CN1614415A - Quality determining method for Relinqing preparation - Google Patents
Quality determining method for Relinqing preparation Download PDFInfo
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- CN1614415A CN1614415A CN 200410081383 CN200410081383A CN1614415A CN 1614415 A CN1614415 A CN 1614415A CN 200410081383 CN200410081383 CN 200410081383 CN 200410081383 A CN200410081383 A CN 200410081383A CN 1614415 A CN1614415 A CN 1614415A
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- quercetin
- reference substance
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- relinqing
- methyl alcohol
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Abstract
A method for detecting drug quality includes preparing sample solution as collecting 0.3 g of drug in bottle, adding 20 ml of extraction-hydrolysis solution in volume ratio of 70:4:6=methyl alcohol/sulfuric acid/water, neutralizing it to pH 4-5 by 20% NaOH and using 70% methyl alcohol for constant volume, preparing reference solution as collecting set weight of quercetin and adding methyl alcohol to make each 1ml solution contain 18-20 microng quercetin and carrying out detection by filling 10 micron L, each of the two into liquid phase chromatograph for confirming quercetin content in the sample.
Description
Technical field
The invention belongs to the Chinese traditional patent formulation formulation art, relate in particular to a kind of quality determining method of 'Relinqing '.
Background technology
The 'Relinqing ' made from the headdress flower knotweed has clearing heat and detoxicating, inducing diuresis for treating strangurtia.Be used for the treatment of damp-heat accumulation, the disease of dark urine, odynuria, urinary tract infections, pyelonephritis are seen above-mentioned card marquis person, effect is obvious.Yet because the Chinese medicinal ingredients more complicated contains many unknown compositions, can effectively control the product quality of 'Relinqing ', and easy to operate detection method, yet there are no report.
Summary of the invention
The object of the present invention is to provide and a kind ofly can effectively control 'Relinqing ' quality, the quality determining method of the 'Relinqing ' of accuracy height, advanced technology.
The quality determining method of a kind of 'Relinqing ' of the present invention is got 3333 parts of headdress flower knotweeds, adds 10 times of water gagings and soaks 0.5 hour, decocted 1.5 hours, filter, the dregs of a decoction add 8 times of water gagings, decoct 1.5 hours, filter, merge filtrate twice, filtrate is concentrated into the medicinal extract that relative density is 1.15～1.20 (50), gets 70% medicinal extract spray drying, get spray powder, standby; Residue medicinal extract and spray powder boiling granulating, drying, sieve (20 order) adds 11.4 parts of sodium carboxymethyl starches and 1.0 parts of mixings of dolomol, is pressed into 1000, and the bag film-coating promptly, is characterized in that may further comprise the steps:
(1) preparation of need testing solution: get 10 of this product, remove coatings, the accurate title, decide, porphyrize, precision takes by weighing 0.3g, places conical flask, accurate to add volume ratio be the extraction-hydrating solution 20ml of methyl alcohol/sulfuric acid/water of 70: 4: 6, and close plug was in 80 ℃ of water-bath refluxing extraction 2 hours, put coldly, be neutralized to PH4～5, be transferred in the 50ml volumetric flask with 20%NaOH, use 70% methanol constant volume, shake up, filter, get subsequent filtrate as need testing solution;
(2) preparation of reference substance solution: it is an amount of that precision takes by weighing the Quercetin reference substance, adds methyl alcohol and make the reference substance solution that every 1ml contains Quercetin 18-22 μ g;
(3) content assaying method: accurate respectively reference substance solution and each 10 μ l of need testing solution of drawing, inject liquid chromatograph, to measure, quercetin content is with control 'Relinqing ' quality in the calculation sample.
(4) chromatographic condition: with octadecylsilane chemically bonded silica is filling agent, volume ratio is that 50: 50 methyl alcohol-0.4% phosphoric acid solution is a moving phase, and flow velocity 1.0ml/min detects wavelength 360nm, 25 ℃ of column temperatures, theoretical cam curve calculate by the Quercetin peak should be not less than 3000.
The quality determining method of 'Relinqing ' of the present invention, the wherein preparation of (2) reference substance solution: precision takes by weighing Quercetin reference substance 10.5mg and places the 100ml measuring bottle, add dissolve with methanol and be diluted to scale, shake up, the accurate absorption in 20ml to the 100ml volumetric flask, add dissolve with methanol and be diluted to scale, shake up, promptly make the reference substance solution that every 1ml contains 21.0 μ g.
