DOI QR코드

DOI QR Code

Study on The System Suitability Test for Alcohols Separation by GCOTC

GCOTC에 의한 알코올류 분리를 위한 시스템 적합성에 관한 연구

  • Oh, Doe Seok (Korea Industrial Health and Evaluation Co., Ltd.) ;
  • Kim, Sung Hwa (Korea Industrial Health and Evaluation Co., Ltd.) ;
  • Lee, Seul (Korea Industrial Health and Evaluation Co., Ltd.) ;
  • Choi, Jae Gu (Dongnam Health University)
  • Received : 2017.02.08
  • Accepted : 2017.06.20
  • Published : 2017.06.30

Abstract

Objectives: The purpose of this study is to enhance the application of analytical method of polar solvents(alcohols) by GCOTC (gas chromatography open tubular column) through the system suitability test(SST) to estimate the whole chromatographic system performance(integral part). Methods: To perform the SST, carried out repeatability(n=6) as analytical method of polar solvents by GCOTC, got the retention time($t_R$), standard deviation(${\sigma}_{n-1}$) of $t_R$, baseline width($w_b=4{\sigma}_{n-1}$) and calculated dead time($t_m$) by $v_m=d^2{\pi}L(f/4)$ and $v_m=t_m$ x flow rate. Results: In this experiment, obtained the basic data, there were $t_m=2$ min, methanol($t_R=3.569$, ${\sigma}_{n-1}=0.01$, $w_b=0.04$), ethanol ($t_R=3.892$, ${\sigma}_{n-1}=0.004$, $w_b=0.016$), isopropanol($t_R=4.209$, ${\sigma}_{n-1}=0.004$, $w_b=0.016$). By using these data, calculated the corrected retention time($t_R{^{\prime}}$), capacity factor(k), separation factor(${\alpha}$), number of theoretical plate(n) and resolution($R_s$) for SST and got the good results. Conclusions: Through the SST, could reconfirm the whole chromatographic performance system(integral part) for analytical method of polar solvents by GCOTC. Therefore, this analytical method expect to be widely applied at the related areas.

Keywords

References

  1. Agalloco J, "Validation: an unconventional review and reinvention". Validation: an unconventional review and reinvention, 1995, 49 (4): 175-179.
  2. Agilent technologies ; http://www.chem.agilent.com
  3. Center for Drug Evaluation and Research(CDER), Reviewer Guidance, Validation of Chromatographic Methods, 11.1994
  4. DEEPAK BAHNOT, How to calculate System Suitability in Chromatography, Posted on 2.27.2013
  5. Hsu, H.; Chien, C. S. J. Food Drug Anal. 1994, 2(3), 161-176
  6. Linda L. Ng, Reviewer Guidance, Center for Drug Evaluation and Research(CDER), Validation of Chromatographic Methods, 11.1994
  7. Oh Doe Seok, Kim Sung Hwa, Lee Seul, and Hwang Kyung Chul, Study on Development of Analytical Method for Polar Solvent by GC, Journal of Korean Society and Environmental Hygiene, 2016, 26(1), 20-29 https://doi.org/10.15269/JKSOEH.2016.26.1.20
  8. Osman TDRYAKD, Dilan BAYSOYU, Gulizar AYDIN, Emine SECER, Setting System Suitability Parameters for Performance Optimization of GC-NPD Detection for Pesticide Residue Analysis, G.U. Journal of Science, 2009, 22(3): 149-150
  9. USP29, 2006.6.1.
  10. Wikipedia, the free encyclopedia, Validation(drug manufacture), 2013