CN111408733A - Antibacterial and antiviral nano silver colloidal solution and preparation method and application thereof - Google Patents
Antibacterial and antiviral nano silver colloidal solution and preparation method and application thereof Download PDFInfo
- Publication number
- CN111408733A CN111408733A CN202010326618.2A CN202010326618A CN111408733A CN 111408733 A CN111408733 A CN 111408733A CN 202010326618 A CN202010326618 A CN 202010326618A CN 111408733 A CN111408733 A CN 111408733A
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- CN
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- Prior art keywords
- solution
- antibacterial
- antiviral
- nano
- silver colloidal
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- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 title claims abstract description 120
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- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims abstract description 52
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims abstract description 52
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims abstract description 34
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Abstract
The embodiment of the invention relates to the technical field of medical health, and particularly discloses an antibacterial and antiviral nano-silver colloidal solution and a preparation method and application thereof. The preparation method of the antibacterial and antiviral nano silver colloidal solution comprises the following steps: slowly adding silver nitrate into the salicylic acid compound solution and fully stirring to prepare an intermediate solution; and sequentially and slowly adding a tannic acid solution, a sodium carbonate solution and a polyvinylpyrrolidone solution into the intermediate solution and fully stirring to prepare the antibacterial and antiviral nano-silver colloidal solution. The embodiment of the invention can solve the technical problem that the nano-silver colloidal solution in the prior art cannot well overcome the instability of the nano-silver, and simultaneously enhances the broad-spectrum antibacterial and antiviral effects of the nano-silver in the nano-silver colloidal solution.
Description
Technical Field
The invention relates to the technical field of medical treatment and health, in particular to an antibacterial and antiviral nano-silver colloidal solution and a preparation method and application thereof.
Background
Since Olympic Gentiansis (Ivanovski) discovered Nicotiana tabacum virus in 1898, more than 400 kinds of viruses associated with human diseases were discovered, and it was counted that more than 90% of human respiratory infectious diseases are caused by viruses, and many viral diseases such as smallpox, measles, poliomyelitis, etc. were effectively controlled with the development of immunology, however, many viruses which are not very antigenic and are liable to mutation, such as influenza Virus, SARS (Severe acute respiratory syndrome) coronavirus, avian influenza Virus, Human Immunodeficiency Virus (HIV), and new coronavirus, are difficult to control, are sometimes or currently circulating in a relatively serious situation, and are also diseases caused by bacteria, these pose serious threats to human health, and thus, prevention of bacterial and viral infections remains a major and urgent task for humans.
Among them, respiratory viruses such as influenza virus, SARS coronavirus, avian influenza virus, and novel coronavirus are difficult to control, and the main reason is that these viruses are infected on the mucosal surface, have weak antigenicity, and are prone to antigenic variation and drug-resistant mutation, resulting in poor viral drug resistance and viral vaccine immunization. Therefore, in the face of the characteristics of various human respiratory viruses, mucosal surface infection, weak antigenicity, easy antigenic variation and drug resistance mutation, the active search for a broad-spectrum nonspecific antibacterial and antiviral solution which is safe, effective and suitable for mucosal surface application is of great significance.
The nano silver is prepared by nano technology, the nano metal silver has strong bactericidal capacity, after the nano silver is prepared, the particle size reaches a nano (nm) level state, the nano silver has larger specific surface area, and the smaller the material unit of the nano silver is, the more the nano silver can effectively contact bacteria and viruses. In the prior art, nano silver is prepared into various antibacterial and antiviral products such as nano silver colloidal solution, is safe and effective, has no drug resistance, has multi-target 'attack' effect on various bacteria, fungi and viruses, has broad-spectrum antibacterial, antifungal and antiviral effects, and is suitable for application on the surface of a mucous membrane. However, in the prior art, the nano silver colloidal solution cannot well overcome the defect that nano silver is not stable enough, so that the wide application of nano silver in the field of medicines with broad-spectrum antibacterial and antiviral effects is limited.
Therefore, how to provide a safe, effective, non-drug-resistant, broad-spectrum antibacterial and antiviral nano-silver colloidal solution suitable for mucosal surface application and sufficiently stable is a technical problem to be solved.
