High-Resolution Charge Variant Analysis for Top-Selling Monoclonal Antibody Therapeutics Using a Linear ph Gradient Separation Platform

Similar documents
A Fast and Robust Linear ph Gradient Separation Platform for Monoclonal Antibody (MAb) Charge Variant Analysis

A Novel ph Gradient Separation Platform for Monoclonal Antibody (MAb) Charge-Variant Analysis

HIC as a Complementary, Confirmatory Tool to SEC for the Analysis of mab Aggregates

Development of Ultra-fast ph-gradient Ion Exchange Chromatography for the Separation of Monoclonal Antibody Charge Variants

Lifetime stability of size exclusion chromatography columns for protein aggregate analysis

A universal chromatography method for aggregate analysis of monoclonal antibodies

Developing Robust and Efficient IEX Methods for Charge Variant Analysis of Biotherapeutics Using ACQUITY UPLC H-Class System and Auto Blend Plus

Analysis of Monoclonal Antibodies and Their Fragments by Size Exclusion Chromatography Coupled with an Orbitrap Mass Spectrometer

Separate and Quantify Rituximab Aggregates and Fragments with High-Resolution SEC

An Automated System for At-Line Process Analysis of Biopharmaceutical Fermentation Reactions

Analysis of Intact and C-terminal Digested IgG1 on an Agilent Bio MAb 5 µm Column

Concentration of Human Hormones in Drinking Water Using Solid Phase Extraction and Analysis by High Performance Liquid Chromatography

Separation of Intact Monoclonal Antibody Sialylation Isoforms by ph Gradient Ion-Exchange Chromatography

Analysis of Monoclonal Antibodies and Their Fragments by Size-Exclusion Chromatography Coupled with an Orbitrap Mass Spectrometer

MAbPac SCX-10 Column for Monoclonal Antibody Variant Analysis and Characterization

Application Note. Author. Abstract. Biopharmaceuticals. Verified for Agilent 1260 Infinity II LC Bio-inert System. Sonja Schneider

MAbPac SCX-10 Columns

Characterize Fab and Fc Fragments by Cation-Exchange Chromatography

Practical guidance for switching between anion and cation analysis systems

mab Titer Analysis with the Agilent Bio-Monolith Protein A Column

Application of Agilent AdvanceBio Desalting-RP Cartridges for LC/MS Analysis of mabs A One- and Two-dimensional LC/MS Study

Application Note. Author. Abstract. Biotherapeutics and Biologics. Sonja Schneider Agilent Technologies, Inc. Waldbronn, Germany

Characterization of mab aggregation using a Cary 60 UV-Vis Spectrophotometer and the Agilent 1260 Infinity LC system

mabs and ADCs analysis by RP

Molecular Characterization of Biotherapeutics The Agilent 1260 Infi nity Multi-Detector Bio-SEC Solution with Advanced Light Scattering Detection

Determination of Oxalate and Other Anions in Bayer Liquor Using Ion Chromatography

Monitoring Monoclonal Antibody Heterogeneity by Cation-Exchange Chromatography

Precise Characterization of Intact Monoclonal Antibodies by the Agilent 6545XT AdvanceBio LC/Q-TOF

Disulfide Linkage Analysis of IgG1 using an Agilent 1260 Infinity Bio inert LC System with an Agilent ZORBAX RRHD Diphenyl sub 2 µm Column

Goldman Sachs Key Debates In Biosimilars Conference

Analysis of Glyphosate and AMPA in Environmental Water Samples by Ion Chromatography and On-Line Mass Spectrometry with Minimal Sample Preparation

High-throughput and Sensitive Size Exclusion Chromatography (SEC) of Biologics Using Agilent AdvanceBio SEC Columns

Technical Data. Analytical Data

Analysis of amoxicillin and five impurities on the Agilent 1220 Infinity LC System

Fast and High Resolution Analysis of Intact and Reduced Therapeutic Monoclonal Antibodies (mabs)

Maximizing Chromatographic Resolution of Peptide Maps using UPLC with Tandem Columns

