Graft Copolymers Research Articles

Induction of physico-chemical properties in mercerized Yucca filamentosa fiber-based graft copolymer through response surface methodology and its characterization

Induction of physico-chemical properties in mercerized <i>Yucca filamentosa</i> fiber-based graft copolymer through response surface methodology and its characterization

Synergistic effects of dual reactive compatibilizers for high-performance fully biodegradable polylactic acid/poly (butyleneadipate-co-terephthalate) composites

The PLA-g-(GMA-co-St) graft copolymer (PGS) was prepared using melt-free radical grafting technology, PGS and ESO were simultaneously employed as compatibilizers for the poly (lactic acid)/poly (butylene adipate-co-terephthalate) (PLA/PBAT) blends. The effects of the type and amount of compatibilizers on the properties of the blends were studied. The results reveal that the epoxy groups in PGS and ESO can interact with the terminal groups of PLA and PBAT. The incorporation of either PGS or ESO separately can improve the compatibility between PLA and PBAT to a considerable degree. However, the introduction of both compatibilizers into the PLA/PBAT blends results in a notable shift of the Tg of the two phases, reduces the size of PBAT particles, and makes their dispersion more uniform. This reveals that the dual reactive compatibilizers can achieve a synergistic effect, significantly reducing the interfacial tension between the two phases and facilitating inter-phase dispersion, ultimately forming a more uniform microstructure. Simultaneously, as the amount of ESO added to the blends gradually increases, the vicat softening temperature and complete decomposition temperature of the blends continue to increase, the notched impact strength and elongation at the break of the blend gradually increase and then decrease. When the ESO amount reaches 4 wt%, the performance of each property increases to 88.9 °C, 447.66 °C, 335.16 %, and 23,359.30 J/m2, respectively. At this point, the fracture surface of the blend samples is accompanied by a large-scale plastic deformation. In conclusion, this work represents the first attempt to accomplish synergistic effects via dual reactive compatibilizers. Under the best formulation and processing circumstances, the PLA/PBAT blends greatly increase their overall performance while maintaining biodegradability, hence broadening their application prospects in packaging, agriculture, and disposable tableware.

Surface Modification of Kosa Silk Fiber by Graft Copolymerization with Vinyl Benzyl Trimethylammonium Chloride (VBT) and Its Antibacterial Study

Surface Modification of Kosa Silk Fiber by Graft Copolymerization with Vinyl Benzyl Trimethylammonium Chloride (VBT) and Its Antibacterial Study

Influence of Different Grafted Natural Rubbers on Electrical and Mechanical Properties of Natural Rubber/Carbon Nanotubes Composites

This study investigates the augmentation of electrical and mechanical characteristics of natural rubber (NR) film with different forms by integrating carbon nanotubes (CNTs). NR with different forms (i.e., natural rubber grafted with polystyrene (NR–g–PS) and polybutyl methacrylate (NR–g–PBMA)) were successfully synthesized. The success of these grafting was confirmed through Proton Nuclear Magnetic Resonance (1H–NMR) and Attenuated Total Reflectance–Fourier Transform Infrared (ATR–FTIR) analyses, which showed that the grafting efficiency exceeded 90%. The properties of ungrafted NR and grafted NRs with CNTs were compared and analyzed. It was found that the NR/CNTs composites with grafting displayed significantly improved electrical properties and mechanical strength when compared to the NR/CNTs composites without grafting. It was found that the NR–g–PBMA exhibited an 860% increase in electrical conductivity at 100 kHz compared to ungrafted NR. This might be attributed to the synergistic of the high specific surface of CNTs and the high polarization of functional groups, which gave a higher value for the CNTs filled grafted NR than the ungrafted NR. Moreover, the mechanical properties of NR–g–PS composites showed a 114% increase in 100% modulus, 127% in tensile strength, and 37% in hardness, while the NR–g–PBMA composites exhibited a 159% increase in 100% modulus, 95% in tensile strength, and 34% in hardness compared to ungrafted NR. This enhancement can be attributed to the formation of chemical linkages between the grafted NR matrix and CNTs through functional groups from both. Consequently, it can be concluded that introducing functional groups on grafted NR assists in establishing a crosslinking network, enhancing both the mechanical and electrical properties. Additionally, this research emphasizes the benefits of producing flexible conductive materials with high modulus and enhanced electrical properties. Keywords: Natural rubber latex, Graft copolymerization, Glutaraldehyde, Natural rubber composites, Electrical properties

Preparation of Consolidated Dust Suppression Materials Based on Pectin: Graft Modification Experiment and Reaction Mechanism.

