Anti-Malaria Artemisia Annua Extract Artemisinin 99%
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|Min. Order:||1 kg|
|Production Capacity:||500000 Ton/Year|
|Transport Package:||Packed in Fiber Drum, LDPE Bag Inside; 25kg|
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- Model NO.: 63968-64-9
- Packaging Material: Fiber Drum, LDPE Bag Inside
- Extraction Process: Chemical
- Raw Material: Artemisia Annua Leaf
- Other Names: Qinghaosu, Arteannuin, Artemisinine
- Plant Part Used: Leaf
- Molecular Weight: 282.34
- Trademark: Kingherbs
- Origin: Yongzhou of Hunan Province
- Certification: ISO, Kosher
- Storage Method: Keep Tightly Sealed, Store Away From Moisture
- Application: Anti-Malaria
- Botanical Source: Artemisia Annua L
- CAS No: 63968-64-9
- Molecular Formula: C15h22o5
- Appearance: White Needle Crystal
- Specification: Artemisinin 99% by HPLC
Artemisia annua Extract
Product Name: Artemisia annua Extract
Botanical Source: Artemisia annua L.
Plant Part Used: Aerial parts
Specification: Ratio Extract
Appearance: Fine Brownish Yellow Power
Artemisia annua, also known as sweet wormwood, sweet annie, sweet sagewort, annual mugwort or annual wormwood (Chinese pinyin:qīnghāo), is a common type of wormwood native to temperate Asia, but naturalized in many countries including scattered parts of North America.
Artemisia annua belongs to the plant family of Asteraceae and is an annual short-day plant. Its stem is erect brownish or violet brown. The plant itself is hairless and naturally grows from 30 to 100 cm tall. Although in cultivation it is possible, that plants reach a height of 200 cm. The leaves of A. annua have a length of 3-5 cm and are divided by deep cuts into two or three small leaflets. The intensive aromatic scent of the leaves is characteristic.The Artemisinin content in dried leaves is in between 0% and 1.5%. New hybrids of Artemisia annua developed in Switzerland can reach a leave artemisinin content of up to 2%. The small flowers have a diameter of 2-2.5 mm and are arranged in loose panicles. Their color is green-yellowish. The seeds are brown achenes with a diameter of only 0.6-0.8 milimeter. Their thousand-kernel weight (TKW) averages around 0.03 g (in comparison, wheat has a TKW of approximately 45 g).
The growing period of Artemisia annua from seeding till harvest is 190-240 days, depending on the climate and altitude of the production area. The plant should be harvested at the beginning of flowering. At that time the artemisinin content is the highest. Dry leave yields of Artemisia annua plantations vary between 0.5 and 3 t/ha.
|Growth Phases||Days after sowing|
|Appearance of 1st pair of leaves||15-30|
|Appearance of 2nd pair of leaves||21-50|
|Cessation of growth in height||170-200|
Artemisia annua is best sown in rows. That facilitates weeding, which has to be done mechanically or manually since no chemical crop protection agents are admitted. It is recommended to sow 1.4 - 2 seeds per square meter. The fertilizer requirements are on a low level. Potassium should be used as base fertilizer. It is taken up by the plant during the whole growing season. Nitrogen is required during early branching stages, an amount of approximately 70 kg N/ha is sufficient for the plant. Phosphate on the other hand is required during the blooming stages. Phosphate fertilization can lead to a higher artemsinin content in the leaves. The application of salicylic acid on the leaves shortly before harvesting the plant also can raise its artemisinin content. Besides few viral diseases Artemisia a. has no major diseases that need to be controlled.
The harvest of the plant is best done in the state of flower budding. The whole plant is harvested and cut into branches which are dried in the sun or in an oven. The drying temperature should not exceed 40 °C. The dry branches are shaken or beaten to separate the leaves from the stem. The leaves are then packed into fabric bags and shipped to further processing. It is important that the temperatures during transportation and storage never get higher than 40 °C, otherwise artemisinin gets volatile and is lost into the air. The leaves should not be crushed before long time storage (1 year). The optimal storage conditions are either 20 °C with 85% relative humidity (RH) or 30 °C with 30-40% RH.
In traditional Chinese medicine, A. annua is traditionally used to treat fever.
In 1971, scientists demonstrated the plant extracts had antimalarial activity in primate models, and in 1972, the active ingredient, artemisinin (formerly referred to as arteannuin), was isolated and its chemical structure described. Artemisinin may be extracted using a low boiling point solvent, such as diethylether, and is found in the glandular trichomes of the leaves, stems, and inflorescences, and it is concentrated in the upper portions of plant within new growth. The first isolation of artemisinin from the herb occurred from a military project known as Project 523, following the study of traditional medicine pharmacopoeias performed by Tu Youyou and other researchers within the project.
Apart from the active compound Artemisinin, recent studies show that A. annua is one of the four medical plants with the highest Oxygen radical absorbance capacity (ORAC) level.
