Acrylic Acid Copolymer Research Articles

Ultrasound protein-copolymer microbubble library engineering through poly(vinylpyrrolidone-co-acrylic acid) structure

HypothesisWhile albumin-coated microbubbles are routine contrast agents for ultrasound imaging, their short duration of contrast enhancement limits their use, yet can be improved by incorporating protein-copolymer hybrids into microbubble shells. The incorporation of N-vinyl-2-pyrrolidone and acrylic acid copolymer (P(VP–AA)) has been shown to enhance the performance of bovine serum albumin (BSA)-coated microbubbles. However, the impact of the copolymer structural properties on key microbubble characteristics (i.e., concentration, mean diameter and acoustic response) remains poorly understood. Therefore, we hypothesize that the copolymer structure affects its capacity to form micelle-like nanoaggregates, protein-copolymer hybrids, and microbubble shells, ultimately influencing the physicochemical and acoustic properties of the microbubbles. ExperimentsHere we evaluate the production and performance of BSA@P(VP–AA) microbubbles synthesized using a series of P(VP–AA) copolymers with –C8H17 and –C18H37 end groups and molecular weight cutoffs between 3.5 and 15 kDa. Both simulation and experimental data demonstrate that interactions between BSA and the copolymers significantly influence the performance of the resulting microbubbles across the library of 60 formulations. FindingsThe introduction of –C8H17 terminated copolymers into microbubble shells resulted in up to 200-fold higher concentration, 7-fold greater acoustic response, and 5-fold longer ultrasound contrast enhancement compared to plain BSA microbubbles. The enhanced acoustic performance was sustained during in vivo cardiac ultrasound imaging, without altering liver accumulation after copolymer introduction. These findings underscore how optimizing copolymer structure (specifically the terminal end group and molecular weight) can tailor the formation and performance of protein-copolymer-coated microbubbles, offering valuable insights for designing ultrasound contrast agents.

Methallylsulfonate Polymeric Antiscalants for Application in Thermal Desalination Processes.

Nine copolymers of acrylic acid and sodium methallyl sulfonate were tested as scale inhibitors in thermal desalination. The nine antiscalants covered molar masses between 2000 and 9500 g.mol-1 and concentrations of sulfonated monomer ranging between 10 and 30 mole percent. A pressure measurement and control (P-MAC) unit and a high-temperature pressurized vessel were used to measure the effectiveness of the scale inhibitors in seawater, concentrated seawater, and model solutions at 125 °C. The effectiveness of the novel copolymers was comparable to commercial antiscalant at times up to 15 min and improved at longer times. Molar mass was a more important determinant of effectiveness than degree of sulfonation, with the greatest mitigation of calcium sulfate precipitation observed for antiscalants of molar mass 2000 to 2500 g.mol-1 regardless of sulfonate content. Antiscalants of molar mass 4500 to 5000 g.mol-1 showed a higher threshold effect than antiscalants of molar mass 7000 to 9500 g.mol-1, with a 30% sulfonated polymer of molar mass 4500 g.mol-1 performing appreciably better than other polymers of a similar molar mass.

Vitrimer-like elastomers with rapid stress-relaxation by high-speed carboxy exchange through conjugate substitution reaction

We report vitrimer-like elastomers that exhibit significantly fast stress relaxation using carboxy exchange via the conjugate substitution reaction of α-(acyloxymethyl) acrylate skeletons. This network design is inspired by a small-molecule model that shows the carboxy exchange reaction even at ambient temperature in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO). The acrylate and acrylic acid copolymers are cross-linked using bis[α-(bromomethyl)acrylates] and doped with 10 wt% DABCO, exhibiting processability to obtain a transparent film by hot pressing. The high-speed bond exchange in the network, validated by stress-relaxation tests, allows quick molding with household iron. In addition, the material is applied as an adhesion sheet for plastic and metal substrates. Because dynamic cross-linking with the proposed bond exchange mechanism can be implemented for any polymer bearing carboxyl pendants, our approach can be applied to versatile backbones, which must thus be meaningful in the practical sense.

