CN104546993A - Pharmaceutical composition for treating dark eye circles and preparation method and use thereof - Google Patents

Pharmaceutical composition for treating dark eye circles and preparation method and use thereof Download PDF

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CN104546993A
CN104546993A CN201310506603.4A CN201310506603A CN104546993A CN 104546993 A CN104546993 A CN 104546993A CN 201310506603 A CN201310506603 A CN 201310506603A CN 104546993 A CN104546993 A CN 104546993A
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herba
pharmaceutical composition
black
eyed
skin
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王恩瀚
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Guangzhou Green Biological Technology Co Ltd
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Abstract

The invention discloses a pharmaceutical composition for treating dark eye circles and a preparation method and use thereof. Raw materials of the pharmaceutical composition are all natural active ingredients and are nonirritant to skin. The pharmaceutical composition with a dark eye circle treating effect is prepared from patrinia villosa, strobilanthes affinis, ilex pubescens, incarrillea sinensis, centella asiatica, saussurea involucrata, carpesium divaricatum and eupatorium odoratum, wherein the weight percent of any ingredient is not higher than 30% the overall weight. The raw materials of the pharmaceutical composition disclosed by the invention are simply obtained, and the preparation method is convenient. Proved by clinical trial results, the pharmaceutical composition disclosed by the invention has a good effect on the treatment of the dark eye circles, is nonirritant and non-allergic to the skin, is easily accepted by mass consumers, and has good application prospect and market prospect.

Description

Treat black-eyed pharmaceutical composition and preparation method thereof and purposes
Technical field
The present invention relates to a kind of pharmaceutical composition and preparation method thereof and purposes, particularly a kind of have pharmaceutical composition used for cosmetic for the treatment of black eye effect and preparation method thereof and purposes.
Background technology
Body skin is so that part is the thinnest near the eyes, and melanin activity is very vigorous, adds that the factors such as age growth, external irritant haunt, is easy to occur various problem, and black-eyed appearance is just unavoidable! So-called black eye, be when eye vein blood vessel blood flow rate is too slow, eye part skin red blood cell is supported not enough, in vein blood vessel, carbon dioxide and metabolic waste accumulation are too much, form chronic hypoxia, blood is comparatively dark and formed and be detained and cyanic colours that eye pigmentation is formed at eye or auburn shade.The traditional Chinese medical science claims “ Jian Black-spot ".Clinical manifestation: men and women can fall ill, and female is more than man; Be found in any age, minority was fallen ill from pubarche; The most no conscious sympton of patient; Skin lesion feature is that the skin of upper palpebra inferior presents lividity, boundary clear; Can with psychentonia, face is matt, look wan and sallow, by medical histories such as eyestrain, menoxenia, hyperthyroidisms; Do not have enough sleep, night life is frequent, and smoking and drinking can cause primary disease to be increased the weight of.The natural drug of exploitation treatment black eye better effects if has become the problem in science of medicine scholar and dermatologist general concern.As number of patent application 201110400186.6, disclose in this application and a kind ofly have the Chinese medicine composition, preparation and preparation method thereof of dispelling black eye effect, described compositions is made up of the crude drug of following weight parts proportioning: Radix Astragali 40-60 part, Radix Puerariae 10-30 part, Fructus Aurantii Immaturus 10-30 part, Rhizoma Curcumae Longae 10-30 part.For another example number of patent application 201210245706.5, which disclose a kind of anti-black eye eye cream, its formula comprises following component: jasmine hydrosol 50-60: ermine oil 8-12: Radix Puerariae oil 7-9: olive oil 1-3: little by candle Apis cerana Fabricius 1-2: plant whitening agent 1-2: plant collagen 1-2: antiseptic 0.8-1.2.For another example number of patent application 201210295087.4, which disclose a kind of anti-black eye lipid nanoparticle emulsion and preparation method thereof, described emulsion comprises following component, the mixture 0.5-7.3% of olibanoresin extract, Aesculus hippocastanum L. seed extract, tetrahydrochysene piperine, the mixture 1.0-19.6% emulsifying agent 0.5-11.8% of stearic acid monoglycerides or Vegetable oil lipoprotein or stearic acid monoglycerides and Vegetable oil lipoprotein, antiseptic 0.006-1.3%, surplus is water.For another example number of patent application 201010563016.5, which discloses a kind of black eye whitening wrinkle-resisting frost.Be made up of the diazolidinyl urea of the spirulina maxim extract of the Oleum lavandula angustifolia of the dipalmitoyl hydroxyproline of the coenzyme Q10 of the vitamin E of the Jojoba oil of the sorbitan stearate of the glycerol stearate of the polysorbate-60 of the stearyl alcohol of the water of 70-80%, 5-10% butanediol, 1-3%, 1-3%, 1-3%, 1-3%, 2-6%, 0.5-2%, 0.5-2%, 0.5-2%, 0.1-1%, 0.1-1%, 0.1-1% Maifanitum and 0.1-1%.
In sum, black eye are owing to often staying up late, emotional instability, eye strain, aging, vein blood vessel blood flow rate is too slow, and eye part skin red blood cell is for hypoxgia, in vein blood vessel, carbon dioxide and metabolic waste accumulation are too much, form chronic hypoxia, blood is comparatively dark and formed and remain in a standstill and cause eye pigmentation, namely we " the panda eye " often said.Deep black eye can allow people seem listless, affect image very much, and therefore, the development of new safely and effectively black-eyed product of external curing has good Social and economic benef@.
Summary of the invention
The object of the invention is to overcome weak point of the prior art, a kind of pharmaceutical composition and the preparation technology thereof with the effect for the treatment of black eye are provided.
The pharmaceutical composition with the effect for the treatment of black eye of the present invention, with patrima villosa, Herba Goldffussiae Psilostachydis, Radix Ilicis Pubescentis, Herba speranskiae tuberculatae, Herba Centellae, Herba Saussureae Involueratae, Herba Carpesii Divaricati and Herba Eupatorii Odorati for prepared by raw material, and the weight percentage of any component is all no more than 30% of total amount.