Disclosure of Invention
The embodiment of the invention aims to provide an antibacterial and antiviral nano-silver colloidal solution, a preparation method thereof and application thereof in preparing antibacterial materials or antibacterial drugs, which can solve the technical problem that the nano-silver colloidal solution in the prior art cannot well overcome the instability of nano-silver, and can enhance the broad-spectrum antibacterial and antiviral effects of the nano-silver in the nano-silver colloidal solution.
On one hand, the embodiment of the invention provides a preparation method of an antibacterial and antiviral nano silver colloidal solution, which comprises the following steps: slowly adding silver nitrate into the salicylic acid compound solution and fully stirring to prepare an intermediate solution; and sequentially and slowly adding a tannic acid solution, a sodium carbonate solution and a polyvinylpyrrolidone solution into the intermediate solution and fully stirring to prepare the antibacterial and antiviral nano-silver colloidal solution.
In one embodiment of the present invention, the method for preparing the antibacterial and antiviral nano silver colloid solution further comprises the steps of: and storing the antibacterial and antiviral nano silver colloid solution in a brown bottle for later use.
In one embodiment of the present invention, the salicylic acid compound solution is selected from any one of an acetylsalicylic acid solution, a sodium salicylate solution, a salicylic acid solution, and a calcium acetylsalicylate urea solution.
In one embodiment of the invention, the content of the acetylsalicylic acid in the acetylsalicylic acid solution is 2 mg/ml, the content of the sodium salicylate in the sodium salicylate solution is 2-5 mg/ml, the content of the salicylic acid in the salicylic acid solution is 1-2 mg/ml, and the content of the calcium acetylsalicylic acid urea in the calcium acetylsalicylic acid urea solution is 2-5 mg/ml.
In one embodiment of the invention, the agitation is achieved using a magnetic stirrer.
In one embodiment of the present invention, the content of silver ions in the intermediate solution is 0.4 to 0.8 mg/ml, the content of tannic acid in the tannic acid solution is 5 to 10 mg/ml, the content of sodium carbonate in the sodium carbonate solution is 5 to 10 mg/ml, the content of polyvinylpyrrolidone in the polyvinylpyrrolidone solution is 10 to 20 mg/ml, and the volume ratio of the intermediate solution, the tannic acid solution, the sodium carbonate solution, and the polyvinylpyrrolidone solution is 88: 3: 2: 7.
In one embodiment of the present invention, the average particle size of the nano silver particles in the antibacterial and antiviral nano silver colloidal solution is 42.30 nm.
In one embodiment of the present invention, the zeta potential of the nano silver particles in the antibacterial and antiviral nano silver colloidal solution is-19.8 mv.
In another aspect, an antibacterial and antiviral nano-silver colloidal solution is provided, which is prepared by the method for preparing the antibacterial and antiviral nano-silver colloidal solution according to any one of the embodiments.
In still another aspect, an embodiment of the present invention provides a use of the antibacterial and antiviral nano-silver colloidal solution as described in any one of the preceding embodiments in preparing an antibacterial and antiviral material or an antibacterial and antiviral drug.
The previous embodiment of the present invention is to prepare an intermediate solution by slowly adding silver nitrate to a salicylic acid compound solution and sufficiently stirring; and the tannic acid solution, the sodium carbonate solution and the polyvinylpyrrolidone solution are sequentially and slowly added into the intermediate solution and fully stirred to prepare the safe, effective, drug-resistance-free, broad-spectrum antibacterial and antiviral nano-silver colloidal solution which is suitable for application on the surface of a mucous membrane and is stable enough.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings needed to be used in the description of the embodiments are briefly introduced below, and it is obvious that the drawings in the following description are only some embodiments of the present invention, and it is obvious for those skilled in the art to obtain other drawings based on these drawings without creative efforts.
