Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/78618
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dc.contributor.authorGöttel, Benedikt-
dc.contributor.authorLucas, Henrike-
dc.contributor.authorSyrowatka, Frank-
dc.contributor.authorKnolle, Wolfgang-
dc.contributor.authorKuntsche, Judith-
dc.contributor.authorHeinzelmann, Joana-
dc.contributor.authorViestenz, Arne-
dc.contributor.authorMäder, Karsten-
dc.date.accessioned2022-03-25T08:29:37Z-
dc.date.available2022-03-25T08:29:37Z-
dc.date.issued2020-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/80572-
dc.identifier.urihttp://dx.doi.org/10.25673/78618-
dc.description.abstractThe purpose of our research was the development of Amphotericin B-loaded in situ gelling nanofibers for the treatment of keratomycosis. Different formulation strategies were applied to increase the drug load of the sparingly water-soluble Amphotericin B in electrospun Gellan Gum/Pullulan fibers. These include bile salt addition, encapsulation in poly(lactic-co-glycolic acid) (PLGA) nanoparticles and formation of a polymeric Amphotericin B polyelectrolyte complex. The Amphotericin B polyelectrolyte complex (AmpB-Eu L) performed best and was very effective against the fungal strain Issatchenkia orientalis in vitro. The complex was characterized in detail by attenuated total reflection infrared spectroscopy, X-ray powder diffraction, and differential scanning calorimetry. A heat induced stress test was carried out to ensure the stability of the polyelectrolyte complex. To gain information about the cellular tolerance of the developed polyelectrolyte complex a new, innovative multilayered-stratified human cornea cell model was used for determination of the cellular toxicity in vitro. For a safe therapy, the applied ophthalmic drug delivery system has to be sterile. Sterilization by electron irradiation caused not degradation of pure Amphotericin B and also for the bile salt complex. Furthermore, the developed Amphotericin B polyelectrolyte complex was not degraded by the irradiation process. In conclusion, a new polyelectrolyte Amphotericin B complex has been found which retains the antifungal activity of the drug with sufficient stability against irradiation-sterilization induced drug degradation. Furthermore, in comparison with the conventional used eye drop formulation, the new AmpB-complex loaded nanofibers were less toxic to cornea cells in vitro. Electrospinning of the Amphotericin B polyelectrolyte complex with Gellan Gum/ Pullulan leads to the formation of nanofibers with in situ gelling properties, which is a new and promising option for the treatment of keratomycosis.eng
dc.description.sponsorshipPublikationsfonds MLU-
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc610-
dc.titleIn situ gelling amphotericin B nanofibers : a new option for the treatment of keratomycosiseng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleFrontiers in Bioengineering and Biotechnology-
local.bibliographicCitation.volume8-
local.bibliographicCitation.publishernameFrontiers Media-
local.bibliographicCitation.publisherplaceLausanne-
local.bibliographicCitation.doi10.3389/fbioe.2020.600384-
local.subject.keywordskeratomycosis, electrospinning, amphotericin B, polyelectrolyte complex, PLGA nanoparticle, in situ forming, hydrogel, ocular drug delivery-
local.openaccesstrue-
dc.identifier.ppn1743354940-
local.bibliographicCitation.year2020-
cbs.sru.importDate2022-03-25T08:28:22Z-
local.bibliographicCitationEnthalten in Frontiers in Bioengineering and Biotechnology - Lausanne : Frontiers Media, 2013-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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