Flavonoids were referred to as Vitamin P (probably due to the effect they had on the permeability of vascular capillaries) from the mid-1930s to early 50s, but the term has since fallen out of use.
Flavonoids (or bioflavonoids) (from the Latin word flavus
meaning yellow,
their colour in nature) are a class of plant secondary metabolites.
Flavonoids were referred to as Vitamin P (probably due to the effect they had on the permeability of vascular capillaries) from the mid-1930s to early 50s, but the term has since fallen out of use.
Flavonoids were referred to as Vitamin P (probably due to the effect they had on the permeability of vascular capillaries) from the mid-1930s to early 50s, but the term has since fallen out of use.
Flavonoids
(or bioflavonoids), also collectively known as Vitamin P and citrin, are a
class of plant secondary metabolites.
According to the IUPAC nomenclature, they can be classified into:
- ''flavonoids'', derived from 2-phenylchromen-4-one (2-phenyl-1,4-benzopyrone) structure (examples: quercetin, rutin).
- ''isoflavonoids'', derived from 3-phenylchromen-4-one (3-phenyl-1,4-benzopyrone) structure
- ''neoflavonoids'', derived from 4-phenylcoumarine (4-phenyl-1,2-benzopyrone) structure.
The three
flavonoid classes above are all ketone-containing compounds, and as such, are
flavonoids and flavonols. This class was the first to be termed
"bioflavonoids." The terms flavonoid and bioflavonoid have also been
more loosely used to describe non-ketone polyhydroxy polyphenol compounds which
are more specifically termed flavanoids, flavan-3-ols, or catechins (although
catechins are actually a subgroup of flavanoids).
Flavonoids
are widely distributed in plants fulfilling many functions.
Flavonoids
are the most important plant pigments for flower coloration producing yellow or
red/blue pigmentation in petals designed to attract pollinator animals.
Flavonoids
secreted by the root of their host plant help ''Rhizobia'' in the infection
stage of their symbiotic relationship with legumes like peas, beans, clover,
and soy. Rhizobia living in soil are able to sense the flavonoids and this
triggers the secretion of Nod factors, which in turn are recognized by the host
plant and can lead to root hair deformation and several cellular responses such
as ion fluxes and the formation of a root nodule.
They also
protect plants from attacks by microbes, fungi and insects.
Flavonoids
(specifically flavanoids such as the catechins) are "the most
common group of polyphenolic compounds in the human diet and are found
ubiquitously in plants". Flavonols, the original bioflavonoids such as
quercetin, are also found ubiquitously, but in lesser quantities. Both sets of
compounds have evidence of health-modulating effects in animals which eat them.
The
widespread distribution of flavonoids, their variety and their relatively low
toxicity compared to other active plant compounds (for instance alkaloids) mean
that many animals, including humans, ingest significant quantities in their
diet. Resulting from experimental evidence that they may modify allergens, viruses,
and carcinogens, flavonoids have potential to be biological "response
modifiers", such as anti-allergic,
anti-inflammatory, anti-microbial and anti-cancer
activities shown from in vitro studies.
Antioxidant activity in vitro
Flavonoids
(both flavonols and flavanols) are most commonly known for their antioxidant
activity in vitro.
Consumers
and food manufacturers have become interested in flavonoids for their possible
medicinal properties, especially their putative role in prevention of cancers
and cardiovascular
diseases. Although physiological evidence is not yet established,
the beneficial effects of fruits, vegetables, and tea or even red wine have
sometimes been attributed to flavonoid compounds rather than to known
micronutrients, such as vitamins and dietary minerals.
Alternatively,
research conducted at the Linus Pauling Institute and evaluated by the European
Food Safety Authority indicates that, following dietary intake, flavonoids
themselves are of little or no direct antioxidant value. As body conditions are
unlike controlled test tube conditions, flavonoids and other polyphenols are
poorly absorbed (less than 5%), with most of what is absorbed being quickly
metabolized and excreted.
The increase
in antioxidant capacity of blood seen after the consumption of flavonoid-rich
foods is not caused directly by flavonoids themselves, but most likely is due
to increased uric acid levels that result from metabolism
of flavonoids. According to Frei, "we can now follow the activity of
flavonoids in the body, and one thing that is clear is that the body sees them
as foreign compounds and is trying to get rid of them."
