The potetial for using gene therapy to treat a variety of disease states is
growing rapidly. Many vector types and delivery systems have been develope
d that allow the opimation of protein production levels and kinetics for a
given therapeutic gene production. in cases. In which a transient, localize
d delivery of gene product is desired any determination of the locale of tr
ansfected tissue by non-marker genes is problematic. We describe a techniqu
e by whick the use of fluorescent microspheres can help in identifying pote
ntially transfected tissue. Adenovirus containing the gene for beta-galacto
sidase (beta-gal) was mixed with fluorescent microspheres and injected into
mt skeletal muscle and porcine myocardium. The injection sites could be vi
sualized under ultraviolet light and correlated with beta-gal enzyme expres
sion. This method is simple. inexpensive and generally useful for in vivo g
ene transfer experiments..