Total Amount Of Monomers Research Articles

Leveraging Janus Substrates as a Confined "Interfacial Reactor" to Synthesize Ultrapermeable Polyamide Nanofilms.

Porous substrates act as open "interfacial reactors" during the synthesis of polyamide composite membranes via interfacial polymerization. However, achieving a thin and dense polyamide nanofilm with high permeance and selectivity is challenging when using a conventional substrate with uniform wettability. To overcome this limitation, we propose the use of Janus porous substrates as confined interfacial reactors to decouple the local monomer concentration from the total monomer amount during interfacial polymerization. By manipulating the location of the hydrophilic/hydrophobic interface in a Janus porous substrate, we can precisely control the monomer solution confined within the hydrophilic layer without compromising its concentration. The hydrophilic surface ensures the uniform distribution of monomers, preventing the formation of defects. By employing Janus substrates fabricated through single-sided deposition of polydopamine/polyethyleneimine, we significantly reduce the thickness of the polyamide nanofilms from 88.4 to 3.8 nm by decreasing the thickness of the hydrophilic layer. This reduction leads to a remarkable enhancement in water permeance from 7.2 to 52.0 l/m2·h·bar while still maintaining ~96% Na2SO4 rejection. The overall performance of this membrane surpasses that of most reported membranes, including state-of-the-art commercial products. The presented strategy is both simple and effective, bringing ultrapermeable polyamide nanofilms one step closer to practical separation applications.

Synthesis and Characterization of Maleic Anhydride-Methyl Methacrylate Co-Monomer Grafted Polyethylene Wax for Hot Waxed Wood Process.

The beeswax used in Chinese traditional hot waxed wood technology has several drawbacks, such as high price, scarce resources, and poor heat resistance. To expand the application of hot waxing technology in the field of wood decoration and protection, polyethylene wax was modified by a grafted maleic anhydride-methyl methacrylate co-monomer. A type of modified polyethylene wax with low cost, high melting point, high stability, and strong polarity suitable for hot waxed wood was prepared as a replacement for beeswax. The effects of the grafting conditions on the chemical properties, thermal properties, chemical structure, and crystallization properties of modified polyethylene wax were studied and compared to those of beeswax. The results show that maleic anhydride-methyl methacrylate co-monomer grafting can effectively improve the acid value of polyethylene wax. For the ratio of two monomers of 1/1, the total amount of monomer of 8 wt%, the amount of initiator of 2 wt%, the reaction temperature of 150 °C, and the acid value of modified polyethylene wax was consistent with that of beeswax, realizing the simulation of the main chemical properties of beeswax. The thermal stability and melting temperature of the modified polyethylene wax are significantly higher than those of beeswax, its crystal structure is similar to that of beeswax, and the cyclic anhydride groups and ester groups introduced by co-monomer grafting endow it with polar groups that play an important role in the wood hot waxing process.

The role of mode switching in a population of actin polymers with constraints.

In this paper, we introduce a stochastic model for the dynamics of actin polymers and their interactions with other proteins in the cellular envelop. Each polymer elongates and shortens, and can switch between several modes depending on whether it is bound to accessory proteins that modulate its behaviour as, for example, elongation-promoting factors. Our main aim is to understand the dynamics of a large population of polymers, assuming that the only limiting quantity is the total amount of monomers, set to be constant to some large N. We first focus on the evolution of a very long polymer, of size [Formula: see text], with a rapid switch between modes (compared to the timescale over which the macroscopic fluctuations in the polymer size appear). Letting N tend to infinity, we obtain a fluid limit in which the effect of the switching appears only through the fraction of time spent in each mode at equilibrium. We show in particular that, in our situation where the number of monomers is limiting, a rapid binding-unbinding dynamics may lead to an increased elongation rate compared to the case where the polymer is trapped in any of the modes. Next, we consider a large population of polymers and complexes, represented by a random measure on some appropriate type space. We show that as N tends to infinity, the stochastic system converges to a deterministic limit in which the switching appears as a flow between two categories of polymers. We exhibit some numerical examples in which the limiting behaviour of a single polymer differs from that of a population of competing (shorter) polymers for equivalent model parameters. Taken together, our results demonstrate that under conditions where the total number of monomers is limiting, the study of a single polymer is not sufficient to understand the behaviour of an ensemble of competing polymers.

