TY - JOUR
T1 - Healing of cutaneous and mucosal wounds grafted with collagen-glycosaminoglycan/Silastic bilayer membranes
T2 - A preliminary report
AU - Bertolami, C. N.
AU - Ellis, D. G.
AU - Donoff, R. B.
N1 - Funding Information:
* Shriners Bum Institute, Boston. t Department of Oral and Maxillofacial Surgery, Massachusetts General Hospital, Boston. Supported by NIWHIDR Grants No. DE 07803 (C.N.B.) and DE07086( R.B.D.) and Shriners Hospitals for Crippled Children Grants No. 15880/15878 (C.N.B.). Address correspondence and reprint requests to Dr Bertolami: Department of Oral and Maxillofacial Surgery, Massachusetts General Hospital, Fruit St, Boston, MA 02114.
PY - 1988/11
Y1 - 1988/11
N2 - This report describes the healing of cutaneous wounds in experimental animals grafted with collagen-glycosaminoglycan (GAG) matrix/Silastic (Dow Corning Corp., Midland, MI) bilayers; assesses the feasibility of using collagen-GAG matrix as a vehicle for delivering culture-selected, autogenous fibroblasts to cutaneous wound sites; and evaluates the use of collagen-GAG/Silastic bilayers as mucosal substitutes. Cutaneous and mucosal wounds in New Zealand white rabbits were grafted with either acellular collagen-GAG/Silastic membrane or collagen-GAG/Silastic membrane previously seeded with cultured autogenous fibroblasts. Over 63 days, wound sites were analyzed at intervals based on wound contraction and histology. Cutaneous wounds successfully incorporated grafted collagen-GAG matrix and were significantly inhibited in their rate and extent of wound contraction. Seeding membrane matrices with autogenous, cultured fibroblasts before grafting caused a marked increase in cellularity that persisted throughout the postgraft period. In mucosa, matrices were exteriorized rather than incorporated. This work suggests that collagen-GAG/Silastic bilayer may have value as a dermal substitute and, more significantly, may be appropriate as a vehicle for delivering cultureselected fibroblasts to cutaneous wound sites.
AB - This report describes the healing of cutaneous wounds in experimental animals grafted with collagen-glycosaminoglycan (GAG) matrix/Silastic (Dow Corning Corp., Midland, MI) bilayers; assesses the feasibility of using collagen-GAG matrix as a vehicle for delivering culture-selected, autogenous fibroblasts to cutaneous wound sites; and evaluates the use of collagen-GAG/Silastic bilayers as mucosal substitutes. Cutaneous and mucosal wounds in New Zealand white rabbits were grafted with either acellular collagen-GAG/Silastic membrane or collagen-GAG/Silastic membrane previously seeded with cultured autogenous fibroblasts. Over 63 days, wound sites were analyzed at intervals based on wound contraction and histology. Cutaneous wounds successfully incorporated grafted collagen-GAG matrix and were significantly inhibited in their rate and extent of wound contraction. Seeding membrane matrices with autogenous, cultured fibroblasts before grafting caused a marked increase in cellularity that persisted throughout the postgraft period. In mucosa, matrices were exteriorized rather than incorporated. This work suggests that collagen-GAG/Silastic bilayer may have value as a dermal substitute and, more significantly, may be appropriate as a vehicle for delivering cultureselected fibroblasts to cutaneous wound sites.
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U2 - 10.1016/0278-2391(88)90334-5
DO - 10.1016/0278-2391(88)90334-5
M3 - Article
C2 - 2846805
AN - SCOPUS:0023812628
SN - 0278-2391
VL - 46
SP - 971
EP - 978
JO - Journal of Oral and Maxillofacial Surgery
JF - Journal of Oral and Maxillofacial Surgery
IS - 11
ER -