Methacrylic Acid Copolymer Research Articles

Development and Analysis of Colon-Specific, pH-Responsive Polymer Delivery of Irinotecan Hydrochloride Tablets for Colon Cancer Treatment.

For the formulation of enteric-coated tablets containing irinotecan hydrochloride, this thesis focuses on HPMC and ethylcellulose, both of which are pH- and oxidation-resistant polymers. The integrated polymer-drug tablet mixture was coated with 15% of eudragit S100 and L100, which is a methacrylic acid copolymers, that’s soluble at pH 7. Both the physical characteristics with the invitro release kinetics pattern of the enteric-coated tablets were characterized. In the invitro release study, different pH environments were used, comparable to the gastrointestinal tract (GIT): 0.1 N HCl solution for two hours, pH 6.8 phosphate buffer for three hours, and pH 7.4 phosphate buffer for six hours. Using this device, you can simulate the pH level of the mouth, the digestive tract, and the urinary tract. As a result of consistent release studies, formulation F7 released 88.2% of the drug after 12 hours. Models such as Higuchi, Korsmeyer-Peppas, and zero-order reactions were used to analyze the GIT. This directed the development of a sustained delivery pattern that may be perfect for colonic IRT administration in the eventual treatment of colon cancer. Among the nine formulations, F7 formulated with EC and HPMC extended best sustained release pattern of drug, hence it is suitable for treating colon cancer.

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.

Silica Nanoparticles Tailored with a Molecularly Imprinted Copolymer Layer as a Highly Selective Biorecognition Element.

Molecularly imprinted silica nanoparticles (SP-MIP) are synthesized for the real-time optical detection of low-molecular-weight compounds. Azo-initiator-modified silica beads are functionalized through reversible addition-fragmentation chain transfer (RAFT) polymerization, which leads to efficient control of the grafted layer. The copolymerization of methacrylic acid (MAA) and ethylene glycol dimethacrylate (EDMA) on azo initiator-coated silica particles (≈100nm) using chain transfer agent (2-phenylprop-2-yl-dithiobenzoate) is carried out in the presence of a target analyte molecule (l-Boc-phenylalanine anilide, l-BFA). The chemical and morphological properties of SP-MIP are characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, Brunauer-Emmett-Teller surface analysis, and thermogravimetric analysis. Finally, SP-MIP is located on the gold surface to be used as a biorecognition layer on the surface plasmon resonance spectrometer (SPR). The sensitivity, response time, and selectivity of SP-MIP are investigated by three similar analogous molecules (l-Boc-Tryptophan, l-Boc-Tyrosine, and l-Boc-Phenylalanine) and the imprinted particle surface showed excellent relative selectivity toward l-Boc-Phenylalanine (l-BFA) (k=61), while the sensitivity is recorded as limit of detection=1.72×10-4m.

Methacrylic Acid Co-Polymers: Crucial agents for the Colon Targeted Oral Drug Delivery System

The objective of this research was to formulate an Ornidazole tablet capable of delivering the drug intact to the colon for the treatment of IBD, ulcerative colitis, and Crohn's disease. In the current investigation, pH-independent and pH-dependent polymers were used to target the Ornidazole tablet to the colon. This study evaluated two time-dependent (sustained release) polymers (Eudragit RS and Eudragit RL) and one pH-dependent polymer (Eudragit S100). The influence of the two formulation variables of the colon drug delivery system on the two response variables were examined simultaneously using a statistical 32-Full factorial design. X1 Ratio of Eudragit RS 100 to Eudragit RL 100 and X2 % weight gain with Eudragit S 100 were treated as independent variables in a factorial design, while Y5 and Y12 were treated as dependent variables. Through this procedure, a total of nine F9 samples were produced. Y5 in-vitro release should not exceed 10%, whereas Y12 should surpass 85%. Based on these results, batch B8 is considered the finest of all cohorts. According to the results, the enhanced formulation provides optimal intact drug delivery to the targeted region.

