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  • Elemental Impurities in Pharmaceutical Products

    Elemental impurities in drug substances and drug products may arise from several sources; they may be residual catalysts that were added intentionally in the synthesis or may be present as impurities (e.g., through interactions with processing equipment or container/closure systems or by being present in components of the drug product). Elemental impurities do not provide any therapeutic benefit to the patient, their levels in the drug product should be controlled within acceptable limits. Long-term exposure even to low concentrations of impurities can cause many adverse health effects and even toxicity.

    The following diagram shows an example of typical materials, equipment, and components used in the production of a drug product.

    Classification of Elemental Impurities

    Class Included elemental impurity
    Class 1Arsenic, Lead, Cadmium, Mercury 
    Class 2ACobalt, Vanadium, Nickel
    Class 2BThallium, Gold, Palladium, Iridium, Osmium, Rhodium, Ruthenium, Selenium, Silver, Platinum
    Class 3Lithium, Antimony, Barium, Molybdenum, Copper, Tin, Chromium

    The method used for establishing the PDE for each elemental impurity is discussed in “Q3D (R1) Guideline for elemental impurities” in detail. Elements evaluated in this guideline were assessed by reviewing the publicly available data contained in scientific journals, government research reports and studies, international regulatory standards (applicable to drug products) and guidance, and regulatory authority research and assessment reports.

    Different Analytical techniques for the determination of elemental impurities-

    Many instrumental analytical methods may be employed to measure the concentration level of heavy metals in various samples. The most predominant techniques are Atomic Absorption Spectrometry (AAS); Atomic Emission/Fluorescence Spectrometry (AES/AFS); Inductively Coupled Plasma Mass Spectrometry(ICP-MS); Inductively Coupled Plasma OpticalEmission Spectrometry (ICP-OES); NeutronActivation Analysis (NAA), X-ray Fluorescence(XRF); and Anodic Stripping Voltammetry (AVS).

    The most widely used technique is ICP-OES which has high sample throughput enabling the efficient analysis of a large number of batches, simultaneous determination of multiple elements in each sample, large dynamic linear range, and low chemical and matrix interference effect as well.

    General comparison of different analytical techniques

    Method validation plan

    The general validation plan has been elaborated below and can be used for the method validation approach for elemental testing.

    References:

    1. ICH harmonized guideline “ Guideline for Elemental impurities: Q3D(R1)
    2. https://www.fda.gov/drugs/pharmaceutical-quality-resources/elemental-impurities
    3. Elemental Impurities in Drug Products- Guidance for Industry, U.S. Department of Health, Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER)
    4. Elemental impurity analysis in regulated pharmaceutical laboratories, Agilent technologies

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