N,N,N-Trimethyl chitosan nanoparticles for controlled intranasal delivery of HBV surface antigen

Authors
Subbiah, RameshRamalingam, PrakashRamasundaram, SubramaniyanKim, Do YangPark, KwideokRamasamy, Mohan K.Choi, Kyoung Jin
Issue Date
2012-08-01
Publisher
ELSEVIER SCI LTD
Citation
CARBOHYDRATE POLYMERS, v.89, no.4, pp.1289 - 1297
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.
Keywords
TRIMETHYL CHITOSAN; TMC NANOPARTICLES; VACCINE DELIVERY; DRUG-DELIVERY; CHLORIDE; SYSTEM; IMMUNIZATION; ADJUVANT; MCC; TRIMETHYL CHITOSAN; TMC NANOPARTICLES; VACCINE DELIVERY; DRUG-DELIVERY; CHLORIDE; SYSTEM; IMMUNIZATION; ADJUVANT; MCC; Trimethyl chitosan; Nanoparticles; Controlled intranasal delivery; Atomic force microscopy; In vivo immunological study
ISSN
0144-8617
URI
https://pubs.kist.re.kr/handle/201004/128988
DOI
10.1016/j.carbpol.2012.04.056
Appears in Collections:
KIST Article > 2012
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