Vincenzo Pucci Merck Global Bioanalytics 7 th EBF, November 2014

Similar documents
Jennifer L. Simeone and Paul D. Rainville Waters Corporation, Milford, MA, USA A P P L I C AT ION B E N E F I T S INT RO DU C T ION

High sensitivity assays using online SPE-LC-MS/MS -How low can you go? Mohammed Abrar Unilabs York Bioanalytical solutions, York, UK

Fast, Reproducible LC-MS/MS Analysis of Dextromethorphan and Dextrorphan

SPE, LC-MS/MS Method for the Determination of Ethinyl Estradiol from Human Plasma

MultiQuant Software 2.0 for Targeted Protein / Peptide Quantification

Analysis of the Vitamin B Complex in Infant Formula Samples by LC-MS/MS

How To Test For Contamination In Large Volume Water

Thermo Scientific SOLAµ SPE Plates Technical Guide. Consistent excellence. for bioanalysis

RapidFire High-throughput MS technology. Enhancing Drug Discovery Turning Mass Specs into Plate Readers

LC-MS/MS Method for the Determination of Docetaxel in Human Serum for Clinical Research

8. SUMMARY AND CONCLUSION

Guidance for Industry

Method Development of LC-MS/MS Analysis of Aminoglycoside Drugs: Challenges and Solutions

LC-MS/MS for Chromatographers

How to develop Antibody Drug Conjugates: Bioanalysis Contribution

Rapid and Reproducible Amino Acid Analysis of Physiological Fluids for Clinical Research Using LC/MS/MS with the atraq Kit

DMPK: Experimentation & Data

Lead optimization services

Rapid LC/MS/MS Method Development for Drug Discovery

Guidance for Industry

Accurate Mass Screening Workflows for the Analysis of Novel Psychoactive Substances

Validation and Calibration. Definitions and Terminology

Extraction of Epinephrine, Norepinephrine and Dopamine from Human Plasma Using EVOLUTE EXPRESS WCX Prior to LC-MS/MS Analysis

Fit-For-Purpose Method Validation For Successful Biomarker Measurement To Support MRTP Applications

Daniel M. Mueller, Katharina M. Rentsch Institut für Klinische Chemie, Universitätsspital Zürich, CH-8091 Zürich, Schweiz

Overview. Introduction. AB SCIEX MPX -2 High Throughput TripleTOF 4600 LC/MS/MS System

Guideline on bioanalytical method validation

Therapeutic Drug Monitoring of Antiretroviral Drugs with HPLC-MS

Overview. Purpose. Methods. Results

CONFIRMATION OF ZOLPIDEM BY LIQUID CHROMATOGRAPHY MASS SPECTROMETRY

Introduction. Methods. Sample Processing

DRUG METABOLISM. Drug discovery & development solutions FOR DRUG METABOLISM

Guidance for Industry

Step-by-Step Analytical Methods Validation and Protocol in the Quality System Compliance Industry

Integration of DiscoveryQuant Software into Automated In-Vitro ADME Assay Workflows

UPLC-MS/MS Analysis of Aldosterone in Plasma for Clinical Research

Quantitative analysis of anabolic steroids in control samples from food-producing animals using a column-switching LC-HESI-MS/MS assay

Simultaneous Quantitation of 43 Drugs in Human Urine with a Dilute-and-Shoot LC-MS/MS Method

SIMULTANEOUS DETERMINATION OF NALTREXONE AND 6- -NALTREXOL IN SERUM BY HPLC

Simultaneous qualitative and quantitative analysis using the Agilent 6540 Accurate-Mass Q-TOF

Development and Validation of a LC-MS/MS Method for Plasma Analysis of the Serotonin Metabolite: 5-Hydroxyindoleacetic acid (5-HIAA)

MultiQuant Software Version 3.0 for Accurate Quantification of Clinical Research and Forensic Samples

Advances in LC-MS bioanalysis for drug research and development 液 相 质 谱 生 物 样 品 分 析 技 术 在 新 药 研 发 中 的 新 进 展

Improving the Metabolite Identification Process with Efficiency and Speed: LightSight Software for Metabolite Identification

The Scheduled MRM Algorithm Enables Intelligent Use of Retention Time During Multiple Reaction Monitoring

Fast and Accurate Analysis of Vitamin D Metabolites Using Novel Chromatographic Selectivity and Sample Preparation

API 3200 LC/MS/MS SYSTEM. Performance, productivity and value combined

Draft Agreed by Pharmacokinetics Working Party January End of consultation (deadline for comments) 31 May 2011

METHOD OF ANALYSIS. N methyl 2-pyrrolidone

AbsoluteIDQ p180 Kit. Targeted Metabolite Identifi cation and Quantifi cation. Bringing our targeted metabolomics expertise to your lab.

