CN110305932A - ATP bioluminescence lgCA-lgIAThe method for marking bent method detection plated film antibiotic glass bacteria resistance energy - Google Patents
ATP bioluminescence lgCA-lgIAThe method for marking bent method detection plated film antibiotic glass bacteria resistance energy Download PDFInfo
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/02—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
- C12Q1/04—Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor
- C12Q1/06—Quantitative determination
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/02—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
- C12Q1/18—Testing for antimicrobial activity of a material
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- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2304/00—Chemical means of detecting microorganisms
- C12Q2304/60—Chemiluminescent detection using ATP-luciferin-luciferase system
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/195—Assays involving biological materials from specific organisms or of a specific nature from bacteria
- G01N2333/24—Assays involving biological materials from specific organisms or of a specific nature from bacteria from Enterobacteriaceae (F), e.g. Citrobacter, Serratia, Proteus, Providencia, Morganella, Yersinia
- G01N2333/245—Escherichia (G)
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/195—Assays involving biological materials from specific organisms or of a specific nature from bacteria
- G01N2333/24—Assays involving biological materials from specific organisms or of a specific nature from bacteria from Enterobacteriaceae (F), e.g. Citrobacter, Serratia, Proteus, Providencia, Morganella, Yersinia
- G01N2333/25—Shigella (G)
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/195—Assays involving biological materials from specific organisms or of a specific nature from bacteria
- G01N2333/24—Assays involving biological materials from specific organisms or of a specific nature from bacteria from Enterobacteriaceae (F), e.g. Citrobacter, Serratia, Proteus, Providencia, Morganella, Yersinia
- G01N2333/255—Salmonella (G)
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/195—Assays involving biological materials from specific organisms or of a specific nature from bacteria
- G01N2333/305—Assays involving biological materials from specific organisms or of a specific nature from bacteria from Micrococcaceae (F)
- G01N2333/31—Assays involving biological materials from specific organisms or of a specific nature from bacteria from Micrococcaceae (F) from Staphylococcus (G)
Abstract
The present invention relates to a kind of plated film antibiotic glass bacteria resistance detection methods, and detecting step includes: sample preparation and pretreatment;Lectotype selection and reagent, culture medium are prepared;Culture presevation, activation and bacteria suspension preparation;ATP log concentration value lgCARelative intensity of fluorescence logarithm lgIAMark Qu Jianli and inoculation bacterium solution viable bacteria ATP concentration CACalibration;Sample inoculation, culture and elution recycling;Recovered liquid IAMeasurement and its viable bacteria ATP concentration CAAnd TAIt calculates;Antibiotic rate R or antibacterial activity value A is calculated;Evaluation of result;Its special feature is that: accurate quantitative test can be carried out to the glass bacteria resistance with R or A characterization using ATP fluophotometer.Present invention provide that control sample and antimicrobial sample after elution recycling contact 0h and culture for 24 hours, measure recovered liquid IAAnd with lgIACharacterization and calculating R or A;Evaluation of result foundation is provided.The ATP bioluminescence lgC for the antibiotic glass antibacterium performance detection that the present invention researches and developsA‑lgIABent method is marked, product quality will be supported to be promoted and market order specification with advanced detection technique.
Description
Technical field
The present invention relates to the antibacterium performance test methods of antibiotic glass, specifically a kind of application ATP fluophotometer pair
It can be carried out the ATP bioluminescence of accurate quantitative detection with the antibiotic glass bacteria resistance that antibiotic rate R or antibacterial activity value A is characterized
lgCA-lgIACalibration curve method belongs to antibacterial glass Function detection technical field.
Background technique
Antibiotic glass is as a kind of novel ecological functional material, using nanometer " dispersion ", " modification " technology, by antibacterial agent with
The mode of chemical bonding belongs to coated glass class highest level in conjunction with glass;Medical care, food fresh keeping, the vehicles and
The purposes in the fields such as 3C electronic touch product is very extensive, according to world-wide markets visual report, antibiotic glass market rule in 2017
Mould is 1.8 hundred million dollars, and world market annual compound growth rate is 6.9%, it is contemplated that will break through 2.7 hundred million dollars within 2023.Although generation
First of boundary antibiotic glass production line was gone into operation in 2005 in Chinese Qinhuangdao, and China in 2007 has issued first, the whole world and resisted
Bacterium glass industry standard --- " anti-microbial coating glass " (JC/T 1054-2007);But the lag of existing detection technique is seriously made
About industry development.
Currently, anti-biotic material performance detection technical system is mainly for bacterium and fungi, various countries' bacteria resistance energy both at home and abroad
Test method principle is mostly based on the colony counting method being separately cultured to bacterium, first is that the pad pasting training that Japanese Industrial Standards propose
Support and impregnate quantitative test method;Two are derived from the antibacterial around-France of U.S. textile industry;Third is that international oscillation flask method;Four
It is derived from the dropping method of U.S. textile enterprise;Fifth is that Japanese enterprises are directed to the coverslip method of photocatalyst-type anti-biotic product research and development.Always
For body, there are following common problems in technology contents and practical application for existing antibacterium method for testing performance: first is that involved
Experimental strain is very few, it is difficult to meet the research and development of new product and Quality Control demand that enterprise grows with each passing hour;Second is that experimentation is cumbersome, correlation behaviour
Work is influenced by laboratory technician's professional experiences, and test error is big, lacks comparativity;Third is that test period 48 hours~72 hours it
Between, time and economic cost are high.In recent years, increasingly mature in the development of international Bacteria Detection technical field ATP fluorescence analysis, with
Traditional Plating is 98% compared to the correlation of ATP testing result, and accuracy is high and can realize quick detection;Developed country has incited somebody to action
The method applies in HACCP.Domestic ATP correlative study is started late, and is drawn by application demand, and existing ATP fluorescence detector is
The health supervision specified as China Health department and the relevant special inspecting equipment of food safety.Current foreign countries' anti-biotic material
Energy detection technique is studied to quantification, rapid and summary trend development, and testing result accuracy and comparativity are focused on;It has borrowed
ATP fluorescence analysis principle of reflecting formulates ISO20743:2007-2013 " Textiles-Determination of
Antibacterial activity of textile products (textile-antibiotic finish textile bacteria resistance energy
Measurement) " and ISO13629-1:2012 " Textiles-Determination of antifungal activity of
Textile products.Part1Luminescence (measurement of textile-antibiotic finish textile fungicidal properties) ", it is specified that
With the fluorimetry of anti-thin/mould performance of ATP changes of contents characterization after sample inoculation, but it is only applicable to water imbibition
And control sample it is thin/textile material or poromerics of mould increasing value > 0, closed in viable bacteria way of recycling, test condition for validity etc.
It is not suitable for having glass, ceramics of unwetted property hard surface and control sample bacterium increasing value < 0 etc. inorganic in terms of key technology
Nonmetallic materials etc.;Uncertainty of measurement assessment is not provided simultaneously.In addition, the standard method dependent antimicrobial performance characterization parameter compared with
Be it is single, only relate to antibacterial activity value A, and China then usual antibiotic rate R.
Therefore, to resist foreign technology barrier, specification domestic market order pushes industrial transformation upgrading, it would be highly desirable to research section
It emulates the advanced, accuracy and reproducibility are high, easy-to-use antibiotic glass Performance Testing Technology.The art of this patent highway route design integrates with
The world, detection method belong to the whole world and initiate, and can effectively fill up domestic and international correlative technology field blank.
Summary of the invention
The technical problem to be solved in the present invention is to provide a kind of application ATP fluophotometers to living with antibiotic rate R or antibacterial
Property value A characterization antibiotic glass bacteria resistance can be carried out the ATP bioluminescence lgC of detectionA-lgIACalibration curve method is able to solve
Antibiotic glass or even other product scope anti-biotic materials and product bacteria resistance can accurate quantitative test problems.
In order to solve the above technical problems, the technical solution adopted by the present invention is that:
A kind of detection method of plated film antibiotic glass bacteria resistance energy, comprising: (1) sample preparation and pretreatment;(2) equipment
Type selecting and reagent, culture medium are prepared;(3) culture presevation, activation and bacteria suspension preparation;(4) ATP log concentration value lgCAIt is opposite
Fluorescence intensity logarithm lgIAStandard curve is established and inoculation bacterium solution viable bacteria ATP concentration CACalibration;(5) sample inoculation, cultivate and wash
De- recycling;(6) reclaim liquid phase is to fluorescence intensity level IAMeasurement;(7) the viable bacteria ATP concentration C of recovered liquidAAnd TAReckoning and antibacterial
Rate R and antibacterial activity value A is calculated;(8) evaluation of result;It is characterized in that, using ATP fluophotometer to antibiotic rate R or anti-
The plated film antibiotic glass bacteria resistance of bacterium activity value A characterization can be carried out the ATP bioluminescence lgC of accurate quantitative testA-lgIAMark
Directrix curve method, specific:
In reclaim liquid phase to fluorescence intensity level IAIn measurement:
Quantity, size and the pre-treatment requirement for specifying control sample and antimicrobial sample, testing standard bacterial strain is passed on,
After activation, takes continuous switching 2 times Fresh bacterial cultures to prepare bacteria suspension and primary dcreening operation is carried out to its bacterium number.It is trained with test strain
Nutrient solution is by 1.0 × 10-3The ATP standard stock solution of mol/L is diluted to high and low concentration standard serial solution: 7.0 × 10-9mol/L、
7.0×10-8mol/L、7.0×10-7Mol/L is (if instrument upper limit of detection is unable to reach 10-7Mol/L magnitude or high standard
Curve it is linear poor, its ATP concentration series can be changed to 7.0 × 10-10mol/L、7.0×10-9mol/L、7.0×10- 8) and 4.2 × 10 mol/L-11mol/L、4.2×10-10mol/L、4.2×10-9Mol/L, and measure its relative intensity of fluorescence value
IA;Draw the lgC of two respective concentrationsA-lgIAStandard curve is derived from fitting equation Y=aA0X+bA0(high concentration), Y
=aAX+bA(low concentration) and linearly dependent coefficient RA0 2(high concentration), RA 2(low concentration).It is 6.0 × 10 to bacteria total amount8CFU/
After the bacteria suspension of mL carries out 10 times of gradient dilutions, its relative intensity of fluorescence value I is measuredA, according to high standard fitting equation Y
=aA0X+bA0Calculate corresponding viable bacteria ATP concentration CA;It is adjusted to obtain CARange is 5.0 × 10-8Mol/L~9.0 × 10- 8The inoculation bacterium solution of mol/L.Then, 0.3mL bacterium solution is added dropwise respectively to each group control sample and antimicrobial sample surface to be measured, immediately
Elution recycling is carried out to 6 groups of 0h contact samples with 4.7mL eluent;Using the relatively glimmering of ATP fluorescent spectrophotometer measuring recovered liquid
Light intensity value IAC0ij、IAT0ij, according to low concentration calibration curve equation formula Y=aAX+bACalculate the ATP concentration C of its viable bacteriaAOijWith
TAOij.Meanwhile contacting sample for 24 hours for 6 groups and being sealed in sterilized petri dishes, (37 ± 1) DEG C, (90 ± 2) %RH culture ± 2h for 24 hours
Afterwards;Remained on surface bacterium is recycled using mode identical with 0h contact sample and measures the relative intensity of fluorescence value of its recovered liquid
IACtij、IATtij, calculate corresponding viable bacteria ATP concentration CAtijAnd TAtij;
In antibiotic rate R and antibacterial activity value A is calculated:
According to ATP low concentration standard curve lgCA-lgIALinear equation Y=aAX+bA, contacted with 0h and cultivated for 24 hours
The relative intensity of fluorescence measured value I of every control sample and antimicrobial sample recovered liquid afterwardsAC0ij、IACtijAnd IAT0ij、IATtijBased on
Data;In the case where testing condition for validity, its bacterium increasing value F after cultivating for 24 hours is calculatedij、GijAnd antibiotic rate RijIt is living with antibacterial
Property value Aij;To every group of sample RijAnd AijArithmetic mean of instantaneous value is taken to obtain corresponding RiAnd Ai;Every batch of plated film antibiotic glass sample resists
Bacterium rate R and antibacterial activity value A is its 3 groups of sample RiAnd AiArithmetic mean of instantaneous value;And the clear related data revision of the convention and measurement are uncertain
Degree requires;
In evaluation of result:
With reference to health industry common practice and the requirement of dependent antimicrobial product standard, determine that antibacterium grading performance determines mark
It is quasi-;As the antibiotic rate R of certain group (part) plated film antibiotic glass samplei(Rij) or antibacterial activity value Ai(Aij) and other two groups (four)
When the bacteria resistance of sample can be compared to a levels be at least differed, one group of (part) sample is extracted again and repeats to test;Calculate it
Through ATP bioluminescence lgCA─lgIAThe antibiotic rate or antibacterial activity value that calibration curve method measures.If two groups of front and back (part) plated film
Antibiotic glass sample antibacterium performance level is identical, then abandons it;Take other two groups (four) remaining sample antibiotic rate Ri(Rij) or
Antibacterial activity value Ai(Aij) arithmetic mean of instantaneous value as batch (group) plated film antibiotic glass sample bacteria resistance can evaluation knot
Fruit.
The present invention by adopting the above technical scheme, compared with prior art, beneficial effect is:
(1) advanced: using modern precision instrument-ATP fluophotometer as test equipment, it is dense to have reached viable bacteria ATP
The modernization of degree measurement and glass antibacterium performance detection;Can effectively reduce human factor in experimentation influences, and avoids biography
The generally existing large error of system plate culture;It can ensure the quantification of testing result, while increase substantially testing number
According to accuracy;Detection technique has certain advance.
