CN113633014A - Coffee-flavored refreshing electronic atomized liquid and preparation method thereof - Google Patents
Coffee-flavored refreshing electronic atomized liquid and preparation method thereof Download PDFInfo
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- CN113633014A CN113633014A CN202110893259.3A CN202110893259A CN113633014A CN 113633014 A CN113633014 A CN 113633014A CN 202110893259 A CN202110893259 A CN 202110893259A CN 113633014 A CN113633014 A CN 113633014A
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- 239000007788 liquid Substances 0.000 title claims abstract description 83
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- 239000000284 extract Substances 0.000 claims abstract description 69
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 36
- 235000003599 food sweetener Nutrition 0.000 claims abstract description 30
- 239000003765 sweetening agent Substances 0.000 claims abstract description 30
- 239000003094 microcapsule Substances 0.000 claims abstract description 28
- 238000002156 mixing Methods 0.000 claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 238000000889 atomisation Methods 0.000 claims abstract description 25
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000001816 cooling Methods 0.000 claims abstract description 13
- 239000002994 raw material Substances 0.000 claims abstract description 13
- 239000011259 mixed solution Substances 0.000 claims abstract description 12
- 229960004063 propylene glycol Drugs 0.000 claims abstract description 12
- 238000010438 heat treatment Methods 0.000 claims abstract description 8
- 238000003756 stirring Methods 0.000 claims abstract description 8
- 239000000463 material Substances 0.000 claims description 31
- 239000011162 core material Substances 0.000 claims description 24
- 239000000839 emulsion Substances 0.000 claims description 20
- 239000005913 Maltodextrin Substances 0.000 claims description 18
- 229920002774 Maltodextrin Polymers 0.000 claims description 18
- 229940035034 maltodextrin Drugs 0.000 claims description 18
- 235000019198 oils Nutrition 0.000 claims description 18
- 235000020238 sunflower seed Nutrition 0.000 claims description 17
- 108010073771 Soybean Proteins Proteins 0.000 claims description 15
- 235000019710 soybean protein Nutrition 0.000 claims description 15
- 241000999530 Anisodus Species 0.000 claims description 12
- 244000037364 Cinnamomum aromaticum Species 0.000 claims description 11
- 235000014489 Cinnamomum aromaticum Nutrition 0.000 claims description 11
- 241000241413 Propolis Species 0.000 claims description 11
- 229940069949 propolis Drugs 0.000 claims description 11
- 239000008373 coffee flavor Substances 0.000 claims description 9
- 238000001694 spray drying Methods 0.000 claims description 6
- OEUVSBXAMBLPES-UHFFFAOYSA-L calcium stearoyl-2-lactylate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O.CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O OEUVSBXAMBLPES-UHFFFAOYSA-L 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 210000000582 semen Anatomy 0.000 claims description 5
- 239000003995 emulsifying agent Substances 0.000 claims description 4
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims description 3
- 229940080352 sodium stearoyl lactylate Drugs 0.000 claims description 3
- 235000010957 calcium stearoyl-2-lactylate Nutrition 0.000 claims description 2
- 150000003904 phospholipids Chemical class 0.000 claims description 2
- 229940071440 soy protein isolate Drugs 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 12
- 239000003571 electronic cigarette Substances 0.000 abstract description 12
- 201000007100 Pharyngitis Diseases 0.000 abstract description 5
- 206010068319 Oropharyngeal pain Diseases 0.000 abstract description 3
- 230000000052 comparative effect Effects 0.000 description 16
- 239000003921 oil Substances 0.000 description 15
- 230000001953 sensory effect Effects 0.000 description 12
- 208000024891 symptom Diseases 0.000 description 8
- 244000062730 Melissa officinalis Species 0.000 description 7
- 235000012907 honey Nutrition 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 6
- 229940109850 royal jelly Drugs 0.000 description 6
- 241000208125 Nicotiana Species 0.000 description 5
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 5
- 206010011224 Cough Diseases 0.000 description 4
- NYRXUBDGDSRBGB-UHFFFAOYSA-N Obtusifolin Chemical compound O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(C)C(O)=C2OC NYRXUBDGDSRBGB-UHFFFAOYSA-N 0.000 description 4
- LQGUBLBATBMXHT-UHFFFAOYSA-N chrysophanol Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC(O)=C3C(=O)C2=C1O LQGUBLBATBMXHT-UHFFFAOYSA-N 0.000 description 4
- 230000007794 irritation Effects 0.000 description 4