The quality determining method of 'Relinqing ' of the present invention is got the Quercetin reference substance solution and is carried out the UV spectral scan, at the 360nm place absorption maximum is arranged, so select 360nm as detecting wavelength.
'Relinqing ' of the present invention can be conventional various formulations.
Method of the present invention is preferably come out by following test:
The inventor is according to " technical requirement of study of tcm new drug ", test adopted by " 2000 editions appendix heavy metals of Chinese pharmacopoeia, arsenic salt inspection technique drench to heat that test agent has been done heavy metal respectively in ten batches of the clear sheets, arsenic salt detects, and the result is as follows:
1, heavy metal is all less than 10/1000000ths.
2, arsenic salt is all less than 2/1000000ths.
According to above testing result, illustrate that the content of heavy metal, arsenic salt in the clear sheet of heat pouring is all very low, and all up to specification, therefore do not list quality determining method of the present invention in.
Assay is the assay of the contained active ingredient of meletin of 'Relinqing ' headdress flower knotweed, with reference to the content assaying method of Quercetin in the medicinal material of polygonum capilalum, adopts the content of Quercetin in high effective liquid chromatography for measuring this product headdress flower knotweed.Chromatographic condition is as described in the text, and Quercetin and other component degree of separation, reappearance, precision, the recovery are good, so adopt the content of Quercetin in high effective liquid chromatography for measuring this product.
1, medicine and medicament methyl alcohol are chromatographically pure, and water is double distilled water, and sample is provided by Guiyang Xintian Pharmaceutical Industry Co., Ltd., and the Quercetin reference substance identifies that by the Chinese biological goods institute provides lot number: 10081-9905.
2, instrumental analysis condition instrument is Agilent 1100 high performance liquid chromatographs, VWD detecting device, Agilent 1100 chem workstations.
3, the chromatographic condition octadecyl silane is a filling agent, chromatographic column Elite Hypersil C18,5 μ m, 4.6 * 250mm, moving phase adopts methyl alcohol-0.4% phosphoric acid solution (50: 50), detects wavelength 360nm, and column temperature is 25 ℃, flow velocity is 1.0ml/min, and theoretical cam curve should be not less than 3000 in the Quercetin peak.
4, detect wavelength and select to get the Quercetin reference substance solution and carry out the UV spectral scan, at 360nm place absorption maximum is arranged, so select 360nm as the detection wavelength.
5, reference substance purity test
Adopt high-efficient liquid phase technique, calculate the purity of measuring reference substance with normalization method.
The sample introduction concentration of Quercetin reference substance is 0.21mg/ml, and sample size is 10 μ l, and purity is 100%.
6, the sample-pretreating method described in the text content assaying method is pressed in the need testing solution preparation, by ultrasonic Extraction 1 hour, 2 hours, 3 hours and 1 hour, 2 hours, 3 hours relatively proof of refluxing extraction, reflux and to obtain satisfactory experimental results in 2 hours, can save time again, raise the efficiency, concrete data see Table one.
Table one sample pre-treatment test
| Ultrasonic time (hour) | ????1 | ????2 | ????3 |
| Content (mg/g) | ????4.036 | ????4.247 | ????4.108 |
| Return time (hour) | ????1 | ????2 | ????3 |
| Content (mg/g) | ????4.333 | ????4.720 | ????4.469 |
7, methodological study
7.1 the investigation of linear relationship: precision takes by weighing Quercetin reference substance 10.5mg, put in the 100ml measuring bottle, add dissolve with methanol and be diluted to scale, shake up, the accurate absorption in 20ml to the 50ml volumetric flask adds dissolve with methanol and is diluted to scale, shake up, promptly make the reference substance solution that every 1ml contains 42.0 μ g, accurate respectively absorption above-mentioned reference substance solution 2ml, 5ml, 10ml, 15ml, 20ml place the 20ml measuring bottle, add methyl alcohol to scale.Draw above-mentioned reference substance solution 10 μ l respectively and inject liquid chromatograph, measure by above-mentioned chromatographic condition.(μ g) is horizontal ordinate with the Quercetin sample size, and corresponding peak area (A) is an ordinate, calculates regression equation and is:
A＝3851.4C-45.446???r＝0.9999
Concrete data see Table two
Table two linear relationship is investigated test
| Sample size (μ g) | ????0.042 | ????0.105 | ????0.21 | ????0.315 | ????0.42 |
| Peak area | ????122.7 | ????357.7 | ????757.4 | ????1160.4 | ????1580.3 |
Show that the Quercetin sample size is good in 0.042～0.42 μ g scope internal linear relation.