Preparation and Characterization of Soap-Free Vinyl Acetate/Butyl Acrylate Copolymer Latex.

The soap-free emulsion of vinyl acetate (VAc)/butyl acrylate (BA) copolymer was prepared by a semi-continuous and pre-emulsification polymerization method, using ammonium sulfate allyloxy nonylphenoxy poly(ethyleneoxy) (10) ether (DNS-86) as a reactive emulsifier. The effects of DNS-86 on the stability of the emulsion and the properties of the latex film were investigated. The infrared spectrum, thermal stability, glass transition temperature and micromorphology of latex were also studied. The results showed that the emulsion had the best stability and the conversion rate reached a maximum of 98.46% when the DNS-86 amount was 4 wt % of the total amount of monomers. Compared with the PVAc latex synthesized with octylphenol polyoxyethylene ether (10) (OP-10), the latex prepared with DNS-86 has higher thermal stability and ionic stability, whereas the latex film has better water resistance.

Influence of different light-curing units on monomer elution from bulk fill composites

Objectives: This in vitro study assessed the effect of different light-curing units on the elution of monomers from bulk fill composites with different thicknesses. Methods: Five bulk fill composites (Filtek Bulk Fill Flowable, SonicFill 2, SDR, Tetric N-Ceram Bulk Fill, and Venus Bulk Fill) and one conventional composite (Filtek Z250) were selected for the study. The cylindrical specimens in thickness of 2 mm or 4 mm were prepared and photopolymerized for 20 s with a light-emitting diode (VALO Cordless) or a halogen (Monitex BlueLuxer) light-curing unit. The specimens in glass vials were covered with a 75% ethanol/water solution. Ethanol/water extraction solutions were collected for high-performance liquid chromatography analysis after 24 h, 3 days, and 7 days. The data were analyzed with repeated measures and three-way ANOVA (p < 0.05). Results: The total monomer amount was significantly influenced by light-curing source used and thickness. The highest levels of Bis-GMA and Bis-EMA were eluted from Tetric N-Ceram BulkFill and Venus Bulk Fill, respectively. SonicFill 2 released the highest level of TEGDMA at 4-mm thickness. The highest levels of UDMA release, from 4-mm-thick Filtek Bulk Fill Flowable, were attained using the halogen unit. Conclusions: Light-curing sources affected the number of monomers released by materials. The amount of eluted monomers declined over time. The increased ratio of released monomers to increased thickness is material dependent. The number of residual monomers is highly associated with the resin ratio and crosslinking network of the composites.

Coupled equilibria in H-bond donating ring-opening polymerization: The effective catalyst-determined shift of a polymerization equilibrium

In the classic view of catalysis, a catalyst cannot alter the thermodynamically-determined endpoint of a reversible reaction. This conclusion is predicated on the assumption that the catalyst does not perturb the energy of product or reactant or does so to an equal extent. In the H-bond mediated ring-opening polymerization (ROP) of lactone monomers, the strength of the interactions of thiourea with product and reactant are not equal, and the magnitudes of these interactions are of similar energy to the free energy of reaction. The total monomer concentration at equilibrium in the thiourea/base cocatalyzed ROP of lactones is shown to be a function of the initial concentration of thiourea. Because the binding of thiourea to monomer and the polymerization reaction itself are both reversible, the application of varying amounts of thiourea catalyst directly alters the total amount of monomer in the reaction solution at equilibrium, which can be recovered at the end of the reaction.

High solid content poly(butyl acrylate)/poly(methyl methacrylate) core/shell nanosized spheres synthesised by microemulsion polymerisation

Core–shell nanosized polymer particles with poly(butyl acrylate) (PBA) as core and poly(methyl methacrylate) (PMMA) as shell were synthesised via a semi-continuous two-stage microemulsion polymerisation. A series of experiments were conducted to investigate the maximum solid content of the microemulsion under different surfactant/monomer ratios, and it was found that the maximum solid content could reach around 43.73% with minimum surfactant/monomer at only 5.25 wt%. The particle samples were characterised by proton nuclear magnetic resonance (1H-NMR), scanning electron microscopy, transmission electron microscopy (TEM) and dynamic light scattering (DLS) techniques. 1H-NMR and TEM results revealed that PBA/PMMA core/shell composite latexes were synthesised successfully by microemulsion polymerisation. DLS studies indicated that an optimal dosage of surfactant (1.29 wt% of the total amount of monomers) was found to synthesise particles with desired core–shell structure, which was consistent with the theoretical calculation. The size of nanoparticles increased with the increase in the amount of core monomer, showing an inverse relationship with surfactants.

