Cochlear gene transfer studies in animal models have utilized mainly two de
livery methods: direct injection through the round window membrane (RWM) or
intracochlear infusion through a cochleostomy. However, the surgical traum
a, inflammation, and hearing loss associated with these methods Lead us to
investigate a less invasive delivery method. Herein, we studied the feasibi
lity of a vector transgene-soaked gelatin sponge, Gelfoam, for transgene de
livery into the mouse cochlea through an intact RWM, The Gelfoam absorbed w
ith liposomes and adenovirus, but not with adeno-associated virus (AAV), wa
s successful in mediating transgene expression across an intact RWM in a va
riety of cochlear tissues. The Gelfoam technique proved to be an easy, atra
umatic, and effective, but vector-dependent, method of delivering transgene
s through an intact RWM, Compared with the more invasive gene delivery meth
ods, this technique represents a safer and a more clinically viable route o
f cochlear gene delivery in humans.