Improved sequential injection method for phosphate quantification within a wide dynamic range with in-line pre-concentration to monitor soil leachates

Phosphate is a well-known contaminant and its content is an indicator of water quality, so it is important to have an efficient monitoring of the soil leaching process. In this work, an automatic, low cost flow analysis method, capable of real-time monitoring of the soil leaching processes using spectrophotometric detection, based on the molybdenum blue reaction, was developed. The developed methodology for phosphate determination was based on the molybdenum blue reaction and includes an on-line solid phase extraction (SPE) step, involving an AG1-X8 anionic exchange sorbent. The described SI method enabled phosphate determination within a wide range, 1–80 µM, with a detection limit of 0.52 µM. It was successfully applied to leachates from laboratory scale soil columns (LSSC) and one sample analysis was carried out in triplicate, in less than 10 minutes.info:eu-repo/semantics/publishedVersio

Novel microfluidic paper-based analytical devices (μPADs) for the determination of nitrate and nitrite in human saliva

In this work, two different microfluidic paper-based analytical devices (μPADs) were developed for the quantification of nitrite and nitrate in human saliva samples, in order to aid in the diagnosis of some diseases and health conditions associated with these ions. The development of these nitrite and nitrate μPADs involved several studies to optimize their design and construction, including an interference assessment and stability studies. These μPADs allowed a nitrite determination in a range of 5–250 μM with limits of detection and quantification of 0.05 μM and 0.17 μM, respectively, and a nitrate determination in the range 0.2–1.2 mM with limits of detection and quantification of 0.08 mM and 0.27 mM, respectively. As for the stability, both of the μPADs were stable when stored in vacuum at 4 °C (the nitrite μPAD for at least 60 days and the nitrate μPAD for at least of 14 days) and, after the sample placement, the nitrite and nitrate μPADs could be scanned within the first 4 and 2 h, respectively. The nitrite μPAD measurements were compared with the ones obtained from the standard colorimetric method and there were no statistically significant differences between these two methods. To evaluate the accuracy of nitrate μPAD measurements, 4 certified water samples were used and recovery studies using saliva samples were performed.info:eu-repo/semantics/acceptedVersio

Determination of urinary iron by colorimetric detection with a novel microfluidic paper-based analytical device

info:eu-repo/semantics/publishedVersio