Application of macleaya cordata extractive in veterinary drugs for economic animals
A technology of Boluohui extract and veterinary medicine, which is applied in the application field of Boluohui extract in economic animal veterinary medicine, can solve the problems of economic loss in livestock and poultry breeding industry, and achieve the effect of improving feed conversion rate
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Embodiment 1
[0016] Example 1 The preparation method of Boluohui extract
[0017] Take Boluo fruit pods, extract with 20 times the amount of 0.5% sulfuric acid aqueous solution, then adjust the pH to 8-10 with alkali, separate the precipitate, then extract with 90% ethanol, filter part of the concentrated extract, add concentrated sulfuric acid to precipitate A large amount of orange-red precipitates, after drying, obtain the Boluohui extract. The total biological content measured by HPLC is about 66.4% (total the content of prosanginarine and chelerythrine, the same below), wherein sanguinarine is about 66.4%. For 46.4%, chelerythrine is about 20%.
Embodiment 2
[0018] Example 2 Preparation of Boluohui Extract Premix
[0019] Weigh 100 g of the Boluohui extract prepared by the method in Example 1, use a medicine pulverizer to pulverize, pass through a 120-mesh sieve, and set aside; then weigh 3900 g of medicinal starch. Thoroughly mix the Boluohui extract and medicinal starch with a small mixer for 15 minutes, check that the coefficient of variation is <0.5, and obtain 4000 grams of Boluohui extract premix.
Embodiment 3
[0020] Example 3 In vitro inhibition test of Boluohui extract on common pathogenic bacteria of livestock and poultry
[0021] Select Boluohui extract for use, and measure its content In order to carry out experimental research, the solution prepared by the Boluohui extract prepared in Example 1 is respectively common to livestock and poultry such as Haemophilus, Listeria, Pasteurella, and Streptococcus. In vitro antibacterial test for animal pathogenic bacteria. According to the aseptic operation procedure, under aseptic conditions, dump the medium plate corresponding to the corresponding strain, and apply the corresponding strain inoculum on it. Paper and tablet are tightly bonded. At the same time, a filter paper soaked in aureomycin was used as a control. Three copies of each sample were made, and the results were averaged. Invert culture at 37°C, observe the antibacterial effect at 24 hours, measure the diameter of the antibacterial zone, and judge the sensitivity.
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