Food processing heating ascorbic acid

Ascorbic acid is photosensitive and unstable in aqueous solution at room temperature. During storage of foods, vitamin C is inactivated by oxygen. This process is accelerated by heat and the presence of catalysts. Ascorbic acid concentration in human organs is highest in adrenal and pituitary glands, eye lens, liver, spleen, and brain. Potatoes, citrus fruits, blade currants, sea buckthorns, acerola, rose hips, and red paprika peppers are among the most valuable vitamin C sources [1,2]. 

Another important food processing technology is pasteurisation. It consists of rapid heating to temperatures between 60 and 65°C in order to destroy microorganisms. Oxidoreductases are inactivated at the same time. As the heating is short, the destruction of antioxidants is only moderate. Losses of ascorbic acid are a good indicator of the destructive changes. Losses of ascorbic acid and carotenes are minimised by deaeration. 

Evaporation is the oldest process for the concentration of liquid foods. Temperatures are higher compared to those of the more modern membrane filtration or freeze concentration processes. Tocopherols, carotenes, ascorbic acid, flavonoids and other phenolic antioxidants are partially destroyed by heating. Therefore, it is necessary to minimise the time needed for evaporation, and heating to the evaporation temperature should be carried out very rapidly. The temperature may be decreased if the pressure is reduced. The process is then more expensive, but losses of antioxidants become substantially lower. 

To predict nutrient deterioration, knowledge of the reaction rate as a function of temperature of storage or processing is needed. The kinetics of ascorbic acid destruction have been examined most extensively in model systems, with particular attention being given to intermediate moisture foods (17, 71,78,79). Most of the data available for vitamin C losses in actual food systems are insuflBcient to calculate the kinetic parameters needed to predict losses during heat treatment or storage. 

Effect of Heat Processing on Bioavailability of Added Iron. Several studies in Table III measured directly the effect of heat processing on added iron. These studies compared processed foods to a control group of identical unprocessed food. Studies in Table 111 utilizing unprocessed controls include 15, 19, and 23. Other studies did not employ an unprocessed control, but used a reference dose to enable comparisons from study to study. Reference doses of ferrous sulfate (most animal assays) or ferrous ascorbate (most human tests) were frequently used. Preparation of ferrous ascorbate, usually a 2 1 molar ascorbic acid iron solution, has been detailed by Layrisse et al. (25). These controls enabled measurement of variation in iron absorption from subject to subject, important in view of greater absorption of an iron deficient versus an iron replete subject. When a reference dose was fed as a radiolabeled salt (55Fe), and on alternate times the test diet was fed with a different radiolabel (59Fe), errors due to variation in subject absorption were eliminated, as each subject served as its own control. The different availabilities of various iron sources from baked enriched rolls were established in this manner (17). 

A few trends are evident from the heat-processing data in Table III. Processing increased bioavailability of added iron when the process involved heating a predominantly aqueous food (i.e., wet-heat processing), as well as when ascorbic acid was added before heating. A greater bioavailability resulted after the processing of canned liquid milk-based infant formula (13),... 

In heat treated or stored food products several amino acids are not fully available because of derivatization or crosslinking reactions. Since 30 years furosine is known as a useful indicator of early Maillard reaction which is applied in food science, nutrition and medical biochemistry. Recently more sensitive analytical methods for furosine determination are available which have again increased the attractivity of this important indicator. Lately, N -carboxymethyllysine (CML) became available as another marker of special interest, because CML is a more useful indicator of the advanced heat damage by Maillard reaction than furosine. In addition, CML has the advantage to indicate reactions of lysine with ascorbic acid or ketoses such as fructose. Indicators for protein oxidation of sulfur amino acids are methionine sulfoxide and cysteic acid. An established marker for cross-linking reactions is lysinoalanine, which also indicates protein damages due to processing under alkaline conditions. Other markers formed as a consequence of alkaline treatment are D-amino acids. 

Ascorbate is found in numerous plant foods including green vegetables, citrus fmits, tomatoes, berries, and potatoes. Ascorbate can be lost in foods due to heat processing and prolonged storage. Transition metals and exposure to air will also cause the degradation of ascorbic acid. 

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