Controlled release of dexamethasone acetate from biodegradable and biocompatible polyurethane and polyurethane nanocomposite

被引:35
作者
Da Silva, Gisele Rodrigues [1 ]
Ayres, Eliane [2 ]
Orefice, Rodrigo Lambert [2 ]
Moura, Sandra Aparecida L. [3 ]
Cara, Denise Carmona [3 ]
Cunha, Armando Da Silva, Jr. [1 ]
机构
[1] Univ Fed Minas Gerais, Sch Pharm, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Met & Mat Engn, BR-31270901 Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Inst Biol Sci, Dept Gen Pathol, BR-31270901 Belo Horizonte, MG, Brazil
关键词
Polyurethane; nanocomposite; dexamethasone acetate; in vitro controlled release; in vivo biocompatibility; SUSTAINED-RELEASE; POLY(EPSILON-CAPROLACTONE); POLYMERS; IMPLANTS;
D O I
10.1080/10611860902839510
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polyurethanes and polyurethane nanocomposites can be applied to control the release of drugs previously incorporated into these materials. In this study, dexamethasone acetate (ACT) was incorporated into biodegradable and biocompatible polyurethane and polyurethane containing montmorillonite nanoparticles. Fourier transform infrared spectroscopic technique showed no strong interactions between drug and polymers. Data obtained from X-ray diffraction and small angle X-ray scattering indicated that the incorporation of ACT did not disturb the polymer morphology, but montmorillonite led to a less defined phase separation between hard and soft segments of polyurethane. The in vitro release studies demonstrated that nanoparticles increased the rate of ACT release possibly because these particles have a hydrophilic surface that increases the absorption of water and accelerates the hydrolysis of the polymer. The in vivo short-term biocompatibility studies demonstrated adequate interfacial interaction between polyurethane and subcutaneous tissue and a discreet inflammatory response which was completely resolved in 14 days.
引用
收藏
页码:374 / 383
页数:10
相关论文
共 31 条
  • [1] Polymer-layered silicate nanocomposites: Preparation, properties and uses of a new class of materials
    Alexandre, Michael
    Dubois, Philippe
    [J]. Materials Science and Engineering: R: Reports, 2000, 28 (1-2) : 1 - 63
  • [2] [Anonymous], 2008, US PHARM
  • [3] Phase morphology of hydrolysable polyurethanes derived from aqueous dispersions
    Ayres, Eliane
    Orefice, Rodrigo L.
    Yoshida, M. Irene
    [J]. EUROPEAN POLYMER JOURNAL, 2007, 43 (08) : 3510 - 3521
  • [4] Small-angle X-ray scattering of polymers
    Chu, B
    Hsiao, BS
    [J]. CHEMICAL REVIEWS, 2001, 101 (06) : 1727 - 1761
  • [5] Polyesterurethane foam scaffold for smooth muscle cell tissue engineering
    Danielsson, C
    Ruault, S
    Simonet, M
    Neuenschwander, P
    Frey, P
    [J]. BIOMATERIALS, 2006, 27 (08) : 1410 - 1415
  • [6] Concomitant and controlled release of dexamethasone and 5-fluorouracil from poly(ortho ester)
    Einmahl, S
    Zignani, M
    Varesio, E
    Heller, J
    Veuthey, JL
    Tabatabay, C
    Gurny, R
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 185 (02) : 189 - 198
  • [7] Dexamethasone-loaded poly(ε-caprolactone) intravitreal implants:: A pilot study
    Fialho, Silvia Ligorio
    Behar-Cohen, Francine
    Silva-Cunha, Armando
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 68 (03) : 637 - 646
  • [8] Determination of dexamethasone acetate in cream by HPLC
    Garcia, CV
    Breier, AR
    Steppe, M
    Schapoval, EES
    Oppe, TP
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2003, 31 (03) : 597 - 600
  • [9] The role of apoptosis in wound healing
    Greenhalgh, DG
    [J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1998, 30 (09) : 1019 - 1030
  • [10] Preparation and characterization of highly porous, biodegradable polyurethane scaffolds for soft tissue applications
    Guan, JJ
    Fujimoto, KL
    Sacks, MS
    Wagner, WR
    [J]. BIOMATERIALS, 2005, 26 (18) : 3961 - 3971