Pathway-dependent Shape Transformation of Polymeric Vesicles under UV Light and the Assembly of UV-irradiated Polymer.

Shape transformation of polymer particles is generally a nonequilibrium dynamics process. Controlling the shape transformation of polymers is increasingly attractive and challenging for scientists due to their extensive use in drug delivery and cancer therapy. Herein, we investigated the UV-triggered shape transformation pathway of polymeric vesicles assembled from Polystyrene--poly(4-vinylpyridine) and 4-hydroxyazobenzene (PS--P4VP(Azo-OH)) and the direct assembly pathway of UV-irradiated PS--P4VP(Azo-OH) homogeneous solution.

Well-Ordered Nanoparticles/Block Copolymer Nanosheets with a Controllable Location of Nanoparticles.

Precisely controlling the spatial distributions and arrangements of metal nanoparticles (NPs) into block copolymers is of great importance for fabricating novel nanomaterials with the desired optical and electronic properties. Herein, we develop a simple yet versatile strategy to prepare organic/inorganic nanosheets formed by the coassembly of polystyrene--poly(4-vinylpyridine) (PS--P4VP) and PS tethered gold nanoparticles (AuNPs@PS) within emulsion droplets. The arrangement of the AuNPs@PS building blocks within the block copolymers (BCP)/AuNPs nanosheets can be adjusted by tuning the effective size ratio (λ), which can be controlled by the core diameter of the AuNPs and the molecular weight of the PS.

PolyNC: a natural and chemical language model for the prediction of unified polymer properties.

Language models exhibit a profound aptitude for addressing multimodal and multidomain challenges, a competency that eludes the majority of off-the-shelf machine learning models. Consequently, language models hold great potential for comprehending the intricate interplay between material compositions and diverse properties, thereby accelerating material design, particularly in the realm of polymers. While past limitations in polymer data hindered the use of data-intensive language models, the growing availability of standardized polymer data and effective data augmentation techniques now opens doors to previously uncharted territories.

Storage Stability of 6FDA-DMB Polyamic Acid Solution Detected by Gel Permeation Chromatography Coupled with Multiple Detectors.

Polyamic acid (PAA) is the precursor of polyimide (PI), and its solution's properties have a direct influence on the final performances of PI resins, films, or fibers. The viscosity loss of a PAA solution over time is notorious. A stability evaluation and revelation of the degradation mechanism of PAA in a solution based on variations of molecular parameters other than viscosity with storage time is necessary.

scAnnotate: an automated cell-type annotation tool for single-cell RNA-sequencing data.

Motivation: Single-cell RNA-sequencing (scRNA-seq) technology enables researchers to investigate a genome at the cellular level with unprecedented resolution. An organism consists of a heterogeneous collection of cell types, each of which plays a distinct role in various biological processes. Hence, the first step of scRNA-seq data analysis is often to distinguish cell types so they can be investigated separately.

Effect of Annealing Process and Molecular Weight on the Polymorphic Transformation from Form II to Form I of Poly(1-butene).

Poly(1-butene) (PB-1) resin has excellent mechanical properties, outstanding creep resistance, environmental stress crack resistance and other excellent properties. However, PB-1 resin experiences a crystal transformation for a period, which seriously affects the production efficiency and directly restricts its large-scale commercial production and application. The factors affecting the crystal transformation of PB-1 are mainly divided into external and internal factors.

A Facile Approach to Produce Star Polymers Based on Coordination Polymerization.

Many efforts have been devoted to preparing star polymers. Research into coordination polymerization, the most powerful stereoselective process to endow polymers with superb properties, lags far behind those achieved by radical polymerization and ionic polymerization. Herein, we propose a facile strategy to prepare star polymers with regular arms based on coordination polymerization via an insertion reaction between the carbon-heteroatom unsaturated bond and the metal-alkyl species.

Direct Synthesis of Functional Thermoplastic Elastomer with Excellent Mechanical Properties by Scandium-Catalyzed Copolymerization of Ethylene and Fluorostyrenes.

Herein, we report copolymerizations of ethylene (E) and ortho-/meta-/para-fluorostyrenes (S =oFS/mFS/pFS) by using quinolyl methylene fluorenyl scandium complex (Flu-CH -Qu)Sc(CH SiMe ) . The copolymerizations proceed in a controlled fashion to afford copolymers composed of "soft" ethylene-fluorostyurene (E-S ) random segments (T =-22.2-5.

