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PubMed1994

Effects of water and carboxylic acid monomer on polymerization of HEMA in the presence of N-phenylglycine.

OBJECTIVES: This research was designed to study the effect of water or carboxylic acid monomer on the polymerization of 2-hydroxyethyl methacrylate (HEMA) in order to understand the bonding mechanism of dentin bonding systems using N-phenylglycine (NPG). METHODS: The polymerization of HEMA in the presence of NPG was studied by adding various amounts of water and/or 4-(2-methacryloyloxyethoxycarbonyl) phthalic acid (4-MET) and evaluated using differential scanning calorimetry (DSC). RESULTS: The addition of water promoted the polymerization of HEMA. Polymerization was further promoted through the addition of 4-MET as a carboxylic acid monomer. Polymerization was promoted at the molar ratio of 4-MET to NPG of 1.0-7.0. SIGNIFICANCE: Moisture on the dentin surface could contribute to improving bond strength in dentin bonding systems using NPG by promoting polymerization at the dentin interface.

Analysis of Variance↗
PubMed1993

Methylisocyanate and actin polymerization: the in vitro effects of carbamylation.

Uremia has been implicated in cataractogenesis due to protein carbamylation by cyanate derived from urea. The present study was designed to directly identify the effects of carbamylation on actin polymerization and the possible contribution to cataract formation. The susceptibility of actin to carbamylation is expected because of the 19 lysines distributed along its length. The lysines of actin were selectively carbamylated by methylisocyanate (MIC) at pH 8.0 and 4 degrees C and actin polymerization assayed by high-shear viscometry, fluorescence and transmission electron microscopy. Our results provide evidence that non-enzymatic carbamylation of the lysine residues prevents the polymerization of actin. In addition, this carbamylated actin inhibited the polymerization of nascent, unmodified actin. High-shear viscosity measurements demonstrated decreased initial apparent rates and decreased steady-states (final specific viscosities) of polymerization. Fluorescence measurements showed decreased relative intensities of fluorescence versus control and confirmed the inhibitory effects of carbamylation by MIC on the steady state of F-actin. Transmission electron microscopy (TEM) showed the presence of disorganized filaments when carbamylated actin was added to polymerizing unmodified actin. Our results suggest that carbamylation of actin can cause a loss of ordered filament structure and shape of the lens fiber cell, thus predisposing it to cataract development.

Actins↗
PubMed1988

Phenylmethylsulfonyl fluoride inhibits chemotactic peptide-induced actin polymerization and oxidative burst activity in human neutrophils by an effect unrelated to its anti-proteinase activity.

Stimulation of polymorphonuclear leukocytes with the chemotactic peptide N-formylmethionylleucylphenylalanine (fMet-Leu-Phe) causes conversion of monomeric actin to polymeric actin. We studied the role of proteinase inhibitors phenylmethylsulfonyl fluoride PMSF) and diisopropyl fluorophosphate in fMet-Leu-Phe-induced actin polymerization in polymorphonuclear leukocytes. Pre-incubation of cells with PMSF (2 mM) for 1 min caused inhibition of fMet-Leu-Phe-induced actin polymerization, as studied by 7-nitrobenz-2-oxa-1,3-diazole (NBD) -phallacidin labeling and flow cytometry. PMSF also inhibited fMet-Leu-Phe-induced hydrogen peroxide release, superoxide anion generation and chemiluminescence. In contrast, diisopropyl fluorophosphate (5 mM) was unable to inhibit fMet-Leu-Phe-induced actin polymerization and superoxide generation, but was effective in inhibiting hydrogen peroxide production and chemiluminescence. PMSF did not cause any change in membrane potential by itself and failed to inhibit the membrane potential changes induced by fMet-Leu-Phe, indicating that PMSF does not affect the binding of fMet-Leu-Phe to the receptors. The high concentration of PMSF required coupled with the fact that diisopropyl fluorophosphate was unable to inhibit fMet-Leu-Phe-induced actin polymerization suggested that this activity of PMSF might be unrelated to proteinase inhibitory activity. Polymyxin B, a membrane-active antibiotic, had an effect similar to PMSF on fMet-Leu-Phe-induced actin polymerization. This suggests that PMSF may also be acting via its membrane effect rather than its anti-proteinase effect.