Thermo Scientific EASY-nLC 1200 System. Leading in simplicity. and performance

Separation of Recombinant Human Erythropoietin (repo) Using Agilent Bio SEC-3

Agilent AdvanceBio SEC Columns for Aggregate Analysis: Instrument Compatibility

Effect of Temperature on IC Signal Noise

Application Note USD Purification of Mouse IgM from Cell Culture Supernatant by Cation Exchange Chromatography on CM Ceramic HyperD F Sorbent

Fast mass transfer Fast separations High throughput and improved productivity Long column lifetime Outstanding reproducibility Low carryover

Peptide Mapping: A Quality by Design (QbD) Approach

Fraction Analysis of Cysteine Linked Antibody-Drug Conjugates Using Hydrophobic Interaction. chromatography. Agilent 1260 Infinity II Bio-Inert System

Analysis of Intact Monoclonal Antibodies Using an M3 MicroLC with the TripleTOF 6600

Thermo Scientific Solutions for Intact-Protein Analysis. Better, Faster Decisions for. Biotherapeutic Development

Size Exclusion Chromatography of Biosimilar and Innovator Insulin Using the Agilent AdvanceBio SEC column

Monoclonal Antibody Characterization Achieving Higher Throughput and Productivity

Determination of Cations in Hydraulic Fracturing Flowback Water from the Marcellus Shale

SEC-MS with Volatile Buffers for Characterization of Biopharmaceuticals

2012 Waters Corporation 1

Application Note. Biopharma. Authors. Abstract. James Martosella, Phu Duong Agilent Technologies, Inc Centreville Rd Wilmington, DE 19808

Two-Dimensional LC Protein Separation on Monolithic Columns in a Fully Automated Workflow

Cell Clone Selection Using the Agilent Bio-Monolith Protein A Column and LC/MS

Thermo Scientific BioLC Columns. Monoclonal antibody. characterization

Comparison of Different Brands of Carrier Ampholytes for Monoclonal Antibody Charge Heterogeneity Analysis by Capillary Isoelectric Focusing

Analysis of Illegal Dyes in Food Matrices Using Automated Online Sample Preparation with Liquid Chromatography-Mass Spectrometry

Analysis of biomolecules by SEC and Ion-Exchange UPLC

Size Exclusion BioHPLC Columns

Bioanalysis of Intact Therapeutic Monoclonal Antibodies from Non-Human Primates Using MSIA D.A.R.T. S Technology

Chromatography Column Performance and Data Analysis Success Guide. Hints and Tips for Better Purifications

Determination of Sulfite in Food and Beverages by Ion Exclusion Chromatography with Pulsed Amperometric Detection

Application Note. Author. Abstract. Small Molecule Pharmaceuticals. Sonja Krieger Agilent Technologies, Inc. Waldbronn, Germany

Quantification of Drug Metabolites in Early-Stage Drug Discovery Testing

R R Innovation Way P/N SECKIT-7830 Newark, DE 19711, USA Tel: Fax: Website: Published in November 2013

Optimization of cief to Resolve Challenging MAb Samples of Clinical Immunodiagnostic Relevance

Thermo Scientific Peptide Mapping Workflows. Upgrade Your Maps. Fast, confident and more reliable peptide mapping.

TSKgel STAT Columns for High Performance Ion Exchange Chromatography

Determination of Oversulfated Chondroitin Sulfate and Dermatan Sulfate in Heparin Sodium Using Anion-Exchange Chromatography with UV Detection

Determination of Trace Copper, Nickel, and Zinc in Boiling Water Reactors Using Nonsuppressed Conductivity Detection

Development of Analysis Methods for Therapeutic Monoclonal Antibodies Using Innovative Superficially Porous Particle Biocolumns

Protein-Pak Hi Res HIC Column and HIC Protein Standard

A Generic Kit-Based Approach for Quantifying Monoclonal Antibody Drugs Through Direct Digestion of Discovery Study Samples

Improving Resolution and Column Loading Systematically in Preparative Liquid Chromatography for Isolating a Minor Component from Peppermint Extract

