US20040214926A1 - Materials and food additives free of endocrine disruptive chemicals - Google Patents

Materials and food additives free of endocrine disruptive chemicals Download PDF

Info

Publication number
US20040214926A1
US20040214926A1 US10/852,026 US85202604A US2004214926A1 US 20040214926 A1 US20040214926 A1 US 20040214926A1 US 85202604 A US85202604 A US 85202604A US 2004214926 A1 US2004214926 A1 US 2004214926A1
Authority
US
United States
Prior art keywords
endocrine
polymeric material
chemicals
monomer
endocrine disruptive
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US10/852,026
Inventor
George Bittner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US10/852,026 priority Critical patent/US20040214926A1/en
Publication of US20040214926A1 publication Critical patent/US20040214926A1/en
Priority to US13/033,493 priority patent/US20110168657A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/74Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
    • G01N33/743Steroid hormones
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/34Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
    • A23L3/3454Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
    • A23L3/3463Organic compounds; Microorganisms; Enzymes
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • C08K5/134Phenols containing ester groups
    • C08K5/1345Carboxylic esters of phenolcarboxylic acids
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2500/00Screening for compounds of potential therapeutic value
    • G01N2500/04Screening involving studying the effect of compounds C directly on molecule A (e.g. C are potential ligands for a receptor A, or potential substrates for an enzyme A)
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]

Definitions

  • the present invention relates, generally, to the field of plastics and, more specifically, to plastic materials and food additives that are substantially free of endocrine disruptive chemicals.
  • the present invention also relates to methods for detecting endocrine disruptive activity.
  • endocrine disruptors may act as agonists or antagonists to estrogens or androgens and may interfere in multiple ways with the action of thyroid hormones.
  • endocrine disruptors can mimic or block chemicals naturally found in the body, thereby altering the body's ability to produce hormones, interfering with the ways hormones travel through the body, and altering the concentration of hormones reaching hormone receptors.
  • relatively few chemicals have been examined for their endocrine disruptive effect, those chemicals that have shown such an effect are increasingly found in common food and plastic products.
  • Endocrine disruptors include chemicals such as, for example, polychlorinated biphenyls (PCBs), dioxins and furans. These chemicals are found environmentally in insecticides, herbicides, fumigants, and fungicides that are used in agriculture as well as in the home. Other endocrine disruptors are found in common chemicals such as detergents, dental amalgams and resins that coat the inside of tin cans.
  • PCBs polychlorinated biphenyls
  • dioxins and furans.
  • DEHP di(2-ethylhexyl) phthalate
  • PVC plastic polyvinyl chloride
  • DEHP an estrogen-mimicking chemical
  • DEHP has been found to leach from these plastics, thereby creating problems with the materials in contact with the plastic.
  • DEHP has been found to leach from intravenous bags and tubing into the blood and medications being administered to patients. Exposure to DEHP through intravenous bags and tubing presents a health risk that could be avoided through the use of a plastic material that does not contain endocrine disruptive chemicals.
  • bisphenol A is a monomer used to synthesize a number of plastics, such as polycarbonates, epoxy, phenoxy and polysulfone polymers, and is released in significant amounts when these plastics are exposed to water, particularly when heated. Bisphenol A has been shown to possess deleterious estrogenic activity. Nevertheless, plastics manufactured with bisphenol A, such as polycarbonate, are commonly used for food and beverage containers, baby bottles, baby toys, microwaveable containers and medical items.
  • Endocrine disruptors and natural estrogens share a common mechanism of action.
  • estrogenic activity is produced by binding natural estrogen to an estrogen receptor (ER) within the nucleus of the cell, followed by transcriptional activation of these occupied ERs.
  • ER estrogen receptor
  • antiestrogenic activity is produced by endocrine disruptors which bind to ERs but which do not subsequently activate the occupied ER.
  • SERMs selective estrogen receptor modulators
  • endocrine disruptors When tested in animal model systems, endocrine disruptors produce deleterious estrogenic effects at concentrations less than those concentrations that are released by certain plastics. For example, research has found that very low dosages of endocrine disruptors exhibit behavioral effects on rodents including, for example, learning disabilities, disorders of attention, motivation, emotion, cognitive development, and changes in sexual orientation and aggressive behavior. Other effects include alterations of reproductive organs of infant and adult males and females such as reduced sperm counts, prostate enlargement, ovarian and uterine dysfunction, and the rate of growth and time to sexual maturation.
  • Plastics are made from monomers that are synthesized into polymers, typically by the application of heat, pressure and, in certain cases, catalysts. The most common monomers from which plastics are made are shown in Table 1. TABLE 1 Plastic Production Monomer Exhibits Estrogenic (EA) or Carcinogenic Monomer Polymer Acronym (CA) Activity Ethylene Polyethylene PE 2 (LDPE, NT HDPE, LLDPE) Vinylchloride Polyvinylchloride PVC CA Propylene Polypropylene PP NT Styrene Polystyrene PS NT Bisphenol A Polycarbonate 1,3 PC EA (Epoxy, Polysulfone, Phenoxy, etc Polymers) Terephthalic Polyethylene, PET EA acid + terephthalate ethylene glycol
  • PE polyethylene
  • LDPE low density PE
  • LLDPE linear low density PE
  • HDPE high density PE
  • PET polyethylene terephthalate
  • antioxidants are added to increase the useful life of PE and other plastics by preventing, or at least minimizing, the degradation of oxygen which can often cause breakage of molecular chains leading to other undesirable effects such as, for example, discoloration, loss of surface gloss, surface cracking, and lowering of tensile strength.
  • plastics are typically processed into useful shapes at temperatures in excess of 150° centigrade which can lead to thermo-oxidative degradation of molecular weight, ductility, and strength.
  • Table 2 lists some common antioxidants, all of which, with the possible exception of organo-hosphites and thioethers, have estrogenic, carcinogenic or other toxic effects.
  • additives other than antioxidants are also used in plastic processing.
  • various pigments including, for example, lead chromates, lead molybdates, lead sulphteranges, chromium oxides, ferric ammonium ferrocyanide, carbon black and phthalo blues are used to add color to PE and other polymers. Common pigments are found in Table 3. Many of these pigments exhibit endocrine disruptive activity or other toxic effects.
