Characterization of currently marketed heparin products: key tests for LMWH quality assurance
Research article published in Journal of pharmaceutical and biomedical analysis (2013)
Abstract
During the 2007-2008 heparin crisis it was found that the United States Pharmacopeia (USP) testing monograph for heparin sodium or low molecular weight heparins did not detect the presence of the contaminant, oversulfated chondroitin sulfate (OSCS). In response to this concern, new tests and specifications were developed by the Food and Drug Administration (FDA) and USP and put in place to detect not only the contaminant OSCS, but also to improve assurance of quality and purity of these drug products. The USP monographs for the low molecular weight heparins (LMWHs) approved for use in the United States (dalteparin, tinzaparin and enoxaparin) are also undergoing revision to include many of the same tests used for heparin sodium, including; one-dimensional (1D) 500 MHz (1)H NMR, SAX-HPLC, percent galactosamine in total hexosamine and anticoagulation time assays with purified Factor IIa or Factor Xa. These tests represent orthogonal approaches for heparin identification, measurement of bioactivity and for detection of process impurities or contaminants in these drug products. Here we describe results from a survey of multiple lots from three types of LMWHs in the US market which were collected after the 2009 heparin sodium monograph revision. In addition, innovator and generic versions of formulated enoxaparin products purchased in 2011 are compared using these tests and found to be highly similar within the discriminating power of the assays applied.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
During the 2007-2008 heparin crisis it was found that the United States Pharmacopeia (USP) testing monograph for heparin sodium or low molecular weight heparins did not detect the presence of the contaminant, oversulfated chondroitin sulfate (OSCS).
Por qué esto importa para la hirudoterapia
Este estudio describe la aplicación de pruebas analíticas ortogonales, entre ellas RMN y HPLC, para caracterizar las heparinas de bajo peso molecular comercializadas actualmente y detectar la presencia de contaminantes como el sulfato de condroitina sobresulfatado tras la crisis de la heparina de 2007-2008. La investigación se centra fundamentalmente en la garantía de calidad farmacéutica y en asegurar la pureza de los medicamentos anticoagulantes. Este artículo no aborda sanguijuelas, hirudoterapia ni ningún componente del secretoma de la sanguijuela. En consecuencia, su relevancia para la American Society of Hirudotherapy es estrictamente indirecta, ya que solo atañe a la vigilancia de la seguridad de los anticoagulantes convencionales.
Citación
Characterization of currently marketed heparin products: key tests for LMWH quality assurance
Ye H et al. · Journal of pharmaceutical and biomedical analysis, 2013
Contexto clínico relacionado
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Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: 18 de junio de 2026