Chinese herbal compound microemulsion gel emplastrum, and its preparation method and application
A technology of microemulsion gel and plaster, which can be used in pharmaceutical formulations, non-central analgesics, antipyretics, etc., can solve the problems of easy skin pulling, loss of active ingredients, dull ointment, etc., to avoid active Effects of ingredients and moisture loss, improving formulation stability, and promoting transdermal penetration
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Embodiment 1
[0078] Example 1 Preparation of Huoxue Zhitong Extract
[0079] Huoxue Zhitong ointment (rubber ointment) has been included in the Pharmacopoeia (2010 edition, one part 957 pages, 2015 edition one part, 1294 pages), its prescription and extract preparation method are as follows:
[0080]
[0081] In addition to the menthol, borneol, camphor, methyl salicylate, and belladonna liquid extract in the prescription of Huoxue Zhitong ointment, the other twenty-three medicinal materials such as Angelica dahurica are crushed into coarse powder, and 90% ethanol is used as a solvent, soaked, and infiltrated , collect the percolation liquid, recover ethanol and concentrate it into a clear paste with a relative density of 1.2634 (25°C), add belladonna liquid extract, stir well, and obtain the blood-activating and pain-relieving extract. Above-mentioned menthol, borneol, camphor, methyl salicylate are standby.
Embodiment 2
[0082] Embodiment 2 Preparation example 1 of the microemulsion gel plaster for promoting blood circulation and relieving pain of the present invention
[0083] Prescription 1 (according to 100 grams)
[0084]
[0085]
[0086] Weigh menthol, borneol, camphor, and methyl salicylate according to the prescription in Example 1, first take camphor, menthol, and borneol, mix and grind until partially liquefied, then add methyl salicylate and stir to completely dissolve, as a mixed oil phase .
[0087] Weigh 3.82g of the mixed oil phase, 10.23g of RH40, and 5.09g of PEG400, stir at 20-35°C for 10 minutes at a stirring speed of 300-500 rpm, add water slowly, and stir for 10 minutes to obtain a blank microemulsion.
[0088] Add 1.92 g of the blood-activating and pain-relieving extract prepared in Example 1 into the blank microemulsion, and stir to balance for 30 minutes to obtain the blood-activating and pain-relieving microemulsion.
[0089] Weigh 4.00 g of carbomer and 1.00 g...
Embodiment 3 preparation example 2
[0091] Prescription 2 (according to 100 grams)
[0092]
[0093]
[0094] Take by weighing 6.38g of blood-activating and pain-relieving extract prepared in Example 1, 1.28g of IPM, 15.29g of Tween 80, 5.08g of absolute ethanol, and weigh menthol, borneol, camphor, and salicylic acid according to the prescription of Example 1 Methyl ester was stirred at 20-35°C for 40 minutes at a stirring speed of 300-500 rpm. After the drug was completely dissolved, an appropriate amount of water was slowly added and stirred for 20 minutes to obtain 28.03 g of blood-activating and pain-relieving microemulsion.
[0095] Weigh 4.00g of sodium polyacrylate NP-700, 1.5g of cross-linked polyvinylpyrrolidone, 0.10g of aluminum hydroxide, and 0.05g of EDTA-2Na, add 20.00g of glycerin and stir evenly to prepare Phase A. Weigh Povidone K-30 and add appropriate amount of distilled water to fully swell, add 0.40g of citric acid and stir evenly to obtain phase B, add phase B to phase A and then add...
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