- 210000004185 liver Anatomy 0.000 description 4
- 230000005586 smoking cessation Effects 0.000 description 4
- 230000000391 smoking effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 3
- 239000000739 antihistaminic agent Substances 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000007762 w/o emulsion Substances 0.000 description 3
- 206010050639 Allergic pharyngitis Diseases 0.000 description 2
- 244000201986 Cassia tora Species 0.000 description 2
- 235000014552 Cassia tora Nutrition 0.000 description 2
- VWDXGKUTGQJJHJ-UHFFFAOYSA-N Catenarin Natural products C1=C(O)C=C2C(=O)C3=C(O)C(C)=CC(O)=C3C(=O)C2=C1O VWDXGKUTGQJJHJ-UHFFFAOYSA-N 0.000 description 2
- 239000010282 Emodin Substances 0.000 description 2
- RBLJKYCRSCQLRP-UHFFFAOYSA-N Emodin-dianthron Natural products O=C1C2=CC(C)=CC(O)=C2C(=O)C2=C1CC(=O)C=C2O RBLJKYCRSCQLRP-UHFFFAOYSA-N 0.000 description 2
- YOOXNSPYGCZLAX-UHFFFAOYSA-N Helminthosporin Natural products C1=CC(O)=C2C(=O)C3=CC(C)=CC(O)=C3C(=O)C2=C1O YOOXNSPYGCZLAX-UHFFFAOYSA-N 0.000 description 2
- 208000031226 Hyperlipidaemia Diseases 0.000 description 2
- ZCHGCYXNSBHAEG-UHFFFAOYSA-N Obtusifolin Natural products COc1ccc2C=C(C(=O)Oc2c1C=CC(=C)C)C(C)(C)C=C ZCHGCYXNSBHAEG-UHFFFAOYSA-N 0.000 description 2
- NTGIIKCGBNGQAR-UHFFFAOYSA-N Rheoemodin Natural products C1=C(O)C=C2C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C1O NTGIIKCGBNGQAR-UHFFFAOYSA-N 0.000 description 2
- NZPQWZZXRKZCDU-UHFFFAOYSA-N chrysophanol Natural products Cc1cc(O)c2C(=O)c3c(O)cccc3Oc2c1 NZPQWZZXRKZCDU-UHFFFAOYSA-N 0.000 description 2
- RHMXXJGYXNZAPX-UHFFFAOYSA-N emodin Chemical compound C1=C(O)C=C2C(=O)C3=CC(C)=CC(O)=C3C(=O)C2=C1O RHMXXJGYXNZAPX-UHFFFAOYSA-N 0.000 description 2
- VASFLQKDXBAWEL-UHFFFAOYSA-N emodin Natural products OC1=C(OC2=C(C=CC(=C2C1=O)O)O)C1=CC=C(C=C1)O VASFLQKDXBAWEL-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 2
- 230000004377 improving vision Effects 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- PKUBGLYEOAJPEG-UHFFFAOYSA-N physcion Natural products C1=C(C)C=C2C(=O)C3=CC(C)=CC(O)=C3C(=O)C2=C1O PKUBGLYEOAJPEG-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000208128 Nicotiana glauca Species 0.000 description 1
- 241000533293 Sesbania emerus Species 0.000 description 1
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 244000290333 Vanilla fragrans Species 0.000 description 1
- 235000009499 Vanilla fragrans Nutrition 0.000 description 1
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000001387 anti-histamine Effects 0.000 description 1
- 229940124623 antihistamine drug Drugs 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 229940069765 bean extract Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000012496 blank sample Substances 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 210000001508 eye Anatomy 0.000 description 1
- 210000000232 gallbladder Anatomy 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 229940074968 melissa officinalis extract Drugs 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 208000035824 paresthesia Diseases 0.000 description 1
- 238000013441 quality evaluation Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/10—Chemical features of tobacco products or tobacco substitutes
- A24B15/16—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes
- A24B15/167—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes in liquid or vaporisable form, e.g. liquid compositions for electronic cigarettes
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/302—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by natural substances obtained from animals or plants
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Botany (AREA)
- Tea And Coffee (AREA)
Abstract
The application relates to the technical field of electronic cigarettes, and particularly discloses coffee-flavored refreshing electronic atomized liquid and a preparation method thereof. The electronic atomization liquid is prepared from the following raw materials in parts by weight: 40-60 parts of 1, 2-propylene glycol, 10-30 parts of glycerol, 5-10 parts of coffee extract, 10-20 parts of radix Anisodi Acutanguli extract, 5-10 parts of microcapsule sweetener and 2-20 parts of water. The preparation method comprises the following steps: mixing glycerol, 1, 2-propylene glycol and water at 50-60 deg.C to obtain primary mixed solution; adding coffee extract and radix Anisodi Acutanguli extract into the primary mixed solution, mixing at 50-60 deg.C, stopping heating, adding microcapsule sweetener under stirring, and cooling to room temperature. The electronic cigarette atomized liquid has the effects of refreshing, restoring consciousness, preventing and relieving sore throat.