  • plastic additives include plasticizers and stabilizers.
  • esters of phthalic acid one of the most ubiquitous plasticizers for PVC compounds, all exhibit estogenic disruptive activity and are frequently used in high concentrations, often 40-80% by weight, in plastic materials. This is extremely troublesome because most plasticizers are quite mobile at ambient conditions and, when child-oriented products are made from these materials, children may ingest significant amounts of these compounds when they “taste” their surroundings.
  • Thermal stabilizers for PVC include barium-cadmium soaps, organo-tin compounds, lead compounds, and cadmium-zinc soap. Additives that contain lead and cadmium are clearly toxic. Many of the most common ultraviolet stabilizers for PE such as, for example, benzothiazoles and benzophenones have exhibited endocrine disruptive activity and have rather low molecular weight. Such low molecular weight (1000 daltons) stabilizers are routinely added to PE and are sufficiently mobile to migrate by diffusion from the plastic to the environment. Common stabilizers are found in Table 4.
  • plastics Although tested for carcinogenic activity and acute toxicity, chemicals used in plastics that contact humans directly or that contact food have not been tested for estrogenic activity and, as a result, the disruptive activity has not yet been regulated. Furthermore, the formulations used to manufacture plastics usually are not required to be revealed to other companies, consumers or governmental agencies. Even when the manufacturer divulges the primary monomer or polymer used in a plastic, it rarely reveals all additives used in the formulation.
  • Antioxidants are one of the most important and most widely used food additives.
  • the oldest and most common antioxidants that are deemed suitable for food contact service belong to a class of materials known as hindered phenols.
  • the most ubiquitous of these is BHT. Since 1949, BHT has been widely used as an antioxidant food additive in large part because it is very inexpensive and because it was routinely assumed to be non-toxic. BHT works by intercepting and reducing free radicals that are associated with the oxidation process. However, primary data suggests that BHT exhibits endocrine disruptive activity. BHT is therefore almost certainly unsuitable as an antioxidant in foods.
  • Table 6 lists 12 common food antioxidants. Some antioxidants such as, for example, BHA, BHT, tocopherols, TBHQ, gallates and THBP, are widely used due to their overall efficacy. Others are “natural” antioxidants isolated from plants, although they are less commonly used in the manufacture of food products at present. The estrogenic activity of food antioxidants has not yet been examined, but many food antioxidants would be expected to exhibit estrogenic activity because they contain a phenolic ring. Since many estrogenic chemicals have effects at picomolar to nanomolar levels and antioxidants are often added to foodstuffs in micromolar to millimolar concentrations (i.e. 1000 ⁇ greater), such estrogenic antioxidants could be a significant health hazard, particularly to a developing fetus.
  • Some antioxidants such as, for example, BHA, BHT, tocopherols, TBHQ, gallates and THBP.
  • Others are “natural” antioxidants isolated from plants, although they are less commonly used in the manufacture of food products at present.
  • Tert-Butylhydroquinone 1 2 (2) yes Stabilizes fats, oils, 0-0.2 mg/kg (TBHQ) confectionery products, etc 5.
  • Propyl gallate 1 3 (3) no Stabilizes animal fats and 0-2.5 mg/kg vegetable oils, meat 0.001-0.01%; products, spices and 0.1% (chewing snacks gum base) 6.
  • 2,4,5-Trihydroxy- 1 3 (3) no Stabilizes Vitamin A, 0.02% butyrophenone (THBP) oils, used in packaging Migration ⁇ 0.005% material 6 7.
  • Catechin E 2 4 (4) yes, ⁇ 2.10 from tea 9.
  • CFSAN Center for Food Safety and Applied Nutrition
  • the required toxicological studies include absorption, metabolism, and excretion studies, acute toxicity, short-term studies, long-term and carcinogenicity studies, reproduction, skin toxicity, and mutagenicity. Some of the additional recommended studies include neurotoxicity and immunotoxicity.
  • the current toxicological studies do not adequately address endocrine disruptor issues, in part because the endpoint measurements and the doses at which LD50 or carcinogenic effects and endocrine disruptive effects are observed are markedly different and in part because different assays are needed.
  • plastics synthesized from bisphenol A have deleterious estrogenic activity, but are now commonly used for food and beverage containers, baby bottles, baby toys, microwaveable containers, and medical items.
  • new plastic formulations that lack biologically detectable estrogenic activity but retain the useful characteristics of current plastics.
  • the already daunting task of developing these new plastic formulations is made more complex by fact that the chemistry of effective additives that lack detectable estrogenic activity has not yet been explored.
  • the development of new formulations that are commercially attractive and that lack biologically detectable estrogenic activity requires innovative combinations of scientific knowledge from several disparate scientific fields: endocrine physiology, molecular biology, environmental health science and polymer chemistry.
  • the only way for to reliably determine that plastic formulations do not have biologically detectable estrogenic activity is for all chemicals in a plastic formulation, as well as those chemicals which leach from the plastic, to test negative for such activity in a series of state-of-the-art assays.
  • the only way to determine the effectiveness of any additives lacking detectable estrogenic activity is to perform shelf life, or durability, studies, perhaps in combination with additional studies on plastic sheets that are exposed to harsh conditions such as extreme temperature, UV and microwave radiation, and chlorine exposure.
  • the present invention relates, generally, to the field of plastics and, more specifically, to plastic materials and food additives that are substantially free of endocrine disruptive chemicals.
  • the present invention provides for the use of certain monomers, or the combination of certain monomers and additives, to make plastic compositions and products which are substantially free of endocrine disruptive chemicals and are therefore useful in products and applications where no endocrine disruptive effects are desired.
  • the present invention also relates to the field of food products and food additives and, more specifically, to food products and food additives that are substantially free of endocrine disruptive chemicals.
  • the present invention also relates to methods for detecting endocrine disruptive activity and, more specifically, to a series of assays which, when performed in combination, provide a novel method for determining the presence of endocrine disruptive activity.

