DETERMINATION OF VITAMINS A, E, AND K AND UBIQUINONES IN PLASMA BY VERY HIGH SPEED LIQUID CHROMATOGRAPHY

Similar documents
Necessity of Monitoring HPLC by a X-R Control Chart on Measurement of Serum Fat-Soluble Vitamins

Targeting of Coenzyme Q10 Solubilized with Soy Lecithin to Heart of Guinea Pigs

Type Analysis of Citrus Essential Oils by Multidimensional Supercritical Fluid Chromatography/ Gas Chromatography

Toshio OKANO,3 Naoko MIzuNo,3 Sumiko SHIDA,3 Norlko TAKAHASHI,3 Tadashl KOBAYASHI,3* Elzo KURODA,4 Solchl

Selectivity Comparison of Agilent Poroshell 120 Phases in the Separation of Butter Antioxidants

A Novel Solution for Vitamin K₁ and K₂ Analysis in Human Plasma by LC-MS/MS

TENOFOVIR TABLETS: Final text for addition to The International Pharmacopoeia (June 2010)

The Determination of CBD and General Cannabinoid Content in Hemp Oils Using HPLC with UV Detection

DIRECT EXTRACTION OF BENZODIAZEPINE METABOLITE WITH SUPERCRITICAL FLUID FROM WHOLE BLOOD

The Third Department of Internal Medicine, University of Tokyo Faculty of Medicine, Hongo, Tokyo 113

High-Performance Liquid Chromatographic Determination of Vitamin D3 in Fish Liver Oils and Eel Body Oils

RITONAVIRI COMPRESSI RITONAVIR TABLETS. Final text for addition to The International Pharmacopoeia (July 2012)

Screening of Antihistamine Agents (Diphenhydramine) with Blood and Urine Samples by REMEDi-HS System

3-Acetyldeoxynivalenol. 15-Acetyldeoxynivalenol

DRAFT PROPOSAL FOR THE INTERNATIONAL PHARMACOPOEIA: CARBAMAZEPINI COMPRESSI - CARBAMAZEPINE TABLETS

Analytical Method for 2, 4, 5-T (Targeted to Agricultural, Animal and Fishery Products)

ARTESUNATE TABLETS: Final text for revision of The International Pharmacopoeia (December 2009) ARTESUNATI COMPRESSI ARTESUNATE TABLETS

INTERNATIONAL PHARMACOPOEIA MONOGRAPH ON LAMIVUDINE TABLETS

Title Revision n date

Determination of Amantadine Residues in Chicken by LCMS-8040

Tenofovir disoproxil fumarate (Tenofoviri disoproxili fumaras)

ISSN (Print)

PAPRIKA EXTRACT SYNONYMS DEFINITION DESCRIPTION FUNCTIONAL USES CHARACTERISTICS

Quantitative Method to measure Glycidol Fatty Acid Esters (GEs) in Edible Oils

Normal Phase HPLC Column COSMOSIL SL-II

PDF hosted at the Radboud Repository of the Radboud University Nijmegen

[ APPLICATION NOTE ] Profiling Mono and Disaccharides in Milk and Infant Formula Using the ACQUITY Arc System and ACQUITY QDa Detector

Sheikh R J et al. IRJP 1 (1)

Determination of DDTs and Dicofol Residues in Vegetables by GC/MS and HPLC

Ergovaline. [Methods listed in the Feed Analysis Standards] 1 Liquid chromatography Note 1, 2 [Feed Analysis Standards, Chapter 5, Section 2

Amudha S et al., Asian Journal of Pharmthiaceutical Technology & Innovation, 04 (21); 2016; Research Article

CHAPTER 3: ANALYTICAL METHOD DEVELOPMENT AND VALIDATION

Determination of β2-agonists in Pork Using Agilent SampliQ SCX Solid-Phase Extraction Cartridges and Liquid Chromatography-Tandem Mass Spectrometry

THIN LAYER CHROMATOGRAPHY

ISSN: ; CODEN ECJHAO E-Journal of Chemistry 2011, 8(3),

Title. CitationScientific reports, 6: Issue Date Doc URL. Rights(URL)

SPE-LC-MS/MS Method for the Determination of Nicotine, Cotinine, and Trans-3-hydroxycotinine in Urine

