Nonswellable and swellable ethylene glycol dimethacrylate-acrylic acid copolymer microspheres
Ali Tuncel
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey
Search for more papers by this authorKutay Ecevit
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey
Search for more papers by this authorKemal Kesenci
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey
Search for more papers by this authorCorresponding Author
Erhan Pişkin
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, TurkeySearch for more papers by this authorAli Tuncel
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey
Search for more papers by this authorKutay Ecevit
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey
Search for more papers by this authorKemal Kesenci
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey
Search for more papers by this authorCorresponding Author
Erhan Pişkin
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, Turkey
Hacettepe University, Chemical Engineering Department, 06532, Beytepe, Ankara, TurkeySearch for more papers by this authorAbstract
In this study, nonswellable and swellable poly(ethylene glycol dimethacrylate/acrylic acid) copolymer microspheres, in the size range of 50–150 μm, were produced by conventional and modified suspension copolymerizations of the respective monomers, i.e., ethyleneglycol dimethacrylate (EGDMA) and acrylic acid (AA) in aqueous media. Poly(vinyl alcohol) and benzoyl peroxide were used as the stabilizer and the initiator. The diluent, i.e., toluene was included in the polymerization recipe of the modified suspension polymerization. The microspheres were characterized by optical microscopy, FTIR, and FTIR-DRS, and potentiometric titrations. Highly crosslinked, transparent, and nonswellable poly(EGDMA/AA) microspheres were obtained with the conventional suspension polymerization procedure. The modified suspension polymerization provided swellable, opaque, and crosslinked copolymer microspheres. Acrylic acid incorporation into the copolymeric microspheres were significantly higher in the modified procedure, relative to the conventional procedure. © 1996 John Wiley & Sons, Inc.
References and Notes
- 1 G. Subramanian, B. A. Rhodes, J. F. Cooper, and V. J. Sodd, Eds., Radiopharmaceuticals, Society of Nuclear Medicine, New York, 1975.
- 2 J. Woodward, Ed., Immobilized Cells and Enzymes: A Practical Approach, IRL Press, Oxford, 1985.
- 3 P. D. G. Dean, W. S. Johnson, F. A. Middle, Eds., Affinity Chromatograph: A Practical Approach, IRL Press, Oxford, 1985.
- 4 A. Rembaum and Z. A. Toke, Eds., Microspheres: Medical and Biological Applications, CRC Press, Boca Raton, FL, 1988.
- 5 K. Mosbach, Ed., Methods Enzymol., 137, 443 (1988).
- 6 D. S. Kompala and P. Todd, Eds., Cell Separation Science and Technology, ACS Symposium Series, 464, American Chemical Society, Washington, DC, 1991.
- 7 R. Arshady, Biomaterials, 14, 5 (1993).
- 8 R. Arshady, Colloid Polym. Sci., 270, 717 (1992).
- 9
H. G. Yuan,
G. Kalfas,
W. H. Ray,
JMS-Rev.-Macromol. Chem. Phys.,
31,
215
(1991).
10.1080/15321799108021924 Google Scholar
- 10 E. A. Gruike, Encycl. Polym. Sci. Eng., 19, 443 (1989).
- 11 K. F. Mueller, S. Heiber, W. Flankl, U.S. Pat. 4, 224, 472, (1978).
- 12 J. Seidel, J. Malinsky, K. Dusek, and W. Heitz, Adv. Polym. Sci., 5, 113 (1967).
- 13 J. C. Moore, J. Polym. Sci., Part A–2, 835 (1969).
- 14
J. Coupek,
M. Krivakova, and
S. Pokorny,
J. Polym. Sci. Polym. Symp.,
42,
185
(1973).
10.1002/polc.5070420121 Google Scholar
- 15 W. Heitz, Adv. Polym. Sci., 23, 1 (1977).
- 16 J. Kalal, J. Polym. Sci., Polym. Symp. Ed., 62, 251 (1978).
- 17 D. Horak, Z. Pelzbauer, M. Bleha, M. Havsky, F. Svec, and J. Kalal, J. Appl. Polym. Sci., 26, 411 (1980).
- 18 D. Horak, F. Svec, M. Bleha, and J. Kalal, Angew. Makromol. Chem., 95, 109, (1981).
