Rozou S - Search Results

1

The effect of pH dependent molecular conformation and dimerization phenomena of piroxicam on the drug:cyclodextrin complex stoichiometry and its chromatographic behaviour. A new specific HPLC method for piroxicam:cyclodextrin formulations.

Rozou S, Voulgari A, Antoniadou-Vyza E. Rozou S, et al. Eur J Pharm Sci. 2004 Apr;21(5):661-9. doi: 10.1016/j.ejps.2004.01.007. Eur J Pharm Sci. 2004. PMID: 15066667

2

HPLC analysis, isolation and identification of a new degradation product in carvedilol tablets.

Galanopoulou O, Rozou S, Antoniadou-Vyza E. Galanopoulou O, et al. Among authors: rozou s. J Pharm Biomed Anal. 2008 Sep 10;48(1):70-7. doi: 10.1016/j.jpba.2008.05.004. Epub 2008 May 16. J Pharm Biomed Anal. 2008. PMID: 18584991

3

An improved HPLC method overcoming Beer's law deviations arising from supramolecular interactions in tolfenamic acid and cyclodextrins complexes.

Rozou S, Antoniadou-Vyza E. Rozou S, et al. J Pharm Biomed Anal. 1998 Dec;18(4-5):899-905. doi: 10.1016/s0731-7085(98)00227-1. J Pharm Biomed Anal. 1998. PMID: 9919995

4

Chromatographic behaviour of naproxen-cyclodextrin complexes stationary phase C8 alkyl chain as competitor for the drug release from cyclodextrin cavity.

Rozou S, Antoniadou-Vyza E. Rozou S, et al. J Chromatogr A. 2004 Jul 2;1041(1-2):187-93. doi: 10.1016/j.chroma.2004.05.002. J Chromatogr A. 2004. PMID: 15281268

5

Study of structural features and thermodynamic parameters, determining the chromatographic behaviour of drug-cyclodextrin complexes.

Rozou S, Michaleas S, Antoniadou-Vyza E. Rozou S, et al. J Chromatogr A. 2005 Sep 16;1087(1-2):86-94. doi: 10.1016/j.chroma.2005.02.039. J Chromatogr A. 2005. PMID: 16130701

6

New SPE loading material for affinity-based separation of cyclodextrins from drug:CD complexes in order to overcome Beer's law deviations.

Rozou S, Raftopoulos P, Hatziantoniou S, Antoniadou-Vyza E. Rozou S, et al. J Sep Sci. 2009 Oct;32(20):3521-8. doi: 10.1002/jssc.200900251. J Sep Sci. 2009. PMID: 19777455

7

The application of Quality by Design framework in the pharmaceutical development of dry powder inhalers.

Buttini F, Rozou S, Rossi A, Zoumpliou V, Rekkas DM. Buttini F, et al. Among authors: rozou s. Eur J Pharm Sci. 2018 Feb 15;113:64-76. doi: 10.1016/j.ejps.2017.10.042. Epub 2017 Nov 23. Eur J Pharm Sci. 2018. PMID: 29104067 Review.

8

Dry powder inhalers: An overview of the in vitro dissolution methodologies and their correlation with the biopharmaceutical aspects of the drug products.

Velaga SP, Djuris J, Cvijic S, Rozou S, Russo P, Colombo G, Rossi A. Velaga SP, et al. Among authors: rozou s. Eur J Pharm Sci. 2018 Feb 15;113:18-28. doi: 10.1016/j.ejps.2017.09.002. Epub 2017 Sep 5. Eur J Pharm Sci. 2018. PMID: 28887232 Review.

9

Development and validation of a hydrophilic interaction liquid chromatography method for the quantitation of impurities in fixed-dose combination tablets containing rosuvastatin and metformin.

Machairas G, Panderi I, Geballa-Koukoula A, Rozou S, Antonopoulos N, Charitos C, Vonaparti A. Machairas G, et al. Among authors: rozou s. Talanta. 2018 Jun 1;183:131-141. doi: 10.1016/j.talanta.2018.02.068. Epub 2018 Feb 17. Talanta. 2018. PMID: 29567155

10

Application of a One-Dimensional Computational Model for the Prediction of Deposition from a Dry Powder Inhaler.

Gourgoulianis K, Daniil Z, Athanasiou K, Rozou S, Bontozoglou V. Gourgoulianis K, et al. Among authors: rozou s. J Aerosol Med Pulm Drug Deliv. 2017 Dec;30(6):435-443. doi: 10.1089/jamp.2016.1363. Epub 2017 Jul 6. J Aerosol Med Pulm Drug Deliv. 2017. PMID: 28683222

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