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  1. NTU Theses and Dissertations Repository
  2. 公共衛生學院
  3. 環境衛生研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/42496
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor蔡詩偉
dc.contributor.authorYa-Ting Liuen
dc.contributor.author劉雅婷zh_TW
dc.date.accessioned2021-06-15T01:14:51Z-
dc.date.available2014-09-16
dc.date.copyright2009-09-16
dc.date.issued2009
dc.date.submitted2009-07-28
dc.identifier.citation1. US FDA. Question and answers on the occurrence of furan in food. 2004; Available at: http://www.cfsan.fda.gov/~dms/furanqa.html.
2. Vranova, J. and Z. Ciesarova, Furan in food - a review. Czech journal of food sciences, 2009; 27(1): 1-10.
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4. NTP, Toxicology and carcinogenesis studies of furan (CAS No. 110-00-9) in F344/N rats and B6C3F1 mice (gavage studies). Ntp technical report No. 402. U.S. Department of health and human services, public health service, national institutes of health, research triangle park, nc. 1993.
5. IARC, Dry cleaning, some chlorinated solvents and other industrial chemicals. IARC monographs on the evaluation of carcinogenic risks to humans. IARC Lyon, France, 1995; 63: 393-407.
6. US FDA. Exploratory data on furan in food. 2004; Available at: http://www.cfsan.fda.gov/~dms/furandat.html/.
7. European Food Safety Authority, Report of the scientific panel on contaminants in the food chain on provisional findings on furan in food. The EFSA Journal, 2004; 137: 1-20. Available at : http://www.efsa.europa.eu/en/science/contam/ contam_documents/760.html.
8. Locas, C.P. and V.A. Yaylayan, Origin and mechanistic pathways of formation of the parent furan - a food toxicant. Journal of Agricultural and Food Chemistry, 2004; 52(22): 6830-6836.
9. Mark, J., et al., Quantitation of furan and methylfuran formed in different precursor systems by proton transfer reaction mass spectrometry. Journal of Agricultural and Food Chemistry, 2006; 54(7): 2786-2793.
10. Becalski, A. and S. Seaman, Furan precursors in food: A model study and development of a simple headspace method for determination of furan. Journal of Aoac International, 2005; 88(1): 102-106.
11. Stadler, R., Furan: Summary of industry activities. Report of a workshop held on analytical methods and brainstorming on the elements to be included in a database. Joint DG SANCO/EFSA/DG JRC workshop, Brussels, 19th May 2006.
12. Yaylayan, V.A., Precursors, formation and determination of furan in food Journal für Verbraucherschutz und Lebensmittelsicherheit, 2006; 1(1): 5-9.
13. Limacher, A., et al., Formation of furan and methylfuran by maillard-type reactions in model systems and food. Journal of Agricultural and Food Chemistry, 2008; 56(10): 3639-3647.
14. Senyuva, H.Z. and V. Gokmen, Potential of furan formation in hazelnuts during heat treatment. Food Additives and Contaminants, 2007; 24: 136-142.
15. Egle, J.L. and B.J. Gochberg, Respiratory retention and acute toxicity of furan. American Industrial Hygiene Association Journal, 1979; 40(4): 310-314.
16. Kedderis, G.L. and S.D. Held, Prediction of furan pharmacokinetics from hepatocyte studies: Comparison of bioactivation and hepatic dosimetry in rats, mice, and humans. Toxicology and Applied Pharmacology, 1996; 140(1): 124-130.
17. Burka, L.T.W., K. D. Irwin, R. D., Disposition of [14c] furan in the male f344 rat. Journal of Toxicology and Environmental Health, 1991; 34(2): 245-257.
18. Carfagna, M.A., S.D. Held, and G.L. Kedderis, Furan-induced cytolethality in isolated rat hepatocytes - correspondence with in-vivo dosimetry. Toxicology and Applied Pharmacology, 1993; 123(2): 265-273.
19. Chen, L.J., S.S. Hecht, and L.A. Peterson, Identification of cis-2-butene-1,4-dial as a microsomal metabolite of furan. Chemical Research in Toxicology, 1995; 8(7): 903-906.