Very long-time crystallization kinetics for ethylene-methacrylic acid ionomers neutralized with zinc, sodium, lithium and magnesium

Papers by our group [1] (Grady et al., 2013) and another group [2] (Paul et al. 2012) examined crystallization of random copolymers of ethylene and methacrylic acid after room temperature annealing. Similar conclusions were reached concerning the crystallization process; primary crystals were either unchanged or changed very little after annealing while secondary crystallization occurred over long time scales after annealing. The current work confirms these general conclusions for four different cations (Zn2+, Na+, Li+ and Mg2+), with the latter two not studied in either of the previous studies. Even after 6 years of annealing at room temperature, the crystallization rate is constant with logarithmic time, i.e. the material continues to crystallize. The acid copolymer does not crystallize with room temperature annealing, although secondary crystals of the acid copolymer thicken with annealing.

Characteristics of Lactobacillus casei probiotic microparticles in L-type methacrylic acid copolymer matrix.

Lactobacillus casei (LC) is a type of lactic acid bacterium that is known for its beneficial probiotic properties. However, it is not typically found in the human intestine because it lacks acid resistance. LC thrives in an optimal pH environment of 6.8 and can be initiated in a more acidic environment at a pH of 3.5. This study purposed to compare the effect of L-type methacrylic acid copolymer (MAC) as a matrix (0.50%, 0.75%, and 1.00%) on the physical characteristics of LC probiotic microparticles made by the spray drying process. Probiotic microparticles were also made from a dry suspension of LC FNCC 0090 bacteria and dispersed in a solution of L-type MAC. The results showed that a rise in matrix content by 1.00% increased particle size (4.47 ± 0.19 µm) and reduced moisture content (7.45 ± 0.11%). The analysis of microparticle morphology also indicated a positive correlation between the level of L-type MAC and the production of smooth, nonporous, and almost spherical shapes. In addition, it was observed that encapsulation efficiency (92.46 ± 0.17%) and protection against stomach acid (98.17% ±1.17%) increased with the level of the matrix.

PH-Sensitive Acrylic Terpolymers for the Coating of Orally Administered Drugs Used for Colonic Release.

Polymeric coatings are a promising option for the development of delivery systems for orally administered drugs. However, the gastrointestinal conditions to which they are subjected, which include low pH and solubility as well as peristaltic movements, can limit their applications. In this work, different formulations of polymeric coatings were produced using pH-sensitive materials consisting of copolymers of methyl acrylate, methyl methacrylate, and methacrylic acid. The polymers were synthesized by the emulsion polymerization technique, obtaining small average particle sizes (56-190 nm), molecular weights between 200,000 and 400,000 g/mol, and a glass transition temperature above 35 °C, which are suitable for film formation at room temperature. Thus, they were assessed as coatings for hydroxypropyl methylcellulose capsules (HPMC) using the immersion method, showing adequate capacity to protect the capsule at gastric pH (pH 1.2) and dissolve at the simulated intestinal pH (pH= 7.2). In particular, the higher the content of the acidic monomer, the higher the release time of the test molecule contained in the acrylic terpolymer-coated HPMC capsules proposed, which was a curcuminoid derivative due to their bright color and potential medical benefits. In addition, a minimum number of immersions was required for coating the HPMC capsules at high acidic concentrations, which further facilitates the delayed release needed for colonic treatment. However, too high proportions of methacrylic acid may result in cytotoxicity issues. Consequently, a biocompatible formulation containing a proportion of methyl acrylate, methyl methacrylate, and methacrylic acid of 7:3:3 is proposed as the most adequate for colonic release. Thus, by chemically modulating the molar percentages of the acrylic monomers, it was possible to obtain tailored acrylic terpolymer coatings with different characteristics and desired properties in order to modulate the release kinetics of an active substance in a colonic environment.