HRMS in Clinical Research: from Targeted Quantification to Metabolomics

Thermo Scientific Prelude SPLC System FPO. Making LC/MS accessible. to clinical research and toxicology labs

Quan / Qual Analyses in Clinical Research using a Second Generation Exactive High Resolution Mass Spectrometer

Optimizing the Post-implementation Monitoring of a LC-MS/MS Method

AppNote 1/2012. Rapid Cleanup and Comprehensive Screening of Pain Management Drugs in Urine using Automated Disposable Pipette Extraction and LC-MS/MS

Integrating Automated Systems for Regulated Bioanalysis Farmen, R.H., Struwe, P. and Groeschl, M.

Reversed Phase High Presssure Liquid Chromatograhphic Technique for Determination of Sodium Alginate from Oral Suspension

International GMP Requirements for Quality Control Laboratories and Recomendations for Implementation

A High Throughput Automated Sample Preparation and Analysis Workflow for Comprehensive Forensic Toxicology Screening using LC/MS/MS

IN VITRO BINDING BIOEQUIVALENCE STUDY SUMMARY TABLES AND SAS TRANSPORT FORMATTED TABLES FOR DATASET SUBMISSION

Analytical Test Method Validation Report Template

Appendix 5 Overview of requirements in English

Unique Software Tools to Enable Quick Screening and Identification of Residues and Contaminants in Food Samples using Accurate Mass LC-MS/MS

Overview. Triple quadrupole (MS/MS) systems provide in comparison to single quadrupole (MS) systems: Introduction

The Use of Micro Flow LC Coupled to MS/MS in Veterinary Drug Residue Analysis

Biological importance of metabolites. Safety and efficacy aspects

Draft agreed by Pharmacokinetics Working Party January Adoption by CHMP for release for consultation 17 February 2011

Thermo Scientific SOLA SPE cartridges and plates Technical Guide. Join the revolution. unparalleled performance

Screening and quantitative determination of drugs in diluted urine by UPLC-MS-MS

Comprehensive LC/MS Analysis of Illicit and Pain Management Drugs, Including Their Metabolites, in Urine

AppNote 1/2014. Automated Hydrolysis, DPX Extraction and LC/MS/MS Analysis of Pain Management Drugs from Urine KEYWORDS ABSTRACT

NANOCOMPOSIX'S GUIDE TO ICP-MS MEASUREMENT

Simultaneous Qualitative and Quantitative Data Acquisition for Research of Diabetes Drugs

Quantitation of Drugs in Dried Bloodstains. Thomas Meyer Anna Gomenyuk Nadiah Lester

What Do We Learn about Hepatotoxicity Using Coumarin-Treated Rat Model?

Selective Testosterone Analysis in Human Serum by LC-FAIMS-MS/MS

Quantitative Analysis of Explosives in Surface Water Comparing Off-Line Solid Phase Extraction and Direct Injection LC/MS/MS

Mouse Insulin ELISA. For the quantitative determination of insulin in mouse serum and plasma

Application of ICP-MS and LC-ICP-MS in Drug Development Jaap Wieling. EBF Focus Meeting, Brussels

LC-MS/MS Solutions for the Pharmaceutical and CRO Industries TSQ Series -based Solutions for Drug Discovery and Development

Waters Core Chromatography Training (2 Days)

LC-MS/MS, the new reference method for mycotoxin analysis

Making the Leap to LC/MS/MS: Enhancing and Accelerating Clinical Research and Forensic Toxicology Applications

MRMPilot Software: Accelerating MRM Assay Development for Targeted Quantitative Proteomics

Cliquid Drug Screen & Quant Software for Routine Forensic Toxicology. great interest in forensic, toxicological and clinical research laboratories.

