Polymer materials of medical purpose and materials for dentistry

A wide range of polymer materials for medical purposes based on polysiloxane developed at the State Research Institute of Building Structures is presented. The properties of compositions cured by both end hydroxyl groups and the reaction of hydroxylation are considered and examples of their applications are presented.     

Polymer colloids in photonic materials

Exciting materials known as photonic band-gap materials have come upon the materials science scene and are being studied by many research groups around the world. These new materials operate on light in a way very analogous to the way semiconductors operate on electrons to produce very fast electronic switching and computing circuits. It is imagined that the successful fabrication of these materials will lead to computing machines operating on light and yielding the ultimate speeds in information processing, as electrons typically move only at about one tenth to one half the speed of light. Such devices will require much less heat dissipation and may lead to further miniaturization of computing circuits. New applications in diverse chemical and biochemical sensing are also emerging from these photonic materials. Separation and filtration materials and diverse mesoporous materials and composites are also being developed that rely on such photonic arrays and assemblies as fabrication templates. Polymer colloids in the size range of tens of nm to tens of microns are key components in such new materials and processes. A major limitation in the production of such new materials and devices is that fabrication of such arrays and assemblies is extremely slow and unsuitable for practical manufacturing. Crystallization of charged colloidal suspensions, annealing of core–shell particle arrays, epitaxial growth of crystals from two–dimensional templates, and annealing of thermoreversible gel particle arrays are being explored to ameliorate these limitations. To cite this article: J. Texter, C. R. Chimie 6 (2003).     

Polymer materials for constructing therapeutical nanoparticles in photothermal therapy

Photothermal therapy (PTT) ablates tumors by thermal effects of photothermal agents (PTAs), and attracts wide attention due to the non-invasive characteristic. The ideal PTAs are expected to have high photothermal conversion effect under NIR irradiation, as well as targeting abilities and good biocompatibility satisfying the need of application in vivo. Nanoparticles (NPs) are commonly used as anti-tumor materials, and plenty of researches on therapeutical NPs for PTT treatment have been developed. Among various building blocks for photothermal NPs, polymer materials for biomedical applications have great advantages due to their negligible toxicity, flexibility for functional modification, and ability to integrate multiple therapeutic strategies. This review focuses on the polymer materials utilized in photothermal NP designing, including their application as excellent carriers and powerful PTAs with great PTT effects. Furthermore, the synergy therapy based on polymeric nanoplatform for enhancing PTT therapeutic efficiency will be introduced.     

Polymer blends: materials with versatile properties

During the last fifty years blending of dissimilar polymers has been a major path to tailor materials with new properties in industry. Especially in the area of engineering thermoplastic materials this approach has led to a significant number of large volume products, like Polyphenyleneether/High Impact Polystyrene‐blends (PPE/HIPS), Polycarbonate/Styrenics‐blends (PC/ABS), Polycarbonate/Polybutyleneterephthalate‐blends (PC/PBT) and Polyamide/Polyphenyleneether‐alloys (PA/PPE). The commercial success of these materials is mainly related to their unique combinations of properties, which enables their use in a multitude of applications.     

Polymer colloids and silver nanoparticles hybrid materials

The present study presents two different methods to obtain hybrid material formed by the poly [styrene (ST)–poly(ethylene glycol) methyl ether methacrylate (PEGMA) 1100] and silver (Ag⁰). The aim has been to cover the polymeric particles with Ag⁰ shell. The first method consisted of mixing Ag⁰ nanoparticles dispersion with poly (ST-PEGMA 1100) dispersion, while in the second method, the Ag⁰ nanoparticles have been generated in situ. The hybrid materials have been characterized by MO, dynamic light scattering, scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy, X-ray energy dispersive spectrometry, and ultraviolet–visible spectrophotometry. The results confirm the obtaining of two types of morphologies. In the first case, the nanoparticles have been arranged in the interspatial zones of the polymer particles, while in the second method, the Ag⁰ nanoparticles have covered the polymer particles. Thus, the film obtained using the second method is more suitable for the practical application, as a separation membrane, using the antiseptic properties of Ag⁰.     

Polymer/carrier composites as materials and reactors for organic synthesis

In this work new polymer/carrier composites are described which serve as novel materials in flow-through reactors for polymer-supported organic solution-phase synthesis. Monolithic polymer/carrier columns are prepared by a new precipitation polymerization process inside the void pore volume of megaporous glass carrier materials. Chemical functionalization of the internal polymer phase with chlorosulfonic acid or trimethylamine generates small, interconnected ion-exchange resin beads with a diameter of 1-3 microm which can be used for a large variety of organic syntheses. These monolithic rods are incorporated into an appropriate casing and can conveniently be operated in the flow-through mode. Important successful applications are polymer-assisted solution-phase reductions, oxidations and Horner-Emmons olefinations. Additionally, the use of these monolithic columns as catalytic microreactors and their performance in selected reactions are described.     

