Recent reports on using bio-active paper and bio-active thread to determine human blood type have shown a tremendous potential of using these low-cost materials to build bio-sensors for blood diagnosis. In this work we focus on understanding the mechanisms of red blood cell agglutination in the antibody-loaded paper. We semi-quantitatively evaluate the percentage of antibody molecules that are adsorbed on cellulose fibres and can potentially immobilize red blood cells on the fibre surface, and the percentage of the molecules that can desorb from the cellulose fibre surface into the blood sample and cause haemagglutination reaction in the bulk of a blood sample. Our results show that 34 to 42% of antibody molecules in the papers treated with commercial blood grouping antibodies can desorb from the fibre surface. When specific antibody molecules are released into the blood sample via desorption, haemagglutination reaction occurs in the blood sample. The reaction bridges the red cells in the blood sample bulk to the layer of red cells immobilized on the fibre surface by the adsorbed antibody molecules. The desorbed antibody also causes agglutinated lumps of red blood cells to form. These lumps cannot pass through the pores of the filter paper. The immobilization and filtration of agglutinated red cells give reproducible identification of positive haemagglutination reaction. Results from this study provide information for designing new bio-active paper-based devices for human blood typing with improved sensitivity and specificity.

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Sedimentation field-flow fractionation-inductively coupled plasma-mass spectrometry (SdFFF-ICP-MS) was successfully applied to investigate particle size distribution of titanium dioxide (TiO(2)) in sunscreen samples after hexane extraction to remove organic components from the samples. Three brands of sunscreen products of various sun protection factor (SPF) value were used as samples. Different particle size distribution profiles were observed for sunscreen samples of various brands and SPF values; however, the particle size distributions of titanium dioxide in most sunscreen samples investigated in this work were larger than 100 nm. The titanium dioxide concentrations were higher for the products of higher SPF values. By comparing the results obtained from online SdFFF-ICP-MS and those from the off-line ICP-MS determination of titanium after acid digestion, ICP-MS was found to effectively atomize and ionize the titanium dioxide particle without the need for acid digestion of the samples. Therefore, the online coupling between SdFFF and ICP-MS could be effectively used to provide quantitative information of titanium dioxide concentrations across particle size distribution profiles.

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Interaction between metal ions and humic matter was investigated using a hyphenated technique, field-flow fractionation-inductively coupled plasma mass spectrometry (FFF-ICP-MS). Aggregation of a metal-spiked commercial Aldrich humic acid in an aqueous solution of calcium ion or in seawater was examined over time intervals of 0-4320 min. The aggregation was demonstrated by shifts in peak maximum of humic matter from smaller size (2.9 nm) to larger size (5.1 or 5.8 nm in Ca2+ solution or in seawater, respectively) and also by the broadening of size distribution profiles. With FFF, size distribution of humic aggregate was characterized. Further, dominant particle size (2.9 nm), mean particle size (3.8 nm), and diffusion coefficient (1.51 x 10(-6) cm2/s) of humic acid solution were determined. With FFF-ICP-MS, associations of Cd, Cu, and Pb with humic aggregates were examined. The mean diameters of Cd-, Cu-, and Pb-bound humic aggregates in the metal-spiked humic acid were 4.1, 4.5, and 5.8 nm, respectively. These diameters were shifted to 6.0, 6.0, and 6.9 nm, respectively, in the humic acid incubated with calcium solution, whereas they were shifted to 6.5, 5.7, and 7.4 nm, respectively, in the humic acid incubated with seawater for three days. Humic aggregate of small size showed more affinity for Cu than Cd and Pb, whereas the large aggregate showed more affinity for Pb than Cd and Cu, respectively.

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BackgroundAccumulating evidence suggests a role for silicon in optimal connective tissue health. Further proof of its importance/essentiality may be provided by studies involving imposed depletion followed by 29Si challenge to estimate metabolic balance. Prior to conducting these expensive studies, we first established the variance of estimating normal Si excretion versus intake using a single oral dose of typical dietary Si, orthosilicic acid.MethodsHealthy volunteers were recruited from Loei Rajabhat University, separated into two matched groups (three males and three females/group) and maintained on a standardized diet for the three study days. One group ingested 500 ml water containing orthosilicic acid (28.9 mg Si) and the other group received 500 ml water alone, all on a fasted stomach. Blood samples and total urine and faeces were collected over the 48 h post-dose period and 24 h before-hand (baseline) and analysed for silicon by inductively coupled plasma optical emission spectrometry.ResultsSerum Si analysis confirmed the ready absorption of silicon from the orthosilicic acid solution. Mean total urinary and faecal Si excretions over the 24 h post-dose period accounted for 57 ± 9.5% and 39 ± 9.4% of the ingested dose, respectively. Thus in total 96.3 ± 5.8% of the ingested dose was recovered in faecal plus urinary excretions over the 24 h post-dose period.ConclusionsWe report that in healthy subjects (presumably in Si balance), the ingestion of a soluble dose of dietary Si results in the same quantity (within analytical error) being excreted within 24 h. It is currently not known if this all originated from the dose solution or if there was some exchange with the body Si pool but, given the low variance in these silicon balance data, isotopic studies are now merited.

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