Dual stimuli-responsive delivery system for self-regulated colon-targeted delivery of poorly water-soluble drugs

Inflammatory bowel disease (IBD) are chronic inflammatory conditions which cause significant patient morbidity. Local drug delivery to the colon can improve treatment efficacy and reduce side effects associated with IBD treatment. Smart drug delivery systems are designed to regulate the release of therapeutic agents at the desired site of action. pH-responsive drug carriers have been previously utilised for improved oral drug delivery beyond stomach harsh conditions. Additionally, the colon possesses a diverse microbiome secreting bioactive molecules e.g., enzymes, that can be exploited for targeted drug delivery. We herein synthesised and characterised a 2-hydroxyethyl methacrylate and methacrylic acid copolymer, crosslinked with an azobenzyl crosslinker, that displayed pH- and enzyme-responsive properties. The swelling and drug release from hydrogel were analysed in pH 1.2, 6.5 and 7.4 buffers, and in the presence of rat caecal matter using metronidazole and mesalamine as model BCS Class I and IV drugs, respectively. Swelling studies displayed pH-responsive swelling behaviour, where swelling was maximum at pH 7.4 and minimum at pH 1.2 (69 % versus 32 %). Consequently, drug release was limited in gastric and small intestinal conditions but increased significantly when exposed to colonic conditions containing caecal matter. This system displays promising capacity for achieving colon-targeted drug delivery with enhanced dissolution of poorly water-soluble drugs for local treatment of IBD and other colon-targeted therapies.

Preparation of a Structural Polyimide Foam Plastic Based on a Bulk Copolymer of Acrylonitrile and Methacrylic Acid

Foaming of particles of acrylonitrile–methacrylic acid copolymer in the temperature interval 160–220°С was studied. As shown by IR spectroscopy, the final polymer matrix of the foam plastics consists of glutarimide fragments. Thermogravimetric analysis shows that the products start to degrade at a high temperature (about 350°С). The effect of the prolonged heat treatment at 150–190°С on the physicomechanical characteristics of the foamed plastics was examined.

Spectroscopic and Thermal Investigations on Methyl Methacrylate – co – Methacrylic Acid Copolymer

Gamma irradiation effects on methyl methacrylate (MMA) – methacrylic acid (MAA) copolymer were investigated by spectroscopic (ESR, FTIR) and thermal (DSC) methods. Electron spin resonance (ESR) spectra of the irradiated copolymer are analysed to be caused by different component spectra from the free radicals (~ CH2 – CH – CH2 ~ and – COOH or – COOCH3) as per computer simulation analysis. The ESR signals could be annealed near the transition temperature of the copolymer, and the free radicals formed irradiation might react to form stable structures at transition temperatures. Fourier transform infrared (FTIR) studies suggested that the 3380 cm-1 absorption band (due to COOH groups and or hydrogen bonding) and 1734 cm-1 absorption band (due to carbonyl groups) were mostly affected by irradiation. Differential scanning calorimeter (DSC) thermogram indicated that the copolymer is a two-phase system (PMMA and PMAA), and transition temperatures are influenced by gamma irradiation. The dosimetric application of copolymer is tested by the ESR technique, and it was found suitable for dosimetry.

Real-time in vivo monitoring of the antimicrobial action of combination therapies in the management of infected topical wounds

The increasing prevalence of non-healing infected wounds has become a serious concern in the clinical practice, being associated to population aging and to the rising prevalence of several chronic conditions such as diabetes. Herein, the evaluation of the bactericidal and antibiofilm effects of the natural antiseptic terpenes thymol and farnesol standing alone or in combination with the standard care antiseptic chlorhexidine was carried out both in vitro and in vivo. The in vitro combinatorial treatment of chlorhexidine associated with those terpenes against Staphylococcus aureus in its planktonic and sessile forms demonstrated a superior antibacterial activity than that of chlorhexidine alone. Real-time in vivo monitoring of infection progression and antimicrobial treatment outcomes were evaluated using the bioluminescent S. aureus strain Xen36. In vivo studies on infected wound splinting murine models corroborated the superior bactericidal effects of the combinatorial treatments here proposed. Moreover, the encapsulation of thymol in electrospun Eudragit® S100 (i.e., a synthetic anionic copolymer of methacrylic acid and ethyl acrylate)-based wound dressings was also carried out in order to design efficient antimicrobial wound dressings.