Properties of na‐montmorillonite and cellulose nanocrystal reinforced poly(butyl acrylate‐co‐methyl methacrylate) nanocomposites

Poly(butyl acrylate‐co‐methyl methacrylate) (BA‐co‐MMA) nanocomposite latexes were synthesized in the presence of sodium montmorillonite (Na‐MMT) and cellulose nanocrystal (CNC) as fillers. Nanocomposite preparation with 3 wt% Na‐MMT based upon the total monomer amount was conducted by semi‐batch emulsion polymerization. Furthermore, direct blending of neat copolymer latex with Na‐MMT was performed for comparison. CNC/BA‐co‐MMA nanocomposites were obtained via blending process with varying CNC content (1, 2, and 3 wt %). Good dispersion of both Na‐MMT and CNC within the copolymer matrix was achieved as demonstrated by X‐ray diffraction and transmission electron microscope. Particle size of the nanocomposite latexes was around 120 nm. Thermal, mechanical, and barrier properties of the copolymer showed great improvement with the addition of both Na‐MMT and CNC. CNC nanocomposites displayed enhanced properties with increasing CNC level. Tensile strength of copolymer latex with 3 wt% CNC reached 262.5% of the pristine latex, while tensile strength of Na‐MMT nanocomposite at the same content was 187.5% of the pristine latex. POLYM. ENG. SCI., 55:2922–2928, 2015. © 2015 Society of Plastics Engineers

Iniferter-mediated grafting of molecularly imprinted polymers on porous silica beads for the enantiomeric resolution of drugs.

A surface-imprinted chiral stationary phase for the enantiomeric resolution of the antidepressant drug, citalopram, is presented in this work. N, N'-diethylaminodithiocarbamoylpropyl(trimethoxy)silane has been used as silane iniferter for the surface functionalization of the solid silica support. A molecularly imprinted polymer thin film, in the nm scale, was then grafted on the silanized silica using itaconic acid as the functional monomer and ethylene glycol dimethacrylate as the cross-linker in the presence of the template S-citalopram. The total monomer amount was calculated to obtain the desired thickness. Non-imprinted stationary phases were prepared similarly in the absence of S-citalopram. Characterization of the materials was carried out by scanning electron microscopy, thermogravimetric analysis, elemental analysis and Fourier transform infrared spectroscopy. Stationary phases have been applied to the chromatographic separation of the target. Conditions for best chromatographic resolution of the enantiomers were optimized, and it was found that a mobile phase consisting of a mixture of formate buffer (40 mM, pH 3) and acetonitrile (30:70 v/v) at 40 °C provided best results. Binding behaviour of the developed material was finally assessed by batch rebinding experiments. The obtained binding isotherm was fitted to different binding models being the Freundlich-Langmuir model, the one that best fitted the experimental data. The developed material has shown high selectivity for the target enantiomer, and the stationary phase could be undoubtedly exploited for chiral separation of the drug.

Preparation and characterization of cationic pH-sensitive SiO2/polymer core-shell nanoparticles with amino groups in the shell

Silica/poly(styrene-N,N′-dimethylaminoethyl methacrylate) (SiO2/P(St-DMAEMA)) cationic pH-responsive core-shell particles with a narrow size distribution and diameter of less than 200 nm were synthesized by emulsion polymerization. The effects of the St/DMAEMA molar ratio, SiO2 core size, monomer amount, and cross-linking degree on the morphology and pH-responsiveness of the core-shell particles were investigated by transmission electron microscopy, dynamic light scattering, and conductometric titration. The results showed that core-shell particles with only one SiO2 core could be obtained when the cross-linker divinyl benzene (DVB) was used, and the diameter of the core-shell particles increased with the size of the SiO2 core and the total amount of monomer. It was observed that the amount of surface amino groups, zeta potential, and volume swelling ratio of the core-shell particles were significantly affected by the St/DMAEMA molar ratio, and a high volume swelling ratio was achieved at pH 4 and a DVB content of 3 mol%. The zeta potential was observed to be a function of pH, and the particles were positively charged when the pH value was below approximately 7.2.