Treating black-eyed pharmaceutical composition, is prepare with the raw material of following mass fraction: patrima villosa 1 ~ 60 part, Herba Goldffussiae Psilostachydis 1 ~ 60 part, Radix Ilicis Pubescentis 1 ~ 60 part, Herba speranskiae tuberculatae 1 ~ 60 part, Herba Centellae 1 ~ 60 part, Herba Saussureae Involueratae 1 ~ 60 part, Herba Carpesii Divaricati 1 ~ 60 part, Herba Eupatorii Odorati 1 ~ 60 part.
Treating black-eyed pharmaceutical composition, is prepare with the raw material of following mass fraction: patrima villosa 1 ~ 50 part, Herba Goldffussiae Psilostachydis 1 ~ 50 part, Radix Ilicis Pubescentis 1 ~ 50 part, Herba speranskiae tuberculatae 1 ~ 50 part, Herba Centellae 1 ~ 50 part, Herba Saussureae Involueratae 1 ~ 50 part, Herba Carpesii Divaricati 1 ~ 50 part, Herba Eupatorii Odorati 1 ~ 50 part.
Preferably, described in there is the pharmaceutical composition for the treatment of black eye effect, be prepare with the raw material of following parts by weight:
Patrima villosa 1 ~ 40 part
Herba Goldffussiae Psilostachydis 1 ~ 40 part
Radix Ilicis Pubescentis 1 ~ 40 part
Herba speranskiae tuberculatae 1 ~ 40 part
Herba Centellae 1 ~ 40 part
Herba Saussureae Involueratae 1 ~ 40 part
Herba Carpesii Divaricati 1 ~ 40 part
Herba Eupatorii Odorati 1 ~ 40 part
Preferably, described in there is the pharmaceutical composition for the treatment of black eye effect, be prepare with the raw material of following parts by weight:
Patrima villosa 2 ~ 35 parts
Herba Goldffussiae Psilostachydis 2 ~ 35 parts
Radix Ilicis Pubescentis 2 ~ 35 parts
Herba speranskiae tuberculatae 2 ~ 35 parts
Herba Centellae 2 ~ 35 parts
Herba Saussureae Involueratae 2 ~ 35 parts
Herba Carpesii Divaricati 2 ~ 35 parts
Herba Eupatorii Odorati 2 ~ 35 parts
Preferably, described in there is the pharmaceutical composition for the treatment of black eye effect, be prepare with the raw material of following parts by weight:
Patrima villosa 8 ~ 30 parts
Herba Goldffussiae Psilostachydis 8 ~ 30 parts
Radix Ilicis Pubescentis 8 ~ 30 parts
Herba speranskiae tuberculatae 8 ~ 30 parts
Herba Centellae 10 ~ 30 parts
Herba Saussureae Involueratae 10 ~ 30 parts
Herba Carpesii Divaricati 10 ~ 30 parts
Herba Eupatorii Odorati 10 ~ 30 parts
Most preferred, be prepare with the raw material of following parts by weight:
Patrima villosa 10 parts
Herba Goldffussiae Psilostachydis 10 parts
Radix Ilicis Pubescentis 10 parts
Herba speranskiae tuberculatae 10 parts
Herba Centellae 10 parts
Herba Saussureae Involueratae 10 parts
Herba Carpesii Divaricati 10 parts
Herba Eupatorii Odorati 10 parts
Most preferred, be prepare with the raw material of following parts by weight:
Patrima villosa 8 parts
Herba Goldffussiae Psilostachydis 8 parts
Radix Ilicis Pubescentis 8 parts
Herba speranskiae tuberculatae 12 parts
Herba Centellae 12 parts
Herba Saussureae Involueratae 12 parts
Herba Carpesii Divaricati 12 parts
Herba Eupatorii Odorati 12 parts
Most preferred, be prepare with the raw material of following parts by weight:
Patrima villosa 8 parts
Herba Goldffussiae Psilostachydis 8 parts
Radix Ilicis Pubescentis 15 parts
Herba speranskiae tuberculatae 15 parts
Herba Centellae 15 parts
Herba Saussureae Involueratae 15 parts
Herba Carpesii Divaricati 15 parts
Herba Eupatorii Odorati 15 parts
Most preferred, be prepare with the raw material of following parts by weight:
Patrima villosa 10 parts
Herba Goldffussiae Psilostachydis 10 parts
Radix Ilicis Pubescentis 10 parts
Herba speranskiae tuberculatae 12 parts
Herba Centellae 12 parts
Herba Saussureae Involueratae 12 parts
Herba Carpesii Divaricati 12 parts
Herba Eupatorii Odorati 12 parts
Most preferred, be prepare with the raw material of following parts by weight:
Patrima villosa 8 parts
Herba Goldffussiae Psilostachydis 8 parts
Radix Ilicis Pubescentis 8 parts
Herba speranskiae tuberculatae 10 parts
Herba Centellae 10 parts
Herba Saussureae Involueratae 15 parts
Herba Carpesii Divaricati 15 parts
Herba Eupatorii Odorati 15 parts
The preparation method with the pharmaceutical composition for the treatment of black eye effect of the present invention, comprises the following steps:
(1) each above-mentioned raw material is placed in volumetric concentration be 20% ~ 80% ethanol soak 2 ~ 48 hours, the ethanol consumption soaked is 10 ~ 200 times of each raw material gross weight, filters, obtains soak;
Preferably, filtration residue is the soak with ethanol 2 ~ 48 hours of 20% ~ 80% again by volumetric concentration, merges the solution after soaking, obtains soak.
(2) soak is concentrated into 2 ~ 5% of original weight amount, concentrated solution macroporous resin adsorption, then uses the ethanol repeatedly eluting of volumetric concentration 5 ~ 95%, collects eluent, is the described pharmaceutical composition with the effect for the treatment of black eye;
Preferably, the volumetric concentration of ethanol is 40% ~ 95%;
Described macroporous resin employing Mitsubishi chemical company take polystyrene-divinylbenzene as the HP825L type macroporous resin of matrix; The method that soak concentrates is conventional concentrating under reduced pressure.
Test proves, the pharmaceutical composition with treatment black eye effect of the present invention, has and waits multiple action, can be used in preparing the curative drug for the treatment of black-eyed cosmetics and skin;
The invention still further relates to a kind of skin care cosmetics, there is described in comprising the pharmaceutical composition for the treatment of black eye effect and the adjuvant of cosmetic field use;
The invention still further relates to a kind of curative drug of skin, comprise the pharmaceutical composition with the effect for the treatment of black eye described in claim and medically acceptable carrier.
