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Quantitative PCR and Disaccharide Profiling to Characterize the Animal Origin of Low-Molecular-Weight Heparins
Low-molecular-weight heparins (LMWHs) are widely used in the management of thrombosis and acute coronary syndromes. They are obtained by the enzymatic or chemical depolymerization of porcine intestinal heparin. Enoxaparin sodium, a widely used LMWH, has a unique and reproducible oligosaccharide prof...
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Published in: | Clinical and applied thrombosis/hemostasis 2009-02, Vol.15 (1), p.50-58 |
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creator | Houiste, Céline Auguste, Cécile Macrez, Céline Dereux, Stéphanie Derouet, Angélique Anger, Pascal |
description | Low-molecular-weight heparins (LMWHs) are widely used in the management of thrombosis and acute coronary syndromes. They are obtained by the enzymatic or chemical depolymerization of porcine intestinal heparin. Enoxaparin sodium, a widely used LMWH, has a unique and reproducible oligosaccharide profile which is determined by the origin of the starting material and a tightly controlled manufacturing process. Although other enoxaparin-like LMWHs do exist, specific release criteria including the origin of the crude heparin utilized for their production, have not been established. A quantitative polymerase chain reaction method has been developed to ensure the purity of the porcine origin of crude heparin, with a DNA detection limit as low as 1 ppm for bovine, or 10 ppm for ovine contaminants. This method is routinely used as the release acceptance criterion during enoxaparin sodium manufacturing. Furthermore, when the process removes DNA, other analytical techniques can be used to assess any contamination. Disaccharide profiling after exhaustive depolymerization can determine the presence of at least 10% bovine or 20% ovine material; multivariate analysis is useful to perform the data analysis. Consistent with the availability of newer technology, these methods should be required as acceptance criteria for crude heparins used in the manufacture of LMWHs to ensure their safety, quality, and immunologic profile. |
doi_str_mv | 10.1177/1076029608320831 |
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They are obtained by the enzymatic or chemical depolymerization of porcine intestinal heparin. Enoxaparin sodium, a widely used LMWH, has a unique and reproducible oligosaccharide profile which is determined by the origin of the starting material and a tightly controlled manufacturing process. Although other enoxaparin-like LMWHs do exist, specific release criteria including the origin of the crude heparin utilized for their production, have not been established. A quantitative polymerase chain reaction method has been developed to ensure the purity of the porcine origin of crude heparin, with a DNA detection limit as low as 1 ppm for bovine, or 10 ppm for ovine contaminants. This method is routinely used as the release acceptance criterion during enoxaparin sodium manufacturing. Furthermore, when the process removes DNA, other analytical techniques can be used to assess any contamination. Disaccharide profiling after exhaustive depolymerization can determine the presence of at least 10% bovine or 20% ovine material; multivariate analysis is useful to perform the data analysis. 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Disaccharide profiling after exhaustive depolymerization can determine the presence of at least 10% bovine or 20% ovine material; multivariate analysis is useful to perform the data analysis. Consistent with the availability of newer technology, these methods should be required as acceptance criteria for crude heparins used in the manufacture of LMWHs to ensure their safety, quality, and immunologic profile.</description><subject>Animals</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Disaccharides - isolation & purification</subject><subject>DNA - isolation & purification</subject><subject>Heparin, Low-Molecular-Weight - chemistry</subject><subject>Heparin, Low-Molecular-Weight - isolation & purification</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Swine</subject><issn>1076-0296</issn><issn>1938-2723</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp1kUlLAzEUgIMo7ndPEhC8jWaZyXKUukLFBcXjkMlk2sg0qUlG0V9vSgsFwUNIeO9730vyADjC6Axjzs8x4gwRyZCgJC-8AXaxpKIgnNDNfM7pYpHfAXsxviOEJZNsG-xgIVAlSr4L3NOgXLJJJftp4OPoGSrXwksbldZTFWybg8F3trduApOHoxxUOplgfwxMUwMvnJ2pHj4EO7EO-g6O_Vdx73ujh16F4s3YyTTBWzPPMhcPwFan-mgOV_s-eL2-ehndFuOHm7vRxbjQJapSgUnXUsU40tggjjEVptUNZkTLUkvdkYoKKlsiu6aSje4azRohteSNamTVMroPTpfeefAfg4mpntmoTd8rZ_wQa8YEYajiGTz5A777Ibh8t5rQsiSISr7QoSWlg48xmK6eh_zs8F1jVC8mUf-dRC45XomHZmbadcHq6zNQLIGoJmbd9V_hL50nkFk</recordid><startdate>200902</startdate><enddate>200902</enddate><creator>Houiste, Céline</creator><creator>Auguste, Cécile</creator><creator>Macrez, Céline</creator><creator>Dereux, Stéphanie</creator><creator>Derouet, Angélique</creator><creator>Anger, Pascal</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200902</creationdate><title>Quantitative PCR and Disaccharide Profiling to Characterize the Animal Origin of Low-Molecular-Weight Heparins</title><author>Houiste, Céline ; 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subjects | Animals Chromatography, High Pressure Liquid Disaccharides - isolation & purification DNA - isolation & purification Heparin, Low-Molecular-Weight - chemistry Heparin, Low-Molecular-Weight - isolation & purification Polymerase Chain Reaction - methods Swine |
title | Quantitative PCR and Disaccharide Profiling to Characterize the Animal Origin of Low-Molecular-Weight Heparins |
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