Actins↗
PubMed1993

The effect of a fibre free and fibre supplemented polymeric enteral diet on normal human bowel function.

Although the effects of dietary fibre in a normal diet on intestinal function are well known, the effects of supplementing enteral diet with fibre on intestinal function are not so clear. The aims of the present study were two fold: firstly to compare intestinal function during ingestion of a self selected diet and fibre free polymeric enteral diet and secondly to investigate the effect of adding the fibre source, soy polysaccharide to the same polymeric diet, on bowel function. Six healthy subjects were randomly assigned to 3 treatment periods (7 days) of a self selected diet (SSD), 2 l polymeric enteral diet (ED), or 2 l of the same polymeric enteral diet supplemented with 20 g/l of soy polysaccharide fibre (SPED). Parameters measured were bowel frequency/day, mean daily wet stool weights and whole gut transit time. Highest stool wet weights (g/24 h +/- SEM) were obtained from subjects consuming a SSD (180.3 +/- 30.6). This was significantly higher (p < 0.02) than those consuming an ED (81.9 +/- 14.5) but not a SPED (123 +/- 22.3). Whole gut transit (h +/- SEM) on a SSD (47 +/- 5.9) was significantly (p < 0.05) quicker than on an ED (73 +/- 4.9), but not significantly different from those ingesting a SPED (54 +/- 5.5). Bowel frequency/day (+/- SEM) in subjects consuming a SPED (1.0 +/- 0.1) was significantly (p < 0.02) higher than in subjects ingesting an ED (0.8 +/- 0.1) but was not significantly different when compared to a SSD (1.0 +/- 0.2). We conclude that ingestion of an ED results in significantly longer whole gut transit time, significantly decreased daily stool wet weights and decreased bowel frequency when compared to a SSD. The ingestion of 30 g of soy polysaccharide in a polymeric enteral diet not only tends to normalise whole gut transit time and daily stool wet weights, but also significantly increases bowel frequency when compared with values seen during the consumption of a fibre free polymeric enteral diet.

Journal Article↗
PubMed1982

Di-and triphosphate derivatives of acyclo- and arabinosylguanine. Effects on the polymerization of purified tubulin.

Glutamate- and nucleotide-dependent polymerization of purified calf brain tubulin was used as a model system to study interactions of ribose-modified GDP and GTP analogs with tubulin. Earlier studies (Hamel, E., and Lin, C.M.(1981) Proc. Natl. Acad. Sci. U.S.A. 78,3368-3372) were extended to three additional sets of analogs: the di- and triphosphate derivatives of 9-beta-D-arabinofuranosylguanine (araGDP and araGTP) and acycloguanosine (9-(2-hydroxyethoxymethyl)guanine) (acycloGDP and acycloGTP), as well as the periodate-oxidized and borohydride-reduced derivatives of GDP and GTP (ox-redGDP and ox-redGTP). Disruption of the ribose ring in ox-redGTP resulted in major loss of activity relative to GTP in supporting tubulin polymerization, although the analog's deficiency may result from an inability to displace GDP from the exchangeable site rather than a direct effect on the polymerization reaction itself. The poor activity of ox-redGTP could be largely reversed if nucleoside diphosphate kinase was added to the reaction mixture. Removal of the 2' and 3' carbons entirely, in the form of acycloGTP, resulted in only minimal loss of activity relative to GTP. AraGTP, on the other hand, was more active than GTP in supporting tubulin polymerization. All three GDP analogs were much less effective than GDP in inhibiting tubulin polymerization, although araGDP was significantly more inhibitory than acycloGDP or ox-redGDP. Relative inhibitory activity of these and additional GDP analogs was the same whether GTP or a GTP analog was used to support tubulin polymerization.