Quality-by-Design-Based Method Development Using an Agilent 1290 Infinity II LC

Fast Online Desalting of mabs Using a Reversed-Phase Desalting Cartridge for LC-MS Analysis

N-Glycan Profiling Analysis of a Monoclonal Antibody Using UHPLC/FLD/Q-TOF

Analysis of TCM injections using the Agilent 1290 Infinity LC system

Instructions for Capillary Electrophoresis Peptide Analysis Kit

Method Development Considerations for Reversed-Phase Protein Separations

Determination of Adenovirus pviii (31K) Concentration for Estimation of the Empty Capsid Concentration of the Adenovirus Reference Material (ARM)

Fast and Efficient Peptide Mapping of a Monoclonal Antibody (mab): UHPLC Performance with Superficially Porous Particles

BioHPLC columns. Tim Rice Biocolumn Technical Specialist

UFFLC of the Proteome Ultra High Pressure and Ultra Fast Flow Liquid Chromatography: A New Approach To Proteomics

Bio-Monolith Protein G Column - More Options for mab Titer Determination

INTERNATIONAL PHARMACOPOEIA MONOGRAPH ON ARTEMETHER AND LUMEFANTRINE CAPSULES REVISED DRAFT FOR DISCUSSION

High Resolution Analysis of Heparin and Heparin-like Impurities on Glycomix TM an Anion Exchange Column

Polishing of monoclonal antibodies using Capto S ImpAct

columns IonPac ICE-AS1 Ion-Exclusion Column Superior Chromatographic Performance Separates weakly ionized acids by differences in pk a

SMART Digest Kit User Manual. Version 2

Optimizing the Purification of a Standard Chiral Compound Utilizing a Benchtop, Multi-Purpose, Semi-Preparative to Preparative HPLC System

Size-Exclusion Chromatography (SEC) Optimization Guide

The Quantitative Analysis of Curcuminoids in Food and Food Additives Using Rapid HPLC With Electrochemical, UV, or Fluorescence Detection

PLRP-S Polymeric Reversed-Phase Column for LC/MS Separation of mabs and ADC

Technical Overview. Author. Abstract. Edgar Naegele Agilent Technologies, Inc. Waldbronn, Germany

Affi-Gel Protein A MAPS II Kit Instruction Manual

Microflow Liquid Chromatography Mass Spectrometry System. Nexera Mikros C146-E350

ALLIANCE SYSTEM FOR CARBAMATE ANALYSIS

Thermo Scientific icap 7000 Plus Series ICP-OES. Gain more power. experience more performance

Transcription:

High-Resolution Charge Variant Analysis for Top-Selling Monoclonal Antibody Therapeutics Using a Linear ph Gradient Separation Platform Shanhua Lin and Chris Pohl, Thermo Fisher Scientific, Sunnyvale, CA, USA Application Note 9 Key Words Rituxan, rituximab, Herceptin, trastuzumab, Humira, adalimumab, Avastin, bevacizumab, CX- ph Gradient Buffer Kit, MAbPac SCX-, mab charge variant analysis Goal To develop a high-resolution charge variant analysis for Rituxan (rituximab), Herceptin (trastuzumab), Humira (adalimumab), and Avastin (bevacizumab) using a linear ph gradient separation method. Introduction Monoclonal antibody (mab) therapeutics is a quickly growing market. In, of the top ten bestselling pharmaceutical products, five were monoclonal antibodies (Humira, Remicade, Rituxan, Herceptin, and Avastin). Humira sales revenue alone exceeded $ billion. With the patent protection for these blockbuster drugs expiring in the next few years, many companies are entering the development of biogenerics, also known as the biosimilars. In order to demonstrate the safety and efficacy of the biosimilars and gain approval of the regulatory agency, it is essential to detect, characterize, and quantify impurities as well as structural variants of these biosimilars. Some structural variants, such as charge variants, have been demonstrated as critical quality attributes (CQAs). Charge variants of mabs are due to modifications such as sialylation, deamidation, and C-terminal lysine truncation. Traditionally, salt gradient cation-exchange chromatography has been used with some success in characterizing mab charge variants. However, significant effort is often required to tailor the salt gradient method for each individual mab. In the fast-paced drug development environment, a quick and robust platform method is desirable to accommodate the majority of the mab analyses. Thermo Fisher Scientific recently introduced cation-exchange ph gradient buffers that meet these platform method requirements. The buffer system consists of a low-ph buffer A at ph 5.6 and a high-ph buffer B at ph.. A linear ph gradient from ph 5.6 to ph. is generated over time by running a linear pump gradient from % buffer A to % buffer B. In this study, the charge variants of Rituxan (rituximab), Herceptin (trastuzumab), Humira (adalimumab), and Avastin (bevacizumab) are analyzed on a Thermo Scientific MAbPac SCX- column with a linear ph gradient separation method. The linear gradient from ph 5.6 to ph. is generated over time by running a linear pump gradient from % Thermo Scientific CX- ph Gradient Buffer A (ph 5.6) to % CX- ph Gradient Buffer B (ph.). The results demonstrate the general applicability of the ph gradient method on monoclonal antibody charge variant analysis. The data also show that the ph gradient method delivers higher-resolution power than the traditional salt method. The methods described here can be widely used in the development of the biosimilars of these top-selling mabs.

