CN101928636B - Xenon-containing grease-like liquid and preparation method thereof - Google Patents
Xenon-containing grease-like liquid and preparation method thereof Download PDFInfo
- Publication number
- CN101928636B CN101928636B CN2010102753163A CN201010275316A CN101928636B CN 101928636 B CN101928636 B CN 101928636B CN 2010102753163 A CN2010102753163 A CN 2010102753163A CN 201010275316 A CN201010275316 A CN 201010275316A CN 101928636 B CN101928636 B CN 101928636B
- Authority
- CN
- China
- Prior art keywords
- xenon
- liquid
- milliliters
- grease
- injector
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Images
Landscapes
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention discloses xenon-containing grease-like liquid. 1 to 3.4 volume of xenon is dissolved in 1 volume of grease-like liquid. A preparation method for the grease-like liquid comprises the following steps of: sucking the grease-like liquid by using an injector at normal temperature and normal pressure; adding the xenon into the injector; closing the injector; strongly shaking the injector for at least over 30 minutes; and moving the piston of the injector along with the dissolution of the xenon in a carrier to supplement the volume reduction of the xenon when the xenon is dissolved. The dissolved amount of the xenon can be read according to the scale change of the injector. After the xenon is dissolved in the grease-like liquid, the inoxidizability of the liquid can be improved effectively.
Description
Technical field: the present invention relates to a kind of oils preparation and preparation method thereof, especially a kind of grease-like liquid that contains xenon and preparation method thereof.
Background technology: cosmetics, pharmaceutical agent, food additive, beverage, life active additive etc. generally all contain the oils composition; The material of these oils compositions or lipophilic class externally environmental factors (irradiation of light, temperature, variety of way) acts on down; Be easy to suffer oxidation, thereby lower the characteristic or the biological agent of this liquid.Two kinds of methods of main at present employing are come antioxidation: 1, in these oil substances, add chemical antioxidants, for example: butylhydroxy, dibenzylatiooluene, propyl group, alkyl phenol type etc.This type antioxidant can not bring other special biological activitys, but very big side effect is arranged.2, add natural antioxidant; For example: alpha-tocopherol; But this natural antioxidant generally can bring other biological activity; Thereby bring some unpredictable result to collective, and much this type antioxidant for example alpha-tocopherol can improve the probability that changes skin carcinoma and melanoma.
Xenon is the bigger element of atomic number in the noble gas, and atomic radius is bigger.Atomic number 54, the peripheral electron 5s5p that arranges is positioned at period 50 family, atom covalence radius 209 micromicrons, the first ionization energy 1172kJ/mol.Simple substance is made up of monoatomic molecules.Rare gas, colourless, do not have smell, tasteless, density 5.887 grams per liters, fusing point-111.9 ℃, boiling point-107.1 ± 3 ℃, 110.9 milliliters of solubilized (volume) in every premium on currency in the time of 20 ℃.Can absorb X ray.The chemical property torpescence.Can be with water, hydroquinone, phenol etc. form the weak bond clathrate.Under electric field action, can send intensive white light.Be used to make the high pressure xenon long-arc lamp, produce ultraviolet high-tension electricity arc lamp, flash lamp, neutron counter, X ray enumerator, the ionization chamber of also using as the neutron-absorbing material in anesthetis, the atomic pile, filling thyratron and detection ultra rays.
Summary of the invention: the deficiency to above-mentioned prior art the invention provides a kind of grease-like liquid that contains xenon and preparation method thereof.
For realizing above-mentioned purpose, the technical scheme that the present invention adopts is: contain the grease-like liquid of xenon, the xenon of dissolving 1-3.4 volumes in the grease-like liquid of 1 volume.
The method for preparing that contains the grease-like liquid of xenon; At normal temperatures and pressures, adopt syringe to suck grease-like liquid, in syringe, add xenon then; The closed injection device; At least strongly rock syringe more than 30 minutes, along with syringe piston is moved in the dissolving of xenon in carrier, the minimizing of volume when dissolving with additional xenon.Scale according to syringe changes, and can read the meltage of xenon.