Especially may be used for preparation circumference of eyes skin care cosmetics, comprise eye cream, essence, liniment and lotion, but be not limited to above-mentioned dosage form, according to method known in skin care industry field, after aforementioned pharmaceutical compositions is degerming by known method, various different external preparation can be made;
During preparation skin care cosmetics, can by obtained extracting solution compositions, through being evaporated to 10% ~ 50% of original weight amount, obtain composition concentrated solution, mix mutually with the substrate of known cosmetics and medicine or adjuvant, carrier, additive, conventionally be prepared, wherein, described composition concentrated solution accounts for 5% ~ 10% of cosmetics gross weight.
It is gloomy that black eye often show as skin of lower eyelid color, comprises the poor and transparence of the shade of too much pigmentation, cutis laxa and tear groove formation, skin of lower eyelid, affect face appearance.Medical circle is more and more paid attention to mainly coming from beauty treatment circle to black eye and was more and more paid close attention to it in the last few years, although it both can not pose a health risk, also can not cause disease and cause any pathologic to change, but it can have a strong impact on emotion and oneself's impression of individual.Especially a lot of women is seriously perplexed by it, even has influence on their quality of life.Black eye can make people seem tired, sad, listless, and this makes a lot of people will cover up black eye when work and social activity.The traditional Chinese medical science is thought, black eye is caused by deficiency of the kidney, and black is the true qualities of kidney, the fine nourishing by the five internal organs vital essence of eye, and as sexual strain, kidney essense is lost two orders at least and lacked moistening of vital essence, and the black of kidney floats on upper so two orders are without god, black eye.
Root of the present invention it is documented and great many of experiments screening, from a large amount of natural plants, patrima villosa, Herba Goldffussiae Psilostachydis, Radix Ilicis Pubescentis, Herba speranskiae tuberculatae, Herba Centellae, Herba Saussureae Involueratae, Herba Carpesii Divaricati and Herba Eupatorii Odorati has been selected to be raw material, prepare the described pharmaceutical composition with the effect for the treatment of black eye, wherein, described patrima villosa selects the dry herb of Valerianaceae plant Patrinia villosa Juss.; Herba Goldffussiae Psilostachydis selects the dry aerial parts of acanthaceous plant Xiao chicken coop Taraphochlamys affinis (G riff) Bremekhu [Strobilanthesaffinis (Griff) Y.C.Tang]; Radix Ilicis Pubescentis selects the dry root of Aquifoliaceae Holly Radix Ilicis Pubescentis (Ilx pubescensHook.et Am.); Herba speranskiae tuberculatae selects Bignoniaceae Herba Incarvilleae sinensis to draft a document the dry herb of plant Incarrillea sinensis LaM.; Herba Centellae selects the dry herb of Centella samphire Centella asialica (L.); Herba Saussureae Involueratae selects the dried floral of Compositae Genus Saussurea Herba Saussureae Involueratae subgenus herbaceous plant Saussurea involucrate (Kar.et Kir.) Sch.Bip; Herba Carpesii Divaricati is the dry herb of Compositae Carpesium plant Carpesium divaricatum Sieb.et Zucc.; Herba Eupatorii Odorati selects the dry herb of Compositae Eupatorium herbaceos perennial Eupatorium odoratum L..
Root it is documented:
Herba Goldffussiae Psilostachydis is the dry aerial parts of acanthaceous plant Xiao chicken coop Taraphochlamys affinis (G riff) Bremekhu [Strobilanthes affinis (Griff) Y.C.Tang], it is a kind of Guangxi traditional herbal medicine, supplement to the Herbal records that its root can be invigorated blood circulation, removing heat from blood, soothing the liverly rush down wet, reducing swelling and alleviating pain, is clinically at present mainly used in the sick treatment such as acute, chronic hepatitis, jaundice.
Patrima villosa (Phylanthus urinaria L.) is one of source of Herba Patriniae, for the dry whole herb with root of Valerianaceae herbaceos perennial patrima villosa Patrinia villosa Juss., have another name called Herba Sonchi Oleracei, bitter vegetarian, Radix Scrophulariae, be distributed widely in south China each province, because extensively being eaten containing beneficiating ingredients such as several amino acids, vitamin and mineral.Herba Patriniae begins to be loaded in Shennong's Herbal, has heat-clearing and toxic substances removing, promoting diuresis and pus discharge, blood circulation promoting and blood stasis dispelling, effect of tranquilizing mind, is usually used in treating appendicitis, lung pus carbuncle clinically, tuberculosis scrofula, carbuncle sore tumefacting virus, enteritis, dysentery, hepatitis, tonsillitis, eye conjunctivitis, postnatal blood stasis is suffered from abdominal pain, spitting of blood, epistaxis, neurasthenia, heart neurosis etc.Pharmaceutical research shows, Herba Patriniae has antibacterial, antiviral, hepatic cholagogic, the effect such as calmness and leukocyte increasing, and toxic and side effects is minimum.
Radix Ilicis Pubescentis is dry root or the leaf of Aquifoliaceae Holly Radix Ilicis Pubescentis (Ilx pubescens Hook.et Am.), has effect of blood circulation and channel invigorating, reducing swelling and alleviating pain, heat-clearing and toxic substances removing, is the Chinese crude drug that south China is conventional.The chemical constitution study of Radix Ilicis Pubescentis shows it mainly containing the type compound such as triterpene and glycosides, lignanoid, iridoid, and wherein triterpene and glycoside thereof are the main components of Radix Ilicis Pubescentis.Pharmaceutical research display Radix Ilicis Pubescentis has the effect such as anti-artery and vein thrombosis, expansion peripheral blood vessel, anticoagulant, adjustment immune status, clinically, all kinds of preparation of Radix Ilicis Pubescentis is widely used in the various diseases such as treatment coronary heart disease, cerebral thrombosis, thromboangiitis, diabetic foot.
