背景:普通外科手术中,磁吻合技术以操作简便、吻合迅速、对位准确、吻合质量确定、应用范围广泛等优点备受关注,但磁材料留置体内可能会对机体产生一些不良的影响,生物可降解纳米磁性复合材料有望解决此问题。目的:研制适用于外科吻合...背景:普通外科手术中,磁吻合技术以操作简便、吻合迅速、对位准确、吻合质量确定、应用范围广泛等优点备受关注,但磁材料留置体内可能会对机体产生一些不良的影响,生物可降解纳米磁性复合材料有望解决此问题。目的:研制适用于外科吻合用的生物可降解纳米钕铁硼磁性复合材料,并评价其主要磁性能、体外降解性能。方法:采用高能球磨法制备纳米钕铁硼微粒,以溶剂挥发法将纳米钕铁硼微粒与生物可降解材料聚乳酸/羟基乙酸共聚物复合(聚乳酸/羟基乙酸共聚物含量分别为2.5%、5%、7.5%、10%、20%、30%、40%、50%),在特定温度(60,80,100,120,140℃)、压力(6,8,10,12,14 MPa)条件下,以温压成型工艺压制生物可降解聚乳酸/羟基乙酸共聚物-纳米钕铁硼磁性复合材料,检测其最大磁能积。采用磷酸盐缓冲液恒温振荡浸泡法进行生物可降解聚乳酸/羟基乙酸共聚物-纳米钕铁硼磁性复合材料(聚乳酸与羟基乙酸摩尔比分别为90/10、70/20、50/50)体外降解实验,扫描电镜观察磁体降解前后显微形态结构变化及降解时间与聚乳酸/羟基乙酸共聚物摩尔比的关系。结果与结论:生物可降解纳米钕铁硼磁性复合材料的磁性能在一定范围内与纳米钕铁硼微粒含量、成型温度及成型压力呈正比,与聚乳酸/羟基乙酸共聚物含量呈反比。在工艺参数为温度120℃、压力12 MPa、聚乳酸/羟基乙酸共聚物含量为5%时其磁性能最佳,最大磁能积为45 k J/m3。生物可降解纳米钕铁硼磁性复合材料在体外的降解过程与聚乳酸/羟基乙酸共聚物内部组分的摩尔比密切相关,降解时间与聚乳酸含量呈正比,与羟基乙酸含量呈反比,聚乳酸与羟基乙酸摩尔比90/10、70/20、50/50组的降解高峰期分别为8,6,4周。展开更多
研究了N-氨乙基-γ-氨丙基三甲氧基硅烷在水溶液中以单层形式负载于磁铁矿纳米颗粒表面的方法,并研究了单分子层硅烷负载磁铁矿纳米颗粒吸附剂(monolayer of silane on magnetite nanoparticles,MSMNPs)的除磷性能.结果表明,在低浓度下...研究了N-氨乙基-γ-氨丙基三甲氧基硅烷在水溶液中以单层形式负载于磁铁矿纳米颗粒表面的方法,并研究了单分子层硅烷负载磁铁矿纳米颗粒吸附剂(monolayer of silane on magnetite nanoparticles,MSMNPs)的除磷性能.结果表明,在低浓度下(平衡浓度小于300 mg·L^(-1))硅烷在磁铁矿纳米颗粒表面产生单层吸附,而反应温度90℃以上或离子强度0.1 mol·L^(-1)NaCl以上可以使单层硅烷在磁铁矿纳米颗粒表面的覆盖度达到~100%.FTIR和XPS图谱显示负载的硅烷以化学键的形式与磁铁矿纳米颗粒表面相结合.单层硅烷负载不引起磁性强度的明显变化.MSMNPs对磷的吸附等温线更符合Langmuir模型,拟合得到的最大吸附量为7.59 mg·g^(-1).由于磷吸附位位于MSMNPs的最外面,磷的吸附及脱附均很快,30 min内达到90%以上,1 h内达到平衡.因此,MSMNPs是一种易分离因而可反复使用,并且可快速吸附与脱附污染物的新型吸附剂.展开更多
Soft magnetic composites （SMCs） were prepared from three different ferromagnetic powder particles： iron powder ASC 100.29, spherical FeSi particles and vitroperm （Fe73CulNb3Si16B7） flakes. Two types of hybrid org...Soft magnetic composites （SMCs） were prepared from three different ferromagnetic powder particles： iron powder ASC 100.29, spherical FeSi particles and vitroperm （Fe73CulNb3Si16B7） flakes. Two types of hybrid organic-inorganic phenolic resins modified with either silica nanoparticles or boron were used to design a thin insulating layer perfect- ly covering the ferromagnetic particles. Fourier transform infrared （FTIR） spectrometry confirmed an incorporation of silica or boron into the polymer matrix, which manifested itself through an improved thermal stability of the hybrid resins verified by thermogravimetric-differential scanning calorimetry （TG-DSC） analysis. The core-shell particles prepared from the ferromagnetic powder particles and the modified hybrid resins were further compacted to the cylindrical and toroidal shapes for the mechanical, electrical and magnetic testing. A uniform distribution of the resin between the ferromagnetic particles was evidenced by scanning electron microscope （SEM） analysis, which was also reflected in a rather high value of the electrical resistivity. A low porosity and extraordinary high values of mechanical hardness and flexural strength were found in SMC consisting of the iron powder and phenolic resin modified with boron. The coercive fields of the prepared samples were comparable with the commercial SMCs.展开更多
