Magnetic response release electronic atomized liquid as well as preparation method and application thereof

By using magnetic responsive microcapsules in the electronic atomization liquid and using magnetic fields to control the release of microcapsules, the problems of flavor attenuation and taste adjustment of the electronic atomization liquid are solved, achieving better user experience and diversified choices.

CN119699632APending Publication Date: 2025-03-28ALD GRP
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Patent Information

Application Number
CN202311279753.6
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2023-09-27
Publication Date
2025-03-28

AI Technical Summary

Technical Problem

The existing electronic atomizing liquid has a taste attenuation problem during use and cannot be adjusted according to the taste needs of different groups of people.

Method used

Magnetic responsive microcapsules are used as the key component of the electronic atomization liquid to control the release method of the microcapsules through a magnetic field to achieve controllable release and taste adjustment. Magnetic responsive microcapsules contain magnetic responsive materials, which can heat up and destroy the microcapsule structure under the action of magnetic fields, thereby releasing the active ingredients.

Benefits of technology

It effectively avoids the taste attenuation problem of electronic atomizing liquid during use, realizes adjustable and diverse choices of taste strength, and improves consumers' user experience.

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Abstract

The invention relates to a magnetic response release electronic atomized liquid as well as a preparation method and application thereof. The electronic atomized liquid comprises the following components in percentage by weight: 90-99.99% of polyol and 0.01-10% of magnetic response microcapsules, the magnetic response microcapsule contains a magnetic response material; the magnetic response material comprises at least one of magnetic response metal ions and magnetic response metal oxide nanoparticles. The electronic atomized liquid contains the magnetic response material, controllable release can be achieved under the action of a magnetic field, the problem that the taste of the atomized liquid is attenuated is solved, the taste intensity can be adjusted and diversified selection can be achieved according to different consumers, the consumer taste matching performance is better, and the electronic atomized liquid is suitable for various consumers. And a research and development direction is provided for making more personalized atomized liquid.
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Description

Technical Field

[0001] The present invention relates to the field of electronic atomization, and in particular to a magnetic response-releasing electronic atomization liquid and a preparation method and application thereof. Background Art

[0002] With the widespread development of electronic atomization technology, electronic atomization technology has been widely used in the fields of medicine, electronic cigarettes, etc. In the field of medicine, Chinese medicine has become an important factor for patients to be reluctant to take Chinese medicine because of its strong herbal flavor. In addition, traditional medicines are generally swallowed, which makes it extremely difficult for children and the elderly to take them. Electronic atomization liquid is an emerging atomization technology that generates aerosols for human inhalation by heating atomization liquid. If traditional medicines are atomized for patients to take, it will effectively eliminate the resistance of children to taking medicines and the safety hazards caused by the elderly swallowing medicines.

[0003] Compared with traditional cigarettes, electronic cigarettes are loved by cigarette lovers all over the world because they do not contain carcinogens such as tar and have rich flavors. Flavors and flavors are added to the atomizing liquid of electronic cigarettes. The volatility of flavor and flavor molecules is uncontrollable. During use, there is generally a phenomenon of poor durability and durability. As the number of puffs increases, due to sensory fatigue and the reduction of flavor substances in the atomizing liquid, the taste of the atomizing liquid decreases, which greatly affects the consumer's smoking experience. However, there is no effective way in the prior art to solve the problem of taste attenuation of the atomizing liquid caused by the increase in the number of puffs. In addition, different groups of people have different requirements for taste intensity, and the existing atomizing liquid cannot achieve adjustable release of taste intensity, and cannot meet the taste needs of different groups of people. Summary of the invention

[0004] In order to overcome the problems existing in the prior art, one of the objectives of the present invention is to provide an electronic atomization liquid.

[0005] A second object of the present invention is to provide a method for preparing electronic atomization liquid.

[0006] A third object of the present invention is to provide an electronic atomization device.

[0007] A fourth object of the present invention is to provide an application of electronic atomization liquid in the field of electronic atomization.

[0008] In order to achieve the above object, the technical solution adopted by the present invention is:

[0009] The first aspect of the present invention provides an electronic atomization liquid, comprising the following components in weight percentage: 90-99.99% polyol, 0.01-10% magnetic responsive microcapsules; the magnetic responsive microcapsules contain magnetic responsive materials; the magnetic responsive materials include at least one of magnetic responsive metal ions and magnetic responsive metal oxide nanoparticles. The magnetic responsive material in the present invention refers to a material that heats up under the action of a magnetic field.