Description
Technical Field
The application relates to the technical field of electronic cigarettes, in particular to coffee-flavored refreshing electronic atomized liquid and a preparation method thereof.
Background
The electronic cigarette mainly comprises a battery, an atomizer and electronic cigarette liquid (also called electronic atomization liquid). The principle is that the battery supplies power to the atomizer to atomize the tobacco juice, the tobacco juice is converted into mist, and a user inhales the mist to obtain real smoking feeling.
The electronic atomization liquid is heated by the electronic cigarette atomizer, can generate fog like a cigarette and is a core part of the electronic cigarette. The taste and quality of the electronic atomization liquid directly determine the acceptance and experience of consumers on the mouthfeel of the electronic cigarette.
In the prior art, most smokers can cause or aggravate foreign body feeling and uncomfortable feeling of throat after smoking for a long time; since continuous smoking can further cause or aggravate pharyngolaryngitis and other diseases for a long time, a smoking cessation substitute is needed to be provided, which can help smokers to enhance the prevention and relief effect of electronic atomized liquid on throat discomfort on the basis of ensuring refreshment.
Disclosure of Invention
In order to enhance the prevention and alleviation effects of electronic atomized liquid on throat discomfort on the basis of ensuring refreshing, the application provides coffee-flavored refreshing electronic atomized liquid and a preparation method thereof.
In a first aspect, the application provides a coffee-flavored refreshing electronic atomized liquid, which adopts the following technical scheme:
the coffee-flavored refreshing electronic atomized liquid is prepared from the following raw materials in parts by weight:
the microencapsulated sweetener is added in the form of microcapsules; wherein the core material is one or more of Mel, propolis, Lac Regis Apis and herba Melissae axillaris extract; the wall material comprises soybean protein isolate, maltodextrin and sunflower seed oil; the weight ratio of the core material to the wall material is 1 (5-10).
By adopting the technical scheme, the throat hitting feeling and the smoke quantity of the electronic cigarette atomized liquid in the using process can be improved by adding the 1, 2-propylene glycol and the glycerol, the acutangular anisodus root extract is a main component derived from wild tobacco leaves, the similarity of the electronic cigarette atomized liquid and tobacco can be improved after the acutangular anisodus root extract is added, and the acutangular anisodus root extract is different from the tobacco and also has the effects of eliminating swelling and toxin, relieving pain, promoting the circulation of qi and the like, and the throat discomfort such as pharyngitis, foreign body feeling in throat, sore throat and the like can be effectively prevented or relieved on the basis of refreshing by combining the added coffee extract and the microcapsule sweetening agent.
Preferably, the weight ratio of the soybean protein isolate, the maltodextrin and the sunflower seed oil is (6-8): (6-9).
Preferably, the maltodextrin has a DE value of 15 to 22.
Preferably, the method for preparing the microcapsule sweetener comprises the following steps:
mixing Mel, propolis, Lac Regis Apis and herba Melissae axillaris extract to obtain core material;
dissolving soybean protein isolate in water, keeping the temperature in a water bath at 40-50 ℃ for 20-30min, cooling to room temperature, and adding maltodextrin to obtain an outer wall material;
dispersing the sunflower seed oil and the emulsifier at high speed for 10-15min to obtain an emulsion of an inner wall material;
mixing the emulsions of the core material, the outer wall material and the inner wall material, dispersing at high speed in a water bath at 40-50 ℃ for 20-30min, and homogenizing under 40-50Mpa for 2-3 times to obtain a mixed emulsion;
and carrying out high-speed centrifugal spray drying on the mixed emulsion at the temperature of 180-200 ℃ to obtain the microcapsule sweetener.
Preferably, the emulsifier is selected from one of soft phospholipid, distilled monoglyceride, sodium stearoyl lactylate and calcium stearoyl lactylate.
By adopting the technical scheme, when the soybean protein isolate and the maltodextrin are matched for use, a compact and complete honeycomb structure can be formed under the action of hydrogen bonds, the sunflower seed oil serving as the nonpolar vegetable oil can be filled in the honeycomb structure to form a wall material of the microcapsule together, and meanwhile, the sunflower seed oil can be used as an oil phase in a water-in-oil (W/O) emulsion and can effectively coat honey, propolis, royal jelly and a melissa extract in a core material to form the water-in-oil emulsion, and at the moment, the water-in-oil emulsion can protect the core material from being oxidized by air and can provide a basic condition for subsequent centrifugal spray drying. The microencapsulated sweetener thus produced is effective in prolonging the shelf life of the active ingredient contained in the core material contained therein.
