Investigation of swellable poly (N-isopropylacrylamide) based hydrogels for drug delivery

被引:29
作者
Fu, G. [1 ]
Soboyejo, W. O.
机构
[1] Princeton Inst Sci & Technol Mat PRISM, Princeton, NJ 08544 USA
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2011年 / 31卷 / 05期
基金
美国国家科学基金会;
关键词
Poly (N-isopropylacrylamide) hydrogel; Diffusion; Swelling; Modeling; Controllable drug delivery; RESPONSIVE POLYMERS; NETWORK HYDROGELS; RELEASE; TEMPERATURE; DIFFUSION; NANOPARTICLES; KINETICS; MATRICES; BEHAVIOR; SYSTEMS;
D O I
10.1016/j.msec.2011.03.009
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The thermo-sensitive properties of poly (N-isopropylacrylamide) (PNIPA) hydrogels are modified by the addition of hydrophilic acrylamide comonomers and an interpenetrating network of sodium alginate for drug delivery applications near 37 degrees C. A mathematical model is presented to describe the mass transport kinetics during the hydrogel drug delivery process, which is accompanied by a volume change during phase transition. In this model, the transport in the polymer matrix is described by Fick's second law in cylindrical coordinates, with concentration dependent diffusion coefficients. The moving boundary problems caused by the polymer matrix swelling are also solved by numerical simulation. The models show that the Trypan blue release from the modified PNIPA-based hydrogels is strongly concentration dependent. The sodium alginate component is also shown to effectively facilitate the diffusion process. The results from the simulation are in good agreement with the measurements of diffusion and swelling observed from in vitro experiments. The implications of this work are also discussed for practical drug delivery systems. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1084 / 1090
页数:7
相关论文
共 36 条
[21]   Synthesis and characterization of thermo-sensitive nanoparticles for drug delivery applications [J].
Biomedical Engineering Program, University of Texas Southwestern Medical Center, Dallas, TX, United States ;
不详 ;
不详 ;
不详 .
J. Biomed. Nanotechnol., 2008, 4 (482-490) :482-490
[22]   POLY (N-ISOPROPYLACRYLAMIDE) - EXPERIMENT, THEORY AND APPLICATION [J].
SCHILD, HG .
PROGRESS IN POLYMER SCIENCE, 1992, 17 (02) :163-249
[23]   Synthesis and phase behavior of aqueous poly(N-isopropylacrylamide-co-acrylamide), poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide) and poly (N-isopropylacrylamide-co-2-hydroxyethyl methacrylate) [J].
Shen, Zheyu ;
Terao, Ken ;
Maki, Yasuyuki ;
Dobashi, Toshiaki ;
Ma, Guanghui ;
Yamamoto, Takao .
COLLOID AND POLYMER SCIENCE, 2006, 284 (09) :1001-1007
[24]   HPMC-matrices for controlled drug delivery: A new model combining diffusion, swelling, and dissolution mechanisms and predicting the release kinetics [J].
Siepmann, J ;
Kranz, H ;
Bodmeier, R ;
Peppas, NA .
PHARMACEUTICAL RESEARCH, 1999, 16 (11) :1748-1756
[25]   Calculation of the required size and shape of hydroxypropyl methylcellulose matrices to achieve desired drug release profiles [J].
Siepmann, J ;
Kranz, H ;
Peppas, NA ;
Bodmeier, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 201 (02) :151-164
[26]   Dual release of proteins from porous polymeric scaffolds [J].
Sohier, J ;
Vlugt, TJH ;
Cabrol, N ;
Van Blitterswijk, C ;
de Groot, K ;
Bezemer, JM .
JOURNAL OF CONTROLLED RELEASE, 2006, 111 (1-2) :95-106
[27]   Stimulus-responsive "smart" hydrogels as novel drug delivery systems [J].
Soppimath, KS ;
Aminabhavi, TM ;
Dave, AM ;
Kumbar, SG ;
Rudzinski, WE .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2002, 28 (08) :957-974
[28]  
STOLL R, 1989, SEDIMENT ACOUSTICS, V26, P5
[29]   Thermoresponsive and biodegradable linear-dendritic nanoparticles for targeted and sustained release of a pro-apoptotic drug [J].
Stover, Thomas C. ;
Kim, Young Shin ;
Lowe, Tao L. ;
Kester, Mark .
BIOMATERIALS, 2008, 29 (03) :359-369
[30]   SPECTRUM OF LIGHT SCATTERED FROM A VISCOELASTIC GEL [J].
TANAKA, T ;
HOCKER, LO ;
BENEDEK, GB .
JOURNAL OF CHEMICAL PHYSICS, 1973, 59 (09) :5151-5159