Modeling of Oligomerization of C&lt;sub&gt;9&lt;/sub&gt; Fraction of Petrol Pyrolysis

Process of terpolymerization of basic unsaturated components of liquid products of pyrolysis of straight-run gasoline in toluene solution has been studied as model of oligomerization of C9 fraction under the action of catalytic system TiCl4Al (C2H5)2Cl. Relative reactivity of styrene, indene and dicyclopentadiene (80-85 % from total amount of monomers) was established. On the basis of data of adiabatic thermometry, IR and 1H NMR spectroscopy we revealed possibilityto synthesize polymeric and oligomeric products.These products basically correspondto the industrial petropolymericresinsobtained from C9 fraction.

Facile and controllable fabrication of gold nanoparticles-immobilized hollow silica particles and their high catalytic activity

A facile and controllable method of immobilizing gold nanoparticles (AuNPs) on hollow silica particles (SiO2HPs) is proposed and the resultant SiO2HP/AuNP composite particles exhibit high catalytic activity. The carrier SiO2HPs decorated with amino groups are prepared in a W/O inverse emulsion, having a well-defined hollow structure, mesoporous wall and dense bush-like surface morphology. A large number of ultrafine AuNPs are generated via in situ reduction of chloroauric acid by the amino groups and firmly anchored on the bush-like silica shell. The structure and morphology of the composites are governed by changing the weight percentage of 3-aminopropyltriethoxysilane in the total amount of monomers (wa), which have been extensively characterized. Benefiting from the unique multiple structures, the composite particles exhibited outstanding catalytic efficiency and repeatability, which are confirmed by two oxidation–reduction reactions of 2-nitroaniline/NaBH4 and 4-nitrophenol/NaBH4.

Evaluation of TEGDMA leaching from four resin cements by HPLC

The aim of this study was to evaluate the elution of TEGDMA from dual cured resin cements, used for bonding of ceramic restoration by high performance liquid chromatography (HPLC). Forty freshly extracted caries and restoration free molar teeth used in this study. Standardized Class I preparations were prepared in all teeth. Ceramic inlays were cemented with one of the dual cured resin cements (Variolink II, Rely X ARC, Rely X Unicem and Resilute). After cementation, specimens were stored in 75% ethanol solution. HPLC was used to analyze the amounts of TEGDMA in different time intervals. Two-way ANOVA and Tukey HSD tests were used to evaluate the results (P<.05). The amount of TEGDMA eluted from Resilute was the highest and the amount of TEG-DMA eluted from Rely X Unicem was the lowest (P<.05). The total amount of monomers was the highest after 21 days (P<.05). In the case of resin cements, elution of TEGDMA was the highest in Resilute and lowest in Rely X Unicem. The amount of TEGDMA eluted from resin cements was influenced by the time.

Synthesis of cationic polyacrylamide by aqueous two‐phase polymerization in poly(ethylene glycol) chloride solution

AbstractAqueous two‐phase copolymerization of acrylamide(AM) and acryloyloxyethyl trimethyl ammonium chloride (DAC) was performed in poly(ethylene glycol) (PEG) solution and in PEG chloride(Cl‐PEG) solution, respectively. Series of cationic polyacrylamide(CPAM) aqueous dispersion were prepared using potassium persulfate (KPS) as initiator. The effect of total amount of monomers, the dosage of initiator, the content of dispersant, the mass ratio of AM to DAC, and the temperature on the conversion, molecular weight, cationic degree, and stability of aqueous dispersion were studied in detail. It is found that the increase of initiator and reaction temperature resulted in the increase of the final conversion, whereas the increase of DAC and PEG concentration resulted in the decrease of the final conversion. The optimum reaction conditions of synthesis were as follows: (1) PEG‐H2O system: PEG 7.5 g, AM 8 g, DAC 2 g, KPS 0.05 g, H2O 100 mL, 70°C. In this process conditions, the molecular weight of CPAM was 3.21 × 106, the cationic degree of CPAM was 24.4%, the storage stability of the aqueous dispersion was over 3 months. (2) Cl‐PEG‐H2O system: Cl‐PEG 7.5 g, AM 8 g, DAC 2 g, KPS 0.05 g, H2O 100 mL, 65°C. In this process conditions, the molecular weight was 3.68 × 106, the cationic degree was 23.3%, and the storage stability of the aqueous dispersion was over 6 months. In general, the stability of CPAM aqueous dispersion in Cl‐PEG system is much better than in PEG system. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013