Preferably, the electronic atomization liquid is prepared from the following raw materials in parts by weight:
by adopting the technical scheme, the effects of refreshing the mind and restoring consciousness, and preventing and relieving the sore throat of the electronic atomized liquid can be effectively improved by optimizing the proportion of the components.
Preferably, the electronic atomization liquid also comprises 3-5 parts of cassia seed extract.
By adopting the technical scheme, the cassia seed extract can generate coffee-like aroma after being added and heated, so that the coffee aroma of the electronic atomized liquid is greatly improved together with the coffee extract, and the flavor is better; and the cassia seed extract is rich in emodin, chrysophanol, cassia tora essence, obtusifolin and other active ingredients, can prevent and reduce hyperlipidemia, has the effects of clearing liver and helping detoxification, and can effectively relieve the problems of liver and gallbladder and eyes of old smokers caused by bad habits such as smoking.
In a second aspect, the application provides a preparation method of coffee-flavor refreshing electronic atomized liquid, which adopts the following technical scheme:
a preparation method of coffee-flavor refreshing electronic atomized liquid comprises the following steps:
1) uniformly mixing glycerol, 1, 2-propylene glycol and water according to parts by weight at 50-60 ℃ to obtain a primary mixed solution;
2) adding the coffee extract and the acutangular anisodus root extract into the primary mixed liquid according to the weight parts, uniformly mixing at 50-60 ℃, stopping heating, adding the microcapsule sweetening agent while stirring, and cooling to room temperature to obtain the coffee-flavored refreshing electronic atomized liquid.
Through adopting above-mentioned technical scheme, according to specific charging sequence for the reaction between various raw materials is more abundant, combine inseparabler, is difficult for separating after combining between each raw materials, makes the nature of atomized liquid more stable, when promoting coffee flavor, makes the save time of atomized liquid especially sweetener longer, thereby lets the effect of refreshing of electron atomized liquid and alleviating the uncomfortable sense of throat better.
Preferably, the preparation method of the coffee flavor refreshing type electronic atomized liquid comprises the following steps:
1) uniformly mixing glycerol, 1, 2-propylene glycol and water according to parts by weight at 50-60 ℃ to obtain a primary mixed solution;
2) adding coffee extract, semen Cassiae extract and radix Anisodi Acutanguli extract into the primary mixed solution according to weight parts, mixing at 50-60 deg.C, stopping heating, adding microcapsule sweetener under stirring, and cooling to room temperature to obtain coffee refreshing electronic atomized liquid.
By adopting the technical scheme, the cassia seed extract can generate coffee-like aroma after being added and heated, and the coffee aroma of the electronic atomized liquid is improved together with the coffee extract; and the cassia seed extract is also rich in a large amount of active ingredients such as emodin, chrysophanol, cassia tora essence, obtusifolin and the like, and has the effects of clearing liver and improving vision while preventing and reducing hyperlipidemia.
The coffee-flavor refreshing electronic atomized liquid can be used for preparing an electronic atomization device containing the electronic atomized liquid.
In summary, the present application has the following beneficial effects:
1. the electronic cigarette atomized liquid has the effects of refreshing, preventing and relieving throat discomfort.
2. According to the application, the cassia seed extract is added and heated to generate coffee-like aroma, so that the coffee aroma of the electronic atomized liquid is greatly improved together with the coffee extract; meanwhile, the tea also has the effects of clearing liver and improving vision.
3. The preparation method is simple to operate, the reaction between various raw materials is more sufficient and the combination is tighter, the raw materials are not easy to separate after being combined, the property of the atomized liquid is more stable, and the storage time of the atomized liquid, particularly the sweetener, is longer while the flavor of coffee is improved.
Detailed Description
The present application will be described in further detail with reference to examples.
The raw materials used in the examples of the present application are all commercially available products, except for the following specific descriptions.
The radix Anisodi Acutanguli extract is selected from radix Anisodi Acutanguli extract (specification 10:1, pharmaceutical grade) of Ningxia vanilla biotech GmbH with product number of xcsw 20210507.
The Lac Regis Apis is selected from Lac Regis Apis (purity of 99%, CAS number of 8031-67-2) produced by Zhengzhou Akmm chemical industry Co.
The Mel is selected from Mel (purity of 99%, CAS number of 8028-66-8) produced by Zhengzhou Akmm chemical Co.
The propolis is selected from propolis (purity of 98%, specification: 0.5g, CAS number of 9009-62-5) produced by Shanghai Mingsheng Biochemical reagent Co., Ltd.
The herba Melissae axillaris extract is selected from herba Melissae axillaris extract (also called herba Melissae axillaris powder with specification of 10:1, purity of 10%, and light yellow powder appearance) produced by Sienna Tianrui biotechnology limited.
