Dendritic Polymers Research Articles

Stimuli-responsive rotaxane-branched dendronized polymers with tunable thermal and rheological properties

Aiming at the creation of polymers with attractive dynamic properties, herein, rotaxane-branched dendronized polymers (DPs) with rotaxane-branched dendrons attached onto the polymer chains are proposed. Starting from macromonomers with both rotaxane-branched dendrons and polymerization site, targeted rotaxane-branched DPs are successfully synthesized through ring-opening metathesis polymerization (ROMP). Interestingly, due to the existence of multiple switchable [2]rotaxane branches within the attached dendrons, anion-induced reversible thickness modulation of the resultant rotaxane-branched DPs is achieved, which further lead to tunable thermal and rheological properties, making them attractive platform for the construction of smart polymeric materials.

Hyperbranched Polymers: Recent Advances in Photodynamic Therapy against Cancer.

Hyperbranched polymers are a class of three-dimensional dendritic polymers with highly branched architectures. Their unique structural features endow them with promising physical and chemical properties, such as abundant surface functional groups, intramolecular cavities, and low viscosity. Therefore, hyperbranched-polymer-constructed cargo delivery carriers have drawn increasing interest and are being utilized in many biomedical applications. When applied for photodynamic therapy, photosensitizers are encapsulated in or covalently incorporated into hyperbranched polymers to improve their solubility, stability, and targeting efficiency and promote the therapeutic efficacy. This review will focus on the state-of-the-art studies concerning recent progress in hyperbranched-polymer-fabricated phototherapeutic nanomaterials with emphases on the building-block structures, synthetic strategies, and their combination with the codelivered diagnostics and synergistic therapeutics. We expect to bring our demonstration to the field to increase the understanding of the structure-property relationships and promote the further development of advanced photodynamic-therapy nanosystems.

Synthesis of dendritic urethane acrylates for fabricating a robust honeycomb-like structure acting for SERS detection

In this study, novel dendritic urethane acrylate polymers were developed for the fabrication of robust honeycomb-like surfaces after exposure to a UV-crosslinking process. Through iterative synthesis based on a highly selective intermediate of 4-isocyanate-4′-(3,3-dimethyl-2,4-dioxo-azetidine)-diphenylmethane, poly(urea/malonamide) dendrons bearing peripheral methyl methacrylate end groups with well-defined structures were realized. A coating solution was prepared by the combined use of 30–70 wt% UA dendron acting as dendritic diluents and dendritic UA copolymers acting as amphiphiles that can fabricate honeycomb-like surfaces via a breath figure self-assembly process using water droplets as templates. The resulting film can be cured under UV light to achieve a robust honeycomb-like structure with a hexagonal structure exhibiting solvent-resistant properties in ethanol. Consequently, this solvent-resistant porous array can act as a substrate for the detection of vanishingly low concentrations of analytes that are aqueous insoluble via surface-enhanced Raman scattering analysis.

Construction of dendritic polymers on carbon fiber surfaces to improve the interfacial bonding of carbon fiber/silicone rubber composites

Carbon fiber (CF) reinforced composite materials are highly sought after for their exceptional mechanical properties and functional capabilities, making them promising materials for applications in aerospace and other industries. In this study, we aimed to construct a medium modulus interfacial layer using the layer-by-layer construction (LBL) method. This was achieved by grafting rigid dendritic polymers onto the surface of the carbon fiber, with the branch density being adjustable based on the reaction time. The rigid branched structure of the dendritic polymer and the numerous functional groups provide physical entanglement and stronger mechanical bonding at the interface, great chemical bonding. This distinctive structure improves the interfacial compatibility of the composite and enhances its mechanical properties. Following treatment, the tensile properties of the fibres are increased by approximately 20 %, suggesting that the treatment process effectively repairs surface defects on the fiber. Compared to untreated carbon fiber composites, the tensile properties of CF-M-P3 have improved by approximately 11 %. Furthermore, the thermal weight loss of the composite material is significantly reduced due to the branching of its rigid dendritic structure. The weight loss percentage decreased from 16.84 % to 7.89 % after being held at a temperature of 350 °C for a duration of 4 h.

Dendritic Solid Polymer Electrolytes: A New Paradigm for High-Performance Lithium-Based Batteries.

