TY - JOUR
T1 - Agarose gel as biomaterial or scaffold for implantation surgery
T2 - Characterization, histological and histomorphometric study on soft tissue response
AU - Varoni, Elena
AU - Tschon, Matilde
AU - Palazzo, Barbara
AU - Nitti, Paola
AU - Martini, Lucia
AU - Rimondini, Lia
N1 - Funding Information:
This study was partially supported by Consorzio InterUniversitario per lo Studio della Chimica dei Metalli nei Sistemi Biologici (CIRMSC), Ministero dell’ Istruzione, dell’Università e della Ricerca (MIUR) (POR no. 1291); Rizzoli Orthopaedic Institute, Bologna-Italy. Materials were provided by Ghimas S.p.A.
PY - 2012/12
Y1 - 2012/12
N2 - Maxillofacial, orthopedic, oral, and plastic surgery require materials for tissue augmentation, guided regeneration, and tissue engineering approaches. In this study, the aim was to develop and characterize a new extrudable hydrogel, based on agarose gel (AG; 1.5% wt) and to evaluate the local effects after subcutaneous implantation in comparison with collagen and hyaluronic acid. AG chemical-physical properties were ascertained through Fourier transform infrared (FT-IR) spectroscopy and rheological analysis. In vivo subcutaneous implants were performed, and histological and histomorphometric evaluations were done at 1, 4, 12, and 16 weeks. FT-IR confirmed that spectroscopic properties were the same for the baseline agarose and rheological characterization established that AG is a weak hydrogel. Subcutaneous AG implants induced new vessels and fibrous tissue formation rich in neutrophils; the capsule thickness around AG increased until the 12th week but remained thinner than those around hyaluronic acid and collagen. At 16 weeks, the thickness of the capsule significantly decreased around all materials. This study confirmed that 1.5% wt AG possesses some of the most important features of the ideal biocompatible material: safety, effectiveness, costless, and easily obtained with specific chemical and geometrical characters; the AG can represent a finely controllable and biodegradable polymeric system for cells and drug delivery applications.
AB - Maxillofacial, orthopedic, oral, and plastic surgery require materials for tissue augmentation, guided regeneration, and tissue engineering approaches. In this study, the aim was to develop and characterize a new extrudable hydrogel, based on agarose gel (AG; 1.5% wt) and to evaluate the local effects after subcutaneous implantation in comparison with collagen and hyaluronic acid. AG chemical-physical properties were ascertained through Fourier transform infrared (FT-IR) spectroscopy and rheological analysis. In vivo subcutaneous implants were performed, and histological and histomorphometric evaluations were done at 1, 4, 12, and 16 weeks. FT-IR confirmed that spectroscopic properties were the same for the baseline agarose and rheological characterization established that AG is a weak hydrogel. Subcutaneous AG implants induced new vessels and fibrous tissue formation rich in neutrophils; the capsule thickness around AG increased until the 12th week but remained thinner than those around hyaluronic acid and collagen. At 16 weeks, the thickness of the capsule significantly decreased around all materials. This study confirmed that 1.5% wt AG possesses some of the most important features of the ideal biocompatible material: safety, effectiveness, costless, and easily obtained with specific chemical and geometrical characters; the AG can represent a finely controllable and biodegradable polymeric system for cells and drug delivery applications.
KW - biocompatibility
KW - histocompatibility
KW - histomorphometry
KW - injectable biomaterial/scaffold
KW - polysaccharide gel
UR - http://www.scopus.com/inward/record.url?scp=84869754144&partnerID=8YFLogxK
U2 - 10.3109/03008207.2012.712583
DO - 10.3109/03008207.2012.712583
M3 - Article
SN - 0300-8207
VL - 53
SP - 548
EP - 554
JO - Connective Tissue Research
JF - Connective Tissue Research
IS - 6
ER -