After xenon is dissolved in grease-like liquid, can effectively improve the non-oxidizability of this liquid.
Description of drawings:
Fig. 1 is the non-oxidizability test pattern that in almond oil, adds xenon.
Fig. 2 is the non-oxidizability test pattern that in oleum lini, adds xenon.
Fig. 3 is the non-oxidizability test pattern that in borage oil, adds xenon.
Fig. 4 is the non-oxidizability test pattern that in Oleum Cocois, adds xenon.
Fig. 5 is the non-oxidizability test pattern that in the combination agent of pine-seed oil, oleum lini, soybean oil, Oleum Hippophae, adds xenon.
Fig. 6 is the non-oxidizability test pattern that in the cosmetics of being made up of olive oil, sodium polyacrylate and diformazan basic ring penta siloxanes, adds xenon.
Fig. 7 is the non-oxidizability test pattern that in toothpaste, adds xenon.
Fig. 8 is the non-oxidizability test pattern that in sulphur ointment, adds xenon.
In above figure, the transverse axis of coordinate system is that the time, (unit: week), the longitudinal axis was a non-oxidizability percentage ratio.
The Line 1 representative has added 40 milliliters xenon in Fig. 1-Fig. 5, and No. 2 line representatives have added 20 milliliters xenon, and No. 3 line representatives have added 10 milliliters xenon, and No. 4 line representatives have added 4 milliliters xenon, and No. 5 line has been represented 1 milliliter xenon.
Among Fig. 6, the Line 1 representative has added 200 milliliters xenon, and No. 2 line representatives have added 100 milliliters of xenons, and No. 3 line representatives have added 50 milliliters of xenons, and No. 4 line representatives have added 20 milliliters of xenons, and No. 5 line representatives have added 5 milliliters of xenons.
Among Fig. 7, the Line 1 representative has added 64 milliliters of xenons, and No. 2 line representatives have added 32 milliliters of xenons, and No. 3 line representatives have added 16 milliliters of xenons, and No. 4 line representatives have added 6.4 milliliters of xenons, and No. 5 line representatives have added 1.6 milliliters of xenons.
Among Fig. 8, the Line 1 representative has added 180 milliliters of xenons, and No. 2 line representatives have added 90 milliliters of xenons, and No. 3 line representatives have added 45 milliliters of xenons, and No. 4 line representatives have added 18 milliliters of xenons, and No. 5 line representatives have added 4.5 milliliters of xenons.
The specific embodiment:
Described grease-like liquid can be cosmetics, health pharmaceutical reagent, food, beverage, bioactive additive, food additive, non-traditional pharmaceutical reagent etc., as: almond oil, oleum lini, borage oil, peach kernel oil, cupu oil, awns nut oil, olive oil, Oleum Glycines, Oleum Helianthi, Oleum Hippophae, Semen Juglandis oil, Oleum Ricini, Oleum sesami, Petiolus Trachycarpi oil, Oleum Cocois, cashew nut oil, Semen Maydis oil, vegetable oil, Oleum Arachidis hypogaeae semen, Fructus Tritici aestivi wet goods; Can also be the material that contains the lipophilic constituents, as: Hydrocarbon, aliphatic alcohol, fatty acid, wax, triglycerides, phospholipid, sphingolipid, glycolipid class, lipoprotein, organosilicon lipid, emulsifying agent, solubilizing agent etc., but be not limited only to above-mentioned substance.