Highly Conductive and Uniform PEDOT on Poly(acrylic acid-vinylbenzyl chloride) Functionalized Surfaces

This study demonstrates increasing the uniformity and conductivity of poly(3,4-ethylene dioxythiophene) (PEDOT) thin films synthesized by vapor phase polymerization (VPP) through the utilization of a thin interfacial prime layer on the substrate surface. The prime layer, which is a copolymer of acrylic acid (AA) and vinylbenzyl chloride (VBC), was coated on the substrate surface using initiated chemical vapor deposition (iCVD) method. FTIR and XPS were used to analyze the structure of as-deposited films. The use of P(AA-VBC) copolymer as a prime layer allowed uniform and complete coverage of the oxidant solution on the substrate surface due to the hydrophilic nature of the AA constituent. During the VPP, the existence of the chlorine ions originating from the VBC constituent allowed in-situ doping of the as-deposited polymer, which contributes to the increased uniformity and the conductivity. The experimental studies were carried out to show the increase in uniformity, conductivity and adherence of the as-deposited PEDOT film in the presence of the prime layer. There was nearly a 4-fold increase in the conductivity of as-deposited PEDOT in the presence of the prime layer, with measured conductivity uniformity as high as 96% over a 5×5 cm2 glass surface.

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.

Sorption of non‐ferrous metal ions from aqueous solutions by polymer compositions based on polyacrylic acid and bentonite clay

AbstractComposite hydrogels (CH) were obtained by copolymerization of acrylic acid with N,N‐methylene‐bis‐acrylamide in the suspension of bentonite clay (BC) by the method “in situ.” At this CH of cross‐linking structure was formed in which, in the space between parts of polymer hydrogels (PH) on the base of polyacrylic acid (PAAc), were introduced particles of mineral. The morphology and structure of CH have been investigated by scanning electron microscopy, which has shown that particles of BC are distributed throughout the whole volume of the composite. The sorption of Cu2+, Ni2+, and Cr3+ ions from aqueous solutions of their salts by sorbents using the spectrophotometric method was studied. It has been determined that the introduction of BC particles into the composition of PH leads to a noticeable increase in their sorption capacity. Determination of the elemental analysis of the composition of sorbents after sorption by X‐ray fluorescence analysis showed that the sorption of non‐ferrous metal ions increases in the row Cr3+ < Ni2+ < Cu2+.

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.

PH‐responsive bionanocomposite pectin grafted with dimethylaminoethyl methacrylate and acrylic acid copolymer along with silver nanoparticles for breast cancer drug delivery

AbstractIn this study, we developed a pH‐responsive hydrogel membrane composed of pectin, dimethylaminoethyl methacrylate (DMAEMA), and acrylic acid (AA) through a free radical‐triggered graft copolymerization method. Freshly formed silver nanoparticles (AgNPs) produced from the reduction reaction were embedded in the produced hydrogel. Pectin‐grafted dimethylaminoethyl methacrylate and acrylic acid copolymer [poly (DMAEMA‐co‐AA)‐g‐pectin] and its bionanocomposite with AgNPs were confirmed by Fourier‐transform infrared spectroscopy (FT‐IR), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). The swelling behavior of poly (DMAEMA‐co‐AA)‐g‐pectin in solutions with diverse pH values was assessed. For use as a controlled drug delivery agent, the hydrogel was loaded with 5‐fluorouracil (5‐FU). The incorporation of AgNPs had a great impact on the entrapment efficiency of 5‐FU. At pH 7.4, nearly 48% of the 5‐FU was released in vitro from the polymeric nanocomposite within 24 h. Moreover, poly (DMAEMA‐co‐AA)‐g‐pectin and poly (DMAEMA‐co‐AA)‐g‐pectin/AgNPs presented high cytocompatibility toward normal skin fibroblast cells (BJ1), and the drug delivery system strongly inhibited human Caucasian breast adenocarcinoma cells (MCF‐7). These results demonstrated that these poly (DMAEMA‐co‐AA)‐g‐pectin/AgNPs are an excellent candidate for use in anticancer drug delivery systems.Highlights Free radical polymerization of nanocomposites incorporated with nanoparticles. Nanoparticles improve the bionanocomposites' drug loading. The developed bionanocomposites exhibit control drug release. The novel bionanocomposites acts as an excellent anticancer drug carrier.

Phase boundaries and copolymerization of acrylic acid + butyl methacrylate in supercritical carbon dioxide under high-pressure single-fluid initiation

Associative polymers based on acrylic acid and n-butyl methacrylate were synthesized via precipitation polymerization in pressurized carbon dioxide. Physicochemical characterization confirmed BMA incorporation and good reaction yields (>67.1 mol%). Size exclusion chromatography showed bimodal polymer molar mass distribution with distinct average molar masses. Rheological properties of aqueous polymer solutions were assessed under varying pH, ionic strength, and salt concentrations and demonstrated increased viscosity with higher n-butyl methacrylate content, attributed to hydrophobic associations. The apparent viscosity of the synthesized polymers was strongly influenced by the ionic strength of the aqueous solutions.

