PURPOSE: To demonstrate in vivo that platinum embolic coils can be use
d to deliver genetically modified, growth factor-secreting fibroblast
grafts into the endovascular space with the long-term goal of improvin
g fibrosis with coil-embolized cerebral aneurysms. MATERIALS AND METHO
DS: Murine fibroblasts that contained multiple inserts of the DNA for
human basic fibroblast growth factor were grown in culture onto 10-mm-
long segments of Guglielmi detachable coils. Control (n = 4) and fibro
blast-bearing (n = 4) coils were implanted into the common carotid art
ery in nude rats. The arterial segments that contained the coil were h
arvested after 14 or 35 days. Cellular content and collagen formation
in the treated vessels were assessed histologically. RESULTS: At both
14 and 35 days, samples with control coils showed primarily involuting
blood elements with minimal fibroblast proliferation or collagen form
ation. AT 14 days, samples with fibroblast-bearing coils showed extens
ive fibroblast proliferation. AT 35 days, samples with fibroblast-bear
ing coils showed marked interval fibroblast proliferation and collagen
information. CONCLUSION: Platinum coils can be used as a cell deliver
y device. Direct intravascular implantation of growth factor-secreting
fibroblast grafts leads to improved intravascular scar formation, the
refore theoretically reducing the potential for aneurysm regrowth or c
oil compaction.