“…and the United States Pharmacopoeia (USP) includes the dispersion of the standard compound in anhydrous acetic acid followed by titration with perchloric acid and potentiometric determination of the endpoint [ 8 , 9 ], while for the determination of DS in slow-release tablets, the USP proposes its dispersion in a methanol–water mixture (70:30) and subsequent analysis in a liquid chromatograph with a UV detector, using methanol and phosphate buffer (pH 2.5) as mobile phase components [ 10 ]. In recent decades, several analytical methods have been developed for the determination of diclofenac in drug products, including spectrophotometric [ 7 , 11 , 12 , 13 , 14 , 15 , 16 ], spectroscopic [ 17 , 18 , 19 , 20 , 21 ], fluorimetric [ 22 ], potentiometric [ 22 , 23 , 24 , 25 , 26 , 27 ], and chromatographic methods [ 28 , 29 , 30 , 31 , 32 , 33 , 34 ].…”