Publications by authors named "Claudiu-Augustin Ghiorghita"

Porous hydrogels have brought more advantages than conventional hydrogels when used as chromatographic materials, controlled release vehicles for drugs and proteins, matrices for immobilization or separation of molecules and cells, or as scaffolds in tissue engineering. Polysaccharide-based porous hydrogels, in particular, can address challenges related to bioavailability, solubility, stability, and targeted delivery of natural antioxidant compounds. Their porous structure enables the facile encapsulation and controlled release of these compounds, enhancing their therapeutic effectiveness.

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Biobased porous hydrogels enriched with phytocompounds-rich herbal extracts have aroused great interest in recent years, especially in healthcare. In this study, new macroporous hybrid cryogel constructs comprising thiourea-containing chitosan (CSTU) derivative and a L. extract (HYP), commonly known as St John's wort, were prepared by a facile one-pot ice-templating strategy.

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Article Synopsis
  • Polysaccharides like chitosan and alginate have been used to create versatile hydrogels that can improve the effectiveness of drug delivery and functional foods.
  • These hydrogels help resolve issues related to bioavailability, solubility, stability, and targeted delivery of phytocompounds.
  • The review discusses the preparation, properties, and applications of these hybrid systems, particularly in areas like wound management and the food industry, emphasizing how their structural and functional requirements impact their performance.
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  • Environmental contamination from pesticides is a widespread issue, creating a need for effective and eco-friendly removal methods.
  • The study explored the use of self-assembled hydrogels made from chitosan and carboxymethylcellulose, showing high efficiency in removing various fungicides, especially with the DA-CMC variant.
  • The results demonstrated that the CS/DA-CMC hydrogels could effectively reduce pesticide levels in water, achieving removal rates up to 94% for specific fungicides.
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A new derivative of polyethyleneimine (PEI) with 9% degree of substitution of its primary and secondary amino groups with thiourea moieties (TU-PEI) has been synthesized and investigated as flocculant in model suspensions of commercial fungicide formulations Dithane M45, Melody Compact 49 WG, Cabrio®Top, and their mixtures. The structure of TU-PEI, obtained by an aqueous one-pot strategy involving formaldehyde mediated coupling of PEI and TU, was confirmed by FTIR and H NMR spectroscopy as well as the streaming potential measurements. The settling time, polymer dose, and fungicide type and concentration were the parameters used for assessing the flocculation ability of the new polycation sample.

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The introduction of selective recognition sites toward certain heavy metal ions (HMIs) is a great challenge, which has a major role when the separation of species with similar physicochemical features is considered. In this context, ion-imprinted polymers (IIPs) developed based on the principle of molecular imprinting methodology, have emerged as an innovative solution. Recent advances in IIPs have shown that they exhibit higher selectivity coefficients than non-imprinted ones, which could support a large range of environmental applications starting from extraction and monitoring of HMIs to their detection and quantification.

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Biomass-derived materials with multiple features are seldom reported so far. Herein, new chitosan (CS) sponges with complementary functions for point-of-use healthcare applications were prepared by glutaraldehyde (GA) cross-linking and tested for antibacterial activity, antioxidant properties, and controlled delivery of plant-derived polyphenols. Their structural, morphological, and mechanical properties were thoroughly assessed by Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and uniaxial compression measurements, respectively.

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Designing of economically feasible and recyclable polysaccharide-based materials with thiourea functional groups for removal of specific metal ions such as Ag(I), Au(I), Pb(II) or Hg(II) remains a major challenge for environmental applications. Here, we introduce ultra-lightweight thiourea-chitosan (CSTU) aerogels engineered by combining successive freeze-thawing cycles with covalent formaldehyde-mediated cross-linking and lyophilization. All aerogels exhibited outstanding low densities (0.

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Nowadays, pollution has become the main bottleneck towards sustainable technological development due to its detrimental implications in human and ecosystem health. Removal of pollutants from the surrounding environment is a hot research area worldwide; diverse technologies and materials are being continuously developed. To this end, bio-based composite hydrogels as sorbents have received extensive attention in recent years because of advantages such as high adsorptive capacity, controllable mechanical properties, cost effectiveness, and potential for upscaling in continuous flow installations.