Artemisia annua possesses the capacity to produce high phenolic compounds, which result in high antioxidant activity. Five major groups (coumarins, flavones, flavonols, phenolic acids and miscellaneous) containing over 50 different phenolic compounds were identified analyzing A. annua.
Flavonoids are generally known for their redox properties involved in the delay or inhibition of the initiation or propagation in oxidizing chain reactions.
Even though the beneficial effect of these phenolic compounds in association of a great number of diseases is often discussed, different studies show beneficial effects of flavonoids compound produced by A. annua. It has been stated that there is a negative correlation between the presence of the mentioned components and cardiovascular diseases, cancer and parasitic disease such as malaria.
Artemisinin and Flavonoids
In the last 20 years researchers focused on the activity of artemisinin against malaria. Therefore, less studies were done about the relationship between flavonoids and cancer. Despite that, recent studies show that the flavonoids present in the A. annua leaf are linked to suppression of CYP450 enzymes responsible for altering the absorption and metabolism of artemisinin in the body. Further researches in the synergistic effect of artemisinin and flavonoids and their biological interaction between malaria and cancer are needed.
Research to develop antimalarial drugs led to the discovery of artemisinin, a compound which is extracted from Artemisia annua, in the 1970s by Chinese scientist Tu Youyou, for which she shared the 2015 Nobel Prize in Physiology or Medicine. While most TCM herbs are boiled at high temperature that can damage the active ingredient in Artemisia annua, one traditional source says that this herb is to be steeped in cold water; knowing this, scientists found that a better extract was obtained by using a low-temperature ether-based extraction method, and by adding detoxification and purification processes, they could create a drug with sufficient active ingredient to be effective.
Artemisinin is a sesquiterpene lactone with an endoperoxide bridge and has been produced semisynthetically as an antimalarial drug. The efficacy of tea made from A. annua in the treatment of malaria is dubious. Research has found that artemesinin is not soluble in water and the concentrations in these infusions are considered insufficient to treat malaria. In 2004, the Ethiopian Ministry of Health changed Ethiopia's first line antimalaria drug from sulfadoxine/pyrimethamine (Fansidar), which has an average 36% treatment failure rate, to artemether/lumefantrine (Coartem), a drug therapy containing artemesinin which is 100% effective when used correctly, despite a worldwide shortage at the time of the needed derivative from A. annua. A 2012 review said that artemisinin-based remedies are the most effective drugs for the treatment of malaria. A 2013 review suggested that although Artemisia annua may not cause hepatotoxicity, haematotoxicity, or hyperlipidemia, it should be used cautiously during pregnancy due to a potential risk of embryotoxicity at a high dose.
Despite global efforts in combating malaria, it remains a large burden for the population, particularly in tropical and subtropical regions. Although WHO recommends artemisinin-based remedies for treating uncomplicated malaria, artemisinin resistance can no longer be ignored. The causes that affected the emergence of artemisinin resistance include, for example, the use of artemisinin-based remedies. Encouraging herbal alternatives are in the pipeline, but the only indelible solution for the eradication of malaria would be for the creation of an effective vaccination. Emergence of artemisinin resistance has been identified in Cambodia and the border of Thailand. It will likely spread to other endemic areas across the world in the impending future. As of 2013, it seems that the pathogenic agent of malaria is slowly becoming resistant to artemisinin-based drugs.
Several studies show that flavonoids assimilation beverages treatments such as tea might prevent, delay or help to cure cancer. Recent investigations linked the influence of flavonoids with different enzymes involved in drug metabolism and in chemical Carcinogenesis process. This induces to a therapeutic potential.
Many studies show anti-cancer results analyzing different flavonoids, such as flavones and flavonols. In general it has been shown that specific flavonoid compounds can inhibit specific cancer cell growth as well as cell proliferation. Furthermore, these flavonoids induce cell Apoptosis.
It is proven, that artemisinin has anti-cancer activity as well, because it contains an endoperoxide group. Artemisinin has a high anti-cancer activity due to its interaction with iron complexes in the blood. This shows that artemisinin derivatives induce apoptosis of cancer cells as well.
Synthetic derivatives of artemisinin are being investigated for their potential use as anticancer drugs.
Animal experiments showed that artesunate, a synthetic derivative of artemisinin, has anti-allergic properties, by effecting mast cell degranulation. This makes artesunate a candidate for treatment of allergic asthma. A Metabolomics animal study further strengthens this hope.
The proposed mechanism of action of artemisinin involves cleavage of endoperoxide bridges by iron, producing free radicals (hypervalent iron-oxo species, epoxides, aldehydes, and dicarbonyl compounds) which damage biological macromolecules causing oxidative stress in the cells of the parasite. Malaria is caused by apicomplexans, primarily Plasmodium falciparum, which largely reside in red blood cells and itself contains iron-rich heme-groups (in the form of hemozoin).