The natural material pectin was used as the matrix to prepare a dust suppressant. The regression model in response to the grafting ratio was established, and the optimum modification scheme was determined. The amount of monomer, initiator, cross-linking agent, and reaction temperature was 3.20 g, 0.20 g, and 0.15 g and 92 °C, respectively. Through Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy tests, not only the formation of the product in graft copolymerization reaction was validated but also the wettability of pectin was significantly improved. The surface morphology of pectin before and after modification was observed by a scanning electron microscope. After graft copolymerization treatment, the surface of pectin presented a dense grid structure, which proved that the pectin-modified dust suppressant can play a crucial role in wetting and condensing coal dust. Contact angle tests were used to characterize the effect of pectin modification on the wettability of bituminous coal before and after modification. The results of contact angle tests showed that when the droplets just contacted the bituminous coal flakes, the contact angle of modified pectin droplets on the flakes was the smallest, and the value was 55.21°. Compared with pure water droplets and unmodified pectin droplets, it decreased by 21.66° and 18.50°. The modification reaction process and dust suppression mechanism were explained at the molecular level.

Development of Slow-Release Fertilizers with Function of Water Retention Using Eco-Friendly Starch Hydrogels

Over the past two decades, the development and commercialization of slow-release fertilizers (SRFs) have significantly advanced, with the primary aim of mitigating environmental issues associated with excessive fertilizer use. A range of methodologies, including chemical and physical reactions, incorporation into carriers with porous and layered structures, and coating techniques, have been explored and refined. On the other hand, global challenges such as drought and desertification further underscore the need for SRFs that not only control nutrient release but also improve soil moisture retention. This paper reviews the development and application of eco-friendly starch hydrogels as fertilizer carriers and water retention for SRFs, particularly starch-based superabsorbent polymers (SAPs) produced through grafting copolymerization with acrylamide. This review explores both scientific issues, such as the microstructures and releasing mechanisms of SAPs, and technical development, involving copolymerization technologies, multi-initialization processes, methods of loading fertilizer into hydrogel, etc. Starch, as both a biodegradable and renewable carbohydrate polymer, offers distinct advantages due to its excellent chemical stability and high reactivity. The fabrication techniques of SAPs have been developed from traditional batch polymerization in aqueous solutions to more efficient, solvent-free reactive extrusion. The benefits of SRFs based on SAPs encompass enhanced soil aeration, the prevention of soil deterioration, the minimization of water evaporation, environmental pollution control, reduction in plant mortality, and prolonged nutrient retention within soil. In this review, we summarize the current progress, identify limitations in existing technologies, and propose future research directions to further enhance the performance of starch-based SRFs.

Synthesis and characterization of guar gum xanthate derivative super adsorbent hydrogel for the capturing of heavy metal ions from wastewater

