Disposable devices for the dispensing of oral drops. Study of photoprotectiveness and compatibility

in the first part of this article calorimetric studies on poly (hydroxy ethyl methacrylate) (PHEMA) are presented. In the past the irregular melting curves in this type of experiment have been interpreted as evidence for the existence of different types of water in these gels. The studies presented here demonstrate that the occurrence of a glass transition in the freezing hydrogels may be responsible for this irregular melting behavior, and that this behavior is not (necessarily) an indication for the existence of different types of water. In the second part results are shown of measurements of the mobility of water in hydrogels, made by relaxation NMR. These results indicate that very rapid interchange occurs between the water molecules, and they support the conclusion that the calorimetric data mentioned above are not indicative for the existence of different classes of water in hydrogels. These results are compared with data from other fields of science, especially from fundamental freeze drying studies, which support the alternative interpretation of the calorimetric measurements.     

Investigations into the Mass Spectrometric Method for the Determination of the Mode of Termination in Radical Polymerization

The fraction of termination by disproportionation, λ, in radical polymerization may be determined by a mass spectrometric (MS) analysis of the resulting polymer. It is subjected to an array of stringent consistency checks, working with polymerizations of methyl methacrylate at 85 °C in three different solvents and with four different initiators. λ is shown to be unaffected by the choice of initiator, initiator concentration, or isoviscous solvent. These findings serve to allay any fears about the method being undermined by effects such as primary radical termination or chain transfer to solvent, thereby establishing its robustness. At the same time, direct evidence for the occurrence of chain transfer to the solvent methyl isobutyrate is uncovered, and the importance of knowing other rate‐parameter values accurately, if λ is to be determined accurately, is illustrated. By carrying out MS analyses, it is concluded that electrospray ionization with time‐of‐flight detection gives the best results for the present purpose.

     

Magnetic Polymer/Nickel Hybrid Nanoparticles Via Miniemulsion Polymerization

This work shows a method to synthesize and encapsulate magnetic nickel nanocrystals into polymeric colloidal particles through miniemulsion polymerization. The nickel nanoparticles are produced by a thermal decomposition method in the presence of oleylamine and triphenylphosphine, which results in a hydrophobic surface. However, being compatible with the monomer does not ensure a successful encapsulation by miniemulsion polymerization, as the nickel nanoparticles are expelled from the polymer particles with increasing styrene conversion due to the poor adhesion interaction between the organic shells of the nickel nanoparticles and the polystyrene. Changing the hydrophobic polystyrene to a polymer with higher polarity such as poly(methyl methacrylate) proves to be efficient for encapsulation of nickel nanoparticles when employing a hydrophilic initiator. After encapsulation, these nanoparticles show magnetic response.

     

Effect of different monomer-based composites and acid etching pre-treatment of enamel on the microleakage using self-etch adhesives systems

Objective. To evaluate quantitatively the marginal microleakage of restorations carried out with self-etching adhesives with or without prior phosphoric enamel acid etching of silorane or methacrylate resin-based composite restorations subjected to thermal cycling. Materials and methods. Forty cavities were prepared at the proximal surface of bovine incisors and randomly divided according to the etching of the enamel and restorative system used. The groups were restored with methacrylate [Adper SE Plus adhesive (3M ESPE) + Filtek Z250 (3M ESPE)] or silorane [Filtek LS adhesive (3M ESPE) + Filtek LS composite (3M ESPE)] restorative systems, light-cured using a LED unit (Bluephase 16i, Vivadent). After restorative procedure and thermocycling (1000 cycles), the specimens were immersed in methylene blue for 2 h. The specimens were triturated and the powder was used for analysis in an absorbance spectrophotometer. Data were statistically analyzed by 2-way ANOVA (alpha = 0.05). Results. No statistical difference between the restorative materials tested with or without previous acid etching of enamel in Class II marginal microleakage was observed (p > 0.05). Conclusions. The use of acid etching prior to self-etching adhesives did not interfere on the microleakage of methacrylate- or silorane-based restorations.     