20. Byrns, M.C., D.P. Predecki, and L.A. Peterson, Characterization of nucleoside adducts of cis-2-butene-1,4-dial, a reactive metabolite of furan. Chemical Research in Toxicology, 2002; 15(3): 373-379.
21. Heppner, C.W. and J.R. Schlatter, Data requirements for risk assessment of furan in food. Food Additives and Contaminants, 2007; 24: 114-121.
22. NRC, Spacecraft maximum allowable concentrations for selected airborne contaminants. Washington, DC: National Academy Press, 2000; 4: 307-329,appendix B14, Furan.
23. Becalski, A., et al., Development and validation of a headspace method for determination of furan in food. Food Additives and Contaminants, 2005; 22(6): 535-540.
24. Sanz, C., et al., Optimizing headspace temperature and time sampling for identification of volatile compounds in ground roasted arabica coffee. Journal of Agricultural and Food Chemistry, 2001; 49(3): 1364-1369.
25. Kolb B, E.L., Static headspace-gas chromatography theory and practice. Wiley-VCH, Weinheim, 1997.
26. Senyuva, H.Z. and V. Gokmen, Analysis of furan in foods. Is headspace sampling a fit-for-purpose technique? Food Additives and Contaminants, 2005; 22(12): 1198-1202.
27. Wenzl, T., Methods for the determination of furan in food – outcome of a survey conducted among EU food control laboratories. European Commission Joint Research Centre, 2008.
28. Hasnip, S., C. Crews, and L. Castle, Some factors affecting the formation of furan in heated foods. Food Additives and Contaminants, 2006; 23(3): 219-227.
29. Ridgway, K., S.P.D. Lalljie, and R.M. Smith, Comparison of in-tube sorptive extraction techniques for non-polar volatile organic compounds by gas chromatography with mass spectrometric detection. Journal of Chromatography A, 2006; 1124(1-2): 181-186.
30. Goldmann, T., et al., Rapid determination of furan in heated foodstuffs by isotope dilution solid phase micro-extraction-gas chromatography - mass spectrometry (SPME-GC-MS). Analyst, 2005; 130(6): 878-883.
31. Ho, I.P., S.J. Yoo, and S. Tefera, Determination of furan levels in coffee using automated solid-phase microextraction and gas chromatography/mass spectrometry. Journal of Aoac International, 2005; 88(2): 574-576.
32. Bianchi, F., et al., Development and validation of a solid phase micro-extraction-gas chromatography-mass spectrometry method for the determination of furan in baby-food. Journal of Chromatography A, 2006; 1102(1-2): 268-272.
33. Altaki, M.S., F.J. Santos, and M.T. Galceran, Analysis of furan in foods by headspace solid-phase microextraction-gas chromatography-ion trap mass spectrometry. Journal of Chromatography A, 2007; 1146(1): 103-109.
34. Altaki, M.S., F.J. Santos, and M.T. Galceran, Automated headspace solid-phase microextraction versus headspace for the analysis of furan in foods by gas chromatography-mass spectrometry. Talanta, 2009; 78(4-5): 1315-1320.
35. Yang, X.G. and T. Peppard, Solid-phase microextraction for flavor analysis. Journal of Agricultural and Food Chemistry, 1994; 42(9): 1925-1930.
36. Kataoka, H., H.L. Lord, and J. Pawliszyn, Applications of solid-phase microextraction in food analysis. Journal of Chromatography A, 2000; 880(1-2): 35-62.
37. Wardencki, W., M. Michulec, and J. Curylo, A review of theoretical and practical aspects of solid-phase microextraction in food analysis. International Journal of Food Science and Technology, 2004; 39(7): 703-717.
38. US FDA. Determination of furan in foods. 2004; Available at: http://www.cfsan.fda.gov/~dms/furan.html/.
39. Nyman, P.J., et al., Single-laboratory validation of a method for the determination of furan in foods by using static headspace sampling and gas chromatography/mass spectrometry. Journal of Aoac International, 2006; 89(5): 1417-1424.