Time-dependent mechanical behavior of tough hydrogels under multiaxial stretching

ABSTRACT Understanding the time-dependent mechanical behavior of tough and viscoelastic hydrogels under complex external loading is crucial. In this study, we utilized tough and viscoelastic hydrogels synthesized through the copolymerization of methacrylic acid and methacrylamide as a model system to investigate their mechanical behavior under multiaxial stretching across a wide range of strain rates. Three stretching modes examined were uniaxial, pure shear, and equal biaxial stretching. Our findings show that under equal biaxial stretching, the hydrogels exhibit higher mechanical properties and energy dissipation compared to uniaxial and pure shear stretching, owing to the greater contribution of hydrogen bonds to energy dissipation in the former stretching mode. Additionally, employing the time-elongation separability method during the stretching process, we observed that the relaxation of dynamic hydrogen bonds in the hydrogels only depends on stretching time, independent of the elongation ratio and stretching modes. We anticipate that this study will yield valuable contributions to the design of durable load-bearing soft materials, particularly in dealing with complex deformation and strain rate responses.

Preparation of acidity-sensitive N-isopropylacrylamide and methacrylic acid copolymer monolithic column for the pipette tip solid phase extraction of phenols

An acidity-sensitive poly(N-isopropylacrylamide-methyl acrylic acid-co-divinyl- benzene) monolith was prepared in situ in a pipette tip for solid phase extraction of phenol, m-cresol, o-nitrophenol, 2,4-dichlorophenol and p-tert-butylphenol. The monolith was characterized by FT-IR, BET (surface area = 266.56 m2/g) and thermogravimetric analysis (thermally stable up to 350 °C). The introduction of methyl acrylic acid enhanced the stability in the strong alkaline condition. The adsorption experiments and density function theory calculations indicated NIPAM was the main adsorption sites and the adsorption mechanism of phenol on the monolith was hydrophobic interaction, H-bond interaction, C − H···π interaction of isopropyl group of NIPAM with the phenyl group of phenols. Based on these features and under the optimal extraction conditions, a pipette tip solid phase extraction coupled to high-performance liquid chromatography with ultraviolet detection method was developed for the determination of 5 phenols in the diffusion of polycarbonate cups. Due to the usage of 0.1 M NaOH as the eluent, the method presented selectivity for phenols based on the acidity-sensitive of the monolith. Wide linear range (0.6–200 µg/L), low detection limits (0.2–0.3 µg/L), good reproducibility (%RSD less than 9.8%) and satisfactory recoveries (86.3–114.1%) were obtained. The proposed method was suitable for quantitative analysis of phenollic in water samples.

Novel concrete superplasticizers with sterically hindered amines as stabilizing pendant side chains

In this work, a sterically hindered amine, 2,2,6,6-tetramethyl-4-piperidyl methacrylate (TMPMA), is introduced as a bulky pendant group to achieve steric hindrance, replacing the traditional poly(ethylene oxide) (PEO) side chains of traditional polycarboxylate ether (PCE) superplasticizers (SPs). Note that PCE is the common name for concrete superplasticizers having both carboxylic acid and PEO side-chains in which the bulky PEO pendant group exert large steric hindrance leading to good dispersion and stabilization of cement particles. In this work, the PEO side chains are replaced by a sterically hindered amine. Therefore, copolymers of methacrylic acid (MAA) and TMPMA with different molar ratios were prepared by Reversible-Addition Fragmentation Chain Transfer polymerization (RAFT). The prepared copolymers were characterized by proton nuclear magnetic resonance (1H NMR) and size exclusion chromatography (SEC) to elucidate the chemical structure and molecular weights. Rheological studies and fluidity measurements revealed that poly(MAA-co-TMPMA) SPs, which we introduce here as polycarboxylate amine (PCA) SPs, enhanced cement flowability, workability, and slump retention. Free radical polymerization (FRP) was also employed, as an industrially more relevant, more straightforward and more cost-effective synthesis technique, for the preparation of PCA SPs to reflect the possibility of scaling up these SPs via conventional polymerization methods. The resulting FRP PCA analog exhibited the same plasticizing efficacy as those prepared by RAFT polymerization, demonstrating that these polymers could have high potential in the concrete industry.

