Examples of using Moxidectin in English and their translations into Vietnamese
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Moxidectin Basic Info.
Active ingredients: fipronil(10%), moxidectin(1%).
It contains moxidectin and praziquantel as active ingredients.
It consists of 2 active ingredients: moxidectin and fipronil.
Moxidectin has a detrimental effect on nematodes and ectoparasites.
The active ingredients are imidacloprid and moxidectin.
Moxidectin is a macrocyclic lactone and semisynthetic derivative of nemadectin.
The active ingredients of the droplets are considered fipronil,as well as moxidectin.
Moxidectin is a semisynthetic compound of the macrocyclic lactone group(milbemycin).
The presence of the methyloxime affords moxidectin a greater hydrophobicity and longer biological half-life compared to nemadectin.
Moxidectin is is fou nd in veterinary medicine used to treat animals such as dogs, cats, horses, cattle and sheep.
Nematodes can develop cross-resistance between moxidectin and other similar parasiticides, such as ivermectin, doramectin and abamectin.[9].
Moxidectin is a semi-synthetic milbemycin derived from nemadectin by selective oxidation followed by methyloximation.
These channels are vital to the function of invertebrate nerve and muscle cells;when moxidectin binds to the channels, it disrupts neurotransmission, resulting in paralysis and death of the parasite.
Moxidectin is very rapidly absorbed and penetrates the circulatory system, tissues and organs and is subsequently excreted along with the feces.
Eight different avermectins were isolated in four pairs of homologue compounds, with a major(a-component) and minor(b-component) component usually in ratios of 80:20 to 90:10.[2] Other anthelmintics derived from the avermectins include ivermectin, selamectin, doramectin,eprinomectin, moxidectin, and abamectin.
Moxidectin kills some of the most common internal and external parasites by selectively binding to a parasite's glutamate-gated chloride ion channels.
Main rival products for dogs include ivermectin(trade names Stromectol, Ivermec and others) or milbemycin oxime(Interceptor) for heartworms,imidacloprid and moxidectin(Advantage), fipronil(Frontline) or lufenuron(Program) for fleas, or the combination milbemycin oxime/lufenuron(Sentinel) for both.
Moxidectin binds selectively to parasite glutamate-gated chloride ion channels and disrupts neurotransmission leading to paralysis and death of the parasite.
Two companies filed patents for moxidectin: Glaxo Group and the American Cyanamid Company;[1] in 1988, all patents were transferred to American Cyanamid.[1] In 1990, the first moxidectin product was sold in Argentina.[1].
Moxidectin It is another substance of the insecticidal type, which is absorbed into the skin and enters the bloodstream, after which it has a destructive effect on the parasites.
Moxidectin is an anthelmintic drug used in animals to prevent or control parasitic worms(helminths), such as heartworm and intestinal worms, in dogs, cats, horses, cattle and sheep.
For human use, moxidectin was approved by the United States Food and Drug Administration in June, 2018 for the treatment of onchocerciasis in adults and adolescents aged 12 and older.
Moxidectin, a macrocyclic lactone of the milbemycin class,[6] is a semisynthetic derivative of nemadectin, which is a fermentation product of the bacterium Streptomyces cyanogriseus subsp. noncyanogenus.[13].
Moxidectin is very lipophilic, which causes it to have a high volume of distribution.[11] Moxidectin concentrates in the animal's adipose tissue, from where it is released for up to two months following administration.[11].
If a dog licks moxidectin from the skin which was applied as a"spot-on"(topical) treatment, this has the same effect as an overdose, and may cause vomiting, salivation and neurological signs such as ataxia, tremor, and nystagmus.[1] Collie dogs cannot be administered moxidectin.