CN105510545A - Method for evaluating genetic toxicity of drinking water through multi-genetic-end point biological group tests - Google Patents
Method for evaluating genetic toxicity of drinking water through multi-genetic-end point biological group tests Download PDFInfo
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Abstract
The invention discloses a method for evaluating the genetic toxicity of drinking water through multi-genetic-end point biological group tests. According to the method, water supply plant filter outflow water and disinfected water serve as research objects, biological group genetic toxicity tests: an Ames test, an in vivo micronucleus test in mouse bone marrow polychromatic erythrocyte, a mouse sperm shape abnormality test, a hamster ovary cell micronucleus test and an SOS/umu test serve as evaluation standards, and when 3 positive results exist in the biological group genetic toxicity test, it is shown that biological genetic toxicity safety exists. The method has the following advantages that three genetic end points of gene mutation, chromosomal aberration and DNA damage are contained; test organisms comprise pronuclei, eukaryon and mammals; in-vivo and in-vitro tests are included; sexual cells and body cells are included; the detection means is relatively simple, convenient, rapid, economical and good in laboratory universality.
Description
Technical field
The invention belongs to potable water genetoxic determination and evaluation field, relate to a kind of genotoxic method of biological group test accurate evaluation potable water.
Background technology
Along with the diversification of new high-tech industry, the newborn polluter along with multiple types, difficult degradation enters in drinking water source, brings potential threat to drinking water safety.Although potable water technology obtains larger development, nano-scale, trace, the organism such as hydrophilic are difficult to remove.This type of material cooperates with biosome by modes such as synergy, summation actions, therefore physico-chemical analysis method cannot reflect that the effect of multiple pollutant matter is to the comprehensive toxicity effect of biosome and long-term effect.Separately there are some researches show, potable water mutagenicity power and TOC or COD
mncorresponding relation is there is no etc. index, for 3-chloro-4 (dichloromethyl)-5-hydroxyl-2 (5H)-furanone (MX), its toxicity can be compared with aspergillus flavus, it is the strongest mutagenic matter found in chlorination tap water up to now, its concentration is ng/L level, very micro-to contributions such as TOC, but can 11 ~ 67% be reached to the contribution of potable water mutagenicity, this means that the physics and chemistry water-quality guideline of individual event and the maximum permissible concentration of minority noxious material still can not ensure the security of potable water completely, even if every water-quality guideline meets drinking water sanitary standard (GB5749-2006) 106 water quality standard, as the toxicity accumulation that people drink for a long time, also certain security risk may be there is.
The short-term genetoxic method set up at present has kind more than 200, detect gene mutation, DNA damage and chromosome (group) distortion respectively, Many researchers generally uses one to two kinds of methods wherein test to source water, waterworks water outlet, pipeline water outlet etc. and evaluate.Because subject cell or animal produce individual sensitivity and specificity to toxic contaminants material, can false negative result be caused, cause the erroneous judgement to drinking water safety, and then affect the quality of human gene bank.So set up one and contain many genetic end-points that gene mutation, DNA damage and chromosome (group) distorts, relate to different types of animal subject, accurately feasible, quick economic method is imperative.
Summary of the invention
The present invention is directed to the practical problems of background technology, provide a kind of genotoxic method of many genetic end-point biology group test evaluation potable water.
The object of the invention is to be achieved through the following technical solutions:
A kind of genotoxic method of many genetic end-point biology group test evaluation potable water, with water after the water outlet of filter tank, waterworks and sterilization for research object, with biology group genetic toxicity test: in Salmonella reversion test, body, micronucleus mice bone marrow micronucleus, mouse inbred strain, hamster ovary cell micronucleus test, SOS/umu test are evaluation criterion, namely represent to there is biological genetic toxicity security when there being 3 positive findingses in biology group genetic toxicity test.
Tool of the present invention has the following advantages:
1. gene mutation, chromosome aberration and DNA damage three science of heredity terminals are included;
2. test organism comprises protokaryon, eucaryon and mammality;
3. comprise in body, in vitro test;
4. sexual cell and body cell is comprised;
5. detection means relative ease, quick, economical and laboratory versatility is good.
