(1)PHA 734 BASIC PHARMACEUTICAL PROCESSES IN DESIGN OF DOSAGE FORMS AND THEIR IMPORTANCE Dersi Kaynakları 1

Dash line; 0.04 M Britton–Robinson buffer solution on 0.2% 2.5 μL of MWCNT-modified GCE TX: Tenoxicam, MWCNT: Multiwalled carbon nanotube, GCE: Glassy carbon electrode..

Appropriate volume of the aliquot was transferred to a 10 mL volumetric fask and the volume was adjusted to the mark with the mobile phase to obtain a solution containing 12

Results obtained from the proposed method for the analysis of both drugs in tablets indicate that the proposed technique can be used for simultaneous quantitation and routine quality

The results of the recovery assay indicate that the method is selective, accurate and precise for the analysis of GEM without interference from the excipients used to formulation

Effect of the level of pore forming agent on in-vitro drug release of porous tablets prepared Response curves clearly shown in Figure 8 clearly shows that formulation having least

Each solutions was measured in three replicated and the linearity was evaluated by linear regression analysis, which was calculated by the least square regression method (Table

Certain analytical parameters of original UV-spectrophotometric and second derivative UV spectrophotometric methods such as limit of detection (LOD) and limit of quantification (LOQ)

Drug absorption is defined as the process of movement of unchanged drug from the site of administration to systemic circulation.. Following absorption, the