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Development of dispersive liquid-liquid microextraction methods for the analysis of polar and nonpolar components in liquid samples : 액체 시료중 극성 및 비극성 물질 분석을 위한 분산액체-액체 미량추출법의 개발

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dc.contributor.advisor권성원-
dc.contributor.author이정-
dc.date.accessioned2017-07-13T16:39:37Z-
dc.date.available2017-07-13T16:39:37Z-
dc.date.issued2017-02-
dc.identifier.other000000140663-
dc.identifier.urihttps://hdl.handle.net/10371/120148-
dc.description학위논문 (박사)-- 서울대학교 대학원 : 약학과, 2017. 2. 권성원.-
dc.description.abstractThis study describes a novel sample preparation method for simultaneous identification of 10 phenolic acids from wine using ion pair dispersive liquid-liquid microextraction based on the solidification of a floating organic droplet (IP-DLLME-SFO). For the first time, the ion-pairing technique combined with DLLME-SFO was applied for the detection of phenolic acids. The IP-DLLME-SFO dramatically enhanced the extraction efficiency for very polar phenolic acids, such as gallic acid and protocatechuic acid, which could not be extracted by DLLME-SFO in the absence of an ion-pairing reagent. The effects of the parameters that can affect the extraction efficiency were systematically investigated, including the type and concentration of ion-pairing reagent, type and volume of extraction and dispersive solvents, extraction time, sample pH, and ion strength. And the optimized microextraction conditions yielded high enrichment factors. The combined application of IP-DLLME-SFO and superficially porous particle (SPP) column provided a sensitivity of analysis method, which can separation 10 phenolic acids with similarity chemical structures in 40 min.
The method was validated in terms of linearity, sensitivity, precision and recovery. The coefficient of determination (R2) was higher than 0.994 for all calibration curves. The method linearity was constructed in the range of 0.01 – 15 g/mL, and the sensitivity expressed as limit of detection was as low as 10 ng/mL. The intra- and inter-day precisions were below 7.95 % and 9.33 %, respectively. With a simple dilution, the measured absolute recovery values of around 81.5 ~ 109% were obtained for the compounds, indicating that the extraction efficiency was very high. The method that we developed was successfully applied to the analysis of commercial wine samples with no significant matrix effect, revealing different levels of phenolic acids among these products. The result suggest that the combined use of DLLME-SFO and SPP column may be applicable to the analysis of various polar and non-polar compounds in liquid sample with complex matrices.
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dc.description.tableofcontents1. Introduction 1
2. Materials and methods 5
2.1. Reagents and solutions chemicals 5
2.2. Instrumentation 5
2.3. Preparation of standard solutions and blank, spiked, and real samples 6
2.4. DLLME-SFO procedure 6
2.5. Validation 8
2.6. Statistics 8
3. Results and discussion 10
3.1. Chromatographic separation on a core–shell particle column 10
3.2. Selection of the type and concentration of ion-pairing reagent 12
3.3. Effect of sample pH on extraction efficiency involving THAB 15
3.4. Selection of extraction and dispersive solvents for DLLME-SFO 17
3.5. Optimization of volume of the extraction and dispersive solvents 19
3.6. Salt effect on IP-DLLME-SFO 22
3.7. Facilitation of extraction and optimization of the extraction time 24
3.8. Method validation 26
3.9. Application of the developed method to wine sample analysis 28
4. Conclusions 33
References 34
Appendix 40
1. The principle of DLLME 39
2. DLLME-SFO 40
2.1 Requirments of SFO solvent 40
2.2 Physical properties of the extraction solvents evaluated for SFO method 41
3. SPP column 42
3.1 Concept 42
3.2. Column characteristics 43
3.3. Safety 44
3.4. Application 45
4. Principle and mechanisms of ion-pairing 46
5. The influence of salt 47
6. Validation of analytical procedures 49
6.1. Linearity 26
6.2. Limit of detection 50
6.3. Limit of quantification 51
6.4. Precision 52
6.5. Recovery 53
Publications 55
국문초록 56
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dc.formatapplication/pdf-
dc.format.extent8803668 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectDLLME-SFO-
dc.subjection pairing-
dc.subjectpolar-
dc.subjectphenolic acids-
dc.subjectwine-
dc.subjectCore–shell particle column-
dc.subjectHPLC-
dc.subject.ddc615-
dc.titleDevelopment of dispersive liquid-liquid microextraction methods for the analysis of polar and nonpolar components in liquid samples-
dc.title.alternative액체 시료중 극성 및 비극성 물질 분석을 위한 분산액체-액체 미량추출법의 개발-
dc.typeThesis-
dc.contributor.AlternativeAuthorLi Jing-
dc.description.degreeDoctor-
dc.citation.pages56-
dc.contributor.affiliation약학대학 약학과-
dc.date.awarded2017-02-
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