Development of Gallic Acid-Modified Hydrogels Using Interpenetrating Chitosan Network and Evaluation of Their Antioxidant Activity

In this work, antioxidant hydrogels were prepared by the construction of an interpenetrating chitosan network and functionalization with gallic acid. The poly(2-hydroxyethyl methacrylate) p(HEMA)-based hydrogels were first synthesized and subsequently surface-modified with an interpenetrating polymer network (IPN) structure prepared with methacrylamide chitosan via free radical polymerization. The resulting chitosan-IPN hydrogels were surface-functionalized with gallic acid through an amide coupling reaction, which afforded the antioxidant hydrogels. Notably, gallic-acid-modified hydrogels based on a longer chitosan backbone exhibited superior antioxidant activity than their counterpart with a shorter chitosan moiety; this correlated to the amount of gallic acid attached to the chitosan backbone. Moreover, the surface contact angles of the chitosan-modified hydrogels decreased, indicating that surface functionalization of the hydrogels with chitosan-IPN increased the wettability because of the presence of the hydrophilic chitosan network chain. Our study indicates that chitosan-IPN hydrogels may facilitate the development of applications in biomedical devices and ophthalmic materials

Development of Poly(2-Methacryloyloxyethyl Phosphorylcholine)-Functionalized Hydrogels for Reducing Protein and Bacterial Adsorption

A series of hydrogels with intrinsic antifouling properties was prepared via surface-functionalization of poly(2-hydroxyethyl methacrylate) [p(HEMA)]-based hydrogels with the biomembrane-mimicking zwitterionic polymer, poly(2-methacryloyloxyethyl phosphorylcholine) [p(MPC)]. The p(MPC)-modified hydrogels have enhanced surface wettability, high water content retention (61.0%–68.3%), and good transmittance (>90%). Notably, the presence of zwitterionic MPC moieties at the hydrogel surfaces lowered the adsorption of proteins such as lysozyme and bovine serum albumin (BSA) by 73%–74% and 59%–66%, respectively, and reduced bacterial adsorption by approximately 10%–73% relative to the unmodified control. The anti-biofouling properties of the p(MPC)-functionalized hydrogels are largely attributed to the dense hydration layer formed at the hydrogel surfaces by the zwitterionic moieties. Overall, the results demonstrate that biocompatible and antifouling hydrogels based on p(HEMA)-p(MPC) structures have promising potential for application in biomedical materials

Aggregation-Induced Emission of Tetraphenylethene-Conjugated Phenanthrene Derivatives and Their Bio-Imaging Applications

In this study, a series of rationally designed emissive phenanthrene derivatives were synthesized and their aggregation-induced emission (AIE) properties in tetrahydrofuran (THF)/water mixtures were investigated. Two tetraphenylethene (TPE) segments were conjugated to both ends of the phenanthrene core at the para-positions and meta-positions, resulting in pTPEP and mTPEP derivatives, respectively. While the TPE-conjugated phenanthrene derivatives did not show any emission when dissolved in pure THF, they showed strong sky-blue emissions in water-THF mixtures, which is attributed to the restriction of intramolecular motions of TPE segments by aggregation. Furthermore, silica nanoparticles loaded with these AIE-active compounds were prepared and proved to be promising intracellular imaging agents

Detecting mercury ions in water using a low-cost colorimetric sensor derived from immobilized silver nanoparticles on a paper substrate

The exceptional and specific reactivity of mercury ions (Hg2+) toward plasmonic silver nanoparticles (AgNPs) in aqueous media has motivated the need to develop innovative, low-cost, portable, and robust sensors to help address the detrimental effects of heavy metal contamination particularly in rural communities. In this paper, we present the plasmonic and colorimetric sensing of Hg2+ using a paper-based sensing material derived from thiamine-functionalized (ThAgNPs) that were immobilized on a commercial filter paper. Plasmonic AgNPs with a surface plasmon resonance peak at 420 nm and a size of about 21.3 nm were synthesized by a chemical reduction technique. Fourier transform infrared spectroscopy revealed the characteristic functional groups of thiamine in the spectra of AgNPs, thereby confirming the functionalization of AgNPs. The successful integration of ThAgNPs onto the Whatman filter paper (WFP) matrix was confirmed by the UV–vis and SEM-EDX results. An evident color change from yellowish to white was manifested by the fabricated WFP-ThAgNP sensor in the presence of Hg2+ with an appreciable detection of up to 0.5 µM using the naked eye. The colorimetric response of the sensor was also found to be selective towards Hg2+ after testing with different metal ions. Moreover, the response was consistent for tap, and creek water samples spiked with Hg2+. The results of this work provide a promising baseline technology for the development of an affordable, fast, portable, and reliable sensor that can be used for on-site detection and monitoring of Hg2+ levels in the water