Rheo-Physical Characterization of Microstructure and Flow Behavior of Concentrated Surfactant Solutions

Processing-relevant relationships between the microstructure and flow behavior of concentrated surfactant solutions were determined by a combination of basic rheological experiments, rheo-flow velocimetry tests, and flow birefringence measurements. The most common surfactant microstructures found in liquid soaps and other consumer care products—spherical, worm-like, and hexagonally packed micelles and lamellar structures—were recreated by varying the concentration of sodium laureth sulfate in water from 20 to 70 wt% and adding salt in some cases. It was found that common features of flow curves, such as power-law shear thinning behavior, resulted from a wide variety of material responses including shear-induced wall slip in micellar samples and plug flow in lamellar samples. Knowledge of key processing-structure-property relationships for concentrated solutions will allow engineers to develop more efficient industrial workflows for the scalable manufacturing of materials and feedstocks with reduced economic and environmental costs

Quantitative trait loci for sensitivity to ethanol intoxication in a C57BL/6J × 129S1/SvImJ inbred mouse cross

Individual variation in sensitivity to acute ethanol (EtOH) challenge is associated with alcohol drinking and is a predictor of alcohol abuse. Previous studies have shown that the C57BL/6J (B6) and 129S1/SvImJ (S1) inbred mouse strains differ in responses on certain measures of acute EtOH intoxication. To gain insight into genetic factors contributing to these differences, we performed quantitative trait locus (QTL) analysis of measures of EtOH-induced ataxia (accelerating rotarod), hypothermia, and loss of righting reflex (LORR) duration in a B6 × S1 F2 population. We confirmed that S1 showed greater EtOH-induced hypothermia (specifically at a high dose) and longer LORR compared to B6. QTL analysis revealed several additive and interacting loci for various phenotypes, as well as examples of genotype interactions with sex. QTLs for different EtOH phenotypes were largely non-overlapping, suggesting separable genetic influences on these behaviors. The most compelling main-effect QTLs were for hypothermia on chromosome 16 and for LORR on chromosomes 4 and 6. Several QTLs overlapped with loci repeatedly linked to EtOH drinking in previous mouse studies. The architecture of the traits we examined was complex but clearly amenable to dissection in future studies. Using integrative genomics strategies, plausible functional and positional candidates may be found. Uncovering candidate genes associated with variation in these phenotypes in this population could ultimately shed light on genetic factors underlying sensitivity to EtOH intoxication and risk for alcoholism in humans

Using Ultrasonic Speckle Velocimetry to Detect Fluid Instabilities in a Surfactant Solution

Rheometry is a leading technology used to define material properties of multi-phase viscoelastic fluid-like materials, such as the shear modulus and viscosity. However, traditional rheometry relies on a mechanical response from a rotating or oscillating rotor of various geometries which does not allow for any spatial or temporal quantification of the material characteristics. Further, the setup operates under the assumption of a uniform and homogeneous flow. Thus, only qualitative deductions can be realized when a complex fluid displays inhomogeneous behavior, such as wall slip or shear banding. Due to this lack of capability, non-intrusive imaging is required to define and quantify behavior that occurs in a complex fluid under shear conditions. This thesis outlines the design, fabrication, and experimental examples of an adapted ultrasonic speckle velocimetry device, which enables spatial and temporal resolution of inhomogeneous fluid behavior using ultrasound acoustics. For the experimental example, a commercial surfactant mixture (hair shampoo) was tested to show the utility and precision that ultrasonic speckle velocimetry possesses

Using Ultrasonic Speckle Velocimetry to Detect Fluid Instabilities in a Surfactant Solution

Rheometry is a leading technology used to define material properties of multi-phase viscoelastic fluid-like materials, such as the shear modulus and viscosity. However, traditional rheometry relies on a mechanical response from a rotating or oscillating rotor of various geometries which does not allow for any spatial or temporal quantification of the material characteristics. Further, the setup operates under the assumption of a uniform and homogenous flow. Thus, only qualitative deductions can be realized when a complex fluid displays inhomogeneous behavior, such as wall slip or shear banding. Due to this lack of capability, nonintrusive imaging is required to define and quantify behavior that occurs in a complex fluid under shear conditions. This thesis outlines the design, fabrication, and experimental examples of an adapted ultrasonic speckle velocimetry device, which enables spatial and temporal resolution of inhomogeneous fluid behavior using ultrasound acoustics. For the experimental example, a commercial surfactant mixture (hair shampoo) was tested to show the utility and precision that ultrasonic speckle velocimetry possesses

STAT3/PIAS3 Levels Serve as "Early Signature" Genes in the Development of High-Grade Serous Carcinoma from the Fallopian Tube.

The initial molecular events that lead to malignant transformation of the fimbria of the fallopian tube (FT) through high-grade serous ovarian carcinoma (HGSC) remain poorly understood. In this study, we report that increased expression of signal transducer and activator of transcription 3 (pSTAT3 Tyr705) and suppression or loss of protein inhibitor of activated STAT3 (PIAS3) in FT likely drive HGSC. We evaluated human tissues-benign normal FT, tubal-peritoneal junction (TPJ), p53 signature FT tissue, tubal intraepithelial lesion in transition (TILT), serous tubal intraepithelial carcinoma (STIC) without ovarian cancer, and HGSC for expression of STAT3/PIAS3 (compared with their known TP53 signature) and their target proliferation genes. We observed constitutive activation of STAT3 and low levels or loss of PIAS3 in the TPJ, p53 signature, TILT, and STIC through advanced stage IV (HGSC) tissues. Elevated expression of pSTAT3 Tyr705 and decreased levels of PIAS3 appeared as early as TPJ and the trend continued until very advanced stage HGSC (compared with high PIAS3 and low pSTAT3 expression in normal benign FT). Exogenous expression of STAT3 in FT cells mediated translocation of pSTAT3 and c-Myc into the nucleus. In vivo experiments demonstrated that overexpression of STAT3 in FT secretory epithelial cells promoted tumor progression and metastasis, mimicking the clinical disease observed in patients with HGSC. Thus, we conclude that the STAT3 pathway plays a role in the development and progression of HGSC from its earliest premalignant states.Significance: Concomitant gain of pSTAT3 Tyr705 and loss of PIAS3 appear critical for initiation and development of high-grade serous carcinoma. Cancer Res; 78(7); 1739-50. ©2018 AACR