Enteric coating of tablets containing an amorphous solid dispersion of an enteric polymer and a weakly basic drug: A strategy to enhance in vitro release

Recent work has highlighted that amorphous solid dispersions (ASDs) containing delamanid (DLM) and an enteric polymer, hypromellose phthalate (HPMCP), appear to be susceptible to crystallization during immersion in simulated gastric fluids. The goal of this study was to minimize contact of the ASD particles with the acidic media via application of an enteric coating to tablets containing the ASD intermediate, and improve the subsequent drug release at higher pH conditions. DLM ASDs were prepared with HPMCP and formulated into a tablet that was then coated with a methacrylic acid copolymer. Drug release was studied in vitro using a two-stage dissolution test where the pH of the gastric compartment was altered to reflect physiological variations. The medium was subsequently switched to simulated intestinal fluid. The gastric resistance time of the enteric coating was probed over the pH range of 1.6–5.0. The enteric coating was found to be effective at protecting the drug against crystallization in pH conditions where HPMCP was insoluble. Consequently, the variability in drug release following gastric immersion under pH conditions reflecting different prandial states was notably reduced when compared to the reference product. These findings support closer examination of the potential for drug crystallization from ASDs in the gastric environment where acid-insoluble polymers may be less effective as crystallization inhibitors. Further, addition of a protective enteric coating appears to provide a promising remediation strategy to prevent crystallization at low pH environments, and may mitigate variability associated with prandial state that arises due to pH changes.

Sуnthesis of terpene–methacrylic acid copolymers and their effect on the stability of inorganic dispersions in the presence of cationic surfactants

Copolymers of methacrylic acid and natural terpene monomers (α-pinene; β-pinene; ∆3-karene) with the molecular weight of (0.3–0.5)∙104 and a content of carboxyl groups of 14.5–16.3 % were synthesized. For the synthesized copolymers, hydrodynamic radius and the Kuhn segment, which characterizes flexibility of a polymer chain, were determined, as well as the Huggins constant in aqueous and saline solutions, and concentration regions for formation of supramolecular structures. In the presence of a cationic surfactant (benzetonium chloride, Hyamine), depending on the concentration of copolymers in the system, polymer-surfactant complexes were formed in soluble and insoluble forms. It has been shown that the effectiveness of the stabilizing action of soluble complexes with respect to an aqueous dispersion of calcium carbonate increases with an increase in the content of nonpolar groups in the polymer chain. A cationic surfactant (Hyamine) has been proposed as a precipitant in the method for the quantitative determination of carboxyl-containing polymers in aqueous and saline media.

Effect of the chemical structure of carboxyl-containing polymers on precipitate morphology and carbonate dispersions stability

The influence of the molecular structure of carboxyl-containing polymers on their inhibitory and stabilizing effect in the precipitation processes was studied using a number of polymeric acids with different contents of carboxyl groups (X): polyacrylic acid (Mn = 5100 g-mol–1, X = 61.11 %), polymethacrylic acid (Mn = 5500 g-mol–1, X = 48.79 %), copolymer of methacrylic acid with turpentine terpene (α-pinene) (Mn = 350 g-mol–1, X = 14.54 %). It has been established that polyacid molecules slow down the process of crystal growth and recrystallization of the amorphous phase into more stable crystalline forms, which leads to a change in the morphology and structure of a carbonate precipitate. It has also been shown that polycarboxylic acids increase the colloidal stability of a mixed dispersion of carbonates and kaolin. The synergism of the stabilizing effect of mixtures of different hydrophobicity-polyacids was noted: in the presence of a mixture of polyacrylic acid with a copolymer of methacrylic acid with turpentine terpene, the stabilization effect increases 2 times compared to dispersion without additives and 1.4–1.8 times compared with individual components of the mixture.