- 19 D. Horak, F. Svec, M. Havsky, M. Bleha, and J. Kalal, Angew. Makromol. Chem., 95, 117 (1981).
- 20 A. Guyot and M. Bartholin, Prog. Polym. Sci., 81, 277 (1982).
- 21 Y. Ohtsuka, H. Kawaguchi, and Y. Yamamoto, J. Appl. Polym. Sci., 27, 3279 (1982).
- 22 H. Galina, N. B. Colaz, P. P. Wiezorek, and M. Woiszynska, Br. Polym. J., 17, 215 (1985).
- 23 M. Dimonie, H. D. Schell, G. Hubca, M. A. Mateescu, C. G. Oprescu, S. Todireanu, O. Maior, J. Languri, and M. Iosif, J. Macromol. Sci.-Chem., A22, 729 (1985).
- 24 C. C. R. Robert, P. A. Buri, and N. A. Peppas, J. Appl. Polym. Sci., 30, 301 (1985).
- 25 D. Horak, F. Svec, J. Kalal, K. Gumargalieve, A. Adamyan, N. Skuba, M. Titova, and N. Trostenyuk, Biomaterials, 7, 188 (1986).
- 26 O. Okay, J. Appl. Polym. Sci., 32, 5533 (1986).
- 27 O. Okay, Angew. Macromol. Chem., 143, 209 (1986).
- 28 O. Okay, Angew. Macromol. Chem., 153, 125 (1987).
- 29 B. D. Barr-Howell and N. A. Peppas, Eur. Polym. J., 8, 591 (1987).
- 30 O. Okay, Angew. Macromol. Chem., 157, 1 (1988).
- 31 T. G. Park and A. S. Hoffman, J. Biomed. Mater. Res., 24, 21 (1990).
- 32 T. G. Park and A. S. Hoffman, Biotechnol. Bioeng., 35, 152 (1990).
- 33 O. Okay and W. Funke, Macromolecules, 23, 2623 (1990).
- 34 O. Okay and W. Funke, Makromol. Chem. Commun., 11, 583 (1990).
- 35 T. G. Park and A. S. Hoffman, J. Polym. Sci., Polym. Chem. Ed., 30, 505 (1992).
- 36 N. A. Peppas, Ed., Hydrogels in Medicine and Pharmacy, Vol. II., CRC Press, Boca Raton, FL., 1978.
- 37 J. Kloosterboer, Adv. Polym. Sci., 84, 1 (1988).
- 38 H. Boots, J. Kloosterboer, and G. van de Hei, Br. Polym. J., 17, 219 (1985).
- 39 J. Bastide and L. Leiber, Macromolecules, 21, 2649 (1988).
- 40 G. P. Simon, P. E. M. Allen, D. J. Bennett, D. R. G. Williams, and E. H. Williams, Macromolecules, 22, 3555 (1989).
- 41 W. Funke, Br. Polym. J., 21, 107 (1989).
- 42 J. Kloosterboer, G. G. Litjen, and H. Boots, Makromol. Chem. Makromol. Symp., 24, 223 (1989).
- 43 A. B. Scranton, C. N. Bowman, J. Klier, and N. A. Peppas, Polymer, 33, 1683 (1992).
- 44 A. Tuncel, K. Ecevit and E. Piskin, J. Appl. Polym. Sci., January (1995) to appear.
- 45 K. Ecevit, M. S. Thesis, Hacettepe University, Ankara, Turkey (1995).
- 46 H. Hopff, H. Lussi, and E. Hammer, Makromol. Chem., 82, 175, 184 (1965).
- 47 D. B. Scules, J. Appl. Polym. Sci., 20, 2299 (1976).
- 48 A. Mersmann and H. Grossman, Chem. Eng. Technol., 52, 621 (1980).
- 49 R. Arshady and A. Ledwith, Reactive Polym., 1, 159 (1983).
- 50 R. Arshady, J. Chromatogr., 586, 181, 198 (1991).
- 51 S. M. Ahmed, Dispers. Sci. Technol., 5,, 421 (1984).
- 52 M. Brun, J. F. Quinson, R. Blane, M. Negre, C. Eyr and, and M. Bartholin, Makromol. Chem., 182, 873 (1981).