Herba speranskiae tuberculatae is the dry herb that Bignoniaceae Herba Incarvilleae sinensis drafts a document plant Incarrillea sinensis LaM., another name scabies grass, malicious maggot grass, grass of delivering a child.Mainly be distributed in the ground such as Liaoning, Jilin, Hebei, Henan, Shandong, Shaanxi, nature and flavor sweet, acrid, warm, enter lung, liver two warp, have dispel the wind, dehumidify, relaxing muscles and tendons to promote blood circulation, the effect such as pain relieving, be used for the treatment of rheumatic arthralgia, the disturbance of lower legs due to pathogenic cold and dampness, eczema scrotum clinically, the diseases such as sore swollen toxin.
Herba Centellae is the dry herb of Centella samphire Centella asialica (L.), has another name called Glechota longituba (Nakai) Kupr, ground wire grass, Gotu Kola etc.Herba Centellae is the perennial herbaceous plant that crawls, and often crispaturas into bulk, and its stem is elongated, and tuberosity is taken root.Originate in India, be now distributed widely in the torrid zone, the world, subtropical zone district, be mainly distributed in each province on the south the Changjiang river in China.Herba Centellae happiness is born in moistening riverbank, marsh, meadow.TAO Hong-Jing is said: this grass is gained the name with cold and cool, its property Great Cold, therefore named Herba Centellae.Herba Centellae begins to be loaded in Shennong's Herbal, has effect of heat-clearing and toxic substances removing, detumescence dampness removing.For jaundice due to damp-heat, heatstroke diarrhoea, sand Stranguria stranguria with blood, carbuncle sore tumefacting virus, injury from falling down.Pharmacological research shows: Herba Centellae extract has outstanding healing of wound and cicatrix repair, and its reason is that asiaticoside has and promotes collage synthesis and the important function such as new vascular generation, the growth of stimulation granulation in body, so be conducive to wound healing.As continuous administration, containing the preparation of asiaticoside, can prevent wound infection from suppurating on skin wound, shorten wound healing time, skin hardness can be reduced and improve skin-nourishing, the effect of enhancing metabolism.
Herba Saussureae Involueratae is the dried floral of Compositae Genus Saussurea Herba Saussureae Involueratae subgenus herbaceous plant Saussurea involucrate (Kar.et Kir.) Sch.Bip, has another name called Herba Saussureae Involueratae, snow lotus of big bud.Herba Saussureae Involueratae is the distinctive rare Chinese medicine in Xinjiang, and locals Feng Xuelian is " king of BAICAO ", " in medicine superfine product ".Herba Saussureae Involueratae is grown on the above height above sea level of snow line in the high mountain gravel and crack of stone of 2600-4000 rice.All there is distribution at Southern Tianshan north slope, particularly have rich in natural resources in the Ili Prefecture in Xinjiang.In Qing Dynasty's supplementary Amplifications of the Compendium of Materia Medica, the existing record to Herba Saussureae Involueratae, claims Herba Saussureae Involueratae " extremely hot in nature can mend lean sun "." Chinese Herbal Medicine in Xinjiang " claims: " Herba Saussureae Involueratae hardship warm in nature, micro-, function expelling wind and removing dampness ".Show the result of study of Herba Saussureae Involueratae at present, its effective ingredient is mainly flavone compound and polysaccharide.The effects such as Herba Saussureae Involueratae has wind-damp dispelling, restores menstrual flow and invigorates blood circulation, warm palace dissipating blood stasis, tonifying yang and enriching blood, are clinically used for the treatment of the diseases such as rheumatic arthralgia, menoxenia, the cold pain of cold womb lower abdomen, lumbago due to renal deficiency, measles without adequate eruption.In recent years, Herba Saussureae Involueratae receives much attention as the effect of ethnic drug in antiearly pregnancy, defying age and inhibition tumor cell propagation.
Herba Carpesii Divaricati is Compositae Carpesium plant Carpesium divaricatum Sieb.et Zucc., is grown in hill thick grass, is mainly distributed in the ground such as Sichuan, Guizhou, Hunan, Fujian and northeast.Its root and basal part of stem all can hyoscines.Its acrid in the mouth is pained, is cool in naturely nontoxicly commonly used for formula for clearing heat and removing toxicity, treatment flu, wind syndrome of head, have loose bowels, the disease such as laryngopharynx swelling and pain, acute conjunctivitis, carbuncle sore tumefacting virus, blood stasis are hemorrhage.
Herba Eupatorii Odorati is Compositae Eupatorium herbaceos perennial Eupatorium odoratum L., is mainly distributed in the ground such as Guangdong, Hainan, Guangxi, Yunnan, Guizhou (west and south) in China.Herba Eupatorii Odorati all herbal medicine, is also conventional medical herbs among the people in China, has dissipating blood stasis for subsidence of swelling, removing toxic substances, hemostasis and disinsection efficiency, be mainly used in treating swelling and pain by traumatic injury, sore swollen toxin, dermatitis and traumatic hemorrhage.Modern pharmacology research shows that the extract of aircraft blade of grass has and suppresses bacillus pyocyaneus, escherichia coli, staphylococcus aureus, gonococcal activity, and can promote the healing of wound.
At present, there is not yet both at home and abroad the compositions of patrima villosa, Herba Goldffussiae Psilostachydis, Radix Ilicis Pubescentis, Herba speranskiae tuberculatae, Herba Centellae, Herba Saussureae Involueratae, Herba Carpesii Divaricati and Herba Eupatorii Odorati is used for the treatment of black-eyed relevant report.
In sum, black-eyed formation is main relevant with pigmentation and Blood vessel pattern, its reason mainly with some bad life habits as stayed up late, smoking, drink, emotional disturbance and make the situation of applying some make up relevant.Current black eye lack effective external use skin care, beneficial effect of the present invention is according to the black-eyed cause of disease and pathomechanism, consult a large amount of monograph and document, successively screened multiple natural plants, finally filtered out and can effectively treat black-eyed pharmaceutical composition.Drug regimen raw material of the present invention obtains simple, and preparation method is convenient.Clinical test results confirms: medicine composite for curing black eye effect of the present invention has good effect, to no skin irritation and sensitization, is easy to be accepted by consumers in general, has a good application prospect and market prospect.
