ABSTRACT

Recent regulations on heavy metal testing have required the pharmaceutical industry to monitor a suite of elemental impurities in pharmaceutical raw materials, drug products and dietary supplements. These new directives s are described in the new United States Pharmacopeia (USP) Chapters <232>, <233>, and <2232>, together with Q3D, Step 4 guidelines for elemental impurities, drafted by the ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use), a consortium of global pharmaceutical associations, including the European Pharmacopeia (Ph.Eur.), the Japanese Pharmacopeia (JP) and the USP. This book provides a complete guide to the analytical methodology, instrumental techniques and sample preparation procedures used for measuring elemental impurities in pharmaceutical and nutraceutical materials.

It offers readers the tools to better understand plasma spectrochemistry to optimize detection capability for the full suite of elemental PDE (Permitted Daily Exposure) levels in the various drug delivery categories. Other relevant information covered in the book includes:

  • The complete guide to measuring elemental impurities in pharmaceutical and nutraceutical materials.
  • Covers heavy metals testing in the pharmaceutical industry from an historical perspective.
  • Gives an overview of current USP Chapters <232> <233> and <2232> and ICH Q3D Step 4 Guidelines.
  • Explains the purpose of validation protocols used in Chapter <233>, including how J-values are calculated
  • Describes fundamental principles and practical capabilities of ICP-MS and ICP-OES.
  • Offers guidelines about the optimum strategy for risk assessment
  • Provides tips on how best to prepare and present your data for regulatory inspection.

An indispensable resource, the fundamental principles and practical benefits of ICP-OES and ICP-MS are covered in a reader-friendly format that a novice, who is carrying out elemental impurities testing in the pharmaceutical and nutraceutical communities, will find easy to understand.

chapter |10 pages

Testing for Heavy Metals

An ACS Perspective

chapter |19 pages

Elemental Impurities in Pharmaceuticals

An Overview

chapter |4 pages

An Overview of ICP

Mass Spectrometry

chapter |5 pages

Principles of Ion Formation

chapter |12 pages

Sample Introduction

chapter |8 pages

Plasma Source

chapter |8 pages

Interface Region

chapter |9 pages

Ion-Focusing System

chapter |9 pages

Mass Analyzers

Quadrupole Technologya

chapter |10 pages

Mass Analyzers

Double-Focusing Magnetic Sector Technology

chapter |10 pages

Mass Analyzers

Time-of-Flight Technology

chapter |28 pages

Mass Analyzers

Collision/Reaction Cell and Interface Technology

chapter |10 pages

Ion Detectors

chapter |14 pages

Peak Measurement Protocol

chapter |11 pages

Methods of Quantitation

chapter |12 pages

Review of ICP-MS Interferences

chapter |13 pages

Routine Maintenance

chapter |11 pages

The Risk Assessment Approach

chapter |7 pages

Regulatory Inspection Readiness

chapter |38 pages

How to Select an ICP Mass Spectromete

chapter |48 pages

Plasma Spectrochemistry Glossary of Terms

chapter |3 pages

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