(2) scientific: according to ATP fluorescence analysis test philosophy, to establish the viable bacteria concentration logarithm suitable for multi-cultur es
Value lgCA- relative intensity of fluorescence logarithm lgIAStandard curve;It is real-time to construct antibiotic glass bacteria resistance energy ATP bioluminescence
The mathematical model of quantitative analysis method.Meanwhile country variant consumer perceptions habit is taken into account, take antibiotic rate R and antibacterial activity
Value A is correlated performance evaluation index, improves the science and versatility of detection method.
(3) innovative: compared with the conventional method that existing operation is numerous, error is big, the period is long, this patent method was being tested
Automation and the higher ATP fluophotometer of intelligent level are introduced in journey, are greatly simplified experimental procedure, are realized glass
The precision of antibacterium performance test results and quantification simultaneously have good reproducibility and comparativity;Survey is greatly shortened simultaneously
It tries the period, reduce testing cost;Presently relevant the field of test technology blank can effectively be filled up.
(4) perspective: to establish with lgCA、lgIAStandard curve quantitative analysis method based on linear relationship, innovation is simultaneously
Enrich bacteria suspension viable bacteria content characterization and measuring method, specify control sample, standard liquid concentration, determination step, calculation formula,
The technology contents such as uncertainty;The pioneering recovered liquid viable bacteria relative intensity of fluorescence value I directly measured with instrumentAIt evaluates as a result
Form calculates and determines antibiotic rate R or antibacterial activity value A, and by group and a between-group variation coefficient CV to investigate measurement not true
Fixed degree, technically has centainly perspective.
(5) operability: ATP fluophotometer is cheap, it is easy to operate, be widely used, this patent establish with sample
The plated film antibiotic glass bacteria resistance energy ATP fluorometric investigation method letter that the variation of inoculation viable bacteria ATP concentration is attached most importance to before and after product culture
Easy row, description of Related Art is clear and specific, should be readily appreciated that and grasps;Have stronger operability in implementation process, fits
For the horizontal Experiment on Microbiology personnel of different majors, achievements conversion and popularization and application may advantageously facilitate.
(6) universality: because ATP is prevalent in, life entity is intracellular, and patented method can expand for experimental strain and provide tool
The detection technique support for thering is wide spectrum to be worth;The introducing of pertinent instruments can greatly simplify experimental procedure, reduce testing cost;Be conducive to
Expand inspection, learn, grind, produces all circles promote and apply, can support coated glass bacteria resistance energy detection technique realization generalization, together
When can to the product scopes bacteria resistance energy detection technique research such as ceramics, plastics provide reference.
Further, preferred embodiment of the invention is:
The sample preparation and pretreatment carries out in the steps below:
(1) control sample: in addition to not carrying out anti-microbial coating processing, classification, raw material, technique and the appearance of control sample, ruler
Very little, quantity etc. is identical with antibiotic glass sample to be measured;Each strain test uses 6 groups of samples;Wherein 0h is contacted and is trained for 24 hours
It is each with 3 groups to support test, every group of 5 samples;
(2) antimicrobial sample: the horizontal glass test plate (panel) through antimicrobial component coating film treatment can be sunlight controlling coated glass, low
The product categories such as radiation film coating glass;Sample test surface immaculate, speckle, film surface and glass surface are without scuffing;Having a size of (50 ±
2) mm × (50 ± 2) mm, thickness are not more than 10mm.Antimicrobial sample quantity is identical as control sample, every group of sample to be tested selection one
Group control sample as object of reference and effectively identifies;
(3) sample pre-treatments: impregnating 1min in 75% ethanol solution for control sample and antimicrobial sample before experiment, and
With the abundant cleaning sample of sterile water to remove ethyl alcohol on superclean bench;Sample surface to be measured is put into upwards after natural drying
It is spare in sterilized petri dishes;
The lectotype selection and reagent, culture medium are prepared, and are carried out in the steps below:
(1) General Requirement: test analytical reagents and meet tertiary effluent as defined in GB/T 6682-2008 (distilled water or
Deionized water), laboratory has the safe qualification of two stage biological, and personnel have regular Microbiological Lab's working experience;
(2) instrument and equipment: the superclean bench of two stage biological safety cabinet or lustration class not less than 100;The light of fluorescence containing ATP
The ATP bioluminescence rapid detection system of meter, matched reagent box, pressurizer and inspissator, plastic test tube etc. is spent, wherein ATP is glimmering
Light spectrometer wavelength range 300nm~650nm, ATP Concentration Testing range 10-13Mol/L~10-7mol/L;(20~50) DEG C ± 1
DEG C, the constant temperature and humidity incubator of (50~95) %RH ± 2%RH;The pressuresteam sterilization of (121 ± 2) DEG C, (103 ± 5) kPa
Device;- 20 DEG C~-70 DEG C of low temperature refrigerator;0 DEG C~8 DEG C of refrigerating box;The electronic balance of sensibility reciprocal 0.001g;Frequency range (30~
50) ultrasonic cleaner of kHz;The vortex oscillator of the range of speeds (500~3000) r/min;The pH of precision ± 0.1 (25 DEG C)
Meter;Electric furnace;
(3) material utensil: the sterile measuring pipette of 1mL, 10mL;0.05mL, 0.1mL, 0.2mL, 1mL, 5mL, 10mL (meter
Error is measured less than single track changeable fluid liquid-transfering gun and sterile liquid transfer gun head 1%);The sterile conical flask of capacity 250mL, 500mL;
The sterile petri dish of diameter 90mm;Maxwell bacterium standard opacity tube and mating test tube;Sterile test tube;Diameter connects no more than 4mm's
Kind ring;L stick;Alcolhol burner;Sterilize tweezers;Medical adhesive tape;The ruler of scale division value 1mm;Thermometer;
The stopwatch of precision 0.01s;A6 white copy paper;0.7mm core black gel ink pen;
(4) reagent: 75% ethanol solution;(121 DEG C of high pressure sterilization 15min, 5 DEG C~10 DEG C are deposited 85% physiological saline
Put 30d);
(5) medium/liquid (commercially available medium/liquid can be used): through 121 DEG C of high pressure sterilizations after matched medium/liquid packing
15min, 2 DEG C~8 DEG C storage 30d;
Nutrient agar (NA): 5g beef extract, 10g peptone, 5g sodium chloride, 15g agar are dissolved by heating in 1000mL water
In, adjust pH to 7.0~7.2;
Nutrient broth (NB): 3g beef extract, 10g peptone, 5g sodium chloride are dissolved by heating in 1000mL water, pH is adjusted
To 7.0~7.2;
Salmonella preservation is with brain heart oxoid meat soup (BHI): by 10g peptone, 5g sodium chloride, 2.5g phosphoric acid hydrogen two
Sodium, 2g glucose dissolve by heating in 500mL cattle heart leachate, adjust pH to 7.4 ± 0.2;
The culture solution of escherichia coli and Shigella/staphylococcus aureus and salmonella: by 1:500/1:100
Nutrient broth (NB) mixed with 85% sterile saline solution, adjust pH to 7.0~7.2;
(6) ATP fluorescence reaction reagent (or with commercial reagent): in addition to phosphate buffer solution, matched ATP fluorescence reaction examination
- 20 DEG C~-70 DEG C of agent preservations, use in 6 months;
Dilution buffer: 0.005mol/L and the disodium phosphate soln for containing 0.037% sucrose, adjusting pH to 7.2 ±
0.2;121 DEG C of high pressure sterilizations 15min, 2 DEG C~8 DEG C storage 30d;
ATP standard reagent stoste: by 60.5mg trinosin (C10H14O13P3Na2·3H2O) it is dissolved in 100mL
In water, being configured to concentration is 1 × 10-3The solution of mol/L, -20 DEG C of freezings are sealed 6 months;
ATP fluorescent reagent buffer solution: by 1117mg trishydroxymethylaminomethane, 183mg disodium ethylene diamine tetraacetate,
808mg magnesium acetate, 6.7mg dithiothreitol, the beta-cyclodextrin of 25000mg and 925mg glucose are dissolved by heating in 250mL water
In, adjust pH to 7.5 ± 0.2;It is used in 8h;
ATP lysate: 4.6 international units/ml apyrase (EC:3.6.1.5) and 46 is international single
Adenosine phosphate deaminase (EC:3.5.4.6 or EC:3.5.4.17), 37mg sucrose, the 20mg bovine serum albumin of position/ml is dissolved in
10mL concentration is to adjust in pH to 6.0 ± 0.5,8h in the 2-morpholine ethane sulfonic acid buffer solution of 0.05mol/L and use (1mL cracking
ATP concentration in nutrient broth can be down to 10 in 15min by liquid-13Mol/L or less);
ATP extracting solution: 45mg trishydroxymethylaminomethane is dissolved by heating in 9.8ml water, is 10% with 0.2ml concentration
Benza mix after, adjust pH to 12.0 ± 0.5;
ATP fluorescent reagent: by 16mg luciferase (EC:1.13.12.7), the D- fluorescein of 12.6mg, 56mg cow's serum
Albumen is dissolved in the ATP fluorescent reagent buffer solution of 30mL, and 15min is stored at room temperature after mixing, is used in 3h;
Culture presevation, activation and the bacteria suspension preparation, carries out in the steps below:
(1) test strain: escherichia coli ATCC 8739;Staphylococcus aureus ATCC 6538;Salmonella
ATCC 14028;Shigella CMCC 51105 (or provided by national corresponding culture presevation administrative center and can be traced to the source other
Strain);
(2) culture presevation: opening freeze-drying lactobacillus pipe with sterile working, and adequate nutrition meat soup (sramana is added with capillary syring
Salmonella BHI broth), pressure-vaccum makes strain melt dispersion for several times.Then, a little test strain suspension is instilled and 5mL is housed
In the test tube of~10mL nutrient broth, (37 ± 1) DEG C culture for 24 hours~48h;As slant preservation bacterium, (5 ± 1) DEG C storage (does not surpass
Spend 1 month), inoculation times were no more than for 14 generations;
(3) actication of culture: slant preservation bacterium is transferred nutrient agar slant medium, and (37 ± 1) DEG C culture 18h~for 24 hours;
Switching 1 time daily, continuous switching are no more than 15d.Test is trained using the 3rd generation~the 14th generation and in the interior Fresh bacterial transferred for 24 hours
Support object;
(4) prepared by bacteria suspension: scraping a small amount of Fresh bacterial from strain activation and culture base with oese, test strain is added
Bacteria suspension is made in culture solution;1000r/min shakes test tube 1min or with 30cm amplitude of oscillation shaking test tube 80 times, it is ensured that bacterial suspension is equal
It is even.Appropriate bacteria suspension is moved in sterile test tube matched with Maxwell standard opacity tube, it is white in A6 with 0.7mm core black gel ink pen
The parallel lines that 3 length are 10cm are drawn on color copy paper;Estimate test tube and standard opacity tube (nominal concentration 6.0 × 108CFU/
ML culture solution is added dropwise until the two turbidity is identical in differences in turbidity);
The ATP log concentration value lgCARelative intensity of fluorescence logarithm lgIAStandard curve is established and inoculation bacterium solution is living
Bacterium ATP concentration CACalibration carries out in the steps below:
(1) standard serial solution is determining and prepared by ATP bioluminescence test specimens: using test strain culture solution by 1.0 × 10- 3The ATP standard stock solution of mol/L is diluted to high and low concentration standard serial solution: 7.0 × 10-9mol/L、7.0×10-8mol/L、
7.0×10-7Mol/L is (if instrument upper limit of detection is unable to reach 10-7Mol/L magnitude or high standard curve it is linear compared with
Its ATP concentration series can be changed to 7.0 × 10 by difference-10mol/L、7.0×10-9mol/L、7.0×10-8) and 4.2 × 10 mol/L-11mol/L、4.2×10-10mol/L、4.2×10-9Mol/L is simultaneously mixed.Then, with sterilizing liquid-transfering gun by the ATP standard of 0.1mL
Serial solution is moved to respectively in three sterile test tubes, and phosphate buffer of the 0.9mL containing 0.037% sucrose is successively added dropwise and mixes
It is even;The mixed solution of 0.1mL various concentration is moved to respectively in three instrument sterile test tubes again, as ATP bioluminescence
Test Duplicate Samples;
(2) relative intensity of fluorescence value IAMeasurement: according to relative intensity of fluorescence value I in this patentAMeasuring method, with test organisms
After kind culture solution is as blank sample liquid validation instrument and reagent set background;According to the sequence of concentration from low to high, to various concentration
The ATP that 0.1mL is added dropwise in three Duplicate Samples of ATP standard solution respectively extracts reagent, and the ATP fluorescence examination of 0.1mL is instilled after mixing
