2018
DOI: 10.1016/j.ejpb.2018.05.023
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Prolonged drug release properties for orodispersible films by combining hot-melt extrusion and solvent casting methods

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Cited by 50 publications
(31 citation statements)
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“…Even though rapid disintegrating is the main feature of ODFs, in particular cases prolonged drug release from ODFs would also be beneficial, especially for patients with swallowing deficiencies. Prolonged drug release from ODFs has been achieved by incorporating drug-loaded matrix particles based on Eudragit® RS and silicon dioxide [92]. In that study, the matrix particles, with theophylline as a model drug, were produced by hot melt extrusion (HME), and the ODFs were subsequently produced by the solvent casting method.…”
Section: Prolonged Drug Releasementioning
confidence: 99%
“…Even though rapid disintegrating is the main feature of ODFs, in particular cases prolonged drug release from ODFs would also be beneficial, especially for patients with swallowing deficiencies. Prolonged drug release from ODFs has been achieved by incorporating drug-loaded matrix particles based on Eudragit® RS and silicon dioxide [92]. In that study, the matrix particles, with theophylline as a model drug, were produced by hot melt extrusion (HME), and the ODFs were subsequently produced by the solvent casting method.…”
Section: Prolonged Drug Releasementioning
confidence: 99%
“…The other possibility is to suspend the drug in the aqueous solution of the polymer used for casting the film, which allows uncontrolled recrystallization to be avoided [8,16,17,[19][20][21][22][23][24]. However, the formulation of such biphasic films, containing suspended API, implies serious challenges regarding the uniformity of the content, texture, and appropriate mechanical properties of the films [15].…”
Section: Introductionmentioning
confidence: 99%
“…Other administration formulations can be explored, including a single dose, long-acting injectable, a trans-mucosal gel that children can put under their tongue, or oral nano-suspensions that would be taken up by mucosal cells for slow release. Gummies with delayed release formulations or transdermal patches are also possible delivery systems [67][68][69][70][71][72]. Although not established, we speculate that the ideal dosing target would be once a month, with a maximum frequency of once in every one to two weeks [15].…”
Section: Slow Release Formulation Of Bkis To Achieve Steady State Thementioning
confidence: 93%