A kind of detection method of sodium pantothenate isomer
A detection method and technology of sodium pantothenate, applied in the direction of measuring devices, instruments, scientific instruments, etc., to achieve the effects of good reproducibility, simple operation and high precision
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Embodiment 1
[0045] (1) Experimental materials and instrument conditions
[0046] Instrument: High performance liquid chromatography: Thermo; Chromatographic column: Chiralpak AD-H, 5 μm, 4.6×250 mm; Flow rate: 1.0mL / min; Column temperature: 25°C; Injection volume: 10 μl; Running time: 15min; Detection Wavelength: 210nm. Inject the blank solution, system suitability solution and test solution into the liquid chromatograph respectively, record the chromatogram, and the chromatographic conditions are as follows: Chromatographic column: use amylose-tris(3,5-xylylcarbamate) derivative As filler; flow rate 1.0mL / min; column temperature: 25°C; injection volume: 10μl; running time: 15min; detection wavelength: 210nm; mobile phase: n-hexane-isopropanol-trifluoroacetic acid, gradient elution , and its gradient is shown in Table 1.
[0047] time (min) mobile phase A mobile phase B mobile phase C 0 85 15 0.2 5 85 15 0.2 10 85 15 0.2 15 85 15 0.2
[004...
Embodiment 2
[0062] Embodiment 2 detection method system applicability test of the present invention
[0063] System suitability is achieved by measuring the RSD of the peak area of D-sodium pantothenate in the 5-pin reference solution and the resolution of the peaks of D-sodium pantothenate and L-sodium pantothenate in the system suitability solution. The RSD of the peak area of D-sodium pantothenate is ≤2.0%, and the resolution of the peaks of D-sodium pantothenate and L-sodium pantothenate in the system suitability solution is ≥1.5. Prepare blank solution, reference solution, and system suitability solution as described in Example 1. Under the chromatographic conditions described in Example 1, enter 1 needle of blank solution, 5 needles of reference solution, and 1 needle of system suitability solution to obtain a chromatogram Figure, such as figure 1 , figure 2 , image 3 , Figure 4 , Figure 5 and Figure 6 , according to the formula conversion results are shown in the tab...
Embodiment 3
[0067] Embodiment 3 Detection method specificity test of the present invention
[0068] The specificity of the method is realized by studying the peak identification and selectivity, and it is required that the blank solvent does not interfere with the detection; the D-sodium pantothenate positioning solution has no interference with the detection of L-sodium pantothenate; The resolution of adjacent peaks should be ≥1.5, and the recovery rate of sodium L-pantothenate should be between 90.0% and 110.0%. Prepare blank solution, DL-sodium pantothenate stock solution, L-sodium pantothenate fixing solution (system suitability solution), D-sodium pantothenate fixing solution and selective solution as described in Example 1. After the system is balanced, inject 1 needle of blank solution, 3 needles of L-sodium pantothenate positioning solution, 3 needles of selective solution, and 1 needle of D-sodium pantothenate positioning solution, and record the chromatogram, as figure 1 , fi...
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