STIMULI SENSITIVE POLYMERS FOR DRUG DELIVERY SYSTEMS

被引:37
作者
KWON, IC [1 ]
BAE, YH [1 ]
OKANO, T [1 ]
BERNER, B [1 ]
KIM, SW [1 ]
机构
[1] UNIV UTAH,CTR CONTROLLED CHEM DELIVERY,SALT LAKE CITY,UT 84108
来源
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA | 1990年 / 33卷
关键词
D O I
10.1002/masy.19900330123
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Temperature sensitive and electric field sensitive hydrogels were prepared for use in modulated drug release systems. Crosslinked poly(N‐isopropyl‐acrylamide) and its networks, modified with hydrophobic components by copolymerization or by interpenetrating polymer networks (IPNs) formation, were utilized as temperature sensitive hydrogels. Indomethacin (a model solute)‐release from polymer matrix and permeation through polymer membrane demonstrated “on‐off” regulation with temperature fluctuation. This was the result of polymer surface properties rather than bulk swelling, as temperature was changed past the swelling transition temperature range of the polymer. The on‐off regulation in an electric field was also obtained with a positively charged solute (Edrophonium chloride) release in distilled‐deionized water from a matrix of crosslinked poly(2‐acrylamido‐2‐methylpropanesulfonic acid‐co‐butyl methacrylate). This was attributed to the ion exchange between Edrophonium ion and protons produced at the anode. The swelling changes produced by local pH or ionic strength changes affected non‐charged solute release. Copyright © 1990 Hüthig & Wepf Verlag
引用
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页码:265 / 277
页数:13
相关论文
共 26 条
  • [1] Obie J.F., Cooper C.W., J. Pharm. Expl. Ther., 209, (1979)
  • [2] Davis S.S., Advanced delivery systems for peptides and proteins‐pharmaceutical considerations, Delivery Systems for Peptide Drug, (1986)
  • [3] Vander A.J., Sherman J.H., Luciano D.S., Human Physiology: The Mechanism and Body Function, (1985)
  • [4] Heller J., J. Control. Rel., 8, (1988)
  • [5] Taylor L.D., Cerankowski L.D., J. Polym. Sci., Polym. Chem. Ed., 13, (1975)
  • [6] Okano T., Bae Y.H., Kim S.W., Temperature reponsive controlled drug delivery, Modulated Controlled Release
  • [7] Bae Y.H., Okano T., Kim S.W., Die Makromolekulare Chemie, Rapid Communications, 9, (1988)
  • [8] Heskins M., Guillet J.E., Solution Properties of Poly(N-isopropylacrylamide), Journal of Macromolecular Science: Part A - Chemistry, 2 A, (1968)
  • [9] Hoffman A.S., Afrassiabi A., Dong L.C., J. Control. Rel., 4, (1986)
  • [10] Park T.G., Hoffman A.S., Appl. Biochem. Biotech., 19, (1988)