At normal temperatures and pressures; Adopt syringe to suck 20 milliliters of grease-like liquids, add 1,4,10,20,40 milliliter xenon then respectively, and all add 0.005% vitamin e; To reach the needed full concentration of cell system; The closed injection device rocks syringe more than 30 minutes at least strongly then, and xenon is dissolved in wherein fully.In 20 weeks, these 5 groups of liquid are carried out the test of oxidation resistance.Get respectively and dissolved 10 milliliters of 5 groups of not commensurability liquid,, adopt the bottle cap sealing of polypropylene material, shine with light with the bottle splendid attire of polypropylene material.After through 4,10,16,20 week, by means of diphenyl-its oxidation resistance of picryl hydrazine test.
Embodiment 1:
As shown in Figure 1: the xenon of different volumes joins the raising that has promoted its oxidation resistance in 20 milliliters of almond oil, especially in 20 milliliters of oils and fatss, adds show under the situation that volume is 40 milliliters and 20 milliliters xenons more obvious.
Embodiment 2:
As shown in Figure 2: the xenon of different volumes joins the raising that has promoted its oxidation resistance in 20 milliliters of oleum linis, especially in 20 milliliters of oils and fatss, adds show under the situation that volume is 40 milliliters and 20 milliliters xenons more obvious.
Embodiment 3:
As shown in Figure 3: the xenon of different volumes joins the raising that in 20 milliliters of borage oils, has promoted its oxidation resistance, especially in 20 milliliters of oils and fatss, adds show under the situation that volume is 40 milliliters and 20 milliliters xenons more obvious.
Embodiment 4:
As shown in Figure 3: the xenon of different volumes joins the raising that has promoted its oxidation resistance in 20 milliliters of Oleum Cocois, especially in 20 milliliters of oils and fatss, adds show under the situation that volume is 40 milliliters and 20 milliliters xenons more obvious.
Embodiment 5:
As shown in Figure 5: the xenon of different volumes joins the raising that has promoted its oxidation resistance in 20 milliliters of combination agent of being made up of pine-seed oil (25%), oleum lini (25%), soybean oil (25%), Oleum Hippophae (25%), especially in 20 milliliters of combination agent, adds show under the situation that volume is 40 milliliters of xenons more obvious.
Embodiment 6:
As shown in Figure 6: the xenon of different volumes joins the raising that has promoted its oxidation resistance in 400 milliliters of cosmetics of being made up of olive oil, sodium polyacrylate and diformazan basic ring penta siloxanes, especially in 400 milliliters of cosmetics, adds show under the situation that volume is 200 milliliters of xenons more obvious.
Embodiment 7:
As shown in Figure 7: the xenon of different volumes joins the raising that has promoted its oxidation resistance in 400 milliliters the toothpaste, especially in 400 milliliters of toothpaste, adds show under the situation that volume is 64 milliliters of xenons more obvious.
Embodiment 8:
As shown in Figure 8: the xenon of different volumes joins the raising that has promoted its oxidation resistance in 200 milliliters 10% sulphur ointment, especially in 200 milliliters of toothpaste, adds show under the situation that volume is 180 milliliters of xenons more obvious.
