Method for making a low-acrylamide content snack with desired organoleptical properties

Information

  • Patent Grant
  • 9215886
  • Patent Number
    9,215,886
  • Date Filed
    Friday, December 5, 2008
    16 years ago
  • Date Issued
    Tuesday, December 22, 2015
    9 years ago
Abstract
A method for making a food product with a low acrylamide content having organoleptical properties comparable to traditional food products. Potatoes containing a low reducing sugar concentration are used to make potato flakes. Dextrose is added to the low reducing sugar potato flakes to increase the total reducing sugar concentration.
Description
BACKGROUND OF THE INVENTION

1. Technical Field


The present invention relates to a method of producing a snack having a low level of acrylamide.


2. Description of Related Art


The chemical acrylamide has long been used in its polymer form in industrial applications for water treatment, enhanced oil recovery, papermaking, flocculants, thickeners, ore processing and permanent-press fabrics. Acrylamide precipitates as a white crystalline solid, is odorless, and is highly soluble in water (2155 g/L at 30° C.). Synonyms for acrylamide include 2-propenamide, ethylene carboxamide, acrylic acid amide, vinyl amide, and propenoic acid amide. Acrylamide has a molecular mass of 71.08, a melting point of 84.5° C., and a boiling point of 125° C. at 25 mmHg.


In recent times, a wide variety of foods have tested positive for the presence of acrylamide monomer. Acrylamide has especially been found primarily in carbohydrate food products that have been heated or processed at high temperatures. Examples of foods that have tested positive for acrylamide include coffee, cereals, cookies, potato chips, crackers, french-fried potatoes; breads and rolls, and fried breaded meats. In general, relatively low contents of acrylamide have been found in heated protein-rich foods, while relatively high contents of acrylamide have been found in carbohydrate-rich foods, compared to non-detectable levels in unhealed and boiled foods.


It is presently believed that acrylamide is formed from the presence of amino acids and reducing sugars. For example, it is believed that a reaction between free asparagine, an amino acid commonly found in raw vegetables, and free reducing sugars accounts for the majority of acrylamide found in fried food products. Asparagine accounts for approximately 40% of the total free amino acids found in raw potatoes, approximately 18% of the total free amino acids found in high protein rye, and approximately 14% of the total free amino acids found in wheat.


Acrylamide has not been determined to be detrimental to humans, but its presence in food products, especially at elevated levels, is undesirable. As noted previously, relatively higher concentrations, of acrylamide are found in food products that have been heated or thermally processed. Prior art methods of reducing the level of acrylamide adversely affect the quality and flavor of the finished product. Therefore, it would be desirable to develop a method of reducing the level of acrylamide in the end product of heated or thermally processed foods with minimal flavor impact.


SUMMARY OF THE INVENTION

The present invention is a method for making a thermally processed food product with a low acrylamide content having organoleptical properties comparable to traditional food products. According to one embodiment, dextrose is added to potato flakes with a low reducing sugar concentration to make a dough. The dough is then cooked according to prior aft methods to make a low moisture, ready to eat product with an acrylamide content lower than products made with prior art potato flakes.


The above, as well as additional features and advantages of the invention will become apparent in the following written detailed description.





BRIEF DESCRIPTION OF THE DRAWINGS

The novel features believed characteristic of the invention are set forth in the appended claims. The invention itself, however, as well as a preferred mode of use, further objectives and advantages thereof, will be best understood by reference to the following detailed description of illustrative embodiments when read in conjunction with the accompanying drawings, wherein:



FIG. 1 depicts a general flow chart of a method for making a low-acrylamide snack piece with desired organoleptical properties in accordance with one embodiment of the present invention;



FIG. 2 depicts a chart comparing the acrylamide reaction rates of fructose and dextrose.





DETAILED DESCRIPTION OF THE INVENTION

One embodiment of the present invention is directed towards a method for making a thermally processed food product with a reduced acrylamide content having organoleptical properties comparable to traditional food products. As used herein, a thermally processed food product is defined as a food product that has been thermally processed at a food product temperature of greater than about 120° C. to moisture content of less than about 5% by weight, more preferably less than about 3% by weight, and most preferably less than about 2% by weight. Because, reducing sugars drive both flavor and acrylamide, it can be difficult to lower the level of acrylamide while retaining desired organoleptical properties. The present invention achieves that balance by adding dextrose to potato flakes with a low reducing sugar concentration. As used herein, dextrose means the D-form of glucose and the terms are used interchangeably.


Referring to FIG. 1, the first step of one embodiment of the present invention is to provide potato flakes with a reducing sugar concentration of less than about 0.5% by weight 100. These potato flakes can be made from potatoes with a low reducing sugar concentration, such as chipping variety potatoes or potatoes harvested when the weather is relatively warm. Chipping variety potatoes are those potatoes normally used for frying, such as Saturna, Lady Rosetta, Lady Clair, Hermes, Maris Piper, Erntestolz, Agria, Atlantic, Monona, Norchip, Snowden, Kennebec, Oneida, and Tobique. Of course, such potatoes are provided for purposes of illustration and not limitation. Any potato that can be made into potato flakes having a reducing sugar concentration of less than about 0.5% by weight can be used including, but not limited to proprietary and genetically engineered potatoes. As used herein, “low reducing sugar potato flakes” are potato flakes that comprise a native total reducing sugar concentration of less than about 0.5% by weight. In one embodiment, low reducing sugar flakes comprise a native reducing sugar concentration of less than about 0.5% by weight. In one embodiment, potato flakes are treated with enzymes, fermentation, blanching, or other suitable method to achieve a total reducing sugar concentration of less than about 0.5% by weight. In one embodiment, potato flakes can be made from potatoes having relatively higher reducing sugar concentrations than chipping variety potatoes, including potatoes known to have a tendency to accumulate reducing sugars during low temperature storage such as Russet Burbank potatoes. Potato varieties can also be blended during the flake manufacturing process in accordance with the present invention. Potato flakes can be made from such low reducing sugar potatoes by methods known in the art as exemplified by methods disclosed in U.S. Pat. No. 6,197,358.


In one embodiment, dextrose is added to the low reducing sugar potato flakes 110 so that the enhanced total reducing sugar concentration is less than or about equal the total concentration of native reducing sugars in prior art potato flakes. Consequently, in one embodiment, dextrose is added to the low reducing sugar flakes to provide an enhanced total reducing sugar concentration of less than about 1.2% and more preferably less than or equal to about 0.7% by weight of the potato flakes. These “enhanced” potato flakes contain less than about 0.5% native reducing sugars and less than about 1.0% and preferably less than about 0.7% of dextrose by weight. Dextrose advantageously provides the necessary flavor drivers in the finished product.