Improving immobilization of lipase onto magnetic microspheres with moderate hydrophobicity/hydrophilicity

Magnetic microspheres with carboxyl groups were prepared by copolymerization of vinyl acetate (VAC), acrylamide (AM), and acrylic acid (AA) in the presence of oleic acid-coated Fe3O4 nanoparticles. Scanning electron microscope (SEM) photo showed that the average diameter of magnetic microspheres was about 400nm. Also, FTIR spectra analysis indicated that monomers were successfully enfolded on the microspheres’ surface. They were used as support to immobilize lipase via physical adsorption and covalent binding. To investigate the effect of the microsphere surface properties on lipase immobilization, a series of microspheres with different hydrophobic/hydrophilic surface characteristics were prepared by adjusting molar percentages of different monomers. The results showed that microspheres with different hydrophobicities/hydrophilicities had different immobilized ratios and different activity recovery. Compared with microspheres having hydrophilic characteristics, that with hydrophobic characteristics had a much higher lipase binding efficiency. However, this study further demonstrated that moderate hydrophobicity/hydrophilicity of microsphere surface was very important for elevating activity recovery. When AM (hydrophilic monomer) held 14.3% of total amount of monomers, the activity recovery was the highest (reaching 87%, 418U/g support). Possible reasons for these observations were discussed and a supposed mechanism was speculated.

Synthesis of New Fluorene-Based Copolymers Containing an Anthracene Derivative and Their Applications in Polymeric Light-Emitting Diodes

We report the synthesis of copolymers containing fluorene and highly soluble anthracene derivatives, of general formula, poly{9,9'-bis-(4-octoloxy-phenyl)-fluorene-2,7-diyl-co-9,10-bis-(decy-1-ynyl)-anthracene-2,6-diyl}s (PFAnts). The PFAnts were synthesized via Suzuki coupling and the feed ratios of the anthracene derivative (Ant) were 1, 5, 10, 30, and 50 mol % of the total amount of monomer. PFAnts showed well-defined high molecular weights and were more soluble in conventional organic solvents. The photoluminescence spectra of PFAnts shifted to longer wavelengths with increases in Ant proportion and the PFAnts emitted various colors varying from greenish-blue to orange. The highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels trended toward enhanced hole and electron recombination balance as the Ant proportion increased, due to the better electron-accepting ability of the anthracene moiety compared to the fluorene moiety. Polymeric light-emitting diodes with the configurations ITO/PEDOT:PSS(40 nm)/polymer(60 nm)/Ca(10 nm)/Al(100 nm) (Device A) and ITO/PEDOT:PSS(40 nm)/polymer(60 nm)/Balq(40 nm)/LiF(1 nm)/Al(100 nm) (Device B) were fabricated using the polymers as emissive layers. Especially, Device B with PFAnt01 exhibited the highest measured maximum brightness of 1760 cd/m2 at 14 V, a maximum current efficiency of 1.66 cd/A, and a maximum external quantum efficiency of 0.70%.

HPLC analysis of HEMA released from two different adhesive systems.

The aim of this study was to evaluate in vitro elution of 2-Hydroxyethyl methacrylate (HEMA) from two different adhesive systems, used in two dual polymerized resin cements for bonding of ceramic restoration by high performance liquid chromatography (HPLC). Twenty freshly extracted caries and restoration free molar teeth used in this study. Standardized Class I preparations were prepared in all teeth. A lithium disilicate based (IPS Empress Esthetic; Ivoclar) ceramic inlays were cemented with one of the dual polymerized resin cements (RelyX ARC; 3M ESPE or Nexus 2; Kerr) that have two different adhesive systems (Single Bond; 3M ESPE, Optibond Solo Plus; Kerr). After cementation, specimens were stored in 75% ethanol solution. HPLC was used to analyze the amount of HEMA in the solution (after 10 min, 1 h, 24 h, 3, 7, 14, and 21 days). Two-way analysis of variance and Tukey HSD tests were used to evaluate the results (p < 0.05). There were statistically significant differences between adhesive systems according to the amount of released HEMA (p < 0.01) and also among time periods (p < 0.01). The amount of HEMA eluted from Optibond Solo Plus was significantly higher than Single Bond. The total amount of monomers was the highest after 21 days (p < 0.01). In the case of adhesive systems, Optibond Solo Plus showed the highest amount of HEMA. The amount of HEMA eluted from adhesive systems influenced by the time.