Experimental Chemicals and Reagents Deionized (DI) water, 8. MΩ-cm resistivity MES hydrate [ 99.5%] Sodium chloride [NaCl, 99.5%] Rituxan, Herceptin, Humira, and Avastin were a gift from a biotechnology company. Sample Handling Equipment Polypropylene,. ml vials (P/N 5548) Columns and Buffers MAbPac SCX-, µm, 4 5 mm (P/N 7465) CX- ph Gradient Buffer A (ph 5.6), 5 ml (P/N 87) CX- ph Gradient Buffer B (ph.), 5 ml (P/N 875) LC Separation The LC separation conditions were as follows: Instrumentation Thermo Scientific Dionex UltiMate BioRS system equipped with: SRD-4 Solvent Racks with degasser (P/N 55.945) HPG-4RS Biocompatible Binary Rapid Separation Pump (P/N 5446) WPS-TBRS Biocompatible Rapid Separation Thermostatted Autosampler (P/N 584.) TCC-RS Rapid Separation Thermostatted Column Compartment (P/N 57) VWD-4RS Rapid Separation Variable Wavelength Detector (P/N 574.) equipped with a semi-micro flow cell PEEK,.5 μl volume, 7 mm path length, PCM- ph and Conductivity Monitor (P/N 68.5) ph gradient mobile phase A ph gradient mobile phase B Salt gradient mobile phase A Salt gradient mobile phase B X CX- ph Gradient Buffer A Dilute CX- ph Gradient Buffer A -fold using deionized water. X CX- ph Gradient Buffer B Dilute CX- ph Gradient Buffer B -fold using deionized water. mm MES (ph 5.6) + 6 mm NaCl Add.9 g of MES (Sigma) to 9 ml of deionized water. Adjust the ph with NaOH to 5.6 and add 7.5 g of NaCl, adjust volume to L and filter through a. µm filter before use. mm MES (ph 5.6) + mm NaCl Add.9 g of MES (Sigma) to 9 ml of deionized water. Adjust the ph with NaOH to 5.6 and add 58.44 g of NaCl, adjust volume to L and filter through a. µm filter before use. Full ph gradient ph 5.6 to ph. Time (min) %A %B.. 4. 4. 4 Half ph gradient ph 5.6 to ph 7.9 Time (min) %A %B.. 5 4. 5 4. 4 Full salt gradient 6 mm NaCl to mm NaCl Time (min) %A %B.. 4. 4. 4 Half salt gradient 6 mm NaCl to 8 mm NaCl Time (min) %A %B.. 5 4. 5 4. 4 Flow rate Run time ml/min 4 min Temperature C UV detector wavelength 8 nm Injection volume 5 µl Samples Rituximab, 5 mg/ml; Trastuzumab, 5 mg/ml; Adalimumab, 5 mg/ml; Bevacizumab, mg/ml Data Processing Thermo Scientific Dionex Chromeleon 6.8 Chromatography Data System