Polymer/boron nitride nanocomposite materials for superior thermal transport performance

Boron nitride nanosheets were dispersed in polymers to give composite films with excellent thermal transport performances approaching the record values found in polymer/graphene nanocomposites. Similarly high performance at lower BN loadings was achieved by aligning the nanosheets in poly(vinyl alcohol) matrix by simple mechanical stretching (see picture).     

Polymer/carbon-based quantum dot nanocomposite: forthcoming materials for technical application

This endeavor presents state-of-the-art overview on polymer/carbon-based quantum dot nanocomposite. Carbon-based quantum dot (graphene quantum dot, carbon nanodot, and polymer dot) are ～10nm. Carbon-based quantum dot own exciting features such as tunable optoelectronic and photoluminescence properties, high stability, chemical inertness, low cytotoxicity, and biocompatibility owing to quantum confinement and edge effects. Main emphasis of article was to see the combined effect of polymer and carbon-based quantum dot in nanocomposite. Five major categories have been reviewed in this article including conjugated polymer/carbon-based quantum dot nanocomposite, epoxy/carbon-based quantum dot nanocomposite, polystyrene/carbon-based quantum dot nanocomposite, poly(dimethyl siloxane)/carbon-based quantum dot nanocomposite, and block copolymer/carbon-based quantum dot nanocomposite. The review also refers to cutting edge application areas of polymer/carbon-based quantum dot nanocomposite. Conducting polymer/carbon quantum dot nanocomposite has been integrated in energy storage devices, detectors, and electronic devices. These materials are also promising candidates for bulk heterojunction solar cells and light-emitting diodes. Another important use is the identification and removal of toxic metals. Functional materials have also been used for fluorescence imaging of live cells. Modification of carbon-based quantum dot and incorporation in appropriate polymer matrices can be adopted as powerful future tool enabling desired tailored applicability of nanocomposite in advance high performance technical applications.     

Polymer/silicate composites: new materials for subsurface permeable reactive barriers

Investigations were performed into the suitability of novel composites to serve as materials for subsurface permeable reactive barriers (PRBs). These new materials are Type I composites—they are preformed organic polymers embedded in an inorganic matrix without significant covalent bonding between the components. The required properties for these materials to function efficiently are: (1) a tunable water passing rate to approximate the hydraulic conductivity of the subsurface environment where the PRB will be placed, (2) sufficient mechanical strength (both wet and dry) to maintain barrier integrity, (3) the ability to incorporate selective metal sequestration agents so that they remain active—yet do not leach from the barrier, and (4) to be deployable through direct injection methods such that trenching is not needed. Additionally, there is a need to keep the technology as low cost as possible, while remaining reliable. Results recently obtained in our laboratory show that our materials, remarkably, exhibit all of these properties and show great promise as vadose zone deployable PRBs.     

Polymer modified and stabilized cholesteric liquid crystal materials for flat panel application

Polymer dispersions, even in very low concentrations, can improve the performance of cholesteric liquid crystal materials necessary for their application in flat panel displays. Normal scattering mode, reverse scattering mode and reflective mode cholesteric liquid crystal materials are described. The roll of the polymer in each of these display modes is reviewed as are the unique electro-optic characteristics of the dispersions.     

Natural rheological modifiers for personal care

The development of personal care formulations incorporates the deliberation of the prerequisite product rheology and the right rheology modifier to deliver these effects. While the effectiveness of the finished product will hinge on the selection and level of active ingredients and excipients, the esthetics and even the penetration of these actives into the stratum corneum will be affected by the product rheology. Rheology modifiers are frequently denoted as thickeners, and while increasing the apparent viscosity should enhance the perception of quality in a formulation, this is only one aspect of rheological control. The product itself can be Newtonian or pseudoplastic, thixotropic, existing as a ringing gel or a stringy flowable liquid. This changes the way that the product appears in the bottle, the ease with which aliquots are poured or scooped from the packaging, the process of rubbing it into the skin or along the hair shaft, and upon using, the rinsing and removal of the product. It will also be vital to select the correct rheological characteristics to guarantee the stability of the finished formulation. By changing the structure of polymeric rheology modifiers, the impact on the sensorial properties and performance characteristics can be investigated. Careful selection of monomers, structure and other co‐ingredients will result in products optimized for use in skin care formulations. Copyright © 2016 John Wiley & Sons, Ltd.     

