Determination of plasma Vitamin K by high-performance liquid chromatography with fluorescence detection using Vitamin K analogs as internal standards. Export

@article{citeulike:634903, abstract = {A HPLC fluorescence determination method for Vitamin K derivatives (Vitamin K(1), phylloquinone, PK and K(2), menaquinones, MK-4 and MK-7) using post-column reduction and internal standards was developed. Selectivity and reproducibility were increased by optimized chromatography conditions and satisfactory precision and accuracy were attained by using synthetic internal standards. After addition of internal standards to plasma samples, lipids were extracted with ethanol and hexane. Chromatography was performed by isocratic reverse phase separation on a C18 column. Vitamin K derivatives were detected at 430 nm with excitation at 320 nm for MK-4 and 240 nm for PK and MK-7. The detection limits for MK-4, PK and MK-7 were 4, 2 and 4 pg, respectively. The recoveries of MK-4, PK and MK-7 were greater than 92\% and the inter- and intra-assay R.S.D. values were 5.7-9.2\% for MK-4, 4.9-9.6\% for PK and 6.3-19.3\% for MK-7. The data showed good correlation between proposed method and LC-APCI/MS method for MK-4 (R(2)=0.988), PK (R(2)=0.979) and MK-7 (R(2)=0.986). The method allows the determination of Vitamin K for evaluating their clinical and nutritional status.}, address = {Department of Hygienic Sciences, Kobe Pharmaceutical University, 4-19-1 Motoyamakita-machi, Higashinada-ku, Kobe 658-8558, Japan.}, author = {Kamao, M. and Suhara, Y. and Tsugawa, N. and Okano, T.}, citeulike-article-id = {634903}, citeulike-linkout-0 = {http://dx.doi.org/10.1016/j.jchromb.2004.11.003}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/15664332}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=15664332}, day = {25}, doi = {10.1016/j.jchromb.2004.11.003}, issn = {1570-0232}, journal = {J Chromatogr B Analyt Technol Biomed Life Sci}, keywords = {hplc, vitamink}, month = {February}, number = {1-2}, pages = {41--48}, posted-at = {2006-05-15 02:40:56}, priority = {3}, title = {Determination of plasma Vitamin K by high-performance liquid chromatography with fluorescence detection using Vitamin K analogs as internal standards.}, url = {http://dx.doi.org/10.1016/j.jchromb.2004.11.003}, volume = {816}, year = {2005} }

TY - JOUR ID - citeulike:634903 L3 - citeulike-article-id:634903 N2 - A HPLC fluorescence determination method for Vitamin K derivatives (Vitamin K(1), phylloquinone, PK and K(2), menaquinones, MK-4 and MK-7) using post-column reduction and internal standards was developed. Selectivity and reproducibility were increased by optimized chromatography conditions and satisfactory precision and accuracy were attained by using synthetic internal standards. After addition of internal standards to plasma samples, lipids were extracted with ethanol and hexane. Chromatography was performed by isocratic reverse phase separation on a C18 column. Vitamin K derivatives were detected at 430 nm with excitation at 320 nm for MK-4 and 240 nm for PK and MK-7. The detection limits for MK-4, PK and MK-7 were 4, 2 and 4 pg, respectively. The recoveries of MK-4, PK and MK-7 were greater than 92% and the inter- and intra-assay R.S.D. values were 5.7-9.2% for MK-4, 4.9-9.6% for PK and 6.3-19.3% for MK-7. The data showed good correlation between proposed method and LC-APCI/MS method for MK-4 (R(2)=0.988), PK (R(2)=0.979) and MK-7 (R(2)=0.986). The method allows the determination of Vitamin K for evaluating their clinical and nutritional status. IS - 1-2 JF - J Chromatogr B Analyt Technol Biomed Life Sci SN - 1570-0232 AD - Department of Hygienic Sciences, Kobe Pharmaceutical University, 4-19-1 Motoyamakita-machi, Higashinada-ku, Kobe 658-8558, Japan. EP - 48 TI - Determination of plasma Vitamin K by high-performance liquid chromatography with fluorescence detection using Vitamin K analogs as internal standards. VL - 816 SP - 41 KW - hplc KW - vitamink AU - Kamao, M AU - Suhara, Y AU - Tsugawa, N AU - Okano, T PY - 2005/02/25/ UR - http://dx.doi.org/10.1016/j.jchromb.2004.11.003 ER -