Foregoing invention content part of the present invention has done detailed description to technical scheme of the present invention, and those skilled in the art can repeat the present invention according to foregoing and obtain technique effect of the present invention.Be further explained content of the present invention below by detailed description of the invention, to make those skilled in the art more clearly understand the present invention, not limitation of the present invention, any equivalent replacement or known change all belong to scope.
Detailed description of the invention
Embodiment 1
At room temperature, get patrima villosa 10 kilograms, Herba Goldffussiae Psilostachydis 10 kilograms, Radix Ilicis Pubescentis 10 kilograms, Herba speranskiae tuberculatae 10 kilograms, Herba Centellae 10 kilograms, Herba Saussureae Involueratae 10 kilograms, Herba Carpesii Divaricati 10 kilograms, Herba Eupatorii Odorati 10 kilograms (totally 80 kilograms), with ethanol 800 kilograms of soak extraction of volumetric concentration 70%, soak time is 24 hours, residue soaks with the ethanol 800 kilograms of volumetric concentration 70% and extracts for 24 hours, then the solution after immersion is merged, after 200 object strainer filterings, concentrating under reduced pressure 20 times, again by macroporous resin on concentrated solution, with the ethanol elution of volumetric concentration 50%, containing effective ingredient required in prescription of the present invention in the eluent collected, i.e. pharmaceutical composition.
Embodiment 2
At room temperature, get patrima villosa 8 kilograms, Herba Goldffussiae Psilostachydis 8 kilograms, Radix Ilicis Pubescentis 8 kilograms, Herba speranskiae tuberculatae 12 kilograms, Herba Centellae 12 kilograms, Herba Saussureae Involueratae 12 kilograms, Herba Carpesii Divaricati 12 kilograms, Herba Eupatorii Odorati 12 kilograms (totally 84 kilograms), with ethanol 1680 kilograms of soak extraction of volumetric concentration 50%, soak time is 24 hours, residue soaks with the ethanol 1680 kilograms of volumetric concentration 50% and extracts for 24 hours, then the solution after immersion is merged, after 200 object strainer filterings, concentrating under reduced pressure 40 times, again by macroporous resin on concentrated solution, with the ethanol elution of volumetric concentration 40%, containing effective ingredient required in prescription of the present invention in the eluent collected, i.e. pharmaceutical composition.
Embodiment 3
At room temperature, get patrima villosa 8 kilograms, Herba Goldffussiae Psilostachydis 8 kilograms, Radix Ilicis Pubescentis 15 kilograms, Herba speranskiae tuberculatae 15 kilograms, Herba Centellae 15 kilograms, Herba Saussureae Involueratae 15 kilograms, Herba Carpesii Divaricati 15 kilograms, Herba Eupatorii Odorati 15 kilograms (totally 106 kilograms), with ethanol 1060 kilograms of soak extraction of volumetric concentration 80%, soak time is 24 hours, residue soaks with the ethanol 1060 kilograms of volumetric concentration 80% and extracts for 24 hours, then the solution after immersion is merged, 25 times are concentrated after 200 object strainer filterings, again by macroporous resin on concentrated solution, with the ethanol elution of volumetric concentration 60%, containing effective ingredient required in prescription of the present invention in the eluent collected, i.e. pharmaceutical composition.
Embodiment 4
At room temperature, get patrima villosa 10 kilograms, Herba Goldffussiae Psilostachydis 10 kilograms, Radix Ilicis Pubescentis 10 kilograms, Herba speranskiae tuberculatae 12 kilograms, Herba Centellae 12 kilograms, Herba Saussureae Involueratae 12 kilograms, Herba Carpesii Divaricati 12 kilograms, Herba Eupatorii Odorati 12 kilograms (totally 90 kilograms), with ethanol 2700 kilograms of soak extraction of volumetric concentration 30%, soak time is 24 hours, residue soaks with the ethanol 2700 kilograms of volumetric concentration 30% and extracts for 24 hours, then the solution after immersion is merged, 50 times are concentrated after 200 object strainer filterings, again by macroporous resin on concentrated solution, with the ethanol elution of volumetric concentration 50%, containing effective ingredient required in prescription of the present invention in the eluent collected, i.e. pharmaceutical composition.
Embodiment 5
At room temperature, get patrima villosa 8 kilograms, Herba Goldffussiae Psilostachydis 8 kilograms, Radix Ilicis Pubescentis 8 kilograms, Herba speranskiae tuberculatae 10 kilograms, Herba Centellae 10 kilograms, Herba Saussureae Involueratae 15 kilograms, Herba Carpesii Divaricati 15 kilograms, Herba Eupatorii Odorati 15 kilograms (totally 89 kilograms), with ethanol 1335 kilograms of soak extraction of volumetric concentration 60%, soak time is 24 hours, residue soaks with the ethanol 1335 kilograms of volumetric concentration 60% and extracts for 24 hours, then the solution after immersion is merged, 30 times are concentrated after 200 object strainer filterings, again by macroporous resin on concentrated solution, with the ethanol elution of volumetric concentration 80%, containing effective ingredient required in prescription of the present invention in the eluent collected, i.e. pharmaceutical composition.
Embodiment 6
Liquid embodiment 1 obtained adopts concentrating under reduced pressure, is concentrated into 10% ~ 50% of original weight amount, obtains pharmaceutical composition concentrated solution, and for the preparation of the black-eyed essence for the treatment of, the percentage by weight of component is as follows:
Production technology: hyaluronate sodium is added to the water dispersed with stirring even, then adds other composition successively, stir in 70 DEG C of situations.
Present pre-ferred embodiments matrix components used is described above, and the present embodiment matrix components used can by the efficacy exertion of pharmaceutical composition of the present invention to the best.But the conventional substrate that can be applicable to cosmetics of other manufacturer production also can be used for the present invention, as long as consumption meets national cosmetic additive amount standard, can not affect effect of the present invention, therefore not enumerate.
The present invention's emulsifying equipment used is the FV-30L FISCO vacuum homogeneous emulsifying machine that Shanghai Frock Fluid Machinery Manufacture Co., Ltd. produces, and it has the functions such as homogenizing, stirring and temperature control.The emulsifying equipment prepared for cosmetics of other manufacturer production also may be used for the present invention, as long as operate in strict accordance with technological parameter of the present invention, all can reach effect of the present invention.
