FTIR study of polycaprolactone chain organization at interfaces.

Polycaprolactone (PCL), extensively known as a biomaterial, is the subject of this paper. Knowing well that some biomaterial applications exhibit specific chain organization, we focused our study on the orientation of PCL chains when this polymer is adsorbed (spin-coated) on inert substrates such as gold-coated glass slides. The main technique allowing adsorbed thin films analysis that we chose is polarization-modulation infrared reflection-absorption spectroscopy (PM-IRRAS), which permits qualitative and quantitative determination of chain anisotropy in the confined layers at the interface. Based on our spectroscopic results, we achieved an adsorption model of PCL chains and we calculated orientation angles with respect to the substrate normal. Calculated values show a quasi-perpendicular deposition of PCL chains on the gold substrate. Moreover, PCL thin films remain highly crystalline, a fact which could be the basis of the important anisotropy of PCL chains.

[1]  M. Koenig,et al.  Biodegradable blends and composites of polycaprolactone and starch derivatives , 1995 .

[2]  N. E. Schlotter,et al.  Anisotropic orientation in molecular monolayers by infrared spectroscopy , 1983 .

[3]  Bernhard Schrader,et al.  Infrared and Raman spectroscopy : methods and applications , 1995 .

[4]  J. Schultz,et al.  Quantitative calculation of the orientation angles of adsorbed polyamides nanofilms , 2003 .

[5]  J. Schultz,et al.  Structure, orientation, and conformation of adsorbed polyamides , 2002 .

[6]  Toshihiro Akaike,et al.  A novel degradable polycaprolactone networks for tissue engineering. , 2003, Biomaterials.

[7]  J. Schultz,et al.  Adsorption of polyamides on SAMs: effect of SAM grafting density on polyamide morphology , 2003 .

[8]  J. Schultz,et al.  Molecular orientation of EVA chains adsorbed on chemically controlled surfaces: influence of specific interactions , 2003 .

[9]  P. Degée,et al.  Macromolecular engineering of polylactones and polylactides. 11. Synthesis and use of alkylaluminum dialkoxides and dithiolates, as promoters of hydroxy telechelic poly(.epsilon.-caprolactone) and .alpha.,.omega.-dihydroxy triblock copolymers containing outer polyester blocks , 1993 .

[10]  Yongli Mi,et al.  Miscibility and morphology in crystalline/amorphous blends of poly(caprolactone)/poly(4-vinylphenol) as studied by DSC, FTIR, and 13 C solid state NMR , 2002 .

[11]  Thierry Buffeteau,et al.  Polarization Modulation FT-IR Spectroscopy of Surfaces and Ultra-Thin Films: Experimental Procedure and Quantitative Analysis , 1991 .

[12]  J. Schultz,et al.  Crystallinity measurements of polyamides adsorbed as thin films , 2002 .

[13]  H. Janik,et al.  Biodegradation of polycaprolactone in sea water , 1998 .

[14]  G. Socrates,et al.  Infrared Characteristic Group Frequencies , 1980 .

[15]  Yue Zhao,et al.  Molecular orientation in crystalline miscible blends , 1999 .

[16]  David F. Eggers,et al.  Infrared spectra of complex molecules , 1959 .

[17]  David L. Allara,et al.  Spontaneously organized molecular assemblies. 2. Quantitative infrared spectroscopic determination of equilibrium structures of solution-adsorbed n-alkanoic acids on an oxidized aluminum surface , 1985 .

[18]  A. Elfick Poly(ε-caprolactone) as a potential material for a temporary joint spacer , 2002 .