Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Subbiah, Ramesh | - |
dc.contributor.author | Ramalingam, Prakash | - |
dc.contributor.author | Ramasundaram, Subramaniyan | - |
dc.contributor.author | Kim, Do Yang | - |
dc.contributor.author | Park, Kwideok | - |
dc.contributor.author | Ramasamy, Mohan K. | - |
dc.contributor.author | Choi, Kyoung Jin | - |
dc.date.accessioned | 2024-01-20T14:04:30Z | - |
dc.date.available | 2024-01-20T14:04:30Z | - |
dc.date.created | 2021-09-04 | - |
dc.date.issued | 2012-08-01 | - |
dc.identifier.issn | 0144-8617 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/128988 | - |
dc.description.abstract | Hepatitis 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.language | English | - |
dc.publisher | ELSEVIER SCI LTD | - |
dc.subject | TRIMETHYL CHITOSAN | - |
dc.subject | TMC NANOPARTICLES | - |
dc.subject | VACCINE DELIVERY | - |
dc.subject | DRUG-DELIVERY | - |
dc.subject | CHLORIDE | - |
dc.subject | SYSTEM | - |
dc.subject | IMMUNIZATION | - |
dc.subject | ADJUVANT | - |
dc.subject | MCC | - |
dc.title | N,N,N-Trimethyl chitosan nanoparticles for controlled intranasal delivery of HBV surface antigen | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.carbpol.2012.04.056 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | CARBOHYDRATE POLYMERS, v.89, no.4, pp.1289 - 1297 | - |
dc.citation.title | CARBOHYDRATE POLYMERS | - |
dc.citation.volume | 89 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 1289 | - |
dc.citation.endPage | 1297 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000305593900040 | - |
dc.identifier.scopusid | 2-s2.0-84861602931 | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Applied | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.relation.journalWebOfScienceCategory | Polymer Science | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalResearchArea | Polymer Science | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | TRIMETHYL CHITOSAN | - |
dc.subject.keywordPlus | TMC NANOPARTICLES | - |
dc.subject.keywordPlus | VACCINE DELIVERY | - |
dc.subject.keywordPlus | DRUG-DELIVERY | - |
dc.subject.keywordPlus | CHLORIDE | - |
dc.subject.keywordPlus | SYSTEM | - |
dc.subject.keywordPlus | IMMUNIZATION | - |
dc.subject.keywordPlus | ADJUVANT | - |
dc.subject.keywordPlus | MCC | - |
dc.subject.keywordAuthor | Trimethyl chitosan | - |
dc.subject.keywordAuthor | Nanoparticles | - |
dc.subject.keywordAuthor | Controlled intranasal delivery | - |
dc.subject.keywordAuthor | Atomic force microscopy | - |
dc.subject.keywordAuthor | In vivo immunological study | - |
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