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dc.contributor.authorSubbiah, Ramesh-
dc.contributor.authorRamalingam, Prakash-
dc.contributor.authorRamasundaram, Subramaniyan-
dc.contributor.authorKim, Do Yang-
dc.contributor.authorPark, Kwideok-
dc.contributor.authorRamasamy, Mohan K.-
dc.contributor.authorChoi, Kyoung Jin-
dc.date.accessioned2024-01-20T14:04:30Z-
dc.date.available2024-01-20T14:04:30Z-
dc.date.created2021-09-04-
dc.date.issued2012-08-01-
dc.identifier.issn0144-8617-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/128988-
dc.description.abstractHepatitis B virus surface antigen (HBsAg) loaded N,N,N-trimethyl chitosan nanoparticles (N-TMC NPs) were formulated and studied for controlled intranasal delivery. The size and surface properties of the NPs can be tuned by modifying the concentration of N-TMC and found to be 66 +/- 13, 76 +/- 9 nm for 0.25 and 0.5 wt.% respectively. Loading of 380 and 760 ill of HBsAg yielded 143 +/- 33, 259 +/- 47 nm sized spherical N-TMC NPs with highest loading efficiency and capacity of 90-93%, and 96-97% respectively. In vitro drug release analysis ensured 93% cumulative release of HBsAg antigen over prolonged period (43 days). In vivo immunological study was performed using 6-8 weeks old female BALB mice and reveals adjuvants efficiency of NPs for antigen is highly stable and better than standard. Obtained results show that N-TMC NPs can be extensively used in controlled intra nasal delivery to treat various diseases including hepatitis B and allergic rhinitis. (C) 2012 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.subjectTRIMETHYL CHITOSAN-
dc.subjectTMC NANOPARTICLES-
dc.subjectVACCINE DELIVERY-
dc.subjectDRUG-DELIVERY-
dc.subjectCHLORIDE-
dc.subjectSYSTEM-
dc.subjectIMMUNIZATION-
dc.subjectADJUVANT-
dc.subjectMCC-
dc.titleN,N,N-Trimethyl chitosan nanoparticles for controlled intranasal delivery of HBV surface antigen-
dc.typeArticle-
dc.identifier.doi10.1016/j.carbpol.2012.04.056-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCARBOHYDRATE POLYMERS, v.89, no.4, pp.1289 - 1297-
dc.citation.titleCARBOHYDRATE POLYMERS-
dc.citation.volume89-
dc.citation.number4-
dc.citation.startPage1289-
dc.citation.endPage1297-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000305593900040-
dc.identifier.scopusid2-s2.0-84861602931-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPolymer Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusTRIMETHYL CHITOSAN-
dc.subject.keywordPlusTMC NANOPARTICLES-
dc.subject.keywordPlusVACCINE DELIVERY-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusCHLORIDE-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusIMMUNIZATION-
dc.subject.keywordPlusADJUVANT-
dc.subject.keywordPlusMCC-
dc.subject.keywordAuthorTrimethyl chitosan-
dc.subject.keywordAuthorNanoparticles-
dc.subject.keywordAuthorControlled intranasal delivery-
dc.subject.keywordAuthorAtomic force microscopy-
dc.subject.keywordAuthorIn vivo immunological study-
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