Self-healing of pores in PLGAs

被引:40
作者
Huang, J. [1 ,2 ]
Mazzara, J. M. [3 ,4 ]
Schwendeman, S. P. [3 ,4 ,5 ]
Thouless, M. D. [1 ,2 ]
机构
[1] Univ Michigan, Dept Mech Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, NCRC, Dept Pharmaceut Sci, Ann Arbor, MI 48109 USA
[4] Univ Michigan, NCRC, Biointerfaces Inst, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
关键词
PLGA; Self-healing; Finite element; Simulations; Surface pores; Viscoelasticity; CONTROLLED-RELEASE; DELIVERY; NANOPARTICLES; FORMULATION; RECOVERY; PEPTIDE; STENT;
D O I
10.1016/j.jconrel.2015.02.025
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-healing of pores in Poly(lactic-co-glycolic acid)s (PLGA) plays an important role in the encapsulation and controlled release of drugs from PLGA microparticles. Despite the importance of this phenomenon, neither the mechanics of the deformation nor the material properties that control it have been fully studied. In this study, the material properties of PLGA have been characterized using mechanical tests, and a finite-element model has been developed to predict how pores heal. This model assumes that the healing process occurs by viscous flow resulting from the deviatoric stress field induced by the interaction between the surface curvature and the surface tension of the PLGA. The simulations, which incorporate measured material properties, show good agreement with experimental observations. However, annealing processes that occur over prolonged times increase the viscosity and slow the healing times of PLGA films at intermediate temperatures above the glass-transition temperature. These findings may be reasonably applied towards the prediction of healing processes in PLGA and in related biomaterials for important biomedical applications such as drug delivery. (C) 2015 Published by Elsevier B.V.
引用
收藏
页码:20 / 29
页数:10
相关论文
共 30 条
[1]  
[Anonymous], 2006, Theory of Plasticity
[2]  
Braun PV, 2002, ENCY POLYM SCI TECHN, DOI 1002/0471440264.pst469
[3]   Formulation of functionalized PLGA-PEG nanoparticles for in vivo targeted drug delivery [J].
Cheng, Jianjun ;
Teply, Benjamin A. ;
Sherifi, Ines ;
Sung, Josephine ;
Luther, Gaurav ;
Gu, Frank X. ;
Levy-Nissenbaum, Etgar ;
Radovic-Moreno, Aleksandar F. ;
Langer, Robert ;
Farokhzad, Omid C. .
BIOMATERIALS, 2007, 28 (05) :869-876
[4]   Self-Healing Polymer Coatings [J].
Cho, Soo Hyoun ;
White, Scott R. ;
Braun, Paul V. .
ADVANCED MATERIALS, 2009, 21 (06) :645-+
[5]   STRENGTH RECOVERY BY DIFFUSIVE CRACK HEALING [J].
EVANS, AG ;
CHARLES, EA .
ACTA METALLURGICA, 1977, 25 (08) :919-927
[6]   PLGA-PEG-PLGA tri-block copolymers as in situ gel-forming peptide delivery system: Effect of formulation properties on peptide release [J].
Ghahremankhani, Ali Afshar ;
Dorkoosh, Farid ;
Dinarvand, Rassoul .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2008, 13 (01) :49-55
[7]   Biodegradable nanoparticles for drug delivery and targeting [J].
Hans, ML ;
Lowman, AM .
CURRENT OPINION IN SOLID STATE & MATERIALS SCIENCE, 2002, 6 (04) :319-327
[8]   Surface tension-driven shape-recovery of micro/nanometer-scale surface features in a Pt57.5Ni5.3Cu14.7P22.5 metallic glass in the supercooled liquid region: A numerical modeling capability [J].
Henann, David L. ;
Anand, Lallit .
JOURNAL OF THE MECHANICS AND PHYSICS OF SOLIDS, 2010, 58 (11) :1947-1962
[9]   Pore closing and opening in biodegradable polymers and their effect on the controlled release of proteins [J].
Kang, Jichao ;
Schwendeman, Steven P. .
MOLECULAR PHARMACEUTICS, 2007, 4 (01) :104-118
[10]   Gene delivery from a DNA controlled-release stent in porcine coronary arteries [J].
Klugherz, BD ;
Jones, PL ;
Cui, XM ;
Chen, WL ;
Meneveau, NF ;
DeFelice, S ;
Connolly, J ;
Wilensky, RL ;
Levy, RJ .
NATURE BIOTECHNOLOGY, 2000, 18 (11) :1181-1184