Abstract

The present invention describes plastic materials and food additives that are free or substantially free from endocrine disruptive chemicals. The plastic materials may be used in products which are exposed to individuals in which endocrine disruptive activity is particularly disadvantageous, such as baby bottles, baby toys, food containers, medical containers, animal cages and medical products. The food additives may be used in food products that are ingested by individuals in which endocrine disruptive activity is particularly disadvantageous, such as newborns or the physically infirm. The present invention also describes a series of assays which, when performed in combination, provide a novel method for determining the presence of endocrine disruptive activity.

Description

    CROSS-REFERENCE TO RELATED APPLICATION
  • This application is a continuation of, and incorporates by reference in its entirety, application Ser. No. 10/143,385, filed May 10, 2002. This application claims priority from and incorporates by reference prior U.S. Provisional Patent Application Ser. No. 60/290,595 filed May 10, 2001 in the name of George Bittner, entitled “Materials Void of Adverse Hormonal Activity and Method For Determining the Presence of Hormonally Active Substances in Materials.”[0001]
  • FIELD
  • The present invention relates, generally, to the field of plastics and, more specifically, to plastic materials and food additives that are substantially free of endocrine disruptive chemicals. The present invention also relates to methods for detecting endocrine disruptive activity. [0002]
  • BACKGROUND
  • There is increasing evidence that certain synthetic and natural chemicals, called endocrine disruptors, may act as agonists or antagonists to estrogens or androgens and may interfere in multiple ways with the action of thyroid hormones. For example, endocrine disruptors can mimic or block chemicals naturally found in the body, thereby altering the body's ability to produce hormones, interfering with the ways hormones travel through the body, and altering the concentration of hormones reaching hormone receptors. Although relatively few chemicals have been examined for their endocrine disruptive effect, those chemicals that have shown such an effect are increasingly found in common food and plastic products. [0003]
  • Endocrine disruptors include chemicals such as, for example, polychlorinated biphenyls (PCBs), dioxins and furans. These chemicals are found environmentally in insecticides, herbicides, fumigants, and fungicides that are used in agriculture as well as in the home. Other endocrine disruptors are found in common chemicals such as detergents, dental amalgams and resins that coat the inside of tin cans. In addition, research has found that, because the polymerization process used to make plastics is not complete, unpolymerized monomers with estrogenic activity can migrate out of plastics resulting in deleterious estrogenic, carcinogenic or toxic effects in humans and other species.[0004]
  • By way of example, di(2-ethylhexyl) phthalate (DEHP) is a plasticizer that is a colorless liquid with almost no odor. DEHP is commonly used in producing polyvinyl chloride (PVC) plastic products like toys, vinyl upholstery, shower curtains, adhesives, and coatings. PVC plastic may contain up to 40% DEHP. DEHP, an estrogen-mimicking chemical, has been found to leach from these plastics, thereby creating problems with the materials in contact with the plastic. For example, DEHP has been found to leach from intravenous bags and tubing into the blood and medications being administered to patients. Exposure to DEHP through intravenous bags and tubing presents a health risk that could be avoided through the use of a plastic material that does not contain endocrine disruptive chemicals. [0005]
  • Similarly, bisphenol A is a monomer used to synthesize a number of plastics, such as polycarbonates, epoxy, phenoxy and polysulfone polymers, and is released in significant amounts when these plastics are exposed to water, particularly when heated. Bisphenol A has been shown to possess deleterious estrogenic activity. Nevertheless, plastics manufactured with bisphenol A, such as polycarbonate, are commonly used for food and beverage containers, baby bottles, baby toys, microwaveable containers and medical items. [0006]
  • Molecular Mechanisms by Which Endocrine Disruptors Produce Estrogenic Activity [0007]
  • Endocrine disruptors and natural estrogens share a common mechanism of action. In normal cases, estrogenic activity is produced by binding natural estrogen to an estrogen receptor (ER) within the nucleus of the cell, followed by transcriptional activation of these occupied ERs. When endocrine disruptors are present, normal estrogenic activity is supplanted when endocrine disruptors bind an ER, causing transcriptional activation of the ER even though no natural estrogen is present. Similarly, antiestrogenic activity is produced by endocrine disruptors which bind to ERs but which do not subsequently activate the occupied ER. Finally, selective estrogen receptor modulators (SERMs) bind to ERs, but subsequently activate cellular responses that differ from those activated by the natural estrogens. In general, all but a very small number of molecules that bind to ERs produce some activation of the receptors, as either estrogens or as SERMs. In other words, there are several potential mechanisms by which food antioxidants and other chemicals produce endocrine disruptive activity, but the most common, and best understood, mechanism is via binding to estrogen receptors, thus mimicking the action of natural estrogens. [0008]
  • Effects of Endocrine Disruptors on Human Health [0009]
  • Researchers are exploring the possible link between exposure to endocrine disrupters and breast cancer, testicular cancer, and low sperm count. Deleterious estrogenic effects in humans occur at environmentally-relevant concentrations and include abnormal brain maturation leading to developmental problems or pathologies such as, for example, learning disabilities, attention disorders, abnormalities in motivation, emotion, cognitive development and reproduction, increases in aggressive behavior and changes in sexual orientation. Although the research regarding the effects of these chemicals on human health is just beginning, studies have already been completed on the effect of prenatal exposures to endocrine disruptors on child behavior that have documented developmental injury. [0010]
  • When tested in animal model systems, endocrine disruptors produce deleterious estrogenic effects at concentrations less than those concentrations that are released by certain plastics. For example, research has found that very low dosages of endocrine disruptors exhibit behavioral effects on rodents including, for example, learning disabilities, disorders of attention, motivation, emotion, cognitive development, and changes in sexual orientation and aggressive behavior. Other effects include alterations of reproductive organs of infant and adult males and females such as reduced sperm counts, prostate enlargement, ovarian and uterine dysfunction, and the rate of growth and time to sexual maturation. [0011]
  • As with many hormones, the effects described above are often more dramatic in fetal or developing mammals than in adults. In adults, hormones mainly regulate ongoing physiologic processes. As a result, adult bodies can sometimes compensate or recover from temporary hormonal modulation. Hormonal effects in the fetus are much more profound because they affect gene expression that governs development of organs as well as lifelong hormonal traits, such as receptor numbers and hormonal production. Accordingly, in the case of endocrine disruptors and other developmental toxicants, the timing of exposure may be more important than the dose. [0012]
  • Concern over the effects of endocrine disruptors has increased recently as a result of research showing that plastics commonly used in the home, such as, for example, baby products, food containers and microwaveable products, readily leach endocrine disruptive chemicals. The ubiquity of such plastic items almost certainly contributes to deleterious hormonal effects on human development, beginning prenatally and continuing through puberty and into adulthood. For example, recent data show that levels of bisphenol A in human umbilical cords are 0.2 to 2 micrograms/kg which is consistent with the levels of bisphenol A reported to leach from can linings and plastic baby bottles into vegetable products eaten by babies. Research has shown that a typical daily intake of 700 ml of formula containing 5 ppb bisphenol A from a baby bottle by a 7 kg baby would result in a daily dose of bisphenol A of 0.5 micrograms/kg/day. Furthermore, deleterious developmental changes have been reported in snails, fish, frogs, and rodents at 0.5 to 2 micrograms/kg/day. While it is unlikely that randomized trials will ever directly examine the deleterious developmental effects of bisphenol A on human infants, it is likely that such deleterious effects are produced in humans since basic endocrine mechanisms are not markedly different in rodents and humans. [0013]