The coffee extract is coffee bean extract (with a size of 10:1, brown yellow) produced by Xian Jinkungfang plant technology development Co.
The semen Cassiae extract is selected from semen Cassiae extract (specification of 10:1, pharmaceutical grade) produced by science and technology development limited in Taoism Synthctionss.
Preparation example
Preparation example 1: a microencapsulated sweetener in the form of microcapsules; wherein the core material is honey, propolis, royal jelly and melissa extract, and the weight ratio of the honey, the propolis, the royal jelly and the melissa extract is 1:0.5:0.5: 1; the wall material comprises soybean protein isolate, maltodextrin and sunflower seed oil, and the weight ratio of the soybean protein isolate to the maltodextrin to the sunflower seed oil is 5:6: 6; the weight ratio of the core material to the wall material is 1: 5.
The manufacturing method comprises the following steps:
1) mixing 1kg of Mel, 1kg of propolis, 1kg of Lac Regis Apis and 1kg of Melissa officinalis extract to obtain core material;
2) dissolving 6kg of soybean protein isolate in water, keeping the temperature in a water bath at 40 ℃ for 30min, cooling to room temperature, and adding 7.2kg of maltodextrin (DE 15) to obtain an outer wall material;
3) dispersing 7.2kg sunflower seed oil and 0.141kg lecithin in a T18 high-speed disperser at high speed for 10min to obtain emulsion of inner wall material;
4) mixing the emulsions of the core material, the outer wall material and the inner wall material, preserving in a water bath at a constant temperature of 40 ℃ for 30min, then dispersing in a high-speed disperser T18 for 30min at a high speed, and then homogenizing in an FSH-2 high-pressure homogenizer under 40Mpa for 2 times to obtain a mixed emulsion;
5) and (3) carrying out high-speed centrifugal spray drying on the mixed emulsion in a QZ-5 high-speed centrifugal spray dryer at 180 ℃ for 3min to obtain the microcapsule sweetener.
Preparation example 2: a microencapsulated sweetener in the form of microcapsules; wherein the core material is honey, propolis, royal jelly and melissa extract, and the weight ratio of honey to melissa extract is 1: 0.5; the wall material comprises soybean protein isolate, maltodextrin and sunflower seed oil, and the weight ratio of the soybean protein isolate to the maltodextrin to the sunflower seed oil is 2:3: 3; the weight ratio of the core material to the wall material is 1: 6.
The manufacturing method comprises the following steps:
1) mixing 1kg Mel and 0.5kg herba Melissae axillaris extract to obtain core material;
2) dissolving 2.25kg of soybean protein isolate in water, keeping the temperature in a water bath at 45 ℃ for 25min, cooling to room temperature, and adding 3.375kg of maltodextrin (DE 20) to obtain an outer wall material;
3) dispersing 3.375kg sunflower seed oil and 0.07kg distilled monoglyceride in a T18 high-speed disperser at high speed for 15min to obtain emulsion of inner wall material;
4) mixing the emulsions of the core material, the outer wall material and the inner wall material, preserving in a water bath at 45 ℃ for 25min at constant temperature, dispersing in a T18 high-speed disperser for 20min at high speed, and homogenizing in an FSH-2 high-pressure homogenizer at 40Mpa for 2 times to obtain a mixed emulsion;
5) and (3) carrying out high-speed centrifugal spray drying on the mixed emulsion in a QZ-5 high-speed centrifugal spray dryer for 2min at 190 ℃ to obtain the microcapsule sweetener.
Preparation example 3: a microencapsulated sweetener in the form of microcapsules; wherein the core material is honey, royal jelly and melissa extract, and the weight ratio of the honey, the royal jelly and the melissa extract is 1:0.5: 0.5; the wall material comprises soybean protein isolate, maltodextrin and sunflower seed oil, and the weight ratio of the soybean protein isolate to the maltodextrin to the sunflower seed oil is 8:9: 9; the weight ratio of the core material to the wall material is 1: 10.
The manufacturing method comprises the following steps:
1) mixing 1kg Mel, 0.5kg Lac Regis Apis and 0.5kg herba Melissae axillaris extract to obtain core material;
2) dissolving 10.4kg of soybean protein isolate in water, keeping the temperature in a water bath at 50 ℃ for 20min, cooling to room temperature, and adding 11.7kg of maltodextrin (DE 22) to obtain an outer wall material;
3) dispersing 11.7kg of sunflower seed oil and 0.234kg of sodium stearoyl lactylate in a T18 high-speed disperser at high speed for 15min to obtain emulsion of an inner wall material;
4) mixing the emulsions of the core material, the outer wall material and the inner wall material, preserving in a water bath at 50 ℃ for 20min at constant temperature, dispersing in a T18 high-speed disperser for 20min at high speed, and homogenizing in an FSH-2 high-pressure homogenizer under 50Mpa for 3 times to obtain a mixed emulsion;
5) and (3) carrying out high-speed centrifugal spray drying on the mixed emulsion in a QZ-5 high-speed centrifugal spray dryer for 1min at 200 ℃ to obtain the microcapsule sweetener.
