Rapid quantification of Chinese medicine Zuo Jin Pill using rapid resolution liquid chromatography

Similar documents
Application Note. Author. Abstract. Pharmaceutical QA/QC. Siji Joseph Agilent Technologies, Inc. Bangalore, India

Comprehensive 2D-LC Analysis of Chinese Herbal Medicine

Talanta 66 (2005) Hunan Normal University, Changsha , PR China

Analysis of Stachydrine in Leonurus japonicus Using an Agilent ZORBAX RRHD HILIC Plus Column with LC/ELSD and LC/MS/MS

Extraction Process Validation of Isatis Radix

Application Note. Pharmaceutical QA/QC. Author. Abstract. Siji Joseph Agilent Technologies, Inc. Bangalore, India

Analysis of DNPH-derivatized Aldehydes and Ketones using the Agilent 1220 Infinity LC System with Diode Array Detector

Research of Quality Standards for Stachydrine Hydrochloride in Chinese Medicine TJF Granule

Agilent 1200 Infinity Series HDR DAD Impurity Analyzer System for the Quantification of Trace Level of Genotoxic Impurity

A RP-HPLC METHOD DEVELOPMENT AND VALIDATION OF PARA- PHENYLENEDIAMINE IN PURE FORM AND IN MARKETED PRODUCTS

Automated Switching Between 1D-LC and Comprehensive 2D-LC Analysis

Performance evaluation of the Agilent 1290 Infinity 2D-LC Solution for comprehensive two-dimensional liquid chromatography

High-Resolution Sampling 2D-LC for Pharmaceutical Impurity Analysis

Ultrafast and sensitive analysis of sweeteners, preservatives and flavorants in nonalcoholic beverages using the Agilent 1290 Infinity LC system

Application. Authors. Abstract. Introduction. Hydrocarbon Processing

Performance characteristics of the Agilent 1290 Infinity Quaternary Pump

HKBU Institutional Repository

Accurate quantification of oleanolic acid and ursolic acid in traditional chinese medicine

Achieve confident synthesis control with the Thermo Scientific ISQ EC single quadrupole mass spectrometer

Rapid Screening and Confirmation of Melamine Residues in Milk and Its Products by Liquid Chromatography Tandem Mass Spectrometry

Analysis of Saponins in Spine Date Seed using Agilent ZORBAX Solvent Saver HT (1.8 µm) Columns

Quantification of growth promoters olaquindox and carbadox in animal feedstuff with the Agilent 1260 Infinity Binary LC system with UV detection

Fast methods for the determination of ibuprofen in drug products

Determination of Alkaloids in Goldenseal Using Agilent Bond Elut Plexa Solid Phase Extraction Sorbent for Cleanup and HPLC-DAD Analysis

Method Development and Validation for the Estimation of Darunavir in Rat Plasma by RP-HPLC

Fractionation of Acidic, Basic, and Neutral Drugs from Plasma with an SPE Mixed Mode Strong Cation Exchange Polymeric Resin (Agilent SampliQ SCX)

Development of Validated Analytical Method of Mefenamic Acid in an Emulgel (Topical Formulation)

Development and validation a RP-HPLC method: Application for the quantitative determination of quetiapine fumarate from marketed bulk tablets

Modernizing the USP Monograph for Acetaminophen

Determination of Beta-Blockers in Urine Using Supercritical Fluid Chromatography and Mass Spectrometry

Application Note. Agilent Application Solution Analysis of acaricides in honey. Authors. Abstract. Food

Application Note. Author. Abstract. Xinlei Yang Agilent Technologies Co. Ltd Shanghai, China

Volume 6, Issue 2, January February 2011; Article-015

LC walk-up system using the Agilent 1200 Series LC Method Development Solution and Agilent Easy Access software. Application Note

STABILITY INDICATING METHOD OF RELATED IMPURITIES IN VENLAFAXINE HYDROCHLORIDE SUSTAINED RELEASE TABLETS

Analytical Method Development and Validation of Lafutidine in Tablet dosage form by RP-HPLC

Validated RP-HPLC Method for Estimation of Cefprozil in Tablet Dosage Form

Pharmacophore 2011, Vol. 2 (4), ISSN Pharmacophore. (An International Research Journal)

