Antineoplastic traditional Chinese medicine preparation and preparation method thereof
A traditional Chinese medicine product and anti-tumor technology, which is applied in the fields of medicine, food, and beverage, can solve the problems of high price, poor water solubility, and limited clinical application, and achieve the effect of improving the therapeutic index
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Embodiment 1
[0049] Example 1. Preparation of betulinic acid liposome powder injection
[0050] 1. Preparation method of betulinic acid liposome powder injection
[0051] (1) Preparation of betulinic acid liposome powder injection
[0052] Betulinic acid 0.15g
[0053] Lecithin 0.15g
[0054] Cholesterol 0.15g
[0055] Mannitol 0.30g
[0056] Thin film method (TFV): Weigh 0.15g betulinic acid, 0.15g lecithin and 0.15g cholesterol into a pear-shaped bottle, add 10ml ethanol, shake, add several glass beads, and place on a rotary evaporator at 28~32℃ Evaporate to dry to form a film, vacuum dry until there is no ethanol smell in the pear-shaped bottle, add 7-15ml of phosphate buffered saline solution, shake the film off, sonicate for 10-30min in an ultrasonic instrument to dissolve the film, and pass through a 0.45μm filter membrane , A colorless and transparent liquid is obtained, and the drug encapsulation rate is over 90%. Weigh the prescription amount of mannitol, dissolve it with 15ml of hydr...
Embodiment 2
[0087] Example 2. The effect of betulinic acid and its liposomes on human melanoma cell line A375
[0088] 1 Materials and methods
[0089] 1.1 Drug: betulinic acid liposome was prepared according to Example 1.
[0090] 1.2 Tumor line: Human melanoma cell line A375 was provided by the Chinese Academy of Sciences Cell.
[0091] 1.3 Reagents and equipment: MTT (purchased from Sigma); DMEM, trypsin, calf serum (purchased from GIBCO). Multiskan MK3 microplate reader (Labsystems Dragon)
[0092] 1.4 MTT method to measure the inhibition rate of cell proliferation: collect the human melanoma cell line A375 (2×104 / ml) in logarithmic growth phase, plant them into 96-well culture plate, 100μl per well, add the drug solution according to the design, negative control Use the corresponding culture medium instead, place it in an incubator with 5% CO2 and 37°C for 24 hours. After the treated cells, remove the DMEM medium, wash twice with D-Hank's solution, add 100 μl DMEM medium and 10 μl MTT (5...
Embodiment 3
[0098] Example 3. Effect of betulinic acid liposomes on transplanted tumor of mouse colon cancer cell line (C26)
[0099] 1 Materials and methods
[0100] 1.1 Experimental animals: The mouse colon cancer cell line C26 was provided by Shanghai Medical Engineering Institute; BABL / C+ICR=F1 mice, 19-22 grams, purchased from Shanghai Slack Laboratory Animal Co., Ltd., license number: SCXK (Shanghai) 2003-0003.
[0101] 1.2 Reagents and instruments: cyclophosphamide (specification: 200mg / bottle, batch number: 050206, Shanghai Hualian Pharmaceutical Co., Ltd.); balance (JA2003A, Shanghai Jingtian Electronic Instrument Co., Ltd.)
[0102] 1.3 Establishment of transplanted tumor model of mouse colon cancer (C26) and drug effects Select vigorously growing mouse colon cancer (C26) tumor source, prepare cell suspension by homogenization method (1:8), each mouse is right Inoculate 0.2ml under the axillary skin. At the same time, betulinic acid liposomes (1mg / kg, 10mg / kg) were injected intraper...
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