Examples
Example 1: the proportion and the dosage of the raw materials of the coffee refreshing electronic atomized liquid are detailed in table 1.
The preparation method comprises the following steps
1) Uniformly mixing glycerol, 1, 2-propylene glycol and water according to parts by weight at 50 ℃ to obtain a primary mixed solution;
2) adding coffee extract and radix Anisodi Acutanguli extract in parts by weight into the primary mixed solution, mixing at 50 deg.C, stopping heating, adding the microcapsule sweetener of preparation example 2 under stirring, and cooling to room temperature (25 deg.C) to obtain coffee refreshing electronic atomized liquid.
Example 2: the proportion and the dosage of the raw materials of the coffee refreshing electronic atomized liquid are detailed in table 1.
The preparation method comprises the following steps
1) Uniformly mixing glycerol, 1, 2-propylene glycol and water according to parts by weight at 60 ℃ to obtain a primary mixed solution;
2) adding the coffee extract and the acutangular anisodus root extract in parts by weight into the primary mixed liquid, uniformly mixing at 60 ℃, stopping heating, adding the microcapsule sweetener of the preparation example 1 while stirring, and cooling to room temperature to obtain the coffee-flavored refreshing electronic atomized liquid.
Examples 3 to 7: a coffee flavor refreshing type electronic atomization liquid is different from the coffee flavor refreshing type electronic atomization liquid in the embodiment 1: the electronic atomization liquid has different proportions and dosages of the raw materials, and the details are shown in table 1.
TABLE 1 coffee-flavored refreshing type electronic atomization liquids of examples 1 to 7 with respect to the composition and amount (kg)
Example 8: a coffee-flavored refreshing electronic atomized liquid, which is different from the coffee-flavored refreshing electronic atomized liquid in example 7 in that: the electronic atomization liquid also comprises 3kg of cassia seed extract.
A preparation method of the electronic atomized liquid thereof,
the method comprises the following steps:
1) uniformly mixing glycerol, 1, 2-propylene glycol and water according to parts by weight at 55 ℃ to obtain a primary mixed solution;
2) adding the coffee extract, the cassia seed extract and the acutangular anisodus root extract into the primary mixed liquid according to the weight parts, uniformly mixing at 55 ℃, stopping heating, adding the microcapsule sweetening agent prepared in the preparation example 2 while stirring, and cooling to room temperature to obtain the coffee-flavored refreshing electronic atomized liquid.
Example 9: a coffee-flavored refreshing electronic atomized liquid, which is different from the coffee-flavored refreshing electronic atomized liquid in embodiment 8 in that: the electronic atomization liquid also comprises 5kg of cassia seed extract.
Comparative example
Comparative example 1: an electronic atomization liquid which is different from that in example 7 in that: the electronic atomization liquid does not contain coffee extract.
Comparative example 2: an electronic atomization liquid which is different from that in example 7 in that: the electronic atomized liquid does not contain a microcapsule sweetening agent.
Comparative example 3: an electronic atomization liquid which is different from that in example 7 in that: the electronic atomization liquid does not contain the acutangular anisodus root extract.
Performance detection analysis
Test one:
test subjects: coffee refreshing type electronic atomized liquids prepared in examples 1 to 9 were used as sample samples 1 to 9; the electronic atomization liquids prepared in comparative examples 1 to 3 were used as control samples 1 to 3.
The test method comprises the following steps:
1. sensory evaluation of flavor: the products of examples 1-9 and comparative examples 1-3 were placed in a low temperature atomized electronic device (atomization temperature at 195-: sensory technical requirements the products of examples 1-9 and comparative examples 1-3 were subjected to sensory evaluation, 10 sensory evaluators were selected, and the sensory evaluators were qualified as tobacco sensory evaluators. Wherein, the sensory quality evaluation criteria in GB5606.4-2005 are shown in Table 2.
2. Characteristic sensory evaluation: the products of examples 1 to 9 and comparative examples 1 to 3 were placed in a low-temperature atomized electronic appliance, and sensory evaluation was performed on the throat discomfort and aroma of the products of examples 1 to 9 and comparative examples 1 to 3, 10 sensory evaluators were selected, and the criteria for sensory evaluation are shown in table 2.
