Photothermal therapies
are based on the optical excitation of plasmonic
nanoparticles in the biological environment. The effects of the irradiation
on the biological medium depend critically on the heat transfer process
at the nanoparticle interface, on the temperature reached by the tissues,
as well as on the spatial extent of temperature gradients. Unfortunately,
both the temperature and its biological effects are difficult to be
probed experimentally at the molecular scale. Here, we approach this
problem using nonequilibrium molecular dynamics simulations. We focus
on photoporation, a photothermal application based on the irradiation
of gold nanoparticles by single, short-duration laser pulses. The
nanoparticles, stably bound to cell membranes, convert the radiation
into heat, inducing transient changes of membrane permeability. We
make a quantitative prediction of the temperature gradient around
the nanoparticle upon irradiation by typical experimental laser fluences.
Water permeability is locally enhanced around the nanoparticle, in
an annular region that extends only a few nanometers from the nanoparticle
interface. We correlate the local enhancement of permeability at the
nanoparticle–lipid interface to the temperature inhomogeneities
of the membrane and to the consequent availability of free volume
pockets within the membrane core.