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Natural Products Association


image Type Nonprofit Focus Natural products Location

Dr. Daniel Fabricant, Ph.D., Executive Director and CEO

Dr. Corey Hilmas, MD, Ph.D., Senior Vice President of Scientific and Regulatory Affairs

The Natural Products Association or NPA (formerly the NNFA, or the National Nutritional Foods Association) is the largest and oldest nonprofit organization representing the interests of manufacturers and retailers of the natural products industry, which includes organic and health foods, dietary supplements, natural ingredient cosmetics, and other similar products. The organization includes more than 1,900 members accounting for more than 10,000 retailers, manufacturers, wholesalers and distributors of natural products.

The Natural Products Association was founded in 1936 as the American Health Foods Association (AHFA) to inform consumers about the benefits of the natural nutrition industry. In 1937, the association changed its name to the Natural Health Foods Association (NHFA), representing retailers, manufacturers and distributors. In 1943, NHFA was renamed to the National Dietary Foods Association (NDFA). In 1970, NDFA officially became the National Nutritional Foods Association (NNFA). The organization renamed itself the Natural Products Association or NPA in June 2006. NPA has grown from a small group of members in 1936 to approximately 2,000 in 2013.

The science and regulatory affairs department oversees the association's third-party certification programs.

The NPA Natural Seal is described as the first and only natural products certification in the United States. Currently only personal care and home care products and ingredients can be certified. The association requires that certified products must be at least 95 percent natural ingredients or ingredients from natural sources, excluding water. NPA-certified products must use natural ingredients, avoid ingredients with health risks, don’t use animal testing, and include biodegradable or recycled material in the packaging. Products also must list all ingredients on the package label, and NPA requires 100 percent natural fragrances and colorants. Certified products are said to appear in more than 85,000 stores nationwide. NPA has certified more than 1,200 products and ingredients since 2008, including well-known brands like Burt's Bees and J.R. Watkins.

The Natural Products Association launched the first third-party Good Manufacturing Practices (GMP) program for the manufacturing of dietary supplements and ingredients in 1999. NPA GMP Certification is awarded to companies that comply with the NPA GMP standard as verified through comprehensive third-party inspections of facilities and GMP-related documentation. More than 70 companies are known to have achieved certification. NPA also offers a series of GMP training seminars across the United States each year.



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Nutrament


Nutrament is a nutritional vitamin drink currently supplied by Nestlé Health Science. It was originally distributed by Mead Johnson Nutritionals, beginning in the late 1960s. Current flavors on the market are vanilla, chocolate, strawberry, coconut, banana, cappucino, dulce de leche, mango and eggnog. The product is supplied as individual 12 fluid ounce servings in pull-top cans. According to the product's website, Nutrament currently is available only in regional areas of the United States, mostly in New York and Florida, although internet stores also have it available.

In official records, it is described as "Nutritionally Complete Food Consisting Principally of Milk Solids, Maltose-Dextrins, Soy Flour, Sucrose". The original purpose of Nutrament was as a recovery drink for athletes. Late in the 1960s, a powdered form was offered for mixing with milk, but that brand registration was not renewed in 1988 and officially expired in 1992, still owned by Mead Johnson.

The current formulation is made of skim milk, the sweeteners sugar and corn syrup, various vegetable oils, flavorings, and vitamins and minerals. Because of its high milk content, lactose intolerant people would need to take an enzyme supplement to digest the drink properly, or avoid it altogether. For other persons, the product is considered easy to digest and is a good protein source. It has been used as a meal substitute in dieting, because of its calorie portion control. Because of its low fiber content, it is useful for low-residue diets.



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Nutrilite


Nutrilite is a brand of mineral, vitamin, and dietary supplements created in 1934 by Dr. Carl F. Rehnborg. Nutrilite products are currently manufactured by Access Business Group, a subsidiary of Alticor whose products are sold via the Amway worldwide. The Nutrilite brand is known as Nutriway in Denmark, Finland, Norway, Sweden, Turkey, Australia and New Zealand.

Carl F. Rehnborg created the second multi-vitamin in the 1930s. His time in China between roughly 1917 and 1927 exposed him to experiences in which he realized the role vitamins and nutrients impacted general health. He began selling his vitamins as the California Vitamin company and renamed it in 1939 to Nutrilite. In 1945, he invented the multi-level marketing, door-to-door, selling system to distribute his vitamins. Two men, Lee S. Mytinger and William S. Casselberry became exclusive national distributor in 1945 and operated a company to distribute the vitamins.

