Method of processing edible oil

Abstract

This invention provides a method of using hydrophilic natural antioxidants to improve or preserve oxidative stability of edible oil. The method has been shown to be effective in reducing peroxide values of edible oil over a storage period. As such, it is suitable and safe for wide use in edible oil products.

Claims

1. A method for improving oxidative stability of edible oil, the method comprising: mixing at least one hydrophilic natural antioxidant in a high polarity oil at a temperature of 25-40 C. to obtain an antioxidant oil mixture containing the hydrophilic natural antioxidant 0.04-50 wt; mixing the antioxidant oil mixture in the edible oil so that the hydrophilic natural antioxidant has a concentration of 10-1000 ppm by weight, wherein the hydrophilic natural antioxidant is epigallocatechin gallate (EGCG) or carnosic acid.

2. The method of claim 1, further comprising pretreating the edible oil to remove polar oxidized components therein before mixing with the antioxidant oil, mixture, wherein the pretreating comprises: filtering the edible oil through silica gel chromatography; applying a nonpolar volatile solvent to elute the edible Rom the silica gel; and removing the nonpolar volatile solvent from the edible oil by evaporation.

3. The method of claim 2, wherein the edible oil is fish oil.

4. The method of claim 2, wherein the nonpolar volatile solvent is hexane.

5. The method of claim 2, wherein a volume ratio of silica gel to the edible oil is 1:1 to 1:20.

6. The method of claim 1, wherein the edible oil is soybean oil.

7. The method of claim 1, wherein the antioxidant oil mixture is a solution.

8. The method of claim 7, wherein the high polarity oil is propylene glycol caprylate.

9. The method of claim 1, wherein the antioxidant oil mixture is an emulsion.

10. The method of claim 1, wherein the antioxidant oil mixture contains the hydrophilic natural antioxidant 0.04-20 wt %.

11. The method of claim 1, wherein after mixing the antioxidant oil mixture in the edible oil, the hydrophilic natural antioxidant has a concentration of 100-200 ppm by weight.

12. A method for improving oxidative stability of edible oil, the method comprising: mixing a hydrophilic natural antioxidant in a high polarity oil at a temperature of 5-200 C. to obtain an antioxidant oil mixture containing the hydrophilic natural antioxidant 0.04-50 wt %; mixing the antioxidant oil mixture in the edible oil so that the hydrophilic natural antioxidant has a concentration of 10-1000 ppm by weight, wherein the hydrophilic natural antioxidant is carnosic acid.

13. The method of claim 1, wherein the high polarity oil is propylene glycol caprylate, medium chain monoglyceride, or medium chain triglyceride.

14. The method of claim 13, wherein the medium chain triglyceride is caprylic triglyceride.

15. The method of claim 1, wherein the mixing at least one hydrophilic natural antioxidant in the high polarity oil is performed under ultrasonication.

Description

DETAILED DESCRIPTION

(1) Natural antioxidants are preferable to synthetic antioxidants for use in food products as the former usually has a more desirable safety profile than the latter. The method of this invention utilizes a high polarity oil as an intermediate solvent to distribute a otherwise hydrophilic natural antioxidant into hydrophobic oil such as fish oil and soybean oil. Further, the method can enhance the distribution of the natural antioxidant at an oil/air interface, an area where the natural antioxidant can be more effective preventing lipid oxidation.

(2) The specific examples below are to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever. Without further elaboration, it is believed that one skilled in the art can, based on the description herein, utilize the present invention to its fullest extent. All publications cited herein are incorporated by reference in their entirety.

EXAMPLE 1: Preserving Oxidative Stability of Fish Oil with EGCG

(3) 1.2 g EGCG was dissolved in 8 g of propylene glycol caprylate by ultrasonication to achieve a clear and transparent solution. The dissolution was performed under a temperature between 25 C. and 40 C. and the temperature could be affected by the ultrasonication. The antioxidant oil solution thus obtained had an EGCG concentration of 13 wt %

(4) Next, a silicon gel column was packed using wet packing method with hexane for removing polar oxidized components from fish oil. 90 ml of fish oil (Menhaden oil) was gradually added into the silicon gel column. The volume ratio of silica gel to fish oil is 1:1. A vacuum pump filtration method was applied as follows. The silicon gel column was washed by 180 ml of hexane, which was later evaporated under vacuum. After vacuum evaporation of the hexane, 70 ml of refined fish oil was obtained.

(5) The EGCG-containing antioxidant oil solution was mixed vigorously with the refined fish oil in a ratio of 1:749 with the assistance of vortex until the fish oil mixture became clear and transparent. The fish oil mixture thus obtained had an EGCG concentration of 173 ppm.