[0010] On the one hand, the electronic atomization liquid in the present invention can achieve controlled release. There are two ways to release the magnetic responsive microcapsules, specifically: (1) Under the action of a high-frequency (tens to hundreds of MHz) magnetic field, the magnetic responsive material in the magnetic responsive microcapsule generates local heat and destroys the microcapsule structure, thereby achieving controlled release of the microcapsule. (2) Under the action of a low-frequency alternating magnetic field, the magnetic responsive material moves locally under the action of the magnetic field, causing the microcapsule structure to change, thereby achieving controlled release of the microcapsule. On the other hand, the occurrence of taste attenuation caused by an increase in the number of puffs can be avoided. The magnetic responsive microcapsule contains a magnetic responsive material, which enables the microcapsule to slowly release the active ingredient under the action of the magnetic field and be heated and atomized. The amount of the active ingredient (i.e., the core material) in the atomized aerosol is controlled by the magnetic field, so that the amount of the active ingredient in the aerosol remains constant or increases with the extension of the puffing time, thereby avoiding the occurrence of taste attenuation. In addition, different types of electronic atomization liquids with different magnetic properties (for example, different fragrances or different drugs) can be prepared by adjusting the type and content of the magnetically responsive material in the microcapsule, and then these electronic atomization liquids can be mixed. When used, the magnetic field can be adjusted to selectively release specific types of microcapsules according to the needs of different users. For example, orange-flavored electronic atomization liquid and lemon-flavored electronic atomization liquid with different magnetic strengths are mixed and used, and then when the user wants to use the orange-flavored electronic atomization liquid, the orange-flavored electronic atomization liquid is selectively released through magnetic field regulation, thereby achieving the selective release of the core material in the magnetically responsive microcapsule according to the preferences of different users.

[0011] Preferably, the wall material of the magnetically responsive microcapsule comprises a magnetically responsive material.

[0012] Taking the total mass percentage of the magnetic responsive microcapsules as 100%, the mass percentage of the magnetic responsive material is 0.1-5%.

[0013] Preferably, the core material of the magnetically responsive microcapsule includes at least one of a drug, a fragrance base, and a tobacco flavoring agent. The fragrance base contains unstable components such as esters and aldehydes, which are easy to volatilize or oxidize and deteriorate under high temperature conditions, resulting in the disappearance of the fragrance flavor characteristics when the electronic atomization liquid forms an aerosol, and there is a phenomenon of poor persistence and durability, and even unpleasant odors such as "fermentation taste". Therefore, the present invention uses magnetically responsive microcapsules to embed the core materials such as fragrance bases, which can completely solve the problem of fragrance base volatilization, and thus solve the problem of poor persistence and durability of fragrance bases. On the other hand, the use of magnetically responsive microcapsules to embed the core material can also achieve the controlled release of the microcapsules, thereby meeting the taste intensity and taste diversity needs of different consumers.

[0014] Preferably, the medicine includes Chinese medicine or Western medicine. Chinese medicine has a pungent smell, and many patients resist swallowing Chinese medicine. The present invention can encapsulate the medicine by magnetic responsive microcapsules to avoid the pungent smell of Chinese medicine.

[0015] Preferably, the fragrance base includes at least one of essence and essential oil. The essence used in the atomized liquid of the present invention is food grade fragrance essence.

[0016] Preferably, the flavor includes at least one of blueberry flavor, banana flavor, mint flavor, strawberry flavor, and coconut flavor.

[0017] Preferably, the essential oil includes at least one of sweet orange essential oil, lemon essential oil, peppermint essential oil, lavender essential oil and grapefruit essential oil.

[0018] Preferably, the tobacco flavoring agent is selected from at least one of nicotine and nicotine salt.

[0019] Preferably, the wall material of the magnetic responsive microcapsule further comprises polyphenols. Polyphenols are compounds having a phenolic hydroxyl content of not less than 2. Polyphenols react with metals in the magnetic responsive material to form the wall material.

[0020] Preferably, the polyphenol is at least one selected from compounds containing phenolic hydroxyl functional groups.

[0021] Preferably, the polyphenol is selected from at least one of tannic acid, ellagic acid, gallic acid, anthocyanin and dopamine.

