Bioadhesive properties of poly(alkylcyanoacrylate) nanoparticles coated with polysaccharide

被引:35
作者
Bertholon, Isabelle [1 ]
Ponchel, Gilles [1 ]
Labarre, Denis [1 ]
Couvreur, Patrick [1 ]
Vauthier, Christine [1 ]
机构
[1] Fac Pharm Chatenay Malabry, CNRS, UMR 8612, Lab Physicochim Biopharm Pharmacotech, F-92296 Chatenay Malabry, France
关键词
bioadhesion; gastrointestinal tract; mucus; chain conformation; nanoparticles; polysaccharides;
D O I
10.1166/jnn.2006.418
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Development of bioadhesive nanoparticles is of great interest to improve drug absorption through the intestinal barrier. Various Polysaccharide-coated poly(alkylcyanoacrylate) nanoparticles were prepared. The bioadhesive properties of the nanoparticles coated with dextran or chitosan in end- on or side-on conformation were evaluated with an ex-vivo adsorption experiment on rat intestine. Results show that diffusion of nanoparticles in mucus layer was governed by the nanoparticle diameter and isotherms of adsorption were influenced by the nature of polysaccharide used. High amount of nanoparticles coated with chitosan can be entrapped in the mucus layer even at low nanoparticle concentration in suspension. When nanoparticle concentration increased, a pseudo-plateau was reached. In the case of dextran-coated nanoparticles, linear increase of adsorption was observed and no saturation phenomenon was highlighted over the range of nanoparticle concentration used in this study. These results suggested that interactions involved in bioadhesion mechanism depended on the nature of polysaccharide. Electrostatic interactions are enhanced between chitosan-coated nanoparticles and glycoproteins of mucus leading to a saturated adsorption phenomenon whereas dextran-coated nanoparticles interacted by non-electrostatic interactions with mucus resulting in a non-saturated phenomenon. Polysaccharides grafted at the nanoparticle surface in the brush conformation appeared more favorable to promote interactions of nanoparticles with glycoproteins of mucus in comparison with the more compact loop conformation of polysaccharide chains.
引用
收藏
页码:3102 / 3109
页数:8
相关论文
共 29 条
  • [1] Recent advances on chitosan-based micro- and nanoparticles in drug delivery
    Agnihotri, SA
    Mallikarjuna, NN
    Aminabhavi, TM
    [J]. JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) : 5 - 28
  • [2] MOLECULAR-WEIGHT MANIPULATION OF CHITOSAN .2. PREDICTION AND CONTROL OF EXTENT OF DEPOLYMERIZATION BY NITROUS-ACID
    ALLAN, GG
    PEYRON, M
    [J]. CARBOHYDRATE RESEARCH, 1995, 277 (02) : 273 - 282
  • [3] MOLECULAR-WEIGHT MANIPULATION OF CHITOSAN .1. KINETICS OF DEPOLYMERIZATION BY NITROUS-ACID
    ALLAN, GG
    PEYRON, M
    [J]. CARBOHYDRATE RESEARCH, 1995, 277 (02) : 257 - 272
  • [4] Design of poly-ε-caprolactone nanospheres coated with bioadhesive hyaluronic acid for ocular delivery
    Barbault-Foucher, S
    Gref, R
    Russo, P
    Guechot, J
    Bochot, A
    [J]. JOURNAL OF CONTROLLED RELEASE, 2002, 83 (03) : 365 - 375
  • [5] BERTHOLON I, IN PRESS MACROMOLECU
  • [6] BERTHOLON I, IN PRESS LANGMUIR
  • [7] Influence of the initiator system, cerium-polysaccharide, on the surface properties of poly(isobutylcyanoacrylate) nanoparticles
    Bertholon-Rajot, I
    Labarre, D
    Vauthier, C
    [J]. POLYMER, 2005, 46 (04) : 1407 - 1415
  • [8] Evaluation of the surface properties of dextran-coated poly(isobutylcyanoacrylate) nanoparticles by spin-labelling coupled with electron resonance spectroscopy
    Chauvierre, C
    Vauthier, C
    Labarre, D
    Hommel, H
    [J]. COLLOID AND POLYMER SCIENCE, 2004, 282 (09) : 1016 - 1025
  • [9] Radical emulsion polymerization of alkylcyanoacrylates initiated by the redox system dextran-cerium(IV) under acidic aqueous conditions
    Chauvierre, C
    Labarre, D
    Couvreur, P
    Vauthier, C
    [J]. MACROMOLECULES, 2003, 36 (16) : 6018 - 6027
  • [10] MUCIN INTERACTIONS WITH FUNCTIONALIZED POLYSTYRENE LATEXES
    DURRER, C
    IRACHE, JM
    DUCHENE, D
    PONCHEL, G
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1995, 170 (02) : 555 - 561