As used herein, reducing sugars means all carbohydrate molecules containing a free aldehyde or keto group, and/or hemiacetal group, for example fructose, glucose, maltose, galactose, lactose and pentose sugars such as xylose, and other aldehyde containing compounds. Although reducing sugars are broadly defined, in one embodiment the reducing sugars comprise fructose and glucose because fructose and glucose are the predominant reducing sugars natively present in the potato raw material.


Referring back to FIG. 1, a dough is made by adding water and other minor ingredients as is well known in the art. The dough can then be thermally processed 130 for example by baking or frying, to make a final product with an acrylamide content lower than products made with prior art potato flakes having the same total reducing sugar concentration as the enhanced total reducing sugar concentration. In one embodiment, the dough is sheeted, cut, and thermally processed at a food temperature of at least about 120° C. to a moisture content of less than about 3%.


At higher temperatures, the acrylamide formation rate for fructose is faster than that of dextrose. For example, Table 1 below depicts known second order rate constants of glucose and fructose with asparagine:









TABLE 1







Second order rate constants (×10−3/min) for glucose and


fructose reacting with asparagine.













120° C.
140° C.
160° C.
180° C.
200° C.



(248° F.)
(284° F.)
(320° F.)
(356° F.)
(392° F.)
















Fructose
0.0819
0.369
1.45
5.04
15.8


Glucose/
0.131
0.308
0.668
1.35
2.58


Dextrose









A chart, based on the data provided in Table 1, depicting the comparative second order rate constants of fructose and dextrose is shown in FIG. 2. Curve 201 represents the second order rate constant of fructose as a function of temperature and curve 202 represents the second order rate constant of dextrose as a function of temperature. The rate constants are similar up to about 300° F. At about 320° F. the rate constant of fructose is slightly higher than that of dextrose, at about 350° F. the rate constant of fructose is approximately four times that of dextrose, and at about 390° F., the rate of fructose is approximately six times higher than the rate constant of dextrose.


Through adding dextrose to low reducing sugar flakes it was discovered that the native reducing sugars, including fructose, dextrose and others, found in potatoes have a faster acrylamide formation fate than dextrose alone. Thus, the flavor of a product produced from flakes having a low reducing sugar concentration can be enhanced by the addition of dextrose without suffering the acrylamide level from a product with the same total amount of reducing sugars where only native reducing sugars are present. Of the native reducing sugars present in potatoes, glucose and fructose predominate and are generally present in near equal amounts. Other reducing sugars, such as maltose, are generally present in very small amounts, comprising less than about 5% of the native reducing sugars. By increasing the ratio of dextrose to fructose in the potato flakes to increase the total reducing sugar concentration, the difference in the reaction rates of dextrose and fructose and dextrose and native reducing sugars can be exploited to yield a product with enhanced flavor and lower acrylamide content. In one embodiment, the amount of dextrose added to the low reducing sugar potato flakes increases the molar ratio of dextrose to fructose to at least about 2:1 and in one embodiment at least about 3:1.


In one embodiment, an effective amount of dextrose is added to the low reducing sugar potato flakes. As used herein, an “effective amount” means an amount of dextrose that achieves at least about 25% less acrylamide than products made with prior art flakes having only native reducing sugars at the same total reducing sugar concentration as the enhanced total reducing sugar concentration. In one embodiment, the amount of dextrose added constitutes at least half of the enhanced total reducing sugar concentration in the dough.


Example

Comparative tests were run between a control sample of prior art potato flakes and low reducing sugar flakes (purchased from Washington Potato, in Warden, Wash.) having a native total reducing sugar concentration of 0.2% by weight. Various levels of dextrose were added to the flakes and the total concentration of reducing sugars was recorded. The fabricated chips were fried and tested for acrylamide and moisture content. The results are shown in the Table 2 below.









TABLE 2







Comparative tests of prior art flakes and low reducing sugar


flakes with dextrose added











Acrylamide,

Total Reducing


Sample
ppb
Moisture, %
Sugar, %





Control
343
1.99
1.3


Potato flakes + 0.4%
216
1.83
0.6


dextrose


Potato flakes + 1.0%
294
1.86
1.2


dextrose


Potato flakes + 2.0%
516
1.67
2.2


dextrose









As can be seen, the selective use of dextrose as the primary reducing sugar in potato flakes reduces acrylamide with minimal flavor impact. Adding 0.4% dextrose to low reducing sugar flakes to obtain a total reducing sugar concentration of 0.6% provides a chip having 37% less acrylamide than the control even when fried to a lower moisture content than the control. The addition of 1.0% dextrose to reach a total reducing sugar concentration of that substantially similar to the native reducing sugar level of prior art potato flakes achieves 14% lower acrylamide content at a lower moisture content. In one embodiment, dextrose is added in an amount to obtain a total reducing sugar concentration of about 1.2% or less, which achieves a lower acrylamide level while providing fried potato chips having a flavor profile on parity with fried potato chips made from prior art flakes.


Dextrose advantageously provides many of the same benefits as the native reducing sugars without the higher kinetic acrylamide reaction rates. For example, the flavor drivers provided by native reducing sugars are due to Maillard reaction compounds, Strecker aldehydes, and pyrazines. When the inventive dough was tested for these flavor drivers, the levels of flavor drivers were comparable to fried potato chips made from prior art potato flakes. Interestingly, Maillard reaction compounds in the finished product made with the inventive dough increased with increasing levels of dextrose. Strecker aldehydes were similar to control at 1% dextrose and higher than control at 2% dextrose. Pyrazines in the finished product were similar to control at 2% dextrose.


Though the present invention has been described with reference to potato flakes, it is to be understood that the invention is also applicable to potato granules and corn masa as corn generally contains near equal amounts of fructose and glucose. The examples and explanations given are not meant to limit the present invention.


Having thus described several aspects of at least one embodiment of this invention, it is to be appreciated that various alterations, modifications, and improvements will readily occur to those skilled in the art. Such alterations, modifications, and improvements are intended to be part of this disclosure, and are intended to be within the spirit and scope of the invention. Accordingly, the foregoing description and drawings are by way of example only.