Embodiment 7
The black-eyed clinical experimental study of medicine composite for curing is reported: in following experiment, pharmaceutical composition used is the black-eyed eye cream for the treatment of prepared by the cosmetic formulations of embodiment 6.
1. materials and methods
The routine female patient of case selection 56 of 1.1 black eye patients, 20 ~ 40 years old age, average out to 33 years old, wherein, FitzpatrickIII type skin person 48 example, IV type skin person 8 example.Black eye main manifestations is appearing of inferior palpebral veins, does not do other treatment.Be divided into treatment group (30 example) and matched group (26 is routine) at random, two groups in sex, age, the state of an illness without marked difference.
The eye cream containing pharmaceutical composition of the present invention of 1.2 Therapeutic Method treatment groups is provided by Zhong He International Technology company limited, according to a conventional method eye cream is applied in black eye place, 3 times/day after clean face.Matched group: not containing the eye cream of pharmaceutical composition of the present invention, be also according to a conventional method eye cream is applied in black eye place, 3 times/day after clean face.Treat observe the curative effect after 60 days, carry out therapeutic evaluation, and record untoward reaction.
1.3. parameters for observation on effect and standards of grading: follow up a case by regular visits to after 60 days with treatment before treatment and take pictures, evaluated therapeutic effect by two veteran cosmetologists, focal cleaning rate adopts level Four evaluation criterion, namely fully recovers: black eye disappear and reach 90% ~ 100%; Effective: black eye disappear and reach 70% ~ 89%; Effective: black eye disappear 30% ~ 69%; Invalid: black eye disappear below 30% or without significant change.Effective percentage adds effective adding effectively in recovery from illness.
2. result
Treatment group and matched group have pole significant difference (P < 0.1 improving the curative effect in red blood trace on face patient objective sign, table 1), the eye cream containing pharmaceutical composition of the present invention significantly can improve the black eye of most patient.
A table 1 liang group patient objective sign improves situation
All there is not untoward reaction before and after Product Safety assessment treatment, come off without 1 routine patient.There is not the Adverse Event relevant to the eye cream containing pharmaceutical composition of the present invention in whole research process.
Adopt the pharmaceutical composition with the effect for the treatment of black eye of other embodiment to carry out clinical trial, result also proves to have identical effect.This illustrates that pharmaceutical composition of the present invention treats the desirable external use skin care of black eye at present, and its safety is good, untoward reaction is little, strong adaptability, is worthy of popularization.
Embodiment 8
Treat the skin irritation test research report of black-eyed pharmaceutical composition: by animal experiment, observe that treatment black eye pharmaceutical composition acute ocular of the present invention stimulates, local skin irritant reaction that the intact skin of multiple-contact rabbit and damaged skin produce and anaphylaxis situation.In following experiment, pharmaceutical composition used is the pharmaceutical composition of embodiment 1.
1 animal
16 regular grade adult healthy new zealand rabbits, male and female half and half, 2.5kg ~ 3.5kg, buys in Guangdong Medical Lab Animal Center, and laboratory animal production licence number is SCXK (Guangdong) 2008-0002, the animal quality certification number: Guangdong 2012A016.Raise in Animal House F4 room, general area, new southern Drug safety assessment center (the experimental animal room quality certification number: 0060590.), duration of test, room temperature 20 DEG C ~ 22 DEG C, humidity 40% ~ 67%, illumination 12h/12h round the clock light and shade replaces.
2 methods
(1) according to Ministry of Health of the People's Republic of China " cosmetics health specification (version in 2007) ", adopt consubstantiality self left and right sides matching type, tested rabbit is fixed in rabbit fixed bin, pull open the palpebra inferior of eyes on the right side of test rabbit gently, get 0.1mL pharmaceutical composition to clamp-on in conjunctival sac, and make upper and lower eyelid passive closed 1 second.Left side eye does not process makes own control.After instillation tested material 1,24,48,72h checks rabbit bilateral eyes, and marks to conjunctiva, cornea, iris irritant reaction according to the standards of grading in China's " cosmetics health specification " (version in 2007).To give before tested material 20h and to tested material after 24h apply fluorescein sodium respectively rabbit bilateral eyes checked.Inspection method: by the Fluress of 1% instillation test lagophthalmos, passive closed about 10 seconds, then rinse with normal saline, corneal checked whether that the painted speckle of fluorescein sodium is to judge whether cornea has damage subsequently.
(2) irritant test of intact skin: according to Ministry of Health of the People's Republic of China " cosmetics health specification (version in 2007) ", adopt consubstantiality self left and right sides matching type, prepare before administration: 24h before administration, employing is shaved mao method and is removed family's rabbit back spinal column both sides by hair, the left and right each about 3cm × 3cm of unhairing scope, application area 2.5cm × 2.5cm, not injured skin.Administration: in contrast, pharmaceutical composition (1.0g/ only) is smeared in unhairing district, back, right side to left side bare substrate (normal saline), wraps up, after fixing 4h, clean medicine-feeding part with warm water with clean gauze.Smear 1 every day, continuous 14d.Each remove medicine and again observe erythema and edema before coating, whether coating part has pigmentation, petechia, pachylosis or epidermatic atrophy situation and time of origin and regression time, and erythema and edema to be marked.After last coating, after removal medicine, 30-60min, 24h, 48h and 72h perusal is also recorded and is smeared position with or without the situation such as erythema, edema and pigmentation, petechia, skin emolliency.
(3) irritant test of damaged skin: according to Ministry of Health of the People's Republic of China " cosmetics health specification (version in 2007) ", adopt consubstantiality self left and right sides matching type, before test, 24h cuts off a rabbit back both sides fur, unhairing scope left and right each about 3cm × 3cm, application area 2.5cm × 2.5cm.With blade, standardized groined type is damaged gently, the degree of being with oozing of blood.Then in contrast, pharmaceutical composition (1.0g/ only) is smeared in unhairing district, back, right side, wraps up with clean gauze in left side bare substrate (normal saline) immediately, after fixing 4h, cleans medicine-feeding part with warm water.Smear 1 every day, continuous 14d.Each remove medicine and again observe erythema and edema before coating, whether coating part has pigmentation, petechia, pachylosis or epidermatic atrophy situation and time of origin and regression time, and erythema and edema to be marked.After last coating, after removal medicine, 30-60min, 24h, 48h and 72h perusal is also recorded and is smeared position with or without the situation such as erythema, edema and pigmentation, petechia, skin emolliency.
