CN116042326A - Nucleic acid pollution scavenger - Google Patents

Nucleic acid pollution scavenger Download PDF

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Publication number
CN116042326A
CN116042326A CN202211308288.XA CN202211308288A CN116042326A CN 116042326 A CN116042326 A CN 116042326A CN 202211308288 A CN202211308288 A CN 202211308288A CN 116042326 A CN116042326 A CN 116042326A
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nucleic acid
concentration
sodium
scavenger
potassium carbonate
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刘小龙
刘朝煜
李小花
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Shenzhen Sinang Yiyun Technology Co ltd
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Shenzhen Sinang Yiyun Technology Co ltd
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    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/667Neutral esters, e.g. sorbitan esters
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    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
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    • C11D3/044Hydroxides or bases
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    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/046Salts
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    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates
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    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/10Carbonates ; Bicarbonates
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    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/201Monohydric alcohols linear
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    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/28Heterocyclic compounds containing nitrogen in the ring
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    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/32Amides; Substituted amides
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    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
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    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
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    • C11D3/33Amino carboxylic acids
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    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/34Organic compounds containing sulfur
    • C11D3/349Organic compounds containing sulfur additionally containing nitrogen atoms, e.g. nitro, nitroso, amino, imino, nitrilo, nitrile groups containing compounds or their derivatives or thio urea
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    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/36Organic compounds containing phosphorus
    • C11D3/364Organic compounds containing phosphorus containing nitrogen
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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Abstract

The invention discloses a nucleic acid pollution scavenger, which comprises B vitamins, sodium hydroxide, magnesium sulfate/zinc sulfate, sodium chloride, potassium chloride, sodium trichloroisocyanuric acid and Na 2 HPO 4 、KH 2 PO 4 Potassium carbonate, tween, ethanol and deionized water. The preparation method of the nucleic acid pollution scavenger comprises the following steps: step one: formation of nucleic acid contaminant removal agent: step two: the nucleic acid pollution scavenger is formed into a form which is easy to contact with the surface or space polluted by nucleic acid, and the form which is easy to contact with the surface or space polluted by nucleic acid comprises soaking in a large volume of aqueous solution, droplet spraying, atomizing or wet melt spraying. The active ingredient molecules of the nucleic acid pollution scavenger of the invention break DNA or RNA by contacting with air to generate active oxygen and the secondary derivative acts on phosphodiester bond, thus having a certain degree of selective scavenging effect, mild working condition to be alkalescent, no component with any toxicity risk, high nucleic acid scavenging efficiency and capability of scavenging polluted nucleic acid in 3-5 minutes.

