2016
DOI: 10.1080/22297928.2016.1196148
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Spectrophotometric Methods for Quantitative Determination of Chlorhexidine Gluconate and its Major Impurity, Metabolite and Degradation Product: Para-chloro-aniline

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Cited by 12 publications
(5 citation statements)
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“…After dissolving the polymeric patch, the solution was centrifuged at 3,000 rpm for 10 minutes. The absorbance of the supernatant solution was recorded at 251 nm using a UV spectrophotometer to determine the content of chlorhexidine (Abdelrahman et al, 2016;Fini et al, 2011). To estimate the concentration of chlorhexidine, a calibration was constructed at a concentration range of 0-20 µg/ ml.…”
Section: Phase 2: Determination Of Drug Content and In-vitro Drug Release Studiesmentioning
confidence: 99%
See 1 more Smart Citation
“…After dissolving the polymeric patch, the solution was centrifuged at 3,000 rpm for 10 minutes. The absorbance of the supernatant solution was recorded at 251 nm using a UV spectrophotometer to determine the content of chlorhexidine (Abdelrahman et al, 2016;Fini et al, 2011). To estimate the concentration of chlorhexidine, a calibration was constructed at a concentration range of 0-20 µg/ ml.…”
Section: Phase 2: Determination Of Drug Content and In-vitro Drug Release Studiesmentioning
confidence: 99%
“…The calibration curve was linear with an R 2 value of 0.9605 and the corresponding equation was y = 0.0218x + 0.053. The in-vitro release of chlorhexidine from the polymeric patches was carried out by using a vial method at room temperature for 20 days (Amirthalingam et al, 2017;Shen and Burgess, 2012). The polymeric patch (area: 25 mm 2 ) from each batch was kept in the glass vials containing 1 ml of phosphate buffer pH 6.8.…”
Section: Phase 2: Determination Of Drug Content and In-vitro Drug Release Studiesmentioning
confidence: 99%
“…The evaluation is based on the SD of the response and the slope of the curves of the four studied pesticides, but using a visual non instrumental method regarding to ICH recommendations [15][16][17][18][19][20][21][22][23] for HPTLC method (Table 1).…”
Section: Limits Of Detection and Quantizationmentioning
confidence: 99%
“…In modern analytical laboratories, there is a need for significant stability in analysis techniques, and therefore, analytical methods are continuously changing and developing. Over the past dozen years, numerous papers describing these methods have appeared, such as reversed-phase high-performance liquid chromatography [10][11][12], liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) [13][14][15], spectrophotometric methods [16,17], and electrochemical methods [18][19][20]. The Polish Pharmacopoeia [21] recommends titration in anhydrous acetic acid medium with perchloric acid at 0.1 mol L −1 .…”
Section: Introductionmentioning
confidence: 99%