3 results
(1) result of acute ocular irritation test result table 2 shows the eye irritation of pharmaceutical composition of the present invention to rabbit.Test rabbit right eye is after clamp-oning pharmaceutical composition 0.1mL, and 3 test rabbits all show eye closing, without obvious secretions, without obvious edema.Each time observes eye dripping irritant reaction.Give tested material do not rinse after 1,24,48,72h each time observes eye dripping irritant reaction integration and is 0 point.
A table 2 1.0g/ pharmaceutical composition is to rabbit eyes stimulation
(2) irritant test of intact skin: the result of table 3 shows pharmaceutical composition of the present invention to rabbit intact skin nonirritant.Histopathologic examination's result of the test: matched group and pharmaceutical composition group rabbit skin epithelial cell form no abnormality seen, corium and subcutaneous tissue have no vasodilation and inflammatory cell infiltration and collagen fiber hyperplasia.
A table 3 1.0g/ pharmaceutical composition is to rabbit intact skin stimulation
(3) irritant test of damaged skin: 16 rabbit of pharmaceutical composition group without erythema, without the situation such as edema, pigmentation (table 4).Histopathologic examination's result of the test: matched group and pharmaceutical composition group rabbit skin epithelial cell form no abnormality seen, corium and subcutaneous tissue have no vasodilation, have no obvious collagen fiber hyperplasia, visible mild inflammatory cellular infiltration.Therefore pharmaceutical composition of the present invention is to rabbit damaged skin nonirritant.
A table 4 1.0g/ pharmaceutical composition is to rabbit damaged skin stimulation
Embodiment 10
Treat the hypersensitive experimentation report of black-eyed pharmaceutical composition: by animal experiment, observe treatment black eye pharmaceutical composition of the present invention to the sensitization of Hartley guinea pig skin.The pharmaceutical composition that the pharmaceutical composition used in this experiment is the embodiment of the present invention 1.
1 animal
Select regular grade Hartley Cavia porcellus 50, male and female half and half, weight range 180 ~ 250g, buy in Guangdong Medical Lab Animal Center, laboratory animal production licence number is SCXK (Guangdong) 2008-0002, the animal quality certification number: Guangdong 2012A064.Raise in Animal House F4 room, general area, new southern Drug safety assessment center (the experimental animal room quality certification number: 0060590.), duration of test, room temperature 20 DEG C ~ 22 DEG C, humidity 40% ~ 67%, illumination 12h/12h round the clock light and shade replaces.By number skin dyeing is carried out to Cavia porcellus, with saturated picric acid solution (yellow) dye marker units, with 2% silver nitrate solution (coffee color) dye marker tens; Separately raise by sex, each cage box puts 5 Cavia porcelluss, and cage box is outer labelled, indicates the information such as special topic numbering, animal category, group, sex, route of administration, cage number, number of animals and desired assay commencement date and deadline.The pharmaceutical composition that the pharmaceutical composition used in this experiment is the embodiment of the present invention 1, concentration is 1.0g medicine/only.
2 methods
According to country " drug registration management method ", " Chemical induced irritation, anaphylaxis and hemolytic investigative technique guideline ".Be divided into bare substrate group, positive controls, pharmaceutical composition group at random, wherein bare substrate group 10 Cavia porcelluss, all the other respectively organize 20 Cavia porcelluss.Each group of Cavia porcellus male and female half and half.Successively carry out induction sensitization and contact experiment with exciting, two test between be separated by eluting phase of 10 days.Induction exposure experimental technique is front 24h preserved skin, cut off each 2cm × 2cm region, Cavia porcellus spinal column both sides by hair.Positive controls: get 2.5%2, the acetone soln 0.2g of 4-dinitro-chloro-benzene, cover with two-layer gauze (2.5cm × 2.5cm) and one deck antistaling film respectively, 6h is covered with non-stimulated gauze, remove covering, remove residual given the test agent with warm water, the 7th day and the 14th day, in kind repeat once; Be coated with bare substrate 0.1g in bare substrate treated animal same area, pharmaceutical composition group is coated with 0.1g.Induction exposure is carried out by same step.Contact is excited to be then after last is to tested material sensitization contact 14 days (namely testing the 28th day), at the pharmaceutical composition of pharmaceutical composition group guinea pig back preserved skin place coating 0.1g, package is with fixing, tested material is removed after 6h, observe at once, then again observe skin allergy situation in 24h, 48h and 72h.The positive controls acetone soln 0.2g of 2.5%2,4-dinitro-chloro-benzene, bare substrate treated animal same area is coated with bare substrate 0.1g.1h, 24h and 24h, 48h and 72h observation administration local skin erythema, edema and other abnormal responses after exciting after sensitization.By skin allergy standards of grading, skin erythema and edema are marked, and calculate the anaphylaxis incidence rate of each group, judge anaphylaxis occurrence degree by skin hypersensitivity evaluation criterion.Anaphylaxis incidence rate=(occurring number of animals/this treated animal sum of skin erythema, edema or systemic anaphylaxis in group) × 100%.
3 results:
Excite the rear 24h of contact experiment, 48h and 72h, by not knowing that the professional of experiment content is according to " Chemical induced irritation, anaphylaxis and hemolytic investigative technique guideline " pass judgment on whether occur sensitization of skin reaction (table 5), sensitivity response scoring >=2 timesharing, judge that this animal skin sensitivity response is positive, calculate sensitization rate (>=2 points of number of animals/these treated animal sum × 100%), and by " Chemical induced irritation, anaphylaxis and hemolytic investigative technique guideline " in sensitization of skin reaction test grade scale judge the sensitization intensity (table 6) of pharmaceutical composition of the present invention to guinea pig skin.
Table 5 sensitization of skin extent of reaction standards of grading
First calculate and put each group of integral mean value each observing time, then calculate and to observe in the time limit animal integral mean value every day every, evaluate by " Chemical induced irritation, anaphylaxis and hemolytic investigative technique guideline ".By following formulae discovery every animal average integral every day.