Animals↗
PubMed1990

A general strategy for polymerization, assembly and expression of epitope-carrying peptides applied to the Plasmodium falciparum antigen Pf155/RESA.

Polymerization of DNA fragments in a head-to-tail arrangement provides a convenient way to obtain multimeric expression of a specific gene product, e.g., epitope-carrying peptides for immunological studies. A novel technique for the polymerization and assembly of peptides has been developed, involving the use of the class-IIS restriction enzyme BspMI which enables unidirectional insertion of the DNA fragments to be polymerized [Kim and Szybalski, Gene 71 (1988) 1-8]. One or several DNA fragments are polymerized in subsequent steps, using in vitro DNA polymerization, and the obtained gene constructs containing several repeats are screened and sequenced using polymerase chain reaction techniques. Using a two-step polymerization strategy a peptide, comprising two repetitive sequences from the Plasmodium falciparum malaria blood-stage antigen Pf155/RESA, was assembled and subsequently synthesized in Escherichia coli. Two different fusion proteins suitable for affinity purification were produced using a dual affinity system. Rabbits were immunized with one of the fusion proteins and the antibody response was analyzed by the enzyme-linked immunosorbent assay and immunofluorescence using the second fusion protein.

Amino Acid Sequence↗
PubMed2006

Polymeric diet alone versus corticosteroids in the treatment of active pediatric Crohn's disease: a randomized controlled open-label trial.

BACKGROUND & AIMS: Nutritional therapy has been reported to have an almost equivalent efficacy of corticosteroids in achieving clinical remission in active Crohn's disease (CD). However, the effects of both treatments on intestinal mucosal inflammation rarely are reported. In a randomized controlled trial in children with active CD we compared the efficacy of nutritional therapy alone or corticosteroids on clinical variables and intestinal mucosal healing. METHODS: In a prospective, 10-week open-label trial, children with active, naive CD were randomized to orally polymeric formula alone or oral corticosteroids. The clinical activity index and nutritional and activity serum variables were evaluated at week 0 and then every 2 weeks; intestinal mucosal inflammation was assessed through endoscopy and histology at weeks 0 and 10. Primary efficacy outcomes were clinical remission and mucosal healing. RESULTS: Of the 37 children randomized, 19 received polymeric formula and 18 received corticosteroids. At week 10, on an intention-to-treat basis, the proportion of patients achieving clinical remission was comparable between the 2 groups (polymeric formula: 15/19 [79%; 95% confidence interval (CI), 56%-92%]; corticosteroid group: 12/18 [67%; 95% CI, 44%-84%]; P = .4; not significant). On the contrary, the proportion of children showing mucosa healing was significantly higher in the polymeric (14/19; 74%; 95% CI, 51%-89%) than the corticosteroid group (6/18 [33%; 95% CI, 16%-57%]; P < .05). At week 10 both endoscopic and histologic scores significantly decreased only in the polymeric group (P < .001). CONCLUSIONS: In children with active and recently diagnosed CD, a short course of polymeric diet is more effective than corticosteroids in inducing healing of gut inflammatory lesions.

Administration, Oral↗
PubMed2005

Effects of extracellular polymeric substances on aerobic granulation in sequencing batch reactors.

The effects of extracellular polymeric substances on aerobic granulation in sequencing batch reactors were investigated by evaluating the content and compositions of extracellular polymeric substances, and the relationship between extracellular polymeric substances composition and surface properties of glucose-fed aerobic granules. The results showed that extracellular polymeric substances could affect surface properties of cells, such as surface charge and hydrophobicity, enhance polymeric interaction and promote aerobic granulation. Moreover, extracellular polymeric substances were produced mainly in the exponential phase, and served as carbon and energy source in starvation phase during granulation process, thus regulating the growth of bacteria in the interior and exterior of granules, and maintaining the integrality of granules.

