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Wyszukujesz frazę "Manikandan, S." wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
Development and validation of reversed phase gradient HPLC method for the simultaneous estimation of olmesartan medoxomil and chlorthalidone in dosage forms
Autorzy:
Manikandan, S.
Thirunarayanan, G.
Powiązania:
https://bibliotekanauki.pl/articles/1194011.pdf
Data publikacji:
2015
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
Accuracy
Acetonitrile
Buffer pH 3.0
Chlorthalidone
Forced degradation
Linearity
Olmesartan medoxomil
Precision
RP-gradient HPLC
Robustness
Simultaneous estimation
Opis:
The main objective of the proposed study is to develop and validate a new stability indicating reverse phase HPLC gradient method for the simultaneous estimation of olmesartan medoxomil and chlorthalidone in combined dosage form. The method is optimized by using zorbax phenyl column (250 x 4.6 mm, 5 μ). For pump-A, ammonium dihydrogen orthophosphate and pump-B, acetonitrile: are used. Phosphate buffer pH was adjusted with orthophosphoric acid to 3.0. Water and acetonitrile (45:50) are used as diluent. The flow rate is 1.5 ml/min and the elutant is monitored at 220 nm with uv detector. The retention time of olmesatran medoxomil and chlorthalidone are 10.70 ±0.1 mins and 4.8 ± 0.1 mins respectively. Precision shows that % Relative standard deviation of olmesartan medoxomil and chlorthalidone is about 0.23 and 0.56 respectively. The percentage recoveries of both the drugs olmesartan medoxomil and chlorthalidone from the dosage formulation are 100.3% and 99.20% respectively. Linearity of olmesartan medoxomil and chlorthalidone is in the range of 10.0 to 60.0 μg/ml and 6.25 μg/ml respectively. Calibration curve shows good linearity and range. The correlation coefficient of olmesartan medoxomil and chlorthalidone is 0.999. And the results obtained for Robustness and Ruggedness are well within the acceptance criteria. The proposed method is found to be simple, rapid, accurate and precise. It is found to be economical and suitable for simultaneous determination of olmesartan medoxomil and chlorthalidone in pharmaceutical dosage form.
Źródło:
World Scientific News; 2015, 9; 101-123
2392-2192
Pojawia się w:
World Scientific News
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Development and validation of dissolution method for levocetirizine dihydrochloride by isocratic reverse phase HPLC
Autorzy:
Thirunarayanan, G.
Manikandan, S.
Powiązania:
https://bibliotekanauki.pl/articles/1194036.pdf
Data publikacji:
2015
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
Accuracy
Buffer
Levocetirizine hydrochloride
Precision
Reverse Phase HPLC
Ruggedness
pH
Opis:
Levocetirizine hydrochloride is an orally active, non-sedative antihistamine used in the symptomatic relief of seasonal and perennial allergic rhinitis. The main objective of the proposed study is to develop and validate a dissolution method of Levocetirizine hydrochloride dosage form by reverse phase HPLC isocratic method. The method is optimized by various filteration methods such as centrifuge and whatman 42. The filteration methods are evaluated by reverse phase isocratic HPLC method using column- Phenomenex Luna - C 18 (250 mm x 4.6 mm; 5 µ), mobile phase – mixture of buffer and acetonitrile (580:420), adjusted pH to 6.0 with 10 % sodium hydroxide. buffer - 4.08 g Potassium dihydrogen orthophosphate in 600 mL of water. The flow rate is 1.0 mL/min and the elutant is monitored at 230 nm with UV detector. The retention time of levocetirizine hydrochloride is 5.5. Precision shows that % relative standard deviation is about 1.1%. The percentage recovery of the levocetirizine from the dosage formulation is 99.6%. The results obtained for robustness and ruggedness of levocetirizine hydrochloride are well within the acceptance criteria. The proposed method is found to be simple, rapid, accurate and precise. The proposed methods are validated as per ICH guidelines and successfully applied for the determination of Levocetirizine tablet.
Źródło:
World Scientific News; 2015, 11; 1-17
2392-2192
Pojawia się w:
World Scientific News
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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