7.2 the precision test: precision takes by weighing Quercetin reference substance 10.5mg and places the 100ml measuring bottle, adds dissolve with methanol and is diluted to scale, shakes up, the accurate absorption in 20ml to the 100ml volumetric flask, add dissolve with methanol and be diluted to scale, shake up, promptly make the reference substance solution that every 1ml contains 21.0 μ g.Get this reference substance solution, repeat sample introduction five times, each 10 μ l measure the Quercetin peak area, and RSD is 0.9% as a result, shows that the precision of instrument is good.See Table three.
The test of table precision triple
| The sample introduction number of times | ????1 | ????2 | ????3 | ????4 | ????5 | ??RSD(％) |
| Peak area | ????771.8 | ????781.9 | ????787.4 | ????779.9 | ????771.8 | ??0.9 |
7.3 reappearance test: (lot number: 20030201) test sample is 5 parts, prepares need testing solution and measures content by the text content assaying method, and good reappearance is arranged, and the results are shown in Table four to get same batch.
The test of table four reappearance
| Test sample | ??1 | ??2 | ??3 | ??4 | ????5 | ????RSD(％) |
| Content (mgg -1) | ??4.742 | ??4.727 | ??4.726 | ??4.704 | ????4.736 | ????0.3 |
7.4 stability test:
Sample stability test: get with a need testing solution (lot number: 20030201) measure peak area respectively at different time, measure altogether 6 times by the text content assaying method.RSD is 0.6% as a result, shows that need testing solution is stable in 24h, sees Table five.
The test of table five sample stability
| Minute (hour) | ??1 | ??2 | ??4 | ??8 | ??12 | ??24 | Mean value | ??RSD(％) |
| Peak area | ??1183.3 | ??1195.5 | ??1177.3 | ??1181.8 | ??1177.0 | ??1180.8 | ??1182.6 | ??0.6 |
Reference substance stability test: get with a reference substance solution (21.0 μ g/ml) and measure peak area respectively at different time, measure altogether 6 times by the text content assaying method.RSD is 1.4% as a result, shows that reference substance solution is stable in 24h, sees Table six.
The stability test of table six reference substance
| Minute (hour) | ??0 | ??1 | ??3 | ??5 | ??8 | ??12 | ??24 | Mean value | ??RSD(％) |
| Peak area | ??771.8 | ??788.9 | ??754.6 | ??771.1 | ??761.8 | ??776.7 | ??771.4 | ??770.9 | ??1.4 |
7.5 the average recovery test: precision takes by weighing known content (4.73mgg
-1) 5 parts of same test samples (lot number 20030201), the accurate Quercetin contrast solution (0.042mgml that adds
-1) 5ml, extract and measure by the described method of text by chromatographic condition, with the following formula calculate recovery rate, the results are shown in Table seven, illustrate that this method has the good recovery.
Table seven recovery experimental result
| Sampling amount (g) | The suitable quercetin content (mg) of taking a sample | Add the amount (mg) of Quercetin | Measure the total amount (mg) of Quercetin | The recovery (%) | Average recovery rate (%) | ????RSD％ |
| ??0.0482 | ??0.2280 | ??0.21 | ??0.4310 | ??96.67 | ??100.7 | ????2.7 |
| ??0.0486 | ??0.2299 | ??0.21 | ??0.4383 | ??99.24 | ||
| ??0.0526 | ??0.2488 | ??0.21 | ??0.4660 | ??103.43 | ||
| ??0.0501 | ??0.2370 | ??0.21 | ??0.4520 | ??102.38 | ||
| ??0.0504 | ??0.2384 | ??0.21 | ??0.4524 | ??101.90 |
8, test sample is measured: prepare test sample and reference substance solution by text assay item method, draw 10 μ l respectively and inject liquid chromatograph, the record chromatogram is measured peak area, and the content with Quercetin in the following formula calculation sample the results are shown in Table eight.