Objective：To evaluate the in vitro and in vivo toxicity of self-prepared nanosized Fe2O3, which has the potential implication in tumor hyperthermia. Methods： Fe2O3 nanoparticles were prepared by improving co-precipi...Objective：To evaluate the in vitro and in vivo toxicity of self-prepared nanosized Fe2O3, which has the potential implication in tumor hyperthermia. Methods： Fe2O3 nanoparticles were prepared by improving co-precipitation, which characterization was detected by TEM, XRD, CMIAS, EDS. MTT assay was used to evaluate the in vitro cytotoxicity test; hemolytic test was carried out to estimate whether it has blood toxicity; Fe2O3 suspended in sterile 0.9% NaCl was intraperitoneally injected into Kumning mouse to calculate the LD50 ; micronucleus （MN） were reckoned to identify whether it is genotoxic. Results：The nanoparticles are brown spherical particles with diameter ranging from 8 to 15 nm, which have good decentralization and stability. The experiments also showed that the toxicity of the material on mouse fibroblast （L-929） cell lines was 0 - 1 degree ; it has no hemolysis activity; LD50 arrived at 5.45 g/kg^-1 after intraperitoneal injection of 1 ml suspension; micronucleus test showed that it has no genotoxic effects either. Conclusion： The results showed that the Fe2O3 nanoparticles are prepared successfully, the self-prepared nanosized Fe2O3 is a kind of high biocompatibility materials and perhaps it is suitable for further application in tumor hyperthermia.展开更多
Abstract： Maghemite-silica particulate nanocomposites were prepared by modified 2-step sol-gel process. Superparamagnetic maghemite nanoparticles were successfully produced using Massart＇s procedure. Nanocomposites ...Abstract： Maghemite-silica particulate nanocomposites were prepared by modified 2-step sol-gel process. Superparamagnetic maghemite nanoparticles were successfully produced using Massart＇s procedure. Nanocomposites consisting of synthesized maghemite nanoparticles and silica were produced by dispersing the as-synthesized maghemite nanoparticles into the silica particulate form. The system was then heated at 140 ℃for 3 d. A variety of mass ratios of Fe2O3/SiO2 was investigated. Moreover, no surfactant or other unnecessary precursor was involved. The nanocomposites were characterized using XRD, BET and AGM. The XRD diffraction patterns show the reflection corresponding to maghemite nanoparticles and a visible wide band at 20 from 20° to 35° which are the characteristics of the amorphous phase of the silica gel. The patterns also exhibit the presence of only maghemite and SiO2 amorphous phase, which indicates that there is no chemical reaction between the silica particulate gel and maghemite nanoparticles to form other compounds. The calculated crystallite size for encapsulated maghemite nanoparticles is smaller than the as-synthesized maghemite nanoparticles indicating the dissolution of the nanoparticles. Very