DRAFT MONOGRAPH FOR THE INTERNATIONAL PHARMACOPOEIA EFAVIRENZ, EMTRICITABINE AND TENOFOVIR TABLETS

DRAFT MONOGRAPH FOR THE INTERNATIONAL PHARMACOPOEIA PAEDIATRIC RETINOL ORAL SOLUTION (August 2010)

ANALYTICAL SCIENCES OCTOBER 2018, VOL The Japan Society for Analytical Chemistry

ANALYTICAL TECHNIQUES FOR THE QUALITY OF ANTI- AIDS DRUGS

EMTRICITABINE AND TENOFOVIR TABLETS

Sanjog Ramdharane 1, Dr. Vinay Gaitonde 2

RP-HPLC Analysis of Temozolomide in Pharmaceutical Dosage Forms

REVISED DRAFT MONOGRAPH FOR THE INTERNATIONAL PHARMACOPOEIA RETINOL CONCENTRATE, OILY FORM. (August 2010)

Available online at Scholars Research Library

Determination and pharmacokinetics of manidipine in human plasma by HPLC/ESIMS

SUCROSE OLIGOESTERS TYPE I

IJPAR Vol.3 Issue 4 Oct-Dec-2014 Journal Home page:

10 Sulfaquinoxaline H N O S O. 4-amino-N-quinoxalin-2-ylbenzenesulfonamide C 14 H 12 N 4 O 2 S MW: CAS No.:

Reverse Phase HPLC Analysis of Atomoxetine in Pharmaceutical Dosage Forms

Antioxidant. [Summary of antioxidant]

VITAMINES A / E IN PLASMA BY UV - FAST CODE Z18610

Relative Measurement of Zeaxanthin Stereoisomers by Chiral HPLC

Dienes Derivatization MaxSpec Kit

Comprehensive Two-Dimensional HPLC and Informative Data Processing for Pharmaceuticals and Lipids

Analysis of Phenolic Antioxidants in Edible Oil/Shortening Using the PerkinElmer Altus UPLC System with PDA Detection

Determination of 6-Chloropicolinic Acid (6-CPA) in Crops by Liquid Chromatography with Tandem Mass Spectrometry Detection. EPL-BAS Method No.

Analysis of Triglycerides of Soybean Oil by High- Performance Liquid Chromatography in Combination with Gas Liquid Chromatography

Determination of Tetracyclines in Chicken by Solid-Phase Extraction and High-Performance Liquid Chromatography

Application Note. Author. Abstract. Introduction. Food Safety

International Journal of Pharma and Bio Sciences

vii LIST OF TABLES TABLE NO DESCRIPTION PAGE 1.1 System Suitability Parameters and Recommendations Acidic and Alkaline Hydrolysis 15

Rapid Analysis of Water-Soluble Vitamins in Infant Formula by Standard-Addition

Application Note. Agilent Application Solution Analysis of ascorbic acid, citric acid and benzoic acid in orange juice. Author. Abstract.

A Validated Chiral Liquid Chromatographic Method for The Enantiomeric Separation of Dapoxetine Hydrochloride

A New Stability-Indicating and Validated RP-HPLC Method for the Estimation of Liraglutide in Bulk and Pharmaceutical Dosage Forms

Application Note. Agilent Application Solution Analysis of fat-soluble vitamins from food matrix for nutrition labeling. Abstract.

Naoya Takahashi, Keiya Hirota and Yoshitaka Saga* Supplementary material

LC-MS/MS Method for the Determination of Tenofovir from Plasma

Lutein Esters from Tagetes Erecta

F. Al-Rimawi* Faculty of Science and Technology, Al-Quds University, P.O. Box 20002, East Jerusalem. Abstract

Supporting Information. for. Synthesis of 2,1-benzisoxazole-3(1H)-ones by basemediated. photochemical N O bond-forming

Analysis of HMF by HPLC

Application Note. Authors. Abstract. Petrochemical

METHOD DEVELOPMENT AND VALIDATION BY RP-HPLC FOR ESTIMATION OF ZOLPIDEM TARTARATE

PHOTOCATALYTIC DECONTAMINATION OF CHLORANTRANILIPROLE RESIDUES IN WATER USING ZnO NANOPARTICLES. DR. A. RAMESH, Ph.D, D.Sc.,

