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We report on the fabrication of a novel type of ratiometric fluorescent polymeric probes for fluoride ions (F–) based on self-assembled micellar nanoparticles of P(MMA-co-NBDAE)-b-PF-b-P(MMA-co-NBDAE) coil–rod–coil triblock copolymer, where MMA, NBDAE, and PF are methyl methacrylate, 4-(2-acryloyloxyethylamino)-7-nitro-2,1,3-benzoxadiazole, and polyfluorene, respectively. Blue-emitting conjugated PF block and green-emitting NBDAE moieties with F–turn-off characteristics within the PMMA block serve as fluorescence resonance energy transfer (FRET) donors and switchable acceptors, respectively. For coil–rod–coil triblock copolymer in a good solvent such as THF, the blue emission of PF block dominates due to unimolecularly dissolved state associated with ineffective FRET process. The addition of F–ions only leads to ∼2.92-fold decrease of fluorescence intensity ratio, I515/I417, of characteristic NBDAE and PF emission bands. In acetone, the triblock copolymer spontaneously self-assembles into micelles possessing PF cores and NBDAE-labeled PMMA coronas. In the absence of F–ions, effective FRET processes between micellar cores and coronas occurs, resulting in prominently enhanced NBDAE emission. Upon addition of F–ions, the quenching of NBDAE emission bands leads to ∼8.75-fold decrease in the emission intensity ratio, I515/I417, which is also accompanied by naked eye-discernible fluorometric transition from cyan to blue emissions and colorimetric transition from green to yellowish. At a micellar concentration of 0.1 g/L in acetone at 25 °C, the detection limit of F–ions can be down to ∼4.78 μM (∼0.09 ppm). This work presents a new example of polymeric micelles-based optical F–probes and manifests that, upon proper structural design and optimization of spatial distribution of FRET donors and acceptors, self-assembled micelles of coil–rod–coil triblock copolymers serve as better ratiometric fluorescent F–ion sensors possessing visual detection capability, as compared to that of molecularly dissolved chains. [ABSTRACT FROM AUTHOR]

We report on a robust approach to the size-selective and template-free synthesis of asymmetrically functionalized ultrasmall (<4 nm) gold nanoparticles (AuNPs) stably anchored with a single amphiphilic triblock copolymer chain per NP. Directed NP self-assembly in aqueous solution can be facilely accomplished to afford organic/inorganic hybrid micelles, vesicles, rods, and large compound micelles by taking advantage of the rich microphase separation behavior of the as-synthesized AuNP hybrid amphiphilic triblock copolymers, PEO-AuNP-PS, which act as the polymer-metal-polymer analogue of conventional amphiphilic triblock copolymers. Factors affecting the size-selective fabrication and self-assembly characteristics and the time-dependent morphological evolution of NP assemblies were thoroughly explored. [ABSTRACT FROM AUTHOR]

Solution self-assembly of block copolymers (BCPs) typically generates spheres, rods, and vesicles. The reproducible bottom-up fabrication of stable planar nanostructures remains elusive due to their tendency to bend into closed bilayers. This morphological vacancy renders the study of shape effects on BCP nanocarrier-cell interactions incomplete. Furthermore, the fabrication of single BCP assemblies with built-in drug delivery functions and geometry-optimized performance remains a major challenge. We demonstrate that PEG-b-PCPTM polyprodrug amphiphiles, where PEG is poly(ethylene glycol) and PCPTM is polymerized block of reduction-cleavable camptothecin (CPT) prodrug monomer, with >50 wt % CPT loading content can self-assemble into four types of uniform nanostructures including spheres, large compound vesicles, smooth disks, and unprecedented staggered lamellae with spiked periphery. Staggered lamellae outperform the other three nanostructure types, exhibiting extended blood circulation duration, the fastest cellular uptake, and unique internalization pathways. We also explore shape-modulated CPT release kinetics, nanostructure degradation, and in vitro cytotoxicities. The controlled hierarchical organization of polyprodrug amphiphiles and shape-tunable biological performance opens up new horizons for exploring next-generation BCP-based drug delivery systems with improved efficacy. [ABSTRACT FROM AUTHOR]