Pixel Counting of Fluorescence Spots Triggered by DNA Walkers for Ultrasensitive Quantification of Nucleic Acid

A pixel counting strategy is designed on the basis of DNA walker-triggered fluorescence spots for ultrasensitive detection of nucleic acid. The two-dimensional DNA walker was constructed by hybridization of two types of capture DNAs, which were covalently modified by click chemistry on a glass slide, and dye-labeled hairpin structure (hDNA) as track and swing strand (sDNA) as DNAzyme, respectively. Introduction of target DNA unlocked the sDNA via strand displacement to form the activated DNAzyme, and the latter cut nearby hDNA with Mn²⁺ as cofactor, resulting in fluorescence recovery of dye-labeled hDNA on the substrate due to the separation from the quencher. Meanwhile, the DNAzyme sequence of sDNA was released to cut the next hDNA and, thus, initiated autonomous walking of sDNA for signal amplification. The enhanced fluorescence spots were digitalized as pixels on the basis of DNA walker-built compartments and extracted by a homemade program in MATLAB. The association between fluorescent pixel numbers and DNA concentrations was further proved by a mathematical model and led to an ultrasensitive quantification of nucleic acid with a linear range from 100 fM to 10 pM. The designed pixel counting strategy shows a more sensitive and accurate comparison with conventional methods based on fluorescence intensity or spot counts and provides a new dimension in designing next-type biosensors

Online Monitoring of Intraoperative Exhaled Propofol by Acetone-Assisted Negative Photoionization Ion Mobility Spectrometry Coupled with Time-Resolved Purge Introduction

Online monitoring of exhaled propofol concentration is important for anesthetists to provide adequate anesthesia as propofol concentrations in plasma and breath are correlated reasonably well. Exhaled propofol could be detected by Ni-63 ion mobility spectrometry in negative ion mode; however, the radioactivity of Ni-63 source restricts its clinical application due to safety, environmental, and regulatory concerns. An acetone-assisted negative photoionization ion mobility spectrometer (AANP-IMS) using a side-mounted vacuum ultraviolet (VUV) lamp in the unidirectional (UD) flow mode was developed for sensitive measurement of exhaled propofol by producing a high percentage of O-2(-)(H2O)(n). An adsorption sampling and time-resolved purge introduction system was developed to eliminate the interference of residual inhaled anesthetic sevoflurane based on their different adsorptions between propofol and sevoflurane on the inwall of the fluorinated ethylene propylene (FEP) sample loop. The effects of the inner diameter and the length of the sample loop on the signal intensity of propofol and the time-resolution between propofol and sevoflurane were theoretically and experimentally investigated. A sample loop with 3 mm i.d. and 150 cm length allowed sensitive measurement of exhaled propofol with a response time of 4 s, a linear response range for propofol was achieved to be 0.2 to 14 ppbv with a limit of detection (LOD) of 60 pptv, and the quantification of propofol was not influenced by the change of the sevoflurane concentration. Finally, the performance of monitoring exhaled propofol during surgery was demonstrated on a patient undergoing laparoscopic distal pancreatectomy combined with cholecystectomy

Long-Term Real-Time Monitoring Catalytic Synthesis of Ammonia in a Microreactor by VUV-Lamp-Based Charge-Transfer Ionization Time-of-Flight Mass Spectrometry

With respect to massive consumption of ammonia and rigorous industrial synthesis conditions, many studies have been devoted to investigating more environmentally benign catalysts for ammonia synthesis under moderate conditions. However, traditional methods for analysis of synthesized ammonia (e.g., off-line ion chromatography (IC) and chemical titration) suffer from poor sensitivity, low time resolution, and sample manipulations. In this work, charge-transfer ionization (CTI) with O-2(+) as the reagent ion based on a vacuum ultraviolet (VUV) lamp in a time-of-flight mass spectrometer (CTI-TOFMS) has been applied for real-time monitoring of the ammonia synthesis in a microreactor. For the necessity of long-term stable monitoring, a self-adjustment algorithm for stabilizing O-2(+) ion intensity was developed to automatically compensate the attenuation of the O-2(+) ion yield in the ion source as a result of the oxidation of the photoelectric electrode and contamination on the MgF2 window of the VUV lamp. A wide linear calibration curve in the concentration range of 0.2-1000 ppmv with a correlation coefficient (R-2) of 0.9986 was achieved, and the limit of quantification (LOQ) for NH3 was in ppbv. Microcatalytic synthesis of ammonia with three catalysts prepared by transition-metal/carbon nanotubes was tested, and the rapid changes of NH3 conversion rates with the reaction temperatures were quantitatively measured with a time resolution of 30 s. The high-time-resolution CTI-TOFMS could not only achieve the equilibrium conversion rates of NH3 rapidly but also monitor the activity variations with respect to investigated catalysts during ammonia synthesis reactions

Long-Term Real-Time Monitoring Catalytic Synthesis of Ammonia in a Microreactor by VUV-Lamp-Based Charge-Transfer Ionization Time-of-Flight Mass Spectrometry

With respect to massive consumption of ammonia and rigorous industrial synthesis conditions, many studies have been devoted to investigating more environmentally benign catalysts for ammonia synthesis under moderate conditions. However, traditional methods for analysis of synthesized ammonia (e.g., off-line ion chromatography (IC) and chemical titration) suffer from poor sensitivity, low time resolution, and sample manipulations. In this work, charge-transfer ionization (CTI) with O₂⁺ as the reagent ion based on a vacuum ultraviolet (VUV) lamp in a time-of-flight mass spectrometer (CTI-TOFMS) has been applied for real-time monitoring of the ammonia synthesis in a microreactor. For the necessity of long-term stable monitoring, a self-adjustment algorithm for stabilizing O₂⁺ ion intensity was developed to automatically compensate the attenuation of the O₂⁺ ion yield in the ion source as a result of the oxidation of the photoelectric electrode and contamination on the MgF₂ window of the VUV lamp. A wide linear calibration curve in the concentration range of 0.2–1000 ppmv with a correlation coefficient (<i>R</i>²) of 0.9986 was achieved, and the limit of quantification (LOQ) for NH₃ was in ppbv. Microcatalytic synthesis of ammonia with three catalysts prepared by transition-metal/carbon nanotubes was tested, and the rapid changes of NH₃ conversion rates with the reaction temperatures were quantitatively measured with a time resolution of 30 s. The high-time-resolution CTI-TOFMS could not only achieve the equilibrium conversion rates of NH₃ rapidly but also monitor the activity variations with respect to investigated catalysts during ammonia synthesis reactions