The Guar Gum Xanthate based hydrogel GGmX-g-poly(AA-co-HEMA) has been successfully synthesized by using the graft copolymerization of two monomers, acrylic acid (AA) and 2-hydroxyethyl methacrylate (HEMA) hydrogel. The synthesis follows the free-radical graft polymerization method. UV-visible spectroscopy (UV), Thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), Point zero charge (PZC), and field emission scanning electron microscopy (FESEM) were employed for the characterization of the synthesized hydrogel. This hydrogel has shown a high swelling ratio of 430.2 g/g and retention of 75.82% in distilled water which is a notable result. By using GGmX-g-poly(AA-co-HEMA) hydrogel, the maximum percentage of heavy metal ions removal from wastewater was found to be 98.5(±1.5)% and 97.1(±1.5) at optimum pH 6 and 6.5 for Cu2+ and Ni2+ solutions respectively. The Langmuir adsorption isotherm fits best for the adsorption data indicating a monolayer adsorption with maximum adsorption capacity of 423.72 (±26.1) mg/g and 404.85 (±31.4) mg/g for Cu2+ and Ni2+ ions respectively. The pseudo-second-order kinetic model provides the most accurate depiction of adsorption kinetics with rate constant 9.1 × 10−4 (±1.37×10−4)g/(mg.min) for Cu2+ and 8.3 × 10−4 (±1.24×10−4)g/(mg.min) for Ni2+ ions, respectively. The negative ΔG value (-4.75 kJ/mol for Cu2+ and −3.26 kJ/mol for Ni2+ ions) and positive value of ΔH (57.55 (±5.41) kJ/mol for Cu2+ and 40.60(±5.37) kJ/mol for Ni2+ ions) suggested the process to be spontaneous, endothermic, and feasible. It has been found that the hydrogel has excellent regenerative capacity with the % adsorption has been found to be 84.8% for Cu2+ and 82.4% for Ni2+ ions for the fifth cycle.

Free-radical-induced grafting of rice starch with gallic acid and evaluation of the reaction products' ability to stabilize Pickering emulsions

Pickering emulsions can be stabilized with native rice starch (NRS), but their hydrophobicity is low. Gallic acid (GA) has a simple molecular structure and a rich variety of functional groups. Pickering emulsions can be made more stable by hydrophobically modifying the esterification reaction of NRS with GA to improve its dual wetting properties. In this study, the free radical-induced grafting method was used to prepare rice starch–GA graft copolymer (NRS-g-GA). The addition of GA could improve the crystallinity and orderliness of NRS. The results of Fourier transform infrared spectroscopy and 1H NMR indicated that GA was successfully grafted onto NRS. After modification, the contact angle of NRS increased from 18.2° to 60.2° (NRS-g-GA; 1:1). The emulsion prepared from NRS-g-GA showed better stability than NRS, improving the emulsification of NRS. Its stable emulsion exhibited an emulsion system dominated by elasticity. Thus, GA could be grafted onto NRS to enhance its emulsifying properties, opening up new applications for GA and NRS and promoting the development of starch-based Pickering emulsions in the future.

Enhancing the Biomimetic Mechanics of Bottlebrush Graft-Copolymers through Selective Solvent Annealing.

Self-assembled networks of bottlebrush copolymers are promising materials for biomedical applications due to a unique combination of ultra-softness and strain-adaptive stiffening, characteristic of soft biological tissues. Transitioning from ABA linear-brush-linear triblock copolymers to A-g-B bottlebrush graft copolymer architectures allows significant increasing the mechanical strength of thermoplastic elastomers. Using real-time synchrotron small-angle X-ray scattering, it is shown that annealing of A-g-B elastomers in a selective solvent for the linear A blocks allows for substantial network reconfiguration, resulting in an increase of both the A domain size and the distance between the domains. The corresponding increases in the aggregation number and extension of bottlebrush strands lead to a significant increase of the strain-stiffening parameter up to 0.7, approaching values characteristic of the brain and skin tissues. Network reconfiguration without disassembly is an efficient approach to adjusting the mechanical performance of tissue-mimetic materials to meet the needs of diverse biomedical applications.

Evaluation of a novel non-ionic graft starch-based antiscalant in reduction of CaSO4 scaling by static and reverse osmosis test