Fig. 1 is a schematic flow chart of a method 100 for preparing an antibacterial and antiviral nano silver colloidal solution according to an embodiment of the present invention;
fig. 2 is a graph showing the particle size of nano silver particles in the antibacterial and antiviral nano silver colloidal solution prepared in example 1;
fig. 3 is a zeta potential diagram of nano silver particles in the antibacterial and antiviral nano silver colloidal solution prepared in example 1.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Example one
As shown in fig. 1, an embodiment of the present invention provides a method 100 for preparing an antibacterial and antiviral nano silver colloidal solution, where the method 100 mainly includes:
step S110: silver nitrate was slowly added to the salicylic acid compound solution and stirred well to make an intermediate solution. The silver nitrate may be replaced by other suitable silver salts besides silver nitrate, such as silver sulfate, silver sulfite, silver phosphate, etc. And
step S130: and sequentially and slowly adding a tannic acid solution, a sodium carbonate solution and a polyvinylpyrrolidone solution into the intermediate solution, and fully stirring to prepare the antibacterial and antiviral nano-silver colloidal solution.
Further, the preparation method of the antibacterial and antiviral nano silver colloid solution further comprises the following steps: step S150: and storing the antibacterial and antiviral nano silver colloid solution in a brown bottle for later use. Of course, the antibacterial and antiviral nano silver colloid solution can also be stored in other opaque dark colored bottles for standby.
Wherein the salicylic acid compound solution is selected from any one of an acetylsalicylic acid solution, a sodium salicylate solution, a salicylic acid solution and a calcium acetylsalicylate urea solution. Of course, the salicylic acid compound solution includes, but is not limited to, the above-mentioned acetylsalicylic acid solution, sodium salicylate solution, salicylic acid solution and acetylsalicylic acid calcium urea solution, and other salicylic acid compound solutions such as salicylic acid drug solutions are also possible.
In addition, it should be noted that the concentrations and volume ratios of the raw materials involved in the preparation of the antibacterial and antiviral nano silver colloidal solution in the preparation method 100 of the antibacterial and antiviral nano silver colloidal solution according to the first embodiment of the present invention may be reasonably selected and configured by those skilled in the art according to the technical solutions disclosed in the first embodiment of the present invention, in combination with the practical situations, the protection scope of the present invention includes, but is not limited to, the values or value ranges of the concentrations and volume ratios listed in the first embodiment of the present invention, and the values or value ranges of the concentrations and volume ratios listed in the first embodiment of the present invention are only preferred examples.
It is also worth mentioning that the embodiment of the present invention may further include a step of preparing each raw material involved in the antibacterial and antiviral nano silver colloid solution, for example. In addition, in other embodiments, the raw materials involved in the preparation of the antibacterial and antiviral nano-silver colloidal solution may be replaced by the components before the preparation of the raw materials, and accordingly, the preparation method of the antibacterial and antiviral nano-silver colloidal solution may be suitably modified accordingly.
For example, the salicylic acid compound solution may be an acetylsalicylic acid solution with an acetylsalicylic acid content of 2 mg/ml.
In addition, the salicylic acid compound solution can be sodium salicylate solution with the content of sodium salicylate of 2-5 mg/ml. Specifically, the content of sodium salicylate in the sodium salicylate solution is 2 mg/ml, 2.5 mg/ml, 4 mg/ml, 5 mg/ml and the like, and preferably, the content of sodium salicylate in the sodium salicylate solution is 3 mg/ml.
The salicylic acid compound solution may be salicylic acid solution with salicylic acid content of 1-2 mg/ml. Specifically, the content of salicylic acid in the salicylic acid solution is 1 mg/ml, 1.5 mg/ml, 2 mg/ml and the like, and preferably, the content of salicylic acid in the salicylic acid solution is 1.5 mg/ml.
Alternatively, the salicylic acid compound solution may be a calcium acetylsalicylate urea solution containing calcium acetylsalicylate urea in an amount of 2 to 5 mg/ml, for example. Specifically, the content of calcium acetylsalicylate urea in the calcium acetylsalicylate urea solution is 2 mg/ml, 3.5 mg/ml, 4 mg/ml, 5 mg/ml and the like, and preferably, the content of calcium acetylsalicylate urea in the calcium acetylsalicylate urea solution is 3 mg/ml.
The stirring in steps S110 and S130 is performed by a magnetic stirrer, for example. The stirring can also be achieved by using other suitable stirrers than magnetic stirrers.