TABLE 2 judgment standards
TABLE 3
As can be seen by combining examples 1-9, comparative examples 1-3 and commercially available products 1-2 and tables 2-3, sensory evaluations such as fragrance, irritation, offensive odor and throat discomfort of examples 1-9 are superior to those of comparative examples 1-3 and commercially available products 1-2, and thus it can be seen that the electronic atomized liquids prepared in examples 1-9 have the characteristics of full and fine fragrance, slight irritation, slight offensive odor and slight throat discomfort.
As can be seen by combining examples 7-9 and comparative examples 1-3 with tables 2-3, the coffee extract, the micro-capsule sweetener, the semen cassiae extract and the acutangular anisodus extract can be used together to effectively improve the irritation, miscellaneous gas and throat discomfort of the electronic atomized liquid; in examples 8-9, the coffee aroma is stronger and more prominent due to the addition of the cassia seed extract; meanwhile, the weight of the coffee extract, the acutangular anisodus extract and the microcapsule sweetener is (0.75-1.25): (1.5-2.5): 1, the irritation, the throat discomfort and the amount of mixed smoke are effectively reduced.
And (2) test II:
test subjects: coffee refreshing type electronic atomized liquids prepared in examples 1 to 9 were used as sample samples 1 to 9; the electronic atomization liquids prepared in comparative examples 1 to 3 were used as control samples 1 to 3.
The test method comprises the following steps: 42 old smokers suffering from chronic pharyngitis are searched in the laryngological department of a hospital, and are randomly divided into 3 groups on the basis of 14 days of continuous oral administration of an antihistamine drug, the electronic atomization liquid of examples 1-9 and comparative examples 1-3 is respectively used for assisting smoking cessation, atomization is carried out for 20min every day, and the use amount of each group of samples is 1ml and is divided into 3-4 times. The patients were scored for overall symptoms, cough symptoms and pharyngeal paresthesia at outpatient visits 7 and 14 days post-treatment, with the average score being shown in table 5.
TABLE 4
TABLE 5
As can be seen by combining examples 1-9, comparative examples 1-3 and commercially available products 1-2 with tables 4-5, all patients with allergic pharyngitis of examples 1-9, comparative examples 1-3 and commercially available products 1-2 had significant relief from symptoms after 2 weeks of treatment, and the effect was analyzed after oral administration of antihistamines. Also, the symptoms of the old smoker patients of examples 1-9 were more rapidly controlled, and especially the cough symptoms of the old smoker patients of examples 6-9 were significantly relieved after 1 week of treatment.
The comparison of efficacy between groups also suggests that the adjuvant use of the patients of examples 1-9 more effectively controlled cough and overall pharyngeal symptoms in the patients at 1 week of treatment, and that the improvement in overall pharyngeal symptoms after 2 weeks of treatment is also significantly better than the treatment of the blank samples 1-2.
Conclusion on the basis of antihistamine medication, the electronic cigarette atomized liquids of examples 1 to 9 as smoking cessation products can not only assist smoking cessation, but also have the effect of relieving cough and pharyngeal symptoms of patients with allergic pharyngitis to some extent.
The specific embodiments are merely illustrative of the present application and are not restrictive of the present application, and those skilled in the art can make modifications of the embodiments as required without any inventive contribution thereto after reading the present specification, but only protected by the patent laws within the scope of the claims of the present application.
Claims (9)
1. The coffee-flavor refreshing electronic atomized liquid is characterized by being prepared from the following raw materials in parts by weight:
40-60 parts of 1, 2-propylene glycol;
10-30 parts of glycerol;
5-10 parts of coffee extract;
10-20 parts of acutangular anisodus root extract;
5-10 parts of a microcapsule sweetening agent;
2-20 parts of water;
the microencapsulated sweetener is added in the form of microcapsules; wherein the core material is one or more of Mel, propolis, Lac Regis Apis and herba Melissae axillaris extract; the wall material comprises soybean protein isolate, maltodextrin and sunflower seed oil; the weight ratio of the core material to the wall material is 1 (5-10).
2. The coffee flavor-refreshing type electronic atomized liquid as claimed in claim 1, wherein the weight ratio of the soy protein isolate, the maltodextrin and the sunflower seed oil is (6-8): (6-9).
3. The coffee flavor-refreshing type electronic atomization liquid as claimed in claim 2, wherein the DE value of the maltodextrin is 15-22.
4. The coffee flavor-refreshing electronic atomized liquid as claimed in claim 3, wherein the preparation method of the microcapsule sweetener comprises the following steps:
the method comprises the following steps:
mixing Mel, propolis, Lac Regis Apis and herba Melissae axillaris extract to obtain core material;
dissolving soybean protein isolate in water, keeping the temperature in a water bath at 40-50 ℃ for 20-30min, cooling to room temperature, and adding maltodextrin to obtain an outer wall material;
dispersing the sunflower seed oil and the emulsifier at high speed for 10-15min to obtain an emulsion of an inner wall material;
mixing the emulsions of the core material, the outer wall material and the inner wall material, dispersing at high speed in a water bath at 40-50 ℃ for 20-30min, and homogenizing under 40-50Mpa for 2-3 times to obtain a mixed emulsion;
and carrying out high-speed centrifugal spray drying on the mixed emulsion at the temperature of 180-200 ℃ to obtain the microcapsule sweetener.