Heparin-modified polyether ether ketone hollow fiber membrane with improved hemocompatibility and air permeability used for extracorporeal membrane oxygenation

To expand the selection of raw material for fabricating extracorporeal membrane oxygenation (ECMO) and promote its application in lung disease therapy, polyether ether ketone hollow fiber membrane (PEEK-HFM) with designable pore characteristics, desired mechanical performances, and excellent biocompatibility was selected as the potential substitute for existing poly (4-methyl-1-pentene) hollow fiber membrane (PMP-HFM). To address the platelet adhesion and plasma leakage issues with PEEK-HFM, a natural anticoagulant heparin was grafted onto the surface using ultraviolet irradiation. Additionally, to explore the substitutability of the heparin layer while considering cost and scalability, a heparin-like layer composed of copolymers of acrylic acid and sodium p-styrenesulfonate was also constructed on the surface of PEEK-HFM Even though the successful grafting of heparin and heparin-like layers on the PEEK-HFM surface reduced the pore parameters, improvements in surface hydrophilicity also prevented the platelet-adhesion phenomenon and improved the anticoagulant behaviour, making it a viable alternative for commercial PMP-HFMs in ECMO production. Furthermore heparin-modified and heparin-like modified PEEK-HFMs demonstrated similar performance, indicating that synthetic layers can effectively replace natural heparin. This study holds practical and instructive significance for future research and the application of membranes in the development of oxygenators.

Interfacial Wrinkling Structures Based on a Double Cross-Linking Strategy Enable a Dual-Mode Optical Information Encryption.

Surface wrinkling structures based on a bilayer system are widely employed in storing and encrypting specific optical information. However, constructing a stable wrinkling structure with high-level security remains an extensive challenge due to the delamination issue between the skin layer and the substrate. Herein, a double cross-linking strategy is introduced between a hydrogel layer doped with fluorescent molecules and polydimethylsiloxane to establish a stable interfacial wrinkling structure with dual-mode functionality, in which the light reflection of the wrinkles and fluorescence intensity of fluorescent molecules can be simultaneously regulated by the modulus ratio between the two layers. The spontaneous wrinkling structures with a physically unclonable function can enhance the photoluminescence emission intensity of the wrinkling area under ultraviolet radiation. Meanwhile, the skin layer constructed of acrylamide and acrylic acid copolymer protects the interfacial wrinkling patterns from the loss of a detailed structure for authentication due to external damage. The stable interfacial wrinkling structures with fluorescence can find potential applications in the fields of information storage and encryption.

Hydrophobic Dendritic Modification of a Poly(acrylamide-co-acrylic Acid) Copolymer with Behera′s Amine as Viscous Agent

Hydrophobic Dendritic Modification of a <i>Poly</i>(acrylamide<i>-co-</i>acrylic Acid) Copolymer with Behera′s Amine as Viscous Agent

Highly effective removal of basic fuchsin dye using carboxymethyl konjac glucomannan grafted acrylic acid-acrylamide/montmorillonite composite hydrogel

This study developed a nanocomposite hydrogel, CAM4-MMT, for efficiently removing basic fuchsin dye from water. The hydrogel was prepared by grafting a copolymer of acrylic acid (AA) and acrylamide (AM) onto carboxymethyl konjac glucomannan (CMKGM), and doped with montmorillonite (MMT), exhibited excellent thermal stability, a porous inner structure, large specific surface area (1.407 m2/g), and high swelling capacity (107.3 g/g). The hydrogel achieved a maximum adsorption capacity of 694.1 mg/g and a removal rate of 99.5 %. The Langmuir isotherm and pseudo-second-order kinetic model best described the adsorption process. Regeneration and reuse tests confirmed that the hydrogel has excellent recyclability. In conclusion, the CAM4-MMT composite hydrogel efficiently removed basic fuchsin from water solutions, offering a new scheme for eliminating basic fuchsin using natural polysaccharides with promising applications.

Enhancing asphalt-based waterproof materials for building cement substrates: Modifications, construction, and weathering resistance

Three distinct systems of asphalt-based waterproof material structures were designed for building cement substrates. These asphalt-based waterproof materials were modified using either Styrene Butadiene Rubber (SBR) or Ethylene Acrylic Acid Copolymer (EAA) along with various inorganic fillers. To enhance the adhesion between the waterproof materials and the cement substrate, the surface of the cement substrate was chemically treated with either γ-methacryloyloxypropyltrimethoxy silane (KH-570) or vinyltrimethoxy silane (SG-Si 171) through atomization spraying and infrared irradiation. The adhesion properties and debonding failure modes of waterproof materials for cement substrates were analyzed, and six groups of samples with relatively good adhesion properties were screened for further environmental aging tests. The samples were subjected to temperature fluctuations, water immersion, freeze-thaw cycles, thermal aging, acid, alkali, and salt, to identify favorable asphalt-based waterproof structure systems for five climate zones, acid rain-affected regions, and saline-alkali-affected regions in China. These results provide valuable insights for designing effective waterproof materials for different environments.