The content of silver ions in the intermediate solution prepared in step S110 may be, for example, 0.4 to 0.8 mg/ml, the content of tannic acid in the tannic acid solution may be, for example, 5 to 10 mg/ml, the content of sodium carbonate in the sodium carbonate solution may be, for example, 5 to 10 mg/ml, the content of polyvinylpyrrolidone in the polyvinylpyrrolidone solution may be, for example, 10 to 20 mg/ml, and the volume ratio of the intermediate solution, the tannic acid solution, the sodium carbonate solution, and the polyvinylpyrrolidone solution may be, for example, 88: 3: 2: 7. Specifically, the content of the silver ions in the intermediate solution may be, for example, 0.4 mg/ml, 0.55 mg/ml, 0.7 mg/ml, 0.8 mg/ml, etc., preferably 0.6 mg/ml. The content of tannic acid in the tannic acid solution may be, for example, 5 mg/ml, 7 mg/ml, 8.5 mg/ml, 10 mg/ml, etc., preferably 8 mg/ml. The sodium carbonate solution may contain sodium carbonate in an amount of, for example, 5 mg/ml, 5.5 mg/ml, 6 mg/ml, 8 mg/ml, 10 mg/ml, etc., preferably 7 mg/ml. The content of polyvinylpyrrolidone in the polyvinylpyrrolidone solution may be, for example, 10 mg/ml, 13 mg/ml, 16 mg/ml, 17.5 mg/ml, 20 mg/ml, etc., preferably 15 mg/ml.
Specifically, the average particle diameter of the nano silver particles in the antibacterial and antiviral nano silver colloidal solution is, for example, 42.30 nm.
Specifically, the zeta potential (Zetapontential) of the nano silver particles in the antibacterial and antiviral nano silver colloidal solution is, for example, -19.8 mV.
Several specific examples of the preparation method 100 of the antibacterial and antiviral nano-silver colloidal solution according to the first embodiment of the present invention to prepare the nano-silver colloidal solution will be given below to better illustrate the technical solution of the present invention, and the specific examples are as follows:
example 1: weighing appropriate amount of silver nitrate in the presence of a magnetic stirrer, preparing a solution with silver ion content of 0.4-0.8 mg/ml with 0.2% acetylsalicylic acid solution (acetylsalicylic acid content of 2 mg/ml), then 88 parts (the "parts" referred to herein and hereinafter refer to the volume of the solution) of the solution having the silver ion content of 0.4 to 0.8 mg/ml, in the presence of a magnetic stirrer, 3 parts of 0.5-1.0% tannic acid solution (the content of tannic acid is 5-10 mg/ml), 2 parts of 0.5-1.0% sodium carbonate solution (the content of sodium carbonate is 5-10 mg/ml) and 7 parts of 1.0-2.0% polyvinylpyrrolidone solution (the content of polyvinylpyrrolidone is 10-20 mg/ml) are slowly added in sequence to prepare the antibacterial and antiviral nano silver colloid solution which is stored in a brown bottle for later use. As shown in fig. 2, the Average particle diameter (shown as Z-Average (d.nm)) of the nano silver particles in the prepared antibacterial and antiviral nano silver colloidal solution was 42.30 nm, and as shown in fig. 3, the Zeta Potential (shown as Zeta Potential (mV)) of the nano silver particles was-19.8 mV.
Example 2: weighing appropriate amount of silver nitrate in the presence of a magnetic stirrer, preparing a solution with silver ion content of 0.4-0.8 mg/ml with 0.2-0.5% sodium salicylate solution (sodium salicylate content is 2-5 mg/ml), then 88 parts of the solution with the silver ion content of 0.4-0.8 mg/ml is taken, in the presence of a magnetic stirrer, 3 parts of 0.5-1.0% tannic acid solution (the content of tannic acid is 5-10 mg/ml), 2 parts of 0.5-1.0% sodium carbonate solution (the content of sodium carbonate is 5-10 mg/ml) and 7 parts of 1.0-2.0% polyvinylpyrrolidone solution (the content of polyvinylpyrrolidone is 10-20 mg/ml) are slowly added in sequence to prepare the antibacterial and antiviral nano silver colloid solution which is stored in a brown bottle for later use.