5. The coffee flavor-refreshing electronic atomized liquid as claimed in claim 4, wherein the emulsifier is selected from one of soft phospholipids, distilled monoglyceride, sodium stearoyl lactylate and calcium stearoyl lactylate.
6. The coffee flavor-refreshing electronic atomized liquid as claimed in claim 1, wherein the electronic atomized liquid is prepared from the following raw materials in parts by weight:
40-50 parts of 1, 2-propylene glycol;
10-15 parts of glycerol;
5-8 parts of coffee extract;
10-15 parts of acutangular anisodus root extract;
5-8 parts of a microcapsule sweetening agent;
2-10 parts of water.
7. The coffee flavor-refreshing type electronic atomized liquid as claimed in claim 1, wherein the electronic atomized liquid further comprises 3 to 5 parts of cassia seed extract.
8. A method for preparing coffee refreshing type electronic atomization liquid according to any one of claims 1 to 6, which is characterized by comprising the following steps:
1) uniformly mixing glycerol, 1, 2-propylene glycol and water according to parts by weight at 50-60 ℃ to obtain a primary mixed solution;
2) adding the coffee extract and the acutangular anisodus root extract into the primary mixed liquid according to the weight parts, uniformly mixing at 50-60 ℃, stopping heating, adding the microcapsule sweetening agent while stirring, and cooling to room temperature to obtain the coffee-flavored refreshing electronic atomized liquid.
9. The preparation method of the coffee flavor refreshing type electronic atomized liquid as claimed in claim 7, characterized by comprising the following steps:
1) uniformly mixing glycerol, 1, 2-propylene glycol and water according to parts by weight at 50-60 ℃ to obtain a primary mixed solution;
2) adding coffee extract, semen Cassiae extract and radix Anisodi Acutanguli extract into the primary mixed solution according to weight parts, mixing at 50-60 deg.C, stopping heating, adding microcapsule sweetener under stirring, and cooling to room temperature to obtain coffee refreshing electronic atomized liquid.
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104026730A (en) * | 2014-07-01 | 2014-09-10 | 安徽中烟工业有限责任公司 | Scorch sweet aroma electronic cigarette juice |
CN104126874A (en) * | 2014-07-11 | 2014-11-05 | 张伟滨 | Electronic cigarette atomized liquid and preparation method thereof |
CN104711120A (en) * | 2015-03-31 | 2015-06-17 | 川渝中烟工业有限责任公司 | Essential oil micro-capsule prepared by using tobacco wastes as well as preparation method and application thereof |
CN106942787A (en) * | 2017-03-22 | 2017-07-14 | 云南芯韵科技开发有限公司 | A kind of cigarette microemulsion capsule and preparation method thereof |
CN108902983A (en) * | 2018-06-29 | 2018-11-30 | 深圳职业技术学院 | Double emulsion-spray drying production compound probiotic bilayered microcapsule technical method |
CN112401293A (en) * | 2020-09-17 | 2021-02-26 | 深圳雪雾科技有限公司 | Bitter inhibitor, application, electronic atomized liquid and preparation method thereof |
-
2021
- 2021-08-04 CN CN202110893259.3A patent/CN113633014A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104026730A (en) * | 2014-07-01 | 2014-09-10 | 安徽中烟工业有限责任公司 | Scorch sweet aroma electronic cigarette juice |
CN104126874A (en) * | 2014-07-11 | 2014-11-05 | 张伟滨 | Electronic cigarette atomized liquid and preparation method thereof |
CN104711120A (en) * | 2015-03-31 | 2015-06-17 | 川渝中烟工业有限责任公司 | Essential oil micro-capsule prepared by using tobacco wastes as well as preparation method and application thereof |
CN106942787A (en) * | 2017-03-22 | 2017-07-14 | 云南芯韵科技开发有限公司 | A kind of cigarette microemulsion capsule and preparation method thereof |
CN108902983A (en) * | 2018-06-29 | 2018-11-30 | 深圳职业技术学院 | Double emulsion-spray drying production compound probiotic bilayered microcapsule technical method |
CN112401293A (en) * | 2020-09-17 | 2021-02-26 | 深圳雪雾科技有限公司 | Bitter inhibitor, application, electronic atomized liquid and preparation method thereof |
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