  • In part as a response to the recent concern over the effects of endocrine disruptors, the United States government and foreign governments have become active in the testing and regulation of endocrine disruptors. In the United States, the Food Quality Protection Act of 1996 requires that the United States Environmental Protection Agency to develop an endocrine disrupter screening program. The Safe Drinking Water Act of 1996 authorizes the United States Environmental Protection Agency to screen endocrine disruptors found in drinking water. Outside the United States, a number of countries have adopted regulations of endocrine disruptors. For example, the European Union banned the use of phthalates and PVC, known endocrine disruptors, in toys for children under three years of age. [0014]
  • Plastic Monomers and Additives [0015]
  • Plastics are made from monomers that are synthesized into polymers, typically by the application of heat, pressure and, in certain cases, catalysts. The most common monomers from which plastics are made are shown in Table 1. [0016]
    TABLE 1
    Plastic Production
    Monomer Exhibits
    Estrogenic (EA) or
    Carcinogenic
    Monomer Polymer Acronym (CA) Activity
    Ethylene Polyethylene PE2 (LDPE, NT
    HDPE,
    LLDPE)
    Vinylchloride Polyvinylchloride PVC CA
    Propylene Polypropylene PP NT
    Styrene Polystyrene PS NT
    Bisphenol A Polycarbonate1,3 PC EA
    (Epoxy,
    Polysulfone,
    Phenoxy, etc
    Polymers)
    Terephthalic Polyethylene, PET EA
    acid + terephthalate
    ethylene
    glycol
  • Of the monomers used to produce common plastics, polyethylene (PE) is most frequently used because it is inexpensive to synthesize and has extremely versatile properties. Low density PE (LDPE) and linear low density PE (LLDPE) are also widely used, predominantly for extruded materials and film materials which are commonly used to wrap food products. High density PE (HDPE) is used in applications that involve contact with either food products or potable water, such as, for example, film, plastic bottles, and plastic pipe. Many plastic containers for carbonated beverages are now made of polyethylene terephthalate (PET), an excellent barrier material against the migration of carbon dioxide through the container. [0017]
  • Numerous additives are introduced after the synthesis of plastics to enhance their properties. For example, antioxidants are added to increase the useful life of PE and other plastics by preventing, or at least minimizing, the degradation of oxygen which can often cause breakage of molecular chains leading to other undesirable effects such as, for example, discoloration, loss of surface gloss, surface cracking, and lowering of tensile strength. Furthermore, plastics are typically processed into useful shapes at temperatures in excess of 150° centigrade which can lead to thermo-oxidative degradation of molecular weight, ductility, and strength. Table 2 lists some common antioxidants, all of which, with the possible exception of organo-hosphites and thioethers, have estrogenic, carcinogenic or other toxic effects. [0018]
    TABLE 2
    Some Common Antioxidants
    Predicted Predicted Carcinogenic
    Antioxidants Estrogenic Activity or Other Toxic Effects
    (di)Butyl hydroxy toluene Yes Yes
    (BHT)
    Hindered Phenols Yes NT
    Organo-Phosphites NT NT
    Thio-esters NT NT
    2° Acrylamines NT Yes
  • Depending on the material and its desired use, additives other than antioxidants are also used in plastic processing. For example, various pigments including, for example, lead chromates, lead molybdates, lead sulphteranges, chromium oxides, ferric ammonium ferrocyanide, carbon black and phthalo blues are used to add color to PE and other polymers. Common pigments are found in Table 3. Many of these pigments exhibit endocrine disruptive activity or other toxic effects. [0019]
    TABLE 3
    Some Common Pigments
    Predicted Predicted Carcinogenic
    Pigments Estrogenic Activity or Other Toxic Effects
    Lead chromate Yes
    Lead molybdate Yes
    Lead sulphterange Yes
    Chromium oxides Yes
    Ferric ammonium Yes
    Ferrocyanide Yes
    Carbon black No
    Phthalo blues Yes
  • Other classes of plastic additives include plasticizers and stabilizers. For example, esters of phthalic acid, one of the most ubiquitous plasticizers for PVC compounds, all exhibit estogenic disruptive activity and are frequently used in high concentrations, often 40-80% by weight, in plastic materials. This is extremely troublesome because most plasticizers are quite mobile at ambient conditions and, when child-oriented products are made from these materials, children may ingest significant amounts of these compounds when they “taste” their surroundings. [0020]
  • Stabilizers on the other hand, inhibit or reduce damage caused by electromagnetic radiation to PEs and other polymers. Thermal stabilizers for PVC include barium-cadmium soaps, organo-tin compounds, lead compounds, and cadmium-zinc soap. Additives that contain lead and cadmium are clearly toxic. Many of the most common ultraviolet stabilizers for PE such as, for example, benzothiazoles and benzophenones have exhibited endocrine disruptive activity and have rather low molecular weight. Such low molecular weight (1000 daltons) stabilizers are routinely added to PE and are sufficiently mobile to migrate by diffusion from the plastic to the environment. Common stabilizers are found in Table 4. [0021]
    TABLE 4
    Some Common Stabilizers
    Predicted Predicted Carcinogenic
    Stabilizers Estrogenic Activity or Other Toxic Effects
    Barium-cadmium soaps Yes
    Organo-tin compounds No
    Lead compounds Yes
    Cadmium-zinc soaps Yes
    Benzothiazoles Yes
    Benzophenones Yes
  • Some plastic additives are widely used in the United States in spite of their known endocrine disruptive activity. For example, bisphenol A is a monomer used to synthesize various plastics such as, for example, PCs, epoxy, phenoxy, and polysulfone polymers and is released in significant amounts when the polymer is exposed to water, particularly when heated. Although bisphenol A has been demonstrated to exhibit endocrine disruptive activity, PC products are commonly used for food and beverage containers, baby bottles, baby toys, microwaveable containers, and medical items. PC production has rapidly increased in the United States and, consequently, bisphenol A is now one of the top 50 chemicals produced in the U.S. [0022]
  • Due to federal regulations and commercial concerns, most monomers or additives with carcinogenic or other lethally toxic effects are not found in plastics routinely contacted by humans or that contact food. The U.S. Food and Drug Administration (FDA) has long recognized the problem of migration of chemicals out of plastics and other products and has strictly regulated the antioxidants and other agents in plastic compounds that contact food. The FDA has required that such additives be tested for carcinogenic properties and other acute toxic effects. Less toxic stabilizers such as tin soaps are approved by the FDA for food contact, but less expensive, albeit toxic, stabilizers such as, for example, barium, cadmium, and lead compounds, are approved for use in other applications such as electronics parts that do not contact food. Although tested for carcinogenic activity and acute toxicity, chemicals used in plastics that contact humans directly or that contact food have not been tested for estrogenic activity and, as a result, the disruptive activity has not yet been regulated. Furthermore, the formulations used to manufacture plastics usually are not required to be revealed to other companies, consumers or governmental agencies. Even when the manufacturer divulges the primary monomer or polymer used in a plastic, it rarely reveals all additives used in the formulation. [0023]
  • The United States Food Quality Protection Act requires that chemicals be tested and regulated for endocrine disruptive activity. In furtherance thereof, a multimillion-dollar request for proposal for validation of tests on endocrine disruptive activity has recently been awarded by the U.S. Environmental Protection Administration. The need for, and regulation of, safer plastics with less endocrine disruptive activity is now being driven by well-documented scientific findings. [0024]
