Search

The detection of heavy metals, such as Hg2+ and Fe3+, is of great significance. In this work, fluorescent small-molecule BODIPY (BY-3) bearing C C group was synthesized firstly. And then, the chitosan-based polymer sensor CY-1 was synthesized through the spontaneous NH 2 /C≡C click reaction. The synthesized CY-1 can effectively bind and recognize Hg2+/Hg+ by the –C=N groups formed in the click reaction. Moreover, the macromolecular sensors CS-1 and CS-2 were synthesized by incorporating another recognition sites to CY-1. These synthesized macromolecular sensors can not only recognize Hg2+/Hg+, but also effectively recognize Fe3+/Fe2+. All of them exhibited significant quenching effect, visible to the naked eye under UV irradiation. The detection limit of CY-1 for Hg2+ was 1.51 × 10−6 mol/L, and the detection limit of CS-2 for Fe3+ was 2.30 × 10−6 mol/L. The BODIPY-chitosan sensors synthesized in this work have the functions of removing heavy metal ions besides the identifying ability. The maximum adsorption capacity of 1 g chitosan to Hg2+ was 108 mg as the best one. This article provides a new method to prepare macromolecular sensors for the detection and removal of heavy metal ions. As a useful natural polymer, chitosan's application scope was enlarged. Small-molecule fluorescent monomer BODIPY(BY-3) with C C group was first synthesized. And then, the chitosan-based polymeric sensor CY-1 was synthesized through the NH 2 /C C click reaction. The synthesized macromolecular sensor could not only recognize Hg2+/Hg+, but also effectively recognize Fe3+/Fe2+. [Display omitted] • Solubility of chitosan derived polymer in H 2 O-HAc remains despite the attachment of a large organic group. • By Click reaction, BODIPY fluophores were linked to chitosan with C N, it can recognize Hg2+ and Hg+ well. • By introducing the recognition site S, it can recognize not only Hg2+/Hg+, but also Fe3+/Fe2+. • The functionalized can adsorb and remove heavy metal ions with high efficiency. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fluorescent water-soluble polymer sensors were obtained by RAFT method. • Selective and sensitive recognition of Fe3+ and Fe2+. • Fluorophores could be incorporated as RAFT reagent and/or functional monomer. Fe3+ and Fe2+ are common metal ions in natural water environments and creatures. The development of water-soluble fluorescent sensors for detecting Fe2+/Fe3+ ions was of great significance. In this work, two kinds of boron fluoride dipyrrole (BODIPY) fluorescent small-molecules were synthesized firstly. One of the small molecules contains a thioester bond that can be used as a chain transfer agent to participate in the polymerization process, and the other contains an unsaturated C = C double bond at the meso position. Through the reversible addition-fragmentation chain transfer polymerization (RAFT) polymerization method, methacrylic acid (MAA) and methacrylamide (MAM) were used as the main monomers, and small molecular fluorescent monomers were introduced to the end of the main chain. In this way, fluorescent macromolecules were obtained. The polymers were water soluble owing to the presence of long enough hydrophilic carboxyl and amide chains. These fluorescent probes exhibit high sensitivity to Fe2+/Fe3+, good selectivity, and anti-interference of other ions. The detection limit for Fe2+ was as low as 2.3 × 10−7 M, and the detection limit for Fe3+ can reach up to 4.5 × 10−7 M. The results show that these probes can be used as good sensors to identify Fe2+ and Fe3+. Moreover, the fluorophores could be incorporated into polymer chains as the RAFT reagents and/or functional monomers. [ABSTRACT FROM AUTHOR]

[Display omitted] Over time, functionalized polysulfones have been obtained through various synthetic routes, aiming at the preparation of high-performance materials with targeted functions for specific applications. The successful use of polysulfones and chemically functionalized polysulfones in the fabrication of membranes with applicability in clinical dialyzers, separation of water/organic solvent mixtures, wastewater treatment, gas separation, fuel cells or as a support for composite membranes encourages the study of chemical modification methods of these polymers that lead to the improvement of the properties and the broadening of the applications field. This review summarizes the research progress on the development, investigation, and application of functionalized polysulfones and analyzes why some of their properties, especially surface and morphological ones, should be considered for their extensive use in industrial and environmental scope, membranes for electro-electrodialysis, separation of enantiomer mixtures, ultrafiltration and direct osmosis processes, removal of metals, anion or proton exchange membranes for fuel cells, but also in the biomedical field as hemodialysis membranes, immune response modulators, materials with antimicrobial activity. In addition, the present review highlights the challenges and recent advances achieved through various synthetic approaches that overcome the existing problems and improve the performance of these polymers in medical and industrial fields. [ABSTRACT FROM AUTHOR]