[0022] The present invention uses polyphenols with good biocompatibility as one of the wall materials, which not only achieves the adjustable release of the core material, but also the polyphenols themselves have multiple functions such as antioxidant and antibacterial, so that the electronic atomization liquid has certain antioxidant and antibacterial effects, avoiding the oxidation of components in the electronic atomization liquid or the growth of microorganisms in the electronic atomization liquid, and is healthier and safer when used.

[0023] Preferably, the magnetically responsive metal ions include Fe3+ ion.

[0024] Preferably, the magnetically responsive metal oxide nanoparticles include Fe3O4 nanoparticles.

[0025] Fe 3+ Ions and Fe3O4 nanoparticles used as magnetically responsive materials in electronic atomization liquid are highly safe and will not pose a safety hazard to consumers.

[0026] Preferably, the polyol is selected from at least one of glycerol, propylene glycol, triethylene glycol and ethylene glycol.

[0027] Preferably, the polyols are glycerol and propylene glycol, and the mass ratio of glycerol to propylene glycol is 1:(0.1-8).

[0028] Preferably, the magnetic responsive microcapsules include the following raw materials in parts by weight: 0.01 to 0.05 parts of magnetic responsive material, 0.04 to 0.1 parts of polyphenol, 0.01 to 0.1 parts of emulsifier, 89 to 100 parts of solvent, and 0.1 to 10 parts of core material.

[0029] Preferably, the emulsifier is selected from at least one of Tween 80, Span 60, Span 80, triglycerol, propylene glycol fatty acid ester, lauric acid monoglyceride and sodium stearoyl lactylate.

[0030] Preferably, the solvent is selected from water.

[0031] Preferably, the magnetically responsive microcapsules are prepared by a preparation method comprising the following steps:

[0032] S1: homogenizing and emulsifying the emulsifier, the solvent and the core material to prepare an emulsion;

[0033] S2: Mixing the emulsion, the magnetic responsive material and the polyphenol to prepare the magnetic responsive microcapsule.

[0034] Preferably, the method for preparing the magnetic responsive microcapsules further comprises performing step S3 after step S2, and step S3 is: adjusting the pH to 7-9.

[0035] Preferably, the method for preparing the magnetic responsive microcapsules further comprises performing step S4 after step S3, wherein step S4 comprises: washing with water, and then centrifuging at a speed of 2000-10000 rpm to separate the magnetic responsive microcapsules.

[0036] Preferably, the water washing step is performed 2 to 5 times.

[0037] Preferably, the homogenization and emulsification step takes 5 to 40 minutes.

[0038] Preferably, the step S3 specifically comprises: adjusting the pH to 7-9 and standing for 1-5 hours.

[0039] Preferably, the mixing step in step S2 is specifically: mixing with a vortex mixer for 10 to 30 seconds.

[0040] The second aspect of the present invention provides a method for preparing the electronic atomization liquid provided in the first aspect of the present invention, comprising the following steps: mixing polyols and magnetically responsive microcapsules to obtain the electronic atomization liquid.

[0041] The third aspect of the present invention is to provide an electronic atomization device, which includes the electronic atomization liquid provided in the first aspect of the present invention. The electronic atomization liquid is added to the electronic atomization device when it is needed, and the electronic atomization device atomizes the electronic atomization liquid into aerogel for use by consumers.

[0042] The fourth aspect of the present invention provides the use of the electronic atomization liquid provided by the first aspect of the present invention in the field of electronic atomization.

[0043] The beneficial effects of the present invention are as follows: the electronic atomization liquid of the present invention contains magnetic response materials, which can be controllably released under the action of a magnetic field, which not only solves the problem of flavor attenuation of the atomization liquid, but also can achieve adjustable flavor intensity and diversified choices for different consumers, and has better taste matching for consumers, providing a research and development direction for creating a more personalized atomization liquid.

[0044] In addition, the present invention uses metal polyphenol complex products as wall materials to embed the core material used in the electronic atomization liquid, and the core material can be controlled and released through the magnetic field to meet the taste requirements of different consumers. The polyphenol material also has antibacterial and antioxidant effects, which can make the storage of electronic atomization liquid more stable, avoid oxidation of active ingredients or growth of microorganisms during storage, and have higher safety. BRIEF DESCRIPTION OF THE DRAWINGS

[0045] Figure 1 This is a test diagram of the release rate of the magnetic response fragrance atomization liquid in Example 1 under the action of a magnetic field. DETAILED DESCRIPTION

[0046] The specific implementation of the present invention is further described in detail below in conjunction with the accompanying drawings and examples, but the implementation and protection of the present invention are not limited thereto. It should be noted that if there are processes that are not particularly described in detail below, they can be implemented or understood by those skilled in the art with reference to the prior art. The reagents or instruments used that do not indicate the manufacturer are all conventional products that can be purchased commercially.