Example 3: weighing appropriate amount of silver nitrate in the presence of a magnetic stirrer, preparing a solution with silver ion content of 0.4-0.8 mg/ml with 0.1-0.2% salicylic acid solution (salicylic acid content of 1-2 mg/ml), then 88 parts of the solution with the silver ion content of 0.4-0.8 mg/ml is taken, in the presence of a magnetic stirrer, 3 parts of 0.5-1.0% tannic acid solution (the content of tannic acid is 5-10 mg/ml), 2 parts of 0.5-1.0% sodium carbonate solution (the content of sodium carbonate is 5-10 mg/ml) and 7 parts of 1.0-2.0% polyvinylpyrrolidone solution (the content of polyvinylpyrrolidone is 10-20 mg/ml) are slowly added in sequence to prepare the antibacterial and antiviral nano silver colloid solution which is stored in a brown bottle for later use.
Example 4: weighing appropriate amount of silver nitrate in the presence of a magnetic stirrer, preparing a solution with silver ion content of 0.4-0.8 mg/ml with 0.2-0.5% calcium acetylsalicylate urea solution (the content of calcium acetylsalicylate urea is 2-5 mg/ml), then 88 parts of the solution with the silver ion content of 0.4-0.8 mg/ml is taken, in the presence of a magnetic stirrer, 3 parts of 0.5-1.0% tannic acid solution (the content of tannic acid is 5-10 mg/ml), 2 parts of 0.5-1.0% sodium carbonate solution (the content of sodium carbonate is 5-10 mg/ml) and 7 parts of 1.0-2.0% polyvinylpyrrolidone solution (the content of polyvinylpyrrolidone is 10-20 mg/ml) are slowly added in sequence to prepare the antibacterial and antiviral nano silver colloid solution which is stored in a brown bottle for later use.
The preparation method 100 of the antibacterial and antiviral nano-silver colloidal solution provided by the embodiment of the invention can ensure that the prepared nano-silver colloidal solution has good broad-spectrum antibacterial and antiviral effects, solve the technical problem that the nano-silver colloidal solution in the prior art cannot well overcome the instability of nano-silver, and simultaneously enhance the broad-spectrum antibacterial and antiviral effects of the nano-silver in the nano-silver colloidal solution.
Example two
The second embodiment of the present invention provides an antibacterial and antiviral nano silver colloidal solution, which is prepared from raw materials including silver nitrate, salicylic acid compound solution, tannic acid solution, sodium carbonate solution and polyvinylpyrrolidone solution. The antibacterial and antiviral nano silver colloidal solution is prepared by using the preparation raw material and the preparation method 100 of the antibacterial and antiviral nano silver colloidal solution according to any one of the embodiments, and the preparation method 100 of the antibacterial and antiviral nano silver colloidal solution may refer to the description of the embodiments of the present invention, and is not repeated herein.
The antibacterial and antiviral nano-silver colloidal solution of the second embodiment of the present invention is prepared by the preparation method 100 of the antibacterial and antiviral nano-silver colloidal solution described in any one of the foregoing embodiments, so that the prepared nano-silver colloidal solution can be ensured to have good broad-spectrum antibacterial and antiviral effects, and simultaneously, the technical problem that the nano-silver colloidal solution in the prior art is not stable enough can be solved, and the broad-spectrum antibacterial and antiviral effects of the nano-silver in the nano-silver colloidal solution are enhanced.
Examples of the applications
It should be noted that the antibacterial and antiviral nano-silver colloidal solution according to any one of the embodiments of the present invention is a brand-new colloidal solution with multiple effects of broad-spectrum antibacterial, antifungal, antiviral, analgesic and anti-inflammatory, has no obvious toxic or side effect, has no drug resistance, has various application methods, and can be applied to the surface of an object, the surface of a fabric, the skin and a mucous membrane to inhibit the proliferation of various viruses, bacteria and fungi according to different dosage forms. Specific application methods of the antibacterial and antiviral nano silver colloid solution are shown in table 1, but include, but are not limited to, the application methods listed in table 1.