Accompanying drawing explanation
Fig. 1 is Genetic toxicity combination.
Embodiment
Below in conjunction with accompanying drawing, technical scheme of the present invention is further described; but be not limited thereto; everyly technical solution of the present invention modified or equivalent to replace, and not departing from the spirit and scope of technical solution of the present invention, all should be encompassed in protection scope of the present invention.
Embodiment one: present embodiments provide for one and contain the genotoxic method of many genetic end-points evaluation potable water, its technical measures adopt following scheme:
Though current detection genetoxic method method is many, divides from detection method, following three classes can be divided into substantially: gene mutation test, chromosomal aberration test and DNA damage and repairing test.Mutagenicity test is selected to meet following principle: 1. should include multiple science of heredity terminal; 2. test organism comprises protokaryon, eucaryon and mammality; 3. comprise in body, in vitro test; 4. sexual cell and body cell is comprised; The principles such as 5. detection means relative ease, quick, economic and laboratory versatility be good.In addition, the weight for mutagenicity test evaluation result is worth by following principle: the evolution degree of (1) its test organisms: other higher eucaryotes of mammal > > lower eukaryotes > prokaryotes; (2) contaminating mode: in body, > is external; (3) target cell: reproduction cell > body cell; (4) terminal is observed: gene mutation ≈ chromosome damage > science of heredity interrogatory.In view of above-mentioned, someone proposes weighted method, obtain positive findings to each test macro and give being greater than on the occasion of, the numerical value without activation system and have activation system, acquisition negative findings then gives negative value, and the absolute value without activation system is less than activation system.In view of mentioned above principle, present embodiment proposes a kind of method evaluation potable water genetoxic containing many genetic end-points, sets up methodology respectively, as shown in Figure 1 from gene mutation, chromosome aberration and DNA damage three science of heredity terminals.
One, biological group genetic toxicity test preprocess method
Genetic toxicity test preprocess method adopts two kinds, wherein in Salmonella reversion test, body, micronucleus mice bone marrow micronucleus and mouse inbred strain adopt preconditioned pattern one, and hamster ovary cell micronucleus test and SOS/umu test adopt preconditioned pattern two.
1, preconditioned pattern one: adopt solid phase extraction, with XAD-2 type resin for polymeric adsorbent, granularity 40 ~ 60 order.Before using by resin with heavily steaming methyl alcohol, acetone respectively extracts 8h, loads in port grinding bottle for subsequent use heavily to steam methyl alcohol immersion.Refined resin wet method is loaded special
glass adsorption column in resin height of bed 110mm, and bottom adsorption column and resin bed upper berth through methyl alcohol and acetone extraction glass fiber.Then release methyl alcohol, to methyl alcohol reaches resin bed top just, then distill moisture with 1000 ~ 1200ml and rinse resin column 5 ~ 6 times, after rinsing clean remaining methyl alcohol, retain resin column and be distilled water covering, in case air inlet.Adsorption column upper end is connected with water container by Medical burette, and utilizing syphonic effect to control aqueous sample stream through the flow velocity of resin bed by adjustable screw folder is 50 ~ 70mL/min, and the cumulative volume crossing post water is 250L.Cross post complete, the ether wash-out heavily steamed with 60 ~ 80ml, during wash-out, make ether retain 30 ~ 40min first in pillar.Eluent is collected in beaker and the anhydrous sodium sulfate added after muffle furnace dries 3h in 600 DEG C carries out processed, and be finally concentrated into below 1ml with transferring to KD concentrator under the condition of 43 DEG C of water-baths, 4 DEG C of Refrigerator stores are for subsequent use.
2, preconditioned pattern two: sampling bottle employing 5L is clean, dry Brown Glass Brown glass bottles and jars only.When gathering water sample, with water sample rinse to be measured 3 times in bottle, often kind of water sampling 10L.HLB post enrichment after all water samples is activated again after using the APFF glass fiber filter (U.S. Millipore) in Millipore microfiltration systems that diameter is 142mm and 0.7 μm, aperture to filter.HLB post adopts methylene chloride and methyl alcohol activation pillar.Water sample is connected to the HLB post activated by sample hose, every root HLB post enrichment water sample 2 liters, enrichment is complete and after draining water, with 10mL methylene chloride for eluent divides three times (first time 4mL, second time 3mL and third time 3mL) to carry out wash-out, after concentrated by rotary evaporation, add the anhydrous sodium sulfate through dehydration, dry up rear substitution 0.2mL Bioexperiment solvent DMSO in-20 DEG C of Refrigerator stores for genetoxic biological test with soft high pure nitrogen.
