[Latin Name] Vaccinium myrtillus l.

[Plant Source] Wild bilberry fruit cultivated from Sweden & Finland

[Specifications]

1) Anthocyanidins 25% UV (Glycosyl removed)

2) Anthocyanins 25% HPLC

3) Anthocyanins 36% HPLC

[Particle size] 80 Mesh

[Loss on drying] ≤5.0%

[Heavy Metal] ≤10PPM

[Pesticide residue] EC396-2005, USP 34, EP 8.0, FDA

[Storage] Store in cool & dry area, keep away from the direct light and heat.

[Package] Packed in paper-drums and two plastic-bags inside.

[General feature]

1. 100% extracted from European bilberry fruit, approved ID test from ChromaDex andAlkemist Lab;

2.Without any adultery of other relative species of Berries,such as Blueberry,  Mulberry,Cranberry,etc;

3. Pesticide residue: EC396-2005, USP 34, EP 8.0, FDA

4. Directly import the frozen fruit from North Europe;

5. Perfect water solubility,water insolubles<1.0%
6. Chromatographic fingerprint match EP6 requirement

[What is bilberry fruit]

Bilberry (Vaccinium Myrtillus L.) is a kind of perennial deciduous or evergreen fruit shrubs, mainly found in subarctic regions of the world as in Sweden, Finland and Ukraine, etc. Bilberries contain dense levels of anthocyanin pigments, which was said popularly to have been used by World War II RAF pilots to sharpen night vision. In fork medicine, Europeans have been taking bilberry for a hundred years. Bilberry extracts entered the healthcare market as a kind of dietary supplement for effects on vision enhancement and visual fatigue relief.

[Function]

Protect and regenerate rhodopsin and cure the eye diseases;

Prevent the cardiovascular diseases

Antioxidant and anti-aging

Softening blood capillary, enhancing the heart function and resisting cancer

https://www.iitutor.com
Condensation polymers are formed when monomers join together, and in the process also form a separate small molecule such as a water molecule. The ends of the monomer molecules must have functional groups that can join with other functional groups on neighbouring molecules.
Condensation polymerisation is the process in which two monomers combine with the elimination of a smaller molecule. One way that two different monomers can combine and in doing so lose a molecule of water and represents condensation polymerisation. This process continues and each remaining end joins with another monomer—each time lengthening the chain. One way to think of this is a “head-to-tail” joining.
Synthetic condensation polymers include nylons and polyesters. Natural condensation polymers include cellulose, cotton, wool, and silk.
Cellulose is a complex carbohydrate or polysaccharide. It is the most abundant biopolymer in nature. Carbohydrates consist of molecules containing C, H and O atoms. Carbohydrates contain many alcohol functional groups.
• Cellulose consists of long chains of β-glucose monomers.
• Glucose is an example of a simple carbohydrate or monosaccharide.
Structure of glucose :
Glucose (C6H12O6) is a ring molecule. The carbon atoms in the ring are numbered as shown. The –OH functional groups may be orientated above or below the plane of the ring. These different orientations at C, produce the alpha and beta forms of the glucose monomers.
• Glucose is an organic compound
• Ring can open up in solution to form a straight-chain structure. Open and chain forms are in equilibrium that cause glucose to exist as anomers, β-glucose and α-glucose.
Biopolymer is a naturally occurring polymer such as cellulose, starch, gluten, DNA and protein.
Formation of cellulose:
Cellulose is a condensation polymer which is formed when glucose monomers condense together through beta-1,4-glycosidic bonds. This involves a reaction between the –OH groups at the C1 and C4 carbons of adjacent glucose molecules.
The process begins by the condensation reaction between two glucose monomers to form a beta-maltose dimer. A water molecule is eliminated during this reaction. More glucose monomers condense and the chain grows until about 10 000 glucose monomers are linked in long, unbranched, ribbon-like strands.
Strong hydrogen bonding exists between –OH groups of neighbouring, close-packed strands. This produces a water-insoluble polymer with great strength and rigidity. Plants use cellulose as a structural carbohydrate for their cell walls.

Presente e in vendita ad Imperia ad Olioliva la Stevia rebaudiana la pianta perenne al centro di aspre polemiche tra i sostenitori delle proprietà di questa pianta dolcificante e chi invece al contrario sosteneva che alcuni componenti erano ritenuti sospetti di cancerogenicità.
Tra gli stand di via Bonfante l’Antico Frantoio Sommariva propone oltre ad olio olive piantine di
Stevia reubaudiana, l’uso di questa pianta nei prodotti alimentari è stato in passato limitato in Europa e USA dato che alcuni suoi componenti, alle dosi testate, come lo steviolo e lo stevioside erano ritenuti sospetti di cancerogenicità.
L’utilizzo della Stevia e dei suoi derivati è stato ammesso dalla Unione Europea, come per l’Italia (Regolamento UE N. 1131/2011 della Commissione dell’11 Novembre 2011)
Il possibile uso della Stevia, in paesi diversi da quelli di origine, ha prodotto notevoli controversie e contestazioni, facendo pensare all’esistenza di una cospirazione commerciale, interessata a contrastarne l’uso, ed a favorire invece i dolcificanti artificiali prodotti dalla grandi multinazionali.
In Italia a sostegno dell’utilizzo di questa pianta è nata un’associazione www.nastevia.it