TABLE 1
Type of colloidal solution | Application site | Object of action | Specific method of use |
Example 1 Nano silver colloid solution | Skin, nasal cavity, throat and vagina | Bacteria, fungi and viruses | Spraying, smearing and rinsing |
Example 2 Nano silverColloidal solution | Skin, nasal cavity and object surface | Bacteria, fungi and viruses | Spraying, smearing and rinsing |
Example 3 Nano silver colloid solution | Skin, foot, nail and toenail | Bacteria and fungi | Spraying and smearing |
Example 4 Nano silver colloid solution | Skin, nasal cavity, throat and vagina | Bacteria, fungi and viruses | Spraying, smearing and rinsing |
The antibacterial and antiviral nano-silver colloidal solution provided by the embodiment of the invention has a wide application prospect in the anti-infection field, and can be used for preparing various antibacterial and antiviral materials or antibacterial and antiviral drugs, such as medical dressings, external paints, resin products and the like, and specifically can be used for preparing band-aid, burn patches, burn and scald ointments, hand sanitizer, doors and windows, implantation instruments and the like.
Application effects
The following will describe the antibacterial and antiviral application effects of the antibacterial and antiviral nano-silver colloidal solution of the embodiment of the present invention in detail:
1. broad-spectrum antibacterial application: taking the nano-silver colloidal solution of the example 1, mixing the nano-silver colloidal solution with broth cultures of escherichia coli, staphylococcus aureus, klebsiella pneumoniae, pseudomonas aeruginosa, acinetobacter baumannii and bacillus subtilis and a candida albicans broth culture in equal volume times, acting for different time at room temperature, and then applying a coating method to detect the inhibition effect of the colloidal solution on different bacteria. The experimental results show that the nano silver colloidal solution has extremely strong killing effect on the bacteria and the fungi, and the specific data of the experimental results are shown in table 2.
TABLE 2
Strain (10)4cfu/ml) | 1min | 5min | 15min |
Escherichia coli | 100 | 100 | 100 |
|
100 | 100 | 100 |
|
100 | 100 | 100 |
|
100 | 100 | 100 |
|
100 | 100 | 100 |
|
100 | 100 | 100 |
Candida albicans | 99.10 | 99.50 | 100 |
2. Broad spectrum antiviral applications: the nano-silver colloidal solution of example 1 was mixed with influenza virus (H1N1), influenza virus (H3N2), parainfluenza virus and newcastle disease virus solutions in equal volume, allowed to act at room temperature for 1 hour, and then diluted with physiological saline in equal volume on a 96-well hemagglutination plate, 0.1 ml of 0.5% chicken red blood cells (the content of chicken red blood cells is 5 mg/ml) was added dropwise to each well, mixed, allowed to act at room temperature for 1 hour, and the influence of the nano-silver colloidal solution on the blood coagulation activity of the four viral hemagglutinins was observed. The experimental result shows that the nano silver colloidal solution can obviously inhibit the blood coagulation activity of hemagglutinin of influenza virus (H1N1), influenza virus (H3N2), parainfluenza virus and Newcastle disease virus, and the nano silver colloidal solution has the effect of broad-spectrum resistance to respiratory virus infection, and the specific data of the experimental result is shown in Table 3.
TABLE 3
Viral species | Hemagglutination potency of the experimental group | Hemagglutination titers of virus controls |
Influenza virus (H1N1) | Has no hemagglutination activity | 1280 |
Influenza virus (H3N2) | Has no hemagglutination activity | 1280 |
Parainfluenza virus | Has no hemagglutination activity | 1280 |
Newcastle disease virus | Has no hemagglutination activity | 1280 |
3. Broad-spectrum virucidal applications: the nano silver colloid solution of example 1 was mixed with influenza virus (H1N1), influenza virus (H3N2), parainfluenza virus and newcastle disease virus solution in equal volume for 1 hour at room temperature, then 0.1 ml of the mixed solution was inoculated into the allantoic cavity of 10-day-old chick embryos, 5 chick embryos per group were incubated at 38 ℃ for 72 hours, then placed in a 4 ℃ refrigerator overnight, the allantoic cavity solution was taken the next day, diluted with physiological saline in equal volume on a 96-well hemagglutination plate, 0.1 ml of 0.5% chicken red blood cells (the content of chicken red blood cells was 5 mg/ml) was added dropwise to each well, mixed, and allowed to act for 1 hour at room temperature to observe the inactivation of the nano silver colloid solution on these four viruses. The experimental result shows that the nano silver colloid solution can completely inactivate influenza virus (H1N1), influenza virus (H3N2), parainfluenza virus and Newcastle disease virus, the four viruses do not proliferate in allantoic cavities of 10-day-old chick embryos, and the specific data of the experimental result is shown in Table 4.