Two, biological group genotoxicity testing method
1, Salmonella reversion test method method is summarized as follows: test design is four dosage groups, be converted into the volumescope of the water of organic enriched substance, also the volume being namely equivalent to water sample is 7L/ ware, 5L/ ware, 3L/ ware and 1L/ ware 4 water yield (dosage) gradients, except above-mentioned 4 dosage groups, (TA98 is the Dexon adopted, TA100 is the NaN adopted also to be provided with blank group (certainly beaming back change), solvent control group (DMSO group) and positive controls
3).This test adopts dull and stereotyped incorporation methods, to in the top layer nutrient culture media melted in test, injection test bacterial strain enrichment liquid 0.1mL and tested material solution (pretreated water sample) 0.1mL successively, be injected on bottom culture medium flat plate after being mixed, and 48h is cultivated under 37 DEG C of conditions, then count returning of every ware and become clump count.The each dosage of each test makees 3 parallel wares, repeats once under same test conditions again, finally with 6 ware mean values
calculate test findings.
2, SOS/umu test method :-80 DEG C of Cryopreservation TA1535/PSK1002 bacterium liquid are got and adds appropriate LB nutrient culture media (the bacteriolyze broth bouillon containing ampicillin in right amount, for biochemical molecular experiment preculture bacterial classification) in, keep temperature 37 DEG C, carry out cultivation overnight of vibrating.Second day, use TGA nutrient solution to cultivate 1h in advance to bacterium liquid, test was carried out respectively under+S9 (mediate heredity toxicity) and-S9 (direct genetoxic).Measure the absorbance A595 under nutrient solution 595nm wavelength.1mlZ-buffer solution is injected, 10 μ 1CHCl successively in reaction bacterium liquid
3concussion is shaken all, adds 1ml and carries out vibration containing the buffer solution of ONPG (developer) and shake up, keep temperature to be 30 DEG C, through 60min oscillating reactions, add Na
2cO
3stop reaction, add supernatant toward 96 hole ELISA Plate, under 420nm and 550nm wavelength, measure absorbance A420 and A550 respectively.DMSO is negative control group.The concentration gradient of organic enriched substance water in the 96 every holes of orifice plate is 0.0835L/ hole, 0.0418L/ hole, 0.0209L/ hole, 0.0104L/ hole, 0.0052L/ hole and 0.0026L/ hole.
3, hamster ovary cell micronucleus test method: agent cell uses CHO-K1 cell, this test test method is built by State Key Laboratory of Environmental Aquatic Chemistry, RCEES teacher Ma Mei seminar of Ecological Environment Research Center, Chinese Academy of Sciences, detailed test procedure sees reference document <Assessingofgenotoxicityof16centralizedsour ce-watersinChinabymeansoftheSOS/umuassayandthemicronucle ustest:Initialidentificationofthepotentialgenotoxicantsb yuseofaGC/MSmethodandtheQSARToolbox3.0>.
Chromosome damage effect basis for estimation: when existence in water sample has the hereditary poisonous substance of chromosome damage effect, when cell acute toxicity is less than 50%, along with the increase of water source water sample exposure concentrations, namely remarkable increase presents dosage-response relation to micronuclear rates.By following formulae discovery micronuclear rates (MN%), hypodiploid rate and micronucleus ratio PI:
PI=water sample MN%/negative control MN% (3).
