Pepsin-induced modification of silver nanoparticles in simulated gastric fluid

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dc.contributor.authorT H Jeong-
dc.contributor.authorK B Kim-
dc.contributor.authorS Y Kim-
dc.contributor.authorY R Kim-
dc.contributor.authorJ H Kim-
dc.contributor.authorP T M Thu-
dc.contributor.authorTai Hwan Ha-
dc.contributor.authorS J Ahn-
dc.contributor.authorM D Kim-
dc.contributor.authorY H Kim-
dc.date.accessioned2021-09-07T15:31:06Z-
dc.date.available2021-09-07T15:31:06Z-
dc.date.issued2021-
dc.identifier.issn2215-0382-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/24709-
dc.description.abstractThe behavior of AgNPs in simulated gastric fluids (SGFs) with and without pepsin was studied through time-dependent UV-Vis absorption spectroscopy and transmission electron microscopy. The dissolution at the initial stage and the subsequent particle growth and aggregation were observed in the absence of pepsin in SGF. On the other hand, individual AgNPs were protected via the formation of protein corona when pepsin was introduced into SGF. In addition, the agglomeration of AgNPs continued in SGF with pepsin, and gap narrowing between AgNPs was observed during the agglomeration. Flocculation eventually occurred as a result of continuous agglomeration. In addition, the degree of the agglomeration of AgNPs was found to be determined by the relative quantity of nanoparticles and pepsin. The experimental results indicate that the status of individual NPs and their congregative characteristics should be considered in the evaluation of the safety and toxicity of nanometer-scale materials.-
dc.publisherElsevier-
dc.titlePepsin-induced modification of silver nanoparticles in simulated gastric fluid-
dc.title.alternativePepsin-induced modification of silver nanoparticles in simulated gastric fluid-
dc.typeArticle-
dc.citation.titleColloids and Interface Science Communications-
dc.citation.number0-
dc.citation.endPage100491-
dc.citation.startPage100491-
dc.citation.volume44-
dc.contributor.affiliatedAuthorTai Hwan Ha-
dc.contributor.alternativeName정태현-
dc.contributor.alternativeName김경빈-
dc.contributor.alternativeName김수연-
dc.contributor.alternativeName김유라-
dc.contributor.alternativeName김종훈-
dc.contributor.alternativeNameThu-
dc.contributor.alternativeName하태환-
dc.contributor.alternativeName안상정-
dc.contributor.alternativeName김문덕-
dc.contributor.alternativeName김영헌-
dc.identifier.bibliographicCitationColloids and Interface Science Communications, vol. 44, pp. 100491-100491-
dc.identifier.doi10.1016/j.colcom.2021.100491-
dc.subject.keywordAg nanoparticles-
dc.subject.keywordProtein conona-
dc.subject.keywordPepsin-
dc.subject.keywordPlasmon resonance-
dc.subject.keywordUV-Vis spectroscopy-
dc.subject.keywordTransmission electron microscopy-
dc.subject.localAg nanoparticles-
dc.subject.localProtein conona-
dc.subject.localPepsin-
dc.subject.localPlasmon resonance-
dc.subject.localUV-Vis spectroscopy-
dc.subject.localTransmission electron microscopy-
dc.subject.localtransmission eletron microscopy-
dc.subject.localtransmission electron microscopy-
dc.description.journalClassY-
Appears in Collections:
Division of Bio Technology Innovation > Core Research Facility & Analysis Center > 1. Journal Articles
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