Anionic Microparticles Research Articles

The effect of contact time between CPAM and colloidal silica on the flocculation behavior in the approach flow

Multicomponent wet-end systems have become increasingly common in papermaking, with the objective of improving the retention-formation-dewatering relationship. It is quite common to use at least a cationic polymer, often in combination with an anionic microparticle. In some cases, a fixative is also used. However, there is still debate on the optimal implementation of these systems. In particular, optimizing the contact time of the cationic polymer prior to addition of the anionic microparticle is still poorly understood. In this work, we investigate the effect of the contact time of a cationic polyacrylamide (CPAM) prior to addition of colloidal silica on the flocculation response in a flowing fiber suspension. The effect of using a fixative is also investigated. Focused beam reflectance measurements (FBRM) are combined with zeta-potential measurements for optimizing the addition levels of a two- and three-component system, as well as for elucidating the effect of contact time on CPAM performance. Trials are then performed on a pilot scale flow loop, where the time between addition of these two components is varied and the resulting flocculation response is characterized using high-speed filming and image analysis techniques. It is shown that the efficacy of CPAM can be improved through use of a fixative and that a longer CPAM contact time may be beneficial in terms of immediate flocculation; however, hydrodynamic shear tends to dominate the flocculation response regardless of contact time due to floc rupture.

Effect of network mesh size and swelling to the drug delivery from pH responsive hydrogels

ABSTRACTpH responsive hydrogels are ideal platforms for numerous therapeutic delivery applications, including oral delivery, as they are capable of overcoming the many barriers that must be considered when creating an effective drug delivery system. Understanding of the innate hydrogel network structure and its swelling behavior at environmentally relevant conditions is vital for designing hydrogel network capable of effective controlled drug release. Herein, we explored how to expand traditional techniques of swelling and pore characterization to gain better insight into the performance of anionic microparticles composed of the poly(methyl methacrylate‐co‐acrylic acid) with varying molar percentage of 10, 20, and 30 mol% of MMA, for controlled release of low‐molecular‐weight drugs. By evaluating these carrier systems at environmental conditions, we can observe changes in swelling and pore size of the anionic hydrogel networks as a function of MMA, which was then correlated with the release profiles of the small‐molecular‐weight drug sodium nitrate. With the correlation of the swelling behavior of the networks and the release profiles, we demonstrated how the expansion of swelling parameters at relevant pH values provides further incite for evaluating for the optimal blend for controlled release. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020, 137, 48767.

Influence of Modified Carbon Fiber on Properties of Paper Based Friction Materials

The paper adopts modified carbon fiber with Meldrum's acid and silane coupling agent (KH-550), then add the modified carbon fiber to the paper based friction materials. The paper aims to explore the changes of modified carbon fiber in its surface structure and properties by electron microscopy and infrared spectral analysis, and the effect of anionic microparticle forming retention aid system comprised of lithium soapstone-cationic polyacrylamide (CPAM) on mechanical properties and retention of paper based friction materials. Compared with the addition of unmodified carbon fiber to paper based friction materials, the addition of modified carbon fiber with Meldrum's acid, silane coupling agent, Meldrum's acid and silane coupling agent enhance the tensile strength of paper based friction materials. The tensile index of paper based friction materials was separately enhanced by 64.87 %, 91.38 % and 28.88 %. Compared with the paper based friction materials without the anionic microparticle forming retention aid system, the basis weight of paper based friction materials increased by 13.97 %.

Coaggregation of mineral filler particles and starch granules as a basis for improving filler-fiber interaction in paper production

The sustainable, efficient use of renewable bio-based additives in the production of various materials fits well into the concept of sustainability. Here, the concept of coaggregation of mineral filler particles and starch granules for improving filler-fiber interaction in paper-based cellulosic networks is presented. Coaggregation of precipitated calcium carbonate filler particles and uncooked, unmodified corn starch granules by cationic polyacrylamide (a cationic high molecular weight polymer flocculant) in combination with bentonite (an anionic microparticle) prior to addition to cellulosic fiber slurry delivered enhanced filler bondability with cellulosic fibers. For instance, under the conditions studied, preaggregation resulted in an increase in filler bondability factor from 9.24 to 15.21 at starch dosage of 1% (on the basis of the dry weight of papermaking stock). The swelling and gelatinization of the starch granules in starch-filler preaggregates or hybrids enabled the “bridging” of the gaps in cellulosic networks, leading to structural consolidation and strength enhancement.