Agent;It mixes again, with its relative intensity of fluorescence value of ATP fluorescent spectrophotometer measuring and records immediately and (ensure each link operating time
Unanimously, cross contamination is avoided).Each Duplicate Samples minute is no more than 15s, with each three Duplicate Samples of concentration ATP standard solution
The arithmetic mean of instantaneous value of relative intensity of fluorescence value is its IAMeasured value;
(3) ATP log concentration value lgCARelative intensity of fluorescence logarithm lgIAStandard curve is established: with ATP standard series
The relative intensity of fluorescence logarithm lgI of solutionAAs abscissa, with its corresponding ATP log concentration value lgCAFor ordinate work
Figure;Calibration curve is carried out to mathematical relationship between the two, draws the lgC of two respective concentrationsA-lgIAStandard curve;And it applies
Least square fitting method is derived from the linear equation Y=a of curveA0X+bA0(high concentration), Y=aAX+bA(low concentration) and phase
Close coefficients RA0 2(high concentration), RA 2(low concentration).Work as RA0 2And RA 2>=0.98, it when confidence level >=0.95, is done according to this patent
Measurement it is effective;
(4) it is inoculated with the viable bacteria ATP concentration C of bacterium solutionACalibration: according to relative intensity of fluorescence value I in this patentAMeasuring method is right
Bacteria total amount is 6.0 × 10 after the turbidimetry primary dcreening operation of Maxwell8The relative fluorescence of 10 times of gradient dilution liquid of bacteria suspension of CFU/mL is strong
Angle value IAIt is measured;According to high standard fitting equation Y=aA0X+bA0It calculates and demarcates its viable bacteria ATP concentration CA.Through
Test strain culture solution adjusts to obtain CARange is 5.0 × 10-8Mol/L~9.0 × 10-8The inoculation bacterium solution of mol/L, measures and remembers
Record relative intensity of fluorescence value I of the 0.3mL inoculation bacterium solution after the dilution of 4.7mL eluent in 1minA0;
Sample inoculation, culture and the elution recycling, carries out in the steps below:
(1) sample inoculation culture: 0.3mL inoculation bacterium solution is added dropwise respectively in each group control sample and is resisted with sterilizing liquid-transfering gun
Bacterium sample surface to be measured is (with curve lgCA-lgIACalibration is derived from same branch test strain stoste test tube with bacterium solution, and 2 DEG C ± 0.2 DEG C
Save, used in 2h), bacterium solution is smeared uniformly with L stick (attachment is inoculated with bacterium solution but does not hang drop), it is made to cover sample whole table
Face.Ware lid is covered, is sealed the plate for contacting sample for 24 hours equipped with 6 groups with medical adhesive tape;(37 ± 1) DEG C, (90 ± 2) %RH training
Support ± 2h for 24 hours;
(2) elution recycling: (0.2% sterile surfaces activity can be added using 4.7mL test strain culture solution as eluent
Agent), after 6 groups of 0h contact sample inoculation bacteriums, sufficiently eluted using solid or liquid swab method immediately;6 groups cultivate for 24 hours
Sample uses type of elution identical with 0h contact sample to recycle bacterium.Solid swab method is to be soaked with saturation eluent with head
Aseptic cotton carrier is uniformly embrocated 10 times in each sample surfaces back and forth anyhow respectively, and rotates with it cotton swab;Cut off experimenter's hand
Cotton swab is placed in the sterile test tube equipped with remaining eluent, as recovered liquid (if recovered liquid after mixing by the swab stick of contact portion
Less than 5mL, eluent is added to 5mL).Liquid swab method draws 4.7mL eluent with sterilizing liquid-transfering gun, in plate repeatedly
It rinses each sample surfaces at least 4 times, sufficiently elute and moves into washing lotion in sterile test tube, as recovered liquid (if returning after mixing
Liquid is received less than 5mL, adds eluent to 5mL);
The reclaim liquid phase is to fluorescence intensity level IAMeasurement carries out in the steps below:
(1) instrument and reagent set relative intensity of fluorescence background value calibration: use sterilizing liquid-transfering gun by 0.1mL test strain culture
The ATP lysate of liquid, 0.8mL phosphate buffer solution and 0.1mL containing 0.037% sucrose is separately added into same branch sterile test tube
In and mix well, then the above-mentioned mixed solution of 0.1mL is successively moved in three instrument sterile test tubes, stand 5min~
30min, as skip test Duplicate Samples.The ATP that 0.1mL is added dropwise respectively into three Duplicate Samples extracts reagent, instills after mixing
The ATP fluorescent reagent of 0.1mL;It mixes again, uses its relative intensity of fluorescence value of ATP fluorescent spectrophotometer measuring I immediatelyAAnd it records
(ensuring that each link operating time is consistent, avoid cross contamination).Each Duplicate Samples minute is no more than 15s, with three blank
The arithmetic mean of instantaneous value of Duplicate Samples relative intensity of fluorescence value is tested (or to use according to pertinent instruments as instrument and reagent set background values
Illustrate to calibrate background values);
(2) reclaim liquid phase is to fluorescence intensity level IAMeasurement: it if blank reagent group background level meets instrument requirement, uses
The ATP lysate for phosphate buffer solution and 0.1mL of the liquid-transfering gun by 0.1mL recovered liquid, 0.8mL containing 0.037% sucrose that sterilize
Be separately added into same branch sterile test tube, after mixing well by the above-mentioned mixed solution of 0.1mL successively move to three instruments without
In bacterium test tube, 5min~30min is stood, as ATP fluorometric investigation Duplicate Samples.It is added dropwise 0.1mL's respectively into three Duplicate Samples
ATP extracts reagent, and the ATP fluorescent reagent of 0.1mL is instilled after mixing;It mixes again, uses its phase of ATP fluorescent spectrophotometer measuring immediately
To fluorescence intensity level IAAnd it records and (ensures that each link operating time is consistent, avoid cross contamination).Each Duplicate Samples minute
No more than 15s, using the arithmetic mean of instantaneous value of three ATP fluorometric investigation Duplicate Samples relative intensity of fluorescence values as the I of recovered liquidAMeasurement
Value (or instrument matched reagent box is used, it is required according to operation instructions, directly upper machine measures the opposite of three Duplicate Samples of recovered liquid
Fluorescence intensity level IA);
The recovered liquid viable bacteria ATP concentration CAAnd TAIt calculates and antibiotic rate R and antibacterial activity value A is calculated, by following steps
It is rapid to carry out:
(1) the viable bacteria ATP concentration C of recovered liquidAAnd TAIt calculates
According to ATP low concentration standard curve lgCA-lgIALinear equation Y=aAX+bA, calculate control sample and antibacterial
After sample is contacted through 0h and is cultivated for 24 hours, the viable bacteria ATP concentration C of recovered liquidAAnd TA;Relevant calculation (uses instrument matched reagent box
When, the viable bacteria ATP concentration C of 1mL recovered liquid is calculated according to its practical sample volumeAAnd TA) see formula (1)~(12):
In formula:
CA0And CAtThe average ATP concentration that -3 groups of 0h are contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);
CA0iAnd CAtiThe average ATP concentration that-every group 0h is contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are
Mole every liter (mol/L);Sample group i=1,2,3;
CA0ijAnd CAtijThe ATP concentration that-every 0h is contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;bA- low concentration standard curve lgCA-lgIAIn vertical axis intercept;
TA0And TAtThe average ATP concentration that -3 groups of 0h are contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);
TA0iAnd TAtiThe average ATP concentration that-every group 0h is contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are
Mole every liter (mol/L);Sample group i=1,2,3;
TA0ijAnd TAtijThe ATP concentration that-every 0h is contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
(2) condition for validity is tested
If recovered liquid and 0.3mL inoculation the bacterium solution 1min after the dilution of 4.7mL eluent of every 0h contact control sample
Interior relative intensity of fluorescence measured value is close, i.e.,Every after cultivating for 24 hours control sample recovered liquid relative fluorescence it is strong
Spend the logarithm of measured valueThat is CAtij≥0.1×CA0ij.Then when 3 groups of 0h contact control sample reclaim liquid phase
To fluorescent strength determining valueGroup in and when between-group variation coefficient CV≤10% (involved calculation formula is shown in this patent correlation
Uncertainty of measurement requirement), the measurement carried out according to this patent method is effective.
(3) bacterium increasing value Fij、GijIt calculates
Every control sample and antimicrobial sample after cultivating for 24 hours, bacterium increasing value Fij、GijRespectively according to formula (13),
(14) it calculates:
In formula:
FijAnd GijThe bacterium increasing value of-every control sample and antimicrobial sample after cultivating for 24 hours, sample group i=1,
2,3;Every group of sample number into spectrum j=1,2,3,4,5;
CA0ijAnd CAtijThe ATP concentration that-every 0h is contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
TA0ijAnd TAtijThe ATP concentration that-every 0h is contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;
(4) antibiotic rate R is calculated
It tests under condition for validity, the antibiotic rate R of every plated film antibiotic glass sampleij, every group and every batch of sample antibiotic rate
RiIt is calculated respectively according to formula (15), (16), (17) with R:
In formula:
RijThe antibiotic rate of-every plated film antibiotic glass sample, %;Sample group i=1,2,3;Every group of sample number into spectrum j=
1,2,3,4,5;
RiThe antibiotic rate of-every group plated film antibiotic glass sample, %;Sample group i=1,2,3;
R-every batch of plated film antibiotic glass sample antibiotic rate, %;
CAtijAnd TAtij- every antimicrobial sample and control sample recycle the average ATP concentration of viable bacteria after cultivating for 24 hours, single
Position is mole every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
WithAfter cultivating for 24 hours, the relative intensity of fluorescence of recovered liquid is measured for-every antimicrobial sample and control sample
Value, RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;
(5) antibacterial activity value A is calculated
It tests under condition for validity, the antibacterial activity value A of every plated film antibiotic glass sampleij, every group and every batch of sample it is anti-
Bacterium activity value AiIt is calculated respectively according to formula (18), (19), (20) with A:
In formula:
AijThe antibacterial activity value of-every plated film antibiotic glass sample;Sample group i=1,2,3;Every group of sample number into spectrum j=
1,2,3,4,5;
AiThe antibacterial activity value of-every group plated film antibiotic glass sample, sample group i=1,2,3;
A-every batch of plated film antibiotic glass sample antibacterial activity value;
FijAnd GijThe bacterium increasing value of-every control sample and antimicrobial sample after cultivating for 24 hours, wherein sample group i
=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;
(6) data revision of the convention requirement: the concentration of calibration ATP standard serial solution and the work for being inoculated with bacterium solution, sample recovered liquid
Bacterium ATP concentration CAWhen, with reference to the data revision of the convention regulation in GB 4789.2-2016 in relation to clump count;Work as CALess than 100mol/L
When, " rounding up " round numbers;Work as CAWhen not less than 100mol/L, preceding 2 bit digital is taken after the 3rd bit digital " rounding up ", after
Face replaces digit with 0;It can also be indicated with 10 exponential form, " rounding up " uses two effective digitals afterwards.Control sample and
After antimicrobial sample is contacted through 0h and cultivated for 24 hours, reclaim liquid phase is to fluorescent strength determining value round numbers, antibiotic rate Rij、Ri, R calculate
As a result three effective digitals are taken;Bacterium increasing value Fij、GijWith antibacterial activity value Aij、Ai, A calculated result take two effective digitals;
(7) uncertainty of measurement: this patent method, which mainly passes through, to be calculated control sample and antimicrobial sample and contacts through 0h and for 24 hours
After culture, reclaim liquid phase is in the group of fluorescent strength determining value and between-group variation coefficient CV=σ ÷ μ × 100% (μ, σ and C
V calculated result remains into 2 significant digits), judge ATP fluorimetric assay for biological materials method being applied to plated film antibiotic glass antibacterium
The reproducibility of performance test;In regulation group and between-group variation coefficient CV≤10%.
