas, Ian Acworth, Bruce Bailey, Marc Plante Thermo Fisher Scientific, Chelmsford, MA, USA

Overview Purpose: To develop fast and sensitive HPLC methods suitable to measure the purity of immunological adjuvant formulations. Methods: Adjuvant mixtures and individual components were analyzed by ultra-high performance liquid chromatography (UHPLC) employing octylsilyl (C8) and perfluorophenyl l (PFP) stationary ti phases on either sub-2 micron porous silica or 2.6 micron solid core silica particles. Analytes were detected by both charged aerosol detection and photodiode array detection. Results: Charged aerosol detection is shown to be suitable for measuring components including triterpenoid saponins, cholesterol, phospholipids, and surfactants with sensitivity often superior to that obtained by UV absorbance detection. Introduction A vaccine adjuvant is any substance that helps promote the effectiveness of a vaccine by reducing the amount or frequency of the required dose, by prolonging the duration of immunological memory, or by modulating the involvement of humoral or cellular responses. This functional definition of adjuvants encompasses a very diverse group of substances whose chemical structures and mechanisms of action vary widely. Adjuvants for human or animal vaccines are typically subjected to rigorous standards of analysis including quantification of strength, purity, stability, and degradation behavior, even though they are not currently regulated in the same manner as active pharmaceutical ingredients in the United States. Complicating such analysis, many adjuvants under investigation contain components that are not readily analyzed by traditional HPLC with UV detection. These include various mixtures of lipids, fatty acids, and glycosides that lack suitable UV chromophores. In this work, the lack of a detectable chromophore in several adjuvant compounds and degradation products was overcome by using HPLC with charged aerosol detection, a detector that can measure any non-volatile compound. Adjuvant mixtures and individual components were analyzed by UHPLC employing octylsilyl (C8) and perfluorophenyl (PFP) stationary phases on either sub-2 micron porous silica or 2.6 micron solid core silica particles. Analytes were detected by both charged aerosol detection and diode array detection. The charged aerosol detector is a sensitive, mass-based detector, especially well- suited for the determination of any nonvolatile analyte independent of chemical characteristics. As shown in Figure 1, the detector nebulizes the mobile phase to create aerosol droplets. The mobile phase evaporates in the drying tube, leaving analyte particles, which become charged in the mixing chamber. The charge is then measured by a highly sensitive electrometer, providing reproducible, nanogram-level sensitivity. This technology has greater sensitivity and precision than evaporative light scattering detection and refractive index detection and it is simpler to operate than a mass spectrometer. FIGURE 1. Charged Aerosol Detector and Principle of Operation HPLC eluent Nebulization and Impactor Drying tube Signal out Liquid waste Ion trap Collector / Electrometer Dried particles Mixing chamber Corona wire 2 Direct Analysis of Multicomponent Adjuvants by HPLC with Charged Aerosol Detection

Methods Liquid Chromatography Thermo Scientific Dionex UltiMate 3000 RSLC system with a Diode Array Detector DAD 3000 RS and a Corona ultra RS Charged Aerosol Detector: Nebulizer Temperature: 25 C Power function: 1.00 Data collection rate: 20 Hz Reagents: HPLC- or LCMS-grade or better Data Analysis CDS: Thermo Scientific Dionex Chromeleon Chromatography Data System 7.1 SR1 AbISCO- Thermo Scientific Hypersil GOLD PFP 1.9 µm, 2.1 mm Column Temp: 45 C 0.47 ml/min Injection Vol.: 10 µl Mobile Phase A: 0.1% formic acid in water Mobile Phase B: 0.1% formic acid in 10:90 acetonitrile:reagent alcohol Gradient: Time, %B: -5, 35; 0, 35; 7, 80; 12, 80. ABISCO- (ISCONOVA, Uppsala Sweden) was diluted 5-fold with Milli-Q water and transferred to a glass HPLC autosampler vial. AddaVax Thermo Scientific Accucore C8 2.6 µm, 4.6 150 mm Column Temp: 40 C 0.80 ml/min Injection Vol.: 10 µl Mobile Phase A: 1 mm ammonium acetate in water Mobile Phase B: 2-propanol, Fisher Scientific Optima 2 LC/MS Gradient: Time, %B: 0, 65; 3, 65; 13, 90; 18, 90; 18.1, 65; 30, 65. AddaVax (InvivoGen, San Diego, CA) was diluted 10-fold with Milli-Q water and transferred to a glass HPLC autosampler vial. Squalene-tocopherol-PS80 mixture Thermo Scientific Accucore PFP 2.6 µm, 2.1 mm Column Temp: 45 C 0.50 ml/min Injection Vol.: 1 or 3 µl Mobile Phase A: 0.1% formic acid in water Mobile Phase B: 8% formic acid in 2-propanol, Optima 2 LC/MS Gradient: Time, %B: -5, 30; 0, 30; 13, 95; 18, 95 Dissolve 24.3 mg DL-α-tocopherol (Acros Organics, NJ) in 24.3 ml 2-propanol. Dissolve 48.7 mg squalene in 9.64 ml 2-propanol; dilute 5-fold with 2-propanol. Combine 214 µl squalene solution, 237 µl DL-α-tocopherol solution, 97 µl polysorbate 80 and 452 µl of 2-propanol. Synthetic MPLA Thermo Scientific Accucore C8 2.6 µm, 4.6 150 mm Column Temp: 40 C 0.80 ml/min Injection Vol.: 10 µl Mobile Phase A: 1 mm ammonium acetate in water Mobile Phase B: 2-propanol, Optima 2 LC/MS Gradient: Time, %B: 0, 65; 3, 65; 13, 90; 18, 90; 18.1, 65; 30, 65. Synthetic MPLA (Avanti Polar Lipids, GA) was dissolved in chloroform:methanol:water (CMW) 80:20:4 at a concentration of about 1 mg/ml and transferred to a glass HPLC autosampler vial. AddaVax, shown in Figure 4, is prepa (SPAN 85) in squalene oil (5% v/v) buffer (10 mm ph 6.5) 2. Thermo Scientific Poster Note PN70333_e 11/12S 3