Positionable vertical microfluidic cell based on electromigration in a theta pipet.

A microscale vertical fluidic cell system has been implemented, based on a simple theta pipet pulled to a sharp point (ca. 10-20 μm diameter for the studies herein) and positioned with a high degree of control on a surface. The dual channel arrangement allows an electric field to be generated between an electrode in each compartment of the pipet that can be used to control the electromigration of charged species between the two compartments, across a thin liquid meniscus in contact with the substrate of interest. By visualizing the interfacial region using laser scanning confocal microscopy, the adsorption of fluorescently-labeled materials on surfaces is monitored quantitatively in real time, exemplified through studies of the adsorption of anionic microparticles (1.1 μm diameter) on positively and negatively charged substrate surfaces of poly-L-lysine (PLL) and poly-L-glutamic acid (PGA), respectively, on glass. These studies highlight significant electrostatic effects on adsorption rates and also that the adsorption of these particles is dominated by the three phase meniscus/solid/air boundary. The technique is easily modified to the case of a submerged substrate, resulting in a much larger deposition area. Finite element method modeling is used to calculate local electric field strengths that are used to understand surface deposition patterns. To demonstrate the applicability of the technique to live biological substrates, the delivery of fluorescent particles directly to the surface of a single root hair cell of Zea mays is demonstrated. The mobile pipet allows deposition to be directed to specific regions of the cell, allowing discrete sites to be labeled with particles. Finally, the technique is used to study the uptake of fluorescent polymer molecules to single root hair cells, with quantitative analysis of the adsorption rates of vinyl-sulfonic acid copolymers, with varying rhodamine B content.

Cellulose nanofibers prepared from TEMPO‐oxidation of kraft pulp and its flocculation effect on kaolin clay

ABSTRACTCellulose nanofibers were prepared using TEMPO/NaBr/NaClO oxidation of kraft pulp and successive ultrasonic treatment, and the properties were characterized by conductimetric titration, X‐ray diffraction, and atomic force microscopy. The resulting product was then applied as an anionic microparticle to constitute a microparticulate system with cationic polyacrylamide (CPAM), to induce the flocculation of the kaolin clay suspension. The flocculation effect was evaluated by determining the relative turbidity of clay suspension. The results showed that the obtained cellulose nanofibers had cellulose I structure with higher crystallinity than that of the kraft pulp, and their cross‐sectional dimension was in the range of 3–5 nm. They had more negative zeta potential at neutral and alkaline conditions. It was found that the microparticulate system showed high flocculation effect on kaolin clay at a very low level of nanofiber addition, and a high shear level after CPAM addition was helpful for the flocculation. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40450.

Application of Nano-Materials as Synergistic Retention Aid in Paper Making

Various negatively charged and positively charged inorganic nano-materials have been suggested to constitute the so-called microparticle retention systems with cationic or anionic polymers. Anionic microparticle retention systems consisted of cationic polymers and negatively charged inorganic nano-materials with various aspect ratios were reviewed while their working mechanism were analyzed. Cationic microparticle retention systems made up of either naturally or organo-modified cationic nano-materials were introduced.

Proteomic Analysis of Serum Opsonins Impacting Biodistribution and Cellular Association of Porous Silicon Microparticles

Mass transport of drug delivery vehicles is guided by particle properties, such as size, shape, composition, and surface chemistry, as well as biomolecules and serum proteins that adsorb to the particle surface. In an attempt to identify serum proteins influencing cellular associations and biodistribution of intravascularly injected particles, we used two-dimensional gel electrophoresis and mass spectrometry to identify proteins eluted from the surface of cationic and anionic silicon microparticles. Cationic microparticles displayed a 25-fold greater abundance of Ig light variable chain, fibrinogen, and complement component 1 compared to their anionic counterparts. Anionic microparticles were found to accumulate in equal abundance in murine liver and spleen, whereas cationic microparticles showed preferential accumulation in the spleen. Immunohistochemistry supported macrophage uptake of both anionic and cationic microparticles in the liver, as well as evidence of association of cationic microparticles with hepatic endothelial cells. Furthermore, scanning electron micrographs supported cellular competition for cationic microparticles by endothelial cells and macrophages. Despite high macrophage content in the lungs and tumor, microparticle uptake by these cells was minimal, supporting differences in the repertoire of surface receptors expressed by tissue-specific macrophages. In summary, particle surface chemistry drives selective binding of serum components impacting cellular interactions and biodistribution.

