The problem of a polymer chain immersed in a critical fluid, e.g. a mi
xture of low molecular weight solvent close to its critical point, is
studied and reformulated in a field theoretic framework. The starting
point is a path integral formulation of the polymer chain which intera
cts with the solvent molecules. If the critical solvent is approximate
d by a Gaussian model all classical results are recovered, i.e. the po
lymer chain collapses close to the critical point. These results becom
e modified at the critical point where non-classical exponents determi
ne the precise form of the fluctuation induced interaction potential b
etween two monomers of the chain, and so its conformation.