5 control samples, 5 antimicrobial samples and 5 control samples after cultivating for 24 hours of every group of 0h contact, 5 it is anti-
Bacterium sample, arithmetic mean of instantaneous value of the reclaim liquid phase to fluorescent strength determining valueAnd Respectively according to formula
(21), (22) calculate (sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=
1,2,3;In formula With Respectively every group of control sample and antimicrobial sample are contacted through 0h and are cultivated for 24 hours
Afterwards, the relative intensity of fluorescence measured value of each Duplicate Samples):
15 control samples, 15 antimicrobial samples and 15 control samples, 15 after cultivating for 24 hours that 3 groups of 0h are contacted
Part antimicrobial sample, arithmetic mean of instantaneous value of the reclaim liquid phase to fluorescent strength determining value And Respectively according to formula
(23), (24) calculate (sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=
1,2,3;In formula With Respectively every group of control sample and antimicrobial sample are contacted through 0h and are cultivated for 24 hours
Afterwards, the relative intensity of fluorescence measured value of each Duplicate Samples):
5 control samples, 5 antimicrobial samples and 5 control samples after cultivating for 24 hours of every group of 0h contact, 5 it is anti-
Bacterium sample, standard deviation of the reclaim liquid phase to fluorescent strength determining value And Respectively according to formula (25)
(26) (sample group i=1,2,3 is calculated;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=1,2,
3;In formula With After respectively every group of control sample and antimicrobial sample are contacted through 0h and cultivated for 24 hours, respectively
The relative intensity of fluorescence measured value of Duplicate Samples):
15 control samples, 15 antimicrobial samples and 15 control samples, 15 after cultivating for 24 hours that 3 groups of 0h are contacted
Part antimicrobial sample, standard deviation of the reclaim liquid phase to fluorescent strength determining value And Respectively according to formula
(27) and (28) calculate (sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=
1,2,3;In formula With Respectively every group of control sample and antimicrobial sample are contacted through 0h and are cultivated for 24 hours
Afterwards, the relative intensity of fluorescence measured value of each ATP test Duplicate Samples):
The evaluation of result of the plated film antibiotic glass sample bacteria resistance energy, carries out in the steps below:
(1) with reference to health industry common practice and the requirement of dependent antimicrobial product standard, following classification criterion is taken:
If using antibiotic rate R as correlated performance evaluation index: working as Rij/Ri(staphylococcus aureus when/R < 90%
With salmonella Rij/Ri/ R < 80%), sample is without antibacterial actions;As 90%≤Rij/Ri(golden yellow grape when/R < 99%
80%≤R of coccus and salmonellaij/Ri/ R < 90%), sample has antibacterial actions;As 99%≤Rij/Ri/ R < 99.9%
When (90%≤R of staphylococcus aureus and salmonellaij/Ri/ R < 99%), sample antibacterial actions are stronger;Work as Rij/Ri/R
(staphylococcus aureus and salmonella R when >=99.9%ij/Ri/ R >=99%), sample antibacterial actions are extremely strong;
If using antibacterial activity value A as correlated performance evaluation index: working as Aij/Ai(Staphylococcus aureus when/A < 1.0
Bacterium and salmonella Aij/Ai/ A < 0.5), sample is without antibacterial actions;As 1.0≤Aij/Ai(Staphylococcus aureus when/A < 2.0
0.5≤A of bacterium and salmonellaij/Ai/ A < 1.0), sample has antibacterial actions;As 2.0≤Aij/AiIt is (golden yellow when/A < 3.0
1.0≤A of color staphylococcus and salmonellaij/Ai/ A < 2.0), sample antibacterial actions are stronger;Work as Aij/Ai(gold when/A >=3.0
Staphylococcus aureus and salmonella Aij/Ai/ A >=2.0), sample antibacterial actions are extremely strong;
(2) as the antibiotic rate R of certain group (part) plated film antibiotic glass samplei(Rij) or antibacterial activity value Ai(Aij) with other two
When the bacteria resistance of group (four) sample can be compared to a levels be at least differed, one group of (part) sample is extracted again and is repeated in fact
It tests;It is calculated through ATP bioluminescence lgCA─lgIAThe antibiotic rate or antibacterial activity value that calibration curve method measures.If front and back two
Group plated film antibiotic glass sample antibacterium performance level is identical, then abandons it;Take other two groups (four) remaining sample antibiotic rate Ri
(Rij) or antibacterial activity value Ai(Aij) arithmetic mean of instantaneous value as batch (group) plated film antibiotic glass sample bacteria resistance can
Evaluation result;
Specific embodiment
Below with reference to preferred embodiment, the present invention will be described in detail, so that advantages and features of the invention can be easier to
It is readily appreciated by one skilled in the art, so as to make a clearer definition of the protection scope of the present invention.
The present embodiment is added to the plated film antibiotic glass sample bacteria resistance that nanometer silver-series antibacterial agent is process with surface
It can be illustrated for detection.
Specific detection method carries out in the steps below:
(1) sample preparation and pretreatment
1.1 control samples: in addition to not carrying out anti-microbial coating processing, classification, raw material, technique and the appearance of control sample, ruler
Very little, quantity etc. is identical with antibiotic glass sample to be measured;Each strain test uses 6 groups of samples;Wherein 0h is contacted and is trained for 24 hours
It is each with 3 groups to support test, every group of 5 samples.
1.2 antimicrobial samples: the horizontal glass test plate (panel) through antimicrobial component coating film treatment can be sunlight controlling coated glass, low
The product categories such as radiation film coating glass;Sample test surface immaculate, speckle, film surface and glass surface are without scuffing;Having a size of (50 ±
2) mm × (50 ± 2) mm, thickness are not more than 10mm.Antimicrobial sample quantity is identical as control sample, every group of sample to be tested selection one
Group control sample as object of reference and effectively identifies.
1.3 sample pre-treatments: impregnating 1min in 75% ethanol solution for control sample and antimicrobial sample before experiment, and
With the abundant cleaning sample of sterile water to remove ethyl alcohol on superclean bench;Sample surface to be measured is put into upwards after natural drying
It is spare in sterilized petri dishes.
(2) lectotype selection and reagent, culture medium are prepared
2.1 General Requirements: test analytical reagents and meet tertiary effluent as defined in GB/T 6682-2008 (distilled water or
Deionized water), laboratory has the safe qualification of two stage biological, and personnel have regular Microbiological Lab's working experience.
2.2 instrument and equipments: the superclean bench of two stage biological safety cabinet or lustration class not less than 100;The light of fluorescence containing ATP
The ATP bioluminescence rapid detection system of meter, matched reagent box, pressurizer and inspissator, plastic test tube etc. is spent, wherein ATP is glimmering
Light spectrometer wavelength range 300nm~650nm, ATP Concentration Testing range 10-13Mol/L~10-7mol/L;(20~50) DEG C ± 1
DEG C, the constant temperature and humidity incubator of (50~95) %RH ± 2%RH;The pressuresteam sterilization of (121 ± 2) DEG C, (103 ± 5) kPa
Device;- 20 DEG C~-70 DEG C of low temperature refrigerator;0 DEG C~8 DEG C of refrigerating box;The electronic balance of sensibility reciprocal 0.001g;Frequency range (30~
50) ultrasonic cleaner of kHz;The vortex oscillator of the range of speeds (500~3000) r/min;The pH of precision ± 0.1 (25 DEG C)
Meter;Electric furnace.
2.3 material utensils: the sterile measuring pipette of 1mL, 10mL;0.05mL, 0.1mL, 0.2mL, 1mL, 5mL, 10mL (meter
Error is measured less than single track changeable fluid liquid-transfering gun and sterile liquid transfer gun head 1%);The sterile conical flask of capacity 250mL, 500mL;
The sterile petri dish of diameter 90mm;Maxwell bacterium standard opacity tube and mating test tube;Sterile test tube;Diameter connects no more than 4mm's
Kind ring;L stick;Alcolhol burner;Sterilize tweezers;Medical adhesive tape;The ruler of scale division value 1mm;Thermometer;
The stopwatch of precision 0.01s;A6 white copy paper;0.7mm core black gel ink pen.
2.4 reagents: 75% ethanol solution;(121 DEG C of high pressure sterilization 15min, 5 DEG C~10 DEG C are deposited 85% physiological saline
Put 30d).
2.5 medium/liquids (can use commercially available medium/liquid): through 121 DEG C of high pressure sterilizations after matched medium/liquid packing
15min, 2 DEG C~8 DEG C storage 30d;
Nutrient agar (NA): 5g beef extract, 10g peptone, 5g sodium chloride, 15g agar are dissolved by heating in 1000mL water
In, adjust pH to 7.0~7.2;
Nutrient broth (NB): 3g beef extract, 10g peptone, 5g sodium chloride are dissolved by heating in 1000mL water, pH is adjusted
To 7.0~7.2;
Salmonella preservation is with brain heart oxoid meat soup (BHI): by 10g peptone, 5g sodium chloride, 2.5g phosphoric acid hydrogen two
Sodium, 2g glucose dissolve by heating in 500mL cattle heart leachate, adjust pH to 7.4 ± 0.2;
The culture solution of escherichia coli and Shigella/staphylococcus aureus and salmonella: by 1:500/1:100
Nutrient broth (NB) mixed with 85% sterile saline solution, adjust pH to 7.0~7.2.
2.6ATP fluorescence reaction reagent (or with commercial reagent): in addition to phosphate buffer solution, matched ATP fluorescence reaction examination
- 20 DEG C~-70 DEG C of agent preservations, use in 6 months;
Dilution buffer: 0.005mol/L and the disodium phosphate soln for containing 0.037% sucrose, adjusting pH to 7.2 ±
0.2;121 DEG C of high pressure sterilizations 15min, 2 DEG C~8 DEG C storage 30d;
ATP standard reagent stoste: by 60.5mg trinosin (C10H14O13P3Na2·3H2O) it is dissolved in 100mL
In water, being configured to concentration is 1 × 10-3The solution of mol/L, -20 DEG C of freezings are sealed 6 months;
ATP fluorescent reagent buffer solution: by 1117mg trishydroxymethylaminomethane, 183mg disodium ethylene diamine tetraacetate,
808mg magnesium acetate, 6.7mg dithiothreitol, the beta-cyclodextrin of 25000mg and 925mg glucose are dissolved by heating in 250mL water
In, adjust pH to 7.5 ± 0.2;It is used in 8h;
ATP lysate: 4.6 international units/ml apyrase (EC:3.6.1.5) and 46 is international single
Adenosine phosphate deaminase (EC:3.5.4.6 or EC:3.5.4.17), 37mg sucrose, the 20mg bovine serum albumin of position/ml is dissolved in
10mL concentration is to adjust in pH to 6.0 ± 0.5,8h in the 2-morpholine ethane sulfonic acid buffer solution of 0.05mol/L and use (1mL cracking
ATP concentration in nutrient broth can be down to 10 in 15min by liquid-13Mol/L or less);
ATP extracting solution: 45mg trishydroxymethylaminomethane is dissolved by heating in 9.8ml water, is 10% with 0.2ml concentration
Benza mix after, adjust pH to 12.0 ± 0.5;
ATP fluorescent reagent: by 16mg luciferase (EC:1.13.12.7), the D- fluorescein of 12.6mg, 56mg cow's serum
Albumen is dissolved in the ATP fluorescent reagent buffer solution of 30mL, and 15min is stored at room temperature after mixing, is used in 3h.
(3) culture presevation, activation and bacteria suspension preparation
3.1 test strains: escherichia coli ATCC 8739;Staphylococcus aureus ATCC 6538;Salmonella
ATCC 14028;Shigella CMCC 51105 (or provided by national corresponding culture presevation administrative center and can be traced to the source other
Strain).
3.2 culture presevation: opening freeze-drying lactobacillus pipe with sterile working, and adequate nutrition meat soup (sramana is added with capillary syring
Salmonella BHI broth), pressure-vaccum makes strain melt dispersion for several times.Then, a little test strain suspension is instilled and 5mL is housed
In the test tube of~10mL nutrient broth, (37 ± 1) DEG C culture for 24 hours~48h;As slant preservation bacterium, (5 ± 1) DEG C storage (does not surpass
Spend 1 month), inoculation times were no more than for 14 generations.
3.3 actication of culture: slant preservation bacterium is transferred nutrient agar slant medium, and (37 ± 1) DEG C culture 18h~for 24 hours;
Switching 1 time daily, continuous switching are no more than 15d.Test is trained using the 3rd generation~the 14th generation and in the interior Fresh bacterial transferred for 24 hours
Support object.
The preparation of 3.4 bacteria suspensions: a small amount of Fresh bacterial is scraped from strain activation and culture base with oese, test strain is added
Bacteria suspension is made in culture solution;1000r/min shakes test tube 1min or with 30cm amplitude of oscillation shaking test tube 80 times, it is ensured that bacterial suspension is equal
It is even.Appropriate bacteria suspension is moved in sterile test tube matched with Maxwell standard opacity tube, it is white in A6 with 0.7mm core black gel ink pen
The parallel lines that 3 length are 10cm are drawn on color copy paper;Estimate test tube and standard opacity tube (nominal concentration 6.0 × 108CFU/
ML culture solution is added dropwise until the two turbidity is identical in differences in turbidity).
(4) ATP log concentration value lgCARelative intensity of fluorescence logarithm lgIAStandard curve is established and inoculation bacterium solution viable bacteria
ATP concentration CACalibration
4.1 standard serial solutions are determining and prepared by ATP bioluminescence test specimens: using test strain culture solution by 1.0 × 10- 3The ATP standard stock solution of mol/L is diluted to high and low concentration standard serial solution: 7.0 × 10-9mol/L、7.0×10-8mol/L、
7.0×10-7Mol/L is (if instrument upper limit of detection is unable to reach 10-7Mol/L magnitude or high standard curve it is linear compared with
Its ATP concentration series can be changed to 7.0 × 10 by difference-10mol/L、7.0×10-9mol/L、7.0×10-8) and 4.2 × 10 mol/L-11mol/L、4.2×10-10mol/L、4.2×10-9Mol/L is simultaneously mixed.Then, with sterilizing liquid-transfering gun by the ATP standard of 0.1mL
Serial solution is moved to respectively in three sterile test tubes, and phosphate buffer of the 0.9mL containing 0.037% sucrose is successively added dropwise and mixes
It is even;The mixed solution of 0.1mL various concentration is moved to respectively in three instrument sterile test tubes again, as ATP bioluminescence
Test Duplicate Samples.
4.2 relative intensity of fluorescence value IAMeasurement: according to relative intensity of fluorescence value I in this patentAMeasuring method, with test organisms
After kind culture solution is as blank sample liquid validation instrument and reagent set background;According to the sequence of concentration from low to high, to various concentration
The ATP that 0.1mL is added dropwise in three Duplicate Samples of ATP standard solution respectively extracts reagent, and the ATP fluorescence examination of 0.1mL is instilled after mixing
Agent;It mixes again, with its relative intensity of fluorescence value of ATP fluorescent spectrophotometer measuring and records immediately and (ensure each link operating time
Unanimously, cross contamination is avoided).Each Duplicate Samples minute is no more than 15s, with each three Duplicate Samples of concentration ATP standard solution
The arithmetic mean of instantaneous value of relative intensity of fluorescence value is its IAMeasured value.
4.3ATP log concentration value lgCARelative intensity of fluorescence logarithm lgIAStandard curve is established: with ATP standard series
The relative intensity of fluorescence logarithm lgI of solutionAAs abscissa, with its corresponding ATP log concentration value lgCAFor ordinate work
Figure;Calibration curve is carried out to mathematical relationship between the two, draws the lgC of two respective concentrationsA-lgIAStandard curve;And it applies
Least square fitting method is derived from the linear equation Y=a of curveA0X+bA0(high concentration), Y=aAX+bA(low concentration) and phase
Close coefficients RA0 2(high concentration), RA 2(low concentration).Work as RA0 2And RA 2>=0.98, it when confidence level >=0.95, is done according to this patent
Measurement it is effective.
