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Hydrochloric acid cefepime raw material and method for measuring content of N-methyl pyrrolidine in preparation thereof

A technology for cefepime hydrochloride and cefepime hydrochloride is applied in the field of determination of the content of N-methylpyrrolidine in cefepime hydrochloride raw materials and preparations thereof, and can solve the problems of poor reproducibility of retention time, influence of measurement results, complicated and other problems, to achieve the effect of short sample measurement time, accurate measurement method and stable baseline.

Active Publication Date: 2012-02-29
GUANGZHOU BAIYUSN TIANXIN PHARMA
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Foreign Pharmacopoeia has only USP.26 at present, and JPXIV is recorded, and the silica gel column that is all bonded sulfonic acid groups is the high-performance liquid chromatography of analytical column, when using this method to measure, the chromatographic system is difficult to balance and the measuring time is long (detection one sample about two hours), retention time reproducibility is poor, baseline drift is obvious, column life is short
In the 8th issue of volume 13 of Chinese Journal of New Drugs in 2004, "the comparison of the determination method of N-methylpyrrolidine in cefepime hydrochloride" was reported in "influenced by the main drug cephalosporin hydrochloride, N-methylpyrrolidine in the test solution The peak shape is poor, the retention time drifts greatly, and the retention time difference with the N-methylpyrrolidine peak in the reference solution is often more than 10%", "time-consuming, a sample injection takes 2h", and there are domestic literature reports Determine its content with gas chromatography, but because N-methylpyrrolidine is both a synthetic raw material and a degradation product of cefepime, and cefepime hydrochloride is an acidic substance, and N-methylpyrrolidine is an alkaline substance, the two Part of the N-methylpyrrolidine is neutralized to form a salt when they coexist, and the salt-forming N-methylpyrrolidine cannot be directly gasified. complicated
If direct sample injection is adopted, the high temperature during gasification will degrade cefepime hydrochloride, and the salted N-methylpyrrolidine cannot be gasified, thereby affecting the measurement results; Encapsulate N-methylpyrrolidine, on the other hand cefepime hydrochloride is acidic, and the extraction of N-methylpyrrolidine that forms a salt under acidic conditions is not complete, so the organic solvent extraction method cannot accurately determine the concentration of cefepime hydrochloride. Content of N-Methylpyrrolidine
At present, gas chromatography cannot accurately measure the content of trace N-methylpyrrolidine impurities in cefepime hydrochloride

Method used

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  • Hydrochloric acid cefepime raw material and method for measuring content of N-methyl pyrrolidine in preparation thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] 1. Instrument: Japan Shimadzu LC-10A high performance liquid chromatograph, including LC-10AT pump, CDD-10A conductivity detector, CTO-10A column temperature phase, HW-2000 workstation, chromatographic column: 6.1010.2X0 METROSEP C 2 .

[0022] 2. Reagent: Acetonitrile: Tidea Company, chromatographically pure, batch number: AS-1122

[0023] Nitric acid: Guangzhou Chemical Reagent Factory, analytically pure, batch number: 20060512

[0024] Water: ultrapure water

[0025] 3. Determination method of N-methylpyrrolidine content

[0026] Liquid chromatography conditions and system adaptability: according to the Chinese Pharmacopoeia high-performance liquid chromatography test, the silica gel column bonded with carboxylic acid groups is used as the analytical column, 0.01mol / L nitric acid solution-acetonitrile (99:1) is used as the mobile phase, and the column The temperature is 35°C. Take several injections of the reference substance solution, and its relative standard d...

example 2

[0031] With embodiment 1, just mobile phase is 0.001mol / L sulfuric acid solution-acetonitrile (95: 5), 10 ℃ of column temperatures, need testing solution contains 1mg cefepime hydrochloride raw material or the solution of preparation in every 1ml. Each 1ml of the reference substance solution contains a solution of 0.1mg of N-methylpyrrolidine reference substance. The diluent is 0.001mol / L sulfuric acid solution. In the assay method, 30ul of the test solution and the reference solution were injected into the liquid chromatograph respectively, and the chromatograms were recorded.

Embodiment 3

[0033] With embodiment 1, just mobile phase is 0.05mol / L nitric acid solution-methanol (90: 10), 50 ℃ of column temperatures, need testing solution contains 10mg cefepime hydrochloride raw material or the solution of preparation in every 1ml. Each 1ml of the reference substance solution contains a solution of 1mg of N-methylpyrrolidine reference substance. The diluent is 0.05mol / L nitric acid solution. In the assay method, 10ul of the test solution and the reference solution were injected into the liquid chromatograph respectively, and the chromatograms were recorded.

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Abstract

The invention relates to a measurement method of N-methylpyrrolidine content of cefepime dihydrochloride material and relative agent, for evaluating the quality of cefepime dihydrochloride material and relative agent. The invention discloses a liquid chromatograph which comprises using carboxylic cationic column as analysis column, uses a conductive detector to check, preparing flow phase, preparing sample solution and reference substance solution, using test method to respectively inject the sample solution and reference substance solution into a liquid chromatograph, recording high pressureliquid chromatographs, and calculating the N-methylpyrrolidine content of the sample. The inventive chromatograph system has easy balance, short sample test time, better repeatability in preserved time, stable baseline, durable column, high quality of chromatograph peak of N-methylpyrrolidine, better repeatability, accurate, simple and reliable process.

Description

technical field [0001] The invention relates to a quality detection and determination method for cefepime hydrochloride raw materials and preparations thereof. Background technique [0002] N-methylpyrrolidine is not only the raw material in the synthesis process of cefepime hydrochloride but also its degradation product. Currently, the 2005 edition of the Chinese Pharmacopoeia does not include cefepime and its preparations. There is no determination of N-methylpyrrolidine for other species. Foreign Pharmacopoeia has only USP.26 at present, and JPXIV is recorded, and the silica gel column that is all bonded sulfonic acid groups is the high-performance liquid chromatography of analytical column, when using this method to measure, the chromatographic system is difficult to balance and the measuring time is long (detection one The sample is about two hours), the retention time reproducibility is poor, the baseline drift is obvious, and the column life is short. In the 8th is...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N30/02
Inventor 谭胜连闵翠娥陆媛傅红燕
Owner GUANGZHOU BAIYUSN TIANXIN PHARMA
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