Available online Research Article

Scholars Research Library. Der Pharmacia Lettre, 2015, 7 (5):44-49 (

PHOSPHOLIPIDS RECOVERY FROM DEOILED SOYBEANS USING SUPERCRITICAL CARBON DIOXIDE EXTRACTION

ARTENIMOLUM ARTENIMOL. Adopted revised text for addition to The International Pharmacopoeia

Concurrent analysis of fat and water soluble vitamins in biological fluids using reverse phase-high performance liquid chromatography technique

Measuring Phytosterols in Health Supplements by LC/MS. Marcus Miller and William Schnute Thermo Fisher Scientific, San Jose, CA, USA

Draft monograph for inclusion in. The International Pharmacopoeia. Dextromethorphani solutionum peroralum - Dextromethorphan oral solution

Comparison of a UPLC Method across Multiple UHPLC Systems

Study of the British Pharmacopeia method on methimazole (thiamazole) content in carbimazole tablets

Ultra High Performance Liquid Chromatograph. Nexera X2 C196-E079

IDENTIFICATION AND CONTROLOFRESIDUALSOLVENTS Identification and control of residual solvents EUROPEAN PHARMACOPOEIA 6.

LEVONORGESTREL AND ETHINYLESTRADIOL TABLETS. (January 2012) DRAFT FOR COMMENT

A Sensitive and Simple High Performance Liquid Chromatographic Method for Quantification of Tadalafil in Human Serum

Validation of UV Spectrophotometric and HPLC Methods for Quantitative determination of Iloperidone in Pharmaceutical Dosage Form

Determination of Clarithromycin in Human Plasma by LC-EI Tandem Mass Spectrometry: Application to Bioequivalence Study

Determination of Aflatoxins in Food by LC/MS/MS. Application. Authors. Abstract. Experimental. Introduction. Food Safety

Development and Validation for Simultaneous Estimation of Sitagliptin and Metformin in Pharmaceutical Dosage Form using RP-HPLC Method

Detection of Low Level of Chloramphenicol in Milk and Honey with MIP SPE and LC-MS-MS

Isolation of five carotenoid compounds from tangerine tomatoes

Simultaneous Estimation of Gemcitabine Hydrochloride and Capecitabine Hydrochloride in Combined Tablet Dosage Form by RP-HPLC Method

ZIDOVUDINE, LAMIVUDINE AND ABACAVIR TABLETS Draft proposal for The International Pharmacopoeia (September 2006)

Transcription:

BUNSEKI KAGAKU Vol. 33, pp.e309-e314, 1984 The Japan Society for Analytical Chemistry, 1984 DETERMINATION OF VITAMINS A, E, AND K AND UBIQUINONES IN PLASMA BY VERY HIGH SPEED LIQUID CHROMATOGRAPHY Kouichi ABER, Kenichi KUSUBE, Keeko MUKASA, Yoshinobu ISHIGURO, Tadashi SATO, Seiji ISHIKAWA, and Haruhiko HOSHIDA Tsukuba Research Laboratories, Eisai Co., Ltd., 1-3 Tokodai 5-chome, Toyosato-machi, Tsukuba-gun, Ibaraki 300-26, Japan A quantitative method for analyzing vitamins A, E and K and ubiquinones in plasma, based on recently developed very high speed liquid chromatography, is described. Vitamins A, E, and K and ubiquinones are extracted from 20-50 ƒêl of plasma with 5 ml of hexane after addition of 1 ml of water and 2 ml of ethanol containing each internal standard. Hexane extracts ( 4 ml ) are evaporated under a nitrogen stream at 40 Ž. The residue is dissolved in 100 ƒêl of isopropanol or hexane. The solution is subjected to the very high speed liquid chromatography. Total time required for sample preparation and analysis is some 10 min. The actual chromatographic separation is completed in about 5 min. The detection limits for vitamin A ( retinol ), vitamin E ( ƒ -tocopherol ), vitamin K1 and ubiquinone-10 obtained with a UV detector are 0.056, 0.28, 0.28 and 0.49 ng, respectively. This method offers significant advantages in terms of sensitivity and speed of sample treatment compared to conventional methods. Very high speed liquid chromatography ( VHSLC ) has recently been established by DiCesare et al1)-3). VHSLC represents a major advance in high performance liquid chromatographic technology which enables the separation of compounds in 1-5 min. This paper describes the application of VHSLC to the analysis of vitamins A, E and K and ubiquinones ( UQ ) in plasma, with emphasis on the practical aspects including rapid sample preparation and quantification procedures. EXPERIMENTAL Material Vitamin A ( retinol ) and (3-naphthyl myristate were obtained from Sigma Chemical Co., Ltd. ƒ -, ƒà- ƒá- and ƒâ-tocopherols were individually isolated from soy bean scum or wheat germ oil, and were purified according to the method of Kijima4). Tocol, eicosanyl naphthoate, UQ-7, UQ-8, UQ-9 and 2,3, 6-trimethy1-5- decaprenyl-1, 4- benzoquinone ( TQ-10 ) were synthesized according to the conventional methods5)6), and purified by column chromatography and recrystallization. Methanol, ethanol, hexane and isopropanol of analytical grade were used without further purification.

