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1.
Handb Exp Pharmacol ; (207): 99-125, 2012.
Article in English | MEDLINE | ID: mdl-22566223

ABSTRACT

In late 2007 and early 2008, a cluster of adverse events in patients receiving Heparin Sodium Injection occurred in the United States and in some countries in Europe. The adverse events were reported as being "allergic type" reactions, chiefly characterized by acute hypotension, nausea, and shortness of breath. The root cause of the cluster of adverse events was determined to be a contamination of the heparin by oversulfated chondroitin sulfate. The isolation and structure determination of this contaminant was accomplished by an FDA-led consortium of academic and government laboratories and independently by Baxter Healthcare, whose vial products were first identified in the USA as being associated with the adverse events. Oversulfated chondroitin sulfate was shown to produce acute hypotension in animal models, demonstrating that it was most likely the causative agent responsible for certain of the reported adverse events in patients receiving the contaminated heparin products.


Subject(s)
Chondroitin Sulfates/chemistry , Heparin/chemistry , Chondroitin Sulfates/analysis , Electrophoresis, Capillary , Heparin/analysis , Magnetic Resonance Spectroscopy , Spectrometry, Mass, Electrospray Ionization
2.
J Pharm Biomed Anal ; 49(2): 319-26, 2009 Feb 20.
Article in English | MEDLINE | ID: mdl-19155153

ABSTRACT

Oversulfated chondroitin sulfate (OSCS), an impurity found in some porcine intestinal heparin samples was separated from intact heparin by capillary electrophoresis (CE) using a 600mM phosphate buffer, pH 3.5 as the background electrolyte in a 56cm x 25microm i.d. capillary. This method was confirmed in two separate labs, was shown to be linear, reproducible, robust, easy to use and provided the highest resolution and superior limits of detection compared to other available CE methods. Glycosoaminoglycans such as dermatan sulfate and heparan sulfate were separated and quantified as well during a single run. The heparin peak area response correlated well to values obtained using the official assay for biological activity. A high speed, high resolution version of the method was developed using 600mM lithium phosphate, pH 2.8 in a 21.5cm x 25microm i.d. capillary which provided limits of detection for OSCS that were below 0.1%.


Subject(s)
Anticoagulants/chemistry , Chondroitin Sulfates/chemistry , Dermatan Sulfate/chemistry , Drug Contamination , Heparin/chemistry , Heparitin Sulfate/chemistry , Phosphates/chemistry , Animals , Anticoagulants/analysis , Buffers , Calibration , Chondroitin Sulfates/analysis , Chondroitin Sulfates/isolation & purification , Dermatan Sulfate/analysis , Dermatan Sulfate/isolation & purification , Electrolytes/chemistry , Electrophoresis, Capillary/instrumentation , Electrophoresis, Capillary/methods , Heparin/analysis , Heparitin Sulfate/analysis , Heparitin Sulfate/isolation & purification , Hydrogen-Ion Concentration , Molecular Structure , Osmolar Concentration , Reproducibility of Results , Sensitivity and Specificity , Sus scrofa , Temperature , Time Factors
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