Claims
  • 1. A method for making a potato product, said method comprising the steps of: a) providing potato flakes having a reducing sugar concentration of less than about 0.5% by weight,b) adding an effective amount of dextrose to said potato flakes to make a dough, wherein said effective amount of dextrose raises the total reducing sugar concentration of said potato flakes to less than about 1.2%, and wherein the amount of dextrose added to the potato flakes increases a molar ratio of dextrose to fructose in said dough to at least about 2:1; andc) cooking the dough at a temperature of at least about 120° C. to a moisture content of less than about 3%, thereby producing a low moisture ready to eat product.
  • 2. The method of claim 1 wherein said effective amount of dextrose raises the total reducing sugar concentration of said potato flakes to less than about 0.7%.
  • 3. The method of claim 1 wherein said potato flakes are made from potatoes with a native reducing sugar concentration of about 0.2% by weight.
  • 4. The method of claim 1 wherein said potato flakes are made from potatoes or potato flakes treated with enzymes.
  • 5. The method of claim 1 wherein said potato flakes are made from potatoes or potato flakes treated with yeast.
  • 6. The method of claim 1 wherein said potato flakes are made from potatoes or potato flakes treated by fermentation.
  • 7. The method of claim 1 wherein said potato flakes are made from potatoes or potato flakes treated by blanching.
  • 8. The method of claim 1 wherein said dextrose added at step b) comprises at least 50% of an enhanced total reducing sugar content.
  • 9. The method of claim 1 wherein the ratio of dextrose to fructose in said dough is at least about 3:1.
  • 10. Potato flakes for making a thermally processed food product, said potato flakes comprising less than about 0.5% reducing sugars and less than about 1.0% of added dextrose by weight of said flakes, wherein the ratio of dextrose to fructose is at least about 2:1.
  • 11. The potato flakes of claim 10, wherein a total reducing sugar concentration of said potato flakes is less than about 0.7% by weight of said flakes.
  • 12. The potato flakes of claim 10 wherein said potato flakes are made from potatoes with a low reducing sugar concentration.
  • 13. The potato flakes of claim 10 wherein said potato flakes are made from potatoes or potato flakes treated with enzymes.
  • 14. The potato flakes of claim 10 wherein said potato flakes are made from potatoes or potato flakes treated with yeast.
  • 15. The potato flakes of claim 10 wherein said potato flakes are made from potatoes or potato flakes treated by fermentation.
  • 16. The potato flakes of claim 10 wherein said potato flakes are made from potatoes or potato flakes treated by blanching.
  • 17. The potato flakes of claim 10 wherein said dextrose comprises at least 50% of an enhanced total reducing sugar content.
  • 18. The potato flakes of claim 10 wherein the ratio of dextrose to fructose is at least about 3:1.
  • 19. The method of claim 1 wherein said potato flakes of step a) are made from potatoes comprising glucose and fructose in near equal amounts.
  • 20. The method of claim 1 wherein said potato product comprises less than 294 ppb of acrylamide.
US Referenced Citations (287)
Number Name Date Kind
1053 Hatfield Dec 1838 A
1782960 Erysin Nov 1930 A
2448152 Patton Aug 1948 A
2490431 Greene Dec 1949 A
2498024 Baxter Feb 1950 A
2584893 Lloyd Feb 1952 A
2611705 Hendel Sep 1952 A
2704257 deSellano Mar 1955 A
2744017 Baldwin May 1956 A
2759832 Cording, Jr. Aug 1956 A
2762709 Janis Sep 1956 A
2780552 Willard Feb 1957 A
2893878 Simon Jul 1959 A
2905559 Anderson Sep 1959 A
2910367 Melnick Oct 1959 A
2959487 Notter et al. Nov 1960 A
2987401 Johnston Jun 1961 A
3026885 Eytinge Mar 1962 A
3027258 Markakis Mar 1962 A
3038810 Akerboom Jun 1962 A
3044880 Bogyo Jul 1962 A
3085020 Backinger Apr 1963 A
3219458 Higby Nov 1965 A
3278311 Brown Oct 1966 A
3305366 Sutton Feb 1967 A
3359123 Katucki Dec 1967 A
3365301 Lipoma Jan 1968 A
3369908 Gonzalez Feb 1968 A
3370627 Willard Feb 1968 A
3404986 Wimmer Oct 1968 A
3436229 Simpson Apr 1969 A
3460162 Sijbring Aug 1969 A
3545979 Ghafoori Dec 1970 A
3578463 Smith May 1971 A
3608728 Trimble Sep 1971 A
3620925 Mochizuki Nov 1971 A
3627535 Davidson Dec 1971 A
3634095 Willard Jan 1972 A
3652402 Chibata Mar 1972 A
3687679 Sijbring Aug 1972 A
3690895 Amadon Sep 1972 A
3725087 Miller Apr 1973 A
3773624 Wagner Nov 1973 A
3782973 Pittet Jan 1974 A
3812775 Sijbring May 1974 A
3849582 Blagdon Nov 1974 A
3851572 Lazzarini Dec 1974 A
3870809 Green Mar 1975 A
3914436 Nakadai Oct 1975 A
3917866 Purves Nov 1975 A
3925568 Rao Dec 1975 A
3987210 Cremer Oct 1976 A
3997684 Willard Dec 1976 A
3998975 Liepa Dec 1976 A
4005225 Craig Jan 1977 A
4073952 Standing Feb 1978 A
4084008 Yueh Apr 1978 A
4122198 Wisdom Oct 1978 A
4124727 Rockland Nov 1978 A
4136208 Light Jan 1979 A
4140801 Hilton et al. Feb 1979 A
4167137 van Remmen Sep 1979 A
4192773 Yoshikawa Mar 1980 A
4199612 Fragas Apr 1980 A
4210594 Logan Jul 1980 A
4251895 Caridis Feb 1981 A
4272554 Schroeder Jun 1981 A
4277510 Wicklund Jul 1981 A
4293582 Hamann et al. Oct 1981 A
4312892 Rubio Jan 1982 A
4317742 Yamaji Mar 1982 A
4348417 Greup et al. Sep 1982 A
4366749 Caridis Jan 1983 A
4394398 Wilson Jul 1983 A
4418088 Cantenot Nov 1983 A
4461832 Tschang Jul 1984 A