The paper reports new hydrogels based on quaternary ammonium salts of chitosan designed as biocidal products. The chitosan derivative was crosslinked with salicylaldehyde via reversible imine bonds and supramolecular self-assemble to give dynamic hydrogels which respond to environmental stimuli. The crosslinking mechanism was demonstrated by 1H NMR and FTIR spectroscopy, and X-ray diffraction and polarized light microscopy. The hydrogel nature, self-healing and thixotropy were proved by rheological investigation and visual observation, and their morphology was assessed by scanning electron microscopy. The relevant properties for application as biocidal products, such as swelling, dissolution, bioadhesiveness, antimicrobial activity and ex-vivo hemocompatibility and in vivo local toxicity and biocompatibility on experimental mice were measured and analyzed in relationship with the imination degree and the influence of each component. It was found that the hydrogels are superabsorbent, have good adhesivity to skin and various surfaces and antimicrobial activity against relevant gram-positive and gram-negative bacteria, while being hemocompatible and biocompatible. Besides, the hydrogels are easily biodegraded in soil. All these properties recommend the studied hydrogels as ecofriendly biocidal agents for living tissues and surfaces, but also open the perspectives of their use as platform for in vivo applications in tissue engineering, wound healing, or drug delivery systems. [Display omitted] [ABSTRACT FROM AUTHOR]

The purpose of the study was to develop new antimicrobial hydrogels from natural resources that may promote wound healing and prevent bacterial skin infection. The new hydrogels were synthesized by crosslinking chitosan with a vanillin isomer, 5-methoxysalicylaldehyde, by a friendly and easy method. To characterize these hydrogels, their structural and morphological properties were explored by FTIR, 1H NMR, SEM, POM, and TGA. In view of the targeted application, swelling behavior, biodegradability, antimicrobial activity and biocompatibility were investigated in vitro. Structural and morphological studies confirmed the formation of new hydrogels via the imination reaction concomitant with the supramolecular organization. The hydrogels were highly porous with the average pore diameter around 80 μm, and a swelling rate controlled by the crosslinking density and medium pH. The hydrogels showed a progressive weight loss in the presence of lysozyme up to 35%, during 21 days of testing. They proved non-cytotoxic effect on Normal Human Dermal Fibroblasts using MTS test and powerful antifungal activity against Candida Albicans , as determined by disk diffusion assay. All these properties indicate the new hydrogels as a promising option for the treatment of various skin lesions. [Display omitted] • New hydrogels based on chitosan and a vanillin isomer were synthetized via imine linkage. • The hydrogels were highly porous, thermally stable and biodegradable. • The reversible imine linkage prompted a self-healing behavior. • The hydrogels had no cytotoxic effect on normal human dermal fibroblasts. • They exhibited antifungal activity. [ABSTRACT FROM AUTHOR]

Vitamin B6 is an essential micronutrient in the mammalian diet, with role of coenzyme and synergistic effect with some antibiotics and antitumor drugs. Based on these, we hypothesized that its use for the preparation of hydrogels can yield multifunctional biomaterials suitable for in vivo applications. To this aim, chitosan was reacted with the active form of vitamin B6, pyridoxal 5-phosphate, via acid condensation, when clear hydrogels were obtained. Their investigation by structural characterization methods proved that the hydrogelation was a consequence of both covalent imine formation and physical interactions. The novel hydrogels had microporous morphology and showed shrinking effect in phosphate buffer, indicating good shape preservation and slow dissolution in in vivo environment. Their enzymatic biodegradation could be controlled by the imination degree, varying from 40 to 61% in 21 days. They demonstrated very good in vitro cytocompatibility on normal human dermal fibroblasts cells and no harmful effect on experimental mice, confirming their safely use for in vivo application. [Display omitted] [ABSTRACT FROM AUTHOR]

The paper presents the synthesis and characterization of poly(trimethylene carbonate) grafted chitosan as a new water soluble biopolymer suitable for in vivo applications. The synthesis was performed via ring-opening polymerization of 1,3-dioxan-2-one (trimethylene carbonate) (TMC) monomer, initiated by the functional groups of chitosan in the presence of toluene as solvent/swelling agent. By varying the molar ratio between the glucosamine units of chitosan and TMC, a series of chitosan derivatives with different content of poly(trimethylene carbonate) chains was synthetized. The structural characterization of the polymers was realized by FTIR and 1H NMR spectroscopy and their solubility was assessed in water and in organic solvents as well. The biocompatibility was investigated by MTS assay on Normal Human Dermal Fibroblasts, and the biodegradability was evaluated in lysozyme buffer solution. Further, the surface properties of the polymer films were analyzed by polarized optical microscopy, atomic force microscopy and water-to-air contact angle measurements. It was established that, by 5% substitution of chitosan with poly(trimethylene carbonate) chains having an average polymerization degree of 7, a water soluble polymer can be attained. Compared to the pristine chitosan, it has improved biocompatibility in solution and moderate wettability and higher biodegradability rate in solid state, pointing its suitability for in vivo applications. [ABSTRACT FROM AUTHOR]

