Thermally Responsive PM(EO)2MA Magnetic Microgels via Activators Generated by Electron Transfer Atom Transfer Radical Polymerization in Miniemulsion

被引:70
作者
Dong, Hongchen [1 ]
Mantha, Venkat [2 ]
Matyjaszewski, Krzysztof [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Ctr Macromol Engn, Pittsburgh, PA 15213 USA
[2] Magee Womens Hosp, Dept Anesthesiol, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
DRUG-DELIVERY; ARGET ATRP; BLOCK-COPOLYMERS; AGET ATRP; MICROSPHERES; NANOPARTICLES; POLYMERS; FUNCTIONALIZATION; PARTICLES; RELEASE;
D O I
10.1021/cm901143e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Activators generated by electron transfer atom transfer radical polymerization (AGET ATRP) of di(ethylene glycol) methyl ether methacrylate (M(EO)(2)MA) was successfully conducted in miniemulsion at 65 degrees C. The reaction system was stable without diffusion of monomer and polymer into the aqueous phase because the monomer is water-insoluble and PM(EO)(2)MA becomes hydrophobic above 25 degrees C. The polymerization was well-controlled with a mild water-soluble reducing agent, hydrazine, yielding PM(EO)(2)MA homopolymer with narrow molecular weight distribution (M-w/M-n = 1.2-1.6). Using this technique, well-defined PM(EO)(2)MA microgels were prepared with degradable disulfide cross-linker. The microgels became magnetic after physically loading oleic acid-coated Fe3O4 nanoparticles, which could not diffuse out of the microgels due to their hydrophobicity. Thermally responsive and drug loading-releasing behavior of the magnetic microgels was studied using Rhodamine B as it model for hydrophilic drugs. The drug releasing behavior call be well-controlled by both temperature and addition of reducing agent, indicating that the PM(EO)(2)MA magnetic microgels could find potential application for controlled targeted drug delivery.
引用
收藏
页码:3965 / 3972
页数:8
相关论文
共 80 条
[1]
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3578
[2]
Well-defined amphiphilic thermosensitive copolymers based on poly(ethylene glycol monomethacrylate) and methyl methacrylate prepared by atom transfer radical polymerization [J].
Ali, MM ;
Stöver, HDH .
MACROMOLECULES, 2004, 37 (14) :5219-5227
[3]
Responsive polymers in controlled drug delivery [J].
Bajpai, A. K. ;
Shukla, Sandeep K. ;
Bhanu, Smitha ;
Kankane, Sanjana .
PROGRESS IN POLYMER SCIENCE, 2008, 33 (11) :1088-1118
[4]
Controlled/living radical polymerization: Features, developments, and perspectives [J].
Braunecker, Wade A. ;
Matyjaszewski, Krzysztof .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (01) :93-146
[5]
Smart microgel studies. Polyelectrolyte and drug-absorbing properties of microgels from polyether-modified poly(acrylic [J].
Bromberg, L ;
Temchenko, M ;
Hatton, TA .
LANGMUIR, 2003, 19 (21) :8675-8684
[6]
Neurotransplantation of magnetically labeled oligodendrocyte progenitors: Magnetic resonance tracking of cell migration and myelination [J].
Bulte, JWM ;
Zhang, SC ;
van Gelderen, P ;
Herynek, V ;
Jordan, EK ;
Duncan, ID ;
Frank, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15256-15261
[7]
RETRACTED: Cysteine and glutathione secretion in response to protein disulfide bond formation in the ER (Retracted Article) [J].
Carelli, S ;
Ceriotti, A ;
Cabibbo, A ;
Fassina, G ;
Ruvo, M ;
Sitia, R .
SCIENCE, 1997, 277 (5332) :1681-1684
[8]
Fabrication of Colloidal Stable, Thermosensitive, and Biocompatible Magnetite Nanoparticles and Study of Their Reversible Agglomeration in Aqueous Milieu [J].
Chanana, Munish ;
Jahn, Sabrina ;
Georgieva, Radostina ;
Lutz, Jean-Francois ;
Baeumler, Hans ;
Wang, Dayang .
CHEMISTRY OF MATERIALS, 2009, 21 (09) :1906-1914
[9]
A novel approach for preparation of thermoresponsive polymer magnetic microspheres with core-shell structure [J].
Deng, YH ;
Yang, WL ;
Wang, CC ;
Fu, SK .
ADVANCED MATERIALS, 2003, 15 (20) :1729-+
[10]
Thermosensitive magnetic latex particles for controlling protein adsorption and desorption [J].
Elaïssari, A ;
Bourrel, V .
JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 2001, 225 (1-2) :151-155