Phase behavior of electrostatically complexed polyelectrolyte gels using an embedded fluctuation model

被引:58
作者
Audus, Debra J. [1 ,2 ]
Gopez, Jeffrey D. [1 ,2 ]
Krogstad, Daniel V. [1 ,3 ]
Lynd, Nathaniel A. [1 ]
Kramer, Edward J. [1 ,2 ,3 ]
Hawker, Craig J. [1 ,3 ,4 ]
Fredrickson, Glenn H. [1 ,2 ,3 ]
机构
[1] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[4] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会;
关键词
OPPOSITELY CHARGED POLYELECTROLYTES; DIBLOCK POLYAMPHOLYTE SOLUTIONS; BLOCK-COPOLYMER MELTS; DRUG-DELIVERY; MONTE-CARLO; POLYSTYRENE SURFACES; COMPUTER-SIMULATION; STATISTICAL-THEORY; EXCLUDED-VOLUME; GIBBS ENSEMBLE;
D O I
10.1039/c4sm02299h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanostructured, responsive hydrogels formed due to electrostatic interactions have promise for applications such as drug delivery and tissue mimics. These physically cross-linked hydrogels are composed of an aqueous solution of oppositely charged triblocks with charged end-blocks and neutral, hydrophilic mid-blocks. Due to their electrostatic interactions, the end-blocks microphase separate and form physical cross-links that are bridged by the mid-blocks. The structure of this system was determined using a new, efficient embedded fluctuation (EF) model in conjunction with self-consistent field theory. The calculations using the EF model were validated against unapproximated field-theoretic simulations with complex Langevin sampling and were found consistent with small angle X-ray scattering (SAXS) measurements on an experimental system. Using both the EF model and SAXS, phase diagrams were generated as a function of end-block fraction and polymer concentration. Several structures were observed including a body-centered cubic sphere phase, a hexagonally packed cylinder phase, and a lamellar phase. Finally, the EF model was used to explore how parameters that directly relate to polymer chemistry can be tuned to modify the resulting phase diagram, which is of practical interest for the development of new hydrogels.
引用
收藏
页码:1214 / 1225
页数:12
相关论文
共 72 条
[21]   Shear-thinning hydrogels for biomedical applications [J].
Guvendiren, Murat ;
Lu, Hoang D. ;
Burdick, Jason A. .
SOFT MATTER, 2012, 8 (02) :260-272
[22]   Chain length recognition: Core-shell supramolecular assembly from oppositely charged block copolymers [J].
Harada, A ;
Kataoka, K .
SCIENCE, 1999, 283 (5398) :65-67
[23]   FORMATION OF POLYION COMPLEX MICELLES IN AN AQUEOUS MILIEU FROM A PAIR OF OPPOSITELY-CHARGED BLOCK-COPOLYMERS WITH POLY(ETHYLENE GLYCOL) SEGMENTS [J].
HARADA, A ;
KATAOKA, K .
MACROMOLECULES, 1995, 28 (15) :5294-5299
[24]   Oppositely charged polyelectrolytes. Complex formation and effects of chain asymmetry [J].
Hayashi, Y ;
Ullner, M ;
Linse, P .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (39) :15266-15277
[25]   Complex formation in solutions of oppositely charged polyelectrolytes at different polyion compositions and salt content [J].
Hayashi, Y ;
Ullner, M ;
Linse, P .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (32) :8198-8207
[26]   A Monte Carlo study of solutions of oppositely charged polyelectrolytes [J].
Hayashi, Y ;
Ullner, M ;
Linse, P .
JOURNAL OF CHEMICAL PHYSICS, 2002, 116 (15) :6836-6845
[27]   Hydrogels in drug delivery: Progress and challenges [J].
Hoare, Todd R. ;
Kohane, Daniel S. .
POLYMER, 2008, 49 (08) :1993-2007
[28]  
Hubbell JA, 1995, NAT BIOTECHNOL, V13, P565, DOI DOI 10.1038/NBT0695-565
[29]   Tunable, High Modulus Hydrogels Driven by Ionic Coacervation [J].
Hunt, Jasmine N. ;
Feldman, Kathleen E. ;
Lynd, Nathaniel A. ;
Deek, Joanna ;
Campos, Luis M. ;
Spruell, Jason M. ;
Hernandez, Blanca M. ;
Kramer, Edward J. ;
Hawker, Craig J. .
ADVANCED MATERIALS, 2011, 23 (20) :2327-+
[30]   Molecular dynamics simulations of polyampholyte-polyelectrolyte complexes in solutions [J].
Jeon, J ;
Dobrynin, AV .
MACROMOLECULES, 2005, 38 (12) :5300-5312