Evaluation of asymmetrical structure dialysis membrane by tortuous capillary pore diffusion model

The tortuous capillary pore diffusion model (TCPDM) has been used for estimating diffusive and pure water permeability from simple structure parameters such as pore diameter, surface porosity, wall thickness and tortuosity. The validity of this model for evaluation of homogeneous membrane has been already confirmed. Recently, there is a trend toward the use of asymmetrical dialysis membranes made of synthetic polymer such as poly(acrylonitrile) (PAN), polysulfone (PS) and a polyethersulfone polyarylate (PEPA) blend polymer. The purpose of the present study is to apply the TCPDM to evaluation of commercially available hollow-fiber dialysis membranes with asymmetrical structures by simplifying them to a double-layer membrane. The TCPDM is capable of estimating pore tortuosity of asymmetrical dialysis membranes having skin and supporting layers from data on membrane thickness, pore diameter, pure water permeability and water content. Values for diffusive permeability obtained by the TCPDM are in a good agreement with experimental data. This TCPDM model is useful for evaluation of not only homogeneous membrane but also asymmetrical membrane.     

Asymmetrical flow field-flow fractionation with multi-angle light scattering detection for the analysis of structured nanoparticles

Synthesis and applications of new functional nanoparticles are topics of increasing interest in many fields of nanotechnology. Chemical modifications of inorganic nanoparticles are often necessary to improve their features as spectroscopic tracers or chemical sensors, and to increase water solubility and biocompatibility for applications in nano-biotechnology. Analysis and characterization of structured nanoparticles are then key steps for their synthesis optimization and final quality control. Many properties of structured nanoparticles are size-dependent. Particle size distribution analysis then provides fundamental analytical information. Asymmetrical flow field-flow fractionation (AF4) with multi-angle light scattering (MALS) detection is able to size-separate and to characterize nanosized analytes in dispersion. In this work we focus on the central role of AF4-MALS to analyze and characterize different types of structured nanoparticles that are finding increasing applications in nano-biotechnology and nanomedicine: polymer-coated gold nanoparticles, fluorescent silica nanoparticles, and quantum dots. AF4 not only size-fractionated these nanoparticles and measured their hydrodynamic radius (r_h) distribution but it also separated them from the unbound, relatively low-M_r components of the nanoparticle structures which were still present in the sample solution. On-line MALS detection on real-time gave the gyration radius (r_g) distribution of the fractionated nanoparticles. Additional information on nanoparticle morphology was then obtained from the r_h/r_g index. Stability of the nanoparticle dispersions was finally investigated. Aggregation of the fluorescent silica nanoparticles was found to depend on the concentration at which they were dispersed. Partial release of the polymeric coating from water-soluble QDs was found when shear stress was induced by increasing flowrates during fractionation.     

基于信噪歪度比的二次相位耦合信号增强新算法

提出了信噪歪度比分析法,在这个分析法中用三阶累积量切片首次定义了信噪歪度比的概念,导出了其理论计算公式。从理论分析可知:当背景噪声为对称分布噪声时,信噪歪度比为无限值;当背景噪声为非对称分布噪声时,在一定条件下,其大于等于输入信噪比。理论分析和仿真结果表明:用三阶累积量切片从非高斯非对称分布的噪声中提取二次相位(动态)耦合信号是有效的,且无需对背景噪声的分布作任何假定。这在工程实践中是非常有意义的。     

Affinity purification of viral protein having heterogeneous quaternary structure: Modeling the impact of soluble aggregates on chromatographic performance

