высокоэффективная жидкостная хроматография

The chromatographic behavior of atorvastatin, rosuvastatin and simvastatin in the presence of the main modifi ers of the mobile phase: elution strength and buff er solution, has been studied by means of the reverse-phase high-performance liquid chromatography (HPLC) method. Optimal modifi cation conditions have been found and their application for the determination of statins under study in the pharmaceutical preparations Atorvastatin-OBL, Liprimar and Tulip has been shown. The Sr value is 0.03. The relative determination error does not exceed 7%.

Выявлен эффект экзогенного индола в отношении ростовых
характеристик базидиомицета Lentinula edodes при глубинном
культивировании, проявляющийся в снижении биомассы мице-
лия в интервале значений концентрации добавки 10?
4–10?1 г/л.
Индол стимулировал продукцию индолил-3-уксусной и индолил-
3-пировиноградной кислот. Набор экстраклеточных соединений
индольной природы на обогащенных индолом средах включал,
кроме того, триптамин, триптофан, индолил-3-ацетамид, био-

It is shown that in the analysis of medicines fluoroquinolone by reversed-phase HPLC with fluorimetric detection modification mobile phase ?-cyclodextrin leads to a decrease in the detection limit of antibiotics to 8 times. The possibility of determination of cipro- floxacin in the presence of tetracycline and quinolone derivative series. The proposed method is tested in the analysis of pharmaceutical preparations containing ciprofloxacin.

Sorption properties of simazine, atrazine, propazine and prometrin on commercial chromatographic columns of LiChrospher 60 RP select B, Hypersil BDS-C18, and Zorbax SB-C18 were studied by reversed-phase high-performance liquid chromatography with photodiode matrix detection. The influence of the composition of the mobile phase on the chromatographic characteristics of the separation is considered. It was found that with the content of acetonitrile in a mixture of PF from 10 to 30 vol/vol. the chromatographic peak of atrazine is practically not manifested.

The paper presents the results of optimizing the conditions for the chromatographic determination of 2,4-dichlorophenoxyacetic acid and deltamethrin for two capillary columns (Supelcosil LC-18, Kromasil C-18). The modes of individual chromatography of pesticides were selected. The use of the isocratic elution mode in the joint presence of 2,4-dichlorophenoxyacetic acid and deltamethrin was shown and experimentally proved to be invalid. Three options were proposed for the conditions of the gradient mode of the separate detection of analytes in a mixture.