4. mice bone marrow micronucleus method: test dose designs according to adult's water requirement, average daily water requirement of being grown up comprises drinking-water, food water and metabolic water, be respectively 1200mL, 1000mL and 300mL, adult's body weight calculates with 55kg, can derive from the total amount of drinking-water and food water for (1200+1000) mL/55kg=40mL/kgbw.Experiment on white mice dosage designs by 1000 times, 100 times of day for human beings water requirement and the gradient of 10 times respectively, also namely: 1000 ×: 40mL/kgbw × 1000=40000mL/kgbw=40L/kgbw; 100 ×: 40mL/kgbw × 100=4000mL/kgbw=4L/kgbw; 10 ×: 40mL/kgbw × 10=400mL/kgbw=0.4L/kgbw.Negative control group is separately established (to be also Vehicle controls, by 50% water and 50% salad oil and 2 ~ 3 emulsion that tween is formed through jolting fast, nursing dosage is 20mL/kgbw) and positive controls (adopt endoxan, nursing dosage is 40mg/kgbw).Small white mouse adopts per os gavage approach to cast tested material.30h is adopted to cast tested material (and tester) method, also namely interval 24h casts tested material or tester bis-times, and 6h adopts cervical dislocation mode to put to death small white mouse after second time gavage, obtain femur, use eye scissors to deduct the two ends of femur, ossis come out, the 2mL syringe filling calf serum in using goes out a marrow, blood film method smear routinely, about 2 ~ 3cm length.After using methyl alcohol to fix 5 ~ 10min after natural drying, dye 10 ~ 15min in Giema application liquid, after distilled water flushing, and natural drying.Select cell dispersal evenly and the region that dyeing is good and form is complete, adopt double-blind study diagosis, every small white mouse observes 1000 PCE, calculates and has micronucleus cell number and micronucleus cell rate (‰).
5, method of sperm aberration test in mice is see " mouse inbred strain " (GB15193.7-2003): in test, small white mouse adopts per os gavage approach to cast tested material.Feed 5d once a day continuously, within the 35th day after giving tested material first, adopt cervical dislocation mode to put to death, and take out its both sides epididymis, be positioned in the plate filling 1mL physiological saline in advance.Eye scissors is used longitudinally to cut off epididymis, after leaving standstill 3 ~ 5min, shake gently, then use four layers of lens paper to filter, draw filtrate smear, in atmosphere after natural drying, use methyl alcohol to fix more than 5min, after natural drying, adopt the eosin stains 1h of 1 ~ 2%, then rinse gently with distilled water, diagosis after its drying.Every small white mouse at least checks 1000 complete sperms, the sperm count of record deformity and type, and calculates abnormal rate.
Three, evaluation method
Namely there is biological genetic toxicity in 3 one-way metrics positives.
Embodiment two: present embodiment is evaluated a certain waterworks, domestic south.Water intaking factory's filter tank water outlet and the rear water of sterilization, carry out Genotoxic Assessment according to method described in embodiment one.
1, Salmonella reversion test analysis
The salmonella typhimurium histidine deficient (TA98 and TA100 bacterial strain) used is needed directly to be provided by UnitedStatesUniversityofCaliforniaAmes laboratory in this test, qualification strain properties Pass Test requirement.
Count returning of each plate and become clump count, and obtain average number and the standard deviation of 6 parallel wares, draw the mutagenesis rate MR of TA98 and TA100 respectively, acquired results is as shown in table 1.It is generally acknowledged, the Rule of judgment that Salmonella reversion test presents the positive (can cause the gene mutation of base replacement type) result must meet two conditions simultaneously: 1. returning of tested material group (TA98 or TA100) becomes clump count and ratio MR >=2 of certainly beaming back change group clump count; 2. dose-response response relation (level of signifiance is p=0.01 or 0.05) is had.As shown in Table 1, after the sterilization of waterworks, water is positive findings when dosage is 7L/ ware, and return change bacterium colony with negative control than there were significant differences when 3L/ ware and 5L/ ware with the increase of dosage, but 2 times (i.e. MR < 2) not yet reaching from beaming back change, also can be judged as Ames negative findings.
Water and rear water Salmonella reversion test the results list of sterilizing after waterworks filter evaluated by table 1
2, SOS/umu analysis of experiments
Salmonella typhimurtum S.typhimuriumTA1535/PSK1002 (hereinafter referred TA1535/PSK1002) bacterial strain (purchased from Osaka, Japan public health association) and S9 (purchased from Chinese Disease Control and Prevention Center) can be used in this process of the test.
