2016
DOI: 10.15259/pcacd.21.06
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Physicochemical Characterization and Dissolution Studies of Solid Dispersions of Clotrimazole With Chitosan

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Cited by 2 publications
(2 citation statements)
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“…In the range 900–1200 cm −1 were shown the bands of peaks for the following bonds: 1150 cm −1 (asymmetric stretching of C-O-C bridge), 1059 cm −1 (C-O stretch, secondary hydroxyl group), and 1026 cm −1 (C-O stretch, primary hydroxyl group). The peak at 1150 cm −1 was characteristic of glycoside linkages [ 60 , 61 , 62 , 63 ]. These results illustrated that no change occurred in the chemical structure of the S. baicalensis radix extract after being mixed with chitosan.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In the range 900–1200 cm −1 were shown the bands of peaks for the following bonds: 1150 cm −1 (asymmetric stretching of C-O-C bridge), 1059 cm −1 (C-O stretch, secondary hydroxyl group), and 1026 cm −1 (C-O stretch, primary hydroxyl group). The peak at 1150 cm −1 was characteristic of glycoside linkages [ 60 , 61 , 62 , 63 ]. These results illustrated that no change occurred in the chemical structure of the S. baicalensis radix extract after being mixed with chitosan.…”
Section: Resultsmentioning
confidence: 99%
“…Surprisingly, after mixing the lyophilized extract with chitosans, a slight increase in the dissolution rate of wogonin was observed ( Figure 3 c). The previously published studies indicated that chitosan is a proper carrier for poorly water-soluble drugs [ 61 , 64 ].…”
Section: Resultsmentioning
confidence: 99%