Other potential health benefits
Cancer
Physiological
processing of unwanted flavonoid compounds induces so-called Phase II enzymes
that also help to eliminate mutagens and carcinogens, and therefore may be of
value in cancer
prevention. Flavonoids could also induce mechanisms that may kill
cancer cells and inhibit tumor invasion.
Research
also indicated that only small amounts of flavonoids may be needed for possible
benefits. Taking large dietary supplements likely provides no extra benefit and
may pose risks. However, certainty of neither a benefit nor a risk has been
proven yet in large-scale human intervention trials.
Capillary stabilizing agents
Bioflavonoids
like rutin, monoxerutin, diosmin, troxerutin and hidrosmin have potential
vasoprotective proprieties still under experimental evaluation.
PROBLEM :
I'm looking for a flavonoid extraction and i dont find any exact one.
how to exact flavonoids, the process, and i heard something about i can extract it from the orange or any other fruit.
PROBLEM :
I'm looking for a flavonoid extraction and i dont find any exact one.
how to exact flavonoids, the process, and i heard something about i can extract it from the orange or any other fruit.
i find an article that tell about this: Flavonoids in plants typically consist of flavonoid glycones... the flavonoid "nucleus" with a sugar "tail". The glycones are fairly soluble in polar solvents, including water -- but alcohol is more typically used.
BalasHapusFlavonoid aglycones (with the sugar removed) are soluble in non-polar solvents.
You can make a first pass at the problem with chucking some plant tissue in a blender or tissue macerator with a fairly minimal volume of 95% EtOH (a sparkproof blender is nice, otherwise things can get exciting!). Blend well, then vacuum filter and wash with more EtOH, and concentrate the material in a vacuum dryer. You can further extract any aglycones by re-macerating the tissue with ethyl acetate and refiltering and then drying down the extract under vacuum. In orange, you're going to get a bunch of carotenoids, too.
If you're just interested in the aglycones, macerate the tissue in weak HCl (I've forgotten the concentration we used) in a hot water bath. Extract with ethyl acetate.
You can finetune these procedures for various species and various chemical species you wish to extract, but for quick survey work, these do pretty well. Supercritical fluids are used some now, but that's a bit more specific than I think you want.
PROBLEM :
BalasHapusI'm looking for a flavonoid extraction and i dont find any exact one.
how to exact flavonoids, the process, and i heard something about i can extract it from the orange or any other fruit.
extraction and identification of flavonoid compounds contained in the plant Tanacetum Balsamita L
Hapusmaybe this could help you rara :).
here are images, processes, schemes of work, and its outcomes.
but because it is too long to display,
maybe you can download the file pdf at the address :
http://www.google.co.id/url?sa=t&rct=j&q=&esrc=s&source=web&cd=1&ved=0CB4QFjAA&url=http%3A%2F%2Fpasche08.files.wordpress.com%2F2009%2F05%2Fcopy-of-copy-of-makalah-quercetin-2003.pdf&ei=f0F0UIemC4rjrAftx4DYBQ&usg=AFQjCNFAKwJagREZGqQO46Ufli1T_2Ic9Q&sig2=2bSD4mfG8xjEpCJsenD8vg
i hope can help u.
thanks before :)
I also find the other answer about how to extracting flavonoid? The other answer Tempuyung (Sonchus arvensis) from the Asteraceae tribe is one of the
BalasHapusplants that have multiple classes of flavonoids. Have done the isolation of compounds
methanol extracts of the flavonoid to use dry herbs tempuyung
paper chromatography with the eluent n-butanol-acetic acid-water (4:1:5). Analysis conducted on
blots were obtained using a UV-vis spektrofotometeri method with the help of reagent
sliding sodium hydroxide, aluminum (III) chloride, sodium acetate and boric acid. Results of analysis
showed that the flavonoid compounds obtained belongs to a class of flavone
substituted the 7.4 '-hydroxy flavone.
for more complete you may open this link
http://www.iptek.net.id/ind/pustaka_pangan/pdf/Senaki_V/SRININGSIH.pdf
Hi rara
BalasHapusI have a question for you
how to identify in vitro flavonoids and vitamin C?