A novel nonionic starch-based antiscalant (St-g-GMA) was designed and obtained by graft copolymerization of starch and glycidyl methacrylate (GMA). St-g-GMA not only achieved an obvious reduction of CaSO4 scaling in static test, but also effectively mitigated the flux decrease in dynamic reverse osmosis (RO) system. This improvement is ascribed to the grafted poly(GMA) chains on St-g-GMA. A suitable grafting ratio of this starch-based antiscalant achieve a high performance cost in control of CaSO4 scaling. Combination of the apparent antiscaling performance, observation under scanning electron microscopy, energy dispersive x-ray spectroscopy unit, x-ray diffraction pattern, conductivity measurement, and dispersion experiment, the scale-inhibition mechanism of St-g-GMA was investigated and mainly attributed to chelation, dispersion and lattice distortion effects. The oxygen-containing groups on poly(GMA) chains such as epoxy groups can chelate with Ca2+, causing the induction time of crystallization prolonged; St-g-GMA with the distinct branched chain configuration can well disperse the formed microcrystal of CaSO4. Moreover, molecular dynamics simulations confirmed that the grafted poly(GMA) chains well bind to the crystal surfaces and the oxygen-containing groups could even enter the crystal lattice to inhibit the crystal growth and change the morphologies. St-g-GMA still mitigated the flux decrease notably in treatment of a synthetic seawater during a 24-h RO measurement. This study provided an efficient, environmentally-friendly and low-cost antiscalant with high application potentials.

Synthesis and characterization of amphiphilic Poly(2-hydroxyethyl acrylate-g-α-Methyl-β-Alanine) by Nitroxide-Mediated Polymerization Using “grafting through” approach

Oligomeric poly(α-methyl-β-alanine)with vinyl end-group (PmBA) was synthesized via base-catalyzed hydrogen-transfer polymerization (HTP) of molten methacrylamide (MAm) in the presence of sodium tert-butoxide (t-BuONa). The PmBA was used as a comonomer in the synthesis of amphiphilic poly(2-hydroxyethyl acrylate-g-α-methyl-β-alanine) (PHEA-g-PmBA)via nitroxide-mediated polymerization (NMP)and "grafting through" approach.The graft copolymer formation was confirmed byproton nuclear magnetic resonancespectroscopy (1H-NMR), Fourier-transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and static light scattering (SLS)measurements. Thermogravimetric analysis of the amphiphilicPHEA-g-PmBAexhibited a multi-step decomposition curve corresponding to the α-methyl-β-alanine and the 2-hydroxyethyl acrylate blocks at about 306, 369, and 403 °C.DSC curve of the copolymer has a baseline shift at −12.87 °C attributed to the glass transition temperature. SLS analysis of the final product resulted in a weight average molecular weight of 83.6 kDa. The spectroscopic and thermal analyses proved that amphiphilicPHEA-g-PmBA was successfully synthesized through HTP and NMP.

Time and Temperature Dependence of Drug Crystallization─The Role of Molecular Mobility.

Using the time-temperature-transformation diagrams, we demonstrated a correlation between molecular mobility and crystallization in amorphous solid dispersions of nifedipine (NIF) with each polyvinylpyrrolidone vinyl acetate (PVPVA64) and polyvinyl caprolactam polyvinyl acetate-polyethylene glycol graft copolymer (Soluplus). The behavior was compared with the NIF dispersions prepared with each polyvinylpyrrolidone (PVP) and hydroxypropyl methylcellulose acetate succinate (HPMCAS) [Lalge et al., Mol. Pharmaceutics 2023, 20(3), 1806-1817]. Each system was characterized by a unique temperature at which the crystallization onset time was the shortest. Below this temperature, a coupling was observed between the α-relaxation time determined by dielectric spectroscopy and crystallization onset time. Above this temperature, the activation barrier for crystallization had a more significant role than molecular mobility. In the solid state, PVP and PVPVA64 dispersion exhibited higher resistance to crystallization than HPMCAS and Soluplus. The role of polymers in inhibiting crystal growth in nucleated systems was discerned by monitoring crystallization following wetting of the amorphous dispersion with the dissolution medium. PVPVA64 and Soluplus dispersions exhibited higher resistance to crystal growth than PVP and HPMCAS.

