Fat-Soluble Vitamins Analysis on an Agilent ZORBAX Eclipse PAH Polymeric C18 Bonded Column

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Fat-Soluble Vitamins Analysis on an Agilent ZORBAX Eclipse PAH Polymeric C8 Bonded Column Application Note Food Authors Rongjie FU Agilent Technologies (Shanghai) Co. Ltd. Ying Lun Road Waigaoqiao Free Trade Zone Shanghai 00 P.R. China Jianzhong LI and Ying Wang Agilent Technology Inc. P.R. China Abstract Fat-soluble vitamins are highly lipophilic molecules which are analyzed by normal phase HPLC or reversed phase HPLC with a methanol/acetonitrile mobile phase. A new reversed phase HPLC method was developed for the Agilent ZORBAX Eclipse PAH column for vitamins A, D, D and E. This polymeric C8 phase column provides baseline separation of vitamins D and D, with a short analysis time of only three minutes. The methanol and water mobile phase made this compatible with LC/MS/MS with electrospray ionization.

Introduction Vitamins are essential nutrients that are necessary in small amounts for various functions in the human body. Vitamins are divided into two groups: water-soluble (such as B-complex and C vitamins) and fat-soluble (such as vitamins A, D, E and K). Fat-soluble vitamins perform many functions in the body. Vitamin A plays an important role in helping the eyes adjust to light changes, bone growth, tooth development, reproduction, cell division and gene expression. Vitamin D helps the body to use calcium and phosphorous, and it increases the amount of calcium absorbed from the small intestine to help form and maintain bones. Children especially need adequate amounts of vitamin D to develop strong bones and healthy teeth. Vitamin E acts as an antioxidant, protecting vitamins A and C, red blood cells and essential fatty acids from destruction. [] Though fat-soluble vitamins are beneficial for human health, they have a toxic effect if taken at very high levels. Therefore, the quantity of fat-soluble vitamins in fortified foods must be controlled. HPLC methods are usually used to analyze for these vitamins. Vitamins A and D are often analyzed by normal phase LC as described in the USP method for vitamin A and D. [] Vitamin D has different forms; vitamins D and D are the most important compounds. They have similar structures that make them difficult to separate by HPLC. Recent research showed vitamin D is much less effective than vitamin D in humans. [] Therefore, most foods fortified with Vitamin D use cholecalciferol (vitamin D). Some analytical methods for Vitamin D in food use ergocalciferol (Vitamin D) as an internal standard (for example, The Association of Official Analytical Chemists International (AOACI) method 00.0: cholecalciferol (vitamin D) in selected foods, such as milk and cheese). Therefore, it is important that any method used is capable of accurately separating vitamins D and D. [] This application note describes a method for simultaneously analyzing vitamins A, D, D and E on a polymeric bonding C8 phase. This C8 phase gives the selectivity necessary for polynuclear aromatic hydrocarbons PAH s, some of which separate on the basis of shape. The selectivity of this phase compared to that of typical monomeric bonding C8 phases makes it ideal for separating vitamins D and D, using the same principle of shape selectivity but with a shorter analysis time. The simple mobile phase of methanol and water is also ideal for LC/MS with electrospray ionization (ESI). Experimental HPLC conditions: Instrument: Agilent 00SL series LC system with binary pump Column: Agilent ZORBAX Rapid Resolution HT Eclipse PAH,.6 mm 0 mm,.8 µm Temperature: 0 C Mobile phase: 9% methanol/8% water Flow rate: ml/min (0.6 ml/min for MS detector) Wavelength: nm for VA/80 nm for VD and VE Injection: µl Standards: Vitamin A, ergocalciferol (vitamin D), cholecalciferol (vitamin D) and Vitamin E in methanol Mass conditions: Mass instrument: Agilent 660 triple quadrupole LC/MS system Ion source: ESI Polarity: Postive/Negative Source temp: C Gas flow: L/min Nebulizer: psi Sheath gas temp: 00 C Sheath gas flow: L/min Nozzle voltage: Negative 000 V; Positive 0 V Ion spray voltage: 000 V Resolution: Q (unit) Q (unit) Scan mode: Multiple Reaction Monitoring (MRM) Compound Precursor Product Collision name ion ion Fragmentor Energy Polarity Vitamin A 69.. 0 7 Positive Vitamin D 97. 79. 0 Positive Vitamin D 8. 67. 0 Positive Vitamin E 9. 6. 0 Negative Delta EMV: 00 V

