2010
DOI: 10.1007/s10847-010-9901-6
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A comparative study of complexation methods for cefdinir-hydroxypropyl-β-cyclodextrin system

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Cited by 14 publications
(8 citation statements)
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“…These results agree with those obtained by Mohitm et al , who studied the effect of the complexation method on cefdinir–β‐CD complex formation and who suggested that MWI leads to a higher rate of dissolution compared with the complexes prepared by kneading or by co‐evaporation.…”
Section: Resultssupporting
confidence: 92%
See 1 more Smart Citation
“…These results agree with those obtained by Mohitm et al , who studied the effect of the complexation method on cefdinir–β‐CD complex formation and who suggested that MWI leads to a higher rate of dissolution compared with the complexes prepared by kneading or by co‐evaporation.…”
Section: Resultssupporting
confidence: 92%
“…wileyonlinelibrary.com/jsfa More than simply increasing the effectiveness of the process, MWI also provides technological and economic advantages for the industrial scaling up of the process. 27,28 These results agree with those obtained by Mohitm et al, 35 who studied the effect of the complexation method on cefdinir--CD complex formation and who suggested that MWI leads to a higher rate of dissolution compared with the complexes prepared by kneading or by co-evaporation.…”
Section: Effect Of Encapsulation Methods On Essential Co and -Cd Complsupporting
confidence: 81%
“…These results agree with those previously described by Mohit, for the complexation of cefdinir with β ‐CDs by MWI (60° C, 90 s), in a 1:1 molar ratio, adding 66% ethanol to the mixture.…”
Section: Resultsmentioning
confidence: 99%
“…However, to the best of our knowledge, a comprehensive review of the available techniques for preparation of the inclusion complexes in the solid state is missing. The selection of the preparation method of the inclusion complex in the solid state is one of the critical steps in the development of a CD-based product, as it could determine the overall properties and functionality of the developed formulation [19,20]. It has been shown that an efficient CD complexation of the drug provides significantly faster dissolution rate and greater bioavailability enhancement than the corresponding samples, where only partial or no complexation (such as in the simple physical mixture) is achieved [21].…”
Section: Introductionmentioning
confidence: 99%