Results and Discussion The CX- ph gradient buffer kit generates a linear ph gradient when a linear pump gradient is run from % CX- buffer A to % buffer B. This ph gradient method serves as a platform method for the mab charge variant analysis, covering the ph range from 5.6 to.. Most of the therapeutic mabs have pi values falling within this ph range. Rituxiamab (Figure a), trastuzumab (Figure a), adalimumab (Figure 5a), and bevacizumab (Figure 7a) were analyzed on a MAbPac SCX- column using the full ph gradient method. Satisfactory separations of multiple variants were observed with all four samples. After the initial survey runs of the full ph gradient, the subsequent runs were aimed at improving resolution by decreasing the ph range and gradient slope. The fact that the ph gradient was linear made the method optimization simple. Rituximab (Figure b), trastuzumab (Figureb), adalimumab (Figure 5b), and bevacizumab (Figure 7b) were analyzed using a shallower ph gradient with half the ph range. The variants were identified as peaks,, in the chromatograms. Improved separations of the variants were observed in all cases. Traditionally, the salt gradient method has been used for mab charge variants analysis. The salt gradient method development usually requires screening at different ph values using different buffers. In addition, the minimum salt concentration required to elute the mab off the cation exchange column must be individually determined. For comparison and speed, the same initial conditions and buffers ( mm MES and 6 mm NaCl at ph 5.6) were used for all the samples in this study. Rituxiamab (Figures a and b), trastuzumab (Figures 4a and 4b), adalimumab (Figures 6a and 6b), and bevacizumab (Figures 8a and 8b) were each analyzed by two salt gradient methods: one with steeper gradient slope and the other one with shallower gradient slope. The separation profiles obtained by the ph and salt gradient methods were similar for the same molecule. In order to simplify the comparison, the acidic variant adjacent to the major variant was labeled as peak, the major variant was labeled as peak, and the basic variant adjacent to the major variant was labeled as peak for each chromatogram (Figures 8). In the case of the trastuzumab salt gradient chromatogram, the minor acidic variant was very close to the major peak and could be not be determined, but this was resolved by the ph gradient. Table lists the retention time of peak (RT), peak (RT), and peak (RT) and the difference between RT and RT ( RT-), as well as RT and RT ( RT-). In the case of rituximab, trastuzumab, and bevacizumab, it is clear that the RTs between variants were greater when using the ph gradient profile. In the case of adalimumab, the RTs were similar between the ph gradient profile and the salt gradient profile. Table. Retention time of mab charge variants analyzed by linear ph gradient and salt gradient methods. Method Gradient RT (min) RT (min) RT (min) RT (min) RT (min) Rituxan/rituximab Herceptin/trastuzumab Humira/adalimumab Avastin/bevacizumab ph salt ph salt ph salt ph salt full 7.497 7.86 8.477.6.67 half.98.7.77.7.67 full.97..54.8.94 half.44.78.567.4.784 full 5.57 5.744 6.7.487.46 half 7.44 7.94 8.88.5.94 full n.a..4.477 n.a..7 half n.a..494.844 n.a..5 full 6.6 6.6 6.59.97. half 8.84 9.44 9.97.4.66 full 5.54 5.56 5.9 6.4 half 6.877 7.67 7.947.9.68 full.57.84.64.87.44 half 9.977.55.4.576.88 full.494.74 4...86 half.6.87 4.587.457.77

