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Wyświetlanie 1-2 z 2
Tytuł:
DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF TIZANIDINE HCL AND MELOXICAM IN BILAYER MUCOADHESIVE BUCCAL FILMS
Autorzy:
Zaman, Muhammad
hanif, Muhammad
Murtaza, Hassan
Powiązania:
https://bibliotekanauki.pl/articles/895591.pdf
Data publikacji:
2018-08-31
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
RP-HPLC
method development
simultaneous determination
Recoveries
Opis:
Tizanidine HCl (TZN HCl) is a muscle relaxant and Meloxicam (MLX) is a non-steroidal anti-inflammatory drug used for various pain disorders. They are extensively used as combination therapy in various pain disorder and the need is to develop a suitable method for their simultaneous determination loaded in a single dosage form. Objective of the study was to develop a simple, specific, and accurate reverse phase high performance liquid chromatographic (RP-HPLC) method was developed for the simultaneous determination of TZN HCl and MLX. A kromasil C18 (250×4.60 mm dimensions, 5 μm particle size) column with mobile phase consisting of methanol:water (80:20) was used at isocratic mode. pH of the mobile phase was adjusted to 3.0 by using ortho phosphoric acid and 228nm was taken as lambda max for the detection of drugs. Flow rate was adjusted to 0.8ml/min at ambient temperature with average operating pressure of 140 bar. The retention time of TZN HCl was 2.613 min and of MLX was 6.992 min with resolution of 3.23 and both drugs showed satisfactory linearity in the range of 5-50 μg/mL with correlation coefficient (R2) 0.09997 and 0.9993 respectively. The method was validated as per ICH guidelines and found to be précised with less than 2% relative standard deviation (%RSD). % Recoveries of TZN HCl and MLX were in the range of 99.01% to 100.47% and 98.18% to 100.88% respectively. From the result, it was concluded that the method is suitable for the simultaneous quantification of TZN HCl and MLX.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2018, 75, 4; 851-859
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
BOX BEHNKEN DESIGN: A STATISTICAL APPROACH TO EVALUATE THE EFFECT OF CROSSLINKED CARBOXYMETHYL CELLULOSE AND SODIUM STARCH GLYCOLATE ON RELEASE KINETICS OF DRUG
Autorzy:
Hanif, Muhammad
Abbas, Ghulam
Rasul, Akhtar
Khan, Sajid M.
Amir, Muhammad N.
Powiązania:
https://bibliotekanauki.pl/articles/895395.pdf
Data publikacji:
2018-08-31
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
FTIR
XRD
DSC
quality by design
domperidone maleate
drug release kinetics
Opis:
The aim of study was to evaluate the release kinetics of domperidone maleate (DM) from immediate release (IR) tablets prepared by wet granulation method. Box behnken design (BBD) was used to optimize and evaluate the main, interaction and quadratic effects of independent variables i.e. crosslinked carboxymethyl cellulose (CMC) (X1), sodium starch glycolate (SSG) (X2) and starch (X3) on responses R2 of first order (YI) and β value of weibull model (Y2). Prepared tablets were characterized by various physical tests, in-vitro drug release, fourier transform infrared spectroscopy (FTIR), X-ray diffractometry (XRD) and differential scanning calorimetry (DSC). Accelerated stabilities studies were performed on optimized formulation D9. Y1 and Y2 were ranged from 0.9959 to 0.9994 and 0.041 to 0.912 respectively. β value of weibull model indicated the parabolic shape of dissolution curve. The quadratic model fit the data well and the resulting equations were used to predict the responses in the box behnken design. FTIR spectra showed the compatibility of DM with CMC and SSG. XRD presented diffraction lines indicates crystalline nature of drug. DSC thermograms indicated endothermic peak at 220 0C for DM. Stabilities studies revealed that no significant change in hardness, friability, disintegration time and dissolution release profile of DM. It is concluded that a combination of CMC and SSG can be used to enhance the dissolution and release kinetics of IR tablets of DM.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2018, 75, 4; 965-975
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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