Journals / Turkish Journal of Chemistry / 2018 / Cilt: 42 - Sayı: 3

A simple automated microplate metho d for determining reducing sugars in fo o d extracts and synthetic serum using cupric-neo cuproine as reductant

Pages
794–807
Publication Date
2022-11-04
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The proposed method offers many advantages whencompared to classical methods, such as (sample and reagent) volume reduction (20-fold), simplicity, multiple sampleanalysis (32 samples in 4 h), and environmental friendliness

📌 3 Key Takeaways

🎯
Objective & Hypothesis:In the present work, a simple automated microplate method based on cupric ion reduction is described fordetermining total reducing sugars in food extracts and synthetic serum.
📊
Key Findings & Data:The reaction of Cu(II)-Nc (cupric-neocuproine)with reducing sugars was performed in alkaline medium in microplates, and the absorbance of the formed highly coloredCu(I)-Nc chelate in a plate reader at 450 nm was recorded.
💡
Conclusion & Impact:The proposed method offers many advantages whencompared to classical methods, such as (sample and reagent) volume reduction (20-fold), simplicity, multiple sampleanalysis (32 samples in 4 h), and environmental friendliness
🔬Design:Research Article
📍Scope:32 samples
⚙️Variables:Domain Parameters

Abstract

In the present work, a simple automated microplate method based on cupric ion reduction is described fordetermining total reducing sugars in food extracts and synthetic serum. The reaction of Cu(II)-Nc (cupric-neocuproine)with reducing sugars was performed in alkaline medium in microplates, and the absorbance of the formed highly coloredCu(I)-Nc chelate in a plate reader at 450 nm was recorded. The proposed method was applied to reducing sugars(glucose, fructose, galactose, maltose, and lactose) and their linear calibration curves were constructed. The detectionand quantification limits (LOD and LOQ) for glucose were 0.14 and 0.46 µ M, respectively. Absorbances of glucosewere linear within the concentration range 2.5–54.2 µ M and the method showed high linearity (r = 0 . 9998) over arelatively broad concentration range of analyte. This automated microplate method was validated through linearity,additivity, precision (RSD%, 2.33–6.65), and recovery (101%–103%), revealing that the method is reliable and robustfor determining reducing sugars. Total reducing sugar contents of synthetic sugar mixtures, fruit juices, milk, andsynthetic serum samples were successfully determined with the proposed method. The results were compared to thoseof the conventional alkaline Cu(II)-Nc spectrophotometric method. The proposed method offers many advantages whencompared to classical methods, such as (sample and reagent) volume reduction (20-fold), simplicity, multiple sampleanalysis (32 samples in 4 h), and environmental friendliness

🔖

Cite This Article

APAK, R., BAŞKAN, K. S., TÜTEM, E., BENER, M., ŞEN, F. B., AKYÜZ, E. (2022). A simple automated microplate metho d for determining reducing sugars in fo o d extracts and synthetic serum using cupric-neo cuproine as reductant. Turkish Journal of Chemistry, Cilt: 42 - Sayı: 3, 794–807. https://ajindex.com/articles/601791

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (30)

  1. Wang, Q.; Fang, Y. J. Chromatogr. B 2014, 812, 309-324
  2. Gropper, S. S.; Smith, J. L. Advanced Nutrition and Human Metabolism; Wadsworth Cengage Learning: Belmont, CA, USA, 2012
  3. Gandhi, Y. S.; Bankar, V. H.; Vishwakarma, R. P.; Satpute, S. R.; Upkare, M. M. Imperial Journal of Interdisciplinary Research (IJIR) 2017, 3, 602-606
  4. Cumings, J. H.; Stephen, A. M. Eur. J. Clin. Nutr. 2007, 61, 5-18
  5. Shao, Y.; Lin, A. H. M. Food Chem. 2018, 240, 898-903
  6. Gomis, D. B.; Tamayo, D. M.; Alonso, J. M. Anal. Chim. Acta 2001, 436, 173-180
  7. Neeley, W. E. Clin. Chem. 1972, 18, 509-515
  8. Chen, M.; Zhao, J.; Xia, L. Carbohyd. Polym. 2008, 71, 411-415
  9. Marquez, G.; An´o´n, M. C. J. Food Sci. 1986, 51, 157-160
  10. Pedreschi, F.; Moyano, P.; Kaack, K.; Granby, K. Food Res. Int. 2005, 38, 1-9
  11. Elmore, J. S.; Briddon, A.; Dodson, A. T.; Muttucumaru, N.; Halford, N. G.; Mottram, D. S. Food Chem. 2015, 182, 1-8
  12. Al-Zuhair, S. Bioresource Technol. 2008, 99, 4078-4085
  13. Araujo, A. N.; Lima, J. L.; Rangel, A. O.; Segundo, M. A. Talanta 2000, 52, 59-66
  14. Nelson, N. J. Biol. Chem. 1944, 153, 375-380
  15. Somogyi, M. J. Biol. Chem. 1952, 119, 741-747
  16. Park, J. T.; Johnson, M. J. J. Biol. Chem. 1949, 181, 149-151
  17. Negrulescu, A.; Patrulea, V.; Mincea, M. M.; Ionascu, C.; Vlad-Oros, B. A.; Ostafe, V. J. Braz. Chem. Soc. 2012, 23, 2176-2182
  18. Fox, J. D.; Robyt, J. F. Anal. Biochem. 1991, 195, 93-96
  19. McFeeters, R. Anal. Biochem. 1980, 103, 302-306
  20. Brown, M. E. Diabetes 1961, 10, 60-62
  21. Dygert, S.; Li, L. H.; Florida, D.; Thoma, J. A. Anal. Biochem. 1965, 13, 367-374
  22. McCleary, B.; McGeough, P. Appl. Biochem. Biotechnol. 2015, 177, 1152-1163
  23. McIntyre, A. P.; Mukerjea, R.; Robyt, J. F. Carbohyd. Res. 2013, 380, 118-123
  24. S¨ozgen Ba¸skan, K.; T¨utem, E.; Aky¨uz, E.; Ozen, S.; Apak, R.¨ Talanta 2016, 147, 162-168
  25. Hizukuri, S.; Takeda, Y.; Yasuda, M.; Suzuki, A. Carbohyd. Res. 1981, 94, 205-213
  26. Masuko, T.; Minami, A.; Iwasaki, N.; Majima, T.; Nishimura, S. I.; Lee, Y. C. Anal. Biochem. 2005, 339, 69-72
  27. Leyva, A.; Quintana, A.; S´anchez, M.; Rodr´ıguez, E. N.; Cremata, J.; S´anchez, J.C. Biologicals 2008, 36, 134-141
  28. Armenta, S.; Garrigues, S.; De la Guardia, M. TrAC-Trend. Anal. Chem. 2008, 27, 497-511
  29. Farr´e, M.; P´erez, S.; Goncalves, C.; Alpendurada, M. F.; Barcel´o, D. TrAC-Trend. Anal. Chem. 2010, 29, 1347- 1362
  30. Galuszka, A.; Migaszewski, Z. M.; Konieczka, P., Namiesnik, J. TrAC-Trend.