High performance liquid chromatography for detecting quinine sulfate content
A high-performance liquid chromatography, quinine sulfate technology, which is applied to measurement devices, instruments, scientific instruments, etc., can solve the problems of low detection result accuracy, obstacles to accurate detection of quinine sulfate content, and cumbersome operation methods.
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Embodiment 1
[0029] According to the above-mentioned chromatographic conditions, the quinine sulfate purchased from Malaysia with a calibrated content of 98.0% was assayed.
[0030] Preparation of standard solution: Accurately weigh 25.0mg of standard, place it in a 10ml volumetric flask, add mobile phase and ultrasonic to dissolve the sample and set the volume to the mark.
[0031] Preparation of the sample to be tested: Accurately weigh 25.0 mg of Malaysian quinine sulfate sample, place it in a 10 ml volumetric flask, add mobile phase ultrasound to dissolve the sample and set the volume to the mark.
[0032] Three standard solutions and samples to be tested were prepared respectively, and 5 μl were respectively put into the chromatographic column, and the average value of the obtained peak areas was brought into the above formula for calculation. The calculation results are shown in Table 1.
[0033] Among them, chromatographic column: C18 (4.6 * 250mm5 μ m); mobile phase is methanol-1% ...
Embodiment 2
[0037] According to the above-mentioned chromatographic conditions, the quinine sulfate purchased from India with a calibrated content of 99.4% was assayed.
[0038] Preparation of standard solution: Accurately weigh 25.0mg of standard, place it in a 10ml volumetric flask, add mobile phase and ultrasonic to dissolve the sample and set the volume to the mark.
[0039] Sample preparation to be tested: Accurately weigh 25.0mg of quinine sulfate sample purchased from India, place it in a 10ml volumetric flask, add mobile phase ultrasound to dissolve the sample and set the volume to the mark.
[0040] Three standard solutions and samples to be tested were prepared respectively, and 5 μl were respectively taken into the chromatographic column, and the average value of the obtained peak areas was brought into the above formula for calculation. The calculation results are shown in Table 2.
[0041] Among them, chromatographic column: C18 (4.6 * 250mm5 μ m); mobile phase is methanol-1%...
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