Description

Nucleic acid pollution scavenger
Technical Field
The invention relates to the technical field of biology, in particular to a nucleic acid pollution scavenger.
Background
At present, PCR and related nucleic acid amplification detection laboratories have nucleic acid pollution with different severity, and the phenomenon of false positive results is extremely common. Ultraviolet irradiation is a widely used method, but it is not effective against nucleic acid contamination in various contamination forms (aerosol contamination, laboratory table contamination, etc.). Meanwhile, comprehensive analysis literature reports and market information show that most of functional components and using modes of the nucleic acid pollution scavenger have obvious defects, such as extremely poor scavenging effect of common 75% ethanol, and the peroxide has the defects of long acting time, low efficiency (more than half an hour) and poor scavenging effect. Although the highly oxidative hypochlorite removal efficiency is relatively high, high concentrations of the hypochlorite are required to be effective, but this is unavoidable for human health. In addition, scavengers such as strongly acidic (pH < 2.5) present a risk of corrosion to the equipment and environment.
Therefore, a nucleic acid contamination scavenger is proposed for purifying or scavenging PCR experimental environment and other solutions of nucleic acid amplified DNA and RNA contamination.
Disclosure of Invention
The present invention is directed to a nucleic acid contaminant removal agent that solves the above-mentioned problems of the prior art.
In order to achieve the above purpose, the present invention provides the following technical solutions:
a nucleic acid pollution scavenger comprises vitamin B, sodium hydroxide, magnesium sulfate/zinc sulfate, sodium chloride, potassium chloride, sodium trichloroisocyanuric acid, na 2 HPO 4 、KH 2 PO 4 The vitamin B group is 0.038-0.76 g/L, preferably 0.038g/L, the magnesium sulfate/zinc sulfate is 0.01-0.4 g/L, preferably 0.01g/L, the potassium carbonate is 0.01-0.19 g/L, preferably 0.01g/L, the sodium hydroxide is 0.001-0.01 g/L, preferably 0.001g/L, the sodium hydroxide is 0.01-0.1 g/L, preferably 0.01g/L, the sodium chloride is 0.001-0.01 g/L, the potassium chloride is 0.001-0.01 g/L, preferably 0.001g/L, the sodium trichloroisocyanuric acid is 0.001-0.01 g/L, preferably the sodium trichloroisocyanuric acid is 0.001g/L, the Na 2 HPO 4 The concentration is 0.01 to 0.1g/L, preferably Na 2 HPO 4 The concentration is 0.01g/L KH 2 PO 4 The concentration is 0.001-0.01 g/L, preferably KH 2 PO 4 The concentration is 0.001g/L, the concentration of potassium carbonate is 0.10-0.5 g/L, the concentration of potassium carbonate is 0.10g/L preferably, the concentration of Tween is 0.0001-0.001 g/L, the concentration of Tween is 0.0001g/L preferably, the concentration of ethanol is 0.01-0.1 g/L preferably, the concentration of ethanol is 0.01g/L.
As a further scheme of the invention: the B vitamins and magnesium sulfate/zinc sulfate and potassium carbonate act together to degrade nucleic acid.
As still further aspects of the invention: the sodium hydroxide, na 2 HPO 4 ,KH 2 PO 4 The pH value range of the nucleic acid scavenger is maintained between 6 and 10 by the potassium carbonate.
As still further aspects of the invention: the sodium chloride, potassium chloride, sodium trichloroisocyanuric acid, tween, ethanol and the like maintain the water content, viscosity and temperature stability of the nucleic acid scavenger system and improve the activity of the secondary derivative of the B vitamins.
As still further aspects of the invention: the preparation method of the nucleic acid pollution scavenger comprises the following steps:
step one: adding fixed amount of B vitamins, sodium hydroxide, magnesium sulfate/zinc sulfate, sodium chloride, potassium chloride, sodium trichloroisocyanuric acid and Na according to the proportion concentration 2 HPO 4 、KH 2 PO 4 Adding potassium carbonate, tween and ethanol into 1L deionized water, and fully mixing and reacting to form the nucleic acid pollution scavenger:
step two: the nucleic acid pollution scavenger is formed into a morphology mode which is easy to contact with the surface or space polluted by the nucleic acid to efficiently degrade the nucleic acid, thereby realizing the nucleic acid pollution scavenging.
As still further aspects of the invention: the morphology of the surface or space susceptible to nucleic acid contamination includes bulk aqueous immersion, droplet spray, atomization, or wet melt blown distribution.
Compared with the prior art, the invention has the beneficial effects that:
1. the active ingredient molecules of the nucleic acid pollution scavenger of the invention break DNA or RNA by contacting with air to generate active oxygen and the secondary derivative acts on phosphodiester bond, thus having a certain degree of selective scavenging effect, mild working condition to be alkalescent, no component with any toxicity risk, high nucleic acid scavenging efficiency and capability of scavenging polluted nucleic acid in 3-5 minutes.
Drawings
FIG. 1 is a graph showing the comparison of the effects of a nucleic acid contaminant removal agent.
