Drop pills of corydalis tuber, and preparation method
A technology of Corydalis Corydalis and dripping pills, which can be used in pill delivery, pharmaceutical formulations, medical preparations containing active ingredients, etc. It can solve the problems of first-pass bioavailability of the liver and intestines, affect the therapeutic effect, and long dissolution time limit, etc., and achieve storage Convenient, easy to use, no dust pollution effect
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example 1
[0042] Example 1: drug and matrix ratio test
[0043] Fix the drop distance (about 6cm), the length of the condensation column (80cm), the gradient cooling liquid (the temperature of the upper part of the temperature is 30±2°C, the temperature of the lower part of the nozzle is 10±2°C), the temperature of the oil bath is 100±5°C, and then Carry out combination test, take the smooth roundness of dropping pill as the investigation index, the results are shown in Table 1
[0044] Polyethylene glycol-4000
[0045] Calculation method of smooth and roundness rate: the dripping pills have smooth and complete appearance and high roundness as qualified products. Divide the total weight of qualified products by the total output, which is the smooth rounding rate of the sample.
[0046] It can be seen from Table 1 that under the combined conditions of using polyethylene glycol-4000 as the matrix, the mixing ratio of matrix and drug at 8:5, and the dripping temperature at 110±2...
example 2
[0051] Example 2: The way to add the drug to the matrix is selected
[0052] Fixed drop distance (about 6cm), condensation column length (80cm), gradient cooling liquid (temperature at the upper part is 30+2℃, temperature at the lower part of the nozzle is 10±2℃), oil bath temperature is 100±5℃, substrate and The ratio of the drug was 8:5, the dropping temperature was 95±2°C, and the drug was added to the molten matrix in stages. The test results are shown in Table 2.
[0053] Feeding method
[0054] After the drug is added at one time, due to the large amount of drug, it is difficult to mix evenly. The appearance of the dropping pill is often rough, and the formability is not good. When the drug is added to the molten matrix in stages, it can be fully stirred. The smooth rounding rate is also high.
example 3
[0055] Example 3: Experiments with different dripper temperatures
[0056] The drug was added to the molten Matrix comparison, the test results are shown in Table 3.
[0057] Substrate: drug
[0058] When the dropping pills enter the condensate, the temperature of the coolant (20cm) is too low (20±2°C), and the prepared dropping pills often have voids or irregular pill shapes; when the temperature is too high (45±2°C), The density of the coolant here is low, the sinking speed of the prepared drop pills is too fast, and cannot be fully cooled, and flat pills or adhesions often occur; when the temperature of the coolant is controlled to 30±2°C, the roundness of the obtained drop pills is relatively high , The pill shape is smooth, therefore, the coolant should be controlled at 30±2°C.
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