Modified starches have been used for years in many diverse applications. There is a continuing need to improve upon starch modification processes and modified starches to meet various demands of these applications.
One conventional method for modifying starch, hydroxypropylation, involves the addition of sodium sulfate and sodium hydroxide in addition to propylene oxide to a slurry of native or modified starch. Sodium hydroxide raises the pH of the slurry to about 11.5, thereby facilitating the hydroxypropylation reaction between the starch and the propylene oxide. Hydroxypropylated starch, in a high pH environment, will gelatinize, so sodium sulfate is added to the starch slurry, for example, at a level of about 10%1 or more on a dry basis, in order to inhibit gelatinization of the hydroxypropylated starch. After hydroxypropylation has been completed, the pH of the slurry is reduced by adding an acid, and the resulting hydroxypropylated modified starch is washed and dried for further use. A schematic diagram of this conventional process is shown in
The modified starch resulting from the conventional hydroxypropylation reaction contains sodium salt at a level of about 15-25% by dry weight of the modified starch before the washing step. The washing step typically reduces the sodium salt to a level of about 0.5%) or less on a dry basis.
Another conventional method for modifying starch is by cross-linking the starch. This can be done by adding cross-linking agents, including, but not limited to, a mixture of sodium trimetaphospbate (STMP) and sodium tripolyphosphate (STPP), or phosphorus oxychloride and epichlorohydrin, to either a native starch slurry or starch slurry that has previously been hydroxypropylated. About 5% sodium chloride is added to the reaction in order to modulate the cross-linking process to provide uniformity and consistency in this typically fast reaction. The resulting modified starch contains sodium salt at a level of about 5-25% by dry weight (before the washing step).
The present invention is directed to a process for making a modified starch, to modified starch products resulting from this process, and to related products containing the modified starch as an ingredient, processing aid, or formula component. The process and resulting product according to the present invention reduce, substantially reduce, or eliminate the sodium level typically associated with conventional modified starch products.
The process of the present invention can be used as an alternative to conventional starch modification processes, such as substitution and crosslinking. The resulting modified starch product can be used in place of conventionally modified starches in a wide variety of applications, including, but not limited to, food products, pharmaceutical products, nutraceutical products, paper products, personal care products, and the like.
By using the process of the present invention, a modified starch product that has a low or reduced sodium content, or that is substantially free of sodium, can be made. The modified starch of the present invention can be used to reduce, substantially reduce, substantially eliminate, or eliminate the sodium content of many products.
The process of the present invention involves the use of non-sodium salts and non-sodium alkaline compounds to facilitate the hydroxypropylation reaction described above. The hydroxypropylation reaction can take from a few hours to over 20 hours, depending on the reaction conditions and the desired properties of the end product. Generally, a reaction time of about 18-20 hours is suitable. Once the starch has been hydroxypropylated using this process, the pH of the slurry is reduced, and the modified starch is dried for further use. Because the modified starch does not contain sodium, a washing step is not necessary, but in some instances a washing step may be incorporated into the process, depending on the intended use of the modified starch product. schematic diagram of one embodiment of the process of the present invention is shown in
Similarly, the modified starch can be made using other starch modification reactions, such as cross-linking the starch, by replacing sodium-containing compounds used in such reactions with non-sodium compounds. The modified starch can also be made by using a combination of starch modification processes, such as hydroxypropylation and cross-linking, to achieve the desired properties.
The process of the present invention can be used to modify starch from a wide variety of sources, such as, but not limited to, corn/maize, wheat, rice, buckwheat, barley, oat, millet, rye, sorghum, potato, sweet potato, tapioca/cassava, arrowroot, sago, arracacha, banana, plantain, malanga, kudzu, oca, canna, taro, yams, chestnuts, edible beans, such as lentils, favas, mung bean and peas. In addition to modifying a native starch from these or other sources, the process of the present invention can be used to modify a previously modified starch. The modified starch product resulting from the process of the present invention can also be further modified using other starch modification processes.
Non-sodium salts suitable for use in the process of the present invention include, but are not limited to, the following:
Of these salts, the preferred non-sodium salts for use in the present invention include potassium chloride, ammonium chloride, magnesium chloride, calcium chloride, zinc chloride, aluminum chloride, potassium sulfate, magnesium sulfate, potassium bitartrate, and a combination thereof.
