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Enzyme delivery using the 30Kc19 protein and human serum albumin nanoparticles

DC Field Value Language
dc.contributor.authorLee, Hong Jai-
dc.contributor.authorPark, Hee Ho-
dc.contributor.authorKim, Jeong Ah-
dc.contributor.authorPark, Ju Hyun-
dc.contributor.authorRyu, Jina-
dc.contributor.authorChoi, Jeongseon-
dc.contributor.authorLee, Jongmin-
dc.contributor.authorRhee, Won Jong-
dc.contributor.authorPark, Tai Hyun-
dc.creator박태현-
dc.date.accessioned2014-04-02T00:54:52Z-
dc.date.available2014-04-02T00:54:52Z-
dc.date.created2018-07-09-
dc.date.issued2014-02-
dc.identifier.citationBIOMATERIALS, Vol.35 No.5, pp.1696-1704-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://hdl.handle.net/10371/91297-
dc.description.abstractNanoparticles have been widely used for delivering various chemical and biomolecular drugs, such as anti-cancer drugs and therapeutic proteins. Among nanoparticles, protein nanoparticles have advantages of non-cytotoxicity and biodegradability. In this study, a recombinant 30Kc19 protein was applied to human serum albumin (HSA) nanoparticles to enhance cellular uptake and stability of a nanoparticle cargo enzyme. The 30Kc19 protein, which originates from silkworm, has cell-penetrating and enzymestabilizing abilities. Therefore, 30Kc19-HSA nanoparticles were expected to enhance cellular uptake and stability of an enzyme loaded on the nanoparticles. Here, nanoparticles loaded with beta-galactosidase were prepared using the desolvation method. The 30Kc19-HSA nanoparticles were uniformly spherical in shape, dispersed evenly in phosphate buffered saline and cell culture media, and released beta-galactosidase in a sustained manner. The 30Kc19-HSA nanoparticles had negligible toxicity to animal cells and exhibited enhanced cellular uptake and intracellular stability of beta-galactosidase in HeLa and HEK293 cells when compared with those of HSA nanoparticles. These results suggest that 30Kc19-HSA protein nanoparticles could be used as a versatile tool for drug delivery to various cells. (C) 2013 Elsevier Ltd. All rights reserved.-
dc.language영어-
dc.language.isoenen
dc.publisherELSEVIER SCI LTD-
dc.titleEnzyme delivery using the 30Kc19 protein and human serum albumin nanoparticles-
dc.typeArticle-
dc.author.alternative이홍재-
dc.author.alternative박희호-
dc.author.alternative김정아-
dc.author.alternative박주현-
dc.author.alternative류지나-
dc.author.alternative최정선-
dc.author.alternative이종민-
dc.author.alternative이원종-
dc.author.alternative박태현-
dc.identifier.doi10.1016/j.biomaterials.2013.11.001-
dc.citation.journaltitleBIOMATERIALS-
dc.identifier.wosid000330156100034-
dc.identifier.scopusid2-s2.0-84890155567-
dc.description.srndOAIID:oai:osos.snu.ac.kr:snu2014-01/102/0000002410/1-
dc.description.srndSEQ:1-
dc.description.srndPERF_CD:SNU2014-01-
dc.description.srndEVAL_ITEM_CD:102-
dc.description.srndUSER_ID:0000002410-
dc.description.srndADJUST_YN:N-
dc.description.srndEMP_ID:A002014-
dc.description.srndDEPT_CD:458-
dc.description.srndCITE_RATE:7.604-
dc.description.srndFILENAME:1. (2014.2) enzyme delivery using the 30kc19 protein and human serum albumin.pdf-
dc.description.srndDEPT_NM:화학생물공학부-
dc.description.srndEMAIL:thpark@snu.ac.kr-
dc.description.srndSCOPUS_YN:Y-
dc.description.srndCONFIRM:Y-
dc.citation.endpage1704-
dc.citation.number5-
dc.citation.startpage1696-
dc.citation.volume35-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorPark, Tai Hyun-
dc.identifier.srnd2014-01/102/0000002410/1-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusSILKWORM HEMOLYMPH-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusRECOMBINANT PROTEIN-
dc.subject.keywordPlusHSA NANOPARTICLES-
dc.subject.keywordPlusEPO PRODUCTION-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusENHANCEMENT-
dc.subject.keywordAuthorProtein-
dc.subject.keywordAuthorProtein nanoparticle-
dc.subject.keywordAuthorDrug delivery-
dc.subject.keywordAuthorDrug release-
dc.subject.keywordAuthorEnzyme stability-
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