Conformation and persistence length of chitosan in aqueous solutions of different ionic strengths via asymmetric flow field-flow fractionation.

Conformation of chitosan in acidic aqueous solutions is strongly influenced by ionic strength, but the conventional employed size exclusion chromatography is limited to high ionic strength. Here we show that conformation of chitosan in acetate buffer down to millimolar ionic strength can be studied via asymmetric flow field-flow fractionation (AF4), where the separation is governed by the diffusion properties of the chitosan molecules and assisted by the electrostatic repulsion of the polyelectrolyte from the channel membrane. The size of chitosan decreases with ionic strength due to increasing screening of the polyelectrolyte effect.

Mesenchymal stem cell exosomes reverse acute lung injury through Nrf-2/ARE and NF-B signaling pathways.

Acute lung injury (ALI) is associated with histopathological diffuse alveolar damage. The potential role of mesenchymal stem cells (MSCs) in the treatment of various clinical disorders have been widely documented, such as those for ALI. Recent evidence has demonstrated that exosomes from endothelial progenitor cells can improve outcomes of the lipopolysaccharide (LPS)-induced ALI.

Chromatographic mode transition from size exclusion to slalom chromatography as observed for chitosan.

Elution behavior of chitosan was studied using narrow-bore size exclusion chromatography (SEC) columns packed with 8 μm porous particles at different eluent flow rates. Delayed elution of the largest chitosan species from the columns was observed at high flow rates, which was attributable to strong chain deformation rather than chain degradation. In particular, a chromatographic mode transition from SEC to slalom chromatography (SC) was observed for high molar mass chitosan samples with abnormal elution behaviors, which originates from the coil-stretch transition of chitosan chains in elongational flow through the columns.

Influence of Heating Rate on the Structure and Mechanical Properties of Aromatic BPDA-PDA Polyimide Fiber.

Aromatic polyimide fibers (PI) are usually produced in two steps. The precursor fibers of polyamic acid (PAA) are fabricated first, and then the fabricated fibers are converted into PI fibers through thermal treatment. In the second step (thermal treatment), the mechanical properties of the obtained PI fibers are remarkably affected.

Electrostatic Interaction Mediates the Formation of Vesicular Structures from Coassembly of PS--PAA with Quantum Dots.

Vesicular structures of block copolymers and inorganic nanoparticles with good stability have potential applications in therapeutic drug release and bioimaging. Herein, a block copolymer of polystyrene--poly(acrylic acid) (PS--PAA) and water-soluble AgInS/ZnS core/shell quantum dots (QDs) capped with gelatin and thioglycolic acid were coassembled in tetrahydrofuran by adding water. The positively charged QDs bind to negatively charged PAA segments through electrostatic interaction.

Associative behavior of polyimide/cyclohexanone solutions.

Our previous work has demonstrated that soluble polyimide with relatively weak interaction can be transformed from neutral polymer to associative polymer by increasing molecular weight. Thus, it is necessary to find another way to vary the relatively weak interaction strength, variation of solvent quality. Herein, viscoelastic behaviors are examined for 2,2-bis(3,4-dicarboxy-phenyl) hexafluoropropane dianhydride (6FDA)-2,2'-bis(trifluoromethyl)-4,4'-diam (TFDB) polyimide (PI), with a relatively low molecular weight ( ) of 88 000 g mol, dissolved in cyclohexanone (CYC).

Adsorption of poly(vinyl alcohol) on gel permeation chromatography columns depends on the degree of hydrolysis.

Both fully (98%) and partially (88%) hydrolyzed poly(vinyl alcohol) (PVA) are characterized by aqueous gel permeation chromatography (GPC) coupled with multi-angle laser light scattering. Polymer adsorption on hydrophilic GPC columns is observed for partially hydrolyzed PVA but not for fully hydrolyzed PVA, which is driven by the hydrophobic interactions between the residual acetate groups on PVA and the stationary phase. Desorption of these partially hydrolyzed PVA chains from the packing materials is monitored by decay of the light scattering signal.

Strategy to improve the characterization of chitosan by size exclusion chromatography coupled with multi angle laser light scattering.

Here we present SEC-MALLS study for chitosan samples with weight average molar mass M between 33 and 427 kg/mol on columns packed with 8 μm porous particles. A low injection concentration on the order of 0.1-0.

