Application of extract of Chinese angelica and szechuan lovage rhizome composition to preparation of medicament for promoting ovary granular cell proliferation
A technology of granulosa cells and compositions, which is applied in the field of preparation of drugs for promoting the proliferation of ovarian granulosa cells, the extract of angelica and chuanxiong, which can solve the problems of no ovarian granulosa cell proliferation, achieve small side effects, clear active ingredients, The effect of convenience
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Embodiment 1
[0019] Example 1 Effect of the Extract of Angelica and Rhizoma Chuanxiong Composition on the Proliferation of Ovarian Granulosa Cells
[0020] 1. Experimental materials
[0021] 1.1 Main Instruments
[0022] SpectrumMAX190 automatic microplate reader (Molecular Devices, USA), XSZ-D 2 Optical inverted microscope (Chongqing Optical Instrument Factory), NU-4950CO 2 Incubator (NuAire, USA), Z323 centrifuge (Hermile, Germany). Waters 2695 high-performance liquid chromatograph (U.S. waters company), 2996PDA diode array detector (U.S. waters company), automatic sampler; Empower chromatographic workstation (U.S. waters company). KQ-250E ultrasonic cleaner (Kunshan Ultrasonic Instrument Co., Ltd.), EPED ultrapure water system.
[0023] 1.2 Experimental animals
[0024] 21-day-old clean healthy female SD rats, weighing 60-70 g, were purchased from the Experimental Animal Center of Nanjing Medical University, animal license number: SCXK (Su) 2008-0004.
[0025] 2. Experimental meth...
Embodiment 2
[0040] Determination of the dissolution rate of chlorogenic acid, ferulic acid, ligusticolide I, ligustilide H, ligustilide, n-butenyl ligusticolide and other components after the compatibility of angelica and Chuanxiong.
[0041] 1. Investigation of content determination methodology
[0042] 1.1 Chromatographic conditions
[0043] Chromatographic column: Alltima-C18 (250×4.6mm, 5μm); mobile phase: acetonitrile (B)-0.2% formic acid aqueous solution (A), system gradient elution mobile phase. PAD detector wavelength scanning range: 210-400nm. Column temperature: 30°C; injection volume: 10 μL. Components are detected at the wavelength of maximum absorption.
[0044] 1.2 Preparation of mixed reference substance
[0045] Accurately weigh the reference substance chlorogenic acid, ferulic acid, ligustilide I, listonin H, ligustilide, and n-butenyl ligustilide and dilute the mixed standard solution solution to obtain the product.
[0046] 1.3 Preparation of the test solution
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