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  • Ultrasound monitoring of cartilaginous matrix evolution in degradable PEG hydrogels.

Ultrasound monitoring of cartilaginous matrix evolution in degradable PEG hydrogels.

Acta biomaterialia (2008-09-17)
Mark A Rice, Kendall R Waters, Kristi S Anseth
ABSTRACT

Ultrasound has potential as a non-destructive analytical technique to provide real-time online assessments of matrix evolution in cell-hydrogel constructs used in tissue engineering. In these studies, chondrocytes were encapsulated in poly(ethylene glycol) hydrogels, and gel degradation was manipulated to provide conditions with varying distribution of the large cartilage extracellular matrix molecule, collagen. Mechanical properties and matrix accumulations were simultaneously measured for each condition during 9.5 weeks of in vitro culture. Ultrasound data were used to construct cross-sectional B-scan images for qualitative observations of evolving constructs. Ultrasound data were also analyzed to calculate the speed of sound (SoS) and slope of attenuation (SoA) in developing constructs and a non-degrading hydrogel control without encapsulated chondrocytes. SoS and SoA were calculated from 50 and 100MHz ultrasound data, and sample correlation coefficients were calculated to identify important relationships between these ultrasound parameters and mechanical/biochemical properties of the evolving matrix. SoA appears to be more sensitive to the density of accumulated matrix molecules than SoS, while SoS appeared to be more sensitive to mechanical modulus than SoA in measurements performed at 100MHz. Correlation analysis revealed that ultrasound measurements at 100MHz are more likely to be good predictors of matrix evolution and neotissue function than measurements at 50MHz. Rigorous studies of the relationships identified in this study will lead to non-destructive real-time monitoring that will be useful in combination with bioreactors used to promote and study cartilage regeneration.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Poly(ethylene glycol), average Mn 2,050, chips
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 400
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 1,500
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 4,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 3,350
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 3,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 35,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 2,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, for molecular biology, 1,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 600
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 1,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 300
Supelco
Poly(ethylene glycol), analytical standard, for GPC, 108,000
Sigma-Aldrich
Poly(ethylene glycol), average Mn 20,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 8,000
Sigma-Aldrich
Poly(ethylene glycol), average Mw 1,500
Sigma-Aldrich
Poly(ethylene glycol), average Mn 600, waxy solid (moist)
Sigma-Aldrich
Poly(ethylene glycol), average Mn 3,350, powder
Supelco
Poly(ethylene glycol), analytical standard, for GPC, 40,000
Sigma-Aldrich
Poly(ethylene glycol), average Mn 4,000, platelets
Sigma-Aldrich
Poly(ethylene glycol), tested according to Ph. Eur., 4,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, for molecular biology, 6,000
Sigma-Aldrich
Poly(ethylene glycol), average Mn 6,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 10,000
Sigma-Aldrich
Poly(ethylene glycol), BioUltra, 6,000
Sigma-Aldrich
Poly(ethylene glycol), tested according to Ph. Eur., 400
Sigma-Aldrich
Poly(ethylene glycol), average Mv ~8,000, powder (crystalline)
Sigma-Aldrich
Poly(ethylene glycol), average Mn 400
Sigma-Aldrich
Poly(ethylene glycol), average Mn 4,600
Sigma-Aldrich
Poly(ethylene glycol), average Mn 300