3种义齿基托材料抛光后表面粗糙度的比较研究

目的研究3种义齿基托材料抛光前后的表面粗糙度度。方法选择聚甲基丙烯酸基托树脂（PMMA）、弹性义齿材料和不碎胶等3种义齿基托材料,将材料制成12mm×12mm×2mm的标准试件,每种材料各20个,对试件进行打磨和抛光后,采用表面轮廓测量仪检测材料抛光前后的表面粗糙度,通过扫描电镜对材料表面形貌进行表面观察。结果PMMA、弹性义齿材料和不碎胶抛光后表面粗糙度分别为（0．160±0．018）μm、（0．110±0．011）μm和（0．141±0．017）μ。弹性义齿材料和不碎胶的表面粗糙度低于PMMA（P〈0．05）,表面划痕也少于PMMA。结论弹性义齿材料和不碎胶更能获得抛光效果,表面粗糙度优于PMMA。     

Biological and physicochemical properties of carbon-graphite fibre-reinforced polymers intended for implant suprastructures

The aim of this study was to determine water sorption, water solubility, dimensional change caused by water storage, residual monomers, and possible cytotoxic effects of heat-polymerized carbon-graphite fibre-reinforced composites with different fibre loadings based on methyl methacrylate/poly(methyl methacrylate) (MMA/PMMA) and the copolymer poly (vinyl chloride-co-vinyl acetate). Two different resin systems were used. Resin A contained ethylene glycol dimethacrylate (EGDMA) and 1,4-butanediol dimethacrylate (1,4-BDMA); the cross-linker in Resin B was diethylene glycol dimethacrylate (DEGDMA). The resin mixtures were reinforced with 24, 36 and 47 wt% surface-treated carbon-graphite fibres. In addition, polymer B was reinforced with 58 wt% fibres. Water sorption was equal to or below 3.34±1.18 wt%, except for the 58 wt% fibre loading of polymer B (5.27±1.22 wt%). Water solubility was below 0.36±0.015 wt%, except for polymer B with 47 and 58 wt% fibres. For all composites, the volumetric increase was below 0.01±0.005 vol%. Residual MMA monomer was equal to or below 0.68±0.05 wt% for the fibre composites. The filter diffusion test and the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) (MTT) assay demonstrated no cytotoxicity for the carbon-graphite fibre-reinforced composites, and residual cross-linking agents and vinyl chloride were not detectable by high-performance liquid chromatography (HPLC) analysis.     

Ablation Zones and Weight-Bearing Bones: Points of Caution for the Palliative Interventionalist

PurposeTo evaluate and classify underlying mechanisms of adverse outcomes after percutaneous computed tomography (CT)–guided cryoablation for palliation of painful musculoskeletal metastatic disease.Materials and MethodsData were collected for patients who underwent CT-guided percutaneous palliative cryoablation for painful musculoskeletal metastatic disease between January 2010 and December 2012. Cases with adverse outcomes or suboptimal response were identified and classified according to the Society of Interventional Radiology (SIR) classification system for complications by outcome and according to underlying mechanism of the outcome as delineated on follow-up examination.ResultsThere were 61 patients who received ablation for painful musculoskeletal metastatic disease. Six patients with adverse outcomes were identified. Two were minor complications (A, n = 1; B, n = 1), and four were major complications (C, n = 1; D, n = 3). Four patients incurred sequelae related to damage of ancillary structures included in the ablation zone, and two patients developed complete fractures after ablation of lesions in weight-bearing bones.ConclusionsComplete cryoablation of a painful musculoskeletal metastatic lesion may lead to ancillary damage of adjacent structures or fracture in weight-bearing bones.     

负载抗菌药物的骨水泥的药物释放实验研究

目的 揭示负载抗菌药物的骨水泥的药物释放浓度、持续时间、药物残留程度及低于最小有效抑菌浓度的释放时间,为合理应用抗菌药物提供理论依据。方法 通过对负载盐酸万古霉素和亚胺培南西司他丁钠的骨水泥进行体外洗提实验,采用高效液相色谱法检测分析两种负载抗菌药物的骨水泥的药物释放浓度、释放持续时间和药物残留程度。结果 ①负载抗菌药物的骨水泥第一天药物释放量最大,后逐渐持平,且释放时间较长,释放浓度较低;②截止到第7周盐酸万古霉素、亚胺培南西司他丁释放量分别只占总负载量的15%、25%;③盐酸万古霉素第1周后释放浓度低于最小有效抑菌浓度,亚胺培南西司他丁钠第7周后释放浓度低于最小有效抑菌浓度。结论 载抗菌药物骨水泥存在长时间药物残留现象,是导致持续低于最小有效抑菌浓度的主要原因。此种现象不但对细菌起不到抑菌作用,而且是诱导细菌耐药性的危险因素。