By the light absorption value measured according to beta galactosidase induced activity U value:
Wherein, the dilution ratio (being 0.0656 in this test) of t to be reaction time (20min), v be bacterium liquid.
Calculate the IR value of water sample:
Wherein, U
sampleand U
dMSOthe U value of sample and negative control group respectively.
In general, the Rule of judgment that SOS/umu test (i.e. DNA damage effect) is positive is meet when acute toxicity < 50% simultaneously: 1. IR >=2 (the minimum positive induction value of international acceptance); 2. there is dosage-response relation.Positive then the hereditary poisonous substance existing in water and can cause DNA damage effect is described.For DNA damage effect positive, can compare according to its intensity and positive compound 4-NQO (-S9) and BaP (+S9) damage effect intensity, obtain the equivalent toxic concentration of 4-NQO and BaP in water sample respectively, be expressed as TEQ
4-NQOand TEQ
baP, and calculate corresponding carcinogenic risk P (adult human body weight W=70kg, every daily drink 2L calculates).
By the testing result of water and disinfectant after the filter of waterworks, obtain each water sample IR value and sample concentration, as shown in table 2, without under metabolism activation condition (-S9), after the filter of waterworks, water SOS is negative, after sterilization, water outlet SOS is positive (when maximum dose level is 0.0835L/ hole IR>=2), output water TEQ
4-NQOscope is 0.0444 ~ 0.0582ug/L, and carcinogenic risk is in 4.68 × 10
-7~ 6.14 × 10
-7between, lower than the safe carcinogenic risk control interval 1.0 × 10 of U.S. EPA
-6~ 1.0 × 10
-4(this research takes 10
-5as safety standard), this also shows that sterilization process can increase the rear water outlet genetic toxic effect of filter.
The TEQ of rear water outlet and water outlet after sterilizing filtered by table 2 under evaluating-S9 and+S9 condition
4-NQO, its carcinogenic risk value and TEQ
baPvalue
Note: "-" indicates without dosage-response relation.
3, hamster ovary cell micronucleus test is analyzed
Testing initial water sample exposure concentrations is 0.5mg/L, 0.25mg/L, 0.125mg/L, 0.0625mg/L, 0.03125mg/L and 0.015625mg/L, found that sample exposure concentrations is that the cell acute toxicity of 0.5mg/L is more than 50% according to acute toxicity testing, therefore have selected 0.25mg/L, 0.125mg/L and 0.0625mg/L tri-gradients and carry out observation micronuclear rates and hypodiploid rate, detailed results is shown in Table 3.
It is generally acknowledged, CHO-K1 micronucleus test (chromosome damage effect) positive findings decision condition is: when acute toxicity < 50%, MN% presents dosage-response relation with water sample exposure concentrations.This test adopts One-WayANOVA micronuclear rates compared with control group of upchecking to have conspicuousness to increase, and level of significance is p=0.05.Wherein, micronuclear rates and hypodiploid rate be used for analyze micronucleus produce MOA, for the micronucleus produced by fracture mode, hypodiploid rate can not increase along with the increase of micronucleus; And by the micronucleus that the euploid mode of coming off produces, hypodiploid rate increases along with the increase of micronucleus.
As shown in Table 3, after the filter under water-supply plant C-I and C-II two kinds of operating modes, water and the micronucleus test in vitro of output water under all test doses all present negative findings, and this illustrates that these samples all show as chromosome not damaged effect.There is not the hereditary poisonous substance with chromosome damage effect in water and output water after this shows water-supply plant filter, and reuse backwashing wastewater and mixture manufacturing waste water also can not there is impact to this.
Table 3 filters rear water and output water CHO-K1 chromosome damage effect the results list
4, mice bone marrow micronucleus
SPF level Kun Ming mice is selected in this test, and body weight (W) is about 25 ~ 35g.Each water sample need use 50, each half of male and female.Be divided into 5 groups at random, often organize 10, each 5 of male and female (purchased from Harbin Medical University's Experimental Animal Center), test and carry out after laboratory conforms 3 days small white mouse.