The viable bacteria ATP concentration C of 4.4 inoculation bacterium solutionsACalibration: according to relative intensity of fluorescence value I in this patentAMeasuring method is right
Bacteria total amount is 6.0 × 10 after the turbidimetry primary dcreening operation of Maxwell8The relative fluorescence of 10 times of gradient dilution liquid of bacteria suspension of CFU/mL is strong
Angle value IAIt is measured;According to high standard fitting equation Y=aA0X+bA0It calculates and demarcates its viable bacteria ATP concentration CA.Through
Test strain culture solution adjusts to obtain CARange is 5.0 × 10-8Mol/L~9.0 × 10-8The inoculation bacterium solution of mol/L, measures and remembers
Record relative intensity of fluorescence value I of the 0.3mL inoculation bacterium solution after the dilution of 4.7mL eluent in 1minA0。
(5) sample inoculation, culture and elution recycling
5.1 sample inoculation cultures: 0.3mL inoculation bacterium solution is added dropwise respectively in each group control sample and is resisted with sterilizing liquid-transfering gun
Bacterium sample surface to be measured is (with curve lgCA-lgIACalibration is derived from same branch test strain stoste test tube with bacterium solution, and 2 DEG C ± 0.2 DEG C
Save, used in 2h), bacterium solution is smeared uniformly with L stick (attachment is inoculated with bacterium solution but does not hang drop), it is made to cover sample whole table
Face.Ware lid is covered, is sealed the plate for contacting sample for 24 hours equipped with 6 groups with medical adhesive tape;(37 ± 1) DEG C, (90 ± 2) %RH training
Support ± 2h for 24 hours.
5.2 elution recycling: (0.2% sterile surfaces activity can be added using 4.7mL test strain culture solution as eluent
Agent), after 6 groups of 0h contact sample inoculation bacteriums, sufficiently eluted using solid or liquid swab method immediately;6 groups cultivate for 24 hours
Sample uses type of elution identical with 0h contact sample to recycle bacterium.Solid swab method is to be soaked with saturation eluent with head
Aseptic cotton carrier is uniformly embrocated 10 times in each sample surfaces back and forth anyhow respectively, and rotates with it cotton swab;Cut off experimenter's hand
Cotton swab is placed in the sterile test tube equipped with remaining eluent, as recovered liquid (if recovered liquid after mixing by the swab stick of contact portion
Less than 5mL, eluent is added to 5mL).Liquid swab method draws 4.7mL eluent with sterilizing liquid-transfering gun, in plate repeatedly
It rinses each sample surfaces at least 4 times, sufficiently elute and moves into washing lotion in sterile test tube, as recovered liquid (if returning after mixing
Liquid is received less than 5mL, adds eluent to 5mL).
(6) reclaim liquid phase is to fluorescence intensity level IAMeasurement
6.1 instruments and reagent set relative intensity of fluorescence background value calibration: use sterilizing liquid-transfering gun by 0.1mL test strain culture
The ATP lysate of liquid, 0.8mL phosphate buffer solution and 0.1mL containing 0.037% sucrose is separately added into same branch sterile test tube
In and mix well, then the above-mentioned mixed solution of 0.1mL is successively moved in three instrument sterile test tubes, stand 5min~
30min, as skip test Duplicate Samples.The ATP that 0.1mL is added dropwise respectively into three Duplicate Samples extracts reagent, instills after mixing
The ATP fluorescent reagent of 0.1mL;It mixes again, uses its relative intensity of fluorescence value of ATP fluorescent spectrophotometer measuring I immediatelyAAnd it records
(ensuring that each link operating time is consistent, avoid cross contamination).Each Duplicate Samples minute is no more than 15s, with three blank
The arithmetic mean of instantaneous value of Duplicate Samples relative intensity of fluorescence value is tested (or to use according to pertinent instruments as instrument and reagent set background values
Illustrate to calibrate background values).
6.2 reclaim liquid phases are to fluorescence intensity level IAMeasurement: it if blank reagent group background level meets instrument requirement, uses
The ATP lysate for phosphate buffer solution and 0.1mL of the liquid-transfering gun by 0.1mL recovered liquid, 0.8mL containing 0.037% sucrose that sterilize
Be separately added into same branch sterile test tube, after mixing well by the above-mentioned mixed solution of 0.1mL successively move to three instruments without
In bacterium test tube, 5min~30min is stood, as ATP fluorometric investigation Duplicate Samples.It is added dropwise 0.1mL's respectively into three Duplicate Samples
ATP extracts reagent, and the ATP fluorescent reagent of 0.1mL is instilled after mixing;It mixes again, uses its phase of ATP fluorescent spectrophotometer measuring immediately
To fluorescence intensity level IAAnd it records and (ensures that each link operating time is consistent, avoid cross contamination).Each Duplicate Samples minute
No more than 15s, using the arithmetic mean of instantaneous value of three ATP fluorometric investigation Duplicate Samples relative intensity of fluorescence values as the I of recovered liquidAMeasurement
Value (or instrument matched reagent box is used, it is required according to operation instructions, directly upper machine measures the opposite of three Duplicate Samples of recovered liquid
Fluorescence intensity level IA)。
(7) recovered liquid viable bacteria ATP concentration CAAnd TAIt calculates and antibiotic rate R and antibacterial activity value A is calculated
7.1 recovered liquid viable bacteria ATP concentration CsAAnd TAIt calculates
According to ATP low concentration standard curve lgCA-lgIALinear equation Y=aAX+bA, calculate control sample and antibacterial
After sample is contacted through 0h and is cultivated for 24 hours, the viable bacteria ATP concentration C of recovered liquidAAnd TA;Relevant calculation (uses instrument matched reagent box
When, the viable bacteria ATP concentration C of 1mL recovered liquid is calculated according to its practical sample volumeAAnd TA) see formula (1)~(12):
In formula:
CA0And CAtThe average ATP concentration that -3 groups of 0h are contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);
CA0iAnd CAtiThe average ATP concentration that-every group 0h is contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are
Mole every liter (mol/L);Sample group i=1,2,3;
CA0ijAnd CAtijThe ATP concentration that-every 0h is contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;bA- low concentration standard curve lgCA-lgIAIn vertical axis intercept;
TA0And TAtThe average ATP concentration that -3 groups of 0h are contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);
TA0iAnd TAtiThe average ATP concentration that-every group 0h is contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are
Mole every liter (mol/L);Sample group i=1,2,3;
TA0ijAnd TAtijThe ATP concentration that-every 0h is contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5.
7.2 test conditions for validity
If recovered liquid and 0.3mL inoculation the bacterium solution 1min after the dilution of 4.7mL eluent of every 0h contact control sample
Interior relative intensity of fluorescence measured value is close, i.e.,Every after cultivating for 24 hours control sample recovered liquid relative fluorescence it is strong
Spend the logarithm of measured valueThat is CAtij≥0.1×CA0ij.Then when 3 groups of 0h contact control sample reclaim liquid phase
To fluorescent strength determining valueGroup in and when between-group variation coefficient CV≤10% (involved calculation formula is shown in this patent correlation
Uncertainty of measurement requirement), the measurement carried out according to this patent method is effective.
7.3 bacterium increasing value Fij、GijIt calculates
Every control sample and antimicrobial sample after cultivating for 24 hours, bacterium increasing value Fij、GijRespectively according to formula (13),
(14) it calculates:
In formula:
FijAnd GijThe bacterium increasing value of-every control sample and antimicrobial sample after cultivating for 24 hours, sample group i=1,
2,3;Every group of sample number into spectrum j=1,2,3,4,5;
CA0ijAnd CAtijThe ATP concentration that-every 0h is contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
TA0ijAnd TAtijThe ATP concentration that-every 0h is contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are to rub
You are every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope.
7.4 antibiotic rate R are calculated
It tests under condition for validity, the antibiotic rate R of every plated film antibiotic glass sampleij, every group and every batch of sample antibiotic rate
RiIt is calculated respectively according to formula (15), (16), (17) with R:
In formula:
RijThe antibiotic rate of-every plated film antibiotic glass sample, %;Sample group i=1,2,3;Every group of sample number into spectrum j=
1,2,3,4,5;
RiThe antibiotic rate of-every group plated film antibiotic glass sample, %;Sample group i=1,2,3;
R-every batch of plated film antibiotic glass sample antibiotic rate, %;
CAtijAnd TAtij- every antimicrobial sample and control sample recycle the average ATP concentration of viable bacteria after cultivating for 24 hours, single
Position is mole every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
WithAfter cultivating for 24 hours, the relative intensity of fluorescence of recovered liquid is measured for-every antimicrobial sample and control sample
Value, RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope.
7.5 antibacterial activity value A are calculated
It tests under condition for validity, the antibacterial activity value A of every plated film antibiotic glass sampleij, every group and every batch of sample it is anti-
Bacterium activity value AiIt is calculated respectively according to formula (18), (19), (20) with A:
In formula:
AijThe antibacterial activity value of-every plated film antibiotic glass sample;Sample group i=1,2,3;Every group of sample number into spectrum j=
1,2,3,4,5;
AiThe antibacterial activity value of-every group plated film antibiotic glass sample, sample group i=1,2,3;
A-every batch of plated film antibiotic glass sample antibacterial activity value;
FijAnd GijThe bacterium increasing value of-every control sample and antimicrobial sample after cultivating for 24 hours, wherein sample group i
=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope.
7.6 data revisions of the convention requirement: the concentration of calibration ATP standard serial solution and the work for being inoculated with bacterium solution, sample recovered liquid
Bacterium ATP concentration CAWhen, with reference to the data revision of the convention regulation in GB 4789.2-2016 in relation to clump count;Work as CALess than 100mol/L
When, " rounding up " round numbers;Work as CAWhen not less than 100mol/L, preceding 2 bit digital is taken after the 3rd bit digital " rounding up ", after
Face replaces digit with 0;It can also be indicated with 10 exponential form, " rounding up " uses two effective digitals afterwards.Control sample and
After antimicrobial sample is contacted through 0h and cultivated for 24 hours, reclaim liquid phase is to fluorescent strength determining value round numbers, antibiotic rate Rij、Ri, R calculate
As a result three effective digitals are taken;Bacterium increasing value Fij、GijWith antibacterial activity value Aij、Ai, A calculated result take two effective digitals.
7.7 uncertainties of measurement: this patent method, which mainly passes through, to be calculated control sample and antimicrobial sample and contacts through 0h and for 24 hours
After culture, reclaim liquid phase is in the group of fluorescent strength determining value and between-group variation coefficient CV=σ ÷ μ × 100% (μ, σ and C
V calculated result remains into 2 significant digits), judge ATP fluorimetric assay for biological materials method being applied to plated film antibiotic glass antibacterium
The reproducibility of performance test;In regulation group and between-group variation coefficient CV≤10%.
5 control samples, 5 antimicrobial samples and 5 control samples after cultivating for 24 hours of every group of 0h contact, 5 it is anti-
Bacterium sample, arithmetic mean of instantaneous value of the reclaim liquid phase to fluorescent strength determining value And Respectively according to formula
(21), (22) calculate (sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=
1,2,3;In formula With Respectively every group of control sample and antimicrobial sample are contacted through 0h and are cultivated for 24 hours
Afterwards, the relative intensity of fluorescence measured value of each Duplicate Samples):
15 control samples, 15 antimicrobial samples and 15 control samples, 15 after cultivating for 24 hours that 3 groups of 0h are contacted
Part antimicrobial sample, arithmetic mean of instantaneous value of the reclaim liquid phase to fluorescent strength determining value And Respectively according to formula
(23), (24) calculate (sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=
1,2,3;In formula With Respectively every group of control sample and antimicrobial sample are contacted through 0h and are cultivated for 24 hours
Afterwards, the relative intensity of fluorescence measured value of each Duplicate Samples):
5 control samples, 5 antimicrobial samples and 5 control samples after cultivating for 24 hours of every group of 0h contact, 5 it is anti-
Bacterium sample, standard deviation of the reclaim liquid phase to fluorescent strength determining value And Respectively according to formula (25)
(26) (sample group i=1,2,3 is calculated;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=1,2,
3;In formula With After respectively every group of control sample and antimicrobial sample are contacted through 0h and cultivated for 24 hours, respectively
The relative intensity of fluorescence measured value of Duplicate Samples):
15 control samples, 15 antimicrobial samples and 15 control samples, 15 after cultivating for 24 hours that 3 groups of 0h are contacted
Part antimicrobial sample, standard deviation of the reclaim liquid phase to fluorescent strength determining value And Respectively according to formula
(27) and (28) calculate (sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=
1,2,3;In formula With Respectively every group of control sample and antimicrobial sample are contacted through 0h and are cultivated for 24 hours
Afterwards, the relative intensity of fluorescence measured value of each Duplicate Samples):
(8) evaluation of result
8.1, with reference to health industry common practice and the requirement of dependent antimicrobial product standard, take following classification criterion:
If using antibiotic rate R as correlated performance evaluation index: working as Rij/Ri(staphylococcus aureus when/R < 90%
With salmonella Rij/Ri/ R < 80%), sample is without antibacterial actions;As 90%≤Rij/Ri(golden yellow grape when/R < 99%
80%≤R of coccus and salmonellaij/Ri/ R < 90%), sample has antibacterial actions;As 99%≤Rij/Ri/ R < 99.9%
When (90%≤R of staphylococcus aureus and salmonellaij/Ri/ R < 99%), sample antibacterial actions are stronger;Work as Rij/Ri/R
(staphylococcus aureus and salmonella R when >=99.9%ij/Ri/ R >=99%), sample antibacterial actions are extremely strong;
If using antibacterial activity value A as correlated performance evaluation index: working as Aij/Ai(Staphylococcus aureus when/A < 1.0
Bacterium and salmonella Aij/Ai/ A < 0.5), sample is without antibacterial actions;As 1.0≤Aij/Ai(Staphylococcus aureus when/A < 2.0
0.5≤A of bacterium and salmonellaij/Ai/ A < 1.0), sample has antibacterial actions;As 2.0≤Aij/AiIt is (golden yellow when/A < 3.0
1.0≤A of color staphylococcus and salmonellaij/Ai/ A < 2.0), sample antibacterial actions are stronger;Work as Aij/Ai(gold when/A >=3.0
Staphylococcus aureus and salmonella Aij/Ai/ A >=2.0), sample antibacterial actions are extremely strong.
