Poison purification - a four in one solution for preventing mold, removing mold, detoxifying, and regulating intestines.
Product Composition:
Fungal toxin degrading enzymes (aflatoxin B1 degrading enzyme, vomitoxin degrading enzyme, zearalenone degrading enzyme), enzymatic hydrolysis of yeast cell wall polysaccharides (β - glucan, enzymatic hydrolysis of mannan oligosaccharides), toxin degrading probiotics, glucose oxidase.
Product Principle:
2.1 Using technologies such as biology and genetic engineering, extract and purify degradation enzymes that can be used to degrade mycotoxins from screened and isolated microbial strains, destroy the toxic active centers of mycotoxins, and ultimately convert them into non-toxic degradation products.
Degradation principle of aflatoxin:
Degradation principle of vomitoxin:
Degradation principle of zearalenone: Degradation enzyme destroys the lactone ring of zearalenone
2.2 After enzymatic hydrolysis of yeast cell wall, it becomes β - glucan and mannooligosaccharides (MOS), which can bind various fungal toxins through hydrogen bonding, ionic bonding, and hydrophobic interactions, effectively adsorbing toxins and exerting detoxification effects; At the same time, as the most immunologically active and easily absorbed special ultrafine spiral molecular structure, it can activate macrophages in the body and improve the immune level of the body.
2.3 Glucose oxidase and catalase form an oxidoreductase system that consumes oxygen in the intestine while inhibiting the proliferation of harmful bacteria in the intestine. By enhancing the oxidation of liver microsomes, the body biologically converts mycotoxins, breaks down their functional atomic groups, and converts toxins into non-toxic metabolites. Cooperate with beneficial microorganisms to repair intestinal mucosa and improve intestinal health.
Product Advantages:
Ø Quick Detoxification: Du Li Jing only takes 1 minute to initiate enzymatic hydrolysis reaction in the stomach. After feeding, mycotoxins are absorbed into the bloodstream within 30 minutes and begin to affect the animal's production performance. Therefore, the ideal solution for fungal toxins must adsorb or degrade fungal toxins within 10-30 minutes;
The time required for the aggregation and degradation of zearalenone by mycophenolate mofetil
Safe and efficient: A very small amount can have a detoxifying effect. Non toxic, harmless, does not produce side effects, and does not pollute the environment;
Comparison of the ability of different products to degrade mycotoxins
Good stability: high temperature resistance, storage resistance, and no deterioration or deactivation during the granulation process;
The effect of Du Li Jing on fungal toxins during the granulation process of pig feed
Strong specificity: does not adsorb nutrients, resulting in loss of nutritional value.
Product Efficacy
Ø Quickly decompose various fungal toxins in feed, inhibit the proliferation of fungi in feed in vitro, and reduce the production of new toxins; Neutralizing and degrading absorbed toxins in the body, repairing the decline in animal productivity caused by poisoning.
Ø Protect the liver and kidneys, restore the metabolic function of injured organs; Strengthen the body's antioxidant level, regulate the intestines, and ensure intestinal homeostasis.
Ø Directly activate macrophages, repair immune system damage caused by mycotoxins in feed, quickly restore and improve animal immunity.
Ø Can be used as a comprehensive detoxification and detoxification plan for treating symptoms such as oral ulcers and animal wig infections caused by fungal toxin poisoning.
1. In vitro simulation of the degradation ability of toxin by Du Lijing in gastric juice
Samples of corn were taken from a company in the market, and the contents of aflatoxin B1, vomitoxin, and zearalenone were tested to be 30ug/kg, 3mg/kg, and 0.5mg/kg. 10g of corn was added to 0.1mg/kg of toxin and 20g of artificial simulated gastric juice in a 250ml volumetric flask, and shaken at 39 ℃ to mix thoroughly. The toxin content was detected by sampling at 1h, 2h, and 4h of reaction.
Result analysis: As shown in the above figure, after 4 hours of degradation in simulated gastric juice environment, the degradation rate of aflatoxin B1, zearalenone, and vomitoxin in corn was 90.93%, 89.76%, and 92.87%, respectively.
2. Study on the efficiency of toxin degradation in bran by Du Li Jing
Weigh 10g of bran from a certain company in the market and place it in three 250mL triangular flasks. After testing, the contents of aflatoxin B1, vomitoxin, and zearalenone in the samples were 15.7ug/kg, 88.2ug/kg, and 818.5ug/kg, respectively. Add 0.1mg of toxin to each and shake thoroughly at 37 ℃ for 4 hours. After the reaction is complete, take a sample to test the toxin content.
The results showed that the degradation rates of aflatoxin B1, vomitoxin, and zearalenone in the bran samples were 76.43%, 63.83%, and 74.10%, respectively.
Dosage and usage: Depending on the degree of fungal toxin contamination
Ø The national limit for toxins is within 3 times: 1000g/2-3 tons of water.
Ø The national limit for toxins is 3-10 times: 1000g/ton of water;
Packaging: 1000g per bag; 20 bags/box