Li-ions battery is widely used and recognized, but its energy density based on organic electrolytes has approached the theoretical upper limit, while the use of organic electrolytes also brings some safety hazards (leakage and flammability). Polymer electrolytes (PEs) are expected to fundamentally solve the safety problem and improve energy density. Therefore, Li-ions battery based on solid PE has become a research hotspot in recent years. However, low ionic conductivity and poor mechanical properties, as well as a narrow electrochemical window limit its further development. Dendritic PEs with unique topology structure has low crystallinity, high segmental mobility, and reduced chain entanglement, providing a new avenue for designing high-performance PEs. In this review, the basic concept and synthetic chemistry of dendritic polymers are first introduced. Then, this story will turn to how to balance the mechanical properties, ionic conductivity, and electrochemical stability of dendritic PEs from synthetic chemistry. In addition, accomplishments on dendritic PEs based on different synthesis strategies and recent advances in battery applications are summarized and discussed. Subsequently, the ionic transport mechanism and interfacial interaction are deeply analyzed. In the end, the challenges and prospects are outlined to promote further development in this booming field.

Magnetic Dendritic Polymer Nanospheres for High-Performance Separation of Histidine-Rich Proteins.

Magnetic nanospheres are becoming a promising platform for a wide range of applications in pharmacy, life science, and immunodiagnostics due to their high surface area, ease of synthesis and manipulation, fast separation, good biocompatibility, and recyclable performance. In this work, an innovative and efficient method is developed by in situ reducing and growing Ni(OH)2 for the preparation of dendritic mesoporous nanocomposites of silica@Fe3O4/tannic acid@nickel hydroxide (dSiO2@Fe3O4/TA@Ni(OH)2). The flower-like nanospheres have good magnetic response, large surface area, and high histidine-rich protein (His-protein) purification performance. The dSiO2@Fe3O4/TA@Ni(OH)2 nanospheres were synthesized on the basis of a φ(NaSal/CTAB) of 1/1 and a mass of ferrous chloride tetrahydrate of 0.3 g, resulting in a saturation magnetization value of 48.21 emu/g, which means it can be collected within ∼1 min using a magnetic stand. Also, the BET test showed that the surface area is 92.47 m2/g and the pore size is ∼3.9 nm for dSiO2@Fe3O4/TA@Ni(OH)2 nanocomposites. Notably, the nickel hydroxide with unique flower-like structural features enables the combination of a large number of Ni2+ ions and His-proteins for high performance. The isolation and purification experiments of the synthesized dSiO2@Fe3O4/TA@Ni(OH)2 were performed by separating His-proteins from a matrix composed of bovine hemoglobin (BHb), bovine serum albumin (BSA), and lysozyme (LYZ). The result showed that the nanospheres have a high combination capacity of ∼1880 mg/g in a rapid equilibrium time of 20 min, which was selective for the adsorption of BHb. In addition, the stability and recyclability of BHb are 80% after seven cycles. Furthermore, the nanospheres were also used to isolate His-proteins from fetal bovine serum, proving its utility. Therefore, the strategy of separating and purifying His-proteins using dSiO2@Fe3O4/TA@Ni(OH)2 nanospheres is promising for practical applications.

A conductometric enzymatic methanol sensor based on polystyrene - PAMAM dendritic polymer electrospun nanofibers

Methanol (MeOH) is a solvent and cleaning agent used in industry, but it is poisonous when ingested. The recommended release threshold for MeOH vapor is 200 ppm. We present a novel sensitive micro-conductometric MeOH biosensor created by grafting alcohol oxidase (AOX) onto electrospun polystyrene-poly(amidoamine) dendritic polymer blend nanofibers (PS-PAMAM-ESNFs) on interdigitated electrodes (IDEs). The analytical performance of the MeOH microsensor was evaluated using gaseous MeOH, ethanol, and acetone samples collected from the headspace above aqueous solution with known concentration. The sensor's response time (tRes) fluctuates from 13 s to 35 s from lower to higher concentrations. The conductometric sensor has a sensitivity of 150.53 μS.cm-1 (v/v) for MeOH and a detection limit of 100 ppm in the gas phase. The MeOH sensor is 7.3 times less sensitive to ethanol and 136.8 times less sensitive to acetone. The sensor was verified for detecting MeOH in commercial rubbing alcohol samples.