High-Throughput 3-D Chromatography Through Ion Exchange SPE

High Sensitivity MS Determination of Carryover in a New Autosampler Design

VALIDATION OF ANALYTICAL PROCEDURES: TEXT AND METHODOLOGY Q2(R1)

Increasing the Multiplexing of High Resolution Targeted Peptide Quantification Assays

ProteinPilot Report for ProteinPilot Software

Supplementary Materials and Methods (Metabolomics analysis)

Utilization of Rapid LC-MS for Screening and Quantitative Analysis of Pesticides in Food Matrix using an Exactive Plus Benchtop Orbitrap Platform

Pesticide Analysis by Mass Spectrometry

A feasibility study of the determination of B-group vitamins in food by HPLC with Mass Spectrometric detection. LGC/R/2011/181 LGC Limited 2011

CORESTA RECOMMENDED METHOD N 72

MEPS - Micro Extraction by Packed Sorbent Online SPE for GC and LC sample preparation - Extraction to injection in a single process

Oasis HLB Cartridges and 96-Well Plates

A4: Reference standards and reagents

Transcription:

Merck global bioanalytical strategy to ensure data quality in the discovery space and successful LC-MS/MS methods transfer to preclinical GLP and clinical bioanalytical groups Vincenzo Pucci Merck Global Bioanalytics 7 th EBF, November 2014

Outline Role of Global Bioanalytics in PPDM Drug discovery and assay deployment High Data Quality Maintaining High Throughput Standardized routine analytical platforms MS performance check Minimizing errors Merck bioanalytical acceptance criteria From Discovery to Regulated Bioanalysis Assay validation components Regulated method development Method development experiments 2

Role of Global Bioanalytics in PPDM Discovery Preclinical Clinical DMPK Screening Assays Pharmacokinetics Studies Bio/Efficacy/Engagement Markers Metabolite Identification Tissue Analysis Program-Specific Assays Throughput Reproducibility Accuracy 3

Drug Discovery Assay Deployment and Consideration Hit Enzyme Assay Cell Assay In vivo PK/PD Efficacy Model, SLO Ancillary Pharmacology, DLT PCC Confidence Complexity/resources Decreasing throughput PK/BioA Screening PK Insight into challenges Expanded PK support PK incl. metabolites in add t species/matrices Tox./ancillary pharm. enabling PK Multidose/Formulation In vitro/adme MSIC and MetID In microsomes or S9 (liver/gi/ lung), hepatocytes DDI: TDI CYP (k obs or KI, k inact ), hep. induction, UGT inhib., add t transporter Disposition Quantitative in vivo assessment of ADME Pgp, P eff PXR* CYP inhib.* PPB, B/P and Plas. Stab. Quant./qual. metabolism In vitro/in vivo met. profiles and ID 4

High Data Quality Maintaining High Throughput Today s standardization is the necessary foundation on which tomorrow s improvement will be based Henry Ford Standard process designs and platforms reduce data variability and subsequently create greater flexibility and more predictable outcomes Standardization and in turn increased data confidence are the foundation of speed 5

Harmonization of Routine Analytical Platforms Standard platform for routine quantitative assays to ensure data quality and high throughput MS/MS Method Development Nanomate/FIA based compound tuning platform with global database of MRM parameters (DiscoveryQuant) LC-MS/MS Sample Analysis Sciex triple quadrupole mass spectrometer Thermo LX-2 parallel UHPLC system Standardized UHPLC conditions for discovery quantitative assays Generic internal standard mix Sample Preparation: Automation/Optimization Hamilton Liquid Handler Platform Acceptance Criteria for Discovery Assays 6

Scientifically Qualified and Properly Maintained Instruments System suitability tests are recommended to ensure success Performance of mass spectrometry systems are checked periodically to ensure that the system is operating properly MS performance checks are routinely conducted for our standard chromatographic methods to ensure that the system is sufficiently sensitive, specific, and reproducible The MS performance tests do not replace the required run acceptance criteria with calibration standards and QC samples 7

LC-MS/MS Performance Check Performance check data is displayed in three plots for analyte retention time, peak height, and peak area, as well as a summary table 8

Minimizing Errors: Matrix Effect PEG400 and PEG300 are common vehicles used in drug discovery known to cause matrix effect For studies with PEG based vehicles, QCs containing PEG (0.1, 1%) are incorporated in analytical runs Use of APCI as an alternative to ESI as well as different columns or chromatographic method (e.g. HILIC) Sample dilution (e.g., 1x, 10x and 100x) Selection a new internal standard (i.e. structural analog) Alternative sample extraction methods (e.g. LLE, SPE, SCX) When PEG suppression is difficult to solve analytically, alternative vehicles should be evaluated 9