In general, PCEMNR micronucleus causes positive findings decision condition and is: 1. micronuclear rates > 5 ‰; Or the microkernel incidence of 2. negative control group and positive controls has significant difference (p < 0.01 or 0.05), has dosage-response relation.As shown in Table 4, output water high (1000 ×) dosage group and in (100 ×) dosage group male and female PCEMNR (PCE) micronucleus cell rate all can be induced to increase (with negative control ratio, p < 0.01 or p < 0.05), namely under this experiment condition, these two samples are that mutagenesis is positive, and these two kinds of dosage of water are feminine gender after filter, illustrate under high dose group and middle dosage group, causing mouse marrow cell chromosome distortion effect may be caused by sterilization.All the other water samples, dosage are all negative result.Therefore, deducibility go out sterilization may increase filter after water cause chromosome damage effect.
Table 4 evaluates the rear water of filter and disinfectant mice bone marrow micronucleus
5, mouse inbred strain
The small white mouse source that this test is selected is identical with micronucleus test with dose design, is specifically grouped into each water sample and uses 35, be divided into 5 groups at random, often organize 7, terminate rear often group have 5 animals at least with warranty test.
In general, judge that the condition of the mouse sperm deformity positive is: 1. the mouse group casting tested material compared with negative control group, the negative control group abnormal rate of rate of teratosperm at least >=2 times; Or 2. have significant difference (p < 0.01) through statistics, and there is dose-response relationship.As shown in table 5, after sterilization, water outlet has the effect that male sex-cell is undergone mutation.
Table 5 filters rear water and the rear water mouse inbred strain result of sterilization
Note: with negative control ratio, * *: P < 0.01.
6, many genetic end-point biology group test evaluation water factories genetoxic is comprehensively analyzed
The toxicological test result of different science of heredity terminal is comprehensively analyzed, as shown in table 6.After filter, the different science of heredity terminal Genotoxicity assays of water all present negative findings under all test doses, are the genetoxic pollutant detecting and significantly cause gene mutation, cause DNA damage, cause chromosome damage and cause germinal mutation after this shows the filter of FB water-supply plant in water.Although water testing result occurs positive after Salmonella reversion test, SOS/umu test (-S9), micronucleus test, mouse inbred strain sterilization, this show sterilization can increase in output water cause gene mutation, cause DNA damage (directly causing damage effect), the genetoxic pollutant levels that cause chromosome damage and cause germinal mutation.But these positive findingses occurred all appear at animal subject, cell or bacterial exposure when high dose tested material (if Ames is at 7L/ ware, mouse inbred strain is under the dosage of 40L/kgbw (1000 ×)) detect the positive, Genotoxic content is caused in water outlet very low after this shows the sterilization of FB water factory, and when normally being drunk for a long time by SOS/umu test finder, its carcinogenic risk is far below EPA security risk controlling value, and Salmonella reversion test shows that after sterilization, water presents negative findings when the dosage of 3L/ ware.
In a word, shown by the Genotoxicity assay of many science of heredity terminal, under the condition casting experimental animal, cell and bacterium with the tested material being equivalent to adult's normal water amount (test 10 times of adult normals as Salmonella reversion test 3L/ ware, micronucleus and mouse sperm and drink the water yield), after filter, water and disinfectant Genotoxicity assay result all present feminine gender.
Table 6 different science of heredity terminal Genotoxicity assay result summary sheet
Claims (8)
1. the genotoxic method of the biology of genetic end-point more than kind group test evaluation potable water, it is characterized in that described method with water after the water outlet of filter tank, waterworks and sterilization for research object, with biology group genetic toxicity test: in Salmonella reversion test, body, micronucleus mice bone marrow micronucleus, mouse inbred strain, hamster ovary cell micronucleus test, SOS/umu test are evaluation criterion, namely represent to there is biological genetic toxicity security when there being 3 positive findingses in biology group genetic toxicity test.
2. the genotoxic method of many genetic end-point biology group test evaluation potable water according to claim 1, before it is characterized in that described biology group genetic toxicity test carries out, pre-service must be carried out to research object, wherein, in Salmonella reversion test, body, micronucleus mice bone marrow micronucleus and mouse inbred strain adopt same preconditioned pattern, and hamster ovary cell micronucleus test and SOS/umu test adopt same preconditioned pattern.
