A noninvasive method to predict fluid viscosity and nanoparticle size using total internal reflection fluorescence microscopy (TIRFM) imaging

This study examines the development of an automated particle tracking algorithm to predict the hindered Brownian movement of fluorescent nanoparticles within an evanescent wave field created using total internal reflection fluorescent microscopy. The two-dimensional motion of the fluorescent nanoparticles was tracked, with sub-pixel resolution, by fitting the intensity distribution of the particles to a known Gaussian distribution, thus providing the particle center within a single pixel. Spherical yellow-green polystyrene nanoparticles (200, 500, and 1000 nm in diameter) were suspended in deionized water (control), 10 wt% d-glucose, and 10 wt% glycerol solutions, with 1 mM of NaCl added to each. The motion of tracked nanoparticles was compared with the theoretical tangential hindered Brownian motion to estimate particle diameters and fluid viscosity using a nonlinear regression technique. The automatic tracking algorithm was initially validated by comparing the automated results with manually tracked particles, 1 µm in size. Our results showed that both particle size and solution viscosity were accurately predicted from the experimental mean square displacement. Specifically, the results show that the error of particle size prediction is below 10 % and the error of solution viscosity prediction is less than 1 %. The proposed automatic analysis tool could prove to be useful in bio-application fields for examination of single protein tracking, drug delivery, and cytotoxicity. Furthermore, the proposed tool could be useful in microfluidic areas such as particle tracking velocimetry and noninvasive viscosimetry.     

Spherulitic formation and characterization of partially fluorinated copolymers and their nanohybrids with functional fillers

Poly[vinylidenefluoride‐co‐(tetrafluoroethylene)] (P(VDF‐TeFE)) exhibited clear spherulitic texture with negative birefringence. The number and growth rates of the spherulites decreased at high crystallization temperature than at low crystallization temperature. Nonetheless, overall larger spherulites were found at high crystallization temperature and the brightness of the spherulites increased very fast at low crystallization temperature, thereafter it seemed as diminution of birefringence. AFM was used to investigate the impact of organo modified nanodiamond(ND) on spherulitic textures, lamellar thickness, and thickness distribution of P(VDF‐TeFE) copolymer. Poly[ethylene‐co‐(tetrafluoroethylene)] (ETFE) also confirmed spherulites structure and the boundaries could be clearly observed. By incorporation of the organo modified nanodiamond (ND) and organo‐modified montmorillonite (MMT) in fluropolymer matrix, it was found that spherulitic texture was seriously disordered and their nanohybrids was found only to have poorly developed spherulite structure. Both of the nanohybrids samples show better crystallization temperature as compared to their neat copolymer samples. Furthermore, the incorporation of nanoparticles decreased the size of the spherulites. POLYM. ENG. SCI., 57:161–171, 2017. © 2016 Society of Plastics Engineers     

Advance application of Raman spectroscopy for quantitative analysis of noncrystalline components in thin films of poly(ε-caprolactone)/poly(butadiene) blends

A quantitative analysis method for the distribution of noncrystalline poly(butadiene) component in poly(ε-caprolactone)/poly(butadiene) (PCL/PB) binary blends have been analyzed by advance application of Raman spectroscopy, optical microscopy, and differential scanning calorimetry (DSC) techniques. Thin films of different compositions of PCL/PB binary blends were prepared from solution and isothermally crystallized at a certain temperature. After calibration with real data, quantitative analyses by Raman spectroscopy revealed the amorphous PB are trapped inside the PCL crystals. Polarized optical microscopy and real time atomic force microscopy were used to collect data for the crystal morphology and crystal growth rate. For pure PCL crystals, a morphology of truncated lozenge shape was observed, independent of crystallization temperature and regardless of the blends compositions. For the pure PCL and their blends, almost unique crystal growth rate was found. The miscibility behaviors using DSC were drawn through melting point depression method. The Hoffman-Weeks extrapolations of the blends were found to be linear and identical with those of the neat PCL. The interaction parameter for the blends indicating that the PCL and PB blends have no intermolecular interaction, confirming the blends are immiscible. Despite the immiscibility of the blend, the PCL crystals do not bend during the growth process and do not reduce the growth rate as they do for miscible blend systems.     

