Fast-Disintegrating nanofibrous web of Pullulan/Griseofulvin-Cyclodextrin inclusion complexes
buir.contributor.author | Dursun, Engin | |
buir.contributor.orcid | Durgun, Engin|0000-0002-0639-5862 | |
dc.citation.epage | 2633 | en_US |
dc.citation.issueNumber | 5 | |
dc.citation.spage | 2624 | |
dc.citation.volumeNumber | 29 | |
dc.contributor.author | Hsiung, Emmy | |
dc.contributor.author | Celebioglu, Asli | |
dc.contributor.author | Kilic, Mehmet Emin | |
dc.contributor.author | Durgun, Engin | |
dc.date.accessioned | 2024-03-12T13:19:56Z | |
dc.date.available | 2024-03-12T13:19:56Z | |
dc.date.issued | 2023-04-04 | |
dc.department | Institute of Materials Science and Nanotechnology (UNAM) | |
dc.description.abstract | Griseofulvin (GSF) is one of the most widely used antifungal suffering from low water solubility and limited bioavailability. Here, cyclodextrin (CD) derivatives of hydroxypropyl-beta-CD (HPβCD) known for its high-water solubility were used to form inclusion complexes (ICs) with GSF. Here, the molecular modeling study revealed the more efficient complex formation with 1:2 (guest:CD) stoichiometry, so ICs of GSF-HPβCD were prepared using a 1:2 molar ratio (GSF:HPβCD) and then mixed with pullulan (PULL) to generate nanofibers (NFs) using the electrospinning technique. PULL is a nontoxic water-soluble biopolymer and the ultimate PULL/GSF-HPβCD-IC NF was obtained with a defect-free fiber morphology having 805 ± 180 nm average diameter. The self-standing and flexible PULL/GSF-HPβCD-IC NF was achieved to be produced with a loading efficiency of ∼98% corresponding to ∼6.4% (w/w) of drug content. In comparison, the control sample of PULL/GSF NF was formed with a lower loading efficiency value of ∼72% which equals to ∼4.7% (w/w) of GSF content. Additionally, PULL/GSF-HPβCD-IC NF provided an enhanced aqueous solubility for GSF compared to PULL/GSF NF so a faster release profile with ∼2.5 times higher released amount was obtained due to inclusion complexation between GSF and HPβCD within the nanofibrous web. On the other hand, both nanofibrous webs rapidly disintegrated (∼2 s) in the artificial saliva medium that mimics the oral cavity environment. Briefly, PULL/GSF-HPβCD-IC NF can be a promising dosage formulation as a fast-disintegrating delivery system for antifungal oral administration owing to the improved physicochemical properties of GSF. © 2023 American Chemical Society. | |
dc.embargo.release | 2024-04-04 | |
dc.identifier.doi | 10.1021/acs.molpharmaceut.3c00074 | |
dc.identifier.eissn | 1543-8392 | |
dc.identifier.issn | 1543-8384 | |
dc.identifier.uri | https://hdl.handle.net/11693/114615 | |
dc.language.iso | en | |
dc.publisher | American Chemical Society | |
dc.relation.isversionof | https://dx.doi.org/10.1021/acs.molpharmaceut.3c00074 | |
dc.source.title | Molecular Pharmaceutics | |
dc.subject | Cyclodextrin | |
dc.subject | Antifungal | |
dc.subject | Electrospinning | |
dc.subject | Fast Disintegrating Drug Delivery | |
dc.subject | Griseofulvin | |
dc.subject | Pullulan | |
dc.title | Fast-Disintegrating nanofibrous web of Pullulan/Griseofulvin-Cyclodextrin inclusion complexes | |
dc.type | Article |
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