DEVELOPMENT AND VALIDATION OF A HPLC METHOD FOR IN-VIVO STUDY OF DICLOFENAC POTASSIUM

Low-level Determination of 4-Hydrazino Benzoic Acid in Drug Substance by High Performance Liquid Chromatography/Mass Spectrometry

Analysis of Positional Isomers of Lapatinib with Agilent Poroshell 120 PFP Columns

RP-HPLC Method Development and Validation of Dapagliflozin in Bulk and Tablet formulation

A comparative study on analytical method of total alkaloids from cortex Phellodendri amurens by reversed phase high performance

Agilent 1290 Infinity Quaternary LC Stepwise Transfer to Methods with MS-Compatible Mobile Phases

Determination of underivatized aflatoxins B2, B1, G2, and G1 in ground hazelnuts by immunoaffinity solid-phase extraction with HPLC-FLD detection

Technical Procedure for Concentration Determination of Methamphetamine in Liquids via HPLC

Figure 1. Structures for Vitamin B2 and Vitamin B1.

Available online Journal of Chemical and Pharmaceutical Research, 2014, 6(8): Research Article

Promotion of quality standard of herbal medicine by constituent removing and adding

International Journal of Pharmacy and Pharmaceutical Sciences Vol 2, Issue 1, 2010

Development and Validation of Stability Indicating RP-HPLC Method for the Determination of Anagrelide HCl in Pharmaceutical Formulation

The Agilent InfinityLab 2D-LC Solution with Active Solvent Modulation

VALIDATION OF A UPLC METHOD FOR A BENZOCAINE, BUTAMBEN, AND TETRACAINE HYDROCHLORIDE TOPICAL SOLUTION

LC/MS/MS qua ntitation of β-estradiol 17-acetate using an Agilent 6460 Triple Quadrupole LC/MS working in ESI negative ion mode

Department of Chemistry, JNTUACE, Kalikiri

Figure 1. Structures for Vitamin B2 and Vitamin B1.

Application Note. Edgar Naegele. Abstract

Maximizing Triple Quadrupole Mass Spectrometry Productivity with the Agilent StreamSelect LC/MS System

Rapid and simultaneous determination of paracetamol, ibuprofen and related impurity of ibuprofen by UPLC/DAD

Impact factor: 3.958/ICV: 4.10 ISSN:

TLC Densitometric Quantification of Vasicine, Vasicinone and Embelin from Adhatoda zeylanica leaves and Embelia ribes fruits

7. Stability indicating analytical method development and validation of Ramipril and Amlodipine in capsule dosage form by HPLC.

Mashhour Ghanem 1 and Saleh Abu-Lafi 2 * ABSTRACT ARTICLE INFO

Rapid method development to study plasma stability of diverse pharmaceutical compounds using Rapid Resolution LC and triple quadrupole MS

Determination of Hormones in Drinking Water by LC/MS/MS Using an Agilent InfinityLab Poroshell HPH Column (EPA 539)

Development and validation of RP-HPLC method for determination of marker in polyherbal marketed Kankasava formulations

Analysis of Beer by Comprehensive 2D-LC with the Agilent 1290 Infinity 2D-LC system

Open Access Simultaneous HPLC Determination of Costunolide and Dehydrocostuslactone in Xin-ke-shu Preparations

Fast and Flexible Optimization of Modifier Concentrations Using an Agilent 1290 Infinity LC System with Blend Assist

Macrolides in Honey Using Agilent Bond Elut Plexa SPE, Poroshell 120, and LC/MS/MS

Analytical method development and validation of gabapentin in bulk and tablet dosage form by using UV spectroscopic method

Using the Agilent 1290 Infinity II Multicolumn Thermostat with Extreme Temperatures and Flow Rates

Validation Aspect In Multicomponent Fraction From Gokshur (Tribulus terrestris Linn.) By RP- HPLC Method

Development And Validation Of Rp-Hplc Method For Determination Of Velpatasvir In Bulk

Application Note Pharmaceutical QA/QC. Agilent Application Solution. Authors. Abstract. Syed Salman Lateef Agilent Technologies, Inc.