4537786 Bernard Aug 1985 A
4555409 Hart Nov 1985 A
4582927 Fulcher Apr 1986 A
4594260 Vaqueiro Jun 1986 A
4595597 Lenchin Jun 1986 A
4645679 Lee Feb 1987 A
4673581 Fulcher Jun 1987 A
4706556 Wallace Nov 1987 A
4721625 Lee Jan 1988 A
4749579 Haydock Jun 1988 A
4751093 Hong Jun 1988 A
4756916 Dreher Jul 1988 A
4806377 Ellis Feb 1989 A
4844930 Mottur Jul 1989 A
4844931 Webb Jul 1989 A
4863750 Pawlak Sep 1989 A
4884780 Ohashi Dec 1989 A
4889733 Willard Dec 1989 A
4900576 Bonnett Feb 1990 A
4917909 Prosise Apr 1990 A
4931296 Shanbhag Jun 1990 A
4933199 Neel Jun 1990 A
4937085 Cherry Jun 1990 A
4963373 Fan Oct 1990 A
4966782 Heidolph Oct 1990 A
4971813 Strobel Nov 1990 A
4978684 Cerami Dec 1990 A
4985269 Irvin Jan 1991 A
5002784 Pare Mar 1991 A
5009903 deFigueiredo Apr 1991 A
5035904 Huang Jul 1991 A
5045335 DeRooij Sep 1991 A
5071661 Stubbs Dec 1991 A
5087467 Schwank Feb 1992 A
5126153 Beck Jun 1992 A
5134263 Smith Jul 1992 A
5137740 Benson Aug 1992 A
5167975 Tsurumaki Dec 1992 A
5171600 Young Dec 1992 A
5176933 Fulcher Jan 1993 A
5196225 Lush Mar 1993 A
5232721 Polansky Aug 1993 A
5279840 Baisier Jan 1994 A
5292542 Beck Mar 1994 A
5298274 Khalsa Mar 1994 A
5356646 Simic-Glavaski Oct 1994 A
5362511 Villagran Nov 1994 A
5368879 White Nov 1994 A
5370898 Zussman Dec 1994 A
5389389 Beck Feb 1995 A
5391384 Mazza Feb 1995 A
5391385 Seybold Feb 1995 A
5393543 Laufer Feb 1995 A
5394790 Smith Mar 1995 A
5441758 Lewis Aug 1995 A
5447742 Malvido Sep 1995 A
5458903 Colson Oct 1995 A
5464642 Villagran Nov 1995 A
5464643 Lodge Nov 1995 A
5505978 Roy Apr 1996 A
5514387 Zimmerman May 1996 A
5534280 Welch Jul 1996 A
5554405 Fazzolare Sep 1996 A
5558886 Martinez-Bustos Sep 1996 A
5580598 Benson Dec 1996 A
5589213 Desai Dec 1996 A
5603972 McFarland Feb 1997 A
5603973 Benson Feb 1997 A
5620727 Gerrish Apr 1997 A
5676042 Sakuma Oct 1997 A
5690982 Fazzolare Nov 1997 A
5695804 Hnat Dec 1997 A
5707671 Beck Jan 1998 A
5747084 Cochran May 1998 A
5776531 Aasman Jul 1998 A
5792499 Atwell Aug 1998 A
5846589 Baker Dec 1998 A
5858429 Wallace Jan 1999 A
5858431 Wiedersatz Jan 1999 A
5887073 Fazzari Mar 1999 A
5919691 Schulein Jul 1999 A
5945146 Twinam Aug 1999 A
5947010 Barry Sep 1999 A
5972367 Inoue Oct 1999 A
5972397 Durance Oct 1999 A
6001409 Gimmler Dec 1999 A
6016096 Barnes Jan 2000 A
6025011 Wilkinson Feb 2000 A
6033707 Lanner Mar 2000 A
6039978 Bangs Mar 2000 A
6066353 Villagran May 2000 A
6068872 Hashiguchi May 2000 A
6068873 Delrue May 2000 A
RE36785 Colson Jul 2000 E
6139884 Shifferaw Oct 2000 A
6159530 Christiansen Dec 2000 A
6207204 Christiansen Mar 2001 B1
6210720 Leusner Apr 2001 B1
6227421 Richard May 2001 B1
6287672 Fields Sep 2001 B1
6290999 Gerrish Sep 2001 B1
6299914 Christiansen Oct 2001 B1
6335048 Swarvar Jan 2002 B1
6358544 Henry, Jr. Mar 2002 B1
6383533 Soeda May 2002 B1
6419965 Douaire Jul 2002 B1
6436458 Kuechle Aug 2002 B2
6521871 Shelton Feb 2003 B1
6528768 Simic-Glavaski Mar 2003 B1
6531174 Barrett Mar 2003 B2
6558730 Gisaw May 2003 B1
6599547 Villagran Jul 2003 B1
6602533 Smith Aug 2003 B1
6607777 Walsh Aug 2003 B1
6638554 Rubio Oct 2003 B1
6638558 Brubacher Oct 2003 B2
6716462 Prosise Apr 2004 B2
6770469 Yamaguchi Aug 2004 B2
6778887 Britton Aug 2004 B2
6828527 Simic-Glavaski Dec 2004 B2
6872417 Freudenrich Mar 2005 B1
6896528 Kubota May 2005 B2
6929812 Van Der Doe Aug 2005 B2
6989167 Howie Jan 2006 B2
7037540 Elder May 2006 B2
7122719 Hakimi Oct 2006 B2
7169417 Lang Jan 2007 B2
7189422 Howie Mar 2007 B2
7190813 Daley Mar 2007 B2
7220440 Dria May 2007 B2
7267834 Elder Sep 2007 B2
7291380 Nyholm Nov 2007 B2
7393550 Barry Jul 2008 B2
7514113 Zyzak Apr 2009 B2
7524519 Zyzak Apr 2009 B2
7527815 Teras May 2009 B2
7534934 Rommens May 2009 B2
7763306 Barry et al. Jul 2010 B2
20020018838 Zimmerman Feb 2002 A1
20020025367 Koehler Feb 2002 A1
20020129713 Caridis Sep 2002 A1
20030049359 Kulkarni Mar 2003 A1
20030183092 Barber Oct 2003 A1
20030198725 Cardenas Oct 2003 A1
20030219518 Li Nov 2003 A1
20040047973 Bourhis Mar 2004 A1
20040058046 Zyzak et al. Mar 2004 A1
20040086597 Awad May 2004 A1
20040101607 Zyzak May 2004 A1
20040105929 Tomoda Jun 2004 A1
20040109926 Tomoda Jun 2004 A1
20040115321 Tricoit Jun 2004 A1
20040126469 Tomoda Jul 2004 A1
20040131737 Tomoda Jul 2004 A1
20040180125 Plank Sep 2004 A1
20040180129 Plank Sep 2004 A1
20040197012 Bourg Oct 2004 A1
20040224066 Lindsay Nov 2004 A1
20050064084 Elder et al. Mar 2005 A1
20050068535 Bond Mar 2005 A1
20050074538 Elder Apr 2005 A1
20050079254 Corrigan Apr 2005 A1
20050118322 Elder Jun 2005 A1
20050152811 Taylor Jul 2005 A1
20050196504 Finley Sep 2005 A1
20050214411 Lindsay et al. Sep 2005 A1
20060019007 Baas Jan 2006 A1
20060029992 Grune Feb 2006 A1
20060088633 Barber Apr 2006 A1
20060110503 Bates May 2006 A1
20060127534 Elder Jun 2006 A1
20060193964 Eckhoff Aug 2006 A1
20060210693 Oftring Sep 2006 A1
20060216376 Milici Sep 2006 A1
20060216388 Christensen Sep 2006 A1
20070042080 Plomp Feb 2007 A1
20070087101 Gusek Apr 2007 A1
20070141225 Elder Jun 2007 A1
20070141226 Elder Jun 2007 A1
20070141227 Boudreaux Jun 2007 A1
20070148318 Rubio Jun 2007 A1
20070166439 Soe Jul 2007 A1
20070178219 Boudreaux Aug 2007 A1
20070184175 Rubio Aug 2007 A1
20070196556 Van Der Meer Aug 2007 A1
20070281062 Bourg Dec 2007 A1
20070292589 Elder Dec 2007 A1
20080003340 Karwowski Jan 2008 A1
20080008780 Streekstra Jan 2008 A1
20080101657 Durkin May 2008 A1
20080138480 Bows Jun 2008 A1
20080144880 DeLuca Jun 2008 A1
