The study of naproxen desorption from the silica by RP-HPLC | 12589
Biochemistry & Pharmacology: Open Access

Biochemistry & Pharmacology: Open Access
Open Access

ISSN: 2167-0501

The study of naproxen desorption from the silica by RP-HPLC

Joint Event on 10th World Congress on Pharmacology & 6th International Conference and Exhibition on Advances in Chromatography & HPLC Techniques

August 02-03, 2018 | Barcelona, Spain

Monika Sulekova

University of Veterinary Medicine and Pharmacy in Kosice, Slovakia

Scientific Tracks Abstracts: Biochem Pharmacol (Los Angel)

Abstract :

Naproxen, a non-steroidal anti-inflammatory drug (NSAID) is widely used to moderate pain relief in the treatment of many diseases. Naproxen has analgesic and antipyretic properties. Mesoporous silica SBA-15 was prepared to evaluate its application as naproxen drug delivery system. The amount of naproxen released from the pores of mesoporous silica SBA-15 into the solutions was determined by the method of a reverse-phase high performance liquid chromatography (RP-HPLC). SBA-15 having 3-aminoprophyl-, methyl-, fenyland cyclohexyl-surface groups was successfully prepared by the grafting of SBA-15 with the corresponding alkoxysilanes. The release of the drug was performed in two different media, in a simulated body fluid (pH 7.40) and in a simulated gastric fluid (pH 2.06). The HPLC system Dionex Ultimate 3000 RS (Thermo Fisher Scientific, Germany) consisted of a quaternary pump, a degasser, an automated injector, a column oven and a diode array detector DAD. HPLC system was used, with stationary phase ODS Hypersil C18 column (150x4.6 mm, 3 �?¼m). To determine the concentration of naproxen, the calibration curve has been established based on five solutions of different concentrations of naproxen. The linearity was determined by threefold repeating measurement of each concentration step. The mixture of acetonitrile and water (55:45, v/v) adjusted with ortho-phosphoric acid to pH 3 was selected as the best mobile phase. The flow rate was 1 mL/min and detection was carried out at a wavelength of 229 nm. During the chromatographic separation, the mobile phase was kept isocratic. The release of the drug was studied as a function of time and the results are shown in Figure.
Recent Publications
1. Reitznerov�?¡ A, �? ulekov�?¡ M, Nagy J, Marcin�?�?¡k S, Semjon B, �?�?ert�?­k M and Klempov�?¡ K (2017). Lipid peroxidation process in meat and meat products: a comparison study of malondialdehyde determination between modified 2-thiobarbituric acid spectrophotometric Method and reverse-phase high-performance liquid chromatography. Molecules DOI: 10.3390/ molecules22111988.
2. �? ulekov�?¡ M, Smr�?ov�?¡ M, Hud�?¡k A, He�?¾elov�?¡ M and Fedorov�?¡ M (2017) Organic colouring agents in the pharmaceutical industry. Folia Veterinaria 61(3):32-46.
3. �? ulekov�?¡ M, Hud�?¡k A and Smr�?ov�?¡ M (2016) The determination of food dyes in vitamins by RP-HPLC. Molecules 21(10):1368.
4. �? ulekov�?¡ M and Hud�?¡k A (2015) Determination of the colorants in vitamin E by HPLC with photodiode array detection. �?�?es. slov. Farm. 64(6):279.
5. Telep�?�?¡kov�?¡ M, Andruch V and Balogh IS (2005) Indirect extraction-spectrophotometric determination of chromium. Chem. Pap. 59(2):109.

Biography :

Monika Šuleková has completed her Graduation at the University of Pavol Josef Šafárik in Košice, Slovakia. During her university studies, she spent half a year at Friedrich-Schiller University in Jena, Germany where she studied Analytical Chemistry. Nowadays she works as a Teacher at the University of Veterinary Medicine and Pharmacy in Košice, Slovakia as well as a Researcher in the field of desorption of drugs from mesoporous silica modified by different functional groups, and in determination of synthetic dyes in pharmaceutical products by the RP-HPLC method.