Minimizing Errors: Carryover Ad hoc MultiQuant queries highlights carryover as well as other acceptance criteria failures Autosamplers and washing solutions were optimized in order to reduce carryover DLW autosamplers Sol 1: Water/ACN/Formic Acid Sol 2: ACN/IPA/Acetone/Formic Acid For analytes that show significant carryover with the above conditions, analysts may increase the number of wash cycles or rinse times, or an alternative wash method using acidic/basic solutions Sol 1: 2% ammonium hydroxide in 5 mm aqueous ammonium acetate/acetone/isopropanol/acetonitrile/methanol Sol 2: Methanol/Water/Formic Acid, 10/89/1 (v/v/v) Assessment and solution flowchart (column and autosampler carryover)

Merck Acceptance Criteria for Discovery Assays Study Type PGP, PPB, Non-definitive PK/PD Single and Cassette PK, Definitive PK/PD, Cold- BDC Studies Definitive PK and PK/PD Studies, TK, CV, DLT Definitive Formulation Safety Formulation, Post- PCC PK Studies Level Criteria Level 1 Level 2 Level 3 Level 4 X X X X 11

Level 3/4 Calibration Standard and Quality Control Acceptance Criteria Powder for stock solutions preparation Calibration curve must have a minimum of 6 standards Calibration Standards and QC sample accuracy of 25% Minimum of two QC sets (n=3) Low = 1 or 5-fold LLOQ High = 75-100% ULOQ 2/3 of the QC samples must be within ± 25% of nominal concentration Extrapolation below the LLOQ and above ULOQ is not allowed Dilution integrity QCs for samples > ULOQ at nominal concentration expected. Dilution integrity QCs samples should be frozen for at least 8 h and then analyzed. The mean (n 3) accuracy should be within 25% of the nominal concentration. The LLOQ must be greater than three times the mean of the back calculated value of the zero standards When the assay range is not known, several QC levels should be prepared at or near the expected LLOQ and ULOQ If the calibration standard criteria specified are not met, the analysis will be repeated 12

Level 3/4 Blank Matrix Samples, Carryover Calculations and Interference Carryover Test Carryover test must be ran by assaying one Single Blank after the highest standard Carryover < LLOQ no further checking is needed Carryover LLOQ then it needs to be converted to percent carryover Percent Carryover = [Carryover] / [High STD] 100 Re-assay is required when percent carryover is >25% Analyte interference test The peak area Single Blank <3 peak area of LLOQ The Double Blank will be used to monitor internal standard interference Single Blank (SB) is made from the calibration curve matrix with no analyte added Double Blank (DB) is made from the calibration curve matrix with no analyte or internal standard added 13

Level 3/4 Internal Standard Criteria Scientific judgment should be used when monitoring the internal standard response during an analytical run. IS response unknown 1.5 IS response STD and QC Level 3 The internal standard can be a combination (cocktail) of generic internal standards (e.g. labetalol, imipramine and diclofenac) unless a structural analog or stable isotope label is chosen for a particular structural class/program Level 4 The internal standard (IS) should be a structural analog or stable isotope labeled IS, when available

Level 4 Analyte Matrix Stability Testing Analyte matrix stability testing will be conducted using QCs at low and high concentrations (n 3) Room Temperature Analyte Matrix Stability 3 aliquots of low and high QCs for at least 2 hours Freeze/Thaw Analyte Matrix Stability A minimum of one freeze and thaw cycle 3 aliquots of low and high QCs frozen for at least 8h Long-Term Storage Analyte Matrix Stability Equal or higher the period of time between sample collection and sample analysis 3 aliquots of low and high QCs should be stored under the same storage conditions as the study samples

Preclinical Studies Variability Analysis Dog 30 25 Group Variability Histogram Inter-subject Variability Study Variability 20.4 % (Row Count) 20 15 10 24.0% 76.0% 79.6 % 5 0 1.00 < x 2.00 2.00 < x 3.00 3.00 < x 5.00 5.00 < x 10.00 10.00 < x 2 Bin By Specific Limits ([Variability], 0, 1, 2, 3, 5, 10, 20, 30, 50, 100) Statistical analysis of 25 compounds in 54 Dog Studies (n=3, 65 treatment groups 2-10 mg/kg oral dosing). Variable and Variability: AUC and metric cutoff of 3 Analyses does not take into account difference in formulations and possible non-linear PK 16