Claims (1)
1. xenon is characterized in that as the application of antioxidant in grease-like liquid: the xenon of dissolving 1-3.4 volumes in the grease-like liquid of 1 volume; At normal temperatures and pressures, adopt syringe to suck grease-like liquid, in syringe, add xenon then; The closed injection device; At least strongly rock syringe more than 30 minutes, along with syringe piston is moved in the dissolving of xenon in carrier, the minimizing of volume when dissolving with additional xenon; Described grease-like liquid is cosmetics.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2010102753163A CN101928636B (en) | 2010-09-08 | 2010-09-08 | Xenon-containing grease-like liquid and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2010102753163A CN101928636B (en) | 2010-09-08 | 2010-09-08 | Xenon-containing grease-like liquid and preparation method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101928636A CN101928636A (en) | 2010-12-29 |
CN101928636B true CN101928636B (en) | 2012-11-14 |
Family
ID=43368070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2010102753163A Expired - Fee Related CN101928636B (en) | 2010-09-08 | 2010-09-08 | Xenon-containing grease-like liquid and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101928636B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2024076263A1 (en) * | 2022-10-07 | 2024-04-11 | Александр Юрьевич ВЕРХОВСКИЙ | Method for improving the bioavailability of functional food products |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1255065A (en) * | 1997-03-10 | 2000-05-31 | 迈克尔·乔治夫 | Medicinal preparation containing lipophilicity inert gas |
-
2010
- 2010-09-08 CN CN2010102753163A patent/CN101928636B/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1255065A (en) * | 1997-03-10 | 2000-05-31 | 迈克尔·乔治夫 | Medicinal preparation containing lipophilicity inert gas |
Non-Patent Citations (2)
Title |
---|
GC-MS测定氙在不同浓度脂肪乳中的分配系数;曹伟等;《华西药学杂志》;20070831(第4期);423-425 * |
曹伟等.GC-MS测定氙在不同浓度脂肪乳中的分配系数.《华西药学杂志》.2007,(第4期),423-425. |
Also Published As
Publication number | Publication date |
---|---|
CN101928636A (en) | 2010-12-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Cottica et al. | Antioxidant activity and composition of propolis obtained by different methods of extraction | |
Al-Dhabi et al. | Quantification of phytochemicals from commercial Spirulina products and their antioxidant activities | |
CN101019833B (en) | Oil-in-oil nonaqueous microemulsion used as medicine carrier and its medicine preparation | |
CN103202772A (en) | Cream composition with stable liquid crystal structure and preparation method thereof | |
Telmesani | Oral rehydration salts, zinc supplement and rota virus vaccine in the management of childhood acute diarrhea | |
CN100375621C (en) | Vinorelbine liposome micro ball injection and its prepn | |
Lou et al. | Antioxidant activity and chemical composition of the fractions from burdock leaves | |
CN101928636B (en) | Xenon-containing grease-like liquid and preparation method thereof | |
KR20140017701A (en) | Low-concentration nutritional composition | |
Li et al. | Antiproliferative ability and fluorescence tracking of α-linolenic acid-loaded microemulsion as label-free delivery carriers in MDA-MB-231 cells | |
CN103520103B (en) | A kind of vitamin E nano-emulsion and preparation method thereof | |
CN102048742A (en) | Nano-scale liquid composite vitamin preparation | |
CN101700229B (en) | Prostaglandin E1 long-circulation fat microsphere preparation for intravenous injection and preparation method thereof | |
CN102973636A (en) | Common threewingnut root microemlusion-based gel preparation and preparation method thereof | |
CN101884658A (en) | Compound angelica medicament injection preparation containing polyethylene glycol 12-hydroxystearate and preparation method thereof | |
CN115400080B (en) | Pickering emulsion stabilized by luteolin and preparation method and application thereof | |
Song et al. | Preparation and physicochemical stability of tomato seed oil microemulsions | |
CN101204373A (en) | Paclitaxel lipid microspheres injection and preparation method thereof | |
Ali et al. | Assessment of Physical Stability and Antioxidant Activity of Polysiloxane Polyalkyl Polyether Copolymer‐Based Creams | |
CN103610640A (en) | Alprostadil medium-and-long-chain lipid emulsion for injection and preparation method thereof | |
CN105726360A (en) | Cleansing lotion and preparation method thereof | |
Awaad et al. | Insulin-like 3 expression and fibrosis induction after intra-testicular injection of magnetic nanoparticles in rat testis and the ameliorative role of Echinacea purpurea extract | |
JP6418305B2 (en) | Oral liquid composition | |
CN103919841B (en) | Method for prolonging shelf life of eucommia ulmoides seed oil soft capsules | |
Liu et al. | Microemulsion-based lutein extraction from marigold petals: Process optimization and stabilization evaluation |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20121114 Termination date: 20180908 |
|
CF01 | Termination of patent right due to non-payment of annual fee |