The advantage of the modified starch product made by the process of the present invention is that the modified starch can be used in reduced sodium, low sodium or sodium-free products, such as thud products, and can provide all the textural properties obtained by using a conventionally modified starch ingredient without adding a significant amount of sodium to the food product or other type of product.
As will be appreciated by those skilled in the art, although the process of the present invention does not utilize sodium-containing reactants to make the modified starch product, some trace levels of sodium may be present in the modified starch made by the process of the present invention due to factors other than the modification process itself.
One key advantage of the modified starch of the present invention is that the modified starch can be used as an ingredient or formula component to reduce the sodium content in a wide variety of products, such as food products, while providing the same or similar textural and other organoleptic or physical properties obtained by using a conventionally modified starch ingredient in such products.
As used herein, the expressions “substantially free of sodium,” “low sodium,” “reduced sodium”, and “sodium-free” shall refer to a sodium level or levels that are less than the sodium content of comparable reference products containing conventionally modified starch ingredients. In a preferred embodiment, a low sodium modified starch made in accordance with the present invention is used to prepare food products that are low sodium, reduced sodium, or sodium-free, and that have substantially the same texture, viscosity and taste properties of comparable sodium-containing reference food products made using a conventionally modified starch. As used herein, the expression “reference food” shall refer to a food product having substantially the same formula as a food product comprising a low sodium modified starch, but without the low sodium modified starch and related formula modifications.
Products made using the modified starch of the present invention may be labeled to reflect the sodium reduction if the products meet labeling, regulations or guidelines regarding the sodium content of a given product or type of product.
For example, for food products, “reduced sodium” as defined by the U.S. Food and Drug Administration means at least 25% less than an appropriate reference food, as defined in 21 CFR §101.61(b)(6), and “low sodium” means 140 mg sodium or less per RACC, or “reference amounts customarily consumed”, as defined in 21 CFR §101.61(b)(4). In one embodiment of the present invention, the modified starch product of the present invention is used to make a reduced sodium food product which contains at least about 25% less sodium than an appropriate reference food. In another embodiment of the present invention, the modified starch product of the present invention is used to make a low sodium food product containing about 140 mg sodium or less per RACC.
Although the following Example I describes a hydroxypropylation reaction, the process of the present invention can be applied to any starch modification reaction which conventionally involves a sodium salt, in order to reduce or eliminate the sodium content of the resulting modified starch, such as, but not limited to, the starch modification reactions described in 21 CFR §172.892. Included in these starch modification reactions are substitution and cross-linking reactions. The modified starch product of the present invention can be made using a combination of starch modification reactions to obtain a modified starch product having the desired functional and organoleptic properties.
The modified starch product can be mechanically blended with any native starches and/or modified starches described in 21 CFR §172.892 in various ratios to produce modified starch products with functionality suitable to a variety of food and other applications.
It has been observed that modified starch products made with different salts have different effects on the gelling and pasting properties of the modified starch products, and require different levels of non-sodium salts to complete the modification process. By using a particular non-sodium salt during the starch modification process, it is possible to make a low sodium modified starch with the desired gelatinization and other properties for a particular application. For example, if a magnesium salt is used during the starch modification process instead of a sodium salt, the gel onset temperature of the low sodium modified starch is lower, i.e., the low sodium modified starch gels at a lower temperature, than if a calcium salt is used. Using these properties, it is possible to select and combine various low sodium modified starches, and native and conventionally modified starches, to customize the modified starch characteristics, such as texture, viscosity, taste and sodium content, as needed for a particular application.
To evaluate the properties of the modified starches made by the process of the present invention, a variety of non-sodium salts were used in the hydroxypropylation of native starch, and properties of the resulting modified starch product were compared to those of a native starch and a conventionally modified starch.
Waxy corn starch was obtained from a commercial source and modified according to the procedure by Wang and Wang (Starch/Stärke 52 (2000) 406-412) with modifications.
To make the modified starch products of the present invention, a starch slurry containing dry starch at 35% solid concentration (dry starch basis) was prepared and salt (NH4Cl, KCl, CaCl2, or MgCl2 at their respective maximum concentrations) was added. Then the pH of the starch slurry was adjusted to 11.5 by KOH, instead of NaOH, in order to reduce the sodium content. Propylene oxide was added at 8% on a dry weight basis to initiate the hydroxypropylation, and the reaction took place for 18 hours. Afterward, the slurry pH was neutralized to 5.5-6.0 with HCl, and the modified starch product of the present invention was recovered and dried at 40° C. to moisture content below about 12%.