A Catalytically Independent Physiological Function for Human Acute Phase Protein Group IIA Phospholipase A2: CELLULAR UPTAKE FACILITATES CELL DEBRIS REMOVAL

Human group IIA phospholipase A2 (IIA PLA2) is an acute phase protein first identified at high concentrations in synovial fluid from patients with rheumatoid arthritis. Its physiological role has since been debated; the enzyme has a very high affinity for anionic phospholipid interfaces but expresses almost zero activity with zwitterionic phospholipid substrates, because of a lack of interfacial binding. We have prepared the cysteine-containing mutant (S74C) to allow the covalent attachment of fluorescent reporter groups. We show that fluorescently labeled IIA was taken up by phorbol 12-myristate 13-acetate-activated THP-1 cells in an energy-dependent process involving cell surface heparan sulfate proteoglycans. Uptake concurrently involved significant cell swelling, characteristic of macropinocytosis and the fluorescent enzyme localized to the nucleus. The endocytic process did not necessitate enzyme catalysis, ruling out membrane phospholipid hydrolysis as an essential requirement. The enzyme produced supramolecular aggregates with anionic phospholipid vesicles as a result of bridging between particles, a property that is unique to this globally cationic IIA PLA2. Uptake of such aggregates labeled with fluorescent anionic phospholipid was dramatically enhanced by the IIA protein, and uptake involved binding to heparan sulfate proteoglycans on activated THP-1 cells. A physiological role for this protein is proposed that involves the removal of anionic extracellular cell debris, including anionic microparticles generated as a result of trauma, infection, and the inflammatory response, and under such conditions serum levels of IIA PLA2 can increase approximately 1000-fold. A similar pathway may be significant in the uptake into cells of anionic vector DNA involving cationic lipid transfection protocols.

Encapsulation of the immune potentiators MPL and RC529 in PLG microparticles enhances their potency

Purpose Monophosphoryl lipid A (MPL) and the synthetic LPS mimetic RC529, encapsulated in poly(lactide-co-glycolide) (PLG) microparticles, were evaluated as immune potentiators in the presence of either HIV-1 gp120 protein or antigen from Neisseria meningitidis serotype B (Men B). The immunogenicity of these formulations was evaluated in mice and compared to CpG containing oligonucleotide. This work was done as part of an ongoing effort to enhance the potency of vaccine candidates against HIV and Men B. Methods Microparticles were made by a solvent evaporation method. Blank microparticles as well as microparticles with encapsulated MPL or RC529 were made using the PLG polymer RG503 and the ionic surfactant Dioctylsulfosuccinate by the water-in-oil-in-water emulsion technique. Antigens from HIV-1 and Men B were adsorbed on the surface of these anionic microparticles and the final formulations characterized for protein loading, release, and integrity. The formulations were then tested in mice for their ability to elicit antibodies and bactericidal activity in comparison with CpG containing oligonucleotide. Results We have found that adding soluble immune potentiators to Men B antigen formulated on PLG microparticles significantly enhanced the immune response to a level comparable to that obtained using CpG. In a separate study, we found that encapsulating MPL or RC529 in PLG microparticles further enhanced the response in comparison to soluble CpG, which is our control group. Similarly, adding soluble immune potentiators to gp120 antigen formulated on PLG microparticles resulted in a significant enhancement of the immune response. Moreover, delivering MPL or RC529 encapsulated in PLG microparticles with gp120 adsorbed on PLG microparticles, resulted in even further enhancement of serum titers over those obtained with soluble immune potentiators. These titers were comparable to or greater than those obtained with soluble CpG, the control group. This effect was observed for both antigens regardless of whether or not the immune potentiator and the antigen were used with the same or with separate particles. In conclusion, the advantages of encapsulating MPL and RC529 lie not only in the enhanced immune response they elicit, but also in the convenience of handling these relatively insoluble compounds, and flexibility in vaccine design. The fact that MPL and RC529 are readily soluble in methylene chloride used for the manufacturing of PLG microparticles makes it easy to avoid solubility issues. Moreover, formulating antigen and immune potentiator with the same particle offers an attractive approach to vaccine delivery.

