Preparation method for gel
A gel and inclusion compound technology, applied in the field of drug preparation, can solve problems such as inability to guarantee, and achieve the effects of convenient medication, long-lasting effect and fast dissolution
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2014-01-22
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
Figure 1
Abstract
Description
technical field
[0001] The invention relates to the field of medicine preparation, in particular to a preparation method of a gel. Background technique
[0002] Gel refers to a homogeneous, suspension or emulsion-type latex thick liquid or semi-solid preparation made of a drug and suitable auxiliary materials. Both traditional Chinese medicine and chemical medicine can be made into gel. The bases used to prepare gels can be divided into two categories, namely aqueous gel bases and oily gel bases. Aqueous gel base Carbomer, methyl cellulose, ethyl cellulose, sodium carboxymethyl cellulose, hydroxypropyl methyl cellulose, gelatin, starch, tragacanth, etc. The oily gel base is mainly made of liquid paraffin and polyoxyethylene or fatty oil and colloidal silicon or aluminum soap, zinc soap. In addition to the gel base, the preparation of the gel also requires additives such as βH regulators, humectants, solubilizers, cosolvents, preservatives, and transdermal absorption accel...
Examples
Embodiment 1
[0044] Crush 120g of dried Cnidium into coarse powder, soak in 60% ethanol solution for 12 hours, extract by percolation, extract by percolation with 12 times the amount of 60% ethanol solution, percolation speed 0.3mL / min, collect percolation liquid Concentrate and dry the percolating liquid to obtain a dry paste; dissolve the dry paste in absolute ethanol to form a nearly saturated alcohol solution, and slowly add it to a 60°C saturated solution prepared by dissolving 20 grams of β-cyclodextrin in about 250 mL of water. In the aqueous solution, stir at a constant temperature of 60° C. for 2 hours; cool, stand still for 6 hours, filter, wash with water and absolute ethanol, and dry to obtain the clathrate of the Cnidium mongolica extract.
[0045] Grind 2 grams of clindamycin hydrochloride finely, and slowly add 20 grams of β-cyclodextrin dissolved in about 250 mL of water into a 60°C saturated aqueous solution; place the solution at a constant temperature of 60°C and stir for...