Title :
Controlling sol-gel polymerization by solvent selection to create tissue engineering scaffolds
Author :
Lippincott, H.W. ; Schmidt, D.F.
Author_Institution :
Biomed. Eng. & Biotechnol. Program, Univ. of Massachusetts, Lowell, MA
Abstract :
Polyurethane xerogels with open pore networks were created via solution-gelation (sol-gel) polymerization. The solubility parameters of the solvent(s) and prepolymers and equilibrium swelling and extraction data were both used to select solvent(s) giving porous xerogels. Polycaprolactone (PCL) diol was combined with either poly(tetramethylene glycol) (PTMEG) or castor oil (CO), and the prepoplymer mixture gelled in an array of solvents through reaction with a triisocyanate. The behavior of the PCL/PTMEG system was mapped vs. all pure solvents used as well as several binary blends, and regions generating porous bodies were identified. Both this and the PCL/CO system were also prepared as dense materials, with equilibrium swelling and extractable fraction data generated in various solvents Analysis of this data also allowed for selection of appropriate solvents for porous xerogel formation. Porous xerogels were characterized via scanning electron microscopy and mercury intrusion porosimetry.
Keywords :
aerogels; biochemistry; biomedical materials; polymerisation; sol-gel processing; tissue engineering; castor oil; equilibrium swelling; mercury intrusion porosimetry; polycaprolactone diol; polytetramethylene glycol; polyurethane xerogels; porous xerogel formation; prepolymers; scanning electron microscopy; solution-gelation polymerization; tissue engineering; triisocyanate; Biomedical engineering; Chemistry; Data mining; Glass; Petroleum; Polymers; Silicon compounds; Solvents; Tellurium; Tissue engineering;
Conference_Titel :
Bioengineering Conference, 2009 IEEE 35th Annual Northeast
Conference_Location :
Boston, MA
Print_ISBN :
978-1-4244-4362-8
Electronic_ISBN :
978-1-4244-4364-2
DOI :
10.1109/NEBC.2009.4967746