Message Board

Respected readers, authors and reviewers, you can add comments to this page on any questions about the contribution, review,        editing and publication of this journal. We will give you an answer as soon as possible. Thank you for your support!

Name
E-mail
Phone
Title
Content
Verification Code

XIANG Jingjie, ZHONG Yanqiang, LU Yiming, LU Ying. Preparation of DNA-loaded chitosan nanoparticle vaccine[J]. Journal of Pharmaceutical Practice and Service, 2016, 34(1): 19-23,40. doi: 10.3969/j.issn.1006-0111.2016.01.006
Citation: XIANG Jingjie, ZHONG Yanqiang, LU Yiming, LU Ying. Preparation of DNA-loaded chitosan nanoparticle vaccine[J]. Journal of Pharmaceutical Practice and Service, 2016, 34(1): 19-23,40. doi: 10.3969/j.issn.1006-0111.2016.01.006

Preparation of DNA-loaded chitosan nanoparticle vaccine

doi: 10.3969/j.issn.1006-0111.2016.01.006
  • Received Date: 2015-08-24
  • Rev Recd Date: 2015-11-16
  • Objective To study and optimize the preparation condition of pVAX1-wapA-loaded nanoparticles and determine the transfection efficiency. Methods The related effects of the crucial factors for the formation of nanoparticles: concentration of chitosan and TPP, pH value, N/P ratio were studied by single-factor experiment, with nanoparticles size and zeta potential as index. Cell transfection test was carried out to indicate that enhancement of cell transfection efficiency of nano-carrier. Results Nanoparticles loaded DNA vaccine were nearly spherical shape with uniform particle size chitosan nanoparticle(CS),(219.2±18.2) nm;quaternary ammonium chitosan nanoparticles(CSTM),(222.5±15.6) nm. Zeta potential of CS and CSTM was (24.7±3.5) mV, (19.6±1.2) mV and encapsulation efficiency was 91.24%, 87.66%,respectively.CSTM nanoparticle could enhance cellular uptake of pVAX1-wapA obviously. Conclusion CSTM nanoparticle was proved to be an efficient DNA vaccine delivery vector.
  • [1] 樊明文,边 专. 防龋疫苗主动免疫的现状与未来[J]. 中华口腔医学杂志, 2002,37(6):401-403.
    [2] 刘善奎,高 申,钟延强,等. DNA 疫苗微球给药系统的研究进展[J]. 中国药学杂志,2004,38(11):828-831.
    [3] 白 枫,孙大庆. DNA疫苗递送系统研究进展[J]. 国际免疫学杂志,2008,31(3):236-239.
    [4] 李艳红,胡四海. 壳聚糖纳米粒介导基因转染的影响因素及改性修饰[J]. 微生物学免疫学进展,2010,38(3):50-53.
    [5] Erbacher P,Zou S, Bettinger T,et al. Chitosan-based vector/DNA complexes for gene delivery: Biophysical Characteristics and Transfection Ability[J].Pharm Res,1998,15(9):1332-1339.
    [6] Lee M,Nah JW,Kwon Y,et al. Water-soluble and low molecular weight chitosan-based plasmid DNA delivery[J]. Pharm Res,2001,18(4):427-431.
    [7] Ishii T,Okahata Y,Sato T. Mechanism of cell transfection with plasmid/chitosan complexes[J]. Biochim Biophys Acta,2001,1514(1):51-64.
    [8] Huang M,Fong CW,Khor E,et al. Transfection efficiency of chitosan vectors: effect of polymer molecular weight and degree of deacetylation[J]. J Control Release,2005,106(3):391-406.
    [9] 杨晓容,宗 莉,朱敏艳,等. 荧光探针示踪pDNA/壳聚糖纳米粒在细胞内转运[J].中国药学杂志,2009,43(10):727-731.
    [10] 王江峰,鲁 莹,黄景彬,等.聚氨基酯载基因纳米粒的研究[J].第二军医大学学报,2011,32(5):473-476.
    [11] Qian F,Cui F,Ding J,et al. Chitosan graft copolymer nanoparticles for oral protein drug delivery: preparation and characterization[J].Biomacromolecules,2006,7(10):2722-2727.
    [12] 刘世伟,孙 逊,聂 宇,等。载基因壳聚糖纳米粒的制备及 其相关性质的初步研究[J].华西药学杂志,2005,19 (6):409-411.
    [13] Mao HQ,Roy K,Troung-Le VL,et al.Chitosan-DNA nano-particles as gene carriers: synthesis, characterization and transfection efficiency [J]. J Control Release,2001,70 (3): 399-421.
    [14] Goldmann K,Ensminger SM,Spriewald BM.Oral gene appli-cation using chitosan-DNA nanoparticles induces transferable tolerance[J].Clin Vaccine Immunol,2012,19 (11):1758-1764.
  • 加载中
通讯作者: 陈斌, [email protected]
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Article Metrics

Article views(3715) PDF downloads(135) Cited by()

Related
Proportional views

Preparation of DNA-loaded chitosan nanoparticle vaccine

doi: 10.3969/j.issn.1006-0111.2016.01.006

Abstract: Objective To study and optimize the preparation condition of pVAX1-wapA-loaded nanoparticles and determine the transfection efficiency. Methods The related effects of the crucial factors for the formation of nanoparticles: concentration of chitosan and TPP, pH value, N/P ratio were studied by single-factor experiment, with nanoparticles size and zeta potential as index. Cell transfection test was carried out to indicate that enhancement of cell transfection efficiency of nano-carrier. Results Nanoparticles loaded DNA vaccine were nearly spherical shape with uniform particle size chitosan nanoparticle(CS),(219.2±18.2) nm;quaternary ammonium chitosan nanoparticles(CSTM),(222.5±15.6) nm. Zeta potential of CS and CSTM was (24.7±3.5) mV, (19.6±1.2) mV and encapsulation efficiency was 91.24%, 87.66%,respectively.CSTM nanoparticle could enhance cellular uptake of pVAX1-wapA obviously. Conclusion CSTM nanoparticle was proved to be an efficient DNA vaccine delivery vector.

XIANG Jingjie, ZHONG Yanqiang, LU Yiming, LU Ying. Preparation of DNA-loaded chitosan nanoparticle vaccine[J]. Journal of Pharmaceutical Practice and Service, 2016, 34(1): 19-23,40. doi: 10.3969/j.issn.1006-0111.2016.01.006
Citation: XIANG Jingjie, ZHONG Yanqiang, LU Yiming, LU Ying. Preparation of DNA-loaded chitosan nanoparticle vaccine[J]. Journal of Pharmaceutical Practice and Service, 2016, 34(1): 19-23,40. doi: 10.3969/j.issn.1006-0111.2016.01.006
Reference (14)

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return