Food or edible material: processes – compositions – and products – Meat filled casing – sausage type
Reexamination Certificate
2001-11-07
2004-05-04
Bhat, N. (Department: 1761)
Food or edible material: processes, compositions, and products
Meat filled casing, sausage type
C426S138000, C426S578000, C426S661000
Reexamination Certificate
active
06730340
ABSTRACT:
BACKGROUND OF THE INVENTION
For a number of years, edible films have been used to replace membranes and casings made of animal viscera, in the production of smoked meat products such as ham and sausages. Currently available edible films include collagen films, modified cellulose films and carrageenan-based films.
Collagen films are composed of edible collagen, plasticized with glyerol or other polyols. They are manufactured by extrusion onto a belt followed by drying to remove the moisture. The collagen slurry is applied to the belt cold, and requires high-temperature drying to remove all the excess moisture and bring the film to a final moisture content of approximately 10%. Apart from the difficulty in processing films of this kind, these materials can bring about allergic reactions in certain consumers. Too, being derived from the coum layer of beef or pork, collagen may be an unacceptable casing or film material for religious and dietary reasons.
Modified cellulose films are for the most part composed of modified hydroxypropyl methylcellulose. To date, almost all films of this kind which have been produced are cold water-soluble films which begin to disintegrate on contact with water. For this reason, they have not been used in meat processing.
Carrageenan is a polyanionic polysaccharide derived from red algae. The material is an excellent film-former and has been used in the formulation of edible food packaging films (U.S. Pat. No. 4,851,394) and heat-sealable edible films (U.S. Pat. No. 5,089,307—Ninomiya et al.). Films composed primarily of carrageenan additionally exhibit excellent strength, are not soluble in cold water and bind well to meat
However, because carrageenan forms a thermoreversible gel, films composed of a predominant carrageenan proportion tend to disintegrate in hot water, i.e. above 70° C. The hot carrageenan aqueous solution then re-gels upon contact with cooler water, less than 50° C.
It was one of our objectives to develop carrageenan-based films which can effectively and economically replace edible collagen films currently utilized in ham and sausage production, while providing high yields and high-quality product.
Collagen film is typically wrapped around hams during production, for ease in netting removal after the ham has been cooked. Collagen films appear to the consumer to be part of the ham after cooking and, indeed, are usually not taken note of by the average consumer. Many styles of meats are processed using collagen films, including various ham, chicken and turkey products.
General Description and Objects of the Invention
It is an object of the present invention to provide polysaccharide films which would function well by satisfying all of the following key attributes:
composed of food ingredients which meet Food Chemical Codex Specifications and are approved for usage, i.e. GRAS rated in the United States (generally regarded as safe).
a film that would maintain its composition during the cooking cycle, until the ham forms its own natural protein skin.
after cooking, film adheres to the finished product, in that it does not fully disintegrate after a prolonged exposure to hot water or steam.
film is tender to eat following processing of the meat product.
film binds to the meat surface during and subsequent to processing.
film is permeable to flavouring smoke.
film imparts an appealing shine and colour to the cooked product.
We have found that excellent properties for edible films can be achieved by including, along with the carrageenan, suitable non-thermoreversible gel-forming polymers, preferably Konjac and Gellan gums. Konjac is extracted from the konjac tuber. This polysaccharide hydrates immediately and can form either thermoreversible or non-thermoreversible gels, depending on the conditions under which the gel is formed. Gellan gum is a polysaccharide gum produced from bacterial fermentation. It is a strong gel former and produces gels that are non-thermoreversible in the presence of Ca
+2
and other multivalent anions. Both Konjac and Gellan gums are edible and GRAS rated. We observed that Konjac tends to form gels having a higher degree of elasticity than Gellan, which forms gels having a more brittle texture.
According to present invention, edible films and casing materials comprise a polymer base of carrageenan/Konjac/Gellan, and also a suitable starch, alginate or other polysaccharide, depending on the specific attributes required.
Starch functions to reduce water absorption of the film and it is preferred that a high-amylose starch be used, as high-amylose starch is inherently a better film-former than other starches.
“Alginate” herein refers to the alginates which are commonly used in the food industry, namely polypropylene glycol alginate, sodium alginate or calcium alginate. Alginate in compositions according to the present invention tend to produce strong films exhibiting good adhesion.
Specific methods and formulations are described in more detail below, but generally we have found the following compositions to provide useful edible films:
Suggested Range
Component
Low (wt. %)
High (wt. %)
Carrageenan
2
35
Gellan*
0
35
Konjac*
0
35
Locust bean gum (LBG)
0
10
Protein
0
15
Starch**
0
20
Alginate**
0
35
Sodium Citrate
1
5
Sorbitan Monostearate
0.25
3
Glycerol
1.0
35
Other Plasticizer
†
0
25
Water
8
35
**
total
of Gellan & Konjac gums should be no less than about 5 wt % and up to about 35 wt %
*
total
of starch + alginate should be no less than about 5 wt % and up to about 35 wt %
†
polyhydric alcohols, other than glycerol
The synergistic effects of the main polymers, Gellan Konjac and carrageenan, function to produce a film of high tensile strength, hot and cold water resistance and gum substrate adherence.
The use of a protein source is desirable to provide the film with both improved adhesion and shine functionality. The presence of some (at least about 5%) of alginatge or starch component is necessary to give sufficient film casing adhesion.
Other polysaccharides, as discussed below, may be added to impart specific desired properties to the film. Glyerol was added for its elasticizing effects. Optionally, calcium chloride or potassium carbonate may be utilized to improve the film strength and hot water resistance.
From other formulations tested it is possible to significantly alter the relative amounts of each gel-forming polymer in the film to produce films exhibiting some varying degree of hot water solubility.
DETAILED DESCRIPTION OF THE INVENTION
Polymer solutions were prepared for film casting as follows: glyerol or other plasticizers were added to the requisite amount of hot water. While maintaining the solution at an elevated temperature (80-90° C.), then the dry ingredients were added and the solution vigorously mixed to homogeneity. The polymer solution was then continuously mixed under slow agitation for 1-2 hours to remove trapped air bubbles.
Once the polymer solution appeared to be smooth and free of lumps, it was cast into film, using either a casting box or with a standard draw down bar. Care must be taken to ensure that the hot solution is cast in a uniform thin layer. In all of the experimental examples given below, film was formed by drawing the solution down onto a hot (90° C.) stainless steel belt with a Gardener dye. The films were either air dried overnight at room temperature, or dried over a hot water bath and then removed for testing.
Films produced this way would initially be tested for thickness using a micrometer (Gauge) and tensile/tear strength.
The methods for measuring tear strength and elongation are those specified in ASTMD638. Normally 5 specimens are tested from each of 5 samples with the following conditions
20 lbf load cell
Crosshead speed: 2 in./minute
Die “C” cut specimens
Films that met these requirements would then be tested for hot water solubility by placing strips of the film in boiling water and then allowing the water to cool with the film sample in it. After cooling, the water would then be drained off and non-solubilized material would be placed with the dr
Macquarrie Reg
Schupp Kurt
Taylor Peter
Bhat N.
Shlesinger & Arkwright & Garvey LLP
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