Development, Characterization, and Evaluation of Potential Systemic Toxicity of a Novel Oral Melatonin Formulation.

The need to create safe materials for biomedical and pharmaceutical applications has become a significant driving force for the development of new systems. Therefore, a chitosan-coated copolymer of itaconic acid, acrylic acid, and N-vinyl caprolactam (IT-AA-NVC) was prepared by radical polymerization and subsequent coating via nanoprecipitation to give a system capable of sustained delivery of melatonin. Although melatonin brings undoubted benefits to the human body, aspects of the optimal dose, route, and time of administration for the obtaining of suitable treatment outcomes remain under discussion. The entrapment of melatonin in biocompatible polymeric systems can prevent its oxidation, decrease its toxicity, and provide an increased half-life, resulting in an enhanced pharmacokinetic profile with improved patient compliance. The structures of the biopolymer and conjugate were proven by FTIR, thermal properties were tested by DSC, and the morphologies were followed by SEM. The loading efficiency and in vitro release profile were studied by means of HPLC, and a delayed release profile with an initial burst was obtained. The potential systemic toxicity of the formulation was studied in vivo; a mild hepatotoxicity was observed following administration of the melatonin-loaded formulation to mice, both by histopathology and blood clinical biochemistry. Histopathology showed a mild nephrotoxicity as well; however, kidney clinical biochemistry did not support this.

Synthesis and Performance Evaluation of Modified Polyaspartic-Acid-Based Scale Inhibitor

This paper focuses on the selection and application of scale inhibitor by studying the problem of pipeline scaling in geothermal well development. Adding scale inhibitor can effectively reduce the treatment cost and achieve a good scale resistance effect, but the commonly used polyaspartic acid scale inhibitor has problems such as poor scale inhibition effect and large use limitations. Therefore, a new modified polyaspartic acid scale inhibitor (His-Tyr-SA-PASP) was prepared using polysuccinimide (PSI) as the raw material and histidine (His), tyrosine (Tyr), and sulfonic acid (SA) as the modification reagent. When the dosage of His-Tyr-SA-PASP was 8 mg/L, the scale inhibition rate of CaCO3 was 94.40%. In addition, the scale inhibition effect of His-Tyr-SA-PASP on CaCO3 was better than that of PASP. At the same time, under the condition of a static experiment at 75 °C, according to the ion concentration of water samples in different scale zones, this paper also identified the ratio of four composite scale inhibitors. When the dosage of compound scale inhibitor was 100 mg/L, Sodium of Polyaspartic Acid–Diethylene Triamine Penta (Methylene Phosphonic Acid)–2-Phosphonobutane-1,2,4-Tricarboxylic Acid–Amino Trimethylene Phosphonic Acid–Copolymer of Maleic and Acrylic Acid = (10:10:5:1:9), (15:10:5:2.5:2.5), (12.5:5:10:1:6.5), and (15:5:10:4:1) and the scale inhibition rate was more than 95%. Under the condition of a dynamic experiment, the optimized composite scale inhibitor still showed a scale inhibition rate of more than 90%. It provides a useful reference for the practical application of water treatment in geothermal wells and has the prospect of industrial application.

Facile construction of pH-responsive graphene oxide-based aerogel and its efficient and selective adsorption performance toward methylene blue

In regard to serious environmental pollution by methylene blue (MB) dye, it was crucial to design an efficacious adsorbent for the elimination of MB. Utilizing tannic acid (TA) to functionalize graphene oxide (GO) and employing acrylic acid (AA) and sodium p-styrenesulfonate (SSS) as the monomers, a pH-responsive TGO/P(SSS-co-AA) aerogel (where TGO represented TA-modified GO, and P(SSS-co-AA) denoted the copolymer of SSS and AA) was synthesized by a facile and green one-pot method. The resulting aerogel was subjected to a variety of characterizations, and its adsorption behaviors were systematically explored with MB as the model dye. The results indicated the pH-responsive TGO/P(SSS-co-AA) aerogel possessed the maximum theoretical adsorption capacity of 1782.5 mg/g, and the adsorption process could be accurately described by quasi-second order kinetics model and Langmuir model. The adsorption thermodynamics revealed that the adsorption was a spontaneous, endothermic, and entropy-increasing process. TGO/P(SSS-co-AA) aerogel exhibited highly selective adsorption property and excellent regeneration performance. Even following five regeneration cycles, adsorption capacity of the aerogel could still maintain 936.09 mg/g. In conclusion, TGO/P(SSS-co-AA) aerogel exhibited exceptional performance as an adsorbent for removing MB, providing an inspiration for the construction of GO-based composite aerogel and its actual application in efficient and selective wastewater treatment.