20080166450 Corrigan Jul 2008 A1
20080166452 Corrigan Jul 2008 A1
20080253648 Mulder Oct 2008 A1
20080268111 Grune Oct 2008 A1
20080279994 Cantley Nov 2008 A1
20080299273 Bhaskar Dec 2008 A1
20090047725 Elder Feb 2009 A1
20090074915 Hendriksen Mar 2009 A1
20090098265 Kock Apr 2009 A1
20090191310 Zyzak Jul 2009 A1
20100040729 Sahagian Feb 2010 A1
20100040750 Assaad Feb 2010 A1
20100051419 Desai Mar 2010 A1
20100055259 Bourg Mar 2010 A1
20100062123 Anderson Mar 2010 A1
20100080868 Crosby et al. Apr 2010 A1
20100112177 Bourg, Jr. May 2010 A1
20100255167 Bourg Oct 2010 A1
20110050880 Bourg, Jr. Mar 2011 A1
Foreign Referenced Citations (50)
Number Date Country
4032002 Jun 2003 CL
2743230 Apr 1979 DE
113940 Jul 1984 EP
1419702 May 2004 EP
1419703 May 2004 EP
2019044 Feb 1990 ES
874453 Aug 1942 FR
156905 Jan 1921 GB
1132296 Oct 1968 GB
1519049 Jul 1978 GB
335214 Sep 1980 GB
68006927 Sep 1965 JP
70009815 Oct 1966 JP
57100179 Dec 1980 JP
62048351 Mar 1987 JP
4104753 Apr 1992 JP
6030782 Feb 1994 JP
06169713 Jun 1994 JP
05123126 May 1998 JP
10136883 May 1998 JP
11056280 Mar 1999 JP
11178536 Jul 1999 JP
2004180563 Jul 2004 JP
2004-313183 Nov 2004 JP
2004313183 Nov 2004 JP
2005278448 Oct 2005 JP
910006619 Aug 1991 KR
2048512 Nov 1995 RU
2078797 May 1997 RU
2140927 Nov 1999 RU
2216574 Nov 2003 RU
1822863 Jun 1993 SU
9601572 Jan 1996 WO
0004784 Feb 2000 WO
0191581 Dec 2001 WO
2004004484 Jan 2004 WO
2004026043 Apr 2004 WO
2004028276 Apr 2004 WO
2004028277 Apr 2004 WO
2004028278 Apr 2004 WO
2004032647 Apr 2004 WO
2004032648 Apr 2004 WO
2004039174 May 2004 WO
2004040999 May 2004 WO
2004047559 Jun 2004 WO
2004060078 Jul 2004 WO
2004080205 Sep 2004 WO
2006128843 Dec 2006 WO
2007106996 Sep 2007 WO
2008061982 May 2008 WO
Non-Patent Literature Citations (128)
Entry
Coffin: Effect of Low Temperature Storage on Sugar Concentrations and Chip Color of Certain Processing Potato Cultivars and Selections. Journal of Food Science, 52: 639-645; 1987.
Medical Dictionary: definition of dextrose; published Sep. 7, 2003; http://web.archive.org/web/20030907233102/http://www.medterms.com/script/main/art.asp?ArticleKey=7040.
Dobarganes, Carmen, et al., “Interactions between fat and food during deep-frying,” Eur. J. Lipid Sci. Tech. 2000, vol. 102, pp. 521-528.
Erickson, Michael D., ed., Book entitled “Deep Frying—Chemistry, Nutrition and Practical Applications,” 2d edition, pp. 262, 263, 274, 275.
Farid, M.M., et al., “The analysis of heat and mass transfer during frying of food using a moving boundary solution procedure,” Heat and Mass Transfer, vol. 34, 1998, pp. 69-77.
Fleck, Fiona, “Experts launch action on acrylamide in staple foods,” British Medical Journal, Jul. 20, 2002, p. 120.
Jackson, Lauren, “Formation of acrylamide in food,” US FDA Centre for Food Safety and Applied Nutrition, National Centre for Food Safety and Technology, Summit—Argo, IL, Dec. 4-5, 2002 presentation, 32 pages.
Lotfi, Ehsan, et al. “A new approach for automatic quality control of fried potatoes using machine learning,” Islamic Azad University, Mashad Branch, Ferdowsi University of Mashad, Khorasan Research Center for Technology Development, Mar. 11, 2009, 4 pages.
Pedreschi, Franco, et al. “Acrylamide content and color development in fried potato strips,” ScienceDirect Journal of Food Engineering 39 (2006) pp. 40-46.
Research Disclosure 15172, New process for the manufacture of potato-chips from different types of potatoes (not selected), Nov. 1976, 1 page.
Talburt & Smith (eds.), Potato Processing 4th Ed. 1987, “Improving the Color of Potato Chips,” pp. 406-413.
Tareke, E., et al., “Acrylamide: A Cooking Carcinogen?” Chem. Res. Toxicol. 2000, vol. 13, pp. 517-522, Published on Web May 27, 2000 (6 pages).
NFRI Report, published Jul. 1, 2004, Report on the symposium named “Chemistry and Safety of Acrylamide in Food” held by the Agricultural and Food Chemistry Division of the American Chemical Society held on Mar. 28-31, 2004 in Anaheim, CA, USA, published by the National Food Research Institute (NFRI) of the National Agricultural and Food Research Organization of Japan (NARO), available at http://oasys2.confex.com/acs/227nm/techprogram/D941.HTM.
Summary Report of “2004 Acrylamide in Food Workshop: Update—Scientific Issues, Uncertainties, and Research Strategies,” held on Apr. 13-15, 2004 in Chicago, IL, USA, published on Aug. 6, 2004, by the National Food Research Institute (NFRI) of the National Agricultural and Food Research Organization of Japan (NARO), available at http://222.jifsan.umd.edu/docs/acry2004.
Decision of Rejection, Japanese Pat. App. No. 2007-544461 dated Mar. 16, 2010, translated into English (2 pages).
“Kagaku Dai-jiten (Encyclopedia of Chemistry),” edited by Ohki Michinori, et al., 1989, pp. 317, 96, and 1661 (6 pages).
“Shokuhin Tenkabutsu Binran (List of Food Additives),” 1964, p. 249 (2 pages).
Martinez-Bustos, F., “Effect of the components of maize on the quality of masa and tortillas during the traditional nixtamalisation process,” Journal of the Science of Food and Agriculture, vol. 81, pp. 1455-1462, Aug. 13, 2001, 8 pages.
Sefa-Dedeh, S., “Effect of nixtamalization on the chemical and functional properties of maize,” Food Chemistry, vol. 86, pp. 317-324, Aug. 14, 2003, 8 pages.
Note of the Meeting of Experts on Industrial Contaminants in Food (European Commission): Acrylamide Workshop, Oct. 20-21, 2003, Information on Ways to Lower the Levels of Acrylamide Formed in Food, 6 pages.
