Abstract
Carotenoids, precursors of vitamin A, are natural pigments synthesized by plants and some microorganisms. Humans and animals are not able to synthesize and need to acquire them by alimentation. Beyond the health benefits promoted by vitamin A, these compounds have antioxidant capacity which gives protection for cardiovascular and degenerative diseases. The presence of conjugated double bonds in carotenoid structure contributes for their pigmentation, absorption of ultraviolet/visible radiation, and antioxidant activity but also is the main reason of their chemical instability. Some factors such as heat, light, acids, organic solvent reflux, crystal melting, and iodine treatment can promote carotenoid cis–trans isomerization and oxidation. In the carotenoid qualitative and quantitative analysis, steps of extraction and storage are important to prevent degradation and total recovery. The extraction is generally realized using organic solvents in addiction or not a saponification step. The high-performance liquid chromatography is the most widely used technique, but others may be employed. The industrial production of carotenoids can be made by simple extraction or microbial process.
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Abbreviations
- BHT:
-
2,6-bis(1,1-dimethylethyl)-4-methylphenol
- CEC:
-
Capillary electrochromatography
- DAD:
-
Diode array detector
- DXP:
-
1-Deoxy-d-xylulose-5-phosphate
- GC:
-
Gas chromatography
- HPLC:
-
High-performance liquid chromatography
- IPP:
-
Isopentenyl diphosphate
- MS:
-
Mass spectrometry
- MVA:
-
Mevalonic acid
- NIRS:
-
Near-infrared reflectance spectroscopy
- NMR:
-
Nuclear magnetic resonance
- OCC:
-
Open column chromatography
- TDN:
-
1,1,6-Trimethyl-1,2-dihydronaphthalene
- THF:
-
Tetrahydrofuran
- UHPLC:
-
Ultrahigh-performance liquid chromatography
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Ribeiro, B.D., Grando de Oliveira, R. (2013). Carotenoids as Colorants. In: Ramawat, K., MĂ©rillon, JM. (eds) Natural Products. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-22144-6_172
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DOI: https://doi.org/10.1007/978-3-642-22144-6_172
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