8.2 work as the antibiotic rate R of certain group (part) plated film antibiotic glass samplei(Rij) or antibacterial activity value Ai(Aij) with other two
When the bacteria resistance of group (four) sample can be compared to a levels be at least differed, one group of (part) sample is extracted again and is repeated in fact
It tests;It is calculated through ATP bioluminescence lgCA─lgIAThe antibiotic rate or antibacterial activity value that calibration curve method measures.If front and back two
Group plated film antibiotic glass sample antibacterium performance level is identical, then abandons it;Take other two groups (four) remaining sample antibiotic rate Ri
(Rij) or antibacterial activity value Ai(Aij) arithmetic mean of instantaneous value as batch (group) plated film antibiotic glass sample bacteria resistance can
Evaluation result.
Laboratory biosafety qualification, instrument and equipment, medium/liquid, chemical reagent, reference culture used in the present embodiment:
(1) Laboratory biosafety qualification
In the two stage biological safety experiment room that institute registration number is CNAS BL0059, by having secondary advanced techniques academic title
Microorganism detection professional complete related experiment.
(2) instrument and equipment
2.1 two stage biological safety cabinets: Thermo Scientific1300 series of secondary B2 type Biohazard Safety Equipment, workbench
Surface area 0.55m2, capacity 1130m3/ h, filter efficiency 99.99% (0.3 μm).
2.2 superclean benches: American blend Thermo ScientificTM HeraguardTM, model ECO ultra-clean work
Make platform, inside width × depth × height=920mm × 585mm × 645mm;Air velocity is 0.15m/s~0.25m/s and 0.36m/s
~0.45m/s.
2.3ATP bioluminescence rapid detection system: the portable system SURE ATP fluorescence of Hygiena company, the U.S.
Detector, box containing matched reagent, plastics Special test tube etc.;ATP content detection lower limit 4 × 10-18Mol/ml, the inspection of microorganism total amount
Rising limit 1.0CFU/ml, RLU range of readings 0~9999, detection time 10s, 1000 times/s of sampling rate, measurement error ± 5%.
2.4 constant temperature and humidity incubators: Guan Sen biotechnology (Shanghai) Co., Ltd. model WS-380H, volume 380L, temperature control
The constant temperature and humidity incubator of ± 0.8 DEG C of range (0~50) DEG C, wet range (30~95) %RH ± 2%RH of control.
2.5 pressure steam sterilizers: the autoclave of Japanese Sanyo company model MLS-3780, volume 75L, sterilizing
± 2 DEG C of temperature (105~135) DEG C, maximum pressure 0.235MPa, timing range (1~250) min.
2.6 low temperature refrigerators: the superfreeze storage of Zhong Kemeiling low temperature Science and Technology Co., Ltd. model DW-HL398
Case, dischargeable capacity 398L, -10 DEG C~-86 DEG C of storage temperature.
2.7 refrigerating boxes: the Medical refrigerator of Zhong Kemeiling low temperature Science and Technology Co., Ltd. model YC-968L effectively holds
Long-pending 968L, ± 0.1 DEG C of storage temperature (2~8) DEG C.
2.8 electronic balances: the electronic balance of Japanese Shimadzu model AUX220, range 220g, precision ± 0.1mg.
2.9 ultrasonic cleaners: the supersonic wave cleaning machine of Shanghai Yi Jing ultrasonic instrument Co., Ltd model YQ-120C,
Capacity 3.2L, supersonic frequency 40KHz/28KHz/25KHz, timing range 1min~30min/99min.
2.10 vortex oscillators: the vortex oscillator of American blend Coleparmer Votex-Genie2, the range of speeds
(500~3000) r/min ± 3r/min, timing range 1s~60s.
2.11pH meter: the accurate pH meter of Shanghai precision instrumentation Co., Ltd model MP512-03, range ability (-
2.000~19.999) pH ± 0.002pH, ± 0.4 DEG C of temperature range (- 10~110) DEG C.
2.12 electric furnaces: the 1KW closed temp.-adjustable electric furnace of Changzhou Deco Instrument Ltd. model DLD-1KW.
(3) medium/liquid
The medium/liquid of Beijing overpass technical concern Co., Ltd production.
(4) chemical reagent
Trinosin standard items and prepare ATP fluorescent reagent buffer solution, ATP lysate, ATP extracting solution and
A series of biochemical reagents needed for ATP fluorescent reagent are purchased from U.S.'s Amresco product of Shanghai Jin Pan Biotechnology Co., Ltd agency
Board.
(5) reference culture
Escherichia coli ATCC 8739 and staphylococcus aureus ATCC 6538 is purchased from Chinese industrial microorganism fungus kind
Preservation administrative center.
The detection data and result of the present embodiment calculate:
Using ATP fluophotometer through lgCA-lgIACalibration curve method can be into the bacteria resistance of plated film antibiotic glass sample
Row detection, coherent detection data and Calculation of Measuring Uncertainty result be shown in Table respectively 1~table 4 (Shigella and salmonella
Testing result is close with escherichia coli and the testing result of staphylococcus aureus respectively).
1 relative intensity of fluorescence measured value of table and antibiotic rate R, antibacterial activity value A calculated result (escherichia coli)
2 relative intensity of fluorescence value Calculation of Measuring Uncertainty result (escherichia coli) of table
3 relative intensity of fluorescence measured value of table and antibiotic rate R, antibacterial activity value A calculated result (staphylococcus aureus)
4 relative intensity of fluorescence Calculation of Measuring Uncertainty result (staphylococcus aureus) of table
The above description is only an embodiment of the present invention, is not intended to limit the scope of the invention, all to utilize this hair
Equivalent transformation made by bright description, is applied directly or indirectly in other relevant technical fields, and is included in this hair
In bright scope of patent protection.
Claims (9)
1. a kind of detection method of plated film antibiotic glass bacteria resistance energy, comprising: (1) sample preparation and pretreatment;(2) equipment is selected
Type and reagent, culture medium are prepared;(3) culture presevation, activation and bacteria suspension preparation;(4) ATP log concentration value lgCAIt is relatively glimmering
Luminous intensity logarithm lgIAStandard curve is established and inoculation bacterium solution viable bacteria ATP concentration CACalibration;(5) sample inoculation, culture and elution
Recycling;(6) reclaim liquid phase is to fluorescence intensity level IAMeasurement;(7) recovered liquid viable bacteria ATP concentration CAAnd TACalculate and antibiotic rate R and
Antibacterial activity value A is calculated;(8) evaluation of result;It is characterized in that, using ATP fluophotometer to antibiotic rate R or antibacterial activity
The plated film antibiotic glass bacteria resistance of value A characterization can be carried out the ATP bioluminescence lgC of accurate quantitative testA-lgIAStandard curve
Method, specific:
In reclaim liquid phase to fluorescence intensity level IAIn measurement:
Quantity, size and the pre-treatment requirement for specifying control sample and antimicrobial sample, testing standard bacterial strain is passed on, is activated
Afterwards, it takes continuous switching 2 times Fresh bacterial cultures to prepare bacteria suspension and primary dcreening operation is carried out to its bacterium number, with test strain culture solution
By 1.0 × 10-3The ATP standard stock solution of mol/L is diluted to high and low concentration standard serial solution: 7.0 × 10-9mol/L、7.0×
10-8mol/L、7.0×10-7Mol/L is (if instrument upper limit of detection is unable to reach 10-7Mol/L magnitude or high standard curve
It is linear poor, its ATP concentration series can be changed to 7.0 × 10-10mol/L、7.0×10-9mol/L、7.0×10-8mol/L)
With 4.2 × 10-11mol/L、4.2×10-10mol/L、4.2×10-9Mol/L, and measure its relative intensity of fluorescence value IA;Draw two
The lgC of respective concentrationA-lgIAStandard curve is derived from fitting equation Y=aA0X+bA0(high concentration), Y=aAX+bAIt is (low
Concentration) and linearly dependent coefficient RA0 2(high concentration), RA 2(low concentration) is 6.0 × 10 to bacteria total amount8The bacteria suspension of CFU/mL
After carrying out 10 times of gradient dilutions, its relative intensity of fluorescence value I is measuredA, according to high standard fitting equation Y=aA0X+bA0It pushes away
Calculate corresponding viable bacteria ATP concentration CA;It is adjusted to obtain CARange is 5.0 × 10-8Mol/L~9.0 × 10-8The inoculation bacterium of mol/L
Then 0.3mL bacterium solution is added dropwise to each group control sample and antimicrobial sample surface to be measured in liquid respectively, use 4.7mL eluent pair immediately
6 groups of 0h contact samples carry out elution recycling;Using the relative intensity of fluorescence value I of ATP fluorescent spectrophotometer measuring recovered liquidAC0ij、
IAT0ij, according to low concentration calibration curve equation formula Y=aAX+bACalculate the ATP concentration C of its viable bacteriaAOijAnd TAOij, meanwhile, by 6 groups
Contact sample is sealed in sterilized petri dishes for 24 hours, and (37 ± 1) DEG C, (90 ± 2) %RH culture are for 24 hours after ± 2h;Sample is contacted using with 0h
The identical mode of product recycles remained on surface bacterium and measures the relative intensity of fluorescence value I of its recovered liquidACtij、IATtij, calculate corresponding
Viable bacteria ATP concentration CAtijAnd TAtij;
In antibiotic rate R and antibacterial activity value A is calculated:
According to ATP low concentration standard curve lgCA-lgIALinear equation Y=aAX+bA, every after being contacted with 0h and being cultivated for 24 hours
The relative intensity of fluorescence measured value of control sample and antimicrobial sample recovered liquidWith For basic data;?
It tests under condition for validity, calculates its bacterium increasing value F after cultivating for 24 hoursij、GijAnd antibiotic rate RijWith antibacterial activity value Aij;
To the R of every group of sampleijAnd AijArithmetic mean of instantaneous value is taken to obtain corresponding RiAnd Ai;The antibiotic rate R of every batch of plated film antibiotic glass sample
It is its 3 groups of sample R with antibacterial activity value AiAnd AiArithmetic mean of instantaneous value;And the clear related data revision of the convention and uncertainty of measurement are wanted
It asks;
In evaluation of result:
With reference to health industry common practice and the requirement of dependent antimicrobial product standard, antibacterium grading performance criterion is determined;When
The antibiotic rate R of certain group (part) plated film antibiotic glass samplei(Rij) or antibacterial activity value Ai(Aij) and other two groups (four) samples
Bacteria resistance when can be compared to a levels are at least differed, extract one group of (part) sample again and repeat to test;It is calculated through ATP
Bioluminescence lgCA─lgIAThe antibiotic rate or antibacterial activity value that calibration curve method measures, if two groups of front and back (part) plated film antibacterial
Glass sample antibacterium performance level is identical, then abandons it;Take other two groups (four) remaining sample antibiotic rate Ri(Rij) or antibacterial
Activity value Ai(Aij) arithmetic mean of instantaneous value as batch (group) plated film antibiotic glass sample bacteria resistance can evaluation result.
2. the detection method of plated film antibiotic glass bacteria resistance energy according to claim 1, which is characterized in that the sample
Product preparation and pre-treatment, carry out in the steps below:
(1) control sample: in addition to not carrying out anti-microbial coating processing, classification, raw material, technique and the appearance of control sample, size, number
Amount etc. is identical with antibiotic glass sample to be measured;Each strain test uses 6 groups of samples;Wherein 0h contact and for 24 hours culture examination
Test each with 3 groups, every group of 5 samples;
(2) antimicrobial sample: the horizontal glass test plate (panel) through antimicrobial component coating film treatment can be sunlight controlling coated glass, Low emissivity
The product categories such as coated glass;Sample test surface immaculate, speckle, film surface and glass surface are without scuffing;Having a size of (50 ± 2) mm
× (50 ± 2) mm, thickness are not more than 10mm, and antimicrobial sample quantity is identical as control sample, and every group of sample to be tested selects one group pair
Product as object of reference and effectively identify in the same old way;
(3) sample pre-treatments: control sample and antimicrobial sample are impregnated into 1min in 75% ethanol solution before experiment, and super
With the abundant cleaning sample of sterile water to remove ethyl alcohol on net workbench;Sample surface to be measured is put into upwards after natural drying sterile
It is spare in plate.