Robert, Fabien, et al.“Acrylamide Formation from Asparagine under Low-Moisture Maillard Reaction Conditions. 1. Physical and Chemical Aspects in Crystalline Model Systems,” J. Agric. Food Chem, 2004, 52, 6837-6842, 6 pages.
Afssa, French Food Safety Agency, “Acrylamide: Information Point,” Jul. 24, 2002 (11 pages).
Weisshaar, Rudiger, et al. “Formation of Acrylamide in Heated Potato Products—Model Experiments Pointing to Asparagine as Precursor” Pub. Oct. 3, 2002, Deutsche Lebensmittel-Rundschau 98 Jahrgang, Heft (4 pages).
Williams, J.S.E., “Influence of Variety and Processing Conditions on Acrylamide Levels in Fried Potato Crisps,” ScienceDirect Food Chemistry 90 (2005), pp. 875-881.
Wulfsberg, Gary, Inorganic Chemistry book, University Science Books, 2000,p. 289.
Yarnell, Amanda, “Acrylamide Mystery Solved,” Chemical & Engineering News, Oct. 4, 2002 found at http://pubs.acs.org/cen/today/oct4.html (3 pages).
Yaylayan, Varoujan A., et al., “Why Asparagine Needs Carbohydrates to Generate Acrylamide,” J. Agric. Food Chem. 2003, vol. 51, pp. 1753-1757.
Zhang, Yu, et al., “Study on Formation of Acrylamide in Asparagine-Sugar Microwave Heating Systems Using UPLC-MS/MS Analytical Method,” ScienceDirect, Food Chemistry 108 (2008), pp. 542-550.
Zyzak David V. et al., “Acrylamide Formation Mechanism in Heated Foods,” J. Agric. Food Chem. 2003, vol. 51, pp. 4782-4787.
Zyzak, David, et al. v. Elder, Vincent Allen, et al., Board of Patent Appeals and Interferences, Judgment-Arbitration-Bd.R. 126(f),Apr. 14, 2008, 2 pages.
Health Canada Food & Nutrition “Acrylamide and Food” Dec. 1, 2005 (3 pages).
Health Canada Food & Nutrition “Major pathway of formation of acrylamide in foods and possible approaches to mitigation” Mar. 11, 2005 (2 pages).
Health Canada OCAPI Involving You publication, “Acrylamide and Food,” vol. 2, No. 1, Autumn 2002, 2 pages.
Heldman, Dennis R., et al. “Principles of Food Processing” book, 1997, p. 193.
Hughes B.P. “The amino acid composition of potato protein and of cooked potato” British J. of Nutrition, vol. 12, Issue 02, May 1958, pp. 188-195.
Igoe, Robert, Dictionary of Food Ingredients, 4th ed., (Aspen Publishers 2001), pp. 24, 35, 43, 109, and 167.
Institute of Food Science & Technology (UK) “Acrylamide Information and News” found at http://www.ifst.org/acrylmd.htm Sep. 6, 2002, 5 pages.
Ishihara, Katsuyuki, et al. “Examination of Conditions inhibiting the Formation of Acrylamide in the Model System of Fried Potato” Biosci. Biotechnol. Biochem., 70(7), 2006, pp. 1616-1621.
Jacobs, Morris B., Ph.D. “The Chemistry and Technology of Food and Food Products” textbook, 1951, pp. 221-226.
Jespersen, Neil “Chemistry” from Barron's College Review Series on Science, 1997, p. 210.
Jung, M.Y. et al. “A Novel Technique for Limitation of Acrylamide Formation in Fried and Baked Corn Chips and in French Fries”, J. Food Science vol. 68, No. 4, 2003, pp. 1287-1290.
Kim, Kyu-Won, et al. “Asparaginase II of Saccharomyces cerevisiae” J. Biological Chem. 263 (24), Aug. 25, 1988, pp. 11948-11953.
Kim, Cheong Tae, et al. “Reducing Acrylamide in Fried Snack Products by Adding Amino Acids” J. Food Science vol. 70, No. 5, 2005, pp. C354-C358.
Kirk, Raymond E., et al. “Enciclopedia de Tecnologia Quimica” 1962, pp. 986-998.
Kita, Agnieszka, et al. “Effective Ways of Decreasing Acrylamide Content in Potato Crisps During Processing” J. Agric. Food Chem., Oct. 15, 2004, vol. 52, pp. 7011-7016.
Kretovich, V.L. “Plant Biochemistry” book, 1986, pp. 8-11 (English translation).
Lawrence, James E., “Acrylamide in Food” memorandum, Health Canada Food Program publication, Sep. 23, 2002, 1 page.
Low, Mei Yin, et al. “Effect of Citric Acid and Glycine Addition on Acrylamide and Flavor in a Potato Model System” J. Agric. Food Chem. 2006, 54, pp. 5976-5983.
Martin, Fiona L., et al. “Formation of Strecker Aldehydes and Pyrazines in a Fried Potato Model System” J. Agric. Food Chem. 2001, 49, pp. 3885-3892.
May, N.J., et al. “Acrylamide formation in deep-fried potato products and removal of acrylamide precursors” Food Australia 58 (10) Oct. 2006, pp. 488-493.
Mizukami, Yuzo, et al. “Analysis of Acrylamide in Green Tea by Gas Chromatography—Mass Spectrometry” J. Agric. Food Chem. 2006, 54, pp. 7370-7377.
Mottram, Don—The University of Reading, “Acrylamide in Cooked Foods—the Latest ‘Food Scare’” 2002 (44 pages).
Mottram, Donald S. “Acrylamide is formed in the Maillard reaction” Nature Magazine, Oct. 3, 2002, found at www.nature.com/nature (1 page).
Murray, Lindsay, “Acrylamide” Center for Clinical Toxicology, Vanderbilt Univ. Med. Ctr., Jul. 1996 found at http://www.inchem.org/documents/pims/chemical/pim652.htm, Jun. 1998 (8 pages).
Mustafa, Arwa, et al. “Factors Influencing Acrylamide Content and Color in Rye Crisp Bread” J. Agric. Food Chem. 2005, 53, pp. 5985-5989.
Neergaard, Lauran “Scientists: Chemical Reaction May Create Carcinogen” Health Zone found at http://www.cjonline.com/stories/093002/hea—carcinogen.shtml, Sep. 30, 2002 (3 pages).
Nielsen, Per Munk “Enzyme Technology for Production of Protein-Based Flavours” Novo Nordisk A/S 1995 (6 pages).
Ou, Shiyi, et al. “Reduction of Acrylamide Formation by Selected Agents in Fried Potato Crisps on Industrial Scale” ScienceDirect, Innovative Food Science and Emerging Technologies 9 (2008) pp. 116-121.