The founders of Amway, billionaires Jay Van Andel and Rich DeVos, began as independent distributors selling Nutrilite products in 1949, at a time when the product's previous distributors (Mytinger and Casselberry, Inc.) were involved in a dispute with the U.S. Food and Drug Administration (FDA), which accused them of false advertising. They rose rapidly to being top-selling distributors. Concerned about the FDA dispute, Van Andel and DeVos launched a new company, the American Way, (later known as Amway), to use the MLM system for other household products. The FDA/Mytinger-Cassleberry dispute, which went to the United States Supreme Court, was resolved in favor of the FDA in the 1960s.

Amway bought a controlling interest in the company in 1972, and took over complete ownership in 1994.

In 2001, five Nutrilite products were the first dietary supplements to be certified by NSF International.



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NutriRice


NutriRice is a kind of recomposed fortified rice. The NutriRice process is a way of rice fortification utilized hot extrusion technology not only addresses the problem of hidden hunger but also meets the challenge of implementing rice fortification.

Rice fortification presents numerous technical problems. Micronutrients cannot be simply added to the kernels, because they do not stay where they are needed and the traditional soaking and rinsing of rice with water prior to cooking removes most of the added nutrients.

In the hot extrusion process, rice flour and micronutrients are transformed into a product visually resembling natural rice. Thereby, vitamins and minerals are embedded and protected from segregation and from being removed through rinsing or leaching out during washing and cooking.

The production of NutriRice offers the unique possibility to efficiently fortify rice with multiple micronutrients. Vitamins and minerals such as vitamin A and B family as well as iron and zinc can be chosen for inclusion.

Most Ultra Rice products are designed for blending with white rice in a ratio of 1:100 and intended to be as close as possible to rice in smell, taste, and texture.

It was originally used in Brazil, Colombia, and India, but through a partnership with World Vision the product is slated to be used in many developing countries receiving aid.

With respect to fortified rice properties, such as wash stability, shelf stability, cooking behavior, visual appearance, and cooked rice texture, hot extrusion can be recommended to produce the fortified rice kernel. The fortified rice kernel through hot extrusion most closely resembles natural rice after cooking.

The children of 600 migrant workers attend the Dandelion Middle School in Beijing, some of them as resident pupils. In 2008, as part of a pilot project, all pupils at the school were given NutriRice for a period of 8 months. During the eight-month trial period, the effects of malnutrition were reduced by 50%, thus raising the pupils’ general nutritional status to the average urban level.



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Nutriway


Nutrilite is a brand of mineral, vitamin, and dietary supplements created in 1934 by Dr. Carl F. Rehnborg. Nutrilite products are currently manufactured by Access Business Group, a subsidiary of Alticor whose products are sold via the Amway worldwide. The Nutrilite brand is known as Nutriway in Denmark, Finland, Norway, Sweden, Turkey, Australia and New Zealand.

Carl F. Rehnborg created the second multi-vitamin in the 1930s. His time in China between roughly 1917 and 1927 exposed him to experiences in which he realized the role vitamins and nutrients impacted general health. He began selling his vitamins as the California Vitamin company and renamed it in 1939 to Nutrilite. In 1945, he invented the multi-level marketing, door-to-door, selling system to distribute his vitamins. Two men, Lee S. Mytinger and William S. Casselberry became exclusive national distributor in 1945 and operated a company to distribute the vitamins.

The founders of Amway, billionaires Jay Van Andel and Rich DeVos, began as independent distributors selling Nutrilite products in 1949, at a time when the product's previous distributors (Mytinger and Casselberry, Inc.) were involved in a dispute with the U.S. Food and Drug Administration (FDA), which accused them of false advertising. They rose rapidly to being top-selling distributors. Concerned about the FDA dispute, Van Andel and DeVos launched a new company, the American Way, (later known as Amway), to use the MLM system for other household products. The FDA/Mytinger-Cassleberry dispute, which went to the United States Supreme Court, was resolved in favor of the FDA in the 1960s.

Amway bought a controlling interest in the company in 1972, and took over complete ownership in 1994.

In 2001, five Nutrilite products were the first dietary supplements to be certified by NSF International.



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Papain


imagePapain

Papain, also known as papaya proteinase I, is a cysteine protease (EC 3.4.22.2) enzyme present in papaya (Carica papaya) and mountain papaya (Vasconcellea cundinamarcensis).