As used herein, “HP” shall refer to “hydroxypropylated”.
As used herein, “HP-NH4Cl”, “HP-KCl”, “HP-CaCl2” and “HP-MgCl2” shall refer to a modified starch product of the present invention made by replacing sodium chloride in the modification process with ammonium, potassium, calcium or magnesium chloride, respectively.
Thermal Properties
The gelatinization temperature and enthalpy of the modified starch products, and of a native starch and a conventionally modified starch, were measured with a differential scanning calorimeter (DSC), and the results are summarized in Table 1. As used herein, “HP-(salt)” refers to a modified starch product that has been hydroxypropylated using the named salt and without a subsequent washing step. HP-NH4Cl waxy corn had the highest gelatinization temperature and HP-MgCl2 had the lowest onset gelatinization temperature and enthalpy, as shown in Table 1. The significantly lower enthalpy values of the modified starch products made in accordance with the present invention suggest that some of their crystalline structures were disrupted during the modification process. Commercial HP waxy corn starch had a significantly lower gelatinization temperature due to the added hydroxypropyl groups that weaken the crystalline structure.
Pasting Properties
The pasting properties, including pasting temperature, peak viscosity, breakdown, and final viscosity, of the modified starches were evaluated at 6% (db) by a Micro ViscoAmyloGraph®, available from C.W. Brabender Instruments, Inc., South Hackensack, N.J. The results, and the results of the same analysis performed on a native starch and a conventionally hydroxypropylated starch, are summarized in Table 2.
HP-NH4Cl waxy corn had the lowest overall viscosity profile, whereas HP-KCl waxy corn had the highest peak and final viscosity among all the modified starch samples, as shown in Table 2 and
The low sodium modified starch of the present invention may include the salt residue remaining after the modification reaction has taken place. In a conventional sodium-based reaction, the residual sodium salt associated with a modified starch is typically washed out. The non-sodium salt residues associated with the low sodium modified starch of the present invention may or may not be washed out, depending on the desired effect of the low sodium modified starch. Table 3 summarizes the various salt residue levels of some embodiments of the low sodium modified starch.
§The highest level of salts in modified starch occurs when salt was added its saturation point and no wash step was applied at the end of reaction process.
In some embodiments, it may be desirable to retain or optimize the residual non-sodium salt levels due to the nutritive significance of a particular salt residue. The low sodium modified starch in these embodiments serves to provide an additional source of the nutritive salt in the finished product.
The following examples present a variety of food products made with the modified starch product of the present invention. Although these examples describe food products, the modified starch product can also be used in any type of non-food products in which a conventionally modified starch is used.
In the Examples below, the columns marked as “A” describe conventional food product formulas, and the columns marked “B” describe food product formulas made with the modified starch product of the present invention. The food products are made using conventional methods, but utilize the modified starch product of the present invention as an ingredient in place of or in combination with conventionally modified starches. The “B” formulas containing the modified starch product resulted in finished food products having texture, viscosity and taste properties that were comparable to the products made using the “A” formulas, but with lower or significantly lower sodium levels. All percentages are given as percent by weight unless otherwise indicated.
The present invention is described in the embodiments discussed above, but the embodiments are not intended to limit the scope of the present invention in any way.