The paper reports new chitosan-based nanofibers, designed to address the healing of burn wounds. To this aim, mesoporous chitosan fiber mats were prepared by electrospinning using poly(ethylene oxide) as sacrificial additive, followed by loading with norfloxacin and coating with an antifungal agent via dynamic imine bonds. Dynamic vapor sorption experiment proved intra-fiber mesopores around 2.7 nm, and UV–vis, FTIR, and NMR spectroscopy confirmed the norfloxacin embedding and the imination reaction. SEM, AFM and POM techniques displayed semicrystalline nanofibers with average diameter around 170 nm entangled into a non-woven mat. Their mesoporous nature favored a rapid adsorption of fluids up to 17 g/g, and a biodegradation rate fitting the wound healing rate, i.e. up to 30 % mass loss in media of pH characteristic to wound exudate and total degradation in that characteristic to normal dermis. The composite fibers released the NFX and 2FPBA in a controlled manner, and showed antimicrobial activity against gram positive, gram negative and fungal strains. They had no cytotoxic effect on normal human dermal fibroblasts, and showed biocompatibility on experimental rats. The investigation of wound healing ability on second/third-degree burn model in rats revealed wound closure and total restoration of the fully functional dermis and epidermis. [Display omitted] [ABSTRACT FROM AUTHOR]

Chitosan based nanofibers are emerging biomaterials with a plethora of applications, especially in medicine and healthcare. Herein, binary quaternized chitosan/chitosan fibers are reported for the first time. Their preparation strategy consisted in the electrospinning of ternary chitosan/quaternized chitosan/poly(ethylene oxide) solutions followed by the selective removal of poly(ethylene oxide). Their morphology and performances were systematically investigated and discussed in detail. It was found that the fibers had reversible water vapor adsorption/desorption and showed swelling degrees similar to commercial wound dressings. They presented good mechanical properties and the content of quaternized chitosan modulated their bioadhesion, mucoadhesion and biodegradation rate and conferred them strong antimicrobial activity. Tests on normal human fibroblasts confirmed their safely use in contact with tissues and the biocompatibility investigation on rats showed no harmful effect when subcutaneous implanted. All these proved the binary quaternized chitosan/chitosan fibers as bioactive materials suitable for tissue regeneration, wound healing and drug delivery systems. [Display omitted] [ABSTRACT FROM AUTHOR]

The present study reports the synthesis and characterization of 12 drug delivery systems (DDS) for the co-delivery of antifungal and antiviral agents. The systems were obtained by an in situ hydrogelation method of 6 chitosan oligomers with values of the polymerization degree between 14 and 51, with 2-formylphenylboronic acid, in the presence of tenofovir. The structural characterization by NMR and FTIR spectroscopy demonstrated the formation of imine linkages, while WXRD revealed the 3D layered architecture of the systems. SEM and POM images demonstrated the uniform distribution of tenofovir into the matrix, while the Zeta potential measurements revealed the strong interactions which develop between system components. The obtained DDSs presented biodegradability, hemocompatibility and in vivo biocompatibility, which along with their ability to release both the drug and the antifungal aldehyde make them promising materials for the treatment of HIV infection and its associated co-infections' symptoms. [Display omitted] [ABSTRACT FROM AUTHOR]

The paper reports hydrogels prepared from chitooligosaccharides with different polymerization degrees (14 to 51), by crosslinking with 2-formylphenylboronicacid in three molar ratios of their functionalities. The structural, morphological and supramolecular characterization confirmed a hydrogelation mechanism based on self-assembling of newly formed imine units and porous morphology. Rheological measurements confirmed the formation of thixotropic hydrogels, and swelling tests indicated mass equilibrium swelling values up to 25 in water and 9 in phosphate buffer saline. The monitoring of enzymatic degradability demonstrated the enhancing of biodegradation rate as long as the polymerization degrees of the oligomers decreased, the mass loss increasing from 16% to 43%. In vivo and ex-vivo biocompatibility investigation on experimental mice showed no cytotoxic effect, and in vitro antimicrobial tests revealed remarkable antimicrobial properties on nine strains, with a maximum inhibition diameter of 49 mm on Aspergilius brasiliensis and very good results on Cladosporium cladosporioides , Penicillium crysogenum and different Candida species. [Display omitted] [ABSTRACT FROM AUTHOR]