3. the detection method of plated film antibiotic glass bacteria resistance energy according to claim 1, which is characterized in that described sets
Alternative type and reagent, culture medium are prepared, and are carried out in the steps below:
(1) General Requirement: test analytical reagents and meet tertiary effluent as defined in GB/T 6682-2008 (distilled water or go from
Sub- water), laboratory has the safe qualification of two stage biological, and personnel have regular Microbiological Lab's working experience;
(2) instrument and equipment: the superclean bench of two stage biological safety cabinet or lustration class not less than 100;Fluorophotometric containing ATP
The ATP bioluminescence rapid detection system of meter, matched reagent box, pressurizer and inspissator, plastic test tube etc., wherein ATP fluorescence
Spectrometer wavelength range 300nm~650nm, ATP Concentration Testing range 10-13Mol/L~10-7mol/L;(20~50) DEG C ± 1
DEG C, the constant temperature and humidity incubator of (50~95) %RH ± 2%RH;The pressuresteam sterilization of (121 ± 2) DEG C, (103 ± 5) kPa
Device;- 20 DEG C~-70 DEG C of low temperature refrigerator;0 DEG C~8 DEG C of refrigerating box;The electronic balance of sensibility reciprocal 0.001g;Frequency range (30~
50) ultrasonic cleaner of kHz;The vortex oscillator of the range of speeds (500~3000) r/min;The pH of precision ± 0.1 (25 DEG C)
Meter;Electric furnace;
(3) material utensil: the sterile measuring pipette of 1mL, 10mL;(metering misses by 0.05mL, 0.1mL, 0.2mL, 1mL, 5mL, 10mL
Difference is less than single track changeable fluid liquid-transfering gun and sterile liquid transfer gun head 1%);The sterile conical flask of capacity 250mL, 500mL;Diameter
The sterile petri dish of 90mm;Maxwell bacterium standard opacity tube and mating test tube;Sterile test tube;Diameter is not more than the oese of 4mm;
L stick;Alcolhol burner;Sterilize tweezers;Medical adhesive tape;The ruler of scale division value 1mm;Thermometer;Precision
The stopwatch of 0.01s;A6 white copy paper;0.7mm core black gel ink pen;
(4) reagent: 75% ethanol solution;85% physiological saline (121 DEG C of high pressure sterilization 15min, 5 DEG C~10 DEG C storages
30d);
(5) medium/liquid (commercially available medium/liquid can be used): through 121 DEG C of high pressure sterilization 15min after the packing of matched medium/liquid, 2
DEG C~8 DEG C of storage 30d;
Nutrient agar (NA): 5g beef extract, 10g peptone, 5g sodium chloride, 15g agar are dissolved by heating in 1000mL water, adjusted
Save pH to 7.0~7.2;
Nutrient broth (NB): by 3g beef extract, 10g peptone, 5g sodium chloride dissolve by heating in 1000mL water, adjust pH to
7.0~7.2;
Salmonella preservation is with brain heart oxoid meat soup (BHI): by 10g peptone, 5g sodium chloride, 2.5g disodium hydrogen phosphate, 2g
Glucose dissolves by heating in 500mL cattle heart leachate, adjusts pH to 7.4 ± 0.2;
The culture solution of escherichia coli and Shigella/staphylococcus aureus and salmonella: by the battalion of 1:500/1:100
It supports meat soup (NB) to mix with 85% sterile saline solution, adjusts pH to 7.0~7.2;
(6) ATP fluorescence reaction reagent (or with commercial reagent): in addition to phosphate buffer solution, matched ATP fluorescence reaction reagent-
20 DEG C~-70 DEG C preservations, use in 6 months;
Dilution buffer: 0.005mol/L and the disodium phosphate soln for containing 0.037% sucrose adjust pH to 7.2 ± 0.2;
121 DEG C of high pressure sterilizations 15min, 2 DEG C~8 DEG C storage 30d;
ATP standard reagent stoste: by 60.5mg trinosin (C10H14O13P3Na2·3H2O it) is dissolved in 100mL water,
Being configured to concentration is 1 × 10-3The solution of mol/L, -20 DEG C of freezings are sealed 6 months;
ATP fluorescent reagent buffer solution: by 1117mg trishydroxymethylaminomethane, 183mg disodium ethylene diamine tetraacetate, 808mg
Magnesium acetate, 6.7mg dithiothreitol, the beta-cyclodextrin of 25000mg and 925mg glucose dissolve by heating in 250mL water, adjust
Save pH to 7.5 ± 0.2;It is used in 8h;
ATP lysate: by 4.6 international units/ml apyrase (EC:3.6.1.5) and 46 international units/ml
Adenosine phosphate deaminase (EC:3.5.4.6 or EC:3.5.4.17), 37mg sucrose, that 20mg bovine serum albumin is dissolved in 10mL is dense
Degree is in the 2-morpholine ethane sulfonic acid buffer solution of 0.05mol/L, and adjusting use in pH to 6.0 ± 0.5,8h, (1mL lysate exists
The ATP concentration in nutrient broth can be down to 10 in 15min-13Mol/L or less);
ATP extracting solution: 45mg trishydroxymethylaminomethane is dissolved by heating in 9.8ml water, the benzene for being 10% with 0.2ml concentration
After pricking the mixing of oronain solution, pH to 12.0 ± 0.5 is adjusted;
ATP fluorescent reagent: by 16mg luciferase (EC:1.13.12.7), the D- fluorescein of 12.6mg, 56mg bovine serum albumin
It is dissolved in the ATP fluorescent reagent buffer solution of 30mL, 15min is stored at room temperature after mixing, is used in 3h.
4. the detection method of plated film antibiotic glass bacteria resistance energy according to claim 1, which is characterized in that the bacterium
Kind preservation, activation and bacteria suspension preparation, carry out in the steps below:
(1) test strain: escherichia coli ATCC 8739;Staphylococcus aureus ATCC 6538;Salmonella ATCC
14028;Shigella CMCC 51105 (or other strains that is provided and can be traced to the source by national corresponding culture presevation administrative center);
(2) culture presevation: opening freeze-drying lactobacillus pipe with sterile working, and adequate nutrition meat soup (salmonella is added with capillary syring
With BHI broth), pressure-vaccum make for several times strain melt dispersion, then, by a little test strain suspension instill equipped with 5mL~
In the test tube of 10mL nutrient broth, (37 ± 1) DEG C culture for 24 hours~48h;As slant preservation bacterium, (5 ± 1) DEG C storage (is no more than
1 month), inoculation times were no more than for 14 generations;
(3) actication of culture: slant preservation bacterium is transferred nutrient agar slant medium, and (37 ± 1) DEG C culture 18h~for 24 hours;Daily
Switching 1 time, continuously switching is no more than 15d, and test is using the 3rd generation~the 14th generation and in the interior Fresh bacterial cultures transferred for 24 hours;
(4) prepared by bacteria suspension: scraping a small amount of Fresh bacterial from strain activation and culture base with oese, test strain culture is added
Bacteria suspension is made in liquid;1000r/min shakes test tube 1min or with 30cm amplitude of oscillation shaking test tube 80 times, it is ensured that and bacterial suspension is uniform,
Appropriate bacteria suspension is moved in sterile test tube matched with Maxwell standard opacity tube, with 0.7mm core black gel ink pen in A6 white
The parallel lines that 3 length are 10cm are drawn on copy paper;Estimate test tube and standard opacity tube (nominal concentration 6.0 × 108CFU/mL)
Differences in turbidity, be added dropwise culture solution until the two turbidity it is identical until.
5. the detection method of plated film antibiotic glass bacteria resistance energy according to claim 1, which is characterized in that described
ATP log concentration value lgCARelative intensity of fluorescence logarithm lgIAStandard curve is established and inoculation bacterium solution viable bacteria ATP concentration CAMark
It is fixed, it carries out in the steps below:
(1) standard serial solution is determining and prepared by ATP bioluminescence test specimens: using test strain culture solution by 1.0 × 10-3mol/
The ATP standard stock solution of L is diluted to high and low concentration standard serial solution: 7.0 × 10-9mol/L、7.0×10-8mol/L、7.0×
10-7Mol/L is (if instrument upper limit of detection is unable to reach 10-7Mol/L magnitude or high standard curve it is linear poor, can will
Its ATP concentration series is changed to 7.0 × 10-10mol/L、7.0×10-9mol/L、7.0×10-8) and 4.2 × 10 mol/L-11mol/
L、4.2×10-10mol/L、4.2×10-9Mol/L is simultaneously mixed, then, with sterilizing liquid-transfering gun that the ATP standard series of 0.1mL is molten
Liquid is moved to respectively in three sterile test tubes, and phosphate buffer of the 0.9mL containing 0.037% sucrose and mixing is successively added dropwise;Again will
The mixed solution of 0.1mL various concentration is moved to respectively in three instrument sterile test tubes, parallel as the test of ATP bioluminescence
Sample;
(2) relative intensity of fluorescence value IAMeasurement: according to relative intensity of fluorescence value I in this patentAMeasuring method is trained with test strain
After nutrient solution is as blank sample liquid validation instrument and reagent set background;According to the sequence of concentration from low to high, marked to various concentration ATP
The ATP that 0.1mL is added dropwise in three Duplicate Samples of quasi- solution respectively extracts reagent, and the ATP fluorescent reagent of 0.1mL is instilled after mixing;Again
Secondary mixing, immediately with its relative intensity of fluorescence value of ATP fluorescent spectrophotometer measuring and record (ensure that each link operating time is consistent,
Avoid cross contamination), each Duplicate Samples minute is no more than 15s, relatively glimmering with each three Duplicate Samples of concentration ATP standard solution
The arithmetic mean of instantaneous value of light intensity value is its IAMeasured value;
(3) ATP log concentration value lgCARelative intensity of fluorescence logarithm lgIAStandard curve is established: with ATP standard serial solution
Relative intensity of fluorescence logarithm lgIAAs abscissa, with its corresponding ATP log concentration value lgCAFor ordinate mapping;It is right
Mathematical relationship between the two carries out calibration curve, draws the lgC of two respective concentrationsA-lgIAStandard curve;And application is minimum
Two multiply the linear equation Y=a that fitting process is derived from curveA0X+bA0(high concentration), Y=aAX+bA(low concentration) and phase relation
Number RA0 2(high concentration), RA 2(low concentration), works as RA0 2And RA 2>=0.98, when confidence level >=0.95, the survey done according to this patent
It is fixed effective;
(4) it is inoculated with the viable bacteria ATP concentration C of bacterium solutionACalibration: according to relative intensity of fluorescence value I in this patentAMeasuring method, to through wheat
Bacteria total amount is 6.0 × 10 after family name's turbidimetry primary dcreening operation8The relative intensity of fluorescence value I of 10 times of gradient dilution liquid of bacteria suspension of CFU/mLA
It is measured;According to high standard fitting equation Y=aA0X+bA0It calculates and demarcates its viable bacteria ATP concentration CA, through test organisms
Kind culture solution adjusts to obtain CARange is 5.0 × 10-8Mol/L~9.0 × 10-8The inoculation bacterium solution of mol/L, measures and records
0.3mL is inoculated with relative intensity of fluorescence value I of the bacterium solution after the dilution of 4.7mL eluent in 1minA0。
6. the detection method of plated film antibiotic glass bacteria resistance energy according to claim 1, which is characterized in that the sample
Product inoculation, culture and elution recycling, carry out in the steps below:
(1) sample inoculation culture: 0.3mL inoculation bacterium solution is added dropwise respectively in each group control sample and antibacterial sample with sterilizing liquid-transfering gun
Product surface to be measured is (with curve lgCA-lgIACalibration is derived from same branch test strain stoste test tube with bacterium solution, and 2 DEG C ± 0.2 DEG C saves,
Used in 2h), bacterium solution is smeared uniformly with L stick (attachment is inoculated with bacterium solution but does not hang drop), so that it is covered sample whole surface, covers
Ware lid is sealed the plate for contacting sample for 24 hours equipped with 6 groups with medical adhesive tape;(37 ± 1) DEG C, (90 ± 2) %RH culture for 24 hours ±
2h;
(2) elution recycling: using 4.7mL test strain culture solution as eluent (0.2% sterile surfaces activating agent can be added), 6
After group 0h contact sample inoculation bacterium, sufficiently eluted using solid or liquid swab method immediately;6 groups of samples cultivated for 24 hours
Bacterium is recycled using type of elution identical with 0h contact sample, solid swab method is to be soaked with the sterile of saturation eluent with head
Cotton swab is uniformly embrocated 10 times in each sample surfaces back and forth anyhow respectively, and rotates with it cotton swab;Cut off the contact of experimenter's hand
Cotton swab is placed in the sterile test tube equipped with remaining eluent, as recovered liquid (if recovered liquid is insufficient after mixing by partial swab stick
5mL, addition eluent to 5mL), liquid swab method draw 4.7mL eluent, the repeated flushing in plate with sterilizing liquid-transfering gun
It each sample surfaces at least 4 times, sufficiently elutes and moves into washing lotion in sterile test tube, as recovered liquid (if recovered liquid after mixing
Less than 5mL, eluent is added to 5mL).