Aerobiosis↗
PubMed2005

Evaluation of micro-tensile bond strengths of composite materials in comparison to their polymerization shrinkage.

OBJECTIVE: The present study determined the influence of polymerization shrinkage of eight commercially available hybrid, micro-filled and nano composites (Z100 and Filtek Supreme, 3M-ESPE; Charisma and Durafill, Heraeus Kulzer; Tetric and InTen-S, Ivoclar Vivadent; Enamel plus HFO, GDF; Palfique Estelite Low Flow, Tokuyama) placed in large class 1 cavities on the bond strength to dentin. METHODS: Polymerization shrinkage was recorded for 300 s at room temperature with a Stress-Strain-Analyzer (C(FACTOR)=0.3). The maximum contraction stresses after 300 s, the time until gelation (t(0.5 N)) and the coefficient of near linear fit of contraction force/time (gradient) were analysed. For the evaluation of the micro-tensile-bond-strength (micro-TBS), hourglass shape samples obtained from a total of 32 no carious extracted human third and second molars, randomly divided into 8 groups, were used. Micro tensile bond strengths were determined by computing the ratio of maximum load by the adhesion area of the hourglass shape. In order to analyze the quality of the polymerization within fillings, hardness profiles of a surface cut thought the middle of the restored tooth and along the tooth axis were made. Further, the modulus of elasticity, determined in a three-point-bending test, as well as the variation of the modulus of elasticity and of the hardness within a filling were considered. The statistical analyses were conducted by ANOVA (alpha=0.05) and post-hoc Tukey's test. RESULTS: A significant correlation between polymerization shrinkage and micro-TBS was found (Pearson; -0.44). The correlation between modulus of elasticity in bending test and shrinkage stress (Pearson; 0.77), coefficient of near linear fit m (Pearson; 0.72), time until gelation (Pearson; -0.52) and micro-tensile-bond-strength (Pearson; -0.45) was also significant. A high polymerization tension and modulus of elasticity negatively affected the adhesion of the composite to the tooth hard substance. Further, the number of samples lost during the slice cutting and the hourglass shape preparation was found to correlate highly significantly with the shrinkage stress (Pearson; 0.97), coefficient of near linear fit m (Pearson; 0.94) and modulus of elasticity (Pearson; 0.82). All materials showed sufficient polymerization within the filling in comparison to the filling surface, the hardness at the bottom of the filling was greater than 80% of the maximum hardness value. The modulus of elasticity was not considerably reduced within the filling. SIGNIFICANCE: High contraction stress and modulus of elasticity, fast development of contraction force and an early start of stress build-up of materials placed in restrictive cavities cause tension in the material with a possible subsequent distortion of the bond to the tooth structure. A low modulus of elasticity is not necessarily associated with high bond strength. However, it causes a more uniform stress distribution at the restorative composite-tooth interface. This is also evident in a reduced sample loss during the different stages of sample preparation.

Analysis of Variance↗
PubMed2006

Long-term bond between dual-polymerizing cementing agents and human hard dental tissue.

OBJECTIVES: To examine the long-term adhesion of seven dual-polymerizing cementing agents to human dentin in vitro. METHODS: Two hundred and eighty extracted non-carious human molars were ground flat to expose dentin surfaces. The bond strengths of cementing agents with their respective bonding systems were examined: one compomer cement (PermaCem), five resin cements (RelyX ARC, Panavia F, Variolink II, Nexus 2, Calibra) and one self-adhesive universal resin cement (RelyX Unicem). One subgroup (n=10) was tested after 150 days of storage in water at 37 degrees C (time t(1)), the other subgroup (n=10) was tested after 150 days of storage plus 37,500 thermal cycles (time t(2)). All specimens were stressed in shear at a constant crosshead speed of 0.5mm/min until failure. Statistical analysis was performed by ANOVA, taking effect interactions into account. The Tukey method was used for multiple paired comparisons (alpha=0.05). RESULTS: The three-way ANOVA (cementing agents, polymerization methods, times of measurements) showed Variolink II to have the highest strength at 9.9+/-4.5MPa. Values were slightly higher at t(1) (5.9+/-4.7MPa) than at t(2) (4.9+/-4.2MPa) (p=0.0044). Polymerization with light activation (6.5+/-5.1MPa) yielded higher strengths than polymerization without (4.3+/-3.3MPa) (p<0.0001). Separate two-way ANOVAs for t(1) and t(2) showed that the two main effects (cementing agent, polymerization method) and their interactions differed significantly. SIGNIFICANCE: Cementing agents/adhesive systems and the polymerization method influence the long-term bond to hard dental tissues.

