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A Novel Method for Scatterers Type Enumeration in Polydisperse Suspensions through Fiber Trapping and Unsupervised Scattering Analysis

机译:通过纤维束缚和无监督散射分析的多分散悬浮液中散射体类型枚举的新方法

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摘要

Colloids and suspensions are part of our daily routines. Even the blood is considered a "naturally" occurringcolloid. However, the majority of colloids are complex and composed by a diversity of nano to microparticles.The characterization of both synthetic and physiological uids in terms of particulate types, size and surfacecharacteristics plays a vital role in products formulation, and in the early diagnosis through the identication ofabnormal scatterers in physiological uids, respectively. Several methods have been proposed for characterizingsuspensions, including imaging, electrical sensing counters, hydrodynamic or eld ow fractionation. However,the Dynamic Light Scattering (DLS) has evolved as the most convenient method from these. Based also onthe scattering signal, we propose a novel, simple and fast method able to determine the number of differentscatterers type present in a suspension, without any previous information about its composition (in terms ofparticle classes). This is achieved by collecting features from a 980 nm laser back-scattered signal acquiredthrough a polymeric lensed optical fiber tip dipped into the solution. Unlike DLS, this technique allows thetrapping of particles whose diameter ≥1 μm. For smaller particles, despite not guaranteeing their immobilization,it is also able to determine the number of different nanoparticles classes in an ensemble. The number of particletypes was correctly determined for suspensions of synthetic particles and yeasts; different bacteria; and 100 nmnanoparticles types, using both Principal Component Analysis and K-means algorithms. This method couldbe a valuable alternative to complex and time-consuming methods for particles separation, such as field owfractionation.
机译:胶体和悬浮液是我们日常工作的一部分。甚至血液也被认为是“天然”胶体。但是,大多数胶体是复杂的,并且由多种多样的纳米颗粒组成。\ r \ n根据颗粒类型,大小和表面,合成和生理学的表征\在产品配方中起着至关重要的作用,并在早期诊断中分别通过识别生理\ rui中的\ r \ nabnormal散射体。已经提出了几种表征悬浮液的方法,包括成像,电感应计数器,流体动力学或行分馏。但是,动态光散射(DLS)已发展成为其中最方便的方法。还基于散射信号,我们提出了一种新颖,简单,快速的方法,该方法能够确定悬浮液中存在的不同散射体类型的数量,而无需任何有关其组成的先前信息(就\ r \ nparticle类)。这是通过收集980 nm激光反向散射信号的特征来实现的,该信号是通过浸入溶液中的聚合物透镜光纤尖端采集的。与DLS不同,该技术可以捕获直径≥1μm的颗粒。对于较小的粒子,尽管不能保证固定,但也可以确定集合体中不同纳米粒子类别的数量。正确确定了合成颗粒和酵母菌的悬浮液的颗粒数量。不同的细菌;和100 nm \ r \ nnanoparticles类型,同时使用主成分分析和K-means算法。该方法可能不是复杂而耗时的粒子分离方法(例如场\ row \ r \ nfractionation)的有价值的替代方法。

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    INESC Technology and Science, INESC TEC, Portugal Faculty of Sciences, University of Porto, Physics and Astronomy Department, Portugal Faculty of Engineering, University of Porto, Portugal jipaiva@inesctec.pt;

    INESC Technology and Science, INESC TEC, Portugal Rita S. R. Ribeiro is currently with 4Dcell and Elvesys, Paris, France.;

    INESC Technology and Science, INESC TEC, Portugal Faculty of Sciences, University of Porto, Physics and Astronomy Department, Portugal;

    INESC Technology and Science, INESC TEC, Portugal Faculty of Sciences, University of Porto, Physics and Astronomy Department, Portugal;

    i3S - Instituto de Investigação e Inovaçãao em Saúde;

    INESC Technology and Science, INESC TEC, Portugal Faculty of Engineering, University of Porto, Portugal;

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