40. Nyman, P.J., et al., Single-laboratory validation of a method for the determination of furan in foods by using headspace gas chromatography/mass spectrometry, part 2 - low-moisture snack foods. Journal of Aoac International, 2008; 91(2): 414-421.
41. Kersting, M., et al., Measured consumption of commercial infant food products in German infants: Results from the donald study. Journal of Pediatric Gastroenterology and Nutrition, 1998; 27(5): 547-552.
42. Shin Jiuan Wu, Y.H.C., Chia Wen Fang and Wen Harn Pan, Food sources of weight, calories, and three macro-nutrients-nahsit 1993-1996. Nutritional Sciences Journal, 1999; 24(1): 41-58.
43. Crews, C. and L. Castle, The determination of furan in foods - challenges and solutions. Lc Gc Europe, 2007; 20: 498-503.
44. Yoshida, I., et al., Rapid and improved determination of furan in baby foods and infant formulas by headspace GC/MS. Journal of the Food Hygienic Society of Japan, 2007; 48: 83-89.
45. Zoller, O., F. Sager, and H. Reinhard, Furan in food: Headspace method and product survey. Food Additives and Contaminants, 2007; 24: 91-107.
46. Merritt, C., et al., Mass spectrometric determination of volatile components from ground coffee. Journal of Agricultural and Food Chemistry, 1963; 11(2): 152-155.
47. Kuballa, T., S. Stier, and N. Strichow, Furan concentrations in coffee and coffee beverages. Deutsche Lebensmittel-Rundschau, 2005; 101(6): 229-235.
48. Crews, C. and L. Castle, A review of the occurrence, formation and analysis of furan in heat-processed foods. Trends in Food Science & Technology, 2007; 18(7): 365-372.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/42496-
dc.description.abstract呋喃是無色、易揮發的環狀醚類物質,一般用於化學製造工業。由於呋喃於動物實驗中有致癌性,加上近年來陸續有研究及報告指出食物經熱處理後(如:罐頭食品)可能會產生呋喃,因此人體在長時間低劑量接觸情況下有潛在之健康風險。
由於國內仍缺乏食品呋喃含量的基礎資料,為了評估國人經由飲食造成呋喃暴露的可能健康風險,本研究首先建立經熱處理加工食品之呋喃含量檢驗方法,同時收集常見市售食品,並利用頂空固相微萃取技術及結合氣相層析質譜儀(Headspace-solid phase microextraction gas chromatography-mass spectrometry, HS-SPME-GC-MS)、及標準添加法(Standard addition)進行樣本之分析。
本研究首先以 Carboxen/polydimethylsiloxane (CAR/PDMS)纖維進行15分鐘之頂空萃取,接著再以氣相層析質譜儀分析,而所建立的HS-SPME-GC-MS 分析條件,針對不同種類食物的回收率及偵測極限為: 回收率介於75.7% ~126.3%;偵測極限為0.003 ng/g ~0.39 ng/g;定量極限為0.01 ~1.19 ng/g。
本研究針對市售食物產品調查的結果發現,食物中呋喃檢出範圍為0.44至150 ng/g,其中以嬰兒食品、咖啡、及醬汁高湯類,所含呋喃濃度較高。另一方面,本研究亦參考衛生署「國民營養狀況變遷調查1993-1996」等相關資料,進一步推算國人經由飲食造成呋喃暴露的可能劑量,結果發現:咖啡為成人飲食中主要呋喃暴露來源;19-64歲成人經飲用咖啡暴露之平均暴露量為:男性298.32 ng/kg b.w./day,女性176.25 ng/kg b.w./day; 而6個月之嬰兒經奶粉之平均暴露量為0.05 μg/kg b.w./day;開始使用嬰兒副食品之嬰兒經飲食暴露呋喃的量則為1.19 μg/kg b.w./day。
zh_TW
dc.description.abstractFuran is a colorless, volatile liquid used in some chemical manufacturing industries. Researches have demonstrated that furan forms as a result of traditional heat treatment techniques, such as restoring food in cans and jars. The presence of furan in heat-processed foods is of potential health concern because furan is carcinogenic in mice and rats and has been classified as “possibly carcinogenic to humans” by the International Agency for Research on Cancer (IARC).
