Method for detecting No and/or propofol in expiratory gas
A technology of exhaled breath and propofol, applied in the direction of measuring devices, material analysis by electromagnetic means, instruments, etc., can solve problems such as accidents, lack of understanding or timely diagnosis, etc., achieve less consumables, convenient continuous monitoring, and reduce The effect of the influence of the background
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Embodiment 1
[0036] Separately measure NO and propofol standard gases according to the above-mentioned embodiment. image 3 -5 are the ion mobility spectra of reagent ion peak (RIP), NO and different injection amounts of propofol in negative ion mode, respectively. The migration time of the RIP peak in the negative ion mode is 9.28ms, the migration time of the NO ion peak is 8.30ms, and propofol only has an ion peak at 15.33ms at a lower concentration, and when the concentration increases, the migration time There is also an ion peak at 20.40ms, which has been confirmed to be the ion peak of propofol dimer.
Embodiment 2
[0038] NO and propofol standard gas mixtures were measured according to the above-mentioned embodiment.
[0039] Image 6 Simultaneous measurement of ion mobility spectra of NO and propofol in a clean air atmosphere after drying the system. It can be seen from the figure that when the two are measured at the same time, the two will undergo a complex reaction to form a new complex, and its ion migration time is 15.82ms, and the ion of the propofol monomer at 15.33ms behind the peak. It shows that the two can be measured at the same time, and the complexes of the two can also confirm the existence of each other.
Embodiment 3
[0041] The NO and propofol gas in the exhaled breath were separately measured according to the above-mentioned embodiment.
[0042] Figure 7 -8 are the ion mobility spectra of the background of exhaled breath, NO and propofol in the simulated exhaled breath, respectively. It can be seen from the figure that there are more unknown substances in the background of exhaled breath, and more peaks appear near the RIP peak, but relatively fewer peaks appear at longer migration times. When NO is added into the exhaled air, it enters the transfer tube together with the exhaled air for measurement, and the ion peak of NO can be obtained at 8.34ms. Similarly, when propofol is added into the exhaled breath and enters the migration tube together for measurement, the peaks of propofol monomer and dimer will also appear at about 15.31ms and 20.38ms. This demonstrates that ion mobility spectrometry can measure both NO and propofol anesthetics in exhaled breath alone.
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