TABLE 4
Viral species | Hemagglutination potency of the experimental group | Hemagglutination titers of virus controls |
Influenza virus (H1N1) | Has no hemagglutination activity | 2560 |
Influenza virus (H3N2) | Has no hemagglutination activity | 2560 |
Parainfluenza virus | Has no hemagglutination activity | 1280 |
Newcastle disease virus | Has no hemagglutination activity | 1280 |
In conclusion, in the embodiment of the invention, tannic acid and sodium carbonate are used as reducing agents in a salicylic acid compound solution, silver ions in silver nitrate are reduced to be nano silver, then a proper amount of polyvinylpyrrolidone is added to prepare a stable nano silver colloidal solution, the prepared nano silver colloidal solution has stable performance, is safe and effective, cannot generate drug resistance, and can directly act on proteins or enzyme proteins of various virosomes under the synergistic action of the salicylic acid compound and the nano silver, so that the capacity of virus infection of cells is reduced, and a broad-spectrum antiviral effect is exerted; the nano silver prepared by reducing tannic acid can inhibit the activity of surface protein and enzyme protein of bacteria, fungi and viruses, destroy the cell membrane structure of the bacteria, the fungi and the viruses, inhibit the template function of nucleic acid of the bacteria, the fungi and the viruses and play a broad-spectrum antibacterial and antiviral role.
Finally, it should be noted that: the above examples are only intended to illustrate the technical solution of the present invention, but not to limit it; although the invention has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art that: the technical solutions described in the foregoing embodiments can be modified, or some technical features can be equivalently replaced; and such modifications or substitutions do not depart from the spirit and scope of the corresponding technical solutions of the embodiments of the present invention.
Claims (10)
1. The preparation method of the antibacterial and antiviral nano silver colloidal solution is characterized by comprising the following steps:
slowly adding silver nitrate into the salicylic acid compound solution and fully stirring to prepare an intermediate solution; and
and sequentially and slowly adding a tannic acid solution, a sodium carbonate solution and a polyvinylpyrrolidone solution into the intermediate solution, and fully stirring to prepare the antibacterial and antiviral nano-silver colloidal solution.
2. The method for preparing an antibacterial and antiviral nano-silver colloidal solution according to claim 1, further comprising the steps of: and storing the antibacterial and antiviral nano silver colloid solution in a brown bottle for later use.
3. The method for preparing an antibacterial and antiviral nano-silver colloidal solution according to claim 1, wherein the salicylic acid-based compound solution is any one selected from the group consisting of an acetylsalicylic acid solution, a sodium salicylate solution, a salicylic acid solution and a calcium acetylsalicylic acid urea solution.
4. The method for preparing nano silver colloidal solution for antibacterial and antiviral according to claim 3, wherein the content of acetylsalicylic acid in the acetylsalicylic acid solution is 2 mg/ml, the content of sodium salicylate in the sodium salicylate solution is 2 mg/ml to 5 mg/ml, the content of salicylic acid in the salicylic acid solution is 1 mg/ml to 2 mg/ml, and the content of calcium acetylsalicylic acid urea in the calcium acetylsalicylic acid urea solution is 2 mg/ml to 5 mg/ml.
5. The method for preparing an antibacterial and antiviral nano-silver colloidal solution according to claim 1, wherein the stirring is performed by a magnetic stirrer.
6. The method of preparing an antibacterial and antiviral nano silver colloidal solution as set forth in claim 1, wherein the content of silver ions in the intermediate solution is 0.4-0.8 mg/ml, the content of tannic acid in the tannic acid solution is 5-10 mg/ml, the content of sodium carbonate in the sodium carbonate solution is 5-10 mg/ml, the content of polyvinylpyrrolidone in the polyvinylpyrrolidone solution is 10-20 mg/ml, and the volume ratio of the intermediate solution, the tannic acid solution, the sodium carbonate solution and the polyvinylpyrrolidone solution is 88: 3: 2: 7.