Prokaryote-expressed polyomavirus structural protein VP1 with an N-terminal glutathione-S-transferase tag (GST-VP1) self-assembles into pentamer structures that further organize into soluble aggregates of variable size (3.4 × 10²–1.8 × 10⁴ kDa) [D.I. Lipin, L.H.L. Lua, A.P.J. Middelberg, J. Chromatogr. A 1190 (2008) 204]. The adsorption mechanism for the full range of GST-VP1 soluble aggregates was described assuming a dual-component model [T.Y. Gu, G.J. Tsai, G.T. Tsao, AICHE J. 37 (1991) 1333], with components differentiated by size, and hence pore accessibility, rather than by protein identity. GST-VP1 protein was separated into two component groups: aggregates small enough to access resin pores (LMW: 3.4 × 10²–1.4 × 10³ kDa) and aggregates excluded from the resin pores (HMW: 9.0 × 10²–1.8 × 10⁴ kDa). LMW aggregates bound to resin at a higher saturation concentration (29.7 g L⁻¹) than HMW aggregates (13.3 g L⁻¹), while the rate of adsorption of HMW aggregates was an order of magnitude higher than for LMW aggregates. The model was used to predict both batch and packed bed adsorption of GST-VP1 protein in solutions with known concentrations of HMW and LMW aggregates to Glutathione Sepharose HP resin. Asymmetrical flow field flow fractionation with UV absorbance was utilized in conjunction with adsorption experimentation to show that binding of HMW aggregates to the resin was strong enough to withstand model-predicted displacement by LMW aggregates. High pore concentrations of LMW aggregates were also found to significantly inhibit the diffusion rate of further protein in the resin pores. Additional downstream processing experimentation showed that enzymatic cleavage of LMW aggregates to remove GST tags yields more un-aggregated VP1 pentamers than enzymatic cleavage of HMW aggregates. This model can be used to enhance the chromatographic capture of GST-VP1, and suggests an approach for modeling chromatographic purification of proteins that have a range of quaternary structures, including soluble aggregates.     

Polyelectrolyte complexes of poly(methacryloxyethyl trimethylammonium chloride) and poly(ethylene oxide)-block-poly(sodium methacrylate) studied by asymmetrical flow field-flow fractionation and dynamic light scattering

Polyelectrolyte complex (PEC) formation between cationic poly(methacryloxyethyl trimethylammonium chloride) (PMOTAC) and anionic poly(ethylene oxide)-block-poly(sodium methacrylate) (PEO-b-PMANa) was studied by asymmetrical flow field-flow fractionation and dynamic light scattering. The influence of ionic strength and mixing ratios of the charged units of the polyelectrolytes on the complex formation was evaluated. The diffusion coefficients and the hydrodynamic diameter distributions of the free and complexed polyelectrolytes were measured. In the absence of salt, the weight averaged hydrodynamic diameters were 48 and 28 nm for PMOTAC and PEO-b-PMANa, respectively. In the presence of salt, the particles were smaller, with weight averaged hydrodynamic diameters of 44-45 and 8-10 nm, respectively. In salt-free solution, at 1:1 mixing ratio of the charged monomer units of PMOTAC and PEO-b-PMANa, polydisperse particles with diameters of 2000-4000 nm were formed. In the presence of 20, 80, and 160 mM of sodium chloride, the 1:1 complexes were relatively monodisperse particles with weight averaged hydrodynamic diameters of 93, 124, and 120 nm, respectively.     

Ultrafast cyclic voltammetry with asymmetrical potential scan

Based on the perfect ohmic drop compensation by online electronic positive feedback, ultrafast cyclic voltammetry with asymmetrical potential scan is achieved for the first time, with the reduction of anthracene acting as the test system. Compared with the traditional cyclic voltammetry utilizing symmetrical triangular waveform as the excitation one, the new method allows a simpler approach to mechanistic analysis of ultrafast chemical reactions coupled with a charge transfer. And perhaps more important, it also provides a way to eliminate the interference of the adsorbed product in dynamic monitoring. 2007 Zhi Yong Guo. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.     

