Extensive clinical and laboratory studies have demonstrated that growth fac
tors accelerate and modulate the wound-healing process. The purpose of this
experiment was to apply the principles of growth factor-enhanced wound hea
ling to an in vitro rat tendon model. A method was developed for covalently
binding a biologically active peptide to nonabsorbable braided polyester s
uture (Mersilene). Sutures were treated with various growth factors, which
included epidermal growth factor, platelet-derived growth factor, and kerat
inocyte growth factor, and bovine serum albumin was the control. Spectropho
tometric assessment was used to verify the peptide's activity. The suture w
as subsequently placed through individual harvested rat flexor tendons, whi
ch were arranged in standard tissue culture conditions. Markedly increased
cellular proliferation along the suture was appreciated on the tendons trea
ted with epidermal growth factor-bound suture. Platelet-derived growth fact
or was shown to have a lesser effect, whereas keratinocyte growth factor ha
d no visible effect on cellular proliferation. This preliminary study descr
ibes a new technique of binding growth factors to suture. It also demonstra
tes that the presence of growth factors may help facilitate flexor tendon h
ealing and allow early postoperative rehabilitation to decrease adhesion fo
rmation.