In this research work, an innovative method for measurement of thermal conductivity of a small volume of liquids, microsphere, and the single cancer cell is demonstrated using a micro-pipette thermal sensor (MPTS). The method is based on laser point heating thermometry (LPHT) and transient heat transfer. When a single pulse of a laser beam heats the sensor tip which is in contact with the surrounding liquids or microsphere/cells, the temperature change in the sensor is reliant on the thermal properties of the surrounding sample. We developed a model for numerical analysis of the temperature change using the finite element method (FEM) in COMSOL. Then we used MATLAB to fit the simulation result with experiment data by multi-parameter fitting technique to determine the thermal conductivity. To verify the accuracy in the measurement of the thermal conductivity by the MPTS method, a 10µl sample of de-ionized (DI) water, 50%, and 70% propylene glycol solution were measured with deviation less than 2% from reported data. Also, to demonstrate that the method can be employed to measure microparticles and a single spherical cell, we measured the thermal conductivity of poly-ethylene microspheres with a deviation of less than 1% from published data. We estimated the thermal conductivity of two types of cell culture growth media for the first time and determined the thermal conductivity of cancerous Jurkat Clone E6-1 to be 0.538 W/m.K ± 2%. Using the sensor of 1-2μm tip size, we demonstrated the MPTS technique as a highly accurate technique for determining the thermal conductivity of microfluidic samples, microparticles, biological fluids, and a non-invasive method for measuring the thermal conductivity of single cancer cell. This MPTS technique can be beneficial in developing a diagnosis method for the detection of cancer at an early stage. We also compared three effective thermal conductivity models for determining the weight percentage of Jurkat cell, considering water and protein as the major constituents. We discovered that a combination of Maxwell-Euken and effective medium theory model provides the closest approximation to published data and, therefore, recommend for the prediction of the cell composition.

Background. Endocrine disruptors (EDC) are exogenous compounds that mimic the action of natural hormones and alter the normal endocrine system. Life-long chronic exposure to Bisphenol A (BPA), a putative EDC, has been linked with risk of metabolic disorders in epidemiological studies. Objectives. The aim was to study the human health effects of exposure to BPA, using an integrated approach combining environmental epidemiology and toxicology. Methods. Urinary levels of BPA exposure were measured in participants of the InChianti longitudinal study, a representative population-based study of Italian adults, at the Baseline (1998-00) and nine years later (3rd Wave, 2007-09). Hormones levels and the gene expression of specific target genes were the end points considered. Results were validated in laboratory studies on a human leukemic T-cell line (Jurkat cells). Results. In general, urinary BPA (uBPA) concentrations were higher among men and younger respondents, and within subjects uBPA concentrations were correlated (r=0.58; p=0.013, model adjusted for age, sex, urinary creatinine). At baseline, uBPA concentration were associated with higher total testosterone concentrations in men (β = 0.05; 95% CI, 0.02–0.08). In the 3rd wave, gene expression analysis revealed positive associations between uBPA concentrations and ESR2 (estrogen receptor beta) expression (β=0.18; 95% CI: 0.04, 0.32) and ESRRA (estrogen related receptor alpha) expression (β= 0.17; 95% CI: 0.02, 0.32). In a following in vitro study, BPA exposure (0.001-1 micro molar) led to enhanced expression of ESRRA and ESR2 in Jurkat cells over a period of 72 hours. Conclusions. Results indicate that BPA is bioactive in the human body and is able to alter circulating hormone concentrations and estrogen receptor/estrogen-related receptr gene expression. In particular, given the role of ERRα as a major control point for oxidative metabolism and heart development, this research provides indications on the possible molecular mechanisms of action of BPA in metabolic diseases.