Preclinical Studies Variability Analysis Rat (Row Count) 65 60 55 50 45 40 35 30 25 20 15 10 5 0 Group Variability Histogram 1.00 < 2.00 < x 3.00 < 5.00 < 10.00 < 20.00 < 30.00 < 50.00 < Bin By Specific Limits ([Variability], 0, 1, 2, 3, 5, 10, 20, 30, 50, 100) Inter-subject Variability 29.8% 70.2% Study Variability 27.5% 72.5% Statistical analysis of 40 compounds in 94 Rat Studies (n=3, 115 treatment groups 2-10 mg/kg oral dosing). Variable and Variability: AUC and metric cutoff of 3 Analyses does not take into account difference in formulations and possible non-linear PK

Discovery PK and GLP TK Data PK data comparison shows good agreement between discovery and GLP TK studies 100 40 R 2 = 0.759 Average AUC Norm in GLP Studies 10 4 1 0.4 0.1 0.04 0.01 0.004 0.001 0.0004 0.001 0.004 0.01 0.04 0.1 0.4 1 4 10 40 100 Average AUC Norm in Discovery Studies

From Discovery to Regulated Bioanalysis Bioanalytical information is passed across different groups across the organization Discovery BioA Regulated Method Development GLP BioA Clinical BioA Discovery Acceptance Criteria evaluates essential parameters such as accuracy, precision, selectivity, sensitivity, reproducibility, limit of detection, and stability Information such as compound instability, plasma stabilization, presence of metabolites and possible interference with parent, method conditions (e.g. HILIC, SPE, LLE) move from Discovery to Regulated Method Development

Assay Requirements for all SA Studies Assay Validation Components Discovery Exploratory GLP Acceptance Criteria Level 3 4 SOP Accuracy ± 25% ± 25% ± 15% (± 20% LLOQ) Precision ± 25% ± 25% ± 15% (± 20% LLOQ) Analytical Standard DMSO solution or solid for PCC Solid Solid Analytical Reference Standard Solution Stability No, prepared daily Yes ± 7% Yes ± 7% Stability Check Not Typical Yes, some ± 25% Yes (exhaustive) ± 15% Dilution Recommended Yes ± 25% Yes ± 15% Validation (pass/fail) Pre-study Validation Investment P&A same day None/Ad Hoc Pre-study validation 5-7 business days Pre-study validation ~ 20 business days

Comparison of Assay Validation Components Assay Validation Components Exploratory GLP 3 Days Precision and Accuracy Carryover Specificity Selectivity 1 Freeze Thaw Cycle in Matrix 2h Short-Term Stability in Matrix Long-Term Freezer Stability in Matrix 6 h @ RT & Long Term Stock & Working Standard Stability Dilution Post-Preparative Stability Recovery Matrix Effect

Regulated Method Development Strategic Intent Develops robust regulated analytical methods Leverages information from assays developed for discovery programs Ensures the effective implementation of these methods for GLP and Clinical sample analysis Assists with resolution of issues during both validation and sample analysis Focuses on developing new techniques and approaches for new modalities, expanding BA science into innovative areas 22

Regulated Method Development: Principles Apply a standardized approach as much as possible Intended as starting point for routine small molecules, capturing ~70% of work in this space Do enough to ensure that the method won t fail during validation Transfer method 3-4 weeks prior to sample collection Communication with PK, Regulated GLP BioA and Clinical BioA groups is a key

Regulated Method Development: When? First method is for support of GLP Tox studies md initiated ~2-3 weeks from API 1 st delivery LLOQ 2-5 ng/ml - small molecules 0.1-1 ng/ml - large molecules Once FIH is scheduled, clinical method development is planned md initiated ~2 month before FIH LLOQ 0.1-1 ng/ml - small molecules 0.05-0.5ng/ml - large molecules (has been a challenge)

Method Development Experiments Optimize MS/MS conditions for analytes/is Evaluate standard HPLC conditions Columns, mobile phase and gradient profiles Cross talk and/or metabolite interference as appropriate Standards and QCs preparation methods Solvents, % organic Sample Preparation Volumes, methods (protein precipitation, liquid-liquid extraction etc.) Assay evaluation Linearity and STD curve reproducibility (n=5) Intraday precision and accuracy using freshly spiked QCs Selectivity Carryover Stability QCs Dilution Integrity Ruggedness

Conclusions Standard platforms and protocols reduce variability Work can be easily shared across groups and sites Judgment calls allow discovery groups to work in a highthroughput environment with minimal analyst oversight Essential parameters for bioanalytical method validation are evaluated at early discovery stage Documentation and interactions for successful LC-MS/MS methods transfer to preclinical GLP and clinical bioanalytical groups

Acknowledgments Jane Harrelson Kevin Bateman Lucinda Cohen Bart Emary Dina Goykhman Eric Woolf Rena Zhang