Structural modeling and topological characterization of three kinds of dendrimer networks.

Dendrimers, also known as dendritic polymers, have various applications due to their unique properties, such as their monodisperse structure and their ability to be synthesized with precise control over their size, shape, and surface functionality. Dendrimers are used in drug delivery systems to improve drug solubility, bioavailability, and targeting. They can carry drugs to specific sites, such as cancer cells, and release them in a controlled manner, reducing side effects. Dendrimers can be used as gene delivery vehicles to deliver genetic material to cells in a controlled and targeted manner. Mathematical chemistry is useful to model chemical reactions and predict the behavior of chemical systems. It provides a quantitative understanding of chemical phenomena, which can aid in the design of new molecules and materials. It is used to develop molecular descriptors, which are mathematical representations of molecular structures that can be used to quantify the properties of molecules. These descriptors can be useful in structure-activity relationship studies to predict the biological activity of compounds. The topological descriptors are parameters of any molecular structure that gives a mathematical formula to model such molecular structures. In the current study, our concern is to calculate some useful topological indices for three kinds of dendrimer networks and derive closed mathematical formulas for them. The comparisons of these calculated topological indices are also investigated. Our obtained results will be helpful in investigating QSPRs/QSARs of such molecules in many fields of science, such as chemistry, physics and biochemistry. The dendrimer structure (left). From first (G0) to third (G3) generation, the dendrimer's increasing generations are shown schematically (right).

Self-Assembly of a Linear-Dendritic Polymer Containing Cisplatin and Norcantharidin into Raspberry-like Multimicelle Clusters for the Efficient Chemotherapy of Liver Cancer.

Combination chemotherapy has been proved to be an effective strategy in the clinic, and nanoformulations have drawn much attention in the field of drug delivery. However, conventional nanocarriers suffer from shortcomings such as inefficient coloading and undesired molar ratios of the combined drugs, preleakage of cargos during systemic circulation, and lack of cancer-selective drug release. To achieve tumor-specific codelivery of cisplatin (CDDP) and norcantharidin (NCTD) for synergistic treatment of liver cancer, a novel linear-dendritic polymer, termed as G1(PPDC)x, was designed and synthesized, where a prodrug consisting of cisplatin (CDDP) and norcantharidin (NCTD) was conjugated to PEG2000 via ester bonds to fabricate linear polymer-drug conjugates, and the conjugates were subsequently grafted to the terminal hydroxyls of a dendritic polycarbonate core. Benefiting from the hydrogen bond interactions, G1(PPDC)x could spontaneously self-assemble into a unique type of raspberry-like multimicelle clusters in solution (G1(PPDC)x-PMs). G1(PPDC)x-PMs possessed an optimal synergistic ratio of CDDP and NCTD, without obvious premature release or disassembly in biological environments. Intriguingly, upon extravasation into the interstitial tumor tissues, G1(PPDC)x-PMs (132 nm in diameter) could disassemble and reassemble into smaller micelles (40 nm in diameter) in response to the mildly acidic tumor microenvironment, which would enhance the deep tumor penetration and cellular accumulation of drugs. In vivo delivery of G1(PPDC)x-PMs led to a significantly prolonged blood circulation half-life, which is beneficial to achieve sufficient tumor accumulation through the enhanced permeability and retention (EPR) effect. G1(PPDC)x-PMs displayed the best antitumor activity in H22 tumor-bearing mice with a tumor inhibition rate of 78.87%. Meanwhile, G1(PPDC)x-PMs alleviated both myelosuppression toxicities of CDDP and vascular irritation of NCTD. Our results demonstrated that G1(PPDC)x-PMs could serve as an effective drug delivery system for codelivery of CDDP and NCTD to treat liver cancer efficiently.