Development And Validation Of Stability Indicating RP-HPLC Method For Estimation Of Ledipasvir And Sofosbuvir

Simultaneous Determination of 10 Bioactive Components of Lophatherum gracile Brongn by HPLC-DAD

Available online Journal of Chemical and Pharmaceutical Research, 2012, 4(6): Research Article

Developing a fast, generic method for rapid resolution LC with quadrupole MS detection. Application Note

Novus International Journal of Analytical Innovations 2012, Vol. 1, No. 3

Application Note. Authors. Abstract. Energy & Chemicals, Biofuels & Alternative Energy

SIMULTANEOUS ESTIMATION OF CILOSTAZOL AND ASPIRIN IN SYNTHETIC MIXTURE USING HPTLC METHOD

Computer-assisted analysis of complex natural product extracts

Simultaneous Determination of Five Hydrophilic and Lipophilic Components from roots of Salvia miltiorrhiza by HPLC

Received: ; Accepted:

Application Note. Author. Abstract. Pharmaceutical QA/QC. Vinayak A.K Agilent Technologies Bangalore, India

The new Agilent 1290 Infinity Quaternary LC

RP-HPLC Estimation of Trospium Chloride in Tablet Dosage Forms

DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD TO DETERMINE CINITAPRIDE HYDROGEN TARTARATE IN BULK AND PHARMACEUTICAL FORMULATION

Available online Research Article

Analysis of Phthalates in Body Wash using Solid-Supported Liquid-Liquid Extraction

SIMULTANEOUS ESTIMATION OF MEFENAMIC ACID AND PARACETAMOL IN SUSPENSION FORM BY USING UPLC

INTERNATIONAL JOURNAL OF UNIVERSAL PHARMACY AND BIO SCIENCES

NEVIRAPINE ORAL SUSPENSION Final text for addition to The International Pharmacopoeia (February 2009)

STABILITY INDICATING RP HPLC METHOD FOR ANALYSIS OF DORZOLAMIDE HCl IN THE BULK DRUG AND IT S PHARMACEUTICAL DOSAGE FORM

J Pharm Sci Bioscientific Res (4): ISSN NO

World Journal of Pharmaceutical and Life Sciences WJPLS

Reverse Phase High Performance Liquid Chromatography method for determination of Lercanidipine hydrochloride in bulk and tablet dosage form

Journal of Chemical and Pharmaceutical Research, 2012, 4(6): Research Article. Estimation of zaleplon by a new RP-HPLC method

CHAPTER 19 PARACETAMOL + IBUPROFEN

Transcription:

Rapid quantification of Chinese medicine Zuo Jin Pill using rapid resolution liquid chromatography Application Note Traditional Chinese Medicine Authors Xu Liang, Xi Zhang School of Pharmacy Second Military Medical University, Shanghai 2433 China Zhixiu Xu Agilent Technologies Shanghai, Shanghai 2131 China Abstract This Application Note describes the development of a rapid resolution LC method for the separation of the Chinese herbal prescription Zuo Jin Pill into its six major constituents: magnoflorine, jatrorrhizine, coptisine, palmatine, berberine and evodiamine. The method uses an Agilent 12 Series Rapid Resolution Liquid Chromatography (RRLC) system coupled with an Agilent 12 Series Diode Array Detector (DAD). The separation was carried out on an Agilent ZORBAX Eclipse Plus C 18 column (4.6 15 mm, 1.8 µm). The linear gradient was eluted with the mobile phase of an acetonitrile acetate buffer. All calibration curves showed good linearity (r 2 >.9998) within the test range 1.2-12 µg/ml. The results demonstrate that this analytical method is simple, sensitive and reliable for rapidly analyzing six major bioactive compounds in ZJPs. It is useful for the comprehensive evaluation of the quality of this traditional Chinese Medicine (TCM).

