A detection method for flupentixol-melitracen compound drug impurities, new identifiable impurities and safer compound drugs
A flupentixol and detection method technology, which can be used in measurement devices, pharmaceutical formulations, medical preparations containing active ingredients, etc., and can solve problems such as unclear source attribution and unknown impurity control amount
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Embodiment 1
[0081] Verification of impurities:
[0082] Take blank excipients, flupenthixol hydrochloride, melitracen hydrochloride, flupentixol hydrochloride plus blank excipients, melitracen hydrochloride plus blank excipients, flupentixol hydrochloride plus melitracen hydrochloride, flupenthixine hydrochloride Tonmelitracen Capsules (hereinafter referred to as the test product) was subjected to drug degradation test; and the degraded sample was analyzed by high performance liquid chromatography, and its chromatogram was recorded; other spectra except the test product were superimposed , and compared with the spectrum measured by the test product, as attached figure 1 Shown, by comparing the same retention time chromatographic peak and its full spectrum in different solution chromatograms, it can be seen that in the test sample, impurities are derived from flupenthixol except known impurity G, impurity Lu-28-159, There are also 6 unknown impurities, which are consistent with the substa...
Embodiment 2
[0085] Detect and calculate the impurities and their content in flupentixol melitracen compound drug according to the following process:
[0086] (1) Take the standard reference substances of impurity A and impurity G, accurately weigh them, dilute and dissolve with methanol to constant volume, and make impurity stock solutions containing about 0.2 mg of impurity A and 0.1 mg of impurity G in every 1 mL of the mixed solution;
[0087] (2) Take flupentixol hydrochloride standard reference substance, melitracen hydrochloride standard reference substance, impurity Lu-28-159 standard reference substance (during actual operation, use the salt Lu 28-159-HCl of impurity Lu-28-159 For the injection object), accurately weighed and dissolved with an appropriate amount of diluent, the diluent includes mobile phase A solution and methanol with a concentration of 0.01mol / L, and the volume ratio of the two is 35:65 to obtain the second stock solution;
[0088] (3) Measure the impurity stock...
Embodiment 3
[0145] Embodiment 3, comparative example
[0146] Detect and calculate the impurities and their content in flupentixol melitracen compound drug according to the following process:
[0147] (1) Take the standard reference substances of impurity A and impurity G, accurately weigh them, dilute and dissolve with methanol to constant volume, and make impurity stock solutions containing about 0.2 mg of impurity A and 0.1 mg of impurity G in every 1 mL of the mixed solution;
[0148] (2) Take flupentixol hydrochloride standard reference substance, melitracen hydrochloride standard reference substance, impurity Lu-28-159 standard reference substance (during actual operation, use the salt Lu 28-159-HCl of impurity Lu-28-159 For the injection object), accurately weighed and dissolved with an appropriate amount of diluent, the diluent includes mobile phase A solution and methanol with a concentration of 0.01mol / L, and the volume ratio of the two is 35:65 to obtain the second stock soluti...
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