4 Rituxan ph Gradient % B Rituxan ph Gradient 5% B a b 7 8 5 6 4 7.5-8.. 4. 6. 8.. 4. 6. 8. Mobile Phase A: X CX- ph gradient buffer A, ph 5.6 Mobile Phase B: X CX- ph gradient buffer B, ph. ph Gradient: % B to % B from to min Sample: Rituxan/rituximab (5 mg/ml).5-8.. 4. 6. 8.. Mobile Phase A: X CX- ph gradient buffer A, ph 5.6 Mobile Phase B: X CX- ph gradient buffer B, ph. ph Gradient: % B to 5% B from to min Sample: Rituxan/rituximab (5 mg/ml) Figure. Rituxan/rituximab charge variant analysis using linear ph gradient. (a) Full ph gradient; (b) Half ph gradient. Rituxan Salt Gradient % B a 4 Rituxan Salt Gradient 5% B b 9 6 75 5 4 5-8.. 4. 6. 8.. 4. 6. 8. Mobile Phase A: mm MES (ph 5.6) + 6 mm NaCl Mobile Phase B: mm MES (ph 5.6) + mm NaCl Salt Gradient: % B to % B from to min Sample: Rituxan/rituximab (5 mg/ml) - 8.. 4. 6. 8.. Mobile Phase A: mm MES (ph 5.6) + 6 mm NaCl Mobile Phase B: mm MES (ph 5.6) + mm NaCl Salt Gradient: % B to 5% B from to min Sample: Rituxan/rituximab (5 mg/ml) Figure. Rituxan/rituximab charge variant analysis using salt gradient. (a) Full salt gradient; (b) Half salt gradient.

Herceptin ph Gradient % B Herceptin ph Gradient 5% B 5 a b 7 8 5 6 4 7.5.5-8.. 4. 6. 8.. 4. 6. 8. Mobile Phase A: X CX- ph gradient buffer A, ph 5.6 Mobile Phase B: X CX- ph gradient buffer B, ph. ph Gradient: % B to % B from to min Sample: Herceptin/trastuzumab (5 mg/ml) - 8.. 4. 6. 8.. Mobile Phase A: X CX- ph gradient buffer A, ph 5.6 Mobile Phase B: X CX- ph gradient buffer B, ph. ph Gradient: % B to 5% B from to min Sample: Herceptin/trastuzumab (5 mg/ml) Figure. Herceptin/trastuzumab charge variant analysis using linear ph gradient. (a) Full ph gradient; (b) Half ph gradient. Herceptin Salt Gradient % B a 8 Herceptin Salt Gradient 5% B b 7 5 6 4 7.5.5-8.. 4. 6. 8.. 4. 6. 8. Mobile Phase A: mm MES (ph 5.6) + 6 mm NaCl Mobile Phase B: mm MES (ph 5.6) + mm NaCl Salt Gradient: % B to % B from to min Sample: Herceptin/trastuzumab (5 mg/ml) - 8.. 4. 6. 8.. Mobile Phase A: mm MES (ph 5.6) + 6 mm NaCl Mobile Phase B: mm MES (ph 5.6) + mm NaCl Salt Gradient: % B to 5% B from to min Sample: Herceptin/trastuzumab (5 mg/ml) Figure 4. Herceptin/trastuzumab charge variant analysis using salt gradient. (a) Full salt gradient; (b) Half salt gradient.

6 Humira ph Gradient % B Humira ph Gradient 5% B a b 8. - 8.. 4. 6. 8.. 4. 6. 8. Mobile Phase A: X CX- ph gradient buffer A, ph 5.6 Mobile Phase B: X CX- ph gradient buffer B, ph. ph Gradient: % B to % B from to min Sample: Humira/adalimumab (5 mg/ml) -. 8.. 4. 6. 8.. Mobile Phase A: X CX- ph gradient buffer A, ph 5.6 Mobile Phase B: X CX- ph gradient buffer B, ph. ph Gradient: % B to 5% B from to min Sample: Humira/adalimumab (5 mg/ml) Figure 5. Himira/adalimumab charge variant analysis using linear ph gradient. (a) Full ph gradient; (b) Half ph gradient. Humira Salt Gradient % B a. Humira Salt Gradient 5% B b 4. -. 8.. 4. 6. 8.. 4. 6. 8. Mobile Phase A: mm MES (ph 5.6) + 6 mm NaCl Mobile Phase B: mm MES (ph 5.6) + mm NaCl Salt Gradient: % B to % B from to min Sample: Humira/adalimumab (5 mg/ml) 7.5.5 -. 8.. 4. 6. 8.. Mobile Phase A: mm MES (ph 5.6) + 6 mm NaCl Mobile Phase B: mm MES (ph 5.6) + mm NaCl Salt Gradient: % B to % B from to min Sample: Humira/adalimumab (5 mg/ml) Figure 6. Himira/adalimumab charge variant analysis using salt gradient. (a) Full salt gradient; (b) Half salt gradient.

