Anti-inflammatory analgesic preparation for external application
A technology of anti-inflammatory and analgesic and anti-inflammatory and analgesic drugs, which is applied in the direction of anti-inflammatory agents, non-central analgesics, medical preparations containing active ingredients, etc., can solve the problems of anti-inflammatory and analgesic effects, and achieve transdermal Excellent absorption, alleviating skin irritation, and sufficient curative effect
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[0044] The preparation method of the external preparation provided by the present invention is not particularly limited. According to the desired dosage form, it can be prepared by fully kneading each component and the required matrix components, etc. for preparing an ordinary external preparation.
[0045] When preparing cataplasms and patches, it can be prepared by spreading the kneaded mixture on release paper, drying the kneaded mixture, bonding it to a soft support, and cutting it into a desired size.
[0046] The external preparations provided by the present invention, for example, when they are ointments, liquid preparations (suspensions, emulsions, lotions, etc.), aerosols, and external powders, are used according to the following usual methods of use: direct application by smearing, etc. Use on affected parts of the skin, or after applying or soaking on a support such as cloth.
[0047] In the case of a cataplasm or a patch, these preparations are directly attached to...
Embodiment 1
[0051] Drug-containing matrices of the formulations shown in Table 1 below were prepared. Specifically, felbinac was dissolved in crotamiton, levobupivacaine was dissolved in propylene glycol, and the two were mixed, and then these dissolved substances and other ingredients shown in Table 1 were mixed until uniform, A drug-containing matrix is obtained. The drug-containing matrix prepared in this way was treated with 1000g / m 2 Spread on non-woven fabric, lined with polypropylene, then cut into 10×14cm 2 , to obtain an external patch.
[0052] Table 1
[0053] Element
[0054] Aluminum Dihydroxyacetate
[0055] Unit: parts by weight
Embodiment 2
[0057] Drug-containing matrices of the formulations shown in Table 2 below were prepared. Specifically, indomethacin was dissolved in crotamiton and levobupivacaine was dissolved in propylene glycol.
[0058] Then, these solubilized substances were mixed with other ingredients shown in Table 2 until uniform to obtain a drug-containing matrix. The drug-containing matrix prepared in this way was treated with 1000g / m 2 Spread on non-woven fabric, lined with polypropylene, then cut into 10×14cm 2 , to obtain an external patch.
[0059] Table 2
[0060] Element
[0061] Polyacrylic acid partially neutralized
[0062] Unit: parts by weight
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