2018
DOI: 10.1556/1006.2018.31.6.7
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Comparative high-performance liquid chromatographic and high-performance thin-layer chromatographic study for the simultaneous determination of dapagliflozin and metformin hydrochloride in bulk and pharmaceutical formulation

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Cited by 13 publications
(9 citation statements)
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“…It was found that the recovery percentages were in the range of 98.4–100.4%. The reported methods were used for comparison with the results obtained (Nasser et al, 2018), as shown in Table 2. Comparisons using t‐ and F ‐tests at 95% confidence level were applied, which prove that the difference between the proposed and the reported methods is not significant .…”
Section: Resultsmentioning
confidence: 99%
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“…It was found that the recovery percentages were in the range of 98.4–100.4%. The reported methods were used for comparison with the results obtained (Nasser et al, 2018), as shown in Table 2. Comparisons using t‐ and F ‐tests at 95% confidence level were applied, which prove that the difference between the proposed and the reported methods is not significant .…”
Section: Resultsmentioning
confidence: 99%
“…As a result, they are used in combination therapy with other antidiabetic drugs such as MET (Lajara, 2014). The reported methods for analysis of DAPA and MET in combination include UV spectrophotometry (Bhavyasri & Surekha, 2020; Jani et al, 2015), RP‐HPLC (Abbas et al, 2020; Khalil et al, 2018; Urooj et al, 2017), LC–UV (Hassib et al, 2019), LC–MS/MS (Dias et al, 2019; Shah et al, 2019), capillary electrophoresis (Maher et al, 2019) and TLC–spectrodensitometric methods for simultaneous analysis of DAPA and MET (Abdelrahman et al, 2020; Nasser et al, 2018). These methods are less sensitive with several mobile phases and are applied only to pharmaceutical formulations.…”
Section: Introductionmentioning
confidence: 99%
“…Many spectrophotometric methods [2][3] and chromatographic methods [4][5][6][7][8][9][10][11][12][13] have been reported for estimation of DAPA in bulk and formulation. In combination, DAPA has to be analysed by chromatographic methods [14,15]. A work carried out by Sally et al [14] used acetonitrile: ammonium acetate:10% acetic acid (9:0.9:0.1, v/v) as the mobile phase at 225 nm.…”
Section: Resultsmentioning
confidence: 99%
“…In combination, DAPA has to be analysed by chromatographic methods [14,15]. A work carried out by Sally et al [14] used acetonitrile: ammonium acetate:10% acetic acid (9:0.9:0.1, v/v) as the mobile phase at 225 nm. In another study reported by Parmar et al [15] carried out for simultaneous estimation of DAPA, propanediol and saxagliptin Hydrochloride (SAXA) using Chloroform: Ethyl acetate: methanol: ammonia (6:2:2:2 Drops) as Mobile Phase and 210 nm as detector wave length, the Rf value of DAPA and SAXA was found to be 0.30 and 0.54 respectively.…”
Section: Resultsmentioning
confidence: 99%
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