Introduction Zuo Jin Pill (ZJP), an ancient traditional Chinese medicine (TCM), is widely adopted in China for the clinical treatment of hypochondric and costal pain, stomach ache, acid reflux, nausea and upset. Recent pharmacological studies showed that it also inhibits gastric secretions and provides antiflammatory, antifungal and analgesic benefits. 1 Coptis (coptidis rhizoma) and evodia (evodiae fructus) are the basic components of this Chinese herbal preparation. 2 Coptis dispells heat, dries dampness, purges fever and removes toxins. Evodia warms the middle torso, dispels cold, causes vitality to descend and controls pain. 3 The herb couples are much simpler than complicated formulas in composition and retain the basic therapeutic features. The pharmacologically-active ingredients of coptis are a number of protoberberine alkaloids, 4 and those of evodia are indolequinoline and quinolone alkaloids. 5 Both of these herb drugs have been analyzed well by many different methods. Several studies have been established for simultaneously assaying the two herbs. 6-8 However, current methods need long analysis times, and incorporate complicated sample preparations and solvent systems. In this Application Note, a method using a rapid resolution liquid chromatography (RRLC) coupled with a diode array detector (DAD) was developed for the simultaneous quantification of the main constituents present in various ZJPs. In addition, a comparative study was made between the performance of RRLC and high performance liquid chromatography (HPLC) techniques. During this test, six compounds in the formula, including magnoflorine, jatrorrhizine, coptisine, palmatine, berberine and evodiamine were analyzed. Experimental Equipment The rapid resolution LC (RRLC) method was developed on an Agilent 12 Series RRLC system with the following modules: Agilent 12 Series Binary Pump SL with vacuum degasser Agilent 12 Series High Performance Autosampler SL Agilent 12 Series Thermostatted Column Compartment SL Agilent 12 Series Diode Array Detector SL, with micro flow cell (2- µl volume, 3-mm path length) Agilent ChemStation B.3.2 for data acquisition and evaluation Agilent ZORBAX Eclipse Plus C18 Rapid Resolution High Throughput (RRHT) column (4.6 15 mm, 1.8 µm.) Figure 1 Structures of the constituents in ZJP. Chemicals and materials HPLC grade acetonitrile, acetic acid, and ammoniom acetate were purchased from Merck (Darmstadt, Germany). Pure water was obtained from a Millipore pure water system. All solvents and samples were filtered through.22-µm membrane filters before analysis. The reference standards of jatrorrhizine, coptisine, palmatine, and berberine were purchased from Shanghai Winherb Medical Science Co., Ltd (Shanghai, China). Magnoflorine was purchased from Shanghai Tauto Biotech Co., Ltd (Shanghai, China). Evodiamine was purchased from the Chinese Institute for the Control of Pharmaceutical and Biological Products (Beijing, China). All standards were 98% pure or better. Nine batches of ZJP were collected from different pharmaceutical companies in China. Sample number 1 was prepared by our laboratory according to China Pharmacopoeia. 2

Standard solutions and sample preparation A series of 12 µg/ml standard solutions were prepared in methanol. A calibration curve was formed from analysis of the diluted solutions. The stock solution was used to prepare the reference compound mixture solutions. All the solutions were stored at 4 C in a refrigerator. The ultrasonic extraction was performed by mixing.25 g of pulverized sample and 25 ml of methanol with 1% 1 M hydrochloric acid into a 25-mL volumetric flask. The flask was then sonicated for 1 hour at room temperature. The extract was adjusted to volume. All samples were filtered prior to use through a.22-µm nylon membrane filter. Analytical method Mobile phase A = 5 mm ammonium acetate and.2% acetic acid, B = acetonitrile Flow rate 1.2 ml/min Gradient -3 min, 1%-2% B; 3-9 min, 2%-35% B; 9-15 min, 35%-1% B; 15-18 min, 1%B Column temperature 35 C DAD wavelength 254 nm, 4 Hz, 4 nm slit, save all spectrum Injection volume 5 µl, room temperature, no needle wash. Results and discussion Optimization of the chromatographic conditions The RRLC conditions were optimized to improve detection. Reversed phase RRLC with gradient elution was used according to the literature reports. 6-8 The concentrations of ammonium acetate and acetic acid in the mobile phase were also optimized. The results showed that the addition of.2% acetic acid and 5 mm ammonium acetate in the mobile phase provided the best resolution, peak shape, and signal-to-noise ratio. The solvent system described here was easier to develop than that of mobile phase systems described in previous studies. 6-8 Optimization of the extraction conditions The most important parameters controlling extraction yield were determined to be the choice of solvent, extraction volume, and the extraction time. In order to optimize these parameters, the first set of analyses was performed using different volumes of methanol and ethanol solvent, while altering the concentration of hydrochloric acid. The results showed that 25 ml of methanol with 1% M hydrochloric acid was the most effective solvent, providing the best response. The analyses were then performed using different extraction times, such as 3, 6, and 9 min. The results of these tests showed that 6 min was sufficient to almost completely extract six compounds. mau 2 15 1 5 mau 2 15 1 5 mv 15 125 1 75 5 25 1 1 mv 15 1 5 1 15. 17.5 2. 22. 2 3 4 2 3 4 3 4 2 Comparison of HPLC and RRLC The ZJP sample was analyzed with the RRLC system, and with the HPLC system (Figure 2). Comparable separations were achieved in 7 min on the HPLC, and 18 min with the RRLC method. The shorter run time of the RRLC (25% of that on the HPLC) was due to the analytical column packed with a 1.8 µm stationary phase, which allowed higher pressures and flow rates. Because of its savings in analysis time and solvent, as well as its high performance and efficiency, it was determined that RRLC is the best choice for the analysis of a complex system such as Chinese herbal prescriptions. 2 4 6 8 1 12 14 16 2 4 6 8 1 12 14 16 1 2 3 4 5 6 7 min 5 5 5 mv 25 6 6 6 52.5 55. 57.5 Figure 2 (a, b) RRLC-UV chromatograms of (a) six mixed bioactive markers and (b) ZJP (S4), and (c) HPLC-UV chromatogram of ZJP with the detection at 254 nm: (1) magnoflorine, (2) jatrorrhizine, (3) coptisine, (4) palmatine, (5) berberine, (6) evodiamine. min min 3

