Application of chitosan microspheres for nasal delivery of vaccines

被引:106
作者
Kang, Mi Lan [1 ,2 ]
Cho, Chong Su [3 ]
Yoo, Han Sang [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Vet Med, Dept Infect Dis, KRF Prior Zoonot Dis Res Inst, Seoul 151742, South Korea
[2] Seoul Natl Univ, Program Vet Sci BK21, Seoul 151742, South Korea
[3] Seoul Natl Univ, Res Inst Agr & Life Sci, Dept Agr Biotechnol, Seoul 151921, South Korea
关键词
Mucosal vaccines; Nasal vaccines; Delivery systems; Chitosan microspheres; MUCOSAL IMMUNE-RESPONSES; BORDETELLA-BRONCHISEPTICA ANTIGENS; POLYACRYL STARCH MICROPARTICLES; MANNOSE RECEPTOR; INTRANASAL DELIVERY; CONTROLLED-RELEASE; MUCOADHESIVE MICROSPHERES; ORAL IMMUNIZATION; GENE-TRANSFER; CLEARANCE CHARACTERISTICS;
D O I
10.1016/j.biotechadv.2009.06.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nasal vaccines offer several benefits. such as highly vascular mucous membranes, low enzymatic degradation compared to oral vaccines, and greater acceptability to patients Nasal vaccines, however, have to overcome several limitations. including mucociliary clearance and the inefficient uptake of soluble antigens Therefore, nasal vaccines require potent adjuvants and delivery systems to enhance their immunogenicity and to protect their antigens Chitosan is a cheap, biocompatible, biodegradable, mucoadhesive, and nontoxic natural polymer. Chitosan microspheres have been investigated to determine whether they allow the controlled release of drugs and vaccines They have figured in various studies on the vaccine delivery system through the nasal route. Several researchers have developed modified chitosan microspheres through their concomitant use with adjuvants or immunomodulators for an additive and a synergistic effect, and through the mannosylation of chitosan for receptor-mediated targeting antigen presenting cells. The results of the recent researches on chitosan microspheres used as a nasal vaccine delivery system are discussed in this review (C) 2009 Elsevier Inc. All rights reserved
引用
收藏
页码:857 / 865
页数:9
相关论文
共 91 条
[1]   Chitosan microparticles as oral delivery system for tetanus toxoid [J].
Ahire, Vijay J. ;
Sawant, Krutika K. ;
Doshi, Jignesh B. ;
Ravetkar, Satish D. .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2007, 33 (10) :1112-1124
[2]   Biodegradable mucoadhesive particulates for nasal and pulmonary antigen and DNA delivery [J].
Alpar, HO ;
Somavarapu, S ;
Atuah, KN ;
Bramwell, V .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (03) :411-430
[3]   Permeability issues in nasal drug delivery [J].
Arora, P ;
Sharma, S ;
Garg, S .
DRUG DISCOVERY TODAY, 2002, 7 (18) :967-975
[4]   EFFECT OF CHITOSAN ON THE PERMEABILITY OF MONOLAYERS OF INTESTINAL EPITHELIAL-CELLS (CACO-2) [J].
ARTURSSON, P ;
LINDMARK, T ;
DAVIS, SS ;
ILLUM, L .
PHARMACEUTICAL RESEARCH, 1994, 11 (09) :1358-1361
[5]   Protective immune responses to meningococcal C conjugate vaccine after intranasal immunization of mice with the LTK63 mutant plus chitosan or trimethyl chitosan chloride as novel delivery platform [J].
Baudner, BC ;
Verhoef, JC ;
Giuliani, MM ;
Peppoloni, S ;
Rappuoli, R ;
Del Giudice, G ;
Junginger, HE .
JOURNAL OF DRUG TARGETING, 2005, 13 (8-9) :489-498
[6]   The concomitant use of the LTK63 mucosal adjuvant and of chitosan-based delivery system enhances the immunogenicity and efficacy of intranasally administered vaccines [J].
Baudner, BC ;
Giuliani, MM ;
Verhoef, JC ;
Rappuoli, R ;
Junginger, HE ;
Del Giudice, G .
VACCINE, 2003, 21 (25-26) :3837-3844
[7]   Controlled-release delivery system for the alpha-MSH analog melanotan-I using poloxamer 407 [J].
Bhardwaj, R ;
Blanchard, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (09) :915-919
[8]   The potential of mucoadhesive polymers in enhancing intestinal peptide drug absorption .3. Effects of chitosan-glutamate and carbomer on epithelial tight junctions in vitro [J].
Borchard, G ;
Luessen, HL ;
deBoer, AG ;
Verhoef, JC ;
Lehr, CM ;
Junginger, HE .
JOURNAL OF CONTROLLED RELEASE, 1996, 39 (2-3) :131-138
[9]   Mucoadhesive microspheres for controlled drug delivery [J].
Chowdary, KPR ;
Rao, YS .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2004, 27 (11) :1717-1724
[10]   Pluronic® F127-based systemic vaccine delivery systems [J].
Coeshott, CM ;
Smithson, SL ;
Verderber, E ;
Samaniego, A ;
Blonder, JM ;
Rosenthal, GJ ;
Westerink, MAJ .
VACCINE, 2004, 22 (19) :2396-2405