Core-Shell Nanoparticles Fabricated by Tri-capillary Coaxial Electrospray and Template Removal Method for Protein Delivery

被引:0
作者
Cao, Li-hua [1 ]
Wang, Hong-jun [1 ,2 ]
Tu, Ke-hua [1 ,2 ]
Jiang, Hong-liang [1 ,2 ]
Wang, Li-qun [1 ,2 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
来源
ACTA POLYMERICA SINICA | 2014年 / 09期
关键词
Coaxial electrospray; Nanoparticle; Core-shell; Protein; Drug delivery; BIODEGRADABLE MICROPARTICLES; SIZE; MICROSPHERES; COMPOUND;
D O I
暂无
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A coaxial tri-capillary electrospray and template removal method was proposed to produce nanosized core-shell particles for encapsulating of proteins. Polyethylene glycol (PEG) and poly (D, L-lactide-co-glycolide) (PLGA) were used as corona and shell materials, while Bovine serum albumin (BSA), as a model protein,was entrapped in the core. Microparticles with smooth surfaces and distinct core-shell-corona structures were obtained by coaxial tri-capillary electrospray and nanoparticles with diameter about 100 nm were achieved by removing the corona PEG template from core-shell-corona microparticles. Moreover, the nanoparticle size could be modulated by adjusting the feed rate of shell fluid, and the diameter of nanoparticles could be reduced to (68 +/- 8) nm when the shell fluid feed rate was decreased to 0.5 mL/h. The drug loading content and entrapment efficiency of BSA were 3. 7% and 78. 3%, respectively. It was also found that BSA released from nanoparticles in a typical bi-phased release profile and the process may last for 60 h. The second order structure of BSA released from particles was monitored with circular dichroism spectrum. The results showed that the electrospray process didn ' t affect the second order structure of proteins, implying that the denaturation of the protein didn ' t occur during the process of electrospraying encapsulation.
引用
收藏
页码:1238 / 1243
页数:6
相关论文
共 24 条
  • [1] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [2] Endocytosis at the nanoscale
    Canton, Irene
    Battaglia, Giuseppe
    [J]. CHEMICAL SOCIETY REVIEWS, 2012, 41 (07) : 2718 - 2739
  • [3] A New Method for the Preparation of Monoporous Hollow Microspheres
    Chang, Ming-Wei
    Stride, Eleanor
    Edirisinghe, Mohan
    [J]. LANGMUIR, 2010, 26 (07) : 5115 - 5121
  • [4] Compound-fluidic electrospray: An efficient method for the fabrication of microcapsules with multicompartment structure
    Chen HongYan
    Zhao Yong
    Jiang Lei
    [J]. CHINESE SCIENCE BULLETIN, 2009, 54 (18): : 3147 - 3153
  • [5] The mechanism of uptake of biodegradable microparticles in Caco-2 cells is size dependent
    Desai, MP
    Labhasetwar, V
    Walter, E
    Levy, RJ
    Amidon, GL
    [J]. PHARMACEUTICAL RESEARCH, 1997, 14 (11) : 1568 - 1573
  • [6] Gastrointestinal uptake of biodegradable microparticles: Effect of particle size
    Desai, MP
    Labhasetwar, V
    Amidon, GL
    Levy, RJ
    [J]. PHARMACEUTICAL RESEARCH, 1996, 13 (12) : 1838 - 1845
  • [7] Airway delivery of peptides and proteins using nanoparticles
    Dombu, Christophe Y.
    Betbeder, Didier
    [J]. BIOMATERIALS, 2013, 34 (02) : 516 - 525
  • [8] Conjugates of poly(DL-lactide-co-glycolide) on amino cyclodextrins and their nanoparticles as protein delivery system
    Gao, Hui
    Wang, Yi-Nong
    Fan, Yun-Ge
    Ma, Jian-Biao
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2007, 80A (01) : 111 - 122
  • [9] Encapsulation of BSA in polylactic acid-hyperbranched polyglycerol conjugate nanoparticles: preparation, characterization, and release kinetics
    Gao, Xiujun
    Zhang, Xinge
    Zhang, Xuejiao
    Cheng, Cui
    Wang, Zhen
    Li, Chaoxing
    [J]. POLYMER BULLETIN, 2010, 65 (08) : 787 - 805
  • [10] Biological activity of lysozyme after entrapment in poly (d,l-lactide-co-glycolide)-microspheres
    Ghaderi, R
    Carlfors, J
    [J]. PHARMACEUTICAL RESEARCH, 1997, 14 (11) : 1556 - 1562