high surface area is attained for the produced nanocomposites （360-390 m^2/g）. This enhances the sensitivity and the reactivity of the nanocomposites. The shapes of the magnetization curves for nanocomposites are very similar to the as-synthesized maghemite nanoparticles. Superparamagnetic behaviour is exhibited by all samples, indicating that the size of the maghemite nanoparticles is always within the nanometre range. The increase in iron content gives rise to a small particle growth.展开更多
文摘背景:普通外科手术中,磁吻合技术以操作简便、吻合迅速、对位准确、吻合质量确定、应用范围广泛等优点备受关注,但磁材料留置体内可能会对机体产生一些不良的影响,生物可降解纳米磁性复合材料有望解决此问题。目的:研制适用于外科吻合用的生物可降解纳米钕铁硼磁性复合材料,并评价其主要磁性能、体外降解性能。方法:采用高能球磨法制备纳米钕铁硼微粒,以溶剂挥发法将纳米钕铁硼微粒与生物可降解材料聚乳酸/羟基乙酸共聚物复合(聚乳酸/羟基乙酸共聚物含量分别为2.5%、5%、7.5%、10%、20%、30%、40%、50%),在特定温度(60,80,100,120,140℃)、压力(6,8,10,12,14 MPa)条件下,以温压成型工艺压制生物可降解聚乳酸/羟基乙酸共聚物-纳米钕铁硼磁性复合材料,检测其最大磁能积。采用磷酸盐缓冲液恒温振荡浸泡法进行生物可降解聚乳酸/羟基乙酸共聚物-纳米钕铁硼磁性复合材料(聚乳酸与羟基乙酸摩尔比分别为90/10、70/20、50/50)体外降解实验,扫描电镜观察磁体降解前后显微形态结构变化及降解时间与聚乳酸/羟基乙酸共聚物摩尔比的关系。结果与结论:生物可降解纳米钕铁硼磁性复合材料的磁性能在一定范围内与纳米钕铁硼微粒含量、成型温度及成型压力呈正比,与聚乳酸/羟基乙酸共聚物含量呈反比。在工艺参数为温度120℃、压力12 MPa、聚乳酸/羟基乙酸共聚物含量为5%时其磁性能最佳,最大磁能积为45 k J/m3。生物可降解纳米钕铁硼磁性复合材料在体外的降解过程与聚乳酸/羟基乙酸共聚物内部组分的摩尔比密切相关,降解时间与聚乳酸含量呈正比,与羟基乙酸含量呈反比,聚乳酸与羟基乙酸摩尔比90/10、70/20、50/50组的降解高峰期分别为8,6,4周。
基金Supported by the Slovak Research and Development Agency under the contracts(APVV-0222-10)the Operational Program"Research and Development"financed through European Regional Development Fund(ITMS 26220220105)the Scientific Grant Agency of the Ministry of Education of Slovak Republic and the Slovak Academy of Sciences,projects(VEGA 1/0861/12,VEGA 1/0862/12,VEGA VEGA 2/0155/12)
文摘Soft magnetic composites （SMCs） were prepared from three different ferromagnetic powder particles： iron powder ASC 100.29, spherical FeSi particles and vitroperm （Fe73CulNb3Si16B7） flakes. Two types of hybrid organic-inorganic phenolic resins modified with either silica nanoparticles or boron were used to design a thin insulating layer perfect- ly covering the ferromagnetic particles. Fourier transform infrared （FTIR） spectrometry confirmed an incorporation of silica or boron into the polymer matrix, which manifested itself through an improved thermal stability of the hybrid resins verified by thermogravimetric-differential scanning calorimetry （TG-DSC） analysis. The core-shell particles prepared from the ferromagnetic powder particles and the modified hybrid resins were further compacted to the cylindrical and toroidal shapes for the mechanical, electrical and magnetic testing. A uniform distribution of the resin between the ferromagnetic particles was evidenced by scanning electron microscope （SEM） analysis, which was also reflected in a rather high value of the electrical resistivity. A low porosity and extraordinary high values of mechanical hardness and flexural strength were found in SMC consisting of the iron powder and phenolic resin modified with boron. The coercive fields of the prepared samples were comparable with the commercial SMCs.
