Immunofluorecence technique based method for evaluating activities of cryptosporidium parvum and giardia
A cryptosporidium and evaluation method technology, applied in biological testing, material inspection products, etc., can solve the problems of large errors in the evaluation of the effect of UV inactivation of Cryptosporidium and Giardia, high professional operation level requirements, and high cost. , to achieve the effect of low professional operation requirements, easy promotion and application, and high sensitivity
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example 1
[0037] The method disclosed in this example is to specifically analyze the method for evaluating the activity of two insects by immunofluorescence technology by collecting raw water that has not been subjected to ultraviolet light disinfection treatment as a water sample. Therefore, this example includes a UV disinfection step from the raw water followed by an evaluation of the activity of the two insects. The method for pretreatment of water samples after ultraviolet disinfection treatment disclosed in the above specific embodiments is also applicable to the pretreatment of raw water, and can achieve the same evaluation results.
[0038] Apply the above method for evaluating the activity of Cryptosporidium oocysts and Giardia cysts by UV irradiation, and the specific steps are as follows:
[0039] (1) Provide the water to be treated, and carry out the purification and collection of the two worms: After the water samples to be treated are collected, they are filtered through 6...
example 2
[0048] According to the method described in Example 1, set different light doses Light dosage (mJ / cm 2 ) and light intensity (mW / cm 2 ), irradiate the experimental samples, and evaluate the inactivation rate of the two worms by fluorescent activity staining method (DAPI / PI). Other steps and parameters are the same as Example 1. The irradiation light intensity is respectively: 1.1, 2.3, 4.8mW / cm 2 . Experimental results refer to figure 2 , this figure shows that after different irradiation times, the irradiation light dose Light dosage (mJ / cm 2 ) on the inactivation race (%) of the inactivation rate of the two worms, and the detection took 5 hours. From figure 2 It can be seen from the figure that the UV dose must be greater than 460 mJ / cm when the inactivation rate is 99.9% (3-log) using the fluorescence activity staining method (DAPI / PI). 2 .
example 3
[0050] According to the method described in Example 1, set different light doses Light dosage (mJ / cm 2 ) and light intensity (mW / cm 2 ), irradiate the experimental sample, and evaluate the inactivation rate of the two worms according to the method of Example 1. Other steps and parameters are the same as Example 1. The irradiation light intensity is respectively: 1.1, 2.2, 4.5mW / cm 2 . Experimental results refer to image 3 , this figure shows that after different irradiation times, using the immunofluorescence evaluation method, the irradiation light dose Light dosage (mJ / cm 2 ) on the inactivation race (%) of the inactivation rate of the two worms, and the detection took 6 hours. From image 3 It can be seen from the figure that using the immunological TD (pyrimidine dimer) fluorescence method UV dosage=22 mJ / cm 2 (1.1mW / cm 2 ) can reach 3-log (99.9%) inactivation rate. Explanation: The immunological TD (pyrimidine dimer) fluorescence method has obvious advantages in...
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