Architecting side chain grafted poly (vinylidene fluoride) based graphene oxide composite polyelectrolyte membranes for hydrogen and direct methanol fuel cells

Chemically modified poly (vinylidene fluoride) (PVDF) as polyelectrolyte has generated immense interest due to its high efficiency in electrochemical energy devices. Herein, the design of a polymer electrolyte membrane (PEM) is formulated by the synergistic fusion of graphene oxide (GO) into chemically grafted PVDF with 2-acrylamido-2-methylpropane sulfonic acid (AMPS) by solution phase intercalation producing GO@PVDF-g-PAMPS composite membranes. Ozone-induced graft copolymerization technique is employed to prepare PVDF-g-PAMPS with 18.3% (w/w) degree of grafting. Incorporation of GO into the polymeric membrane generates appropriate hydrophilic-hydrophobic phase separation and constructs well-organized sub-nano slit-like pathways that elevate the proton conduction. PAG-0 membrane without any filler shows a proton conductivity (κ) of 15.1 mS/cm at 80°C whereas PAG-2 membrane (with 2% w/w GO loading) shows a κ of 25.9 mS/cm under similar conditions. The presence of a perfluorinated backbone furnishes excellent oxidative stability to the PEMs by retaining 95% of total mass and 97.3% of κ after dipping in harsh Fenton's reagent at 60°C for 6 h. Representative PAG-2 shows a peak power density of 152.9 mW/cm2 with a maximum current density of 480.6 mA/cm2 (fuel cell operating conditions: 75°C at 100% RH) in hydrogen fuel cell and a peak power density of 37.7 mW/cm2 in methanol fuel cell. Moreover, PAG-2 retains 91% of its initial OCV after 50 h of the durability test.

Synthesis and characterization of self-healable supramolecular hydrogel based on carboxymethyl cellulose for biomedical applications

Hydrogels have been widely used in biomedical fields including tissue engineering, drug delivery and cell delivery and 3D cell delivery due to abundant water content in their hydrophilic three-dimensional networks and having soft tissue similar to the human body. In recent years, supramolecular hydrogels (SHG) formed by the inclusion complex between polyethylene glycol (PEG) and macrocycles such as cyclodextrin (CD) have attracted much interest due to their excellent biocompatibility and great potential in biomedical. In this research, a carboxymethyl cellulose (CMC)-based graft copolymer was prepared by using acrylic acid (AA) and maleic anhydride functionalized β-CD (β-CD-MA) as comonomers and ammonium persulfate (APS) as initiator. Then, a self-healable supramolecular hydrogel was synthesized by formation of a host-guest inclusion complex between CMC-g-poly (AA-co-β-CD-MA) as host molecule and cytosine- and guanine-modified PEG as guest molecules. The prepared hydrogel was characterized by Scanning Electron Microscope (SEM), X-Ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Nuclear magnetic resonance spectroscopy (1H NMR). The thermal stability of hydrogel was also determined by thermal gravimetric (TGA) and differential scanning calorimetry (DSC) methods. In addition, the loading and release profiles of metformin hydrochloride (MH) drug as a model on hydrogel was investigated. The results indicated that the drug release from the hydrogel peaks around 360 min and aligns with the Ritger-Peppas model. The hydrogel's self-healing property was examined at ambient temperature and 37 °C. It showed 70 % healing in 1.5 h and completed recovery after 9 h.

Berberine-Loaded PVCL-PVA-PEG Self-Assembled Micelles for the Treatment of Liver Fibrosis.