Identification and Quantitation of Nicotine Polacrilex in Nicotine Pouches and Other Oral Nicotine Delivery Products

SUMMARY Nicotine polacrilex (CAS-No. 96055-45-7) can be used as the source of nicotine in nicotine pouches and other oral nicotine delivery products such as lozenges, tablets, and gums. The compound is the salt of nicotine with Amberlite IRP64, a copolymer of methacrylic acid and divinylbenzene. Present study describes a unique procedure to identify the presence of the compound nicotine polacrilex in oral nicotine delivery products and to evaluate its level. In oral nicotine delivery products, nicotine polacrilex is used in a mixture with other ingredients such as microcrystalline cellulose (MCC), maltitol, sweeteners, flavors, salts (such as Na2CO3, NaHCO3), water, etc. These ingredients make the analysis of the compound nicotine polacrilex by spectroscopic techniques such as IR or Raman difficult. Also, since nicotine polacrilex is insoluble in common solvents, the analysis using solutions is not possible. The study is also attempting to detect if the product contains only nicotine polacrilex or if it has additional nicotine in a different form (e.g., nicotine or nicotine tartrate). The analysis uses pyrolysis-GC/MS (Py-GC/MS) and the detection and quantitation of nicotine polacrilex is based on measuring the pyrolysis products of divinylbenzene (DVB) moiety from the Amberlite IRP64. The detection was proven very reliable by this procedure, while the quantitation showed some variability caused by the typical variability in the pyrolysis process. [Contrib. Tob. Nicotine Res. 32 (2023) 43–49]

Influence of talc and hydrogenated castor oil on the dissolution behavior of metformin-loaded pellets with acrylic-based sustained release coating

Multi-unit pellet system (MUPS) is of great interest as it is amenable to customization. MUPS comprises multi-particulates, usually as pellets or spheroids, which can be coated with diffusion barrier coatings. One commonly used diffusion barrier coating is the methacrylic acid copolymer, which can be used as a taste masking, enteric or sustained release polymer. While the versatility of methacrylic acid copolymers makes them pliable for pellet coating, there are impediments associated with their use. Additives commonly required with this polymer, including plasticizer and anti-adherent, have been shown to weaken the film strength. The objective of this study was to investigate the impact of osmotic pressure within the core on the sustained release coat integrity and functionality. Hydrogenated castor oil (HCO) was chosen as the additive to be studied. Metformin-loaded pellets, prepared via extrusion-spheronization, were coated with ethyl acrylate and methyl methacrylate copolymer (Eudragit RS 30 D) containing talc, talc-HCO, or HCO to different coat thicknesses. Drug release was investigated using the USP dissolution apparatus 2 and an ultraviolet imager. The swelling of the pellets when wetted was monitored by video imaging through a microscope. When coated to 7.5 % coat weight gain, coats with HCO slowed down drug release more than the other pellets. The pellets also swelled the most, which suggests that they were more resistant to the osmotic pressure exerted by metformin. For drugs which exert high osmotic pressure, HCO can serve as an efficient alternative to talc in the preparation of methacrylic acid copolymer coatings.

Hyperbranched Copolymers of Methacrylic Acid and Lauryl Methacrylate H-P(MAA-co-LMA): Synthetic Aspects and Interactions with Biorelevant Compounds.

The synthesis of novel copolymers using one-step reversible addition-fragmentation chain transfer (RAFT) copolymerization of biocompatible methacrylic acid (MAA), lauryl methacrylate (LMA), and difunctional ethylene glycol dimethacrylate (EGDMA) as a branching agent is reported. The obtained amphiphilic hyperbranched H-P(MAA-co-LMA) copolymers are molecularly characterized by size exclusion chromatography (SEC), FTIR, and 1H-NMR spectroscopy, and subsequently investigated in terms of their self-assembly behavior in aqueous media. The formation of nanoaggregates of varying size, mass, and homogeneity, depending on the copolymer composition and solution conditions such as concentration or pH variation, is demonstrated by light scattering and spectroscopic techniques. Furthermore, drug encapsulation properties are studied by incorporating the low bioavailability drug, curcumin, in the nano-aggregate hydrophobic domains, which can also act as a bioimaging agent. The interaction of polyelectrolyte MAA units with model proteins is described to examine protein complexation capacity relevant to enzyme immobilization strategies, as well as explore copolymer self-assembly in simulated physiological media. The results confirm that these copolymer nanosystems could provide competent biocarriers for imaging and drug or protein delivery/enzyme immobilization applications.