Alkaline weight reduction and dyeing properties of black dope-dyed poly(ethylene terephthalate) microfibre fabrics

Sea–island-type, black dope-dyed poly(ethylene terephthalate) microfibre fabrics were compared with normal sea–island-type PET microfibres in terms of their thermal properties, alkaline weight reduction, and dyeing properties. A comparison of the weight reduction behaviours of the two microfibre yarns revealed that the microfibre yarn containing carbon black exhibited a higher dissolution speed than that containing no carbon black. The incorporation of carbon black particles in the polyester fibre matrix therefore accelerates the degradation of the less crystalline sea component during alkali treatment. A cationic dye staining method was used to monitor the alkaline dissolution behaviour of the sea–island-type PET microfibres, and compared with the K/S values and the colour difference, the f_k value is the most-desirable indicator for determination of the termination point of the alkaline dissolution process. The colour strength and the colour fastness of the dope-dyed sea–island-type PET microfibre fabrics are superior to those of the normal type.     

5-[125I]iodo-2'-deoxyuridine in the radiotherapy of brain tumors in rats

Glial neoplasms of the human central nervous system have defied treatment, in part because of the limited selectivity of available cytotoxic agents. The thymidine analog 5-iodo-2'-deoxyuridine radiolabeled with the Auger electron emitter 125I (125IUdR) is highly toxic to dividing cells when it is deoxyribonucleic acid incorporated, but it is relatively innocuous when located outside the nucleus. Previous studies have shown that 125IUdR has significant antineoplastic potential against mammalian cells in vitro and direct administration of 125IUdR is effective therapy for ovarian ascites tumors in mice and neoplastic meningitis in rats. Studies using external gamma imaging and autoradiography have also shown that direct intratumoral administration of 123IUdR/125IUdR into intracerebral 9L gliosarcomas in rats results in selective uptake of the radionuclide into tumor cells. Based on these encouraging results, we have evaluated the therapeutic potential of 125IUdR in rats bearing intracerebral 9L gliosarcomas. METHODS: Iodine-125-IUdR was infused intracerebrally over a 2-day period into rats bearing 1-day-old 9L tumors and over a 6-day period into animals with 9-day-old 9L tumors; equimolar concentrations of 127IUdR were infused into control animals. Tumor growth was monitored by contrast-enhanced 1H MRI and animal survival was followed over time. RESULTS: Intracerebral tumors (3-7 mm) were readily detected by MRI. Tumor-bearing rats treated with 127IUdR succumbed within 17-24 days, whereas tumor-bearing animals treated with 125IUdR survived significantly longer, and 10%-20% of the animals were cured of tumors. CONCLUSION: These data substantiate the antineoplastic potential of 5-[125I]iodo-2'-deoxyuridine and indicate that it may be a useful agent for the therapy of solid tumors that are accessible to direct radiopharmaceutical administration.     

Generation of intergranular strains during high temperature creep fatigue loading of 316H stainless steel

Abstract

This paper investigates the development of intergranular strains and stresses in AISI type 316H austenitic stainless steel during cyclic loading at high temperature. Isothermal cyclic creep tests at 650°C with 2 h displacement controlled creep dwells at maximum strain are conducted with in situ neutron diffraction monitoring at a time of flight facility. The evolution of intergranular strains in five independent {hkl} grain families were successfully measured during consecutive cycles. The grain family with {111} lattice planes normal to the loading direction exhibited linearly reversible behaviour with cyclic load whereas the {200} planes deformed in a non-linear manner forming a hysteresis loop. Intergranular strains during the first dwell remained unchanged with time, but relaxed with time during later dwells. The start of dwell intergranular strains increased from cycle 1 to cycle 2, but markedly less moving from cycle 2 to cycle 3.     

Three Dimensional Separation with Spiral—Focus in a Decelerating Duct Flow （Effect of Asymmetric Inlet Boundary Layer Thickness）

An experimental apparatus was developed to study the three dimensional separated flow with spiral-foci. The internal decelerating flow was generated by the air suction from a side wall to produce the separation on an opposite-side wall. The relation between the upstream boundary layer and the generation of spiral-foci in the separation region was observed by a tuft method. As a result, it was clarified that the spiral-focus type separation could be produced on the side wall and its behavior was closely related to the vortices supplied into the separation region from the boundary layer developing along top wall or bottom one.