Acid Etching, Dental↗
PubMed2004

Effect of polymerization conditions on the network properties of dex-HEMA microspheres and macro-hydrogels.

Dextran-hydroxy-ethyl-methacrylate (dex-HEMA) hydrogels in the form of microspheres are an attractive system for the controlled delivery of protein drugs. In this work, the microspheres were prepared by a water-in-water emulsion polymerization process. The polymerization reaction was initiated by potassium peroxodisulfate (KPS) and catalyzed by N,N,N',N'-tetramethylethylenediamine (TEMED). The effect of the initiator concentration, reaction temperature and pH on the mechanical and network properties of the microspheres were investigated. The size and size distribution of the microspheres, equilibrium water content, and methacrylate conversion were also determined. The mechanical properties of single microspheres were measured by a micromanipulation technique and the rheological characteristics of the same material in the form of macroscopic hydrogel slabs were determined by a controlled stress rheometer. The results showed that the Young's moduli of the microspheres and of macroscopic slabs measured by these two methods were in good agreement. Higher KPS initiator concentrations resulted in a more rapid polymerization with a shorter gelation and lag time, and a higher Young's modulus of the gels. An increase in temperature also resulted in a more rapid polymerization with a shorter gelation and lag time. However, the Young's modulus of the gels decreased with an increase in polymerization temperature. The pH had no significant effect on the mechanical properties of the microspheres. This study demonstrates that the network properties of dex-HEMA hydrogels can be tailored by the polymerization conditions, which opens the possibility to modulate the release rate of entrapped compounds.

Chemistry, Pharmaceutical↗
PubMed2005

Synthesis and characterization of polyacrylonitrile nanoparticles by dispersion/emulsion polymerization process.

Polyacrylonitrile nanoparticles in sizes ranging from approximately 35 to 270 nm were prepared by dispersion/emulsion polymerization of acrylonitrile in a continuous aqueous phase in the presence of potassium persulfate as initiator and various alkyl-sulfate and sulfonate surfactants. The influence of various polymerization parameters (e.g., concentration of monomer and initiator, type and concentration of surfactant, temperature and time of polymerization, ionic strength, pH and co-solvent concentration) on the properties (e.g., size and size distribution, yield, stability, etc.) of the particles has been investigated. The polymerization of acrylonitrile may occur in two major locations: in the aqueous continuous phase (dispersion polymerization) and/or within the surfactant micelles (emulsion polymerization). A discussion concerning the role of these two mechanisms under different conditions, including comparison with previous literature, is also presented. Surface and bulk characterizations of the particles were performed by methods such as transmission and scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, zeta potential, and gravimetric measurements.

Acrylic Resins↗
PubMed2005

Growth mechanism of soap-free polymerization of styrene investigated by AFM.

To clarify the growth mechanism of polystyrene (PSL) particles in the soap-free polymerization, characteristics of not only particles but also polymeric materials floating in the bulk were investigated on the molecular scale by using atomic force microscope (AFM), where a cationic initiator V-50 is used to make the formed polymeric materials transfer on the mica plate in sampling. Our main attention here is to know the reason why the particle size increases with increasing initiator concentration in the production of PSL particles. The following are found. (1) As far as the initiators and monomers remain in the bulk solution, the polymeric materials are born in the bulk continuously, because of the slow decomposition rate of initiators. (2) The growth of particles at the early stage of t(r) > or = 0.75 h is considered to be attributable mainly to the particle swelling by absorbing monomers from the bulk. The rapid growth at the intermediate stage is due to the deposition of polymeric materials in the bulk on the particle surface and their simultaneous swelling by monomers in the bulk. (3) The reason why the particle size increases with increasing concentration of initiator is that the growth process is controlled by the deposition rate of polymeric materials in the bulk whose amount increases with the initiator concentration. (4) The particle size and the smoothness of particle surface depend on the relative concentration of initiators and monomers remained.