  • Numerous products have been affected by regulations or consumer concerns in other developed countries. For example, several European Union countries recently banned the use of phthalates and PVC plastics in toys for children under three. Consequently, plastic bottles or teething rings in Europe, Japan and the U.S. are no longer made from PVC due to concerns by the public and commercial retailers about the deleterious health effects of phthalates and PVC. As a second example, the use of many PC products such as, for example, baby bottles and dishes, has recently decreased dramatically in Japan due to public awareness that these PCs release bisphenol A whose estrogenic activity has potentially deleterious effects on reproductive functions and many other physiological systems in humans. [0025]
  • Although the concern over the presence of endocrine disruptive chemicals in plastics is escalating, no plastic product on sale in the United States or international market has been demonstrated to be free of endocrine disruptive chemicals. Therefore, the need remains for a plastic material that is substantially free of endocrine disruptive chemicals. [0026]
  • Food Additives [0027]
  • More than 2,800 different food additives are routinely used to maintain product freshness and quality and help retard physical, chemical and biological deterioration. Table 5 lists some commonly used food additives and their intended function. [0028]
    TABLE 5
    Commonly Used Food Additives and Intended Function
    Additive Intended function Examples
    Antimicrobial Prevent microbial Sodium benzoate,
    preservatives growth calcium propionate, potassium
    sorbate, sodium nitrite
    Antioxidants Prevent rancidity BHT, BHA, propyl gallate,
    tocopherols
    Flavor Supplement, enhance or MSG, disodium inosinate,
    enhancers modify original flavor disodium guanylate
    Synergists Increase the effects of Citric acid, tricalcium
    other food additives phosphate and other
    phosphates, ascorbic acid
  • Antioxidants are one of the most important and most widely used food additives. The oldest and most common antioxidants that are deemed suitable for food contact service belong to a class of materials known as hindered phenols. The most ubiquitous of these is BHT. Since 1949, BHT has been widely used as an antioxidant food additive in large part because it is very inexpensive and because it was routinely assumed to be non-toxic. BHT works by intercepting and reducing free radicals that are associated with the oxidation process. However, primary data suggests that BHT exhibits endocrine disruptive activity. BHT is therefore almost certainly unsuitable as an antioxidant in foods. [0029]
  • Table 6 lists 12 common food antioxidants. Some antioxidants such as, for example, BHA, BHT, tocopherols, TBHQ, gallates and THBP, are widely used due to their overall efficacy. Others are “natural” antioxidants isolated from plants, although they are less commonly used in the manufacture of food products at present. The estrogenic activity of food antioxidants has not yet been examined, but many food antioxidants would be expected to exhibit estrogenic activity because they contain a phenolic ring. Since many estrogenic chemicals have effects at picomolar to nanomolar levels and antioxidants are often added to foodstuffs in micromolar to millimolar concentrations (i.e. 1000× greater), such estrogenic antioxidants could be a significant health hazard, particularly to a developing fetus. The need exists, therefore for food additives substantially free of endocrine disruptive activity. [0030]
    TABLE 6
    Antioxidants Permitted in Foods in the United States
    # of # —OHB
    Benzene (on QSARC ADID
    Primary Antioxidants RingsA benz) RBA Use or Origin Approved
    1. Butylated 1 1 (1) yes, −5 Fats and oils, 0-0.5 mg/kg
    hydroxyanisole (BHA) confectioneries, food- 0.01-0.1%
    coating material, and
    2. Butylated 1 1 (1) yes, −5 Low fat foods, fish 0-0.125 mg/kg
    hydroxytoulene (BHT) products, packaging 0.005-0.02%
    materials6
    3. Tocopherols 1 1 (1) yes Major lipid soluble 0.15-2 mg/kg
    antioxidant
    4. Tert-Butylhydroquinone 1 2 (2) yes Stabilizes fats, oils, 0-0.2 mg/kg
    (TBHQ) confectionery products,
    etc
    5. Propyl gallate 1 3 (3) no Stabilizes animal fats and 0-2.5 mg/kg
    vegetable oils, meat 0.001-0.01%;
    products, spices and 0.1% (chewing
    snacks gum base)
    6. 2,4,5-Trihydroxy- 1 3 (3) no Stabilizes Vitamin A, 0.02%
    butyrophenone (THBP) oils, used in packaging Migration <0.005%
    material6
    7. CurcuminE 2 2 (2) yes from tumeric
    8. CatechinE 2 4 (4) yes, −2.10 from tea
    9. SesaminE 2 0 (0) ? from sesame seeds
    10. SesamolinE 2 0 (0) ? from sesame seeds
    11. CarnosineE 0 1 (0) ? from rosemary
    12. Glycyrrhizic AcidE 0 4 (0) ? from licorice
  • Testing [0031]
  • The process of obtaining an approval for food additives for human use is regulated by Center for Food Safety and Applied Nutrition (CFSAN) at the FDA under the Federal Food Drug and Cosmetic Act. The required toxicological studies include absorption, metabolism, and excretion studies, acute toxicity, short-term studies, long-term and carcinogenicity studies, reproduction, skin toxicity, and mutagenicity. Some of the additional recommended studies include neurotoxicity and immunotoxicity. Despite the extensive number of studies required by CFSAN, the current toxicological studies do not adequately address endocrine disruptor issues, in part because the endpoint measurements and the doses at which LD50 or carcinogenic effects and endocrine disruptive effects are observed are markedly different and in part because different assays are needed. [0032]
  • A vast majority of the 80,000 chemicals currently sold on the U.S. and international market have not been tested for estrogenic effects. One significant reason for the lack of testing has been the lack of a reliable test procedure for testing the presence of endocrine disruptive activity. The need exists, therefore for a reliable, comprehensive test for the presence of endocrine disruptors in plastics and foods. [0033]
  • Unique/Innovative Approach in Development of New Plastic Formulations [0034]
  • As discussed above, plastics synthesized from bisphenol A, such as polycarbonate and other plastics, have deleterious estrogenic activity, but are now commonly used for food and beverage containers, baby bottles, baby toys, microwaveable containers, and medical items. Hence, there is a demand for new plastic formulations that lack biologically detectable estrogenic activity but retain the useful characteristics of current plastics. The already daunting task of developing these new plastic formulations is made more complex by fact that the chemistry of effective additives that lack detectable estrogenic activity has not yet been explored. The development of new formulations that are commercially attractive and that lack biologically detectable estrogenic activity requires innovative combinations of scientific knowledge from several disparate scientific fields: endocrine physiology, molecular biology, environmental health science and polymer chemistry. The only way for to reliably determine that plastic formulations do not have biologically detectable estrogenic activity is for all chemicals in a plastic formulation, as well as those chemicals which leach from the plastic, to test negative for such activity in a series of state-of-the-art assays. The only way to determine the effectiveness of any additives lacking detectable estrogenic activity is to perform shelf life, or durability, studies, perhaps in combination with additional studies on plastic sheets that are exposed to harsh conditions such as extreme temperature, UV and microwave radiation, and chlorine exposure. [0035]
  • Summary
  • The present invention relates, generally, to the field of plastics and, more specifically, to plastic materials and food additives that are substantially free of endocrine disruptive chemicals. Specifically, the present invention provides for the use of certain monomers, or the combination of certain monomers and additives, to make plastic compositions and products which are substantially free of endocrine disruptive chemicals and are therefore useful in products and applications where no endocrine disruptive effects are desired. [0036]
  • The present invention also relates to the field of food products and food additives and, more specifically, to food products and food additives that are substantially free of endocrine disruptive chemicals. [0037]
  • The present invention also relates to methods for detecting endocrine disruptive activity and, more specifically, to a series of assays which, when performed in combination, provide a novel method for determining the presence of endocrine disruptive activity. [0038]

