Amphiphilic brush-like block copolymers composed of polynorbonene-cholesterol/poly(ethylene glycol) (P(NBCh9-b-NBPEG)) self-assembled to form a long circulating nanostructure capable of encapsulating the anticancer drug doxorubicin (DOX) with high drug loading (22.1% w/w). The release of DOX from the DOX-loaded P(NBCh9-b-NBPEG) nanoparticles (DOX-NPs) was steady at less than 2% per day in PBS. DOX-NPs were effectively internalized by human cervical cancer cells (HeLa) and showed dose-dependent cytotoxicity, whereas blank nanoparticles were noncytotoxic. The DOX-NPs demonstrated a superior in vivo circulation time relative to that of free DOX. Tissue distribution and in vivo imaging studies showed that DOX-NPs preferentially accumulated in tumor tissue with markedly reduced accumulation in the heart and other vital organs. The DOX-NPs greatly improved survival and significantly inhibited tumor growth in tumor-bearing SCID mice compared to that for the untreated and free DOX-treated groups. The results indicated that self-assembled P(NBCh9-b-NBPEG) may be a useful carrier for improving tumor delivery of hydrophobic anticancer drugs.

The interaction of fields with condensed matter during phase transitions produces a rich variety of physical phenomena. Self-assembly of liquid crystalline block copolymers (LC BCPs) in the presence of a magnetic field, for example, can result in highly oriented microstructures due to the LC BCP's anisotropic magnetic susceptibility. We show that such oriented mesophases can be produced using low-intensity fields (<0.5 T) that are accessible using permanent magnets, in contrast to the high fields (>4 T) and superconducting magnets required to date. Low-intensity field alignment is enabled by the addition of labile mesogens that coassemble with the system's nematic and smectic A mesophases. The alignment saturation field strength and alignment kinetics have pronounced dependences on the free mesogen concentration. Highly aligned states with orientation distribution coefficients close to unity were obtained at fields as small as 0.2 T. This remarkable field response originates in an enhancement of alignment kinetics due to a reduction in viscosity, and increased magnetostatic energy due to increases in grain size, in the presence of labile mesogens. These developments provide routes for controlling structural order in BCPs, including the possibility of producing nontrivial textures and patterns of alignment by locally screening fields using magnetic nanoparticles.

We explore the morphology and phase behavior of a recently introduced architecture of liquid crystalline brushlike block copolymer (LCBBC) as functions of composition and molecular weight. Low-polydispersity materials were prepared by ring-opening metathesis polymerization of n-alkyloxy­cyano­biphenyl and poly­(dl-lactide) (PLA) functionalized norbornene monomers. Well-ordered block copolymer mesophases were observed with transitions from spheres to hexagonally packed cylinders, lamellae, inverse cylinders, and inverse spheres on increasing the weight fraction of the liquid crystalline block, f LC, from 0.15 to 0.85. The microdomain spacing displays a power-law scaling with molecular weight with an exponent of 0.6, L 0 ∼ MW0.6. The simple occurrence of microdomains with curved interfaces, spherical and cylindrical, and the sublinear scaling of microdomain spacing with molecular weight set this system clearly apart from bottlebrush block copolymers. We observe a peculiar morphology dependence of the liquid crystal anchoring condition with the cyanobiphenyl mesogens adopting planar anchoring at cylindrical microdomain interfaces while both homeotropic and planar anchoring were displayed at the block interface in lamellar systems.

We report on the synthesis and properties of cholesteric liquid crystalline random terpolymers with comblike architecture as a modular platform for preparation of stimuli-responsive photonic elastomers. Ring-opening metathesis of norbornene monomers bearing n-alkyloxy cholesteryl (Ch 9 ), n-alkoxy cyanobiphenyl (CB 6 or CB 12 ), and poly(ethylene glycol) (PEG) side chains is efficient and quantitatively yields low polydispersity random terpolymers. This terpolymer scaffold selfassembles to form cholesteric mesophases (N*) in which microphase-segregated domains of PEG side chains are randomly embedded. The cholesteric mesophase provides a 1D photonic band gap structure at optical wavelengths, which is maintained during chemical cross-linking of the norbornene backbone to form elastomers. The presence of cyanobiphenyl mesogens leads to an increase in the helical pitch of the cholesteric mesophase, resulting in a red-shift of the reflectivity relative to the pure cholesteric mesophase. By contrast, the presence of PEG blue-shifts the reflectivity, such that the overall optical properties can be readily tailored by the composition of the terpolymer. Furthermore, the mechanical properties of the materials are enhanced by the presence of the microphase-separated PEG domains which act as physical cross-links and also provide plasticization of the system. The terpolymers described here provide a modular and versatile platform for the realization of photopatternable materials that exhibit shape memory and thermochromic properties.

Phase behavior and dynamics of a LC block copolymer are manipulated by labile mesogens to enable alignment, photopatterning and nanopore orientation at low magnetic fields.