[0047] Embodiment 1:

[0048] The components of the magnetic response flavor release atomization liquid in this example are: 10 g of glycerol, 80 g of propylene glycol, and 10 g of metal polyphenol microcapsules rich in sweet orange essential oil.

[0049] Among them, the metal polyphenol microcapsules rich in sweet orange essential oil are prepared according to the following preparation method, and the specific steps are:

[0050] (1) 99 g of deionized water, 0.94 g of sweet orange essential oil, and 0.01 g of Tween 80 were emulsified in a homogenizer for 10 min to prepare an emulsion;

[0051] (2) 0.01 g FeCl3·6H2O and 0.04 g tannic acid were added to the above emulsion, and the liquid was vigorously mixed for 10 s using a vortex mixer;

[0052] (3) Adjust the pH to 8 using phosphate buffer solution and let stand for 3 h;

[0053] (4) washing three times to remove excess FeCl3·6H2O and tannic acid;

[0054] (5) Metal polyphenol microcapsules rich in sweet orange essential oil were prepared by centrifugation at 2000 rpm.

[0055] The magnetic response flavor release atomized liquid in this example is prepared by the following preparation method, which comprises the following steps: mixing the formulated amounts of glycerin, propylene glycol, and metal polyphenol microcapsules rich in sweet orange essential oil.

[0056] Embodiment 2:

[0057] The components of the magnetic response fragrance release atomization liquid in this example are: 80g of glycerol, 10g of propylene glycol, and 10g of metal polyphenol microcapsules rich in lemon essential oil.

[0058] Among them, the metal polyphenol microcapsules rich in lemon essential oil are prepared according to the following preparation method, and the specific steps are:

[0059] (1) 89.75 g of deionized water, 10 g of lemon essential oil, and 0.1 g of Span 60 were emulsified in a homogenizer for 10 min to prepare an emulsion;

[0060] (2) 0.05 g FeCl3·6H2O and 0.1 g ellagic acid were added to the above emulsion, and the liquid was vigorously mixed for 10 s using a vortex mixer;

[0061] (3) Adjust the pH to 7.5 with phosphate buffer solution and let stand for 4 h;

[0062] (4) washing three times with water to remove excess FeCl3·6H2O and ellagic acid;

[0063] (5) Metal polyphenol microcapsules rich in lemon essential oil were prepared by centrifugation at 4000 rpm.

[0064] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0065] Embodiment 3:

[0066] The components of the magnetic response flavor release atomization liquid in this example are: 40g of glycerol, 55g of propylene glycol, and 5g of metal polyphenol microcapsules rich in peppermint essential oil.

[0067] Among them, the metal polyphenol microcapsules rich in peppermint essential oil are prepared according to the following preparation method, and the specific steps are:

[0068] (1) 99.79 g of deionized water, 0.1 g of peppermint essential oil, and 0.01 g of Span 80 were emulsified in a homogenizer for 15 min to prepare an emulsion;

[0069] (2) 0.04 g FeCl3·6H2O and 0.06 g gallic acid were added to the above emulsion, and the liquid was vigorously mixed using a vortex mixer for 10 s;

[0070] (3) Adjust the pH to 8.5 with phosphate buffer solution and let stand for 2 h;

[0071] (4) washing three times to remove excess FeCl3·6H2O and gallic acid;

[0072] (5) Metal polyphenol microcapsules rich in peppermint essential oil were prepared by centrifugation at 3000 rpm.

[0073] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0074] Embodiment 4:

[0075] The components of the magnetic response flavor release atomization liquid in this example are: 40g of glycerol, 59g of propylene glycol, and 1g of metal polyphenol microcapsules rich in blueberry flavor.