E310 BUNSEKI KAGAKU Vol. 33(1984) Appratus The VHSLC system was consisited of a Shimadzu LC-5A ( Shimadzu Corporation, Kyoto, Japan ) with a Rheodyne loop injector. The UV detector used was a Shimadzu SPD-2A detector. SHIM-PACK PC18-03/S0505 ( PC18 ) and SHIM-PACK ASI-03/S0505 ( ASI ) were used as VHSLC columns. These columns ( 50 mm ~ 4.6 mm I.D. ) have over 5000 theoretical plates per column. PC18 is packed with 3 Đm spherical C18 bonded phase particles and ASI, 3 pm spherical silica gel particles. The conventional columns used for comparison were Nucleosil C18 ( 5 Đm, 150 mm ~ 4.6 mm I.D. ) and Lichrospher ( 5 Đm, 250 mm ~ 4.6 mm I.D. ). VSHLC conditions for the determination of vitamins A, E and K and UQ are shown in Table 1. Table 1 VHSLC conditions for the determination of vitamins A, E and K and UQ Sample treatment Modified procedures, based on the previous methods7)-11), were used. Twenty to fifty 1-11. of plasma was poured into a brown test tube, and then 1 ml of water, 2 ml of ethanol containing each suitable internal standard ( 5-naphtyl myristate, tocol, eicosanyl naphthoate, and TQ-10 for the determinations of vitamins A, E and K and UQ, respectively ) were added with constant mixing. To the mixture, 5 ml of hexane was added and then centrifuged at approximately 3000 rpm for 5 min. Four ml of the hexane layer was transferred to another brown tube and evaporated to dryness under a stream of dry nitrogen gas. The residue was dissolved in 100 Đl of isopropanol or hexane and the resulting solution was subjected to the VHSLC system. RESULTS Separation of vitamins A, E and K and UQ The separations of standards were excellent as shown in Fig. 1. All of them were eluted within 5 min. Minimum detectable quantities and calibration of compounds Since peaks elute very rapidly in VHSLC, quick response of detector is important. The SPD-2A UV detector has three response times : 0.25, 0.55 and 1.55 s. The relation of peak height of UQ 7-10 and TQ-10 to the response time was investigatea ( Table 2 ). To obtain the increased sensitivity of detection, the response time of the detector

E311 was set at 0.25 s. The calibration curves thus obtained were linear through the origin. The minimum detectable quantities of these materials ( S/N = 5 ) were approximately ten times smaller than those obtained by the conventional HPLC ( Table 3 ). A E Fig. 1 Separation of vitamins A, E and K and UQ standards Table 2 Effect of response time on peak height of UQ

E312 BUNSEKI KAGAKU Vol. 33(1984) Table 3 Comparison of the minimum detectable quantities (S/N=5) of VHSLC with those of HPLC Separation of vitamins A, E and K and UQ in plasma Figure 2 shows typical chromatograms of vitamins and UQ obtained with rat plasma. As shown in Table 4, the recoveries of them from rat plasma were satisfactory. The coefficient of variation ( n = 8 ) was ca. 2 % in all cases. A E K UQ Fig. 2 Separation of vitamins A, E and K and UQ inrat plasma