3. the genotoxic method of many genetic end-point biology group test evaluation potable water according to claim 2, it is characterized in that the preconditioned pattern of micronucleus mice bone marrow micronucleus and mouse inbred strain in institute's Salmonella reversion test, body adopts solid phase extraction, with XAD-2 type resin for polymeric adsorbent, concrete steps are as follows:
(1) before using by resin with heavily steaming methyl alcohol, acetone respectively extracts 8h, loads in port grinding bottle for subsequent use heavily to steam methyl alcohol immersion;
(2) resin wet method is loaded
glass adsorption column in resin height of bed 110mm, and bottom adsorption column and resin bed upper berth through methyl alcohol and acetone extraction glass fiber, then release methyl alcohol, to methyl alcohol reaches resin bed top just;
(3) distill moisture with 1000 ~ 1200ml and rinse resin column 5 ~ 6 times, after rinsing clean remaining methyl alcohol, retain resin column and be distilled water covering, in case air inlet;
(4) adsorption column upper end is connected with water container by Medical burette, and utilizing syphonic effect to control aqueous sample stream through the flow velocity of resin bed by adjustable screw folder is 50 ~ 70mL/min, and the cumulative volume crossing post water is 250L;
(5) post is crossed complete, the ether wash-out heavily steamed with 60 ~ 80ml;
(6) eluent to be collected in beaker and the anhydrous sodium sulfate adding oven dry carries out processed, and be finally concentrated into below 1ml with transferring to KD concentrator under the condition of 43 DEG C of water-baths, 4 DEG C of Refrigerator stores are for subsequent use.
4. the genotoxic method of many genetic end-point biology group test evaluation potable water according to claim 3, is characterized in that granularity 40 ~ 60 order of described XAD-2 type resin.
5. the genotoxic method of many genetic end-point biology group test evaluation potable water according to claim 3, is characterized in that in described step (5), wash-out makes ether retain 30 ~ 40min in pillar first.
6. the genotoxic method of many genetic end-point biology group test evaluation potable water according to claim 2, is characterized in that the preconditioned pattern of described hamster ovary cell micronucleus test and SOS/umu test is as follows:
(1) when gathering water sample, with water sample rinse to be measured 3 times in sampling bottle, often kind of water sampling 10L;
(2) all water samples activated again after using the APFF glass fiber filter in Millipore microfiltration systems that diameter is 142mm and 0.7 μm, aperture to filter after the enrichment of HLB post;
(3) water sample is connected to the HLB post activated by sample hose, every root HLB post enrichment water sample 2 liters, enrichment is complete and after draining water, wash-out is carried out three times for eluent divides with 10mL methylene chloride, after concentrated by rotary evaporation, add the anhydrous sodium sulfate through dehydration, dry up rear substitution 0.2mL Bioexperiment solvent DMSO in-20 DEG C of Refrigerator stores for genetoxic biological test with nitrogen.
7. the genotoxic method of many genetic end-point biology group test evaluation potable water according to claim 6, is characterized in that in described step (2), and HLB post adopts methylene chloride and methyl alcohol activation pillar.
8. the genotoxic method of many genetic end-point biology group test evaluation potable water according to claim 6, it is characterized in that in described step (3), when carrying out wash-out three times with 10mL methylene chloride for eluent divides, first time 4mL, second time 3mL and third time 3mL.
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|---|---|---|---|---|
| CN107478795A (en) * | 2017-08-24 | 2017-12-15 | 山东省城市供排水水质监测中心 | A kind of detection method of urban drinking water water body genetoxic |
| CN107764965A (en) * | 2017-10-17 | 2018-03-06 | 中国科学院生态环境研究中心 | Combined pollutant biological genetic toxicity is quick in a kind of drinking water, the method for high flux detection |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107478795A (en) * | 2017-08-24 | 2017-12-15 | 山东省城市供排水水质监测中心 | A kind of detection method of urban drinking water water body genetoxic |
| CN107764965A (en) * | 2017-10-17 | 2018-03-06 | 中国科学院生态环境研究中心 | Combined pollutant biological genetic toxicity is quick in a kind of drinking water, the method for high flux detection |
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