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J Chromatogr B Biomed Appl ; 663(2): 309-13, 1995 Jan 20.
Article in English | MEDLINE | ID: mdl-7735478

ABSTRACT

A simple and rapid HPLC method was developed to determine terguride in terguride hydrogenmaleate, coated tablets and plasma. The assay was carried out on a glass column of SGX CN (150 x 3.3 mm I.D.) using methanol and phosphate buffer solution (pH 7.0) as the mobile phase, with detection at 227 nm. Terguride was quantified using promethazine as an internal standard. The tablet matrix was extracted into methanol. Plasma samples were deproteinated with acetonitrile and the supernatant was injected into the HPLC system. The method is linear, quantitative and reproducible.


Subject(s)
Dopamine Agonists/analysis , Lisuride/analogs & derivatives , Animals , Chromatography, High Pressure Liquid , Dopamine Agonists/blood , Ergot Alkaloids/isolation & purification , Lisuride/analysis , Lisuride/blood , Rats , Tablets
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