Living Self-Assembly of Monodisperse Micron-Sized Polymer Vesicles.

Artificial vesicles are recognized as powerful platforms for a large body of research across the disciplines of chemistry, physics and biology. Despite the great progress, control of the size distribution to make uniform vesicles remains fundamentally difficult due to the highly uncontrollable growth kinetics, especially for micron-sized vesicles. Here we report a template-free living self-assembly method to prepare monodisperse vesicles around 1 µm from an alternating copolymer. The polymer forms nanodisks (ca. 9 nm) in N,N-dimethylformamide (DMF), acting as seeds for subsequent growth. By adding water, the nanodisks gradually grow into larger circular bilayer nanosheets, which bend to crowns and continue to grow into uniform micron-sized vesicles. The first-order growth kinetics as well as the small size polydispersity index (<0.1) suggests the living self-assembly characteristics. This work paves a new way in both living self-assembly and monodisperse polymer vesicles.

Mussel-Inspired Alternating Copolymer as a High-Performance Adhesive Material Both at Dry and Under-Seawater Conditions.

Marine mussels have the ability to cling to various surfaces at wet or underwater conditions, which inspires the research of catechol-functionalized polymers (CFPs) to develop high-performance adhesive materials. However, these polymeric adhesives generally face the problems of complex synthetic route, and it is still high challenging to prepare CFPs with excellent adhesive performance both at dry and underwater conditions. Herein, a mussel-inspired alternating copolymer, poly(dopamine-alt-2,2-bis(4-glycidyloxyphenyl)propane) (P(DA-a-BGOP)), is synthesized in one step by using commercially available monomers through epoxy-amino click chemistry. The incorporation of polar groups and rigid bisphenol A structures into the polymer backbone enhances the cohesion energy of polymer matrix. The alternating polymer structure endows the polymers with high catechol content and controlled polymer sequence. As a result, P(DA-a-BGOP) exhibits a strong bonding strength as high as 16.39 ± 2.13 MPa on stainless steel substrates after a hot pressing procedure and displays a bonding strength of 1.05 ± 0.05 MPa on glass substrates at an under-seawater condition, which surpasses most commercial adhesives.

Laboratory assessment of a multi-target assay for the rapid detection of viruses causing vesicular diseases.

BACKGROUND: The recent mpox outbreak has highlighted the need to rapidly diagnose the causative agents of viral vesicular disease to inform treatment and control measures. Common causes of vesicular disease include Monkeypox virus (MPXV), clades I and II, Herpes simplex viruses Type 1 and Type 2 (HSV-1, HSV-2), human herpes virus 6 (HHV-6), Varicella-zoster virus (VZV) and Enteroviruses (EVs). Here, we assessed a syndromic viral vesicular panel for rapid and simultaneous detection of these 7 targets in a single cartridge. OBJECTIVE: The aim of this study was to evaluate the QIAStat-Dx ® viral vesicular (VV) panel and compare with laboratory developed tests (LDTs). Limit of detection, inter-run variability, cross-reactivity and specificity were assessed. Positive and negative percent agreement, and correlation between assays was determined using 124 clinical samples from multiple anatomical sites. RESULTS: The overall concordance between the QIAstat and LDTs was 96%. Positive percent agreement was 82% for HHV-6, 89% for HSV-1 and 100% for MPXV, HSV-2, EV and VZV. Negative percent agreement was 100% for all targets assessed. There was no cross-reactivity with Vaccinia, Orf, Molluscum contagiosum viruses, and a pooled respiratory panel. CONCLUSION: The QIAstat VV multi-target syndromic panel combine ease of use, rapid turnaround, good sensitivity and specificity for enhanced diagnosis, clinical care and public health responses.

Regioisomer-Directed Self-Assembly of Alternating Copolymers for Highly Enhanced Photocatalytic H2 Evolution.

Porphyrin-based photocatalytic materials have received great attention, and the effect of the substituents, central ions, and aggregated structure on the catalysis performance has been studied up to now. Herein, we report the effect of porphyrin isomerism on their aggregated structures as well as the photocatalytic activity. Two trans- and cis-porphyrin-based alternating copolymers with the same compositions (P1 and P2) are successfully synthesized. It is found that P1 self-assembles into propeller-like nanoparticles and P2 into multilayer hollow nanospheres. Furthermore, the hydrogen production rate of P1 (5533 µmol g-1 h-1) is 30 times higher than that of P2 (173 µmol g-1 h-1). Mechanism studies reveal that the high photocatalytic properties of P1 originate from the more ordered arrangement of porphyrins than P2, which facilitates the mobility and separation of photoinduced carriers. We believe the covalent and noncovalent polymer self-assembly process as well as the isomerism effect as disclosed here will shed new light on the design of high performance photocatalysts.

Revisiting Acetoacetyl Chemistry to Build Malleable Cross-Linked Polymer Networks via Transamidation.

Covalent adaptable networks (CANs) have various potential applications for their dynamic features benefiting from the existence of dynamic covalent bonds (DCBs). Here we exploit acetoacetyl chemistry to design CANs in which acetoacetyl formed amides (AFAs) act as a type of DCBs. We first illuminate that the transamidation of AFAs is ascribed to a "proton-switch" mechanism via model study and DFT calculations. When such AFA linkages are incorporated into cross-linked polymer networks, the malleability and recyclability are demonstrated. After recycling the polymer networks for three times, there are no significant mechanical changes or degradations observed. The study reveals that the transamidation is an economic and efficient exchange reaction in the preparation of CANs.

Versatile Approach to Building Dynamic Covalent Polymer Networks by Stimulating the Dormant Groups.

Despite many efforts, there is no versatile way to realize reversible cross-linking for most polymers. Inspired by the abstraction of hydrogen and the iniferter polymerization of benzophenone (BP), we report a versatile approach for building dynamic covalent networks for polymers containing C-H bonds. Under ultraviolet irradiation, BP can effectively abstract the hydrogen from polymers to form dormant diarylsemipinacol (DASP) groups on the polymer chains. Then, the dormant DASP-based linkages can be homolytically cleaved upon heating, after which they generate carbon-centered aliphatic radicals and DASP-based radicals. Therefore, the cross-linked polymer network can rearrange its topology through the dissociation and association of DASP-based linkages, which endow polymer networks with remodeling and self-healing abilities. Given that most commercially available polymers contain aliphatic C-H bonds, this provides a general method for forming thermal reversible cross-linked networks.