Thiol-End-Group Dendrons Decorated with Gold Nanoparticles Immobilized on Amino-Functionalized Graphene Oxide for SERS Detection

Surface-enhanced Raman scattering (SERS) has abundant chemical fingerprint information to analyze complex analytes under aqueous conditions. However, SERS requires uniform metal particles to generate a hotspot effect and improve sensitivity and enhancement by localized surface plasmon resonance. Therefore, in this study, SERS detection chips have been developed using uniform gold nanoparticle (AuNP) arrays embedded on thiol-end-group dendritic polymers immobilized on amino-functionalized graphene oxide (AGO) thin films of transmission electron microscopy (TEM) grids. The graphene oxide (GO) thin film was fabricated by low-damage plasma with mixed gas (O2/H2) and then further functionalized by diethylenetriamine to form AGO substrates. Based on the efficient building block of dual-functional 4-isocyanato-4′-(3,3-dimethyl-2,4-dioxo-azetidino)-diphenylmethane (IDD), the 0.5 and 1.5 generations of thiol-end-functionalized poly(urea/malonamide) dendrons (DG0.5-SH and DG1.5-SH) were precisely synthesized and grafted onto AGO substrates. The interparticle gap of AuNPs could be well controlled and decorated on these thiol-end-group dendrons to achieve the optimal SERS enhancement effect by manipulating the sizes of AuNPs and generating dendrons. The results indicate that 31 nm AuNPs immobilized on the DG0.5-SH@AGO substrate exhibited reproducible and strong SERS enhancement compared with free AuNPs. Graphene-based SERS substrates provide rapid and stable SERS detection in solutions, which offers great potential for practical applications in detecting biomolecules and environmental pollutants.

Dendritic Polymers in Tissue Engineering: Contributions of PAMAM, PPI PEG and PEI to Injury Restoration and Bioactive Scaffold Evolution.

The capability of radially polymerized bio-dendrimers and hyperbranched polymers for medical applications is well established. Perhaps the most important implementations are those that involve interactions with the regenerative mechanisms of cells. In general, they are non-toxic or exhibit very low toxicity. Thus, they allow unhindered and, in many cases, faster cell proliferation, a property that renders them ideal materials for tissue engineering scaffolds. Their resemblance to proteins permits the synthesis of derivatives that mimic collagen and elastin or are capable of biomimetic hydroxy apatite production. Due to their distinctive architecture (core, internal branches, terminal groups), dendritic polymers may play many roles. The internal cavities may host cell differentiation genes and antimicrobial protection drugs. Suitable terminal groups may modify the surface chemistry of cells and modulate the external membrane charge promoting cell adhesion and tissue assembly. They may also induce polymer cross-linking for healing implementation in the eyes, skin, and internal organ wounds. The review highlights all the different categories of hard and soft tissues that may be remediated with their contribution. The reader will also be exposed to the incorporation of methods for establishment of biomaterials, functionalization strategies, and the synthetic paths for organizing assemblies from biocompatible building blocks and natural metabolites.

Design, synthesis and performance control of dendritic fluorescent liquid crystal polymers with aggregation-induced emission properties

A series of dendritic fluorescent liquid crystal polymers, in which the tetraphenylethylene was linked to the styrene main-chain via flexible spacer with different lengths: poly{3,4,5-tri{[2-(4-oxytetraphenylethylene)-alkoxy]styrene} (denoted as 3P-n, n stands for the length of alkyl spacer and n = 2, 4, 6, 8, 10) were rationally designed and synthesized. The self-assembly behaviors and photophysical properties of 3P-n were investigated in detail by a combination of techniques including differential scanning calorimetry (DSC), polarizing optical microscopy (POM), small-angle X-ray scattering (SAXS), UV–vis absorption spectra (UV–vis spectra) and photoluminescence spectra (PL spectra). Because of the “space volume effect” of side groups and the aggregation-induced emission characteristics of tetraphenylethylene molecule, all of 3P-n are liquid crystal materials with excellent solid-state fluorescence emission performance. Moreover, the self-assembly behaviors and solid-state fluorescence emission efficiency of 3P-n could be effectively regulated by adjusting the flexible spacer length. On one hand, 3P-n could self-assemble into stable columnar nematic phase before decomposition when the flexible spacer was shorter (n = 2, 4, 6, 8). And when the flexible spacer increased to 10, 3P-10 was isotropic at low temperature and formed hexagonal columnar phase at high temperatures, showing typical phase reentrant properties. And the other, the flexible spacer length also made a significant influence on the solid-state fluorescence emission capacity of 3P-n. The solid fluorescence quantum yield of 3P-n first increased with the growth of flexible spacer length (n < 6), and then the solid fluorescence quantum yield of 3P-n would remain unchanged when the flexible spacer increased to a certain length (n≥6).