Journal Article↗
PubMed2005

Class II composite resin restorations with two polymerization techniques: relationship between microtensile bond strength and marginal leakage.

OBJECTIVE: To determine the relationship between leakage and microtensile bond strength in the same specimen of direct Class II composite restorations performed with two polymerization techniques. METHODS: Class II slot preparations were made in 40 non-carious human third molars and restored using Single Bond and P-60 (3M ESPE) according to the manufacturer's indications. Half of the preparations had the cervical margin in enamel and half in dentin. Teeth were incrementally restored either with direct polymerization from occlusal surface or with indirect polymerization through translucent matrices and reflective wedges. Teeth were isolated with nail varnish and immersed in fucsin for 24h. Subsequently, they were sectioned into slabs that were measured for leakage (mm), and trimmed to obtain hour-glass shaped specimens for microtensile bond test. Fractured specimens were examined under magnification (40 x) to evaluate the fracture mode. Data were analyzed with Mann-Whitney and Kruskal-Wallis (microleakage), two-way ANOVA and Student-Newman-Keuls tests (bond strength). The relationship between microleakage and microtensile bond strength were analyzed with Spearman's correlation test. RESULTS: There were no significant effects of polymerization technique and margin location on both leakage and bond strength (p>0.05). Bond strengths were higher in preparations with enamel margins than in preparations with dentin margins, when restored with indirect polymerization technique (p<0.05). No significant correlation was found between leakage and bond strength (p>0.05). CONCLUSIONS: Polymerization techniques had no influence on microleakage and bond strength of Class II composite restorations, and there was no relationship between these variables when evaluated in the same specimen.

Analysis of Variance↗
PubMed2006

Monomeric and polymeric IgA show a similar association with the myeloid FcalphaRI/CD89.

IgA is found in both mucosal secretions and serum and is the dominant immunoglobulin isotype produced in humans. It exists in different molecular forms, namely monomeric IgA, dimeric IgA, polymeric IgA and secretory IgA, all exhibiting interactions with FcalphaRI/CD89 to some extent. CD89 is an activating, gamma-chain associated, Fc receptor for IgA expressed on myeloid cells. Here, we investigated the interaction of monomeric and polymeric IgA purified from human serum with CD89 using surface plasmon resonance. The results demonstrate a similar association for monomeric and polymeric IgA with CD89. In contrast, monomeric IgA dissociated more rapidly from CD89 than polymeric IgA. Removal of N-glycans from mIgA resulted is an increased association with CD89, whereas the dissociation was more rapid, resulting in binding comparable to that of untreated monomeric IgA. We conclude that the initial interaction of monomeric and polymeric IgA with CD89 is similar, whereas monomeric IgA dissociates more rapidly from CD89. In view of the large excess of monomeric IgA in serum, monomeric IgA will compete for CD89 interaction with polymeric IgA, thereby preventing cell activation initiated by receptor aggregation contributing to the anti-inflammatory role of IgA.

Antigens, CD↗
PubMed2006

Increases in intrapulpal temperature during polymerization of composite resin.