Papain belongs to a family of related proteins with a wide variety of activities, including endopeptidases, aminopeptidases, dipeptidyl peptidases and enzymes with both exo- and endo-peptidase activity. Members of the papain family are widespread, found in baculoviruses, eubacteria, yeast, and practically all protozoa, plants and mammals. The proteins are typically lysosomal or secreted, and proteolytic cleavage of the propeptide is required for enzyme activation, although bleomycin hydrolase is cytosolic in fungi and mammals. Papain-like cysteine proteinases are essentially synthesised as inactive proenzymes (zymogens) with N-terminal propeptide regions. The activation process of these enzymes includes the removal of propeptide regions, which serve a variety of functions in vivo and in vitro. The pro-region is required for the proper folding of the newly synthesised enzyme, the inactivation of the peptidase domain and stabilisation of the enzyme against denaturing at neutral to alkaline pH conditions. Amino acid residues within the pro-region mediate their membrane association, and play a role in the transport of the proenzyme to lysosomes. Among the most notable features of propeptides is their ability to inhibit the activity of their cognate enzymes and that certain propeptides exhibit high selectivity for inhibition of the peptidases from which they originate.

The papain precursor protein contains 345 amino acid residues, and consists of a signal sequence (1-18), a propeptide (19-133) and the mature peptide (134-345). The amino acid numbers are based on the mature peptide. The protein is stabilised by three disulfide bridges. Its three-dimensional structure consists of two distinct structural domains with a cleft between them. This cleft contains the active site, which contains a catalytic diad that has been likened to the catalytic triad of chymotrypsin. The catalytic diad is made up of the amino acids - cysteine-25 (from which it gets its classification) and histidine-159. Aspartate-158 was thought to play a role analogous to the role of aspartate in the serine protease catalytic triad, but that has since then been disproved. Nonetheless, it does appear to play a role.



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Phaseolamin



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Pharmavite


imagePharmavite, LLC

Pharmavite is a dietary supplements company based in Northridge, California. The company is the maker of Nature Made, a line of vitamins and nutritional supplements, and SOYJOY, a snack bar made from soy and fruit products.

Pharmavite was founded in 1971 by Oluwason Henry Burdick and Barry Pressman. The Nature Made vitamin brand was launched the following year. The company was purchased in 1989 by Japanese pharmaceutical company Otsuka.

The company is based in Northridge,CA. Manufacturing location is in San Fernando, CA. In 2013 a new manufacturing facility opened in Opelika, Alabama, which produces Softgels and Tablets, and Gummy Vitamins since 2015

In August 2015, a class action lawsuit was filed in the State of California asserting that Pharmavite sells vitamin E dietary supplements products that do not provide the benefits stated on the label and in marketing claims.

Pharmavite's vitamins and supplements product line participates in the United States Pharmacopeia's (USP) Dietary Supplements Verification Program, which verifies the "quality, purity and potency" of dietary supplements through facility audits and random off-the-shelf product testing.



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Pea protein


Pea protein is a food with a neutral taste that is used in dairy alternatives such as cheeses and yogurt. It is extracted from the yellow pea, Pisum sativum, and has a typical legume amino acid profile.

The genotype of the pea plants affects properties of the protein. Pea protein contains Legumin, which has some similar properties to Casein, and pea protein products are promoted as an alternative to whey protein. Some marketing of pea protein is based on consumer concerns around genetic modification of soy plants.




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Phosphatidylserine


imagePhosphatidylserine

Phosphatidylserine (abbreviated Ptd-L-Ser or PS) is a phospholipid and is a component of the cell membrane. It plays a key role in cell cycle signaling, specifically in relationship to apoptosis.

Phosphatidylserine is a phospholipid (more specifically a glycerophospholipid). It consists of two fatty acids attached in ester linkage to the first and second carbon of glycerol and serine attached through a phosphodiester linkage to the third carbon of the glycerol.

Phosphatidylserine coming from plants and phosphatidylserine coming from animals differ in fatty acid composition.

Phosphatidylserine(s) are actively held facing the cytosolic (inner) side of the cell membrane by the enzyme flippase. However, when a cell undergoes apoptosis, phosphatidylserine is no longer restricted to the cytosolic side by flippase. Instead scramblase catalyzes the rapid exchange of phosphatidylserine between the two sides. When the phosphatidylserines flip to the extracellular (outer) surface of the cell, they act as a signal for macrophages to engulf the cells.

Phosphatidylserine plays a role in blood coagulation (also known as clotting). When circulating platelets encounter the site of an injury, collagen and thrombin -mediated activation causes externalization of phosphatidylserine (PS) from the inner membrane layer, where it serves as a pro-coagulant surface. This surface acts to orient coagulation proteases, specifically tissue factor (TF) and factor VII (the tenase complex), facilitating further proteolysis, activation of factor X, and ultimately generating thrombin.

In the coagulation disorder Scott syndrome, the mechanism in platelets for transportation of PS from the inner platelet membrane surface to the outer membrane surface is defective. It is characterized as a mild bleeding disorder stemming from the patient's deficiency in thrombin synthesis.



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