(6) The peroxide value of the fish oil mixture was measured after it was stored at 60 C. in dark for three days. For the peroxide value testing, 2.000.02 g of the fish oil mixture was collected into a 100 ml glass stoppered Erlenmeyer flask as a testing sample. Next, 12 ml of an acetic acid/chloroform solution (v/v, 3:2) was added to the flask followed by swirling the flask until the sample was completely dissolved. 0.2 ml of saturated potassium iodide solution was added into the flask, which was then swirled for exactly one minute before adding 30 ml of distilled water into the flask and shaking the flask vigorously to liberate the iodine from the chloroform layer. Finally, 0.1N sodium thiosulfate was used to titrate oxidized iodine and, with 1 ml of starch solution as indicator, titration was performed until the blue gray color disappeared in the upper aqueous layer.

(7) The results show that the peroxide value of the fish oil mixture having an EGCG concentration of 173 ppm was reduced by 15.2% as compared with a control. Conventionally, the highest amount of BHA in fish oil is 0.2 g/kg (i.e. 200 ppm). A previous study showed that, under the same storage condition, the peroxide value value of a fish oil sample containing 200 ppm BHA was reduced only by 7.8% as compared with a control. Thus, the method of this invention unexpectedly exhibits a better effect in preserving oxidative stability of fish oil.

EXAMPLE 2: Preserving Oxidative Stability of Fish Oil with Carnosic Acid

(8) 1.2 g carnosic acid was dissolved in 8 g of propylene glycol caprylate by ultrasonication to achieve a clear and transparent solution. The dissolution was performed under a temperature between 25 C. and 40 C. and the temperature could be affected by the ultrasonication. The antioxidant oil solution thus obtained had a carnosic acid concentration of 13 wt %

(9) Fish oil was refined through silicon gel chromatography according to the procedure described in Example 1.

(10) The carnosic acid-containing antioxidant oil solution was mixed vigorously with the refined fish oil in a ratio of 1:749 with the assistance of vortex until the fish oil mixture became clear and transparent. The fish oil mixture thus obtained had a carnosic acid concentration of 173 ppm.

(11) The fish oil mixture was stored at 60 C. in dark for three day and the peroxide value was measured according to the procedure described in Example 1. The results show that the peroxide value of the fish oil mixture having a carnosic acid concentration of 173 ppm was reduced by 41.9% as compared with a control. Thus, the method of this invention unexpectedly exhibits a much better effect in preserving oxidative stability fish oil.

EXAMPLE 3: Preserving Oxidative Stability of Soybean Oil with EGCG

(12) 0.2 g EGCG was dissolved in 1.8 g of propylene glycol caprylate by ultrasonication to achieve a clear and transparent solution. The dissolution was performed under a temperature between 25 C. and 40 C. and the temperature could be affected by the ultrasonication. The antioxidant oil solution thus obtained had an EGCG concentration of 10 wt %

(13) The EGCG-containing antioxidant oil solution was mixed vigorously with the soybean oil in a ratio of 1:499 with the assistance of vortex until the soybean oil mixture became clear and transparent. The soybean oil mixture thus obtained had an EGCG concentration of 200 ppm.

(14) The soybean oil mixture was stored at 30 C. in dark for 7 days and the peroxide value was measured according to the procedure described in Example 1. The results indicate no quantitative peroxide value difference among the soybean oil mixture, a control, and a soybean oil sample containing 200 ppm BHA. The study shows that soybean oil is quite stable when stored at 30 C. for 7 days.

EXAMPLE 4: Preserving Oxidative Stability of Soybean Oil with EGCG

(15) 0.2 g EGCG was dissolved in 1.8 g of propylene glycol caprylate by ultrasonication to achieve a clear and transparent solution. The dissolution was performed under a temperature between 25 C. and 40 C. and the temperature could be affected by the ultrasonication. The antioxidant oil solution thus obtained had an EGCG concentration of 10 wt %

(16) The EGCG-containing antioxidant oil solution was mixed vigorously with the soybean oil in a ratio of 1:665.7 with the assistance of vortex until the soybean oil mixture became clear and transparent. The soybean oil mixture thus obtained had an EGCG concentration of 150 ppm.

(17) The soybean oil mixture was stored at 30 C. in dark for 7 days and the peroxide value was measured according to the procedure described in Example 1. The results indicate no quantitative peroxide value difference among the soybean oil mixture, a control, and a soybean oil sample containing 150 ppm BHA. The study shows that soybean oil is quite stable when stored at 30 C. for 7 days.

