Over one million patients per year undergo some type of procedure involving
cartilage reconstruction. Polymer hydrogels, such as alginate, have been s
hown to be effective carriers for chondrocytes in subcutaneous cartilage fo
rmation. The goal of our current study was to develop a method to create co
mplex structures (nose bridge, chin, etc.) with good dimensional tolerance
to form cartilage in specific shapes. Molds of facial implants M ere prepar
ed using Silastic ERTV. Suspensions of chondrocytes in 2% alginate were gel
led by mixing with CaSO4, (0.2 g/mL) and injected into the molds. Construct
s of various cell concentrations (10, 25, and 50 million/mL) were implanted
in the dorsal aspect of nude mice and harvested at times up to 30 weeks. A
nalysis of implanted constructs indicated progressive cartilage formation w
ith time. Proteoglycan and collagen constructs increased with time to appro
ximately 60% that of native tissue. Equilibrium modulus likewise increased
with time to 15% that of normal tissue, whereas hydraulic permeability decr
eased to 20 times that of native tissue. Implants seeded with greater conce
ntrations of cells increased proteoglycan content and collagen content and
equilibrium and decreased permeability. Production of shaped cartilage impl
ants by this technique presents several advantages, including good dimensio
nal tolerance, high sample-to-sample reproducibility, and high cell viabili
ty. This system may be useful in the large-scale production of precisely sh
aped cartilage implants. (C) 2001 John Wiley & Sons, Inc.