Hydrophobically modified poly[(divinyl ether)-co-(maleic anhydride)]: Interactions with cyclodextrin derivatives and hydrogel formation

Polymer International

Volumn 61, Issue 3, 2012, Pages 413-417

  Bernert, Dominika B ^a   Böhm, Indra ^a   Isenbügel, Kathrin ^a   Schönenberg, Lisa ^a   Ritter, Helmut ^a  

^a HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

Cyclocopolymerization; Cyclodextrin; DIVEMA; Gelation; Polyelectrolytes

Indexed keywords

AGGREGATED STRUCTURE; ANTI-TUMOR ACTIVITIES; AVERAGE DIAMETER; CROSSLINKED; CYCLOCOPOLYMERIZATION; CYCLODEXTRIN DERIVATIVES; DISAGGREGATION; DIVEMA; DIVINYL ETHER; DIVINYL ETHER AND MALEIC ANHYDRIDES; DRUG DELIVERY SYSTEM; FUNCTIONALIZED; GEL FORMATION; HOST-GUEST SYSTEM; HYDRODYNAMIC DIAMETER; HYDROGEL FORMATION; PHYSICOCHEMICAL PROPERTY; TEMPERATURE DEPENDENT VISCOSITY;

COAGULATION; CYCLODEXTRINS; DRUG DELIVERY; ETHERS; GELATION; HYDROGELS; HYDROLYSIS; MALEIC ANHYDRIDE; MEDICAL APPLICATIONS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYELECTROLYTES; ZETA POTENTIAL;

BUTADIENE;

EID: 84856678439     PISSN: 09598103     EISSN: 10970126     Source Type: Journal    
DOI: 10.1002/pi.3216     Document Type: Article

References (25)

1. Caliceti P, Schiavon O, Hirano T, Ohashi S and Veronese FM, J Control Release 39: 27 (1996).
2. Izumrudov VA, Gorshkova MY and Volkova IF, Eur Polym J 41: 1251 (2005).
3. Volkova IF, Gorshkova MY, Ivanov PE and Stotskaya LL, Polym Adv Technol 13: 1067 (2002).
4. Butler GB, J Polym Sci 48: 279 (1960).
5. Butler GB and Chu YC, J Polym Sci Pol Chem 17: 859 (1979).
6. Butler GB, J Macromol Sci Chem 1: 219 (1977).
7. Merigant C, Nature 214: 416 (1967).
8. Butler GB, J Polym Sci Pol Chem 38: 3451 (2000).
9. Zhao H, Deng J, Liu Z, Yang P, Liu L, Sun Y, et al, Adv Mater Res 11: 741 (2006).
10. Stotskaya LL, Serbin AV, Munshi K, Kozeletskaya KN, Sominina AA, Kiselev OI, et al, Pharm Chem J 29: 171 (1995).
11. Koopmans C and Ritter H, Macromolecules 41: 7418 (2008).
12. Sangeetha NM and Maitra U, Chem Soc Rev 34: 821 (2005).
13. Peng K, Tomatsu I, Korobko AV and Kros A, Soft Matter 6: 85 (2010).
14. Schmidt M, Makromol Chem Rapid Commun 10: 89 (1989).
15. van der Maarel JRC, Groot LCA, Hollander JG, Jesse W, Kuil ME, Leyte JC, et al, Macromolecules 26: 7295 (1993).
16. Forster S, Schmidt M and Antonietti M, Polymer 31: 781 (1990).
17. Kretschmann O, Choi S, Munteanu M, Tomatsu I, Harada A and Ritter H, Angew Chem Int Ed 45: 4361 (2006).
18. Amajjahe S, Choi S, Munteanu M and Ritter H, Angew Chem Int Ed 47: 3435 (2008).
19. Munteanu M, Choi S and Ritter H, J Incl Phenom Macro 62: 197 (2008).
20. Klee J, Elsner O, Pohle S, Ritter H and Bernert D, Dental composition, Dentsply DeTrey, Konstanz (2010).
21. Butler GB and Chu YC, J Polym Sci 17: 859 (1979).
22. Kunitake T and Tsukino M, J Polym Sci 17: 877 (1979).
23. Magny B, Iliopoulos I, Zana R and Audebertt R, Langmuir 10: 3180 (1994).
24. Guenoun P, Davis HT, Tirrell M and Mays JW, Macromolecules 29: 3965 (1996).
25. Bromberg LE and Barr DP, Macromolecules 32: 3649 (1999).