RRLC method validation The linearity calibration curves were developed from the analyses of six different standard concentrations, in triplicate of chemical markers. The calibration curves and correlation coefficients were determined using a liner regression model. The limits of detection (LOD) were meaured with a signal-tonoise ratio (S/N) of about 3. The limits of quantification (LOQ) were measured with the signal-to-noise ratio (S/N) of about 1. The correlation coefficients (r 2 >.9998), LOD (1.4-12 ng), and LOQ (4.8-3 ng) are shown in Table 1. These resultes confirm good linear correlation and high sensitivity for these chromatographic conditions. Analytes Linear range (µg/ml) Regressive equation* r 2 (n=6) LOD (ng) LOQ (ng) Magnoflorine 2-12 y=.23633x-1.44875.9999 12 3 Jatrorrhizine 3.4-425 y=1.216x-2.96349.9999 2.4 6.8 Coptisine 3.28-477.5 y=1.48691x-4.9647.9998 1.97 6.56 Palmatine 2.6-325 y=.93747x-2.73943.9998 1.56 5.2 Berberine 1.92-12 y=1.2979x-8.926.9998 1.92 5.76 Evodiamine 2.4-3 y=.99174x-2.4918.9998 1.4 4.8 * In the regression equation y = ax + b, y refers to the peak area (A), x is the concentration of the reference (µg/ml), and r 2 is the correlation coefficient of the equation. Table 1 Linear regression equation analysis in the determination of the six compounds. 4

The mixture standard solution was analyzed under the optimal conditions injected five times in one day for intraday variation, then injected five times per day for three consecutive days for inter-day variation. The precision and accuracy of these analyses were calculated. The intra-day precision was within.32%, while the inter-day precision was within.63%. The accuracies were all between 98.6 and 1.78%. Five different solutions from the same sample were analyzed to verify the repeatability of the method. Results of this test showed the relative standard deviation (RSD) of repeatability to be less than 1.59%. Using standard addition, the recovery of this method was established with three different concentration levels (.8, 1., and 1.2 times the matrix concentration) added to the reference standard. Three samples, at each concentration level, were made for the analyses. The solutions were extracted and quantified according to the optimized method, and the mean recoveries calculated for each. The mean recovery results were between 99.1 and 1.14%, with RSD less than 2.47% for ten components. These results indicate a satisfactory assay, with acceptable precision, accuracy, repeatability, and recovery (Table 2). Compound Intra-day (n=6) Inter-day (n=3) Repeatability(n=5) Recovery Accuracy Precision Accuracy Precision RSD (%) Mean RSD (%) (RE, %) (RSD, %) (RE, %) (RSD, %) recovery (%) Magnoflorine 1.6.21 99.47.63.74 99.67 1.5 Jatrorrhizine 98.6.22 99.78.44.57 99.1 1.28 Coptisine 99.46.16 1.26.32.95 1.14 2.47 Palmatine 99.372.32 1.53.33 1.51 99.97 2.4 Berberine 99.5.11 99.98.32 1.59 1.11 1.92 Evodiamine 1.78.25 99.83.43 1.4 1.6 1.8 Table 2 Statistical results of precision, accuracy, repeatability and recovery of the six compounds. 5