FIG. 2 is a graph showing a comparison of curves of a nucleic acid contaminant removal agent.
Detailed Description
The following description of the embodiments of the present invention will be made clearly and completely with reference to the accompanying drawings, in which it is apparent that the embodiments described are only some embodiments of the present invention, but not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
Referring to fig. 1-2, the inventionIn the illustrative embodiment, a nucleic acid contaminant scavenger comprises vitamin B, sodium hydroxide, magnesium sulfate/zinc sulfate, sodium chloride, potassium chloride, na 2 HPO 4 、KH 2 PO 4 Potassium carbonate, tween, ethanol and deionized water, wherein the concentration of vitamin B group is 0.038 to 0.76g/L, preferably the concentration of vitamin B group is 0.038g/L, the concentration of magnesium sulfate/zinc sulfate is 0.01 to 0.4g/L, preferably the concentration of magnesium sulfate/zinc sulfate is 0.01g/L, the concentration of potassium carbonate is 0.01 to 0.19g/L, preferably the concentration of potassium carbonate is 0.01g/L, the concentration of sodium hydroxide is 0.001 to 0.01g/L, preferably the concentration of sodium hydroxide is 0.001g/L, the concentration of sodium chloride is 0.01 to 0.1g/L, preferably the concentration of sodium chloride is 0.01g/L, the concentration of potassium chloride is 0.001g/L, preferably the concentration of sodium trichloroisocyanurates is 0.001 to 0.01g/L, preferably the concentration of sodium trichloroisocyanurates is 0.001g/L, na 2 HPO 4 The concentration is 0.01 to 0.1g/L, preferably Na 2 HPO 4 The concentration is 0.01g/L KH 2 PO 4 The concentration is 0.001-0.01 g/L, preferably KH 2 PO 4 The concentration is 0.001g/L, the concentration of potassium carbonate is 0.10-0.5 g/L, the concentration of potassium carbonate is 0.10g/L preferably, the concentration of Tween is 0.0001-0.001 g/L, the concentration of Tween is 0.0001g/L preferably, the concentration of ethanol is 0.01-0.1 g/L preferably, the concentration of ethanol is 0.01g/L.
The B vitamins and magnesium sulfate/zinc sulfate and potassium carbonate act together to degrade nucleic acid, and the B vitamins comprise vitamin B1, vitamin B2, vitamin B3, vitamin B5, vitamin B7 and vitamin B9.
Sodium hydroxide, na 2 HPO 4 ,KH 2 PO 4 The pH value range of the nucleic acid scavenger is maintained between 6 and 10 by the potassium carbonate.
Sodium chloride, potassium chloride, sodium trichloroisocyanurate, tween, ethanol, etc. maintain the water content, viscosity, temperature stability of the nucleic acid scavenger system and raise the activity of secondary derivative of B vitamins.
The preparation method of the nucleic acid pollution scavenger comprises the following steps:
step one: adding fixed amount of B vitamins, sodium hydroxide, magnesium sulfate/zinc sulfate, sodium chloride, potassium chloride and trichlor according to the proportion concentrationSodium chloroisocyanuric acid, na 2 HPO 4 、KH 2 PO 4 Adding potassium carbonate, tween and ethanol into 1L deionized water, and fully mixing and reacting to form the nucleic acid pollution scavenger:
step two: the nucleic acid pollution scavenger is formed into a morphology mode which is easy to contact with the surface or space polluted by the nucleic acid to efficiently degrade the nucleic acid, thereby realizing the nucleic acid pollution scavenging.
Forms that are susceptible to contact with surfaces or spaces that are contaminated with nucleic acids include bulk aqueous solution immersion, droplet spray, atomization, or wet melt blown distribution.
Embodiment one:
and (3) soaking the PCR tube polluted by the PCR product and a pipette tip (without a filter element) in the nucleic acid scavenger for 3-5 minutes, washing the residual nucleic acid scavenger with pollution-free water, and detecting to remove the pollution of the PCR product.
Embodiment two:
the nucleic acid scavenger is soaked by clean paper towel or cloth, the surface of the liquid transfer device is wiped for 3 to 5 times, the residual nucleic acid scavenger is wiped by the paper towel or cloth which is wet by pollution-free water, and the pollution of PCR products can be removed through detection.
Embodiment III:
spraying the nucleic acid scavenger onto the surface of the instrument or the experiment table by using a spray can for 3-5 minutes, wiping off the residual nucleic acid scavenger by using a paper towel or a rag wetted by water to remove the pollution of the PCR product, and detecting to remove the pollution of the PCR product.
Embodiment four:
the laboratory space is filled with the atomized spray nucleic acid scavenger, and the spraying amount is less than 10mL/m 3 Closing the door for 3-5 minutes, opening the exhaust system for ventilation, and detecting to remove PCR product pollution.
Although the present invention has been described with reference to the foregoing embodiments, it will be apparent to those skilled in the art that modifications may be made to the embodiments described, or equivalents may be substituted for elements thereof, and any modifications, equivalents, improvements and changes may be made without departing from the spirit and principles of the present invention.

