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Methods of Analysis (Extraction, Separation, Identification and Quantification) of Carotenoids from Natural Products
Monica Butnariu*Banat’s University of Agricultural Sciences and Veterinary Medicine “Regele Mihai I al Romanei” Timisoara, Romania.
- *Corresponding Author:
- Butnariu M
Banat’s University of Agricultural Sciences and
Veterinary Medicine King Michael I of Romania from Timisoara
300645, Calea Aradului 119, Timis, Romania
Tel: +40-0-256-277
E-mail: monicabutnariu@yahoo.com
Received Date: May 04, 2016; Accepted Date: June 15, 2016; Published Date: June 21, 2016
Citation: Butnariu M (2016) Methods of Analysis (Extraction, Separation, Identification and Quantification) of Carotenoids from Natural Products. J Ecosys Ecograph 6: 193. doi:10.4172/2157-7625.1000193
Copyright: © 2016 Butnariu M. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Developing techniques for isolation and identification of biocompounds, from natural products, resulted in a rapid enrichment of carotenoid pigments number. For their isolation from biometabolites mixtures, the physical and chemical properties are taken into account. Carotenoids are sensitive to light, heat, oxygen, acids and alkaline bases. The exposure to light (direct sunlight/ UltraViolet), causes cis–trans photoisomerization, which may lead to their photodestruction. Biological materials containing carotenoids and their solutions must be protected from the action of light. Many carotenoids are thermolabile (xanthophylls); their heating being indicated only when it is absolutely necessary. The separation of carotenoids is done at room temperature or up to –20°C, in the dark. In the case of hot saponification they should be protected by a low–boiling solvent (30–60°C). Carotenoids may be oxidized in the presence of oxygen or peroxides, because of their sensitivity to oxygen in the adsorbed state (in thin layer or column chromatograms). It is necessary to operate in inert conditions (under nitrogen or vacuum). The oxidation during the extraction and saponification can be minimized if it is carried out in a nitrogen atmosphere. The exposure of carotenoids to acids, leads to changes such as: the oxidative decomposition, cis–trans isomerization and isomerization of 5,6–epoxides and 5,8–epoxides. The inconveniences are minimized by neutralization (calcium carbonate, pyridine, dimetilalanine). It works with purified solvents, freshly distilled, chlorinated derivatives (dichloromethane or solvents containing hydrochloric acid). The storage of carotenoids should be done in the dark, under an atmosphere of nitrogen or in vacuum, at a temperature of –20°C. The best preservation method is in the crystalline state. The current research techniques are using spectral methods, which provide accurate information on the structure and properties of organic biosubstances. Compared to chemical methods of identification, spectral methods have the advantage that it provides data faster, are accurate, require small amounts of material and enable continuous analysis at different stages of processing of the compound extracted without changing the composition of the biosubstance investigated, which enables its recovery. This chapter presents the main methods of extraction, separation and identification of organic compounds with direct applications on carotenoids.
