Paralytic shellfish poisoning (PSP) standard sample and preparation method and application thereof
A standard sample and shellfish toxin technology, applied in the biological field, can solve the problems of high price and no matrix, and achieve the effects of low raw material cost, guaranteed effectiveness, and simple preparation method
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[0028] Such as figure 2 Shown, the preparation method of paralytic shellfish toxin standard sample of the present invention comprises the following steps: (A) sampling, impurity removal; (B) acidification, homogenate; (C) primary freeze-drying; (D) grinding, sieving (E) freeze-drying again; (F) encapsulation; (G) uniformity and stability inspection; (H) determination of PSP content.
[0029] Specifically, the preparation method of the paralytic shellfish toxin standard sample of the present invention comprises the following steps:
[0030] (A) Take the PSP-positive scallop, wash the shell surface thoroughly with clean water, cut off the adductor muscle, open the shell, rinse the inside with heavy distilled water to remove impurities such as sediment and other foreign objects, and glue the adductor muscle and the connection Separate the tissues at the top and carefully remove all the shellfish;
[0031] (B) adding distilled water and 0.1-0.3 mol / L hydrochloric acid solution ...
Embodiment 1
[0042] Example 1: Take PSP-positive scallops with a PSP content of 46.2 MU / g, wash the shell surface thoroughly with clean water, cut off the adductor muscle, open the shell, and rinse the interior with distilled water to remove impurities such as silt and other foreign substances , separate the adductor muscle from the tissue connected to the glued part, carefully remove all the shellfish, add distilled water, and 0.18mol / L hydrochloric acid solution to make the pH 3, homogenize, and place it in -80℃ for at least 4 hours after mixing. Hours, use a vacuum freeze dryer (CHRiST Epsilon 2-6D) to carry out primary freeze-drying to obtain a PSP positive sample, then carry out tissue grinding, pre-crushing, use a high-alumina porcelain ball mill to finely grind, pass through a 40-mesh sieve, and place it at -80 ° C for pre-treatment. Freeze for at least 4 hours, then freeze-dry again to remove moisture completely. In a room with constant temperature and humidity and aseptic operatio...
Embodiment 6
[0047] Embodiment 6 Uniformity and Stability Inspection
[0048] 6.1 Homogeneity test of samples
[0049] 16 bottles of samples prepared in Example 1 were randomly selected, and 3 groups of samples were taken for 3 times of repeatability detection in each bottle of samples. Use the mouse biological method test in GB / T 5009.213-2008 to analyze the PSP content of the standard sample, expressed in mouse units. All samples are tested in random order under repetitive conditions, that is, in the same laboratory by the same personnel using the same test methods and instruments for a short period of time.
[0050] The uniformity of the test results was evaluated by the single-factor multi-level analysis of variance method, and the following statistical formula was used for the single-factor multi-level analysis of variance. The results are shown in Table 2 and Table 3.
[0051] In order to test the uniformity of the samples, i samples are taken, and each sample is tested j times und...
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