As: the peak area of need testing solution; Ar: the peak area of reference substance solution;
Cs: reference substance concentration (mg/ml);
Ms: test sample sampling amount (g); V: constant volume (ml)
Table eight test sample measurement result
| Lot number | The content of Quercetin (mg sheet -1) | ||
| For the first time | For the second time | Mean value | |
| ????20030201 | ????1.82 | ????1.84 | ????1.8 |
| ????20030202 | ????1.89 | ????1.93 | ????1.9 |
| ????20030203 | ????2.04 | ????2.01 | ????2.0 |
| ????20030204 | ????1.88 | ????1.89 | ????1.9 |
| ????20030205 | ????2.11 | ????2.13 | ????2.1 |
| ????20030301 | ????1.97 | ????1.99 | ????2.0 |
| ????20030302 | ????1.75 | ????1.78 | ????1.8 |
| ????20030303 | ????1.92 | ????1.87 | ????1.9 |
| ????20030304 | ????1.81 | ????1.83 | ????1.8 |
| ????20030305 | ????1.93 | ????1.90 | ????1.9 |
According to the assay result of above 10 batch samples, and the fluctuation of consideration medicinal material content, determine that every of this product contains the headdress flower knotweed with Quercetin (C
15H
10O
72H
2O) meter must not be less than 1.5mg.
Embodiment
Embodiment 1:
(1) preparation of need testing solution: get 10 of this product, remove coatings, the accurate title, decide, porphyrize, precision takes by weighing 0.3g, places conical flask, accurate to add volume ratio be the extraction-hydrating solution 20ml of methyl alcohol/sulfuric acid/water of 70: 4: 6, and close plug was in 80 ℃ of water-bath refluxing extraction 2 hours, put coldly, be neutralized to PH4～5, be transferred in the 50ml volumetric flask with 20%NaOH, use 70% methanol constant volume, shake up, filter, get subsequent filtrate as need testing solution;
(2) preparation of reference substance solution: precision takes by weighing Quercetin reference substance 10.5mg and places the 100ml measuring bottle, add dissolve with methanol and be diluted to scale, shake up, the accurate absorption in 20ml to the 100ml volumetric flask, add dissolve with methanol and be diluted to scale, shake up, promptly make the reference substance solution that every 1ml contains 21.0 μ g;
(3) content assaying method:
With octadecylsilane chemically bonded silica is filling agent, and volume ratio is that 50: 50 methyl alcohol-0.4% phosphoric acid solution is a moving phase, and flow velocity 1.0ml/min detects wavelength 360nm, 25 ℃ of column temperatures, and theoretical cam curve is calculated by the Quercetin peak should be not less than 3000.
Accurate respectively reference substance solution and each 10 μ l of need testing solution of drawing inject liquid chromatograph, select 360nm as detecting wavelength, measure the peak area of reference substance solution and need testing solution, are calculated as follows:
As: the peak area of need testing solution; Ar: the peak area of reference substance solution;
Cs: reference substance concentration (mg/ml);
Ms: test sample sampling amount (g); V: constant volume (ml)
Repeat above-mentioned steps once, calculating quercetin content is that mean value is the 1.8mg/ sheet.
Embodiment 2-10
Quality determining method the results are shown in following table with 1:
| Sequence number | The content of Quercetin (mg sheet -1) | ||
| For the first time | For the second time | Mean value | |
| Embodiment 2 | ????1.89 | ????1.93 | ????1.9 |
| Embodiment 3 | ????2.04 | ????2.01 | ????2.0 |
| Embodiment 4 | ????1.88 | ????1.89 | ????1.9 |
| Embodiment 5 | ????2.11 | ????2.13 | ????2.1 |
| Embodiment 6 | ????1.97 | ????1.99 | ????2.0 |
| Embodiment 7 | ????1.75 | ????1.78 | ????1.8 |
| Embodiment 8 | ????1.92 | ????1.87 | ????1.9 |
| Embodiment 9 | ????1.81 | ????1.83 | ????1.8 |
| Embodiment 10 | ????1.93 | ????1.90 | ????1.9 |
Claims (4)
1, a kind of quality determining method of 'Relinqing ' is got 3333 parts of headdress flower knotweeds, adds 10 times of water gagings and soaks 0.5 hour, decocted 1.5 hours, filter, the dregs of a decoction add 8 times of water gagings, decoct 1.5 hours, filter, merge filtrate twice, filtrate is concentrated into that relative density is 1.15～1.20, temperature is the medicinal extract of 50, gets 70% medicinal extract spray drying, get spray powder, standby; Residue medicinal extract and spray powder boiling granulating, drying is crossed 20 mesh sieves, adds 11.4 parts of sodium carboxymethyl starches and 1.0 parts of mixings of dolomol, is pressed into 1000, and the bag film-coating promptly, is characterized in that may further comprise the steps:
(1) preparation of need testing solution: get 10 of this product, remove coatings, the accurate title, decide, porphyrize, precision takes by weighing 0.3g, places conical flask, accurate to add volume ratio be the extraction-hydrating solution 20ml of methyl alcohol/sulfuric acid/water of 70: 4: 6, and close plug was in 80 ℃ of water-bath refluxing extraction 2 hours, put coldly, be neutralized to PH4～5, be transferred in the 50ml volumetric flask with 20%NaOH, use 70% methanol constant volume, shake up, filter, get subsequent filtrate as need testing solution;
(2) preparation of reference substance solution: it is an amount of that precision takes by weighing the Quercetin reference substance, adds methyl alcohol and make the reference substance solution that every 1ml contains Quercetin 18-22 μ g;
(3) content assaying method: accurate respectively reference substance solution and each 10 μ l of need testing solution of drawing, inject liquid chromatograph, to measure, quercetin content is with control 'Relinqing ' quality in the calculation sample.