Superfast and Reversible Thermoresponse of Poly( N-isopropylacrylamide) Hydrogels Grafted on Macroporous Poly(vinyl alcohol) Formaldehyde Sponges.

Poly( N-isopropylacrylamide) (PNIPAAm), a typical thermoresponsive polymer, exhibits potential application in smart materials. However, bulk PNIPAAm hydrogel monoliths undergo slow volume phase transition at least tens of minutes to hours as determined by the shape and size of polymers due to the formation of the skin layer. In this regard, novel macroporous sponges with rapid thermoresponse are prepared via grafting polymerization of N-isopropylacrylamide (NIPAAm) onto the macroporous poly(vinyl alcohol) formaldehyde (PVF) network as confirmed by attenuated total reflection-infrared (ATR IR) and H NMR spectra.

Viscoelastic behaviour and relaxation modes of one polyamic acid organogel studied by rheometers and dynamic light scattering.

A novel polyamic acid (PAA from BAPMPO-BPDA) organogel was synthesized and characterized via dynamic light scattering (DLS), a classical rheometer, and diffusion wave spectroscopy (DWS). In situ monitoring was performed using a classical rheometer to observe the formation of the PAA organogel. The rheological curves confirm the formation of the PAA gel network and the origin of hydrogen bonding from the -NH- group (donor) and P[double bond, length as m-dash]O group (acceptor).

Fabrication of Hyperbranched Block-Statistical Copolymer-Based Prodrug with Dual Sensitivities for Controlled Release.

Dendrimer with hyperbranched structure and multivalent surface is regarded as one of the most promising candidates close to the ideal drug delivery systems, but the clinical translation and scale-up production of dendrimer has been hampered significantly by the synthetic difficulties. Therefore, there is considerable scope for the development of novel hyperbranched polymer that can not only address the drawbacks of dendrimer but maintain its advantages. The reversible addition-fragmentation chain transfer self-condensing vinyl polymerization (RAFT-SCVP) technique has enabled facile preparation of segmented hyperbranched polymer (SHP) by using chain transfer monomer (CTM)-based double-head agent during the past decade.

Nanoparticle Loading Induced Morphological Transitions and Size Fractionation of Coassemblies from PS-b-PAA with Quantum Dots.

Inorganic nanoparticles play a very important role in the fabrication and regulation of desirable hybrid structures with block copolymers. In this study, polystyrene-b-poly(acrylic acid) (PS48-b-PAA67) and oleic acid-capped CdSe/CdS core/shell quantum dots (QDs) are coassembled in tetrahydrofuran (THF) through gradual water addition. QDs are incorporated into the hydrophilic PAA blocks because of the strong coordination between PAA blocks and the surface of QDs.

Preparation of hydrophilic luffa sponges and their water absorption performance.

Hydrophilic luffa sponges are prepared by grafting polymerization of acrylamide (AM) on luffa cylindrica and subsequent partial hydrolysis under alkaline conditions. Attenuated total reflection infrared spectroscopy is used to verify the composition of the grafted (luffa-g-PAM) and hydrolyzed (luffa-g-(PAM-co-PAANa)) samples. Alkalization conditions, including aqueous NaOH concentrations, alkalization temperature, and time, are studied extensively.

Molar mass fractionation in aqueous two-phase polymer solutions of dextran and poly(ethylene glycol).

Dextran and poly(ethylene glycol) (PEG) in phase separated aqueous two-phase systems (ATPSs) of these two polymers, with a broad molar mass distribution for dextran and a narrow molar mass distribution for PEG, were separated and quantified by gel permeation chromatography (GPC). Tie lines constructed by GPC method are in excellent agreement with those established by the previously reported approach based on density measurements of the phases. The fractionation of dextran during phase separation of ATPS leads to the redistribution of dextran of different chain lengths between the two phases.

pH Dependence of Adsorbed Fibrinogen Conformation and Its Effect on Platelet Adhesion.

Quartz crystal microbalance with dissipation (QCM-D) and dual polarization interferometry (DPI) were used to investigate fibrinogen (Fib) adsorption behavior on different surfaces by changing the pH value. Moreover, integrin adhesion to the adsorbed Fibs was studied using DPI. Qualitative and quantitative studies of platelet adhesion to the adsorbed Fibs were performed using scanning electron microscopy (SEM), confocal laser scanning microscope (CLSM), and released lactate dehydrogenase (LDH) assay.