Sample analysis Once developed, the method was applied to the analysis of 1 batches of ZJP sample. The samples were tested to verify the presence of six marker compounds in the sample. The peaks were identified by comparing the retention times and UV spectra to those obtained from authentic samples. The quantitative analytical results indicated that the six-alkaloid contents in Chinese herbal preparations can vary significantly, depending upon the origin of the sample (Table 3). Multiple constituents are responsible for the therapeutic effects of Chinese herbal preparations, and the concentrations of these constituents may affect these therapeutic benefits. Sample No. Content of each compound in 1 samples (mg/g) Magnoflorine Jatrorrhizine Coptisine Palmatine Berberine Evodiamine 1 14.32 3.88 4.7 19.27 6.22 1.19 2 16.35 3.9 4.15 19.82 61.56 1.45 3 14.28 11.75 5.6 25.24 84.77 1.31 4 14.53 11.8 5.6 24.85 84.44 1.42 5 12.93 8.15 4.48 21.82 73.66.85 6 12.8 7.82 4.32 2.99 71.71.79 7 12.55 8. 4.45 21.42 73.25.84 8 13.22 8.33 4.58 22.16 74.83.77 9 15.76 14.57 5.53 29.79 1.96.78 1 11.7 1.89 3.37 19.44.34 - Table 3 Contents (mg/g) of the six compounds in the 1 samples. 6

Conclusion A rapid RRLC-DAD method was established for the comprehensive analysis of six compounds in ZJP. Validation tests performed in this study indicated that the developed method was sensitive, reliable and rapid. All calibration curves showed good linearity (r 2 >.9998) within the test range of 1.2-12 µg/ml. The detection limits and quantification limits were in the ranges of 1.4-12 ng and 4.8-3 ng, respectively. The described method was successfully applied to the simultaneous separation of the complex constituents in ZJP, and resulted in a shorter time and better fit for effective quality control of this Chinese herbal prescription. 6. X. B. Luo, B. Chen, Simultaneous analysis of protoberberine, indolequinoline and quinolone alkaloids in coptis-evodia herb couple and the Chinese herbal preparations by highperformance liquid chromatographyelectrospray mass spectrometry, Talanta 66 (25) 13-11. 7. C. Y. Chu, S. J. Sheu, Liquid chromatographic separation of the alkaloids in coptis-evodia herb couple, J. Chromatogr. A 756 (1996) 137-144. 8. M. C. Lee, S. J. Sheu, Determination of the Alkaloids in Coptis-Evodia Herb Couple by Capillary Electrophoresis, J. Liq. Chromatogr. 2 (1997) 63-78. References 1. Y. F. Chen, W. W. Chen, R. L. Li, F. Q. Ye, S. F. Xu, H. G. Pan, The study of comparing the protective mechanism of gastric mucosa in rats between Zuo Jin Wan and contra-zuo Jin Wan, J. Guangzhou Univ. Trad. Chin. Med. 2 (23) 133-135. 2. China Pharmacopoeia Committe, China Pharmacopoeia (vol. 1), Chemical Industry Press, Beijing, 25. 3. C. L. Lin, H. Y. Hsu, Herb Couples, Oriental Healing Arts Institute, Los Angeles, CA, 1992, pp. 1 13, 25. 4. L. D. Kong, C. H. Cheng, R. X. Tan, Monoamine oxidase inhibitors from rhizoma of Coptis chinensis, Planta Med. 67 (21) 74-76. 5. Y. Kobayashi, The nociceptive and anti-nociceptive effects of evodiamine from fruits of Evodia rutaecarpa in mice, Planta Med. 69 (23) 425-428. 7

www.agilent.com/chem/12rr Agilent Technologies, Inc., 29 December 7, 29 Publication Number 599-4995EN