基金Grant sponsor:National Natural Science Foundation of China,Grant number:30371830Grant sponsor:National Hi-tech research and development program of China,Grant number:2002AA302207+3 种基金 Grant sponsor:Natural Science Foundation of Jiangsu,Grant number:BK2001003Grant sponsor:Hi-tech research pro-gram of Jiangsu,Grant number:BG2001006 Grant sponsor:Key Project of Chinese Traditional Medicine of Jiangsu,Grant number:H027Grant sponsor:Sci-ence Foundation of Southeast University,Grant number:9223001162
文摘Objective：To evaluate the in vitro and in vivo toxicity of self-prepared nanosized Fe2O3, which has the potential implication in tumor hyperthermia. Methods： Fe2O3 nanoparticles were prepared by improving co-precipitation, which characterization was detected by TEM, XRD, CMIAS, EDS. MTT assay was used to evaluate the in vitro cytotoxicity test; hemolytic test was carried out to estimate whether it has blood toxicity; Fe2O3 suspended in sterile 0.9% NaCl was intraperitoneally injected into Kumning mouse to calculate the LD50 ; micronucleus （MN） were reckoned to identify whether it is genotoxic. Results：The nanoparticles are brown spherical particles with diameter ranging from 8 to 15 nm, which have good decentralization and stability. The experiments also showed that the toxicity of the material on mouse fibroblast （L-929） cell lines was 0 - 1 degree ; it has no hemolysis activity; LD50 arrived at 5.45 g/kg^-1 after intraperitoneal injection of 1 ml suspension; micronucleus test showed that it has no genotoxic effects either. Conclusion： The results showed that the Fe2O3 nanoparticles are prepared successfully, the self-prepared nanosized Fe2O3 is a kind of high biocompatibility materials and perhaps it is suitable for further application in tumor hyperthermia.
基金Project(RP021-2012C)supported by University of Malaya under the UMRG Fund,Malaysia
文摘Abstract： Maghemite-silica particulate nanocomposites were prepared by modified 2-step sol-gel process. Superparamagnetic maghemite nanoparticles were successfully produced using Massart＇s procedure. Nanocomposites consisting of synthesized maghemite nanoparticles and silica were produced by dispersing the as-synthesized maghemite nanoparticles into the silica particulate form. The system was then heated at 140 ℃for 3 d. A variety of mass ratios of Fe2O3/SiO2 was investigated. Moreover, no surfactant or other unnecessary precursor was involved. The nanocomposites were characterized using XRD, BET and AGM. The XRD diffraction patterns show the reflection corresponding to maghemite nanoparticles and a visible wide band at 20 from 20° to 35° which are the characteristics of the amorphous phase of the silica gel. The patterns also exhibit the presence of only maghemite and SiO2 amorphous phase, which indicates that there is no chemical reaction between the silica particulate gel and maghemite nanoparticles to form other compounds. The calculated crystallite size for encapsulated maghemite nanoparticles is smaller than the as-synthesized maghemite nanoparticles indicating the dissolution of the nanoparticles. Very high surface area is attained for the produced nanocomposites （360-390 m^2/g）. This enhances the sensitivity and the reactivity of the nanocomposites. The shapes of the magnetization curves for nanocomposites are very similar to the as-synthesized maghemite nanoparticles. Superparamagnetic behaviour is exhibited by all samples, indicating that the size of the maghemite nanoparticles is always within the nanometre range. The increase in iron content gives rise to a small particle growth.