EXAMPLE 5: Preserving Oxidative Stability of Soybean Oil with EGCG

(18) 0.2 g EGCG was dissolved in 1.8 g of propylene glycol caprylate by ultrasonication to achieve a clear and transparent solution. The dissolution was performed under a temperature between 25 C. and 40 C. and the temperature could be affected by the ultrasonication. The antioxidant oil solution thus obtained had an EGCG concentration of 10 wt %

(19) The EGCG-containing antioxidant oil solution was mixed vigorously with the soybean oil in a ratio of 1:999 with the assistance of vortex until the soybean oil mixture became clear and transparent. The soybean oil mixture thus obtained had an EGCG concentration of 100 ppm.

(20) The soybean oil mixture was stored at 30 C. in dark for 7 days and the peroxide value was measured according to the procedure described in Example 1. The results indicate no quantitative peroxide value difference among the soybean oil mixture, a control, and a soybean oil sample containing 100 ppm BHA. The study shows that soybean oil is quite stable when stored at 30 C. for 7 days.

EXAMPLE 6: Preserving Oxidative Stability of Soybean Oil with EGCG

(21) 0.2 g EGCG was dissolved in 1.8 g of propylene glycol caprylate by ultrasonication to achieve a clear and transparent solution. The dissolution was performed under a temperature between 25 C. and 40 C. and the temperature could be affected by the ultrasonication. The antioxidant oil solution thus obtained had an EGCG concentration of 10 wt %

(22) The EGCG-containing antioxidant oil solution was mixed vigorously with the soybean oil in a ratio of 1:665.7 with the assistance of vortex until the soybean oil mixture became clear and transparent. The soybean oil mixture thus obtained had an EGCG concentration of 150 ppm.

(23) The soybean oil mixture was stored at 40 C. in dark for 7 days and the peroxide value was measured according to the procedure described in Example 1. The results show that the peroxide value of the oil mixture having 150 ppm EGCG was reduced by 4.6% as compared with a control, while the peroxide value of a soybean oil sample containing 150 ppm BHA is almost the same as the control. Thus, the method of this invention exhibits a better effect in preserving oxidative stability of soybean oil.

EXAMPLE 7: Preserving Oxidative Stability of Soybean Oil with EGCG

(24) 0.2 g EGCG was dissolved in 1.8 g of propylene glycol caprylate by ultrasonication to achieve a clear and transparent solution. The dissolution was performed under a temperature between 25 C. and 40 C. and the temperature could be affected by the ultrasonication. The antioxidant oil solution thus obtained had an EGCG concentration of 10 wt %

(25) The EGCG-containing antioxidant oil solution was mixed vigorously with the soybean oil in a ratio of 1:665.7 with the assistance of vortex until the soybean oil mixture became clear and transparent. The soybean oil mixture thus obtained had an EGCG concentration of 150 ppm.

(26) The soybean oil mixture was stored at 60 C. in dark for 7 days and the peroxide value was measured according to the procedure described in Example 1. The results indicate no quantitative peroxide value difference between the EGCG-containing soybean oil mixture and a control.

EXAMPLE 8: Preserving Oxidative Stability of Soybean Oil with Carnosic Acid

(27) 0.2 g carnosic acid was dissolved in 1.8 g of propylene glycol caprylate by ultrasonication to achieve a clear and transparent solution. The dissolution was performed under a temperature between 25 C. and 40 C. and the temperature could be affected by the ultrasonication. The antioxidant oil solution thus obtained had a carnosic acid concentration of 10 wt %

(28) The carnosic acid-containing antioxidant oil solution was mixed vigorously with the soybean oil in a ratio of 1:665.7 with the assistance of vortex until the soybean oil mixture became clear and transparent. The soybean oil mixture thus obtained had a carnosic acid concentration of 150 ppm.

(29) The soybean oil mixture was stored at 60 C. in dark for 7 days and the peroxide value was measured according to the procedure described in Example 1. The results indicate no quantitative peroxide value difference between the carnosic acid-containing soybean oil mixture and a control.

Other Embodiments

(30) All of the features disclosed in this specification may be combined in any combination. Each feature disclosed in this specification may be replaced by an alternative feature serving the same, equivalent, or similar purpose. Thus, unless expressly stated otherwise, each feature disclosed is only an example of a generic series of equivalent or similar features.

(31) Further, from the above description, one skilled in the art can easily ascertain the essential characteristics of the present invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions. Thus, other embodiments are also within the claims.