Adsorption of a Novel Recombinant Glycoprotein from HIV (Env gp120dV2 SF162) to Anionic PLG Microparticles Retains the Structural Integrity of the Protein, Whereas Encapsulation in PLG Microparticles Does Not

To evaluate the delivery of a novel HIV-1 antigen (gp120dV2 SF162) by surface adsorption or encapsulation within polylactide-co-glycolide microparticles and to compare both the formulations for their ability to preserve functional activity as measured by binding to soluble CD4. Poly(lactide-co-glycolide) microparticles were synthesized by a water-in-oil-in-water (w/o/w) emulsification method in the presence of the anionic surfactant dioctylsulfosuccinate (DSS) or polyvinyl alcohol. The HIV envelope glyocoprotein was adsorbed and encapsulated in the PLG particles. Binding efficiency and burst release measured to determine adsorption characteristics. The ability to bind CD4 was assayed to measure the functional integrity of gp120dV2 following different formulation processes. Protein (antigen) binding to PLG microparticles was influenced by both electrostatic interaction and other mechanisms such as hydrophobic attraction and structural accommodation of the polymer and biomolecule. The functional activity as measured by the ability of gp120dV2 to bind CD4 was maintained by adsorption onto anionic microparticles but drastically reduced by encapsulation. The antigen on the adsorbed PLG formulation maintained its binding ability to soluble CD4 in comparison to encapsulation, demonstrating the feasibility of using these novel anionic microparticles as a potential vaccine delivery system.

Novel anionic microparticles are a potent adjuvant for the induction of cytotoxic T lymphocytes against recombinant p55 gag from HIV-1

Microparticles with entrapped antigens have recently been shown to possess significant potential as vaccine delivery systems and adjuvants. However, the potential of microparticles as adjuvants has been seriously limited by the common problem of degradation and denaturation of antigens following encapsulation and release. To overcome these problems, we have developed a novel way to use microparticles as adjuvants, by the adsorption of proteins onto their surface. Anionic microparticles were prepared through the inclusion of an anionic detergent, sodium dodecyl sulphate (SDS), in the microparticle preparation process. The anionic microparticles were capable of the efficient and reproducible adsorption of recombinant p55 gag protein from HIV-1. Microparticles with adsorbed p55 were capable of inducing potent cytotoxic T lymphocyte responses in mice following intramuscular immunization. In addition, the microparticles also exhibited a potent adjuvant effect for antibody induction against p55.

Synergetic Effect of Cationic Polymer Microparticles and Anionic Polymer on Fine Clay Flocculation

Although much research has been done into flocculation systems involving anionic microparticles, few systematic investigations employing cationic polymer microparticles (CPM) have been reported. In the present work, emulsifier-free polymerization was conducted via copolymerization of styrene with three types of cationic monomer. This technique allowed cationic polymer microparticles with well-defined structures to be prepared. Dynamic flocculation experiments showed that the effectiveness of CPM alone as a flocculant for fine clay particles is affected by CPM charge density and by particle size, in the range 0.2 to 0.4 μm. A strong synergetic effect between CPM and anionic polyacrylamide with high molecular weight and low charge density was observed. This significantly reduced the dosage of polymeric flocculant required for effective flocculation. The best flocculation occurred at a value of the anionic polymer:CPM ratio of 1:8 (wt), with anionic polymer dosage approximately 0.06 wt% on clay. Electrostatic interaction between CPM and anionic polymer appears to be an important driving force for flocculation.

An extended model for the estimation of flocculation efficiency factors in multicomponent flocculant systems

Abstract A model for the flocculation efficiency in flocculant systems consisting of up to three components (a low molecular weight (MW) cationic polymer, a high MW cationic polymer and an anionic particle sol) is presented. The model is based on the classical bridging mechanism. Extensions have been carried out to take into account the addition of low MW polymers making surface sites inaccessible for bridging polymers, the flocculation induced by the addition of anionic microparticles, and the conformation of the adsorbed high MW polymer layer. According to this model, the collision efficiency is a function of the degree of surface coverage of the suspended particles by low MW polymer, the degree of surface coverage by high MW polymer, and the addition of a third component which interacts with adsorbed high MW cationic polymers. In the experimental work, the model was tested by determining adsorption isotherms, by flocculation experiments on suspensions of cellulosic fibres and by experiments on a pilot paper machine. The model was found to give a good qualitative description of the experimental results.