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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

Active Publication Date: 2021-02-26
CHENGDU BRILLIANT PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] In the inventor's further research, it was found that in addition to the above-mentioned impurities, the sources of other unknown impurities in the flupentixol-melitracen compound drug were not clear, which led to the emergence of the controlled amount of these unknown impurities. question

Method used

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  • A detection method for flupentixol-melitracen compound drug impurities, new identifiable impurities and safer compound drugs
  • A detection method for flupentixol-melitracen compound drug impurities, new identifiable impurities and safer compound drugs
  • A detection method for flupentixol-melitracen compound drug impurities, new identifiable impurities and safer compound drugs

Examples

Experimental program
Comparison scheme
Effect test

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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PUM

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Abstract

The invention discloses a detection method of flupentixol melitracen compound drug, a new identifiable impurity and a safer compound drug. The process of gradient elution in the high performance liquid chromatography column of silane-bonded silica gel, and further analysis of the spectrum, this detection method can identify various impurities and their accurate content of the flupentixol melitracen compound drug , in particular, 6 new oxidative degradation impurities can be separated and identified, and a safer flupentixol-melitracen compound drug control standard can be obtained accordingly.

Description

technical field [0001] The invention relates to the technical field of flupentixol and melitracen compound medicine. Background technique [0002] Common dosage forms of flupenthixol and melitracen compound drugs, such as flupenthixol and melitracen tablets, flupenthixol and melitracen capsules, etc., all contain two drugs, flupentixol and melitracen, And there is a huge difference in the labeled amounts of the two. For example, each flupentixol and melitracen capsule contains 0.5 mg of flupentixol and 10 mg of melitracen, and the difference in the labeled amounts of the two reaches 20 times. Reasonable, scientific and strict quality control of drug quality is particularly important. [0003] In the existing standards, the impurities of flupenthixol and melitracen compound drug mainly include the degradation impurity Lu-28-159 and impurity G from flupentixol, in addition to the process impurity F, from the degradation of melitracen Impurity impurity A (Lu 23-120), its resp...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N30/02A61K31/496A61K31/382A61K31/122
CPCA61K31/122A61K31/382A61K31/496G01N30/02A61K2300/00
Inventor 陈礼莉胡崇琳徐成福刘丽娟李英富苏忠海
Owner CHENGDU BRILLIANT PHARMA CO LTD
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