Qun-Dong Shen

Light-Activated Hypoxia-Responsive Nanocarriers for Enhanced Anticancer Therapy.

A light-activated hypoxia-responsive conjugated polymer-based nanocarrier is developed for efficiently producing singlet oxygen ((1) O2 ) and inducing hypoxia to promote release of its cargoes in tumor cells, leading to enhanced antitumor efficacy. This dual-responsive nanocarrier provides an innovative design guideline for enhancing traditional photodynamic therapeutic efficacy integrated with a controlled drug-release modality.

Conjugated Polymer Nanoparticles for Fluorescence Imaging and Sensing of Neurotransmitter Dopamine in Living Cells and the Brains of Zebrafish Larvae

Nanoscale materials are now attracting a great deal of attention for biomedical applications. Conjugated polymer nanoparticles have remarkable photophysical properties that make them highly advantageous for biological fluorescence imaging. We report on conjugated polymer nanoparticles with phenylboronic acid tags on the surface for fluorescence detection of neurotransmitter dopamine in both living PC12 cells and brain of zebrafish larvae. The selective enrichment of dopamine and fluorescence signal amplification characteristics of the nanoparticles show rapid and high-sensitive probing such neurotransmitter with the detection limit of 38.8 nM, and minimum interference from other endogenous molecules. It demonstrates the potential of nanomaterials as a multifunctional nanoplatform for targeting, diagnosis, and therapy of dopamine-relative disease.

Layer-by-Layer Assembly of Conjugated Polyelectrolytes on Magnetic Nanoparticle Surfaces

Composite nanoparticles with magnetic core and fluorescent shell were facilely prepared by the layer-by-layer deposition of conjugated polyelectrolytes over the negatively charged nanoparticles (NPs) of superparamagnetic iron oxide. The alternate assembly of cationic and anionic fluorescent polyelectrolytes leads to reversal in the sign of zeta-potentials. The even numbers of adsorption layer corresponding to the anionic polyelectrolyte (PFS) have negative values (-13 to -24 mV), whereas odd numbers of coating relative to the cationic polyelectrolyte (PFN) have positive values (26 to 28 mV). The composite nanoparticles can respond to both external magnetic field and ultraviolet light excitation. Forster resonance energy transfer (FRET) between oppositely charged polyelectrolytes (PFN and ThPFS) layers was also found, indicating dense packing of the polymer coatings. The fluorescence of the positively charged nanoparticles (NPs/PFN) can be quenched with very high efficiency by a small molecule anionic quencher [Fe(CN)6(4-)], while the same quencher has far less effect on the fluorescence of the negatively charged nanoparticles (NPs/PFN/PFS).

Engineered Nanoplatelets for Enhanced Treatment of Multiple Myeloma and Thrombus

A platelet-membrane-coated biomimetic nanocarrier, which can sequentially target the bone microenvironment and myeloma cells to enhance the drug availability at the myeloma site and decrease off-target effects, is developed for inhibiting multiple myeloma growth and simultaneously eradicating thrombus complication.

Greatly Enhanced Energy Density and Patterned Films Induced by Photo Cross-Linking of Poly(vinylidene fluoride-chlorotrifluoroethylene)

Greatly enhanced energy density in poly(vinylidene fluoride-chlorotrifluoroethylene) [P(VDF-CTFE)] is realized through interface effects induced by a photo cross-linking method. Being different from nanocomposites with lowered dielectric strength, the cross-linked P(VDF-CTFE)s possess a high breakdown field as well as remarkably elevated polarization, both of which contribute to the enhanced energy density as high as 22.5 J · cm(-3). Moreover, patterned thin films with various shapes and sizes are fabricated by photolithography, which sheds new light on the integration of PVDF-based electroactive polymers into organic microelectronic devices such as flexible pyroelectric/piezoelectric sensor arrays or non-volatile ferroelectric memory devices.

Anaerobe‐Inspired Anticancer Nanovesicles

Anaerobic bacteria, such as Clostridium and Salmonella, can selectively invade and colonize in tumor hypoxic regions (THRs) and deliver therapeutic products to destroy cancer cells. Herein, we present an anaerobe nanovesicle mimic that can not only be activated in THRs but also induce hypoxia in tumors by themselves. Moreover, inspired by the oxygen metabolism of anaerobes, we construct a light-induced hypoxia-responsive modality to promote dissociation of vehicles and activation of bioreductive prodrugs simultaneously. In vitro and in vivo experiments indicate that this anaerobe-inspired nanovesicle can efficiently induce apoptotic cell death and significantly inhibit tumor growth. Our work provides a new strategy for engineering stimuli-responsive drug delivery systems in a bioinspired and synergistic fashion.

Enhanced electrocaloric effect in poly(vinylidene fluoride-trifluoroethylene)-based terpolymer/copolymer blends

The electrocaloric effect in the blends of poly(vinylidene fluoride–trifluoroethylene–chlorofluoroethylene) (P(VDF-TrFE-CFE)) with small amount of poly(vinylidene fluoride–trifluoroethylene) (P(VDF-TrFE)) is investigated. It was found that small amount of P(VDF-TrFE) (∼10 wt. %) can cause a more than 10% increase in the crystallinity in the blends. Although the two polymers form separate crystalline phases, the interfacial couplings to the random defects in the terpolymer convert the normal ferroelectric P(VDF-TrFE) into a relaxor ferroelectric. As a result, the blends with 10 wt. % of P(VDF-TrFE) exhibit a 30% increase in the adiabatic temperature change over the entire experimental temperature range (20 °C–60 °C).

Self-folded redox/acid dual-responsive nanocarriers for anticancer drug delivery.

Self-folded redox/acid dual-responsive nanocarriers (RAD-NCs) are developed for physiologically triggered delivery of anticancer drugs. The evidenced redox/acid responsiveness, facile decoration of ligands, and active tumor-targeting capability of RAD-NCs suggest their potential as a promising formulation for tumor-targeted chemotherapy.

Nonvolatile data storage using mechanical force-induced polarization switching in ferroelectric polymer

Ferroelectric polymers offer the promise of low-cost and flexible electronic products. They are attractive for information storage due to their spontaneous polarization which is usually switched by electric field. Here, we demonstrate that electrical signals can be readily written on ultra-thin ferroelectric polymer films by strain gradient-induced polarization switching (flexoelectric effect). A force with magnitude as small as 64nN is enough to induce highly localized (40 nm feature size) change in the polarization states. The methodology is capable of realizing nonvolatile memory devices with miniaturized cell size and storage density of tens to hundreds Gbit per square inch.

A type of poly(vinylidene fluoride-trifluoroethylene) copolymer exhibiting ferroelectric relaxor behavior at high temperature (∼100°C)

We report a class of poly(vinylidene fluoride-trifluoroethylene) [P(VDF-TrFE)] copolymers synthesized via reductive dechlorination from P(VDF-CTFE) [termed as the reduced P(VDF-TrFE) copolymer], which exhibit ferroelectric relaxor behavior at high temperature (∼100°C). It was found that the reduced P(VDF-TrFE) 66∕34mol% copolymer has very high content of head-to-head and tail-to-tail defects, which may act as random defects, leading to the observed ferroelectric relaxor at high temperature. Furthermore, the reduced copolymer also exhibits a high melting point (∼200°C), which also makes it attractive for high-temperature dielectric applications.