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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Nanoparticle agglutination: Acceleration of aggregation rates and broadening of the analyte concentration range using mixtures of various-sized nanoparticles
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Nanoparticle agglutination: Acceleration of aggregation rates and broadening of the analyte concentration range using mixtures of various-sized nanoparticles

机译:纳米颗粒凝集:使用各种尺寸的纳米颗粒混合物,可加快聚集速率并扩大分析物浓度范围

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摘要

SiO2 particles of various sizes were prepared and surface modified with biotin-chain-end-functionalized poly(ethylene glycol). Dispersions of these particles were prepared, and their aggregation was induced upon the addition of avidin. The aggregate size and growth rate were monitored by DLS analysis, and SEM and TEM images of freeze-dried samples of the aggregate solutions were used to confirm the DLS data and to image the aggregate size and dimension. A linear correspondence between apparent diameter and time was observed, and both the 20 and 300 nm particles aggregated at slower rates than for the 40 nm particles. These observations were attributed to differences in the average functionality of the systems and the different initial concentrations of particles and avidin. The observed aggregation rates of binary combinations of the three particle sizes (i.e., 20 + 40 nm or 40 + 300 nm) were faster than those of the single-sized mixtures. These results were attributed to the faster flux of smaller particles toward larger particles in the mixture solutions as well as to the potentially larger number of productive collisions possible between mixtures of small particles and large particles versus only similarly sized particles. Combinations of the three sizes of particles were studied to find an empirical optimum formulation for generating large aggregates on a short time scale and over a wide range of analyte concentrations.
机译:制备了各种尺寸的SiO2颗粒,并用生物素链末端官能化的聚乙二醇进行了表面改性。制备这些颗粒的分散体,并在添加抗生物素蛋白时诱导它们的聚集。通过DLS分析监测聚集体的大小和生长速率,并且使用聚集体溶液的冷冻干燥样品的SEM和TEM图像来确认DLS数据并成像聚集体的大小和尺寸。观察到表观直径和时间之间存在线性对应关系,并且20和300 nm粒子的聚集速率均低于40 nm粒子。这些观察结果归因于系统平均功能的差异以及颗粒和抗生物素蛋白的不同初始浓度。观察到的三种粒径(即20 + 40 nm或40 + 300 nm)的二元组合的聚集速率要快于单一尺寸混合物的聚集速率。这些结果归因于较小颗粒向混合物溶液中较大颗粒的流动更快,以及由于小颗粒和大颗粒的混合物与大小相似的颗粒之间可能发生的潜在大量生产冲突。研究了三种尺寸的颗粒的组合,以找到一种经验最佳的配方,可在较短的时间范围内和较大的分析物浓度范围内生成大型聚集体。

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