7. the detection method of plated film antibiotic glass bacteria resistance energy according to claim 1, which is characterized in that described returns
Liquid phase is received to fluorescence intensity level IAMeasurement carries out in the steps below:
(1) instrument and reagent set relative intensity of fluorescence background value calibration: with sterilizing liquid-transfering gun by 0.1mL test strain culture solution,
The ATP lysate of phosphate buffer solution and 0.1mL of the 0.8mL containing 0.037% sucrose is separately added into same branch sterile test tube
And mix well, then the above-mentioned mixed solution of 0.1mL is successively moved in three instrument sterile test tubes, standing 5min~
30min, as skip test Duplicate Samples, the ATP that 0.1mL is added dropwise respectively into three Duplicate Samples extracts reagent, instills after mixing
The ATP fluorescent reagent of 0.1mL;It mixes again, uses its relative intensity of fluorescence value of ATP fluorescent spectrophotometer measuring I immediatelyAAnd it records
(ensuring that each link operating time is consistent, avoid cross contamination), each Duplicate Samples minute is no more than 15s, with three blank
The arithmetic mean of instantaneous value of Duplicate Samples relative intensity of fluorescence value is tested (or to use according to pertinent instruments as instrument and reagent set background values
Illustrate to calibrate background values);
(2) reclaim liquid phase is to fluorescence intensity level IAMeasurement: if blank reagent group background level meets instrument requirement, with sterilizing
The ATP lysate of phosphate buffer solution and 0.1mL of the liquid-transfering gun by 0.1mL recovered liquid, 0.8mL containing 0.037% sucrose is distinguished
It is added in same branch sterile test tube, the above-mentioned mixed solution of 0.1mL is successively moved into three sterile examinations of instrument after mixing well
Guan Zhong stands 5min~30min, and as ATP fluorometric investigation Duplicate Samples, the ATP that 0.1mL is added dropwise respectively into three Duplicate Samples is mentioned
Reagent is taken, the ATP fluorescent reagent of 0.1mL is instilled after mixing;It mixes again, with ATP fluorescent spectrophotometer measuring, it is relatively glimmering immediately
Light intensity value IAAnd record and (ensure that each link operating time is consistent, avoid cross contamination), each Duplicate Samples minute does not surpass
15s is crossed, using the arithmetic mean of instantaneous value of three ATP fluorometric investigation Duplicate Samples relative intensity of fluorescence values as the I of recovered liquidAMeasured value
(or instrument matched reagent box is used, it is required according to operation instructions, directly upper machine measures the relatively glimmering of three Duplicate Samples of recovered liquid
Light intensity value IA)。
8. the detection method of plated film antibiotic glass bacteria resistance energy according to claim 1, which is characterized in that described returns
Receive liquid viable bacteria ATP concentration CAAnd TAIt calculates and antibiotic rate R and antibacterial activity value A is calculated, carry out in the steps below:
(1) recovered liquid viable bacteria ATP concentration CAAnd TAIt calculates
According to ATP low concentration standard curve lgCA-lgIALinear equation Y=aAX+bA, calculate control sample and antimicrobial sample
After contacting through 0h and cultivating for 24 hours, the viable bacteria ATP concentration C of recovered liquidAAnd TA;Relevant calculation (when using instrument matched reagent box, root
The viable bacteria ATP concentration C of 1mL recovered liquid is calculated according to its practical sample volumeAAnd TA) see formula (1)~(12):
In formula:
CA0And CAt- 3 groups of 0h contact and after cultivating for 24 hours control sample recycling viable bacteria average ATP concentration, unit is mole every
It rises (mol/L);
CA0iAnd CAtiThe average ATP concentration that-every group 0h is contacted and control sample recycles viable bacteria after cultivating for 24 hours, unit are mole
Every liter (mol/L);Sample group i=1,2,3;
CA0ijAnd CAtij- every 0h contact and after cultivating for 24 hours control sample recycling viable bacteria ATP concentration, unit is mole every
It rises (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value, RLU;
Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;bA- low concentration standard curve lgCA-lgIAIn vertical axis intercept;
TA0And TAt- 3 groups of 0h contact and after cultivating for 24 hours antimicrobial sample recycling viable bacteria average ATP concentration, unit is mole every
It rises (mol/L);
TA0iAnd TAtiThe average ATP concentration that-every group 0h is contacted and antimicrobial sample recycles viable bacteria after cultivating for 24 hours, unit are mole
Every liter (mol/L);Sample group i=1,2,3;
TA0ijAnd TAtij- every 0h contact and after cultivating for 24 hours antimicrobial sample recycling viable bacteria ATP concentration, unit is mole every
It rises (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value, RLU;
Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
(2) condition for validity is tested
If the recovered liquid and 0.3mL inoculation bacterium solution of every 0h contact control sample are after the dilution of 4.7mL eluent in 1min
Relative intensity of fluorescence measured value is close, i.e.,Every control sample recovered liquid relative intensity of fluorescence survey after cultivating for 24 hours
The logarithm of definite valueThat is CAtij≥0.1×CA0ij, then when 3 groups of 0h contact control sample reclaim liquid phases are to glimmering
Luminous intensity measured value IAC0ijGroup in and when between-group variation coefficient CV≤10% (involved calculation formula is shown in this patent measurement of correlation
Uncertainty requirement), the measurement carried out according to this patent method is effective;
(3) bacterium increasing value Fij、GijIt calculates
Every control sample and antimicrobial sample after cultivating for 24 hours, bacterium increasing value Fij、GijIt is counted respectively according to formula (13), (14)
It calculates:
In formula:
FijAnd GijThe bacterium increasing value of-every control sample and antimicrobial sample after cultivating for 24 hours, sample group i=1,2,3;Often
Group sample number into spectrum j=1,2,3,4,5;
CA0ijAnd CAtij- every 0h contact and after cultivating for 24 hours control sample recycling viable bacteria ATP concentration, unit is mole every
It rises (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value, RLU;
Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
TA0ijAnd TAtij- every 0h contact and after cultivating for 24 hours antimicrobial sample recycling viable bacteria ATP concentration, unit is mole every
It rises (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value, RLU;
Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;
(4) antibiotic rate R is calculated
It tests under condition for validity, the antibiotic rate R of every plated film antibiotic glass sampleij, every group and every batch of sample antibiotic rate RiAnd R
It is calculated respectively according to formula (15), (16), (17):
In formula:
RijThe antibiotic rate of-every plated film antibiotic glass sample, %;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,
3,4,5;
RiThe antibiotic rate of-every group plated film antibiotic glass sample, %;Sample group i=1,2,3;
R-every batch of plated film antibiotic glass sample antibiotic rate, %;
CAtijAnd TAtij- every antimicrobial sample and control sample recycle the average ATP concentration of viable bacteria after cultivating for 24 hours, and unit is
Mole every liter (mol/L);Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every antimicrobial sample and control sample after cultivating for 24 hours, the relative intensity of fluorescence measured value of recovered liquid,
RLU;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;
(5) antibacterial activity value A is calculated
It tests under condition for validity, the antibacterial activity value A of every plated film antibiotic glass sampleij, the antibacterial of every group and every batch of sample it is living
Property value AiIt is calculated respectively according to formula (18), (19), (20) with A:
In formula:
AijThe antibacterial activity value of-every plated film antibiotic glass sample;Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,
3,4,5;
AiThe antibacterial activity value of-every group plated film antibiotic glass sample, sample group i=1,2,3;
A-every batch of plated film antibiotic glass sample antibacterial activity value;
FijAnd GijThe bacterium increasing value of-every control sample and antimicrobial sample after cultivating for 24 hours, wherein sample group i=1,2,
3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours control sample recovered liquid relative intensity of fluorescence measured value, RLU;
Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
With- every 0h contact and after cultivating for 24 hours antimicrobial sample recovered liquid relative intensity of fluorescence measured value, RLU;
Sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;
aA- low concentration standard curve lgCA-lgIASlope;
(6) data revision of the convention requirement: the concentration of calibration ATP standard serial solution and the viable bacteria ATP of inoculation bacterium solution, sample recovered liquid
Concentration CAWhen, with reference to the data revision of the convention regulation in GB 4789.2-2016 in relation to clump count;Work as CAWhen less than 100mol/L, " four
House five enters " round numbers;Work as CAWhen not less than 100mol/L, take preceding 2 bit digital after the 3rd bit digital " rounding up ", behind with 0 generation
Displacement number;It can also be indicated with 10 exponential form, " rounding up " uses two effective digitals, control sample and antimicrobial sample afterwards
After contacting through 0h and cultivating for 24 hours, reclaim liquid phase is to fluorescent strength determining value round numbers, antibiotic rate Rij、Ri, R calculated result take three
Position effective digital;Bacterium increasing value Fij、GijWith antibacterial activity value Aij、Ai, A calculated result take two effective digitals;
(7) uncertainty of measurement: this patent method mainly passes through calculating control sample and antimicrobial sample and contacts through 0h and cultivate for 24 hours
Afterwards, reclaim liquid phase in the group of fluorescent strength determining value and between-group variation coefficient CV=σ ÷ μ × 100% (μ, σ and CV count
Calculate result and remain into 2 significant digits), judge ATP fluorimetric assay for biological materials method being applied to plated film antibiotic glass bacteria resistance energy
The reproducibility of test;In regulation group and between-group variation coefficient CV≤10%;
5 control samples, 5 antimicrobial samples and 5 control samples, the 5 antibacterial samples after cultivating for 24 hours that every group of 0h is contacted
Product, arithmetic mean of instantaneous value of the reclaim liquid phase to fluorescent strength determining valueAnd Respectively according to formula (21),
(22) (sample group i=1,2,3 is calculated;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=1,2,3;
In formulaWithAfter respectively every group of control sample and antimicrobial sample are contacted through 0h and cultivated for 24 hours, respectively
The relative intensity of fluorescence measured value of Duplicate Samples):
15 control samples, 15 antimicrobial samples and 15 control samples after cultivating for 24 hours of 3 groups of 0h contact, 15 it is anti-
Bacterium sample, arithmetic mean of instantaneous value of the reclaim liquid phase to fluorescent strength determining valueAndRespectively according to formula
(23), (24) calculate (sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=
1,2,3;In formulaWithRespectively every group of control sample and antimicrobial sample are contacted through 0h and are trained for 24 hours
After supporting, the relative intensity of fluorescence measured value of each Duplicate Samples):
5 control samples, 5 antimicrobial samples and 5 control samples, the 5 antibacterial samples after cultivating for 24 hours that every group of 0h is contacted
Product, standard deviation of the reclaim liquid phase to fluorescent strength determining valueAnd Respectively according to formula (25) and
(26) (sample group i=1,2,3 is calculated;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=1,2,3;
In formulaWithAfter respectively every group of control sample and antimicrobial sample are contacted through 0h and cultivated for 24 hours, respectively
The relative intensity of fluorescence measured value of Duplicate Samples):
15 control samples, 15 antimicrobial samples and 15 control samples after cultivating for 24 hours of 3 groups of 0h contact, 15 it is anti-
Bacterium sample, standard deviation of the reclaim liquid phase to fluorescent strength determining valueAndRespectively according to formula
(27) and (28) calculate (sample group i=1,2,3;Every group of sample number into spectrum j=1,2,3,4,5;ATP tests Duplicate Samples number k=
1,2,3;In formulaWithRespectively every group of control sample and antimicrobial sample are contacted through 0h and are trained for 24 hours
After supporting, the relative intensity of fluorescence measured value of each Duplicate Samples):
9. the detection method of plated film antibiotic glass bacteria resistance energy according to claim 1, which is characterized in that the knot
Fruit evaluation, carries out in the steps below:
(1) with reference to health industry common practice and the requirement of dependent antimicrobial product standard, following classification criterion is taken:
If using antibiotic rate R as correlated performance evaluation index: working as Rij/Ri(staphylococcus aureus and sand when/R < 90%
Door Salmonella Rij/Ri/ R < 80%), sample is without antibacterial actions;As 90%≤Rij/Ri(staphylococcus aureus when/R < 99%
With 80%≤R of salmonellaij/Ri/ R < 90%), sample has antibacterial actions;As 99%≤Rij/RiWhen/R < 99.9%
(90%≤R of staphylococcus aureus and salmonellaij/Ri/ R < 99%), sample antibacterial actions are stronger;Work as Rij/Ri/R≥
(staphylococcus aureus and salmonella R when 99.9%ij/Ri/ R >=99%), sample antibacterial actions are extremely strong;
If using antibacterial activity value A as correlated performance evaluation index: working as Aij/AiWhen/A < 1.0 (staphylococcus aureus and
Salmonella Aij/Ai/ A < 0.5), sample is without antibacterial actions;As 1.0≤Aij/AiWhen/A < 2.0 (staphylococcus aureus and
0.5≤A of salmonellaij/Ai/ A < 1.0), sample has antibacterial actions;As 2.0≤Aij/Ai(golden yellow Portugal when/A < 3.0
1.0≤A of grape coccus and salmonellaij/Ai/ A < 2.0), sample antibacterial actions are stronger;Work as Aij/AiIt is (golden yellow when/A >=3.0
Staphylococcus and salmonella Aij/Ai/ A >=2.0), sample antibacterial actions are extremely strong;
(2) as the antibiotic rate R of certain group (part) plated film antibiotic glass samplei(Rij) or antibacterial activity value Ai(Aij) and other two groups
When the bacteria resistance of (four) sample can be compared to a levels be at least differed, one group of (part) sample is extracted again and repeats to test;
It is calculated through ATP bioluminescence lgCA─lgIAThe antibiotic rate or antibacterial activity value that calibration curve method measures, if the plating of two groups of front and back
Film antibiotic glass sample antibacterium performance level is identical, then abandons it;Take other two groups (four) remaining sample antibiotic rate Ri(Rij)
Or antibacterial activity value Ai(Aij) arithmetic mean of instantaneous value as batch (group) plated film antibiotic glass sample bacteria resistance can evaluation
As a result.
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Application publication date: 20191008 |