Substituent and Temperature Effect on the Assemblies of Three Lead(II) Coordination Polymers based on Asymmetrical Biphenyl Tritopic Ligands

Three Pb‐based metal‐organic frameworks, [Pb₆(L1)₄] · H₂O ( 1 ), [Pb₂(L2)₂(H₂O)] · H₂O ( 2 ), and [Pb(L2)(H₂O)] · H₂O ( 3 ) were constructed based on two asymmetrical tritopic ligands, 3‐(2′,5′‐dicarboxylphenyl)benzoic acid (H₃L1) and 3‐(2′,5′‐dicarboxylphenyl)pyridine acid (H₂L2), under hydrothermal conditions. The substituents on the two ligands and the induced temperature had effects on the resulting structures. All of the complexes were structurally characterized by X‐ray diffraction analyses and further identified by infrared spectra, elemental analyses, powder X‐ray diffraction, and thermogravimetric analyses. Complexes 1 and 3 are 3D frameworks, which construct from 1D inorganic Pb–O–Pb rod‐shaped secondary building units (SBUs) and H₃L1/H₂L2 ligands as pillars. Complex 2 is a 3D framework based on discrete tetranuclear Pb₄(COO)₈ clusters SBUs and H₂L2 ligands. The effects of both the substituent groups on the aromatic rings and the reaction temperature are discussed in details. The fluorescence properties and thermal stabilities of complexes 1 – 3 were also measured.     

Asymmetrical flow field-flow fractionation with multi-angle light scattering and quasi elastic light scattering for characterization of poly(ethyleneglycol-b-ɛ-caprolactone) block copolymer self-assemblies used as drug carriers for photodynamic therapy

Poly(ethyleneoxide-b-?-caprolactone) (PEO-b-PCL) self-assemblies in water were characterized by asymmetrical flow field-flow fractionation (AsFlFFF), with on-line coupling with quasi-elastic light scattering (QELS), multi-angle light scattering (MALS), refractive index and UV/Vis detection. We report here the AsFlFFF analysis of three different nanoparticular self-assembled systems of PEO-PCL polymers in aqueous media, each polymer differing by the mass of the PEO and PCL fragments. Thus, self-assembled water samples of {PEO(2000)-b-PCL(2600)}, {PEO(5000)-b-PCL(1400)} and {PEO(5000)-b-PCL(4000)} were analyzed by AsFlFFF. In most cases, the size obtained by AsFlFFF was similar to the one characterized by DLS. However, in some instances, only AsFlFFF revealed the presence of several self-assemblies with very different sizes. These nanoparticles being used for the targeted delivery of photosensitizers in photodynamic therapy, it was important to fully characterize the samples in terms of size and size distribution, molecular weight, Ip, aggregation number and also to assess whether the photosensitizer was inside the nanoparticles. AsFlFFF proved to be a very efficient technique which enabled this study without any destruction of the nanoparticles.     

Interactions and stability of silver nanoparticles in the aqueous phase: Influence of natural organic matter (NOM) and ionic strength

The rapid development of nanotechnology and the related production and application of nanosized materials such as engineered nanoparticles (ENP) inevitably lead to the emission of these products into environmental systems. So far, little is known about the occurrence and the behaviour of ENP in environmental aquatic systems. In this contribution, the influence of natural organic matter (NOM) and ionic strength on the stability and the interactions of silver nanoparticles (n-Ag) in aqueous suspensions was investigated using UV–vis spectroscopy and asymmetrical flow field-flow fractionation (AF⁴) coupled with UV–vis detection and mass spectrometry (ICP-MS). n-Ag particles were synthesized by chemical reduction of AgNO₃ with NaBH₄ in the liquid phase at different NOM concentrations. It could be observed that the destabilization effect of increasing ionic strength on n-Ag suspensions was significantly decreased in the presence of NOM, leading to a more stable n-Ag particle suspension. The results indicate that this behaviour is due to the adsorption of NOM molecules onto the surface of n-Ag particles (“coating”) and the resulting steric stabilization of the particle suspension. The application of AF⁴ coupled with highly sensitive detectors turned out to be a powerful method to follow the aggregation of n-Ag particle suspensions at different physical–chemical conditions and to get meaningful information on their chemical composition and particle size distributions. The method described will also open the door to obtain reliable data on the occurrence and the behaviour of other ENP in environmental aquatic systems.