Smart versatile hydrogels tailored by metal-phenolic coordinating carbon and polypyrrole for soft actuation, strain sensing and writing recognition

Biomimetic intelligent conductive hydrogels integrating flexibility, signal sensing, and contactless actuation has become ideal candidates for the production of electronic skins, wearable devices, and soft robotics. However, the development of multifunctional smart hydrogels capable of both sensing and actuating simultaneously to enhance intelligent interaction interfaces remains a significant challenge. Herein, a multifunctional hydrogel composite with integrated sensing and actuating capabilities is proposed through the incorporation of Fe3+-tannic acid (TA) coordination compound-coated carbon nanotubes (Fe-TA@SWNT) and the in-situ formation of conductive polymer polypyrrole (PPy) inside the hydrogel networks composed of carboxymethylcellulose (CMC) and a copolymer of acrylic acid (AA) and [2-(methacryloyloxy) ethyl]dimethyl-(3-sulfopropyl) ammonium hydroxide (SBMA). Benefiting from multiple effective dynamic interactions within the internal matrix, the prepared hydrogel exhibits excellent stretchability (1283.42 % elongation) and toughness (1.11 MJ/m3). Additionally, the catechol groups carried by Fe-TA@SWNT, along with the zwitterionic monomer SBMA, provide the hydrogel with repeatable self-adhesion performance. Based on the outstanding photothermal effect of Fe-TA@SWNT and PPy, the hydrogel demonstrates reversible and stable photothermal responsiveness, exhibiting exceptional actuation performance under near-infrared (NIR) radiation. As a strain sensor, the hydrogel shows excellent sensitivity (GF = 3.32), rapid response time, and reliable stability, enabling precise monitoring of various physiological signals in the human body, including joint movements, facial expressions, and heartbeats. Therefore, this work significantly expands the application prospects of multifunctional smart hydrogels in fields of wearable electronics, soft robotics, and remote light-controlled devices.

Features of Synthesis of Graft Copolymers of Chitosan and Acrylic Acid

Features of Synthesis of Graft Copolymers of Chitosan and Acrylic Acid

The Improved Antigen Uptake and Presentation of Dendritic Cells Using Cell-Penetrating D-octaarginine-Linked PNVA-co-AA as a Novel Dendritic Cell-Based Vaccine.

Cancer immunotherapy using antigen-pulsed dendritic cells can induce strong cellular immune responses by priming cytotoxic T lymphocytes. In this study, we pulsed tumor cell lysates with VP-R8, a cell-penetrating D-octaarginine-linked co-polymer of N-vinylacetamide and acrylic acid (PNVA-co-AA), into the DC2.4 murine dendritic cell line to improve antigen uptake and then determined the anti-tumor effect in tumor-bearing mice. DC2.4 cells were pulsed with the cell lysate of EL4, a murine lymphoma cell line, and VP-R8 to generate the DC2.4 vaccine. For the in vivo study, DC2.4 cells pulsed with EL4 lysate and VP-R8 were subcutaneously injected into the inguinal lymph node to investigate the anti-tumor effect against EL4 and EL4-specific T cell immune responses. VP-R8 significantly improved antigen uptake into DC2.4 compared to conventional keyhole limpet hemocyanin (p < 0.05). The expression of MHC class I, MHC class II, and CD86 in DC2.4 cells significantly increased after pulsing tumor lysates with VP-R8 compared to other treatments (p < 0.05). The intra-lymph node injection of DC2.4 pulsed with both VP-R8 and EL4 lysate significantly decreased tumor growth compared to DC2.4 pulsed with KLH and lysates (p < 0.05) and induced tumor-infiltrating CD8T cells. The DC2.4 vaccine also remarkably increased the population of IFN-gamma-producing T cells and CTL activity against EL4 cells. In conclusion, we demonstrated that VP-R8 markedly enhances the efficiency of dendritic cell-based vaccines in priming robust anti-tumor immunity, suggesting its potential as a beneficial additive for dendritic cell-based immunotherapy.