Redox-active, porous pyrene tetraone dendritic polymers as cathode materials for lithium-ion batteries

Redox active, insoluble pyrene tetraone based dendritic porous polymers were synthesized by using different catalyst loadings and work-up procedures.

Shaping the Future of Macromolecular Chemistry: A Successful Path from the Start

Shaping the Future of Macromolecular Chemistry: A Successful Path from the Start

Dendritic systems for bacterial outer membrane disruption as a method of overcoming bacterial multidrug resistance.

The alarming rise of multi-drug resistant microorganisms has increased the need for new approaches through the development of innovative agents that are capable of attaching to the outer layers of bacteria and causing permanent damage by penetrating the bacterial outer membrane. The permeability (disruption) of the outer membrane of Gram-negative bacteria is now considered to be one of the main ways to overcome multidrug resistance in bacteria. Natural and synthetic permeabilizers such as AMPs and dendritic systems seem promising. However, due to their advantages in terms of biocompatibility, antimicrobial capacity, and wide possibilities for modification and synthesis, highly branched polymers and dendritic systems have gained much more interest in recent years. Various forms of arrangement, and structure of the skeleton, give dendritic systems versatile applications, especially the possibility of attaching other ligands to their surface. This review will focus on the mechanisms used by different types of dendritic polymers, and their complexes with macromolecules to enhance their antimicrobial effect, and to permeabilize the bacterial outer membrane. In addition, future challenges and potential prospects are illustrated in the hope of accelerating the advancement of nanomedicine in the fight against resistant pathogens.

Dendritic magnetic polymeric core-shell and cobalt-wastewater as an efficient peroxymonosulfate activator for degradation of tetracycline antibiotic and methylene blue dye

The residue of antibiotic and carcinogenic dyes in the industrially polluted water has led to increased antibiotic-resistant bacteria, harm to human health, and damage to health-beneficial healthy bacteria, hence, needs to be adequately treated. For this purpose, we prepared and fully identified a series of novel dendritic polymer shelled magnetic beads with generation 2.5 & 1.5 (PSMB-(G2.5/1.5)@Co+2 DPs) with excellent chemical/mechanical strength that can in one sweep recover valuable cobalt ions from hazardous industrial wastewater. In the following, the degradation studies of methylene blue (MB) dye, and tetracycline (TC) antibiotics from effluent, natural saline irrigation water & pharmaceutical wastewater were analyzed by UV–vis spectroscopy and TOC (total organic carbon) measurement. In the following, an understanding of its vital principles and relationship of degradation efficiency with structural, and environmental factors, economic study and long-term stability were assessed in detail. The advantages of this process include a simple reaction set-up, excellent efficiency, mild condition reaction (short time process & wide pH and temperature range), environmentally friendliness solubility in polar/nonpolar media, efficient in the presence of organic and/or inorganic compounds and suitability for real environments, and recyclable capability.

An impedimetric immunosensor based on PAMAM decorated electrospun polystyrene fibers for detection of interleukin-10 cytokine

• Polystyrene (PS) fibers were electrospun and modified by air plasma for their further decoration with PAMAM. • The fabricated three-dimensional (3-D) architecture was employed as the transducer in an impedimetric immunosensor. • An LOD of 0.3 ng/mL of AgIL-10 was obtained. • Detecting AgIL-10 in artificial saliva (AS) as a complex medium was likewise satisfactory. Cytokine storms are known as the uncontrolled overproduction of inflammatory cytokines that can be produced by a variety of viral or non-infectious disorders and inflict significant damage to many organs. Interleukin-10 (IL-10) is an anti-inflammatory cytokine, and rapid detection of its levels in serum and saliva is important for many diseases, including severe COVID-19 patients. In this study, Polystyrene (PS) fibers were electrospun over a gold electrode and modified by air plasma to allow their further decoration with polyamidoamine (PAMAM) dendritic polymer for providing many active sites on the fiber surface. The fabricated three-dimensional (3-D) architecture was employed as a platform in an impedimetric immunosensor for the quantitative detection of interleukin-10 cytokine (AgIL-10). Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), contact angle measurements, fluorescence microscopy, UV–vis spectroscopy, and electrochemical methods including cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used to characterized the proposed electrospun fiber-based platform and electrochemical immunosensor. The PAMAM properties increased not only the amperometric response to the ferro/ferri cyanide redox probe, of the modified gold electrode but also the active surface area available for covalently binding of anti-IL-10 capture antibody, resulting in the sensitive detection of AgIL-10 in the concentration range of (1-50 pg/mL) in phosphate buffer saline (PBS) with a limit of detection (LOD) of 1 pg/mL. The immunosensor's performance in detecting AgIL-10 in artificial saliva (AS) as a complex medium was likewise satisfactory. This immunosensor provides a new opportunity for clinical immunoassays thanks to its great sensitivity, selectivity, and stability.