7. The method of claim 6, wherein the nano silver particles in the nano silver colloidal solution have an average particle size of 42.30 nm.
8. The method of claim 6, wherein the zeta potential of the nano silver particles in the antibacterial and antiviral nano silver colloidal solution is-19.8 mv.
9. An antibacterial and antiviral nano silver colloidal solution, characterized in that it is prepared by the method of any one of claims 1 to 8.
10. The use of the nano silver colloidal solution for antibacterial and antiviral use according to claim 9 for preparing antibacterial and antiviral material or antibacterial and antiviral medicament.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113813287A (en) * | 2021-08-27 | 2021-12-21 | 中国医学科学院皮肤病医院(中国医学科学院皮肤病研究所) | Preparation method of compound medicinal liquid for treating verruca vulgaris |
CN114470131A (en) * | 2020-10-23 | 2022-05-13 | 香港商富斐国际有限公司 | Preparation method of nano silver turmeric material applied to inhibiting novel coronavirus |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002245854A (en) * | 2001-02-20 | 2002-08-30 | Bando Chem Ind Ltd | Colloidal solution of metal, and manufacturing method of the same |
JP2006299329A (en) * | 2005-04-19 | 2006-11-02 | Mitsuboshi Belting Ltd | Method for producing metal nanoparticle |
US20070003603A1 (en) * | 2004-07-30 | 2007-01-04 | Karandikar Bhalchandra M | Antimicrobial silver compositions |
CN101147977A (en) * | 2007-10-17 | 2008-03-26 | 楚雄师范学院 | Method for preparing high activity and long service negative charged colloidal nanometer silver |
CN102579490A (en) * | 2012-02-22 | 2012-07-18 | 大连大学 | Nano-silver antiviral solution and preparation method thereof |
JP2013185213A (en) * | 2012-03-08 | 2013-09-19 | Tokyo Institute Of Technology | Metal nanoparticle, method for producing the same, and conductive ink |
CN103934469A (en) * | 2014-04-03 | 2014-07-23 | 湖北大学 | Method for preparing silver nanoclusters coated with glutathione |
CN110883340A (en) * | 2018-09-10 | 2020-03-17 | 河南金渠银通金属材料有限公司 | Electronegative superfine silver powder and preparation method thereof |
-
2020
- 2020-04-24 CN CN202010326618.2A patent/CN111408733A/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002245854A (en) * | 2001-02-20 | 2002-08-30 | Bando Chem Ind Ltd | Colloidal solution of metal, and manufacturing method of the same |
US20070003603A1 (en) * | 2004-07-30 | 2007-01-04 | Karandikar Bhalchandra M | Antimicrobial silver compositions |
JP2006299329A (en) * | 2005-04-19 | 2006-11-02 | Mitsuboshi Belting Ltd | Method for producing metal nanoparticle |
CN101147977A (en) * | 2007-10-17 | 2008-03-26 | 楚雄师范学院 | Method for preparing high activity and long service negative charged colloidal nanometer silver |
CN102579490A (en) * | 2012-02-22 | 2012-07-18 | 大连大学 | Nano-silver antiviral solution and preparation method thereof |
JP2013185213A (en) * | 2012-03-08 | 2013-09-19 | Tokyo Institute Of Technology | Metal nanoparticle, method for producing the same, and conductive ink |
CN103934469A (en) * | 2014-04-03 | 2014-07-23 | 湖北大学 | Method for preparing silver nanoclusters coated with glutathione |
CN110883340A (en) * | 2018-09-10 | 2020-03-17 | 河南金渠银通金属材料有限公司 | Electronegative superfine silver powder and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
陈艳等: "银溶胶中水杨酸吸附行为的实验和密度泛函理论研究", 《信阳师范学院学报:自然科学版》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114470131A (en) * | 2020-10-23 | 2022-05-13 | 香港商富斐国际有限公司 | Preparation method of nano silver turmeric material applied to inhibiting novel coronavirus |
CN113813287A (en) * | 2021-08-27 | 2021-12-21 | 中国医学科学院皮肤病医院(中国医学科学院皮肤病研究所) | Preparation method of compound medicinal liquid for treating verruca vulgaris |
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