Chitosan and xanthan gum were combined in nine different percentages without using any cross-linking agent. The obtained physical matrices were able to give a burst, delayed, or prolonged release of red yeast rice (RYR) on the basis of xanthan gum percentage. In fact, thermal analysis, swelling behavior, and rheological analysis pointed out that a slight interaction among xanthan gum and RYR was present. This was reflected in a burst release when the amount of xanthan gum was under the 30%. On the contrary, a prolonged release was observed when the xanthan gum percent was higher than 70%. A delayed release was observed using similar percentage of the polymers (i.e., F5-F7). The effect of the formulation on RYR inhibition activity toward 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase and on cholesterol production was also evaluated.
Consumi, M., Leone, G., Pepi, S., Tamasi, G., Lamponi, S., Donati, A., et al. (2018). Xanthan Gum-Chitosan: delayed, prolonged, and burst-release tablets using same components in different ratio. ADVANCES IN POLYMER TECHNOLOGY, 37(8), 2936-2945 [10.1002/adv.21965].
Xanthan Gum-Chitosan: delayed, prolonged, and burst-release tablets using same components in different ratio
Consumi, Marco;Leone, Gemma
;Pepi, Simone;Tamasi, Gabriella;Lamponi, Stefania;Donati, Alessandro;Bonechi, Claudia;Rossi, Claudio;Magnani, Agnese
2018-01-01
Abstract
Chitosan and xanthan gum were combined in nine different percentages without using any cross-linking agent. The obtained physical matrices were able to give a burst, delayed, or prolonged release of red yeast rice (RYR) on the basis of xanthan gum percentage. In fact, thermal analysis, swelling behavior, and rheological analysis pointed out that a slight interaction among xanthan gum and RYR was present. This was reflected in a burst release when the amount of xanthan gum was under the 30%. On the contrary, a prolonged release was observed when the xanthan gum percent was higher than 70%. A delayed release was observed using similar percentage of the polymers (i.e., F5-F7). The effect of the formulation on RYR inhibition activity toward 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase and on cholesterol production was also evaluated.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/1040496