Visible light-regulated cationic polymer coupled with photodynamic inactivation as an effective tool for pathogen and biofilm elimination

BackgroundPathogenic microorganism pollution has been a challenging public safety issue, attracting considerable scientific interest. A more problematic aspect of this phenomenon is that planktonic bacteria exacerbate biofilm formation. There is an overwhelming demand for developing ultra-efficient, anti-drug resistance, and biocompatibility alternatives to eliminate stubborn pathogenic strains and biofilms.ResultsThe present work aims to construct a visible light-induced anti-pathogen agents to ablate biofilms using the complementary merits of ROS and cationic polymers. The photosensitizer chlorin e6-loaded polyethyleneimine-based micelle (Ce6-TPP-PEI) was constructed by an amphiphilic dendritic polymer (TPP-PEI) and physically loaded with photosensitizer chlorin e6. Cationic polymers can promote the interaction between photosensitizer and Gram-negative bacteria, resulting in enhanced targeting of PS and lethality of photodynamic therapy, and remain active for a longer duration to prevent bacterial re-growth when the light is turned off. As expected, an eminent antibacterial effect was observed on the Gram-negative Escherichia coli, which is usually insensitive to photosensitizers. Surprisingly, the cationic polymer and photodynamic combination also exert significant inhibitory and ablative effects on fungi and biofilms. Subsequently, cell hemolysis assessments suggested its good biocompatibility.ConclusionsGiven the above results, the platform developed in this work is an efficient and safe tool for public healthcare and environmental remediation.

Synthesis of Dendronized Polymers on the Au(111) Surface.

Dendronized polymers (DPs) consist of a linear polymeric backbone with dendritic side chains. Fine-tuning of the functional groups in the side chains enriches the structural versatility of the DPs and imparts a variety of novel physical properties. Herein, the first on-surface synthesis of DPs is achieved via the postfunctionalization of polymers on Au(111), in which the surface-confinement-induced planar conformation and chiral configurations were unambiguously characterized. While the dendronized monomer was synthesized in situ on Au(111), the subsequent polymerization afforded only short, cross-linked DP chains owing to multiple side reactions. The postfunctionalization approach selectively produced brominated polyphenylene backbone moieties by the deiodination polymerization of 4-bromo-4″-iodo-5'-(4-iodophenyl)-1,1':3',1″-terphenyl on Au(111), which smoothly underwent divergent cross-coupling reactions with two different isocyanides to form two types of DPs as individual long chains.

Synergistic Activity of Anticancer Polyphenols Embedded in Amphiphilic Dendrimer Nanoparticles

Dendritic polymer nanoparticles (NPs) are promising vehicles for drug delivery. Most dendrimer polymer NPs, however, exhibit positive surface charge which make them, in many instances, cytotoxic. We constructed noncationic, amphiphilic dendrimer NPs embedding curcumin and resveratrol, natural polyphenols exhibiting anticancer properties. The curcumin/resveratrol/dendrimer NPs both effectively shielded the embedded polyphenols and facilitated their slow release and, notably, targeted cancer cells. The experimental data trace the cancer cell toxicity of the curcumin/resveratrol/dendrimer NPs to impairment of mitochondrial functions, specifically giving rise to enhanced intracellular calcium release, inhibition of cytochrome c oxidase enzyme activity, decreased mitochondrial membrane potential, and mitochondrial membrane perturbation. Importantly, synergism between the dendrimer-NP-embedded curcumin and resveratrol was observed, as more pronounced cancer cell death and mitochondrial disruption were induced by the curcumin/resveratrol/dendrimer NPs as compared to either the freely dissolved polyphenols or amphiphilic dendrimer NPs incorporating curcumin or resveratrol separately. This work suggests that amphiphilic dendrimer NPs encapsulating curcumin and resveratrol may constitute a promising anticancer therapeutic platform.