(4) chromatographic condition: with octadecylsilane chemically bonded silica is filling agent, volume ratio is that 50: 50 methyl alcohol-0.4% phosphoric acid solution is a moving phase, and flow velocity 1.0ml/min detects wavelength 360nm, 25 ℃ of column temperatures, theoretical cam curve calculate by the Quercetin peak should be not less than 3000.
2, the quality determining method of 'Relinqing ' as claimed in claim 1, the wherein preparation of (2) reference substance solution: precision takes by weighing Quercetin reference substance 10.5mg and places the 100ml measuring bottle, add dissolve with methanol and be diluted to scale, shake up, the accurate absorption in 20ml to the 100ml volumetric flask, add dissolve with methanol and be diluted to scale, shake up, promptly make the reference substance solution that every 1ml contains 21.0 μ g.
3, the quality determining method of 'Relinqing ' as claimed in claim 1 or 2, wherein every contains the headdress flower knotweed with Quercetin (C
15H
10O
72H
2O) meter must not be less than 1.5mg.
4, the quality determining method of 'Relinqing ' as claimed in claim 3, wherein 'Relinqing ' is conventional various formulations.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100492000C (en) * | 2007-02-13 | 2009-05-27 | 美晨集团股份有限公司 | Method for constructing HPLC standard fingerprint pattern of semen cuscutae medicinal materials and quality identification |
| CN100535655C (en) * | 2006-06-22 | 2009-09-02 | 成都中医药大学 | Medicinal material of polygonum capilalum, extractive, and quality control method |
| CN101140267B (en) * | 2007-10-10 | 2010-09-08 | 广西万寿堂药业有限公司 | Quality detecting method of mountain green tea blood pressure reducing preparations |
| CN103308617A (en) * | 2013-06-03 | 2013-09-18 | 合肥今越制药有限公司 | Fingerprint spectrum detection method for postnatal Gongtai granules |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU1700463A1 (en) * | 1988-08-09 | 1991-12-23 | Кемеровский государственный медицинский институт | Method for separating flavonoids |
| CN1368075A (en) * | 2001-02-05 | 2002-09-11 | 杨孟君 | Nano medicine 'Relinqing' and its preparing process |
| CN1389204A (en) * | 2002-06-14 | 2003-01-08 | 张晴龙 | Chinese medicine extract for treating hepatitis and its prepn. |
| CN1257969C (en) * | 2002-09-12 | 2006-05-31 | 贵州威门药业股份有限公司 | Polygonum capilalum extract , iIts preparation method and use |
| CN1246695C (en) * | 2003-10-16 | 2006-03-22 | 中山大学 | Method for constituting TLC finger-print pyrogram of hypericum-japonicum medicinal herbs and its standard finger-print pyrogram |
-
2004
- 2004-11-29 CN CNB2004100813836A patent/CN1318842C/en active Active
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100535655C (en) * | 2006-06-22 | 2009-09-02 | 成都中医药大学 | Medicinal material of polygonum capilalum, extractive, and quality control method |
| CN100492000C (en) * | 2007-02-13 | 2009-05-27 | 美晨集团股份有限公司 | Method for constructing HPLC standard fingerprint pattern of semen cuscutae medicinal materials and quality identification |
| CN101140267B (en) * | 2007-10-10 | 2010-09-08 | 广西万寿堂药业有限公司 | Quality detecting method of mountain green tea blood pressure reducing preparations |
| CN103308617A (en) * | 2013-06-03 | 2013-09-18 | 合肥今越制药有限公司 | Fingerprint spectrum detection method for postnatal Gongtai granules |
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| CN1318842C (en) | 2007-05-30 |
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