Claims (10)

What is claimed is:
1. A polymeric material substantially void of endocrine disruptive chemicals comprising a monomer wherein said monomer is polymerized to form a polymeric material substantially void of endocrine disruptive chemicals.
2. The polymeric material of claim 1 wherein said monomer is selected from the group consisting of ethylene and propylene.
3. An article made from the polymeric material as recited in claim 1.
4. An article made from the polymeric material as recited in claim 1 selected from the group consisting of baby bottles, baby toys, medical devices, food containers, beverage containers, medical containers and animal cages.
5. A polymeric material substantially void of endocrine disruptive chemicals comprising a monomer wherein said monomer is polymerized in the presence of an antioxidant to form a polymeric material substantially void of endocrine disruptive chemicals.
6. The polymeric material recited in claim 5 wherein said monomer is selected from the group consisting of ethylene and propylene.
7. An article made from the polymeric material as recited in claim 5.
8. A process for preparing a polymeric material substantially void of endocrine disruptive chemicals, said process comprising the steps of:
(a) polymerizing a monomer selected from the group consisting of ethylene and propylene; and
(b) processing said polymerized monomer to form a polymeric material substantially void of endocrine disruptive chemicals.
9. A process for preparing a polymeric material substantially void of endocrine disruptive chemicals, said process comprising the steps of:
(a) polymerizing a monomer selected from the group consisting of ethylene and propylene; and
(b) processing said polymerized monomer with an antioxidant to form a polymeric material substantially void of endocrine disruptive chemicals.
10. A food product substantially void of endocrine chemicals comprised by processing said food product with additives selected from the group consisting of propyl gallate, octyl gallate, dodecyl gallate, ethoxyquin, carnosine, glycyrrhizic acid, sesamin, sesamolin, monoisopropyl citrate and thiodiproprionic acid.
US10/852,026 2001-05-10 2004-05-24 Materials and food additives free of endocrine disruptive chemicals Abandoned US20040214926A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US10/852,026 US20040214926A1 (en) 2001-05-10 2004-05-24 Materials and food additives free of endocrine disruptive chemicals
US13/033,493 US20110168657A1 (en) 2001-05-10 2011-02-23 Materials and Food Additives Free of Endocrine Disruptive Activity

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US29059501P 2001-05-10 2001-05-10
US10/143,385 US6894093B2 (en) 2001-05-10 2002-05-10 Materials free of endorine disruptive chemicals
US10/852,026 US20040214926A1 (en) 2001-05-10 2004-05-24 Materials and food additives free of endocrine disruptive chemicals

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US10/143,385 Continuation US6894093B2 (en) 2001-05-10 2002-05-10 Materials free of endorine disruptive chemicals

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/033,493 Continuation US20110168657A1 (en) 2001-05-10 2011-02-23 Materials and Food Additives Free of Endocrine Disruptive Activity

Publications (1)

Publication Number Publication Date
US20040214926A1 true US20040214926A1 (en) 2004-10-28

Family

ID=23116706

Family Applications (3)

Application Number Title Priority Date Filing Date
US10/143,385 Expired - Lifetime US6894093B2 (en) 2001-05-10 2002-05-10 Materials free of endorine disruptive chemicals
US10/852,026 Abandoned US20040214926A1 (en) 2001-05-10 2004-05-24 Materials and food additives free of endocrine disruptive chemicals
US13/033,493 Abandoned US20110168657A1 (en) 2001-05-10 2011-02-23 Materials and Food Additives Free of Endocrine Disruptive Activity

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US10/143,385 Expired - Lifetime US6894093B2 (en) 2001-05-10 2002-05-10 Materials free of endorine disruptive chemicals

Family Applications After (1)

Application Number Title Priority Date Filing Date
US13/033,493 Abandoned US20110168657A1 (en) 2001-05-10 2011-02-23 Materials and Food Additives Free of Endocrine Disruptive Activity

Country Status (2)

Country Link
US (3) US6894093B2 (en)
WO (1) WO2003000751A1 (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060069809A1 (en) * 2004-07-01 2006-03-30 Bertrand Serlet State based synchronization
US20060288053A1 (en) * 2005-06-21 2006-12-21 Apple Computer, Inc. Apparatus and method for peer-to-peer N-way synchronization in a decentralized environment
US20080034009A1 (en) * 2006-08-04 2008-02-07 Apple Computer, Inc. Method and system for using global equivalency sets to identify data during peer-to-peer synchronization
US20080165807A1 (en) * 2007-01-05 2008-07-10 Apple Computer, Inc. Wide Area Peer-to-Peer Synching in a Decentralized Environment
US20080168183A1 (en) * 2007-01-08 2008-07-10 Apple Computer, Inc. N-way synchronization of data
US20080199595A1 (en) * 2007-02-15 2008-08-21 Mccormick & Company Salt replacing composition, process for its preparation and food systems containing such composition
US20120074091A1 (en) * 2010-09-24 2012-03-29 Himelstein Walter D Safety-coated glass bottle
US8495015B2 (en) 2005-06-21 2013-07-23 Apple Inc. Peer-to-peer syncing in a decentralized environment
US9409219B2 (en) 2011-02-07 2016-08-09 Valspar Sourcing, Inc. Compositions for containers and other articles and methods of using same
US10113027B2 (en) 2014-04-14 2018-10-30 Swimc Llc Methods of preparing compositions for containers and other articles and methods of using same
US10435199B2 (en) 2012-08-09 2019-10-08 Swimc Llc Compositions for containers and other articles and methods of using same
US10526502B2 (en) 2012-08-09 2020-01-07 Swimc Llc Container coating system
US11130881B2 (en) 2010-04-16 2021-09-28 Swimc Llc Coating compositions for packaging articles and methods of coating
US11130835B2 (en) 2015-11-03 2021-09-28 Swimc Llc Liquid epoxy resin composition useful for making polymers

