Long-chain surface-modified red-emitting carbon dots as fluorescent additives for 3D printing vat-photopolymerization.

Carbon dots have recently attracted tremendous scientific attention thanks to their enhanced luminescence properties, photostability and low toxicity. In particular, red-emitting carbon dots (RCDs) are assuming increasing importance in biomedical applications, such as bio-imaging and phototherapy. At the same time, the possibility to create functional and complex objects by means of vat-photopolymerization-based three-dimensional (3D) printing techniques is continuously growing.

Conformation and topology of cyclical star polymers.

We study the conformation and topological properties of cyclical star polymers with f ring arms, each made of n beads. We find that the conformational properties of unlinked cyclical star polymers are compatible with those of linear star polymers with 2f arms made of n/2 beads each. This compatibility vanishes when the topology of the star, measured as the degree of linking between arms, changes.

Gold nanorod-assisted theranostic solution for nonvisible residual disease in bladder cancer.

Residual nonvisible bladder cancer after proper treatment caused by technological and therapeutic limitations is responsible for tumor relapse and progression. This study aimed to demonstrate the feasibility of a solution for simultaneous detection and treatment of bladder cancer lesions smaller than one millimeter. The α5β1 integrin was identified as a specific marker in 81% of human high-grade nonmuscle invasive bladder cancers and used as a target for the delivery of targeted gold nanorods (GNRs).

Universal Time and Length Scales of Polar Active Polymer Melts.

We present an in-depth multiscale analysis of the conformations and dynamics of polar active polymers, comparing very dilute and very dense conditions. We unveil characteristic length and time scales, common to both dilute and dense systems, that recapitulate the conformational and dynamical properties of these active polymers upon varying both the polymer size and the strength of the activity. Specifically, we find that a correlation (or ) length characterizes the polymer conformations and the monomer dynamics.