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, field-effect transistor-based) because of their ability to achieve low and ultralow detection limits
doi: 10.1097/YCO.0000000000000244
The drug is dehalogenated to monochloroacetate and glyoxylate, from which it can be further catabolized to glycolate, glycine, oxalate, and carbon dioxide
J., Pharmacokinetics of NonPrescription Sympathomimetic Agents, Biopharmaceutics & Drug Disposition 10 (1989): 114