Results AbISCO- AbISCO- is a suspension of purified saponins from Quillaja saponaria, cholesterol from sheep wool and egg phosphatidyl choline in phosphate buffered saline 1. As seen in Figure 2, all components elute within 12 min from the Hypersil GOLD PFP column with good resolution. All components and several degradation d products including cholesterol oxidation products (COP) and lyso-pc are detected by the charged aerosol detector, whereas some, such as DPPC, show poor response by UV detection. FIGURE 2. Charged aerosol response is significantly better than UV response for several components of AbISCO- separated by HPLC. 2 pa mau 200 18.0 180 16.0 160 14.0 140 12.0 120 8.0 cholesterol 80 6.0 60 4.0 2.0 saponins lyso PC COP phosphatidyl choline 40 20 0 min -1.0-10 2.0 4.0 6.0 8.0 12.0 13.0 Performance Calibration curves for the three major components of AbISCO (analyzed in duplicate) are presented in Figure 3. The data were fit to a quadratic equation, yielding coefficients of determination, R 2, greater than 0.999 for all three analytes. Table 1 presents a summary of the method s performance, including precision of retention time and peak area, the coefficient of determination, and the limits of detection for the three major components of AbISCO. Figure 3. Calibration data for analysis of AbISCO by HPLC-charged aerosol detection. saponin 3 External CAD_1 Cholesterol External CAD_1 DPPC External CAD_1 6.00 5.50 7.00 pa*min pa*min pa*min 5.50 0 0 4.50 6.00 Area 4.50 4.00 3.50 3.00 2.50 2.00 1.50 1.00 0.50 Area 4.00 3.50 3.00 2.50 2.00 1.50 1.00 0.50 Area 0 4.00 3.00 2.00 1.00 ug/ml ug/ml ug/ml 0 0 0 0 50 150 200 250 300 350 400 450 0 50 150 200 250 300 0 50 150 200 250 300 35 Table 1. Method performance for analysis of AbISCO by HPLC-charged aerosol detection. Component (µg/ml) Ret. Time 1 (%RSD) Peak Area 1 (%RSD) LOD 2 µg/ml Saponins 78.2 6 0.36 13.0 0.9998 Cholesterol 56.8 7 0.39 6.4 0.9999 DPPC 60.2 707 1.27 44 4.4 1.0000 1 for n = 10 replicates 2 Hubaux-Vos method * 7 levels, in duplicate, quadratic fit with no offset AddaVax AddaVax, shown in Figure 4, is prepared by emulsification of sorbitan trioleate (SPAN 85) in squalene oil (5% v/v) and polysorbate 80 (0.5% w/v) in sodium citrate buffer (10 mm ph 6.5) 2. R 2* 2 1-2.5 7.5 1 Tim 4 Direct Analysis of Multicomponent Adjuvants by HPLC with Charged Aerosol Detection

