Method for detecting related substances of dexmedetomidine hydrochloride raw material or preparation
A technology for dexmedetomidine hydrochloride and related substances, which is applied in the field of detection of related substances of dexmedetomidine hydrochloride raw materials or preparations, can solve the problems of low specificity, low sensitivity, and unsatisfactory, and achieve specificity Strong, high-sensitivity, time-shortened effect
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Embodiment 1
[0021] Instruments and conditions: Agilent 1260 liquid chromatography system, DAD detector, chromatographic column: Waters C18 (250×4.6mm, 5μm); detection wavelength: 220nm; phosphate buffer as mobile phase A, acetonitrile as mobile phase B, Gradient elution was carried out according to Table 1.
[0022] Table 1 Concentration gradient of mobile phase
[0023]
[0024] experiment procedure:
[0025] 1. System suitability test: take about 10 mg of dexmedetomidine hydrochloride raw material, put it in a 10 ml measuring bottle, add 1 ml of 6% hydrogen peroxide, heat in an oven at 60° C. for 30 minutes, and use acetonitrile-phosphate buffer (1:1 ) diluted to the mark, shake well, as the system suitability test solution, accurately measure 10 μ l into the liquid chromatograph, record the chromatogram, see the attached HPLC figure 1 .
[0026] Depend on figure 1 It can be seen that the retention time of the main peak of dexmedetomidine hydrochloride is 8.5 minutes, and the s...
Embodiment 2
[0040] Instruments and conditions: Agilent 1260 liquid chromatography system, DAD detector, chromatographic column: Welch Materials C8 (150×4.6mm, 5μm); detection wavelength: 220nm; phosphate buffer as mobile phase A, acetonitrile as mobile phase B, Gradient elution was carried out according to Table 2.
[0041] Table 2 Concentration gradient of mobile phase
[0042]
[0043] Experimental procedure: get about 10mg of dexmedetomidine hydrochloride raw material, put in 10ml measuring bottle, add 6% dioxygen phosphate buffer 1ml, heat in 60 ℃ oven for 30 minutes, with acetonitrile-phosphate buffer (8: 2) Dilute to the mark, shake well, and as a system suitability test solution, accurately measure 10 μl and inject it into a liquid chromatograph, and measure according to the law.
[0044] From the test results, it can be seen that the detection method of the present invention can separate dexmedetomidine hydrochloride from its most difficult oxidative degradation product, while...
Embodiment 3
[0046] Instruments and conditions: Agilent 1260 liquid chromatography system, DAD detector, chromatographic column: N-lycopine M bonded silica gel column (250×4.6mm, 5μm); detection wavelength: 220nm; phosphate buffer as mobile phase A. Acetonitrile is the mobile phase B, and gradient elution is carried out according to Table 3.
[0047] Table 3 Concentration Gradient of Mobile Phase
[0048]
[0049] Experimental procedure: get about 10mg of dexmedetomidine hydrochloride raw material, put in 10ml measuring bottle, add 6% dioxygen phosphate buffer 1ml, heat in 60 ℃ oven for 30 minutes, with acetonitrile-phosphate buffer (9.5: 0.5) Dilute to the mark, shake well, and as a system suitability test solution, accurately measure 10 μl and inject it into a liquid chromatograph, and measure according to the law.
[0050] The preparation steps of the N-lycopine M-bonded silica gel column are: 1) take 20g of activated silica gel in a 500mL three-necked flask, then measure 100mL of t...
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