2013
DOI: 10.1016/j.ejps.2013.02.023
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Drug release from nanoparticles embedded in four different nanofibrillar cellulose aerogels

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Cited by 212 publications
(112 citation statements)
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“…The DCNF aerogel showed controlled release behavior, with 69.205%±2.5% of the drug being released in 24 hours, while almost-complete drug release was seen within 12 hours from the drug solution. The dissolution behavior from the cellulose matrix is primarily dependent on the penetration of medium into the matrix and the swelling properties of the porous matrix formed after lyophilization, 12 in addition to the dissolution of the drug from the matrix.…”
Section: In Vitro Drug Release Studymentioning
confidence: 99%
“…The DCNF aerogel showed controlled release behavior, with 69.205%±2.5% of the drug being released in 24 hours, while almost-complete drug release was seen within 12 hours from the drug solution. The dissolution behavior from the cellulose matrix is primarily dependent on the penetration of medium into the matrix and the swelling properties of the porous matrix formed after lyophilization, 12 in addition to the dissolution of the drug from the matrix.…”
Section: In Vitro Drug Release Studymentioning
confidence: 99%
“…An example of topical drug delivery using hydrophobins is formulation of the drug terbinafine which enhances the permeation of terbinafine through human nails (Vejnovic et al 2010b). Instead of directly coating drug nanoparticles, hydrophobins can also be used to modify the surface stability and biocompatibility of already existing drug-loaded particles of porous silicon (Bimbo et al 2011) and cellulose (Valo et al 2011(Valo et al , 2013.…”
Section: Dispersal Of Hydrophobic Solids Liquids and Airmentioning
confidence: 99%
“…One approach included coating of drug nanoparticles with hydrophobic proteins and embedding them in hydrogels that were subsequently freeze-dried into aerogels [28].…”
Section: Enzymatic Production Of Nanocellulosementioning
confidence: 99%