[0076] The metal polyphenol microcapsules rich in blueberry flavor are prepared according to the following preparation method, and the specific steps are as follows:

[0077] (1) 99.84 g of deionized water, 0.1 g of blueberry flavor, and 0.01 g of triglyceride were emulsified in a homogenizer for 5 min to prepare an emulsion;

[0078] (2) 0.01 g FeCl3·6H2O and 0.04 g anthocyanin were added to the above emulsion, and the liquid was vigorously mixed for 10 s using a vortex mixer;

[0079] (3) Adjust the pH to 7.5 with phosphate buffer solution and let stand for 3 h;

[0080] (4) washing three times to remove excess FeCl3·6H2O and anthocyanins;

[0081] (5) Metal polyphenol microcapsules rich in blueberry flavor were prepared by centrifugation at 6000 rpm.

[0082] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0083] Embodiment 5:

[0084] The components of the magnetic response flavor release atomization liquid in this example are: 40 g of glycerol, 59.5 g of propylene glycol, and 0.5 g of metal polyphenol microcapsules rich in banana flavor.

[0085] Among them, the metal polyphenol microcapsules rich in banana flavor are prepared according to the following preparation method, and the specific steps are:

[0086] (1) 97.82 g of deionized water, 2 g of banana essence, and 0.08 g of propylene glycol fatty acid ester were emulsified in a homogenizer for 15 min to prepare an emulsion;

[0087] (2) 0.02 g FeCl3·6H2O and 0.08 g dopamine were added to the above emulsion, and the liquid was vigorously mixed using a vortex mixer for 15 s;

[0088] (3) Adjust the pH to 7.5 with phosphate buffer solution and let stand for 4 h;

[0089] (4) washing three times with water to remove excess FeCl3·6H2O and dopamine;

[0090] (5) Metal polyphenol microcapsules rich in banana flavor were prepared by centrifugation at 6000 rpm.

[0091] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0092] Embodiment 6:

[0093] The components of the magnetic response fragrance release atomization liquid in this example are: 45g of glycerol, 54.9g of propylene glycol, and 0.1g of metal polyphenol microcapsules rich in lavender essential oil.

[0094] Among them, the metal polyphenol microcapsules rich in lavender essential oil are prepared according to the following preparation method, and the specific steps are:

[0095] (1) 94.85 g of deionized water, 0.5 g of lavender essential oil, and 0.06 g of monolaurin were emulsified in a homogenizer for 10 min to prepare an emulsion;

[0096] (2) 0.03 g FeCl3·6H2O and 0.06 g tannic acid were added to the above emulsion, and the liquid was vigorously mixed for 10 s using a vortex mixer;

[0097] (3) Adjust the pH to 7 with phosphate buffer solution and let stand for 3 h;

[0098] (4) washing three times to remove excess FeCl3·6H2O and tannic acid;

[0099] (5) Metal polyphenol microcapsules rich in lavender essential oil were prepared by centrifugation at 10000 rpm.

[0100] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0101] Embodiment 7:

[0102] The components of the magnetic response fragrance release atomization liquid in this example are: 35g of glycerol, 64.99g of propylene glycol, and 0.01g of metal polyphenol microcapsules rich in grapefruit essential oil.

[0103] The metal polyphenol microcapsules rich in grapefruit essential oil are prepared according to the following preparation method, and the specific steps are as follows:

[0104] (1) 93.89 g of deionized water, 0.6 g of grapefruit essential oil, and 0.04 g of sodium stearoyl lactylate were emulsified in a homogenizer for 10 min to prepare an emulsion;

[0105] (2) 0.02 g FeCl3·6H2O and 0.05 g tannic acid were added to the above emulsion, and the liquid was vigorously mixed for 15 s using a vortex mixer;

[0106] (3) Adjust the pH to 7.5 with phosphate buffer solution and let stand for 3 h;

[0107] (4) washing three times to remove excess FeCl3·6H2O and tannic acid;

[0108] (5) Metal polyphenol microcapsules rich in grapefruit essential oil were prepared by centrifugation at 6000 rpm.

[0109] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0110] Embodiment 8:

[0111] The components of the magnetic response flavor release atomization liquid in this example are: 30g of glycerol, 67g of propylene glycol, and 3g of metal polyphenol microcapsules rich in mint flavor.

[0112] Among them, the metal polyphenol microcapsules rich in mint flavor are prepared according to the following preparation method, and the specific steps are:

[0113] (1) 91.79 g of deionized water, 8 g of mint essence, and 0.1 g of Tween 80 were emulsified in a homogenizer for 10 min to prepare an emulsion;

[0114] (2) 0.04 g FeCl3·6H2O and 0.07 g gallic acid were added to the above emulsion, and the liquid was vigorously mixed using a vortex mixer for 15 s;

[0115] (3) Adjust the pH to 8 using phosphate buffer solution and let stand for 3 h;

[0116] (4) washing three times to remove excess FeCl3·6H2O and gallic acid;

[0117] (5) Metal polyphenol microcapsules rich in mint flavor were prepared by centrifugation at 8000 rpm.