STATEMENT OF PROBLEM: The polymerization of dental composite resins can generate increases in intrapulpal temperature that may damage the pulp. The development of new polymerization devices such as the argon laser makes the assessment of these temperatures important. PURPOSE: This study compared increases in temperature generated by argon laser and halogen light when polymerizing a bonding system and a composite resin, and also sought to determine whether both types of polymerization lights generate temperature increases below the safe limit of 5.5 degrees C. MATERIAL AND METHODS: Thermocouples linked to a temperature reading system were positioned in the pulp chamber of 10 extracted bovine incisors. Class V cavities were prepared, etched, and filled with a 1-bottle bonding system (Single Bond) and composite resin (Z-100). The test groups were as follows (n = 5 for all groups): halogen light for bonding system (HB); halogen light for composite resin (HC); argon laser for bonding system (LB), and argon laser for composite resin (LC). The polymerization parameters were halogen light operated at 600 mW/cm2 for 40 seconds, which served as control, and argon laser operated at 200 mW for 10 seconds. Data were analyzed by a 2-way (light versus material) analysis of variance (ANOVA) (alpha = .05). RESULTS: The average temperature increases were 2.35 degrees C (HB), 2.69 degrees C (HC), 1.25 degrees C (LB), and 1.5 degrees C (LC). Significant differences between halogen light and argon laser (P = .002), but not between composite and bonding system, were demonstrated. CONCLUSIONS: The argon laser produced significantly lower increases in pulpal temperature than the halogen light, independent of the thickness of the polymerized material.

Analysis of Variance↗
PubMed2006

Polystyrene/Fe3O4 magnetic emulsion and nanocomposite prepared by ultrasonically initiated miniemulsion polymerization.

Ultrasonically initiated miniemulsion polymerization of styrene in the presence of Fe3O4 nanoparticles was successfully employed to prepare polystyrene (PS)/Fe3O4 magnetic emulsion and nanocomposite. The effects of Fe3O4 nanoparticles on miniemulsion polymerization process, the structure, morphology and properties of PS/Fe3O4 nanocomposite were investigated. The increase in the amount of Fe3O4 nanoparticles drastically increases the polymerization rate due to that Fe3O4 nanoparticles increase the number of radicals and the cavitation bubbles. Polymerization kinetics of ultrasonically initiated miniemulsion polymerization is similar to that of conventional miniemulsion polymerization. PS/Fe3O4 magnetic emulsion consists of two types of particles: latex particles with Fe3O4 nanoparticles and latex particles with no encapsulated Fe3O4 nanoparticles. Fe3O4 nanoparticles lower the molecular weight of PS and broaden the molecular weight and particle size distribution. Thermal stability of PS/Fe3O4 nanocomposite increases with the increase in Fe3O4 content. PS/Fe3O4 emulsion and nanocomposite exhibit magnetic properties. PS/Fe3O4 magnetic particles can be separated from the magnetic emulsion by an external magnetic field and redispersed into the emulsion with agitation.

Crystallization↗
PubMed1998

Resuscitation of the injured patient with polymerized stroma-free hemoglobin does not produce systemic or pulmonary hypertension.

BACKGROUND: Hemoglobin-based blood substitutes appear poised to deliver the promise of a universally compatible, disease-free alternative to banked blood. However, vasoconstriction following administration of tetrameric hemoglobins has been problematic, likely because of nitric oxide binding. Polymerized hemoglobin is effectively excluded from the abluminal space because of its size, and is thus less likely to perturb vasorelaxation. We therefore hypothesized that hemodynamic responses would be no different in injured patients receiving polymerized hemoglobin versus banked blood. METHODS: Injured patients requiring urgent transfusion were randomized to receive either polymerized hemoglobin or banked blood. Systemic arterial pressure, pulmonary arterial pressure, cardiac index, pulmonary capillary wedge pressure, systemic vascular resistance, and pulmonary vascular resistance were measured serially. RESULTS: There was no difference in any of the measured hemodynamic parameters between patients resuscitated with polymerized hemoglobin versus blood. CONCLUSIONS: Polymerized hemoglobin given in large doses to injured patients lacks the vasoconstrictive effects reported in the use of other hemoglobin-based blood substitutes. This supports the continued investigation of polymerized hemoglobin in injured patients requiring urgent transfusion.

Adult↗