Structural parameters of polyacrylamide hydrogels obtained by the Equilibrium Swelling Theory

In this paper, the synthesis and structural characterization of a series of polyacrylamide hydrogels with different degrees of reticulation are reported. Although the Equilibrium Swelling Theory was recognized as a simple and reliable tool for the determination of structural hydrogels network parameters like equilibrium degree of swelling, cross-link ratio and mesh size, this is the first application of this methodology for polyacrylamide hydrogels. By changing the total monomer content in the synthesis solution (% T) from 5 to 30%, at a fixed value of cross-linker content in the total monomer amount (% C) of 5%, the final parameter obtained, the mesh size, can be tuned from 2 to 0.3 nm. It was also possible to change the mesh size (0.19–0.35) by varying % C from 5 to 12% (at % T = 20%). Scanning Electron Microscopy images for the most different formulations are shown and corroborate data obtained from the theory.

Controlled Loading of Building Blocks into Temporary Self-Assembled Scaffolds for Directed Assembly of Organic Nanostructures

Using temporary self-assembled scaffolds to preorganize building blocks is a potentially powerful method for the synthesis of organic nanostructures with programmed shapes. We examined the underlying phenomena governing the loading of hydrophobic monomers into lipid bilayer interior and demonstrated successful control of the amount and ratio of loaded monomers. When excess styrene derivatives or acrylates were added to the aqueous solution of unilamellar liposomes made from saturated phospholipids, most loading occurs within the first few hours. Dynamic light scattering and transmission electron microscopy revealed no evidence of aggregation caused by monomers. Bilayers appeared to have a certain capacity for accommodating monomers. The total volume of loaded monomers is independent of monomer structure. X-ray scattering showed the increase in bilayer thickness consistent with loading monomers into bilayer interior. Loading kinetics is inversely proportional to the hydrophobicity and size of monomers. Loading and extraction kinetic data suggest that crossing the polar heads region is the rate limiting step. Consideration of loading kinetics and multiple equilibria are important for achieving reproducible monomer loading. The total amount of monomers loaded into the bilayer can be controlled by the loading time or length of hydrophobic lipid tails. The ratio of loaded monomers can be varied by changing the ratio of monomers used for loading or by the time-controlled replacement of a preloaded monomer. Understanding and controlling the loading of monomers into bilayers contributes to the directed assembly of organic nanostructures.

Evaluation of aminoalkylmethacrylate nanoparticles as colloidal drug carrier systems. Part I: synthesis of monomers, dependence of the physical properties on the polymerization methods

Conventional nanoparticles based on acrylic compounds are lipophilic and possess a negative surface charge. This is due to their manufacturing process and to the chemical structure of the polymer. Hence, these particles are not suitable for the adsorption of hydrophilic anionic drugs. In the present investigation, positively charged copolymer nanoparticles prepared from aminoalkyl- and methylmethacrylates were evaluated, with regard to their physical properties. This report provides a detailed description of the synthesis of the non-commercially available monomers and their polymerization procedure. Various parameters were investigated, such as comonomer content, total amount of monomer, concentration of the radical initiator, and the composition of the polymerization medium. The resulting particle diameter and the surface charge were found to be strongly dependent on the polymerization conditions and on the pH. Optimization of the polymerization procedure yielded nanoparticles of about 200 nm exhibiting a positive surface charge. The charges of the different copolymer particles were then compared at different pH values. N-trimethylaminoethylmethacrylate (TMAEMC) nanoparticles with quaternary ammonium groups located at their surfaces, possessed a nearly constant positive zeta potential at various pH values and, consequently, pH-independent particle diameters. The physical characteristics of the other aminoalkyl copolymers correlated with the basicity of the monomers employed and were found to be strongly dependent on the pH of the dispersion medium. Aminoethylmethacrylate (AEMC), methylaminoethylmethacrylate (MMAEMC), and aminohexylmethacrylate (AHMC) as well as aminoethylmethacrylamide (AHMAC) copolymer nanoparticles exhibited a strong positively charged surface even at physiological pH and, therefore, are useful candidates for the adsorption of anionic drugs.