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dc.contributor.authorStie, MB
dc.contributor.authorCorezzi, M
dc.contributor.authorJuncos Bombin, AD
dc.contributor.authorAjalloueian, F
dc.contributor.authorAttrill, E
dc.contributor.authorPagliara, S
dc.contributor.authorJacobsen, J
dc.contributor.authorChronakis, IS
dc.contributor.authorNielsen, HM
dc.contributor.authorFoderà, V
dc.date.accessioned2020-03-03T15:09:50Z
dc.date.issued2020-01-08
dc.description.abstractProtein-based drug carriers are an interesting alternative to traditional polymeric drug delivery systems due to their intrinsic biocompatibility and biodegradability. Electrospinning of neat proteins holds advantages over electrospinning of protein mixtures, e.g., whey isolates, such as better control of the physicochemical and biological function of the resulting nanofiber-based system. In this study, we explore electrospinning of the isolated milk protein α-lactalbumin (ALA), which is a whey protein with important nutritional and pharmacological properties. Via waterborne electrospinning of ALA with a minimum amount of poly(ethylene oxide) (PEO) as a cospininng polymer, nanofibers of high protein content were successfully produced (up to 84% (w/w)). We demonstrate the ability to produce ALA-based nanofibers with a high degree of tunability in terms of size, stability in water, and mechanical properties. The nanofibers displayed excellent biocompatibility in vitro as the viability of cultured TR146 human buccal epithelium and NIH 3T3 murine fibroblast cells was not influenced by exposure to ALA-based nanofibers. ALA-based nanofibers were loaded with up to 6% (w/w) ampicilin, and the nanofibers were capable of maintaining the activity of the antibiotic after electrospinning and cross-linking. Using such a property of the material, we demonstrate that ampicillin-loaded nanofibers successfully inhibit the growth of Gram-negative bacteria in vitro. Importantly, after treatment with ampicillin-loaded nanofibers, no bacterial regrowth was observed, which indicates that this treatment may clear eventual persisters to ampicillin. Finally, the structural properties of the native functional protein were maintained after release of ALA from the nanofibers. This promotes our platform, not only as a sustainable protein-based drug delivery system, but also as an innovative solid form of ALA for food and pharmaceutical applications.en_GB
dc.description.sponsorshipVillum Foundationen_GB
dc.description.sponsorshipDanish Council for Independent Research; Technology and Productionen_GB
dc.description.sponsorshipRoyal Societyen_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.description.sponsorshipWellcome Trusten_GB
dc.identifier.citationVol. 3 (2), pp. 1910-1921en_GB
dc.identifier.doi10.1021/acsanm.9b02557
dc.identifier.grantnumber19175en_GB
dc.identifier.grantnumberDFF-6111-00333en_GB
dc.identifier.grantnumber4093-00282Aen_GB
dc.identifier.grantnumber4217-00048Aen_GB
dc.identifier.grantnumberRG180007en_GB
dc.identifier.grantnumberMC_PC_17189en_GB
dc.identifier.grantnumberMR/P016162/1en_GB
dc.identifier.grantnumberWT097835/Z/11/Zen_GB
dc.identifier.urihttp://hdl.handle.net/10871/120148
dc.language.isoenen_GB
dc.publisherAmerican Chemical Societyen_GB
dc.rights.embargoreasonUnder embargo until 8 January 2021 in compliance with publisher policyen_GB
dc.rights© 2020 American Chemical Societyen_GB
dc.subjectelectrospinningen_GB
dc.subjectα-lactalbuminen_GB
dc.subjectdrug deliveryen_GB
dc.subjectsustainable protein-based materialsen_GB
dc.subjectGram-negative bacteriaen_GB
dc.subjectantibioticsen_GB
dc.subjectgreen chemistryen_GB
dc.titleWaterborne Electrospinning of α-Lactalbumin Generates Tunable and Biocompatible Nanofibers for Drug Deliveryen_GB
dc.typeArticleen_GB
dc.date.available2020-03-03T15:09:50Z
dc.identifier.issn2574-0970
dc.descriptionThis is the author accepted manuscript. The final version is available from the American Chemical Society via the DOI in this recorden_GB
dc.identifier.journalACS Applied Nano Materialsen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2020-01-08
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2020-01-08
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-03-03T15:05:57Z
refterms.versionFCDAM
refterms.panelAen_GB


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