Currently there is no data available regarding the levels of furan in foods in Taiwan, and the potential adverse health effects of furan exposure is unknown. Therefore, the purpose of this research is to develop an analytical method for the determination of furan in foods, and to assess the possible daily intake of furan in humans according to the initial results of furan concentrations measured from local commercial food products.
Furan levels in selected foods were determined by using solid-phase microextraction (SPME) technique for sampling and gas chromatography with mass spectrometry (HS-SPME-GC-MS) for analysis. Due to matrix effects of different food samples, standard addition method was performed in this study.
The results indicated that the 75 μm CAR/PDMS SPME fiber coating provided the highest loading of the analyte. The optimum condition of HS-SPME-GC-MS for extraction of furan in foods was 15 minutes. LODs ranged from 0.003 ng/g in lemon juice to 0.39 ng/g for cereal were determined, while LOQs between 0.01 and 1.19 ng/g were obtained. The recoveries ranged from 75.7% to 126.3%.
The results showed that the concentrations of furan in foods ranged from 0.44 ng/g to 150 ng/g in various kinds of samples. Higher furan levels were found principally in three categories of foods, including baby foods, coffees, and sauces and broths.
Exposures from different food varieties were also estimated. As for adults aged from 16-64 years old, average furan daily intakes were estimated to be 298.32 ng/kg b.w./day for men and 176.25 ng/kg b.w./day for women. It indicated that coffee is the major dietary source of furan for adult. For a six-month-old baby, the average furan daily intake from milk consumption was estimated to be 0.05 μg/kg b.w./day; while for baby food, it was estimated to be 1.19 μg/kg b.w. /day.
en
dc.description.provenanceMade available in DSpace on 2021-06-15T01:14:51Z (GMT). No. of bitstreams: 1
ntu-98-R96844002-1.pdf: 515713 bytes, checksum: f3a79ce1c2bfa1237a75b5ad5a7cf142 (MD5)
Previous issue date: 2009
en
dc.description.tableofcontents中文摘要 I
Abstract II
Table of Contents IV
List of Figures VI
List of Tables VII
Appendixes VIII
Chapter 1. Introduction 1
1.1 Occurrence of furan in foods 1
1.2 Formation of furan 2
1.3 Mechanism and toxicity 4
1.4 Analytical methods of furan in foods 6
1.5 Objectives 8
Chapter 2. Materials and methods 9
2.1 Reagents and standards 9
2.2 Sample collection and preparation 9
2.3 SPME procedure 10
2.4 GC/MS conditions 11
2.5 Method validation 11
2.6 Average daily intake estimations 12
Chapter 3. Results and discussions 14
3.1 Analytical method 14
3.2 Method validation 16
3.3 The concentrations of furan in food in Taiwan 17
3.4 Average furan daily intake estimations 19
Chapter 4. Conclusion 21
References 23
dc.language.isoen
dc.subject健康風險評估zh_TW
dc.subject呋zh_TW
dc.subject喃zh_TW
dc.subject食物zh_TW
dc.subject頂空固相微萃取zh_TW
dc.subjectFooden
dc.subjectHealth Risk Assessmenten
dc.subjectHS-SPMEen
dc.subjectFuranen
dc.title利用頂空固相微萃取技術分析食物中之呋喃zh_TW
dc.titleDeterminations of Furan in Food
by Headspace Solid-Phase Microextraction
en
dc.typeThesis
dc.date.schoolyear97-2
dc.description.degree碩士
dc.contributor.oralexamcommittee陳美蓮,林嘉明
dc.subject.keyword呋,喃,食物,頂空固相微萃取,健康風險評估,zh_TW
dc.subject.keywordFuran,Food,HS-SPME,Health Risk Assessment,en
dc.relation.page47
dc.rights.note有償授權
dc.date.accepted2009-07-28
dc.contributor.author-college公共衛生學院zh_TW
dc.contributor.author-dept環境衛生研究所zh_TW
顯示於系所單位:環境衛生研究所

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