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1997
DOI: 10.1007/bf02234892
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Interaction of drugs with microcrystalline cellulose at the molecular and supermolecular levels

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Cited by 7 publications
(7 citation statements)
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“…For this purpose, nanocomposites grafted with Phos were subjected to a time delay of 12, 18 and 24 h at 37 1C before bacteria inoculation. 34 Our results showed that in spite of strong binding by intermolecular interactions between these components, the released drug retains its medicinal properties against pathogen microorganism and confirmed that the drug molecule and the nanocomposite are compatible with each other. Nanocomposites grafted with Phos in concentration of 10Â MIC reduced bacterial growth compared to control without cellulose nanofibers (data not shown), but did not result in a complete growth inhibition.…”
Section: View Article Onlinesupporting
confidence: 67%
“…For this purpose, nanocomposites grafted with Phos were subjected to a time delay of 12, 18 and 24 h at 37 1C before bacteria inoculation. 34 Our results showed that in spite of strong binding by intermolecular interactions between these components, the released drug retains its medicinal properties against pathogen microorganism and confirmed that the drug molecule and the nanocomposite are compatible with each other. Nanocomposites grafted with Phos in concentration of 10Â MIC reduced bacterial growth compared to control without cellulose nanofibers (data not shown), but did not result in a complete growth inhibition.…”
Section: View Article Onlinesupporting
confidence: 67%
“…Consequently, drug molecule and nanocomposite are compatible with each other. It is important to mention that strong chemical interaction between these components may lead to complete loss of medical properties of drugs 45 . At the same time, there is possibility of intermolecular interactions since the drug molecule contains various functional groups.…”
Section: Preparation and Characterization Of Nanocomposite Tio 2 mentioning
confidence: 99%
“…The formation of similar inclusion complexes was confirmed on the basis of the IR spectra of SD carbendazim (synonym:medamine), ABZ, fenbendazole (FBZ), and triclabendazole (TCB) with PVP and Arabinogalactan (AG) [35]. Under similar conditions, the medamine substance was subjected to joint mechanical treatment with Microcrystalline cellulose (MCC) [41,42], with plant proanthocyanidines [43], and the corresponding SD were obtained, which had increased solubility in water, better permeability through model semipermeable membranes, and, hence, increased bioavailability.…”
Section: Solid Dispersions Of Anthelmintics For Animal Healthmentioning
confidence: 88%