Liver fibrosis is a necessary pathological process in many chronic liver diseases. Studies have shown that the progression of chronic liver disease can be slowed by rational intervention in hepatic fibrosis. Berberine (BBR), a natural extract of Phellodendron amurense, inhibits the development of liver fibrosis through several mechanisms. However, the clinical application of BBR is limited due to its low solubility. Drug delivery systems have been developed to improve the solubility of hydrophobic drugs and increase their efficacy in treating the liver fibrosis. In this study, a biocompatible nanomicelle was constructed by thin-film dispersion method using polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (PVCL-PVA-PEG) as a carrier to encapsulate BBR (PVCL-PVA-PEG/BBR-MCs) to improve the solubility of BBR and reduce the systemic side effects. The ability to inhibit HSC-T6 cell activation of PVCL-PVA-PEG/BBR-MCs was evaluated in vitro. The anti-hepatic fibrosis effects of PVCL-PVA-PEG/BBR-MCs were investigated in vivo. PVCL-PVA-PEG/BBR-MCs have a uniform spherical shape with a mean particle size of 60.04 ± 0.027 nm and a potential of 1.49 ± 0.32 mV. It had an encapsulation efficiency of 98.52% ± 0.70 and drug loading content of 6.16% ± 0.04. Compared to free BBR, PVCL-PVA-PEG/BBR-MCs significantly inhibited HSC-T6 cell activation and TGF-β1-induced HSC-T6 cell migration in vitro. In vivo biodistribution experiments showed significantly improved hepatic distribution of PVCL-PVA-PEG/DiD-MCs compared to free DiD, suggesting that PVCL-PVA-PEG micelles enhance the ability of BBR to enter the liver and improve therapeutic efficacy. After treatment, PVCL-PVA-PEG/BBR-MCs significantly improved fibrotic liver structure and reduced collagen deposition in comparison to the CCl4-treated group; the treatment outcome was more effective than that of the free BBR group. Our results demonstrate the advantages of encapsulating BBR in PVCL-PVA-PEG micelles and highlight the potential of PVCL-PVA-PEG/BBR-MCs as a therapeutic strategy for the treatment of liver fibrosis.

Oral delivery of Sunitinib malate using carboxymethyl cellulose/poly(acrylic acid-itaconic acid)/Cloisite 30B nanocomposite hydrogel as a pH-responsive carrier.

This work aimed to fabricate a Cloisite 30B-incorporated carboxymethyl cellulose graft copolymer of acrylic acid and itaconic acid hydrogel (Hyd) via a free radical polymerization method for controlled release of Sunitinib malate anticancer drug. The synthesized samples were characterized by FTIR, XRD, TEM, and SEM-dot mapping analyses. The encapsulation efficiency of Hyd and Hyd/Cloisite 30B (6 wt%) was 81 and 93%, respectively, showing the effectiveness of Cloisite 30B in drug loading. An in vitro drug release study showed that drug release from all samples in a buffer solution with pH 7.4 was higher than in a buffer solution with pH 5.5. During 240min, the cumulative drug release from Hyd/Cloisite 30B (94.97% at pH 7.4) is lower than Hyd (53.71% at pH 7.4). Also, drug-loaded Hyd/Cloisite 30B (6 wt%) demonstrated better antibacterial activity towards S. Aureus bacteria and E. Coli. High anticancer activity of Hyd/Cloisite 30B against MCF-7 human breast cancer cells was shown by the MTT assay, with a MCF-7 cell viability of 23.82 ± 1.23% after 72-hour incubation. Our results suggest that Hyd/Cloisite 30B could be used as a pH-controlled carrier to deliver anticancer Sunitinib malate.

Reversible fluorescence/photochromic switching of repeated-response cellulose-based hydrogels for information encryption

The rapid development of anti-counterfeiting technology has brought new challenges to the repeatability and stability of reversible fluorescence/photochromic switching hydrogels. To address this issue, a series of chemical cross-linked cellulose-based intelligent responsive hydrogels were synthesized by free-radical graft copolymerization in a hydrothermal process. This strategy allows for the creation of a chemical cross-linked three-dimensional structure that anchors photochromic ammonium molybdate and fluorescent carbon dots together, resulting in enhanced stability and mechanical properties. Especially, the tensile and compressive strength of hydrogel reached a maximum value of 280 kPa and 560 kPa, respectively, which far exceeds that of some reported hydrogels. The resultant hydrogels exhibited desired reversible fluorescence/photochromic switching, reversible printing and erasing of patterns, and information encryption/decryption. Notably, the change of photochromism from yellow to green can be realized, and the self-fading process can be shortened to 25 min at 60 °C instead of 6 h at room temperature. More importantly, the fluorescence quenching phenomenon of the hydrogel occurs gradually after 2 min of continuous irradiation, and it can be recovered by selective treatment with ethanol. Overall, this study provides a simple strategy for the preparation of environmentally friendly reversible fluorescence/photochromic switching cellulose-based hydrogels for information encryption.

