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dc.contributor.authorCheong, Yuen Ki
dc.contributor.authorArce, Mariana
dc.contributor.authorBenito, Alejandro
dc.contributor.authorChen, Daijie
dc.contributor.authorCrisóstomo, Noemi Luengo
dc.contributor.authorKerai, Laxmi
dc.contributor.authorRodríguez, Guillermo
dc.contributor.authorValverde, José L.
dc.contributor.authorVadalia, Mansukhlal
dc.contributor.authorCerpa-Naranjo, Arisbel
dc.contributor.authorRen, Guogang
dc.date.accessioned2020-05-12T00:10:18Z
dc.date.available2020-05-12T00:10:18Z
dc.date.issued2020-04-25
dc.identifier.citationCheong , Y K , Arce , M , Benito , A , Chen , D , Crisóstomo , N L , Kerai , L , Rodríguez , G , Valverde , J L , Vadalia , M , Cerpa-Naranjo , A & Ren , G 2020 , ' Synergistic Antifungal Study of PEGylated Graphene Oxides and Copper Nanoparticles against Candida albicans ' , Nanomaterials , vol. 10 , no. 5 , 819 . https://doi.org/10.3390/nano10050819
dc.identifier.issn2079-4991
dc.identifier.otherORCID: /0000-0001-8865-1526/work/74071644
dc.identifier.otherORCID: /0000-0001-8977-3381/work/74071820
dc.identifier.urihttp://hdl.handle.net/2299/22682
dc.description© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
dc.description.abstractThe coupling reactions of polyethylene glycol (PEG) with two different nano-carbonaceous materials, graphene oxide (GO) and expanded graphene oxide (EGO), were achieved by amide bond formations. These reactions yielded PEGylated graphene oxides, GO-PEG and EGO-PEG. Whilst presence of the newly formed amide links (NH-CO) were confirmed by FTIR stretches observed at 1732 cm−1 and 1712 cm−1, the associated Raman D- and G-bands resonated at 1311/1318 cm−1 and 1584/1595 cm−1 had shown the carbonaceous structures in both PEGylated products remain unchanged. Whilst SEM images revealed the nano-sheet structures in all the GO derivatives (GO/EGO and GO-PEG/EGO-PEG), TEM images clearly showed the nano-structures of both GO-PEG and EGO-PEG had undergone significant morphological changes from their starting materials after the PEGylated processes. The successful PEGylations were also indicated by the change of pH values measured in the starting GO/EGO (pH 2.6–3.3) and the PEGylated GO-PEG/EGO-PEG (pH 6.6–6.9) products. Initial antifungal activities of selective metallic nanomaterials (ZnO and Cu) and the four GO derivatives were screened against Candida albicans using the in vitro cut-well method. Whilst the haemocytometer count indicated GO-PEG and copper nanoparticles (CuNPs) exhibited the best antifungal effects, the corresponding SEM images showed C. albicans had, respectively, undergone extensive shrinkage and porosity deformations. Synergistic antifungal effects all GO derivatives in various ratio of CuNPs combinations were determined by assessing C. albicans viabilities using broth dilution assays. The best synergistic effects were observed when a 30:70 ratio of GO/GO-PEG combined with CuNPs, where MIC50 185–225 μm/mL were recorded. Moreover, the decreased antifungal activities observed in EGO and EGO-PEG may be explained by their poor colloidal stability with increasing nanoparticle concentrations.en
dc.format.extent19
dc.format.extent8514507
dc.language.isoeng
dc.relation.ispartofNanomaterials
dc.subjectantimicrobial nanoparticles; PEGylated graphene oxide; Candida albicans; copper nanoparticles (CuNPs), antifungal; minimum inhibitory concentration (MIC)
dc.titleSynergistic Antifungal Study of PEGylated Graphene Oxides and Copper Nanoparticles against Candida albicansen
dc.contributor.institutionCentre for Engineering Research
dc.contributor.institutionMaterials and Structures
dc.contributor.institutionBioEngineering
dc.contributor.institutionSchool of Physics, Engineering & Computer Science
dc.contributor.institutionDepartment of Engineering and Technology
dc.contributor.institutionDepartment of Clinical and Pharmaceutical Sciences
dc.contributor.institutionCentre for Research into Topical Drug Delivery and Toxicology
dc.contributor.institutionSchool of Life and Medical Sciences
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.3390/nano10050819
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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