FIGURE 4. Chromatograms of AddaVax and emulsifiers by HPLC-charged aerosol detection. 160 0 140 squalene 900 120 800 80 700 600 500 60 40 20 0 AddaVax polysorbate 80 Span-85 400 300 200-20 -10 2.5 7.5 12.5 1 17.5 2 Squalene-based mixture Squalene is mixed with other components in several other adjuvants. The chromatogram shown in Fig 5 illustrates the results obtained with a mixture of squalene, DL-α-tocopherol and polysorbate 80 (PS 80). FIGURE 5. HPLC-charged aerosol detection chromatogram of a mixture of α-tocopherol, squalene and PS 80. pa pa 9.0 alpha-tocopherol 90 8.0 80 7.0 squalene 70 6.0 60 50 4.0 40 3.0 2.0 1.0 mixture squalene α tocopherol 30 20 10 0 min -1.0-5 2.0 4.0 6.0 8.0 12.0 14.0 16.0 18.0 smpla Synthetic monophosphoryl p lipid A, an analog of bacterial lipopolysaccharide p (LPS), has low toxicity while specifically activating TLR4 but not TLR2. smpla contains six acyl groups. Purity analysis is used to quantify contaminants, degradation products, and variants differing in acyl chain number, length, and phosphorylation 3. Figure 6 compares chromatograms obtained from analysis of smpla by inverse gradient HPLC with detection by UV absorbance at 220 nm or charged aerosol detection. FIGURE 6. Purity analysis of smpla by HPLC-UV-charged aerosol detection. 5 pa mau 5 4 4 4 4 3 3 3 3 7 1.27 4.4 1.0000 2 2 smpla 2 2 We would like to thank Isconova, Upp immunological reagent. 1 1 set ared by emulsification of sorbitan trioleate v) and polysorbate 80 (0.5% w/v) in sodium citrate Inverse gradient Standard gradient min - - 2.5 7.5 12.5 1 17.5 2 AddaVax is a trademark of InvivoGen, San Diego Uppsala, Sweden. Span 85 and Tween 80 are tra trademark of EMD Millipore Corporation. All othe subsidiaries. This information is not intended d to encourage use intellectual property rights of others. Thermo Scientific Poster Note PN70333_e 11/12S 5

Table 2. Summary of immunologic adjuvant components investigated in this study. (+) annotation indicates applicable detector. Component UV (220 nm) Charged Aerosol Saponins + + Cholesterol + + Diphosphatidyl choline (DPPC) + Mixed phosphatidyl cholines + Lyso-phosphatidyl choline + Sorbitan trioleate (Span 85) + Polysorbate 80 (Tween 80) + Squalene + + α-tocopherol + + smpla + + Conclusion The HPLC method developed to analyze AbISCO is precise, with retention time precision better than 0.1% RSD and peak area precision between 0.4 and 1.3% RSD for the major components. Charged aerosol detection enables sensitive measurement of adjuvant components not amenable to detection by UV absorbance. Detection limits for saponins, cholesterol, and DPPC were in the low µg/ml (ng on-column) range. By responding uniformly to structurally diverse compounds, charged aerosol detection is able to measure intact adjuvant species along with degradation products and potential impurities, yielding good estimates of relative concentration, even in the absence of pure primary standards. References 1. Picard, M.D.; Cohane, K.P.; Gierahn, T.M.; Higgins, i D.E.; Flechtner, J.B. Highthroughput proteomic screening identifies Chlamydia trachomatis antigens that are capable of eliciting T cell and antibody responses that provide protection against vaginal challenge. Vaccine. 2012, 30(29):4387-93. 2. Mbow M.L.; De Gregorio, E.; Valiante, N.M.; Rappuoli, R. New adjuvants for human vaccines. Curr Opin Immunol. 2010, 2(3):411-6. 3. Raetz, C.R.; Garrett, T.A.; Reynolds, C.M. et al. Kdo 2 -Lipid A of Escherichia coli, a defined endotoxin that activates macrophages via TLR-4. J. Lipid Res. 2006, 47:1097-1111. Acknowledgements We would like to thank Isconova, Uppsala, Sweden for making available the AbISCO immunological reagent. me [min] This information is not intended to encourage use of these products in any manners that might infringe the intellectual property rights of others. PO70333_E 10/12S 6 Direct Analysis of Multicomponent Adjuvants by HPLC with Charged Aerosol Detection

www.thermofisher.com/dionex 2016 Thermo Fisher Scientific Inc. All rights reserved. AddaVax is a trademark of InvivoGen, San Diego, CA. AbISCO- is a registered trademark of ISCONOVA, Uppsala, Sweden. Span 85 and Tween 80 are trademarks of Croda International Plc. Milli-Q is a registered trademark of EMD Millipore Corporation. All other trademarks are the property of Thermo Fisher Scientific Inc. and its subsidiaries. This information is presented as an example of the capabilities of Thermo Fisher Scientific Inc. products. It is not intended to encourage use of these products in any manners that might infringe the intellectual property rights of others. Specifications, terms and pricing are subject to change. Not all products are available in all countries. Please consult your local sales representative for details. Australia +61 3 9757 4486 Austria +43 1 333 50 34 0 Belgium +32 53 73 42 41 Brazil +55 11 3731 5140 China +852 2428 3282 Denmark +45 70 23 62 60 France +33 1 60 92 48 00 Germany +49 6126 991 0 India +91 22 2764 2735 Italy +39 02 51 62 1267 Japan +81 6 6885 1213 Korea +82 2 3420 8600 Netherlands +31 76 579 55 55 Singapore +65 6289 1190 Sweden +46 8 473 3380 Switzerland +41 62 205 9966 Taiwan +886 2 8751 6655 UK/Ireland +44 1442 233555 USA and Canada +847 295 7500 PN70333_E 07/16S