Hydrophobically Functionalized Chitosan Particles

被引:13
作者
Fink, Katharina [1 ,2 ]
Hoehne, Susanne [1 ]
Spange, Stefan [2 ]
Simon, Frank [1 ]
机构
[1] Leibniz Inst Polymer Res Dresden, D-01069 Dresden, Germany
[2] Tech Univ Chemnitz, Dept Polymer Chem, D-09111 Chemnitz, Germany
关键词
Chitosan; grafting of aldehydes and carbonic acid derivatives; NMR; XPS; FT-IR; hydrophobization; super-hydrophobicity; Wilhelmy technique; INTERPENETRATING POLYMER NETWORK; IN-VITRO; HYDROGELS; FILMS; VIVO; DERIVATIVES; COMPOSITE; DELIVERY; PRODUCT; SYSTEM;
D O I
10.1163/156856108X388399
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Particles of chitosan have a very polar surface, and thus they are easily wetted by water and also dissolve in acidic media. The hydroxyl and amino groups offer a high potential for grafting reactions. Aldehydes and carbonic acid derivatives were covalently grafted, preferably onto the amino groups. The reactions were carried out in solution as homogeneous phase reactions as well as on the particle surfaces as heterogeneous phase reactions. Covalently bonded alkyl chains impart the chitosan molecules with hydrophobic properties. We employed different methods such as NMR, XPS, elemental analysis and FT-IR spectroscopy to study the reactions and to estimate the degree of functionalization. The wetting behavior of the particles was investigated by a modified Wilhelmy technique, where an adhesive tape completely coated with the particles was dipped in water. Some of the samples having a high degree of functionalization showed super-hydrophobic surface properties. The observed super-hydrophobic effect results from a combination of the hydrophobic properties of the modified particles and the roughness of the particle coating. (C) Koninklijke Brill NV, Leiden, 2009
引用
收藏
页码:297 / 315
页数:19
相关论文
共 40 条
[1]   FORMATION OF MONOLAYER FILMS BY THE SPONTANEOUS ASSEMBLY OF ORGANIC THIOLS FROM SOLUTION ONTO GOLD [J].
BAIN, CD ;
TROUGHTON, EB ;
TAO, YT ;
EVALL, J ;
WHITESIDES, GM ;
NUZZO, RG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (01) :321-335
[2]  
Batura L. I., 1981, CELL CHEM TECHNOL, V15, P487
[3]   Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications [J].
Berger, J ;
Reist, M ;
Mayer, JM ;
Felt, O ;
Peppas, NA ;
Gurny, R .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 57 (01) :19-34
[4]   Adhesion and viability of two enterococcal strains on covalently grafted chitosan and chitosan/κ-carrageenan multilayers [J].
Bratskaya, S. ;
Marinin, D. ;
Simon, F. ;
Synytska, A. ;
Zschoche, S. ;
Busscher, H. J. ;
Jager, D. ;
van der Mei, H. C. .
BIOMACROMOLECULES, 2007, 8 (09) :2960-2968
[5]   Cross-linking chitosan-Fe(III), an oral phosphate binder:: studies in vitro and in vivo [J].
Bürger, C ;
Valcarenghi, D ;
Sandri, S ;
Rodrigues, CA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 223 (1-2) :29-33
[6]   L-DOPA production by immobilized tyrosinase [J].
Carvalho, GMJ ;
Alves, TLM ;
Freire, DMG .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2000, 84-6 (1-9) :791-800
[7]  
Chen X, 1997, J APPL POLYM SCI, V65, P2257, DOI 10.1002/(SICI)1097-4628(19970912)65:11<2257::AID-APP23>3.3.CO
[8]  
2-L
[9]   Hydrophobic derivatives of chitosan: Characterization and rheological behaviour [J].
Desbrieres, J ;
Martinez, C ;
Rinaudo, M .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 1996, 19 (01) :21-28
[10]   Biodegradation of chitosan-tripolyphosphate beads:: In vitro and in vivo studies [J].
Durkut, S ;
Elçin, YM ;
Elçin, AE .
ARTIFICIAL CELLS BLOOD SUBSTITUTES AND BIOTECHNOLOGY, 2006, 34 (02) :263-276