We conducted an experiment changing the number of students seated between two tablets (Nexus 9) from 9, 5, 3, to 0. When the number of students is 9, students were seated on the chairs by all the desks between the two tablets as shown in Fig. 9.
Differences recorded in the surface roughness for the opposite sides of a given tablet can lead to different dissolution rate of the tablet, and also serve as the basis for screening of fake tablets as will be shown later in the this study.
The ebastine particles could be as clearly identified as the PS microspheres in tablets using the Raman chemical image as shown in Fig. 11b.
Based on Table 3, the size of tablets was observed to be uniform as shown by the low standard deviation value for thickness, diameter, and weight variation.
Two tablets were placed adjacent to each other as shown in Fig. 3.
The radiographs taken after 0.5 h indicated buoyancy of the tablet, in case of volunteers in fed state as shown in Figure 7.
The results of drug content evaluations of tablets prepared by spraying have proved this assumption, as shown in Table 4.
The silymarin content in the seeds and tablet were significantly higher using sonication compared with Soxhlet (F 1,8) = 24.6, p <0.01; F(1,8) = 12.0, p <0.01), as shown in Fig. 4.
The results demonstrated excellent drug uniformity as shown in table 4. Table 4 Results of content uniformity testing of Sirdalud® tablets using the proposed method.
Furthermore, in patients with chronic pain due to osteoarthritis of the hips and/or knees, diclofenac sodium extended-release tablets were shown to be as effective as controlled-release tramadol, an opioid analgesic [ 120].
