A theory is presented for the solvent-mediated force potential between sphe
rical colloidal particles in a solvent. The long range part of the potentia
l Phi(ij)((sol))(r) between the i- and j-species of particles is given as P
hi(ij)((sol)) (r) = -k(B)T Sigma(n) K((n))d(i)((n)) d(j)((n)) 1/r e(-2nr) w
ith the temperature T and the Boltzmann constant k(B), where K(n) and z(n)
are determined by the bulk structure of the solvent and d(j)((n)) is calcul
ated from z(n) and the structure of the solvent near the j-species of collo
idal particle, A similar result is also obtained for the long range part of
the total correlation function h(0j) (r) between colloidal- and solvent-pa
rticles. It is discussed that d(j)((n)) is inversely proportional to the is
othermal compressibility of the solvent. The application of the theory to t
he solvent near its critical point gives extremely, simple and universal ex
pressions for the asymptotic behaviours of h(0j) (r) and Phi(ij)((sol)) (r)
. This Phi(ij)((sol)) (r) is compared with the van der TT Waals potential i
n order to emphasize a role of Phi(ij)((sol)) (r).