Pedreschi, Franco, et al. “Acrylamide reduction under different pre-treatments in French fries” ScienceDirect Journal of Food Engineering 79 (2007) pp. 1287-1294.
Pedreschi, Franco, et al. “Color development and acrylamide content of pre-dried potato chips” ScienceDirect Journal of Food Engineering 79 (2007) pp. 786-793.
Pedreschi, Franco, et al. “Color kinetics and acrylamide formation in NaCl soaked potato chips” ScienceDirect Journal of Food Engineering 79 (2007) pp. 989-997.
Pedreschi, Franco, et al. “Reduction of Acrylamide Formation in Potato Slices During Frying” Lebensm.-Wiss u.-Technol. 37 (2004) pp. 679-685.
Procter & Gamble Press Release Sep. 27, 2002 “Procter & Gamble Makes Significant Advances on Understanding Acrylamide Formation” found at http://biz.yahoo.com/prnews/020927/clf005—1.html (2 pages).
Raloff, Janet, “Hot Spuds: Golden Path to Acrylamide in Food” Science News Online, Oct. 5, 2002, vol. 162 found at http://www.sciencenews.org/20021005/fob5.asp (3 pages).
Rossell, J.B. (ed.) “Frying—Improving Quality” CRC Press, 2001, pp. 198-214 and 306-308.
Rydberg, Per, et al. “Investigations of Factors That Influence the Acrylamide Content of Heated Foodstuffs” J. Agric. Food Chem. 2003, vol. 51, pp. 7012-7018.
Segtnan, Vegard H., et al. “Screening of acrylamide contents in potato crisps using process variable settings and near-infrared spectroscopy” Mol. Nutr. Food Res. vol. 50, 2006, pp. 811-817.
Stadler, Richard H., et al. “Acrylamide from Maillard reaction products” Nature Magazine Oct. 3, 2002 found at www.nature.com/nature (2 pages).
Talburt & Smith (eds.), Potato Processing 4th Ed. 1987, Ch. 12 “Dehydrated Mashed Potatoes—Potato Granules,” pp. 535-555.
Talburt & Smith (eds.), Potato Processing 4th Ed. 1987, “Improving the Color of Potato Chips,” pp. 403-405.
“Temperature and Heat—Local Materials” Mar. 2003 found at http://web.archive.org/web/20030321105136/http://www.pa.uky.edu/sciworks/xtra/local.htm (3 pages).
U.S. Dept. of Health and Human Services, Public Health Service, National Toxicology Program, “9th Report on Carcinogens Revised Jan. 2001” found at http://win2000.kreatiweb.it/sanitaweb/web/Biblioteca/carcinogens/rahc/acrylamide.pdf (5 pages).
U.S. Dept. of Health & Human Services, U.S. Food and Drug Adm., Center for Food Safety and Applied Nutrition “Exploratory Data on Acrylamide in Foods” Dec. 4, 2002 found at http://www.mindfully.org/food/acrylamide-foods-fda (9 pages).
U.S. Food and Drug Administration Public Meeting “Assessing Acrylamide in the U.S. Food Supply,” Sep. 30, 2002(5 pages).
Viklund, Gunilla A., et al., “Variety and Storage Conditions Affect the Precursor Content and Amount of Acrylamide in Potato Crisps,” J. Sci. Food Agric. 2008, vol. 88, pp. 305-312.
Vivanti, Vittorio, et al. “Level of Acrylamide Precursors Asparagine, Fructose, Glucose, and Sucrose in Potatoes Sold at Retail in Italy and in the United States” J. Food Science, vol. 71, No. 2, 2006, pp. C81-C85.
Watson, S.A. (ed.), Corn: Chemistry and Technology, American Association of Cereal Chemists, 1987, pp. 410-420.
Webb, Edwin C., “Enzyme Nomenclature 1992,” Academic Press, p. 422.
Abdel-Kader, Zakia M., “Effect of blanching on the diffusion of glucose from potatoes” (Abstract), Wiley InterScience Journals: Nahrung / Food vol. 36, Iss. 1, 1992, 1 page.
Alternative Medicine Review “Glutathione, Reduced (GSH)” vol. 6, No. 6, 2001, pp. 601-607.
Amrein, Thomas, “Influence of Thermal Processing Conditions on Acrylamide Generation and Browning in a Potato Model System,” J. Agric. Food Chem. 2006, 54, pp. 5910-5916.
Ashoor, S.H. & Zent, J.B., “Maillard Browning of Common Amino Acids and Sugars,” (Abstract), Wiley InterScience Journals: J. Food Science, vol. 49, Issue 4, Jul. 1984, 2 pages.
Associated Press Washington—“Habrian descubierto el origen de sustancia cancerigena en las papas fritas,” Sep. 30, 2002, 2 pages.
Becalski, Adam, et al., “Acrylamide in Foods: Occurrence, Sources, and Modeling,” J. Agric. Food Chemistry, 2003, vol. 51, pp. 802-808.
Becalski, Adam, et al., “Acrylamide in French Fries: Influence of Free Amino Acids and Sugars,” (Abstract), J. Agric. Food Chem. 52 (12), May 22, 2004, 1 page.
Bosset, Dr. Jacques Olivier, et al. “Mitteilungen aus Lebensmitteluntersuchung und Hygiene” Jun. 2002, vol. 93, Offizielles Organ der Schweizerischen Gesellschaft fur Lebensmittel-und Umweltchemie und der Schweizerischen Gesellschaft fur Lebensmittelhygien(79 pages).
Brathen, Erland, et al., “Addition of Glycine Reduces the Content of Acrylamide in Cereal and Potato Products,” J. Agric. Food Chem. 2005, vol. 53, pp. 3259-3264.
CBS News CBC.CA “Food sector told to cut down on toxins in chips, fries” Sep. 19, 2002, 2 pages.
CBC News CBC.CA “Scientists find route for toxin to form in fried, baked foods,” Sep. 30, 2002, 3 pages.
CBC News CBC.CA “Some acrylamide with your fries?” Jan. 14, 2003, 6 pages.
Center for Science in the Public Interest article “New Tests Confirm Acrylamide in American Foods,” found at http://www.cspinet.org/new/200206251.html, Jun. 25, 2002, 2 pages.
Centre for Molecular and Biomolecular Informatics article “An Amino Acid Bedtime Story” found at http://www.cmbi.kun.nl.gvteach/HAN/alg/infopages/bedtime.html, material from Friedli Enterprises, Gert Vriend, Apr. 18, 2000, 4 pages.
chemhelper.com Home Page for Frostburg State University—Organic Chemistry Help, article “Nucleophilic Addition to Carbonyl Groups” found at http://www.chemhelper.com/nucadd.html, 2000 (3 pages).