Creative synthesis of pH-dependent nanoporous pectic acid grafted with acrylamide and acrylic acid copolymer as an ultrasensitive and selective riboflavin electrochemical sensor in real samples

In current research, an innovative pectic acid was grafted with poly (acrylamide-co-acrylic acid) [PA-g-poly (AAm-co-AA)] nanoporous membrane using a free radical-mediated grafting copolymerization process. The optimized parameters for the grafting copolymerization reaction such as initiator concentration, monomer concentrations, polymerization reaction time, and temperature were studied. Additionally, the solid content, graft percentage, and conversion were calculated. The unique polymeric membrane was characterized using Fourier-transform infrared spectroscopy (FT-IR), thermal gravimetry (TG), transmission electron microscopy (TEM), and scanning electron microscopy (SEM) supported by energy dispersive X-ray spectroscopy (EDX). The formulated novel PA-g-poly (AAm-co-AA) had a nanoporous structure with a diameter of 113 nm. pH-dependent swelling and biodegradation measurements were also studied. The electrochemical characterizations of PA-g-poly (AAm-co-AA) were conducted through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Furthermore, the screen-printed electrode (SPE) was modified with pure PA and the new generation of its grafted polymeric nanoparticles to detect and quantify the concentration of riboflavin (RF) in real samples using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques. The modified electrode showed two linear concentration ranges from 0.01 - 2 nM and 2 – 90 nM with low detection limits (LODs) of 0.004 and 0.97 nM, respectively, demonstrating high sensitivity. Besides, the fabricated sensor exhibited more selectivity, simplicity, great reproducibility, repeatability, and good stability. Finally, the PA-g-poly (AAm-co-AA)-modified SPE based sensor was effectively used in real sample analysis of egg yolk, milk, and vitamin B2 drugs with good recovery rates.

Development of Grafted Copolymers from Plant Exudates and Their Application for Site-Specific Drug Delivery: A Systematic Review

Grafted copolymers, extracted from plant exudates, have emerged as promising materials for their potential activity in site-specific drug delivery. These biopolymers, derived from natural sources, provide biocompatibility, biodegradability, and functional diversity. This review focuses on the methods of grafting copolymers onto plant exudates, the characterization of these novel materials, and their potential applications in drug delivery to specific targeted areas. We focus on specific grafted polymers such as Tamarindus indica acrylamide grafted polymer (TIAG), Sterculia urens acrylamide grafted polymer (SUAG), and Eucalyptus obliqua acrylamide grafted polymer (EOAG), among others, to investigate their advantageous characteristics in delivering potent molecules to the intended site of action, thereby enhancing crucial modalities such as the onset and duration of action. This review also highlights the mechanisms of drug release, targeting strategies, and the therapeutic benefits of using these biopolymers in medical applications.

Effect of different initiators on the properties of diacetone acrylamide grafted starch-based adhesive

Environmentally friendly and non-toxic bio-based adhesives are emerging as the most promising substitutes for petroleum-based adhesives, attracting increasing attention. This work involved the synthesis of a starch-based adhesive for particleboards by grafting diacetone acrylamide (DAAM) onto starch. The graft polymerization was initiated using three different initiators: ammonium persulfate (APS), hydrogen peroxide (H2O2)/ammonium ferrous sulfate system, and ceric ammonium nitrate (CAN). A comparative study was conducted to assess the varying effects of these initiators. The results showed that in the graft copolymerization of starch with DAAM, different initiators produced different types of free radicals, and CAN initiation produced alkyl radicals and long-chain alkyl radicals with a peak total spin value of 3.96 × 1015, and thus had the highest grafting efficiency and grafting rate of 72.59 % and 16.75 %, respectively. From the comparison of the total number of spins, it can be seen that CAN is more targeted for starch initiation. In addition, characterization results from Fourier transform infrared spectroscopy and confocal Raman spectroscopy showed that DAAM underwent a graft copolymerization reaction with starch. Notably, the adhesive initiated by CAN demonstrated the highest water resistance and mechanical strength, with an absorption thickness expansion and static bending strength of 8.52 % and 10.56 MPa, respectively.