Efficient Synthesis of Folate-Conjugated Hollow Polymeric Capsules for Accurate Drug Delivery to Cancer Cells.

This study presents an efficient and systematic approach to synthesize bioapplicable porous hollow polymeric capsules (HPCs). The hydroxyl-functionalized nanoporous polymers with hollow capsular shapes could be generated via the moderate Friedel-Crafts reaction without using any hard or soft template. The numerous primitive hydroxyl groups on these HPCs were further converted to carboxyl groups. Owing to the abundance of highly branched carboxyl groups on the surface of the HPCs, biomolecules [such as folic acid (FA)] could be covalently decorated on these organic capsules (FA-HPCs) for drug delivery applications. The intrinsic hollow porosities and specific targeting agent offered a maximum drug encapsulation efficiency of up to 86% and drug release of up to 50% in 30 h in an acidic environment. The in vitro studies against cancer cells demonstrated that FA-HPCs exhibited a more efficient cellular uptake and intracellular doxorubicin release than bare HPCs. This efficient approach to fabricate carbonyl-functionalized hollow organic capsules may open avenues for a new type of morphological-controlled nanoporous polymers for various potential bioengineering applications.

CaO-Nanoparticle-Enriched Polydopamine-Coated Hyper-Crosslinked Polymers as Heterogeneous Catalysts for the Transesterification of Vegetable Oils.

Biodiesel is an alternative fuel produced by the transesterification of vegetable oils in the presence of homogeneous or heterogeneous catalysts. Herein, we report the transesterification of vegetable oils using CaO nanoparticles supported on a polydopamine-coated hyper-crosslinked polymer, CaO@PDA-HCP as a heterogeneous catalyst. The effect of CaO-nanoparticle concentration (5-20 wt%) on catalysis performance was investigated, and the PDA-HCP surface was examined by X-ray diffraction, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, and energy dispersive X-ray spectroscopy. Basicity was shown to greatly influence the methyl ester content, and the best catalyst (15 wt% CaO) was demonstrated to be reusable without any loss of activity.

Porous organic polymers for drug delivery: hierarchical pore structures, variable morphologies, and biological properties.

Porous organic polymers have received considerable attention in recent years because of their applicability as biomaterials. In particular, their hierarchical pore structures, variable morphologies, and tunable biological properties make them suitable as drug-delivery systems. In this review, the synthetic and post forming/control methods including templated methods, template-free methods, mechanical methods, electrospun methods, and 3D printing methods for controlling the hierarchical structures and morphologies of porous organic polymers are discussed, and the different methods affecting their specific surface areas, hierarchical structures, and unique morphologies are highlighted in detail. In addition, we discuss their applications in drug encapsulation and the development of stimuli (pH, heat, light, and dual-stimuli)-responsive materials, focusing on their use for targeted drug release and as therapeutic agents. Finally, we present an outlook concerning the research directions and applications of porous polymer-based drug delivery systems.

Nitrogen-Doped Reduced Graphene Oxide Supported Pd4.7Ru Nanoparticles Electrocatalyst for Oxygen Reduction Reaction.

It is imperative to design an inexpensive, active, and durable electrocatalyst in oxygen reduction reaction (ORR) to replace carbon black supported Pt (Pt/CB). In this work, we synthesized Pd4.7Ru nanoparticles on nitrogen-doped reduced graphene oxide (Pd4.7Ru NPs/NrGO) by a facile microwave-assisted method. Nitrogen atoms were introduced into the graphene by thermal reduction with NH3 gas and several nitrogen atoms, such as pyrrolic, graphitic, and pyridinic N, found by X-ray photoelectron spectroscopy. Pyridinic nitrogen atoms acted as efficient particle anchoring sites, making strong bonding with Pd4.7Ru NPs. Additionally, carbon atoms bonding with pyridinic N facilitated the adsorption of O2 as Lewis bases. The uniformly distributed ~2.4 nm of Pd4.7Ru NPs on the NrGO was confirmed by transmission electron microscopy. The optimal composition between Pd and Ru is 4.7:1, reaching -6.33 mA/cm2 at 0.3 VRHE for the best ORR activity among all measured catalysts. Furthermore, accelerated degradation test by electrochemical measurements proved its high durability, maintaining its initial current density up to 98.3% at 0.3 VRHE and 93.7% at 0.75 VRHE, whereas other catalysts remained below 90% at all potentials. These outcomes are considered that the doped nitrogen atoms bond with the NPs stably, and their electron-rich states facilitate the interaction with the reactants on the surface. In conclusion, the catalyst can be applied to the fuel cell system, overcoming the high cost, activity, and durability issues.

Guided Assembly of Well-Defined Hierarchical Nanoporous Polymers by Lewis Acid-Base Interactions.