Claims (6)

1. A nucleic acid pollution scavenger comprises vitamin B, sodium hydroxide, magnesium sulfate/zinc sulfate, sodium chloride, potassium chloride, sodium trichloroisocyanuric acid, na 2 HPO 4 、KH 2 PO 4 Potassium carbonate, tween, ethanol and deionized water, and is characterized in that: the B vitamins have the concentration of 0.038-0.76 g/L, the concentration of magnesium sulfate/zinc sulfate of 0.01-0.4 g/L, the concentration of potassium carbonate of 0.01-0.19 g/L, the concentration of sodium hydroxide of 0.001-0.01 g/L, the concentration of sodium chloride of 0.01-0.1 g/L, the concentration of potassium chloride of 0.001-0.01 g/L, the concentration of sodium trichloroisocyanuric acid of 0.001-0.01 g/L and Na 2 HPO 4 The concentration is 0.01-0.1 g/L, KH 2 PO 4 The concentration is 0.001-0.01 g/L, the concentration of potassium carbonate is 0.10-0.5 g/L, the concentration of Tween is 0.0001-0.001 g/L, and the concentration of ethanol is 0.01-0.1 g/L.
2. The nucleic acid contaminant removal agent of claim 1, wherein: the B vitamins and magnesium sulfate/zinc sulfate and potassium carbonate act together to degrade nucleic acid.
3. The nucleic acid contaminant removal agent of claim 1, wherein: the sodium hydroxide, na 2 HPO 4 ,KH 2 PO 4 The pH value range of the nucleic acid scavenger is maintained between 6 and 10 by the potassium carbonate.
4. The nucleic acid contaminant removal agent of claim 1, wherein: the sodium chloride, potassium chloride, sodium trichloroisocyanuric acid, tween, ethanol and the like maintain the water content, viscosity and temperature stability of the nucleic acid scavenger system and improve the activity of the secondary derivative of the B vitamins.
5. The nucleic acid contaminant removal agent of claim 1, wherein: the preparation method of the nucleic acid pollution scavenger comprises the following steps:
step one: is concentrated according to the proportionAdding fixed amount of B vitamins, sodium hydroxide, magnesium sulfate/zinc sulfate, sodium chloride, potassium chloride, sodium trichloroisocyanuric acid and Na 2 HPO 4 、KH 2 PO 4 Adding potassium carbonate, tween and ethanol into 1L deionized water, and fully mixing and reacting to form the nucleic acid pollution scavenger:
step two: the nucleic acid pollution scavenger is formed into a morphology mode which is easy to contact with the surface or space polluted by the nucleic acid to efficiently degrade the nucleic acid, thereby realizing the nucleic acid pollution scavenging.
6. The nucleic acid contaminant removal agent of claim 5, wherein: the morphology of the surface or space susceptible to nucleic acid contamination includes bulk aqueous immersion, droplet spray, atomization, or wet melt blown distribution.
CN202211308288.XA 2022-10-25 2022-10-25 Nucleic acid pollution scavenger Pending CN116042326A (en)

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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002060539A1 (en) * 2001-02-01 2002-08-08 Becton Dickinson And Company Surfactant/oxidizing agent solution and methods of use
DE102006018983A1 (en) * 2006-04-25 2007-10-31 Multibind Biotec Gmbh Decontamination solution, useful for degrading, solubilizing and removing protein and nucleic acid molecule from a solution and surface e.g. culture medium, comprises a vitamin, a metal ion and a surface active compound
US20090028961A1 (en) * 2005-04-30 2009-01-29 Multibind Biotec Gmbh Decontamination solution and its use for denaturation, modification, degradation, solubilisation and removal of proteins, nucleic acid molecules and microorganisms
EP2378524A1 (en) * 2010-04-15 2011-10-19 Cristanini Spa Decontamination/detoxification composition
US20120107415A1 (en) * 2008-12-18 2012-05-03 Thomas Lisowsky Combined disinfection and decontamination agent having increased effectiveness
CN112812901A (en) * 2021-01-29 2021-05-18 北京华瑞康源生物科技发展有限公司 Reagent capable of efficiently removing nucleic acid pollution in normal-temperature and low-temperature environments and application
DE102020002883A1 (en) * 2020-04-14 2021-10-14 Van Ba Dam Disinfectant and anti-virus static

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002060539A1 (en) * 2001-02-01 2002-08-08 Becton Dickinson And Company Surfactant/oxidizing agent solution and methods of use
US20090028961A1 (en) * 2005-04-30 2009-01-29 Multibind Biotec Gmbh Decontamination solution and its use for denaturation, modification, degradation, solubilisation and removal of proteins, nucleic acid molecules and microorganisms
DE102006018983A1 (en) * 2006-04-25 2007-10-31 Multibind Biotec Gmbh Decontamination solution, useful for degrading, solubilizing and removing protein and nucleic acid molecule from a solution and surface e.g. culture medium, comprises a vitamin, a metal ion and a surface active compound
US20120107415A1 (en) * 2008-12-18 2012-05-03 Thomas Lisowsky Combined disinfection and decontamination agent having increased effectiveness
EP2378524A1 (en) * 2010-04-15 2011-10-19 Cristanini Spa Decontamination/detoxification composition
DE102020002883A1 (en) * 2020-04-14 2021-10-14 Van Ba Dam Disinfectant and anti-virus static
CN112812901A (en) * 2021-01-29 2021-05-18 北京华瑞康源生物科技发展有限公司 Reagent capable of efficiently removing nucleic acid pollution in normal-temperature and low-temperature environments and application

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