E313 Table 4 Recoveries of vitamins A,E and K and UQ from plasma Comparison of VHSLC and HPLC Table 5 summarizes the contents of vitamins A, E and K and UQ in rat plasma determined by the present VHSLC method and the previous HPLC methods7)9)10)11). They were agreed well each other. Table 5 Comparison of contents of vitamins A, E and K and UQ in rat plasma obtained by VHSLC and those by HPLC DISCUSSION HPLC has been generally used for the separation of vitamins A, E and K and UQ7)- 11) How ever, this procedure has the disadvatages of requiring rather large quantities of samples because of low sensitivity. In case of infant research, HPLC methods are not practical as they need as much as 0.2-0.5 ml of plasma or serum. In addition, the total analysis time of HPLC method is usually 30-60 min per sample and more rapid method has been desired. Therefore, we developed in the present investigation a more sensitive and rapid VHSLC method for vitamins A, E and K and UQ in plasma. DiCesare et al1)-3) already reported that the theoretical plates of their column ( 100 mm x 4.6 mm I.D. ) were over 10000 and many separation are completed in 1 or 2 min. In contrast, we used SHIM-PACK columns whose theoretical plates were over 5000

E314 BUNSEK I KAGAKU Vol. 33(1984) for the separation of vitamins A, E and K and UQ, obtaining excellent separation of them without extraordinary increase of column pressure. As the detector, fluorometers were not suitable since their response times were very slow ; the efficiency on the eluting peak reduced less than 10 %. Therefore, we used the SPD-2A UV detector which response quickly. VHSLC simply means performing modern liquid chromatography in extremely short time. The VHSLC method which we reported here, seems to be more rapid and sensitive than the conventional methods for determining vitamins A, E, and K and UQ. The authors express their deep gratitude to Dr. H. Nakamura, University of Tokyo, Dr. T. Nakamura, Mr. Y. Sawa, Miss Y. Hatori, Eisai Co., Ltd., Dr. H. Higashikuze, Shimadzu Corporation, and Mr. S. Ozawa, Takeda Chemical Co., Ltd., for their valuable discussion and assistances. REFERENCES 1) J.L. DiCesare, M.W. Dong, J.G. Atwood : J. Chromatogr., 217, 369 (1981). 2) J.L. DiCesare, M.W. Dong, L.S. Ettre : Chromatographia, 14, 257 (1981). 3) M.W. Dong, J.L. DiCesare : J. Chromatogr. Sci., 20, 49 (1982) 4) S. Kijima : 'Extraction and purification of natural vitamin E' in S. Shimazono and G. Katsui ( Eds. ) Vitamin E, pp.55 (Asakura,Tokyo) (1973). 5) Y. Yamano, S. Ikenoya, M. Anze, M. Ohmae, K. Kawabe : Yakugaku Zasshi, 98, 774 (1977). 6) R. Rueg, U. Gloor, R.L. Goel, G. Ryster, O. Wiss, O. Isler : Hely. Chin. Acta, 43, 2616 (1960). 7) K. Abe, K. Ishibashi, M. Ohmae, K. Kawabe, G. Katsui : Vitamins(Japan), 51, 275 (1977). 8) K. Abe, G. Katsui : Vitamins(Japan), 49, 259 (1975). 9) K. Abe, O. Hiroshima, K. Ishibashi, M. Ohmae, G. Katsui : Yakugaku Zasshi, 99, 192 (1979) 10) K. Abe, K. Katayama, S. Ikenoya, K. Takada, T. Yuzuriha, K. Hamamura, T. Namura, K. Yasuda, S. Yoshida, B.D. Watson, K. Kogure : 'Level of coenzyme Q in tissue' in K. Folkers and Y. Yamamura ( Eds. ) Biomedical and Clinical Aspects of Coenzyme Q, Vol. 3. Elsevier, Amsterdam, 1981, pp. 53. 11) K.Abe, M. ohmae, K.Kawabe, G. Katsui : Vitamins(Japan), 53, 385 (1979) Keyword phrases very high speed liquid chromatography of vitamins and ubiquinones ; vitamins A, E and K in rat plasma ; UV detection ; pretreatment of plasma ; response time of UV detector ; separation of fat-soluble vitamins and ubiquinones. ( Received February 20, 1984 )