[0118] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0119] Embodiment 9:

[0120] The components of the magnetic response flavor release atomization liquid in this example are: 45g of glycerol, 47g of propylene glycol, and 8g of metal polyphenol microcapsules rich in strawberry flavor.

[0121] Among them, the metal polyphenol microcapsules rich in strawberry flavor are prepared according to the following preparation method, and the specific steps are:

[0122] (1) Take 91.98 g of deionized water, 7 g of strawberry essence, and 0.9 g of Tween 80, and emulsify them in a homogenizer for 10 min to prepare an emulsion;

[0123] (2) 0.05 g FeCl3·6H2O and 0.07 g gallic acid were added to the above emulsion, and the liquid was vigorously mixed using a vortex mixer for 10 s;

[0124] (3) Adjust the pH to 8 using phosphate buffer solution and let stand for 3 h;

[0125] (4) washing three times to remove excess FeCl3·6H2O and gallic acid;

[0126] (5) Metal polyphenol microcapsules rich in strawberry flavor were prepared by centrifugation at 6000 rpm.

[0127] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0128] Embodiment 10:

[0129] The components of the magnetic response flavor release atomization liquid in this example are: 50g glycerin, 48g propylene glycol, and 2g metal polyphenol microcapsules rich in coconut flavor.

[0130] Among them, the metal polyphenol microcapsules rich in coconut flavor are prepared according to the following preparation method, and the specific steps are:

[0131] (1) Take 96.4 g of deionized water, 3 g of coconut essence, and 0.5 g of Tween 80, and emulsify them in a homogenizer for 15 min to prepare an emulsion;

[0132] (2) 0.01 g FeCl3·6H2O and 0.09 g gallic acid were added to the above emulsion, and the liquid was vigorously mixed using a vortex mixer for 10 s;

[0133] (3) Adjust the pH to 8 using phosphate buffer solution and let stand for 3 h;

[0134] (4) washing three times to remove excess FeCl3·6H2O and gallic acid;

[0135] (5) Metal polyphenol microcapsules rich in coconut flavor were prepared by centrifugation at 5000 rpm.

[0136] The magnetically responsive flavor-releasing atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0137] Embodiment 11:

[0138] The components of the magnetic response release of traditional Chinese medicine aerosol liquid in this example are: 50g glycerol, 48g propylene glycol, and 2g magnetic response microcapsules.

[0139] The magnetically responsive microcapsules are prepared according to the following preparation method, the specific steps are:

[0140] (1) 97.11 g of deionized water, 2 g of Momordica grosvenori extract, and 0.8 g of Tween 80 were emulsified in a homogenizer for 15 min to prepare an emulsion;

[0141] (2) 0.03 g FeCl3·6H2O and 0.06 g tannic acid were added to the above emulsion, and the liquid was vigorously mixed for 10 s using a vortex mixer;

[0142] (3) Adjust the pH to 8 using phosphate buffer solution and let stand for 3 h;

[0143] (4) washing three times to remove excess FeCl3·6H2O and tannic acid;

[0144] (5) Magnetic responsive microcapsules were prepared by centrifugation at 5000 rpm.

[0145] The magnetic response release Chinese medicine atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0146] Embodiment 12:

[0147] The components of the magnetic response release of traditional Chinese medicine aerosol liquid in this example are: 50g glycerol, 48g propylene glycol, and 2g magnetic response microcapsules.

[0148] The magnetically responsive microcapsules are prepared according to the following preparation method, the specific steps are:

[0149] (1) 97.8 g of deionized water, 1.5 g of a Chinese medicine honeysuckle extract, and 0.5 g of Tween 80 were emulsified in a homogenizer for 15 min to prepare an emulsion;

[0150] (2) 0.1 g of FeCl3·6H2O and 0.1 g of tannic acid were added to the above emulsion, and the liquid was vigorously mixed for 10 s using a vortex mixer;

[0151] (3) Adjust the pH to 8 using phosphate buffer solution and let stand for 3 h;

[0152] (4) washing three times to remove excess FeCl3·6H2O and tannic acid;

[0153] (5) Magnetic responsive microcapsules were prepared by centrifugation at 5000 rpm.