Claeys, Wendie L., et al. “Quantifying the formation of carcinogens during food processing: acrylamide,” Trends in Food Science & Technology 16 (2005), pp. 181-193.
Database WPI Week 199329 Derwent Publications Ltd., London, GB; AN 1993-234163 XP002473734 & SU 1 750 586 Al (Interbios Res Assoc) Jul. 30, 1992, 1 page.
Database WPI Week 199805 Thomson Scientific, London, GB; AN 1998-042903 XP002503379, Dec. 4, 1996, 1 page.
de Barber, C. Benedito de, et al. “Reversed-Phase High-Performance Liquid Chromatography Analysis of Changes in Free Amino Acids During Wheat Bread Dough Fermentation” Cereal Chemistry, Feb. 26, 1989, vol. 66, No. 4, pp. 283-288.
de Meulenaer, Bruno, et al., “Comparison of Potato Varieties Between Seasons and Their Potential for Acrylamide Formation,” J. Science Food Agric., vol. 88, 2008, pp. 313-318.
de Vleeschouwer, Kristel, et al., “Impact of pH on the Kinetics of Acrylamide Formation/Elimination Reactions in Model Systems,” J. Agric. Food Chem. vol. 54, 2006, pp. 7847-7855.
de Wilde, Tineke, et al., “Influence of Fertilization on Acrylamide Formation during Frying of Potatoes Harvested in 2003,” J. Agric. Food Chem., 2006, vol. 54, pp. 404-408.
Dunlop, Patricia C., et al. “Nitrogen Catabolite Repression of Asparaginase II in Saccharomyces cerevisiae” J. Bacteriology, Jul. 1980, vol. 143, No. 1, pp. 422-426.
El Pais.com, “Hallada la reaccion quimica que produce la acrilamida en las frituras,” Jul. 15, 2009, 1 page.
European Commission—Health and Consumer Protection Directorate-General, “Opinion of the Scientific Committee on Food on new findings regarding the presence of acrylamide in food,” Jul. 3, 2002, 16 pages.
European Food Safety Authority, Report of “Workshop on Acrylamide Formation in Food,” Nov. 17, 2003, Brussels, 22 pages.
“FAO/WHO Joint Consultation on the Health Implications of Acrylamide in Food” Summary Report, Geneva, Switzerland, Jun. 25-27, 2002, 12 pages.
Food Safety Consultations “Health Implications of Acrylamide in Food” Report of a Joint FAO/WHO Consultation, Geneva, Switzerland, Jun. 25-27, 2002, 38 pages.
Joint FAO/WHO Expert Commission on Food Additives, 64th Meeting, Rome, Feb. 8-17, 2005, 47 pages.
Fan, Xuetong, et al. “Effectiveness of Ionizing Radiation in Reducing Furan and Acrylamide Levels in Foods” J. Agric. Food Chem. 2006, 54, pp. 8266-8270.
Fiselier, K., et al., “Brown potato Croquettes Low in Acrylamide by Coating with Egg/Breadcrumbs,” Eur. Food Res. Technol. (2004) 219:111-115.
Fiselier, Katell, et al., “Higher Acrylamide Contents in French Fries Prepared from “Fresh” Prefabricates,” Eur. Food Res. Technol. (2005) 221:376-381.
Food Standards Agency, “Study of Acrylamide in Food,” May 17, 2002, 7 pages.
Francis, Frederick J., “Encyclopedia of Food Science and Technology,” 2nd ed., 2000, pp. 2160-2161.
Freshfields Bruckhaus Deringer “Acrylamide in food—The approach of regulators across Europe” Feb. 2003 (20 pages).
Friedman, Mendel, et al., “Browning prevention in fresh and dehydrated potatoes by SH-containing amino acids,” Food Additives and Contaminants, 1992, vol. 9, No. 5, pp. 499-503.
Friedman, Mendel, “Chemistry, BioChemistry, and Safety of Acrylamide. A Review,” J. Agric. Food Chem., Jul. 3, 2003, vol. 51 (16), pp. 4504-4526.
Friedman, Mendel, et al., “Inhibition of Browning by Sulfur Amino Acids. 1. Heated Amino Acid-Glucose Systems,” J. Agric. Food Chem., 1990, 38, pp. 1641-1647.
Friedman, Mendel “The Impact of the Maillard Reaction on the Nutritional Value of Food Proteins” Ch. 6 from The Maillard Reaction: Consequences for the Chemical and Life Sciences, Ikan, Raphael (ed.), 1996, 24 pages.
Garayo, Jagoba, et al. “Vacuum frying of potato chips” J. Food Engineering 55 (2002), pp. 181-191.
Gertz, Christian, et al. “Analysis of acrylamide and mechanisms of its formation in deep-fried products” Eur. J. Lipid Sci. Technol. 104 (2002), pp. 762-771.
Gokmen, Vural, et al., “Acrylamide formation is prevented by divalent cations during the Maillard reaction,” Food Chemistry (2006) doi: 10.1016/j.foodchem.2006.08.011, 8 pages.
Granda, Claudia, et al., “Effect of Raw Potato Composition on Acrylamide Formation in Potato Chips,” J. Food Science vol. 70, No. 9, 2005, Nov. 16, 2005, pp. E519-E525.
Granda, Claudia, et al. “Kinetics of Acrylamide Formation During Traditional and Vacuum Frying of Potato Chips” J. Food Process Engineering 28 (2005), pp. 478-493.
Granda, C., et al. “Reduction of Acrylamide Formation in Potato Chips by Low-temperature Vacuum Frying”, J. Food Science, vol. 69, No. 8, 2004, Oct. 7, 2004, pp. E405-E411.
Grivas, Prof. Spiros, et al. “Acrylamide in Food—Mechanisms of Formation and Influencing Factors During Heating of Foods”, Report from Swedish Scientific Expert Committee, Apr. 24, 2002 (22 pages).
Harmony House Foods, Inc., http://web.archive.org/web/20050425210612/www.harmonyhousefoods.com/slicedpotato.html, Apr. 25, 2005, 2 pages.
Harrison, Karl “Amino Acids and Proteins” found at http://www.chem.ox.ac.uk/mom/amino—acids/introduction.html, 1996 (2 pages).
Harrison, Karl “Molecules of the Month” found at http://www.chem.ox.ac.uk/mom/, 1996 (1 pages).
Weaver, M.L., et al., “Sugar-End in Russet Burbank Potatoes,” American Journal of Potato Research, 1972, vol. 49, No. 10, pp. 376-382.
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Number Date Country
20100143540 A1 Jun 2010 US