Avastin ph Gradient % B a - 8.. 4. 6. 8.. 4. 6. 8. Mobile Phase A: X CX- ph gradient buffer A, ph 5.6 Mobile Phase B: X CX- ph gradient buffer B, ph. ph Gradient: % B to % B from to min Sample: Avastin/bevacizumab ( mg/ml) Avastin ph Gradient 5% B b -. 8.. 4. 6. 8.. Mobile Phase A: X CX- ph gradient buffer A, ph 5.6 Mobile Phase B: X CX- ph gradient buffer B, ph. ph Gradient: % B to 5% B from to min Sample: Avastin/bevacizumab ( mg/ml) 7 Figure 7. Avastin/bevacizumab charge variant analysis using linear ph gradient. (a) Full ph gradient; (b) Half ph gradient. Avastin Salt Gradient % B a Avastin Salt Gradient 5% B b 4. 7.5.5-8.. 4. 6. 8.. 4. 6. 8. Mobile Phase A: mm MES (ph 5.6) + 6 mm NaCl Mobile Phase B: mm MES (ph 5.6) + mm NaCl Salt Gradient: % B to % B from to min Sample: Avastin/bevacizumab( mg/ml) -. 8.. 4. 6. 8.. Mobile Phase A: mm MES (ph 5.6) + 6 mm NaCl Mobile Phase B: mm MES (ph 5.6) + mm NaCl Salt Gradient: % B to % B from to min Sample: Avastin/bevacizumab ( mg/ml) Figure 8. Avastin/bevacizumab charge variant analysis using salt gradient. (a) Full salt gradient; (b) Half salt gradient.

Conclusion The linear ph gradient method is a platform method for mab charge variant analysis. It can be easily optimized to improve separation and delivers better charge variant separation than the salt gradient method. References http://www.pmlive.com/top_pharma_list/ Top_5_pharmaceutical_products_by_global_sales Lin, S.; Baek, J.; Decrop, W.; Rao, S.; Agroskin, Y.; and Pohl, C. Development of a Cation-Exchange ph Gradient Separation Platform. Presented at 9th International Symposium on High Performance Liquid Phase Separations and Related Techniques, Amsterdam, The Netherlands, June 6-,. Vlasak J. and Ionescu R. Heterogeneity of Monoclonal Antibodies Revealed by Charge-Sensitive Methods, Current Pharmaceutical Biotechnology, 8, 9, 468-48. Application Note 9 For Research Use Only thermoscientific.com/biolc 6 Thermo Fisher Scientific Inc. All rights reserved. Rituxan is a registered trademark of Biogen. Idec, Inc. Herceptin and Avastin are registered trademarks of Genentech, Inc. Humira is a registered trademark of Abbott Laboratories. All other trademarks are the property of Thermo Fisher Scientificand its subsidiaries. This information is presented as an example of the capabilities of Thermo Fisher Scientific 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. USA and Canada + 8 Australia 75 9 (free call domestic) China 8 8 58 (free call domestic) 4 65 58 France + () 6 9 48 4 Germany +49 () 4 94 or India +9 674 9494 +9 7 766 5 AN9-EN66S Japan 75 67 (free call domestic) 75 67 (fax) Korea +8 4 86 United Kingdom +44 () 98 54 New Zealand 8 9 966 (free call domestic) Singapore +65 689 9 All Other Enquiries +44 () 98 54 5 Technical Support For advice and support, please visit our website: www.thermoscientific.com/chromexpert