Table 6 sensitization of skin extent of reaction grade scale
Excite rear 24h, 48h and 72h, the Cavia porcellus of bare substrate group, pharmaceutical composition group excites area skin all not occur erythema, edema situation, also do not occur other abnormal response, anaphylaxis incidence rate is 0, and anaphylaxis evaluation is and has no skin allergy (table 7).
Excite rear 6h, 2,4-dinitro-chloro-benzene group Cavia porcellus excites area skin all to occur erythema, and anaphylaxis incidence rate is 100%, and anaphylaxis is evaluated as extremely strong sensitization.Excite rear 48h, 2,4-dinitro-chloro-benzene Cavia porcellus excites area skin still all to have erythema, and anaphylaxis incidence rate is 100%, and anaphylaxis evaluation is still extremely strong sensitization.
The anaphylaxis of table 7 pharmaceutical composition guinea pig skin is marked
4 conclusions
Under this experiment condition, pharmaceutical composition carries out 3 sensitization to Hartley guinea pig skin and has no skin allergy after exciting for 1 time.

Claims (9)

1. treat black-eyed pharmaceutical composition, it is characterized in that: with patrima villosa, Herba Goldffussiae Psilostachydis, Radix Ilicis Pubescentis, Herba speranskiae tuberculatae, Herba Centellae, Herba Saussureae Involueratae, Herba Carpesii Divaricati and Herba Eupatorii Odorati for prepared by raw material, and the weight percentage of any component is all no more than 30% of total amount.
2. treat black-eyed pharmaceutical composition, it is characterized in that, it is prepare with the raw material of following mass fraction: patrima villosa 1 ~ 60 part, Herba Goldffussiae Psilostachydis 1 ~ 60 part, Radix Ilicis Pubescentis 1 ~ 60 part, Herba speranskiae tuberculatae 1 ~ 60 part, Herba Centellae 1 ~ 60 part, Herba Saussureae Involueratae 1 ~ 60 part, Herba Carpesii Divaricati 1 ~ 60 part, Herba Eupatorii Odorati 1 ~ 60 part.
3. the black-eyed pharmaceutical composition for the treatment of according to claim 2, it is characterized in that, it is prepare with the raw material of following mass fraction: patrima villosa 1 ~ 50 part, Herba Goldffussiae Psilostachydis 1 ~ 50 part, Radix Ilicis Pubescentis 1 ~ 50 part, Herba speranskiae tuberculatae 1 ~ 50 part, Herba Centellae 1 ~ 50 part, Herba Saussureae Involueratae 1 ~ 50 part, Herba Carpesii Divaricati 1 ~ 50 part, Herba Eupatorii Odorati 1 ~ 50 part.
4. the preparation method of the black-eyed pharmaceutical composition of the treatment according to any one of claims 1 to 3, is characterized in that, comprise the following steps:
The first step: each above-mentioned raw material is placed in volumetric concentration be 20% ~ 80% ethanol soak, the ethanol consumption soaked is 10 ~ 200 times of each raw material gross weight, filters, obtains soak;
Second step: soak is concentrated into 2 ~ 5% of original weight amount, concentrated solution macroporous resin adsorption, then be the ethanol elution of 5 ~ 95% by volumetric concentration, collect eluent, be the black-eyed pharmaceutical composition of described treatment.
5. the preparation method of the black-eyed pharmaceutical composition for the treatment of according to claim 4, is characterized in that: in the first step, and the described soak with ethanol time is 2 ~ 48 hours; Or each raw material first uses soak with ethanol 2 ~ 48 hours, residue uses soak with ethanol 2 ~ 48 hours again, merges the solution after soaking, obtains soak.
6. the preparation method of the black-eyed pharmaceutical composition for the treatment of according to claim 4, is characterized in that: in second step, and the volumetric concentration of described eluting ethanol is 40% ~ 95%.
7. the purposes of the black-eyed pharmaceutical composition of the treatment according to any one of claims 1 to 3, is characterized in that: for the preparation of the curative drug of skin care cosmetics or skin.
8. skin care cosmetics, comprise the adjuvant that the black-eyed pharmaceutical composition for the treatment of described in any one of claims 1 to 3 and cosmetic field use.
9. the curative drug of skin, comprises the black-eyed pharmaceutical composition for the treatment of described in any one of claims 1 to 3 and medically acceptable carrier.
CN201310506603.4A 2013-10-18 2013-10-18 Pharmaceutical composition for treating dark eye circles and preparation method and use thereof Pending CN104546993A (en)

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CN105534813A (en) * 2016-01-19 2016-05-04 佛山市芊茹化妆品有限公司 Cosmetic composition with dark circle relieving effect and preparation method and application thereof
FR3036962A1 (en) * 2015-06-03 2016-12-09 Infinitus China Co Ltd COSMETIC COMPOSITION BASED ON CENTELLA ASIATICA
CN107865927A (en) * 2017-09-19 2018-04-03 广州青岚生物科技有限公司 A kind of clarification process and method of quality control of the pharmaceutical composition that there are treatment livid ring around eye to act on
CN108815309A (en) * 2018-07-28 2018-11-16 广州青岚生物科技有限公司 A kind of pharmaceutical composition for treating eyelet periphery melanin deposition disease
CN110051571A (en) * 2018-09-18 2019-07-26 广州青岚生物科技有限公司 A kind of pharmaceutical composition of sun-proof reparation

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3036962A1 (en) * 2015-06-03 2016-12-09 Infinitus China Co Ltd COSMETIC COMPOSITION BASED ON CENTELLA ASIATICA
CN105534813A (en) * 2016-01-19 2016-05-04 佛山市芊茹化妆品有限公司 Cosmetic composition with dark circle relieving effect and preparation method and application thereof
CN107865927A (en) * 2017-09-19 2018-04-03 广州青岚生物科技有限公司 A kind of clarification process and method of quality control of the pharmaceutical composition that there are treatment livid ring around eye to act on
CN108815309A (en) * 2018-07-28 2018-11-16 广州青岚生物科技有限公司 A kind of pharmaceutical composition for treating eyelet periphery melanin deposition disease
CN110051571A (en) * 2018-09-18 2019-07-26 广州青岚生物科技有限公司 A kind of pharmaceutical composition of sun-proof reparation

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