[0154] The magnetic response release Chinese medicine atomized liquid in this example is prepared by the same preparation method as in Example 1.

[0155] Performance Test:

[0156] The release rate of the magnetic response release fragrance atomized liquid in Example 1 under the action of an alternating magnetic field was tested. The specific test method is as follows: the atomized liquid in Example 1 is alternately subjected to a magnetic field and a stirring action, the alternating magnetic field frequency is fixed at 360 kHz, and the stirring rate is 1000 rpm; 0-15 min is the magnetic field action, 15-30 min is the stirring (without the magnetic field action), 30-45 min is the magnetic field action, 45-60 min is the stirring (without the magnetic field action), and 60-75 min is the magnetic field action. The specific test results are shown in FIG. Figure 1 As shown. Figure 1 It can be seen that the atomized liquid in Example 1 breaks the microcapsules under the action of the magnetic field and begins to release the fragrance substances, while the release amount of the microcapsules is still very low even in a high-speed stirring environment without a magnetic field. The atomized liquids in Examples 2 to 12 have the same properties as the atomized liquid in Example 1, that is, the atomized liquid is stable without the action of a magnetic field, the release rate is still very low even in a high-speed stirring environment, and the release is controllable under the action of a magnetic field.

[0157] The above is a detailed description of the embodiments of the present invention, but the present invention is not limited to the above embodiments. Various changes can be made within the knowledge of ordinary technicians in the relevant technical field without departing from the purpose of the present invention. In addition, the embodiments of the present invention and the features in the embodiments can be combined with each other without conflict.

Claims

1. An electronic atomization liquid, characterized in that: The invention comprises the following components in weight percentage: 90-99.99% of polyol and 0.01-10% of magnetic response microcapsules; the magnetic response microcapsules contain magnetic response materials; the magnetic response materials comprise at least one of magnetic response metal ions and magnetic response metal oxide nanoparticles.

2. The electronic atomization liquid according to claim 1, characterized in that: The wall material of the magnetically responsive microcapsule includes a magnetically responsive material; the core material of the magnetically responsive microcapsule includes at least one of a drug, a fragrance base, and a tobacco flavoring agent; preferably, the magnetically responsive metal ion is Fe 3+ ions; and / or, the magnetically responsive metal oxide nanoparticles include Fe3O4 nanoparticles.

3. The electronic atomization liquid according to claim 2, characterized in that: The wall material of the magnetically responsive microcapsule also includes polyphenols; preferably, the polyphenols are selected from at least one of compounds containing phenolic hydroxyl functional groups; preferably, the polyphenols are selected from at least one of tannic acid, ellagic acid, gallic acid, anthocyanin, and dopamine.

4. The electronic atomization liquid according to claim 1, characterized in that: Taking the total mass percentage of the magnetic responsive microcapsules as 100%, the mass percentage of the magnetic responsive material is 0.1-5%.

5. The electronic atomization liquid according to claim 1, characterized in that: The polyol is selected from at least one of glycerol, propylene glycol, triethylene glycol and ethylene glycol; preferably, the polyol is glycerol and propylene glycol, and the mass ratio of glycerol to propylene glycol is 1:(0.1-8).

6. The electronic atomization liquid according to claim 1, characterized in that: The magnetic responsive microcapsule comprises the following raw materials in parts by weight: 0.01 to 0.05 parts of magnetic responsive material, 0.04 to 0.1 parts of polyphenol, 0.01 to 0.1 parts of emulsifier, 89 to 100 parts of solvent and 0.1 to 10 parts of core material.

7. The electronic atomization liquid according to claim 6, characterized in that: The magnetic responsive microcapsules are prepared by a preparation method comprising the following steps: S1: homogenizing and emulsifying the emulsifier, the solvent and the core material to prepare an emulsion; S2: Mixing the emulsion, the magnetic responsive material and the polyphenol to prepare the magnetic responsive microcapsule.

8. The method for preparing the electronic atomization liquid according to any one of claims 1 to 7, characterized in that: The following steps are involved: The polyol and the magnetic responsive microcapsules are mixed to prepare the electronic atomization liquid.

9. An electronic atomization device, characterized in that: Including the electronic atomization liquid as described in any one of claims 1 to 7.

10. Use of the electronic atomization liquid according to any one of claims 1 to 7 in the field of electronic atomization.