Electrospun fibers of acid-labile biodegradable polymers with acetal groups as potential drug carriers

被引:54
作者
Cui, Wenguo [1 ]
Qi, Mingbo [1 ]
Li, Xiaohong [1 ]
Huang, Shaozhou [1 ]
Zhou, Shaobing [1 ]
Weng, Jie [1 ]
机构
[1] SW Jiaotong Univ, Sch Mat Sci & Engn, Minist Educ, Key Lab Adv Technol Mat, Chengdu 610031, Peoples R China
基金
中国国家自然科学基金;
关键词
acid-labile polymer; biodegradable backbone; electrospinning; acetal group; controlled release;
D O I
10.1016/j.ijpharm.2008.05.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The local delivery and controllable release profiles make electrospun ultrafine fibers as potential implantable drug carriers and functional coatings of medical devices. Till date there is no literature report on drug delivery from acid-labile electrospun fibers, whose degradation and drug release behaviors respond to the local pathological pH environment. Acid-labile groups have been incorporated into nonbiodegradable backbones as crosslinkers or linkers of the side chains. A novel strategy was developed in this study to synthesize acid-labile polymers by introducing acetal groups into biodegradable backbone of poly(DL-lactide)-poly(ethylene glycol). In vitro release study showed that the total amount of drug released from acid-labile polymeric fibers was accelerated on account of pH-induced structural and morphological changes of fibrous mats and the degradation of matrix polymers, and the burst release was significant higher for polymers with higher contents of acid-labile segments. During the investigational period, almost no molecular weight reduction and mass loss was detected in neutral buffer solutions, but the degradation was enhanced in acid buffers with a two-stage degradation profile. Surface erosion mechanism was initially detected for fibrous mats with distinct fiber morphologies, and bulk degradation was determined during the following incubation for polymeric films resulting from the morphological changes. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 55
页数:9
相关论文
共 32 条
  • [1] Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: Tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy
    Bae, Y
    Nishiyama, N
    Fukushima, S
    Koyama, H
    Yasuhiro, M
    Kataoka, K
    [J]. BIOCONJUGATE CHEMISTRY, 2005, 16 (01) : 122 - 130
  • [2] BURKERSRODA F, 1997, BIOMATERIALS, V18, P1599
  • [3] Burkersroda F.V., 2002, BIOMATERIALS, V23, P4221, DOI DOI 10.1016/S0142-9612(02)00170-9
  • [4] Acid-cleavable polymeric core-shell particles for delivery of hydrophobic drugs
    Chan, Yannie
    Bulmus, Volga
    Zareie, M. Hadi
    Byrne, Frances L.
    Barner, Leonie
    Kavallaris, Maria
    [J]. JOURNAL OF CONTROLLED RELEASE, 2006, 115 (02) : 197 - 207
  • [5] Investigation on process parameters of electrospinning system through orthogonal experimental design
    Cui, Wenguo
    Li, Xiaohong
    Zhou, Shaobing
    Weng, Jie
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2007, 103 (05) : 3105 - 3112
  • [6] Investigation of drug release and matrix degradation of electrospun poly(DL-lactide) fibers with paracetanol inoculation
    Cui, Wenguo
    Li, Xiaohong
    Zhu, Xinli
    Yu, Guo
    Zhou, Shaobing
    Weng, Jie
    [J]. BIOMACROMOLECULES, 2006, 7 (05) : 1623 - 1629
  • [7] GALLIN JI, 1992, INFLAMMATION BASIC P, V2, P603
  • [8] Tumor pH: Implications for treatment and novel drug design
    Gerweck, LE
    [J]. SEMINARS IN RADIATION ONCOLOGY, 1998, 8 (03) : 176 - 182
  • [9] pH-responsive copolymer assemblies for controlled release of doxorubicin
    Gillies, ER
    Fréchet, JMJ
    [J]. BIOCONJUGATE CHEMISTRY, 2005, 16 (02) : 361 - 368
  • [10] Electrospinning: A fascinating method for the preparation of ultrathin fibres
    Greiner, Andreas
    Wendorff, Joachim H.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (30) : 5670 - 5703