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Chitosan (CS)-based drug delivery systems (DDSs) are often stabilized by chemical cross-linking. A much more friendly approach to deliver drugs in a controlled manner is represented by polyelectrolyte complexes (PECs) physically stabilized by spontaneous interactions between CS and natural or synthetic biocompatible polyanions. PECs with tunable structures, morphologies, and mechanical properties were fabricated in this paper by an innovative and sustainable strategy.

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Article Synopsis
  • A series of experiments demonstrated the effectiveness of APCA-functionalized adsorbents for removing specific heavy metal ions in a batch setting, suggesting the need for further column studies for practical applications.
  • The sorption preference for heavy metals in a fixed-bed column showed that Ni2+ had the highest affinity for the sorbent, while Co2+ had the lowest, with a calculated maximum sorption capacity of 145.55 mg/g for the best-performing composite sorbent.
  • Successful desorption of heavy metals was achieved using a mild 0.1 M HCl solution, and theoretical analyses revealed that minimal energy is needed to favorably configure the APCA sorbents for optimal metal binding.
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Curcumin (CCM) is a natural hydrophobic polyphenol known for its numerous applications in the food industry as a colorant or jelly stabilizer, and in the pharmaceutical industry due to its anti-inflammatory, antibacterial, antioxidant, anti-cancer, and anti-Alzheimer properties. However, the large application of CCM is limited by its poor solubility in water and low stability. To enhance the bioavailability of CCM, and to protect it against the external degradation agents, a novel strategy, which consists in the preparation of semi-interpenetrating polymer networks, (s-IPNs) based on poly(,-dimethylaminoethyl methacrylate) entrapped in poly(acrylamide) networks, by a cryogelation technique, was developed in this work.

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Electrostatically-based layer-by-layer (LbL) assembly is a versatile surface functionalization technique allowing the construction of complex three-dimensional architectures on virtually any type of material using various combinations of nano-bricks. One of the most promising applications of LbL assembled systems is in water purification. The main two strategies developed in this purpose consist in either enhancing the barrier properties of separation membranes and in the construction of core-shell organic/inorganic sorbents.

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Composite solid surfaces with high content of functional groups (FGs) are useful materials in different types of applications requiring stimuli-responsive "hard/soft" architectures, their improved properties rising from the combination of organic-inorganic parts. Among different types of weak polyelectrolytes, poly(ethyleneimine) (PEI) is of great interest in the construction of composite systems with thin layer-by-layer (LbL) organic films due to the large number of amino groups per unit mass of polymer. Herein, the spherical silica microparticles were modified with linear (L) or branched (B) PEI chains using LbL deposition of a copper complex (PEIL-Cu or PEIB-Cu) and poly(acrylic acid) (PAA), glutaraldehyde selective cross-linking, followed by copper and PAA extraction from the multilayer.

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Design of polymeric matrices for loading/release purposes is of great interest in various applications, such as drug delivery systems, antimicrobial surfaces, biosensors, water purification. Compared with other strategies to fabricate materials for such applications, the Layer-by-Layer (LbL) assembly remarked itself by the countless possibilities to tailor the organic architectures at nanoscale owing to the structural diversity of "nano-bricks" suitable for assembly and easiness to control the deposition features. LbL assembled systems have been extensively used as matrices to load/release low molecular compounds such as drugs and dyes, proteins and enzymes, or DNA (RNA).

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The aim of the present work is to construct and investigate the properties of novel polyelectrolyte multilayers consisting of poly(N,N-dimethylamino)ethyl methacrylate (PDMAEMA) and sodium alginate (SA). The influence of PDMAEMA's pH dependent ionization degree on the charge balance, thickness and roughness of the multilayer films was assessed by potentiometric titrations, dye sorption and atomic force microscopy. Moreover, the cross-linking of PDMAEMA/SA films with a dihalogenated aromatic derivative with high reactivity (α,α'-dichloro-p-xylene) by means of Menshutkin reaction and the stability of the multilayer architecture to repeated treatments with NaOH are demonstrated.

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Multilayer thin films are useful materials in fabrication of controlled drug delivery systems and in controlling drug release processes. Herein, we report the fabrication of single polycation multilayers based on branched poly(ethylene imine) (PEI) mediated by dianhydrides (DA), as cross-linker and source of carboxylic groups, deposited onto Daisogel silica microparticles, and their sorption/release properties for some anionic drugs as a function of the cross-linker concentration. Pyromellitic dianhydride (PM) and 3,3',4,4'-benzophenonetetracarboxylic dianhydride (BTCDA) were used as DA reagents.

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