Results and Discussion Vitamins A, D and D are usually separated with normal phase columns due to the highly lipophilic properties of these molecules. The methods developed on reversed phase columns generally use methanol/acetonitrile as the mobile phase, but mostly do not baseline resolve Vitamins D and D. A previous application was developed for fat-soluble vitamins on Agilent ZORBAX Eclipse XDB C8 and Agilent ZORBAX StableBond SB-C8 columns, but with lower resolution of vitamins D and D []. A new application compared the separation of vitamins D and D with Stablebond C8 bonded phase to the same separation with Eclipse Plus C8 bonded phase. The SB-C8 may resolve the D vitamins better because of the accessible silanols on the surface of the stationary phase. However, the longer column increases the resolution but also increases the analysis time. The flow rate can be raised to decrease the time. The method was developed as a UHPLC method for high pressure exceeding 600 bar []. The results of this study determined that a fat-soluble vitamins analysis on an Eclipse PAH column provides better resolution and shorter analysis time compared to Eclipse Plus C8. Vitamins D and D were baseline separated in minutes (Figure ). The polymeric bonding C8 phase made it easy for D and D to resolve completely. The pressure was only 68 bar with a ml/min flow rate, which can be performed on any LC instrument. 0 0 0 Vitamin A Vitamin D Vitamin D Vitamin E (a-ve) Agilent ZORBAX Rapid Resolution HT Eclipse Plus C8.6 mm 0 mm,.8 µm 0 _ 6 7 8 9 min 0 0 0 Rs, =.60 Agilent ZORBAX Rapid Resolution HT Eclipse PAH.6 mm 0 mm,.8 µm 0 _ 6 7 8 9 min Figure. Chromatograms for the separation of four fat-soluble vitamins on different Agilent ZORBAX C8 columns.

Figures and show the total ion chromatogram (TIC) and multiple reaction monitoring (MRM) of four vitamins on the ZORBAX Eclipse PAH column. All four compounds were well resolved with no ion depression, which made it possible to get very high MS sensitivity. 0 7. 7 6. 6..... 0. VA VD VD VE 0...... 6 6. 7 7. 8 8. Counts vs. acquisition time (min) Figure. TIC of four fat-soluble vitamins on an Agilent ZORBAX Eclipse PAH column.

0 0.. 0. 0 6 0...... 6 6. 7 7. 8 8..78 0 0...... 6 6. 7 7. 8 8.. 0...... 6 6. 7 7. 8 8..8 0...... 6 6. 7 7. 8 8. Counts vs. acquisition time (min) Figure. MRM of four fat-soluble vitamins on Agilent ZORBAX Eclipse PAH column.

Conclusion The unique selectivity of a polymerically bonded C8 column, such as the Agilent ZORBAX Eclipse PAH column makes it possible to separate compounds with very similar structures like vitamins D and D. The method developed in this application note resolved four fat-soluble vitamins simultaneously, in minutes, and is compatible with the MS detector. The method can be run on any LC instrument and is suitable for the analysis of fat-soluble vitamins in foods. References. http://www.ext.colostate.edu/pubs/foodnut/ 09.html.. Fat- and Water-Soluble Vitamins with Minerals Tablets, USP0-NF.. A. Laura, G. Armas, Bruce W. Hollis, and Robert P. Heaney, Vitamin D Is Much Less Effective than Vitamin D in Humans. The Journal of Clinical Endocrinology & Metabolism 89():87 9.. John W Henderson Jr and Judy Berry, UHPLC Method Development Options for a Vitamin D and D Separation, Agilent Technologies publication 990-09EN.. R. Ricker, "Comparison of Non-Endcapped Sterically Protected Silanes to Fully Endcapped Dimethylsilane," Hewlett Packard Lab Insights, FD, 998. For More Information For more information on our products and services, visit our Web site at www.agilent.com/chem. www.agilent.com/chem Agilent shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material. Information, descriptions, and specifications in this publication are subject to change without notice. Agilent Technologies, Inc., 00 Printed in the USA February, 00 990-EN