Evaluation and characterization of Pleurotus eryngii extract-loaded chitosan nanoparticles as antimicrobial agents against some human pathogens

dc.contributor.author Acay, Hilal
dc.contributor.author Yıldırım, Ayfer
dc.contributor.author Erdem Güzel, Elif
dc.contributor.author Baran, Mehmet Fırat
dc.contributor.author Baran, Mehmet Fırat
dc.contributor.other 09.03. Department of Nutrition and Dietetics/ Beslenme ve Diyetetik Bölümü
dc.contributor.other 21.02. Department of Medical Services and Techniques / Tıbbi Hizmetler ve Teknikleri Bölümü
dc.contributor.other 09.02. Department of Midwifery/ Ebelik Bölümü
dc.contributor.other 9. Faculty of Health Sciences / Sağlık Bilimleri Fakültesi
dc.contributor.other 21. Vocational School of Health Services / Sağlık Hizmetleri Meslek Yüksekokulu
dc.contributor.other 01. Mardin Artuklu University / Mardin Artuklu Üniversitesi
dc.date.accessioned 2021-06-29T12:00:20Z
dc.date.available 2021-06-29T12:00:20Z
dc.date.issued 2020
dc.description.abstract With the increase of antibiotic resistance, which is present at a worrying rate, research on the use of newly developed nanoparticles as an antimicrobial agent with green biotechnology has intensified. The study aimed to investigate the antimicrobial effects of chitosan nanoparticles (CSNP) synthesized using Pleurotus eryngii extract (PE). Characterization of P. eryngii-loaded chitosan nanoparticles (PE-CSNPs) was performed with Fourier transform infrared spectrophotometer, X-ray diffraction, Field-emission scanning electron microscopy, Brunauer-Emmett-Teller, Differential scanning calorimetry, and zeta potential techniques. The FE-SEM images showed that the surface morphology of nanoparticles is similar to CS, but has more porosity network and smaller dimensions structure. The average particle size of spherical PE-CSNPs was obtained as 330.1 nm. The specific surface area and average pore diameter of the synthesized nanoparticles were found as 3.99 m2g-1 and 2.25 nm, respectively. X-ray diffraction determines the presence of an amorphous peak at 2θ = 21.2° results from CS and PE. PE-CSNPs synthesized using P. eryngii extract showed strong antimicrobial activity against Escherichia coli, Staphylococcus aureus, Bacillus subtilis, and Candida albicans as 0.0156, 0.0625, 0.0625 and 0.0312 mg ml-1, respectively. Thus, it was determined that chitosan nanoparticles formed by the green synthesis of P. eryngii extract showed strong anti-microbial properties. en_US
dc.identifier.citation Acay H, Yildirim A, Erdem Güzel E, Kaya N, Baran MF. Evaluation and characterization of Pleurotus eryngii extract-loaded chitosan nanoparticles as antimicrobial agents against some human pathogens. Prep Biochem Biotechnol. 2020;50(9):897-906. doi: 10.1080/10826068.2020.1765376. Epub 2020 May 18. PMID: 32420792. en_US
dc.identifier.doi 10.1080/10826068.2020.1765376
dc.identifier.scopus 2-s2.0-85085492728
dc.identifier.uri https://pubmed.ncbi.nlm.nih.gov/32420792/
dc.identifier.uri https://doi.org/10.1080/10826068.2020.1765376
dc.identifier.uri https://hdl.handle.net/20.500.12514/2637
dc.indekslendigikaynak Web of Science en_US
dc.indekslendigikaynak Scopus en_US
dc.indekslendigikaynak PubMed en_US
dc.language.iso en en_US
dc.publisher Taylor & Francis Online en_US
dc.relation.ispartof Preparative Biochemistry & Biotechnology en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Antimicrobial effects; DSC; Pleurotus eryngii; chitosan; zeta potential. en_US
dc.title Evaluation and characterization of Pleurotus eryngii extract-loaded chitosan nanoparticles as antimicrobial agents against some human pathogens en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.description.department MAÜ, Fakülteler, Sağlık Bilimleri Fakültesi, Beslenme ve Diyetetik Bölümü en_US
gdc.description.endpage 906 en_US
gdc.description.issue 9 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.startpage 897 en_US
gdc.description.volume 50 en_US
gdc.description.wosquality Q3
gdc.identifier.pmid 32420792
gdc.identifier.wos WOS:000535120000001
gdc.openalex.fwci 0.877
gdc.scopus.citedcount 19
gdc.wos.citedcount 16
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