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6890625B2 (en) * 2001-02-05 2005-05-10 Awi Licensing Company Surface covering having gloss in-register and method of making
US6894093B2 (en) * 2001-05-10 2005-05-17 George D. Bittner Materials free of endorine disruptive chemicals
US20080064795A1 (en) * 2006-09-08 2008-03-13 George Bittner Materials free of endocrine disruptive activity
US20090001101A1 (en) * 2007-06-28 2009-01-01 Ezstella, Llc Powder Dispenser
DE102009023651B4 (en) * 2009-05-26 2021-07-01 Aesculap Ag Process for the production of a polyethylene doped with a stabilizer and use of a polyethylene produced by this process
US8669315B2 (en) 2011-08-22 2014-03-11 Sabic Innovative Plastics Ip B.V. Polycarbonate compositions and methods for the manufacture and use thereof
US20150183929A1 (en) 2013-12-30 2015-07-02 Sabic Innovative Plastics Ip B.V Bisphenol polyether oligomers, methods of manufacture, and polycarbonates made therefrom
US9238609B2 (en) 2014-05-23 2016-01-19 Sabic Global Technologies B.V. Dicarboxylic acid monomers and methods of making and using the same
WO2019113520A1 (en) * 2017-12-07 2019-06-13 Joshua Munoz Edc-free biopolymer based compositions and uses thereof

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2843563A (en) * 1955-01-27 1958-07-15 Eastman Kodak Co Polyethylene compositions stabilized with acyl derivatives of 1, 2, 4-trihydroxybenzene
US2934518A (en) * 1956-06-20 1960-04-26 Union Carbide Corp Poly (ethylene oxide) stabilized with propyl gallate
US3849516A (en) * 1972-04-03 1974-11-19 Exxon Research Engineering Co Grafted polyolefins as stabilizer components in polyolefins
US4824885A (en) * 1986-07-23 1989-04-25 Enichem Sintesi S.P.A. Process of (co) polymerization of alpha-olefins in the presence of antioxidants
US6156361A (en) * 1993-09-17 2000-12-05 Remac, Inc. Method for treating a food product
US6166117A (en) * 1997-06-11 2000-12-26 Kuraray Co., Ltd. Water-soluble film
US6197357B1 (en) * 1998-05-28 2001-03-06 University Of Massachusetts Refined vegetable oils and extracts thereof
US6255413B1 (en) * 1997-12-16 2001-07-03 Phillips Petroleum Company Process to produce branched polymers from ethylene feedstock
US20010031307A1 (en) * 2000-01-14 2001-10-18 Deena Krestel-Rickert Spent hens for use in pet food
US6355215B1 (en) * 1999-03-10 2002-03-12 Implex Corp. Wear-resistant olefinic medical implant and thermal treatment container therefor
US6448315B1 (en) * 1999-02-17 2002-09-10 Bone Support Ab Method for the preparation of UHMWPE doped with an antioxidant and an implant made thereof

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4529606A (en) * 1984-08-20 1985-07-16 General Foods Inc. Citrus flavored beverage in polyethylene containers
US5350786A (en) * 1986-06-30 1994-09-27 Enichem Synthesis S.P.A. Process of (co)polymerization of α-olefins in the presence of stabilizers
US5574118A (en) * 1990-11-02 1996-11-12 Dsm Copolymer, Inc. Olefin polymers containing bound antioxidant
US6143854A (en) * 1993-08-06 2000-11-07 Exxon Chemical Patents, Inc. Polymerization catalysts, their production and use
US5723291A (en) * 1993-09-01 1998-03-03 The Regents Of The University Of California Methods for screening compounds for estrogenic activity
US20010000258A1 (en) * 1994-05-24 2001-04-12 Exxon Chemical Patents Inc. Articles made from polypropylene, higher alpha-olefin copolymers
US6190706B1 (en) * 1997-12-23 2001-02-20 Wm. Wrigley Jr. Company Chewing gum and gum bases having reduced adhesion to environmental surfaces and method for making
JP2000053116A (en) * 1998-08-05 2000-02-22 Grand Polymer:Kk Resin for food container, and resin composition
US6894093B2 (en) * 2001-05-10 2005-05-17 George D. Bittner Materials free of endorine disruptive chemicals

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2843563A (en) * 1955-01-27 1958-07-15 Eastman Kodak Co Polyethylene compositions stabilized with acyl derivatives of 1, 2, 4-trihydroxybenzene
US2934518A (en) * 1956-06-20 1960-04-26 Union Carbide Corp Poly (ethylene oxide) stabilized with propyl gallate
US3849516A (en) * 1972-04-03 1974-11-19 Exxon Research Engineering Co Grafted polyolefins as stabilizer components in polyolefins
US4824885A (en) * 1986-07-23 1989-04-25 Enichem Sintesi S.P.A. Process of (co) polymerization of alpha-olefins in the presence of antioxidants
US6156361A (en) * 1993-09-17 2000-12-05 Remac, Inc. Method for treating a food product
US6166117A (en) * 1997-06-11 2000-12-26 Kuraray Co., Ltd. Water-soluble film
US6255413B1 (en) * 1997-12-16 2001-07-03 Phillips Petroleum Company Process to produce branched polymers from ethylene feedstock
US6197357B1 (en) * 1998-05-28 2001-03-06 University Of Massachusetts Refined vegetable oils and extracts thereof
US6448315B1 (en) * 1999-02-17 2002-09-10 Bone Support Ab Method for the preparation of UHMWPE doped with an antioxidant and an implant made thereof
US6355215B1 (en) * 1999-03-10 2002-03-12 Implex Corp. Wear-resistant olefinic medical implant and thermal treatment container therefor
US20010031307A1 (en) * 2000-01-14 2001-10-18 Deena Krestel-Rickert Spent hens for use in pet food