Polymer materials based on ethylene copolymers with substituted norbornene

The copolymers of ethylene with 5-ethylidene-2-norbornene containing 10–65% of the cyclic comonomer have been prepared with the use of three ansa-metallocene catalysts, namely, Et[Ind]₂ZrCl₂-methylaluminoxane, Et[IndH₄]₂ZrCl₂-methylaluminoxane, and Me₂Si[Ind]₂ZrCl₂-methylaluminoxane. Side groups >C=CH-CH₃ capable of participation in the ozonolysis reaction have been incorporated into polymer chains via the copolymerization of ethylene with the cyclic comonomer. As evidenced by DSC, and X-ray diffraction, and very cold neutron scattering measurements of the supramolecular structure of the copolymers, the enrichment of the copolymer with the cyclic comonomer causes transformation of the ethylene-5-ethylidene-2-norbornene copolymer from the semicrystalline state to the amorphous state. This effect is accompanied by an increase in the density and optical transparency of the material and a rise in its glass transition temperature. Among the copolymers under study, the highest T _g (83°C) is exhibited by the copolymer synthesized with the Et[Ind]₂ZrCl₂-methylaluminoxane catalyst and containing 30 mol % 5-ethylidene-2-norbornene.     

Study of chemical modifiers for the determination of chromium in biological materials by tungsten coil electrothermal atomic absorption spectrometry

The determination of Cr in digest solutions of mussels and non-fat milk powder by tungsten coil electrothermal atomic absorption spectrophotometry (TC-ETAAS) is affected by interferences. This study reports a critical evaluation of chemical modifiers that could be employed to correct these interferences. The chemical modifiers tested were: Mg [as Mg(NO₃)₂], Pd [as Pd(NO₃)₂], NH₄NO₃, ascorbic acid, and mixtures of these compounds. The less effective modifier was NH₄NO₃. The best effects, considering thermal stabilization and sensitivity, were obtained in mixtures of ascorbic acid plus Mg. Chromium was determined by TC-ETAAS in certified reference materials of mussels and non-fat milk powder, and results were comparable with those obtained by graphite furnace atomic absorption spectrophotometry (GFAAS).     

Study of chemical modifiers for the determination of chromium in biological materials by tungsten coil electrothermal atomic absorption spectrometry

The determination of Cr in digest solutions of mussels and non-fat milk powder by tungsten coil electrothermal atomic absorption spectrophotometry (TC-ETAAS) is affected by interferences. This study reports a critical evaluation of chemical modifiers that could be employed to correct these interferences. The chemical modifiers tested were: Mg [as Mg(NO₃)₂], Pd [as Pd(NO₃)₂], NH₄NO₃, ascorbic acid, and mixtures of these compounds. The less effective modifier was NH₄NO₃. The best effects, considering thermal stabilization and sensitivity, were obtained in mixtures of ascorbic acid plus Mg. Chromium was determined by TC-ETAAS in certified reference materials of mussels and non-fat milk powder, and results were comparable with those obtained by graphite furnace atomic absorption spectrophotometry (GFAAS). Received: 19 June 1998 / Revised: 11 January 1999 / Accepted: 16 January 1999     

Chemical modifiers in arsenic determination in biological materials by tungsten coil electrothermal atomic absorption spectrometry

Palladium, iridium, and rhodium are evaluated as possible chemical modifiers in the determination of As in digest solutions of biological materials (human hair and clam) by tungsten coil electrothermal atomic absorption spectrophotometry (TCA-AAS). The modifier in solution was applied onto the coil and thermally pre-reduced; the pre-reduction conditions, the amount of modifier, and the thermal program were optimized. Palladium was not satisfactory, whereas Ir and Rh were effective modifiers and rendered better relative sensitivity for As by a factor of 1.4 and 1.9, respectively compared to the case without modifier. Upon optimization of thermal conditions for As in pre-reduced Ir (2.0 µg) and Rh (2.0 µg) modifiers and in the digest solutions of the study matrices, Rh (2.0 µg) was more effective modifier and was selected as such. The mean within-day repeatability was 2.8% in consecutive measurements (25–100 µg L^–1) (3 cycles, each of n=6) and confirmed good short-term stability of the absorbance measurements. The mean reproducibility was 4.4% (n=20 in a 3-day period) and the detection limit (3 _blank/slope) was 29 pg (n=15). The useful coil lifetime in Rh modifier was extended to 300–400 firings. Validation was by determination of As in the certified reference material (CRM) of Oyster tissue solution with a percentage relative error (E _rel%) of 2% and percentage relative standard deviation (RSD%) of 3% (n=4), and by analytical recovery of As spiked in CRM of human hair [94±8% (n=4)]. The methodology is simple, fast (sample readout frequency 21 h^–1), reliable, of low cost, and was applied to the determination of As in hair samples of exposed and unexposed workers.     

Bitumen latex emulsion mastics for waterproofing and sealing use

Filled bitumen emulsion mastics were developed, and their technological and operational properties (homogeneity, stability, and adhesive strength) were studied. The optimal concentrations of filling the mastics were determined, and they were modified with anionic latex was carried out.     

Polyacrylamide-aluminum pentahydroxochloride-urea formulations as waterproofing agents for oil pool

Gel-forming polyacrylamide (PAA)-aluminum pentahydroxochloride (APHC) formulaitons were studied as waterproofing agents for an oil pool. The optimal formula and the gelation rate were determined.