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Hana Vlčková

Researcher at Charles University in Prague

Publications -  26
Citations -  1055

Hana Vlčková is an academic researcher from Charles University in Prague. The author has contributed to research in topics: Hydrophilic interaction chromatography & Sample preparation. The author has an hindex of 16, co-authored 24 publications receiving 962 citations.

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Journal ArticleDOI

A review of current trends and advances in modern bio-analytical methods: chromatography and sample preparation.

TL;DR: UHPLC has recently become a wide-spread analytical technique in many laboratories which focus on fast and sensitive bio-analytical assays and the key advantages are the increased speed of analysis, higher separation efficiency and resolution, higher sensitivity and much lower solvent consumption as compared to other analytical approaches.
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Hydrophilic interaction chromatography of polar and ionizable compounds by UHPLC

TL;DR: An overview of UHPLC in HILIC mode, including the importance of the final sample diluent, a discussion on available stationary phases and approaches to detection, and a comparison of performance with other chromatographic modes are presented in this paper.
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Ultra high performance liquid chromatography tandem mass spectrometric detection in clinical analysis of simvastatin and atorvastatin.

TL;DR: Simvastatin and atorvastarin as the most widely used statins in clinical treatment and their hydroxy-acid/lactone forms were determined by means of UPLC in connection with triple quadrupole mass spectrometer.
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Microextraction by packed sorbent as sample preparation step for atorvastatin and its metabolites in biological samples—Critical evaluation

TL;DR: Combination of fast MEPS method together with quick UHPLC-MS/MS was used for the determination of atorvastatin and its two metabolites in serum obtained from patients with familiar hypercholesterolemia.
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Determination of pravastatin and pravastatin lactone in rat plasma and urine using UHPLC–MS/MS and microextraction by packed sorbent

TL;DR: The UHPLC-MS/MS method was validated and demonstrated good linearity in range 5-500 nmol/l (r(2)>0.9990) for plasma and urine samples and method recovery was ranged within 97-109% for plasma samples and 92-101% for the urine samples.