Poly(2-isopropyl-2-oxazoline)-
b
-poly(lactide)
(PiPOx-
b
-PLA) diblock copolymers comprise two miscible
blocks: the hydrophilic and thermosensitive PiPOx and the hydrophobic
PLA, a biocompatible and biodegradable polyester. They self-assemble
in water, forming stable dispersions of nanoparticles with hydrodynamic
radii (
R
h
) ranging from ∼18 to
60 nm, depending on their molar mass, the relative size of the two
blocks, and the configuration of the lactide unit. Evidence from
1
H nuclear magnetic resonance spectroscopy, light scattering,
small-angle neutron scattering, and cryo-transmission electron microscopy
indicates that the nanoparticles do not adopt the typical core–shell
morphology. Aqueous nanoparticle dispersions heated from 20 to 80
°C were monitored by turbidimetry and microcalorimetry. Nanoparticles
of copolymers containing a poly(
dl
-lactide) block coagulated
irreversibly upon heating to 50 °C, forming particles of various
shapes (
R
h
∼ 200–500 nm).
Dispersions of PiPOx-
b
-poly(
l
-lactide) coagulated
to a lesser extent or remained stable upon heating. From the entire
experimental evidence, we conclude that PiPOx-
b
-PLA
nanoparticles consist of a core of PLA/PiPOx chains associated via
dipole–dipole interactions of the PLA and PiPOx carbonyl groups.
The core is surrounded by tethered PiPOx loops and tails responsible
for the colloidal stability of the nanoparticles in water. While the
core of all nanoparticles studied contains associated PiPOx and PLA
blocks, fine details of the nanoparticles morphology vary predictably
with the size and composition of the copolymers, yielding particles
of distinctive thermosensitivity in aqueous dispersions.