This application represents a continuation of U.S. application Ser. No. 13/863,328, filed on Apr. 15, 2013, which is a Continuation-In-Part of U.S. patent application Ser. No. 12/436,390, filed on May 6, 2009, which claims the benefit of priority of U.S. Provisional Patent Application No. 61/050,711, filed May 6, 2008, and is also a continuation-in-part of U.S. patent application Ser. No. 12/498,392, filed on Jul. 7, 2009, which claims the benefit of priority of U.S. Provisional Patent Application No. 61/081,125, filed Jul. 16, 2008, each of which applications is incorporated by reference herein in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
3951947 | Schanefelt et al. | Apr 1976 | A |
3969340 | Tessler et al. | Jul 1976 | A |
3970767 | Tessler et al. | Jul 1976 | A |
4000128 | Del Valle et al. | Dec 1976 | A |
4048434 | Speakman | Sep 1977 | A |
4112222 | Jarowenko | Sep 1978 | A |
4120982 | Eastman et al. | Oct 1978 | A |
4120983 | Del Valle et al. | Oct 1978 | A |
4251560 | Dell et al. | Feb 1981 | A |
4379919 | Tessler et al. | Apr 1983 | A |
4431800 | Leusner et al. | Feb 1984 | A |
4623549 | Katt et al. | Nov 1986 | A |
4828833 | Cordon | May 1989 | A |
4847371 | Schara et al. | Jul 1989 | A |
4885180 | Cochran et al. | Dec 1989 | A |
4973447 | Seib et al. | Nov 1990 | A |
4981709 | Furcsik et al. | Jan 1991 | A |
5064633 | Simon et al. | Nov 1991 | A |
5064663 | Murray et al. | Nov 1991 | A |
5110612 | Quarles et al. | May 1992 | A |
5234707 | Merkenich et al. | Aug 1993 | A |
5294453 | Quarles et al. | Mar 1994 | A |
5486375 | Yoder et al. | Jan 1996 | A |
5569480 | De Coninck | Oct 1996 | A |
5576043 | Stankus et al. | Nov 1996 | A |
5641349 | Koubek | Jun 1997 | A |
5851959 | Bernu | Dec 1998 | A |
5976582 | Gonze et al. | Nov 1999 | A |
6102254 | Ross | Aug 2000 | A |
6217921 | Lanner et al. | Apr 2001 | B1 |
6352732 | Lanner et al. | Mar 2002 | B2 |
6488980 | Jeffcoat et al. | Dec 2002 | B1 |
6541060 | Jeffcoat et al. | Apr 2003 | B2 |
6551647 | Lelli | Apr 2003 | B1 |
6689197 | Dick et al. | Feb 2004 | B2 |
6699363 | Moffett | Mar 2004 | B2 |
6821548 | Buwalda et al. | Nov 2004 | B1 |
7094817 | Halley et al. | Aug 2006 | B2 |
20010053401 | Lanner et al. | Dec 2001 | A1 |
20050046356 | Kwak | Mar 2005 | A1 |
20050079598 | Davis | Apr 2005 | A1 |
20050084591 | Shukla et al. | Apr 2005 | A1 |
20050238784 | Shukla et al. | Oct 2005 | A1 |
20060251768 | Bouquerand | Nov 2006 | A1 |
20070020367 | Yoo | Jan 2007 | A1 |
Number | Date | Country |
---|---|---|
491298 | Jun 1992 | EP |
685171 | Dec 1995 | EP |
776610 | Jun 1997 | EP |
1072196 | Jan 2001 | EP |
741742 | Dec 1955 | GB |
741742 | Dec 1955 | GB |
2005029940 | Feb 2005 | JP |
2005171112 | Jun 2005 | JP |
WO 0001251 | Jan 2000 | WO |
WO 0004784 | Feb 2000 | WO |
WO 0132033 | May 2001 | WO |
WO 2004099255 | Nov 2004 | WO |
WO 2005079598 | Sep 2005 | WO |
Entry |
---|
Aziz et al., “Hydroxypropylation and Acetyiation of Sago Starch”, Malaysian Journal of Chemistry, 6:1, 048-054 (2004). |
J. Michaelides PhD., et al., “Alternatives to Sodium Chloride Ingredients and Methods”, Guelph Food Technology Centre Literature, Review, Project: INT 142-6 (Dec. 22, 2008). |
Wattanachant et al., “Characterisation of Hydroxypropylated Crosslinked Sago Starch as Compared to Commercial Modified Starches”, Songklanakarin J. Sci. Technol. 24(3): 439-450 (2002). |
Wattanachant et al., “Effect of Crosslinking Reagents and Hydroxypropylation Levels on Dual—Modified Sago Starch Properties”, Food Chemistry 80, pp. 463-471 (2003). |
Ya-Jane Wang et al., “Effects of Modification Sequence on Structures and Properties of Hydroxypropylated and Crosslinked Waxy Maize Starch”, Starch 52 p. 406-412 (2000). |
Yangsheng Wu et al., “Acetylated and Hydroxypropylated Distarch Phosphates from Waxy Barley: Past Properties and Freeze-Thaw Stability”, Cereal Chem. 67(2):202-208 (1990). |
Number | Date | Country | |
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61081125 | Jul 2008 | US | |
61050711 | May 2008 | US |
Number | Date | Country | |
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Parent | 13863328 | Apr 2013 | US |
Child | 14753806 | US |
Number | Date | Country | |
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Parent | 12498392 | Jul 2009 | US |
Child | 13863328 | US | |
Parent | 12436390 | May 2009 | US |
Child | 13863328 | Apr 2013 | US |