Cited By (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7730026B2 (en) 2004-07-01 2010-06-01 Apple Inc. Method and system using reusable state information for synchronization and maintenance of data
US8868493B2 (en) 2004-07-01 2014-10-21 Apple Inc. Method and system using reusable state information for synchronization and maintenance of data
US20060069809A1 (en) * 2004-07-01 2006-03-30 Bertrand Serlet State based synchronization
US8332352B2 (en) 2004-07-01 2012-12-11 Apple Inc. Method and system using reusable state information for synchronization and maintenance of data
US20100198784A1 (en) * 2004-07-01 2010-08-05 Apple Inc. Method and System Using Reusable State Information for Synchronization and Maintenance of Data
US8495015B2 (en) 2005-06-21 2013-07-23 Apple Inc. Peer-to-peer syncing in a decentralized environment
US7523146B2 (en) 2005-06-21 2009-04-21 Apple Inc. Apparatus and method for peer-to-peer N-way synchronization in a decentralized environment
US20060288053A1 (en) * 2005-06-21 2006-12-21 Apple Computer, Inc. Apparatus and method for peer-to-peer N-way synchronization in a decentralized environment
US8635209B2 (en) 2005-06-21 2014-01-21 Apple Inc. Peer-to-peer syncing in a decentralized environment
US8321374B2 (en) 2005-06-21 2012-11-27 Apple Inc. Peer-to-peer N-way syncing in decentralized environment
US7860826B2 (en) 2006-08-04 2010-12-28 Apple Inc. Method and system for using global equivalency sets to identify data during peer-to-peer synchronization
US20080034009A1 (en) * 2006-08-04 2008-02-07 Apple Computer, Inc. Method and system for using global equivalency sets to identify data during peer-to-peer synchronization
US8868491B2 (en) 2006-08-04 2014-10-21 Apple Inc. Method and system for using global equivalency sets to identify data during peer-to-peer synchronization
US20100299444A1 (en) * 2007-01-05 2010-11-25 Apple Inc. Wide Area Peer-to-Peer Synching in a Decentralized Environment
US7760767B2 (en) 2007-01-05 2010-07-20 Apple Inc. Wide area peer-to-peer synching in a decentralized environment
US20080165807A1 (en) * 2007-01-05 2008-07-10 Apple Computer, Inc. Wide Area Peer-to-Peer Synching in a Decentralized Environment
US20080168183A1 (en) * 2007-01-08 2008-07-10 Apple Computer, Inc. N-way synchronization of data
US8250397B2 (en) 2007-01-08 2012-08-21 Apple Inc. N-way synchronization of data
US20100106687A1 (en) * 2007-01-08 2010-04-29 Apple Inc. N-Way Synchronization of Data
US7657769B2 (en) 2007-01-08 2010-02-02 Marcy M Scott N-way synchronization of data
US20080199595A1 (en) * 2007-02-15 2008-08-21 Mccormick & Company Salt replacing composition, process for its preparation and food systems containing such composition
US11130881B2 (en) 2010-04-16 2021-09-28 Swimc Llc Coating compositions for packaging articles and methods of coating
US20120074091A1 (en) * 2010-09-24 2012-03-29 Himelstein Walter D Safety-coated glass bottle
US11053409B2 (en) 2011-02-07 2021-07-06 Jeffrey Niederst Compositions for containers and other articles and methods of using same
US10294388B2 (en) 2011-02-07 2019-05-21 Swimc Llc Compositions for containers and other articles and methods of using same
US9409219B2 (en) 2011-02-07 2016-08-09 Valspar Sourcing, Inc. Compositions for containers and other articles and methods of using same
US11634607B2 (en) 2011-02-07 2023-04-25 Swimc Llc Compositions for containers and other articles and methods of using same
US10435199B2 (en) 2012-08-09 2019-10-08 Swimc Llc Compositions for containers and other articles and methods of using same
US10526502B2 (en) 2012-08-09 2020-01-07 Swimc Llc Container coating system
US10894632B2 (en) 2012-08-09 2021-01-19 Swimc Llc Compositions for containers and other articles and methods of using same
US11306218B2 (en) 2012-08-09 2022-04-19 Swimc Llc Container coating system
US11628974B2 (en) 2012-08-09 2023-04-18 Swimc Llc Compositions for containers and other articles and methods of using same
US10745514B2 (en) 2014-04-14 2020-08-18 Swimc Llc Methods of preparing compositions for containers and other articles and methods of using same
US10113027B2 (en) 2014-04-14 2018-10-30 Swimc Llc Methods of preparing compositions for containers and other articles and methods of using same
US11525018B2 (en) 2014-04-14 2022-12-13 Swimc Llc Methods of preparing compositions for containers and other articles and methods of using same
US11130835B2 (en) 2015-11-03 2021-09-28 Swimc Llc Liquid epoxy resin composition useful for making polymers

Also Published As

Publication number Publication date
WO2003000751A1 (en) 2003-01-03
US20110168657A1 (en) 2011-07-14
US6894093B2 (en) 2005-05-17
US20030065061A1 (en) 2003-04-03

Similar Documents

Publication Publication Date Title
US20110168657A1 (en) Materials and Food Additives Free of Endocrine Disruptive Activity
Alfei et al. Nanotechnology application in food packaging: A plethora of opportunities versus pending risks assessment and public concerns
Enescu et al. Recent advances and challenges on applications of nanotechnology in food packaging. A literature review
Bang et al. Human risk assessment of endocrine‐disrupting chemicals derived from plastic food containers
Eskandarabadi et al. Active intelligent packaging film based on ethylene vinyl acetate nanocomposite containing extracted anthocyanin, rosemary extract and ZnO/Fe-MMT nanoparticles
CN101200555A (en) Materials free of endocrine disruptive activity
Kumar et al. Toxicity of food additives
Gaikwad et al. Novel polyisoprene based UV-activated oxygen scavenging films and their applications in packaging of beef jerky
Dong et al. Soluble soybean polysaccharide/gelatin active edible films incorporated with curcumin for oil packaging
Garvey Food pollution: a comprehensive review of chemical and biological sources of food contamination and impact on human health
Manoli et al. Food containers and packaging materials as possible source of hazardous chemicals to food
Esfahani et al. Fabrication and characterization of a smart film based on cassava starch and pomegranate peel powder for monitoring lamb meat freshness
Gaikwad et al. The effect of trans-polyisoprene/LDPE based active films on oxidative stability in roasted peanuts
Giordano et al. Maternal diet and the risk of hypospadias and cryptorchidism in the offspring
Du et al. Prevalence of novel and traditional synthetic phenolic antioxidants in baby food from China: A dominant pathway for infant exposure
Lalani et al. Food additives, benefits, and side effects: A review article
JP2009114417A (en) Material without endocrine-disrupting action
Boukoufi et al. Food-inspired innovations to improve the stability of active pharmaceutical ingredients
Nikova et al. Occurrence of meso/micro/nano plastics and plastic additives in food from food packaging
Foltynowicz et al. Oxygen scavengers applications in the dairy industry
US20080182965A1 (en) Materials Free of Endocrine Disruptive Activity
Garban et al. Xenobiochemistry at the interface of packaging materials-food. Note I. Packaging materials and specific interactions in vivo
Stringer et al. Determination of the composition and quantity of phthalate ester additives in pvc children’s toys
Adenuga Occurrence and dietary exposure to phthalates in the US population–a contextual review
Raghul Food, feed, and life on Plastic.

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION