HPLC hodnocení vybraných léčiv II
HPLC evaluation of selected drugs II. THESIS Petr Vyroubal Charles University in Prague, Faculty of Pharmacy in Hradec Králové, Department of Pharmaceutical Chemistry and Drug Control In this thesis was validated method for simultaneous HPLC analysis of paracetamol and tramadol in combined tablet. A...
Main Author: | |
---|---|
Other Authors: | |
Format: | Dissertation |
Language: | Czech |
Published: |
2010
|
Online Access: | http://www.nusl.cz/ntk/nusl-279050 |
id |
ndltd-nusl.cz-oai-invenio.nusl.cz-279050 |
---|---|
record_format |
oai_dc |
spelling |
ndltd-nusl.cz-oai-invenio.nusl.cz-2790502017-06-27T04:40:30Z HPLC hodnocení vybraných léčiv II HPLC evaluation of selected drugs II Vyroubal, Petr Mokrý, Milan Sochor, Jaroslav HPLC evaluation of selected drugs II. THESIS Petr Vyroubal Charles University in Prague, Faculty of Pharmacy in Hradec Králové, Department of Pharmaceutical Chemistry and Drug Control In this thesis was validated method for simultaneous HPLC analysis of paracetamol and tramadol in combined tablet. As stationary phase the chromatographic column Discovery HS F5, 5 µm, 150×3 mm I.D. made by Supelco was used. Mobile phase was formed by mixture of acetonitrile : ammonium acetate solution 0.005 mol/l, acidified with acetic acid at pH 3.2 in the ratio 20:80 (v/v). A flow rate was 1.0 ml/min. Acetylsalicylic acid was used as an internal standard. The detection was performed at λ = 270 nm using an UV detector. The substances were eluted in following order: paracetamol, acetylsalicylic acid and tramadol. The method was validated for linearity (paracetamol R = 0.9996; tramadol R = 0.9998), precision (paracetamol RSD = 0.31 %; tramadol RSD = 0.70 %), accuracy (paracetamol recovery = 99.49 %; tramadol recovery = 98.90 %) and robustness. 2010 info:eu-repo/semantics/masterThesis http://www.nusl.cz/ntk/nusl-279050 cze info:eu-repo/semantics/restrictedAccess |
collection |
NDLTD |
language |
Czech |
format |
Dissertation |
sources |
NDLTD |
description |
HPLC evaluation of selected drugs II. THESIS Petr Vyroubal Charles University in Prague, Faculty of Pharmacy in Hradec Králové, Department of Pharmaceutical Chemistry and Drug Control In this thesis was validated method for simultaneous HPLC analysis of paracetamol and tramadol in combined tablet. As stationary phase the chromatographic column Discovery HS F5, 5 µm, 150×3 mm I.D. made by Supelco was used. Mobile phase was formed by mixture of acetonitrile : ammonium acetate solution 0.005 mol/l, acidified with acetic acid at pH 3.2 in the ratio 20:80 (v/v). A flow rate was 1.0 ml/min. Acetylsalicylic acid was used as an internal standard. The detection was performed at λ = 270 nm using an UV detector. The substances were eluted in following order: paracetamol, acetylsalicylic acid and tramadol. The method was validated for linearity (paracetamol R = 0.9996; tramadol R = 0.9998), precision (paracetamol RSD = 0.31 %; tramadol RSD = 0.70 %), accuracy (paracetamol recovery = 99.49 %; tramadol recovery = 98.90 %) and robustness. |
author2 |
Mokrý, Milan |
author_facet |
Mokrý, Milan Vyroubal, Petr |
author |
Vyroubal, Petr |
spellingShingle |
Vyroubal, Petr HPLC hodnocení vybraných léčiv II |
author_sort |
Vyroubal, Petr |
title |
HPLC hodnocení vybraných léčiv II |
title_short |
HPLC hodnocení vybraných léčiv II |
title_full |
HPLC hodnocení vybraných léčiv II |
title_fullStr |
HPLC hodnocení vybraných léčiv II |
title_full_unstemmed |
HPLC hodnocení vybraných léčiv II |
title_sort |
hplc hodnocení vybraných léčiv ii |
publishDate |
2010 |
url |
http://www.nusl.cz/ntk/nusl-279050 |
work_keys_str_mv |
AT vyroubalpetr hplchodnocenivybranychlecivii AT vyroubalpetr hplcevaluationofselecteddrugsii |
_version_ |
1718468619253317632 |