Three-dimensional hierarchical nanoporous polymers and carbon nanomaterials with well-defined superstructures are of great interest for various intelligent applications, whereas a facile and versatile approach to access those materials with a high surface area, stable well-defined morphology, and ordered pores still remains a significant challenge. Herein, we report a self-regulated Lewis acid-base interaction-mediated assembly strategy for the in situ synthesis of morphology-engineered hyper-cross-linked porous polymers and carbon materials. A series of functionalized aromatic compounds (FAC) is subjected to self-cross-linking via classic Friedel-Crafts chemistry to achieve stable porous polymers with a high surface area. Varying the monomer/catalyst combination had a dramatic effect on the acid-base interaction, facilitating the tailoring of the self-assembled morphologies from nanotubes to hollow nanospheres, and even nanosheets. A mechanistic study showed that the byproducts generated during cross-linking orchestrate the interactions between the catalyst (acid) and FAC (base) and simultaneously drive the self-assembly to yield specific morphologies. Based on the rigid hollow polymer framework and intrinsic hydroxyl functionality, the hyper-cross-linked hollow nanospheres were easily transformed to an acid-functionalized catalyst for efficient biodiesel production. Moreover, high-quality porous carbonaceous nanocounterparts such as carbon nanotubes, hollow carbon nanospheres, and carbon nanosheets could also be produced by direct pyrolysis of the corresponding polymer precursors. These findings may provide guidance for the facile design of morphology-controlled functionalized polymers and carbon nanomaterials for various applications.

Functional Hyper-Crosslinked Polypyrene for Reductive Decolorization of Industrial Dyes and Effective Mercury Removal from Aqueous Media.

A rigid and valuable hyper-crosslinked polymer (HCP) has been synthesized from the polycyclic aromatic hydrocarbon pyrene: hyper-crosslinked polypyrene (HCPPy). HCPPy was prepared through a simple one-step Friedel-Crafts alkylation reaction that involves ZnBr2 -catalyzed crosslinking in the presence of an external crosslinker, bromomethyl methyl ether (BME). Interestingly, the unreacted bromomethyl groups (-CH2 Br) on the surface of HCPPy could be quantified, which later aided in modification as per our requirement. We aimed at modifying with disulfide-containing cystamine dihydrochloride (Cys-HCPPy). Cys-HCPPy exhibited an extended π-conjugated system with uniform (∼1 µm diameter) morphology and high porosity (specific surface area: 445 m2 g-1 ). As a fundamental application, the Cys-HCPPy composite was used as a sorbent to remove Hg2+ ions from aqueous media. Thus, at pH 6, the adsorption capacity for mercury ions reached 1124.82 mg g-1 after 24 h. Furthermore, the immobilization of Ag nanoparticles on the surface of Cys-HCPPy (Ag@Cys-HCPPy) enhanced the catalytic properties, which allowed for the reductive decolorization of industrial dyes such as methylene blue, methyl orange, and Congo Red in the presence of NaBH4 as a reducing agent.

Poly(glycerol sebacate)-Based Polyester-Polyether Copolymers and Their Semi-Interpenetrated Networks with Thermoplastic Poly(ester-ether) Elastomers: Preparation and Properties.

Poly(glycerol sebacate) (PGS), produced from renewable monomers such as sebacic acid and glycerol, has been explored extensively for various biomedical applications. However, relatively less attention has been paid to explore PGS as sustainable materials in applications such as elastomers and rigid plastics, primarily because of serious deficiencies in physical properties of PGS. Here, we present two new approaches for enhancing the properties of PGS; (i) synthesizing block copolymers of PGS with poly(tetramethylene oxide)glycol (PTMO) and (ii) preparing a blend of PGS-b-PTMO with a poly(ester-ether) thermoplastic elastomer. The consequence of molar ratio (hard and soft segments) and M n of soft segment on tensile properties of the material was investigated. The PGS-b-PTMO with 25:75 mole ratios of hard and soft segments and having a medium M n soft segment (5350 g mol-1) exhibits an appreciable increase in percentage of elongation that is from 32% for PGS to 737%. Blends of PGS-b-PTMO and a thermoplastic polyester elastomer, Hytrel 3078, form a semi-interpenetrated polymer network, which exhibits increased tensile strength to 2.11 MPa and percentage of elongation to 2574. An elongation of such magnitude is unprecedented in the literature for predominantly aliphatic polyesters and demonstrates that the simple polyester can be tailored for superior performance.

Hyper-Cross-Linked Polypyrene Spheres Functionalized with 3-Aminophenylboronic Acid for the Electrochemical Detection of Diols.

A sensor for the determination of diols using 3-aminophenylboronic acid (APBA)-functionalized hyper-cross-linked polypyrene (PPy) (APBA@PPy) is presented. The uniform (∼1 µm in diameter) and highly porous (628 m2 g-1 in specific surface area) PPy spheres are fabricated via a one-pot protocol that consists of ZnBr2-catalyzed alkylation of pyrene, a subsequent cross-linking reaction, and concomitant self-assembly. The PPy spheres formed within a few minutes at mild conditions are featured by an excellent structural integrity and inertness to organic solvents. Thus, the APBA@PPy composites (∼1 µm in diameter; 458 m2 g-1 in specific surface area) are prepared simply by substituting unreacted bromomethyl groups on the surface of PPy spheres for APBA. The APBA@PPy composites are successfully applied for the electrochemical sensing of d-glucose and dopamine. A dye displacement assay is also performed using alizarin red dye conjugated to boronic acid in glucose buffer solution.