CN1810256A - Policresulen foam aerosol and its prepn process - Google Patents

Policresulen foam aerosol and its prepn process Download PDF

Info

Publication number
CN1810256A
CN1810256A CN 200510023561 CN200510023561A CN1810256A CN 1810256 A CN1810256 A CN 1810256A CN 200510023561 CN200510023561 CN 200510023561 CN 200510023561 A CN200510023561 A CN 200510023561A CN 1810256 A CN1810256 A CN 1810256A
Authority
CN
China
Prior art keywords
policresulen
sodium
foam
surfactant
acid
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.)
Pending
Application number
CN 200510023561
Other languages
Chinese (zh)
Inventor
李铁军
于云涛
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JINGWEI PHARMACEUTICAL CO Ltd SHANDONG
Original Assignee
JINGWEI PHARMACEUTICAL CO Ltd SHANDONG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by JINGWEI PHARMACEUTICAL CO Ltd SHANDONG filed Critical JINGWEI PHARMACEUTICAL CO Ltd SHANDONG
Priority to CN 200510023561 priority Critical patent/CN1810256A/en
Publication of CN1810256A publication Critical patent/CN1810256A/en
Pending legal-status Critical Current

Links

Landscapes

  • Cosmetics (AREA)
  • Medicinal Preparation (AREA)

Abstract

The present invention discloses one kind of policresulen foam aerosol. The policresulen foam aerosol has softness, fineness, no excitation, excellent adsorption, excellent expansion and other advantages, can penetrate to mucous membrane goffer and other parts common medicine preparation can not reach to, and is suitable for use in body cavity. Clinic application shows that the policresulen foam aerosol is superior to corresponding spraying agent in treating cervicitis and vaginitis. The present invention also provides its preparation process.

Description

Policresulen foam aerosol and preparation technology
Technical field
The present invention relates to pharmaceutical preparation, relate in particular to a kind of policresulen foam aerosol and preparation technology.
Background technology
Policresulen is the local topical medicine.It mainly act as: (1) can optionally act on epithelial cell and the ectopic columnar epithelium that pathological changes takes place, and makes it to solidify, degeneration, comes off, and promote tissue repair, and normal squamous cell is not had influence, does not stay cicatrix after the treatment cervical erosion.(2) recovery of environment in the promotion vagina physiology helps growing again of indigneous flora.(3) can shrink little blood vessel, rapidly hemostasis.(4) can kill multiple pathogenic microorganism, as antibacterial, mycete, infusorian and some virus.Clinical being used for (1) gynecological, increase vaginitis, cervicitis by antibacterial, infusorian, the microbial vagina of beads and cervical secretions; Cervical biopsy or polyp are extractd the treatment of postoperative hemorrhage; (2) surgery and department of dermatologry: the topical therapeutic of skin injury can promote regeneration, antiinflammatory and the healing of slough.
Policresulen is suppository and concentrated solution and spray in gynecological's dosage form commonly used at present, suppository is solid preparation, softening in tract, dissolving is slower, onset is slower, and medicine disperses inhomogeneous, local concentration is higher, simultaneously, need be manipulation when medication, not only unhygienic but also easy cross-contamination, in patient's body foreign body sensation is arranged, bring discomfort to the patient.Concentrated solution need be used cotton balls wiping or dilute with water afterflush when administration, medicine can not fully contact with the tract mucosa, and liquid flows the same inconvenience of use easily in tract.Though the spray that with water is solvent can directly be sprayed at partial wound, the aerosol spray granularity is big, should not go deep into tract mucosa wrinkle wall, and administration is inhomogeneous, influences circulation, makes troubles to the patient.
Washing liquid adopts washout, interior spray in use, but time of contact is short; Can not go deep into the intravaginal lesions position during washout, not have therapeutic effect; Can not fully act on focus, DeGrain during interior the spray.
Suppository is because of the holdup time long (6-8 hour) and to absorb intravaginal moisture zest strong, for recurrence hides some dangers for, but also produce dry and astringent, discomfort such as foreign body sensation, destructible acid-base balance arranged.
These dosage forms produce certain influence to the use of policresulen.
Summary of the invention
Technical problem to be solved by this invention is to overcome the defective of above-mentioned preparation, and the dosage form that research design is new is evenly distributed medicine, better effects if in tract.
The invention provides a kind of policresulen foam aerosol, this aerosol is made up of following component, by weight percentage.
Principal agent: policresulen 1%-40%
Pharmaceutic adjuvant: pH regulator agent 0%-5.0%, foaming agent 0.2%-30%, foam substrate 0%-30%, foam stabiliser 0%-15%, spice 0%-0.5%, solvent 40%-90%, antioxidant 0%-0.5%, antiseptic 0%-0.2%, propellant 3%-40%.
The described pharmaceutic adjuvant of this aerosol comprises: pH regulator agent, foaming agent, foam substrate, foam stabiliser, spice, solvent, antioxidant, antiseptic, propellant etc.
PH value regulator amount ranges 0.000-5.000% (w/w): as sodium hydroxide, sodium bicarbonate, sodium phosphate, sodium citrate etc.;
Foaming agent, foam substrate can adopt surfactant, and its amount ranges 0.200-30.000% (w/w) can be non-ionic surface active agent, anion surfactant, cationic surfactant, amphoteric surfactant or other surfactant;
Available nonionic surfactants, as:
The fatty acid esters of sorbitan class, as: Arlacel-20, Arlacel-60, Arlacel-65, Arlacel-80, Arlacel-85 etc.;
Polyethylene glycols, as: PEG-200, PEG-400, PEG-600, PEG-1000 etc.;
The polyoxyethylene sorbitan fatty acid ester class, as: tween 20, Tween-40, Tween-60, Tween-65, tween 80 etc.;
The polyoxyethylene alkyl ether class, as: Brij30, polyoxyethylene stearyl alcohol ether etc.;
The polyoxyethylene fatty acid ester class, as: Myij-45, Myij-52, Myij-53, Myij-59 etc.;
The polyol-based non-ionic surfactant class, as: glycerol monolaurate, sorbitol lauric acid monoesters etc.;
Available anion surfactant class, as:
The sulfuric ester salt, as: sodium lauryl sulphate, polyoxyethylene lauryl alcohol sodium sulfovinate, glycerol monolaurate sodium sulfate etc.;
The higher fatty acids salt, as: sodium stearate, zinc stearate, aluminium distearate, 12 imido dipropionic acids, the inferior oxygen base of Adeps Bovis seu Bubali disodium beclomethasone, sodium laurate, enuatrol etc.;
Sulfonates, as: dodecylbenzene sodium sulfonate, succinate sodium sulfonate etc.;
Fatty acyl-peptide condensation substance class, as: sodium lauroyl sarcosine, oleoyl glycyl replace propylhomoserin sodium etc.;
Available cationic surfactant class, as:
Amine salt type cationic surfactant class, as: triethanolamine, triethanolamine stearate, Palmic acid triethanolamine etc.;
The quaternary ammonium salt cationic surfactant class, as: dodecyl front three ammonia chloride,
Dodecyl dimethyl benzyl ammonia chloride, myristoyl Propylamino dimethyl benzyl ammonia chloride etc.;
Available amphoteric surfactant class, as:
The amino acid type amphoteric surface active agent class: as: dodecyl base sodium propionate etc.;
Betaine type amphoteric surfac-tant's class: as: dodecyl dimethyl tertiary amine etc.;
Amine oxide type amphoteric surfactant class: as: alkyl dimethyl amine oxide, alkyl diethyl alcohol radical amine oxide etc.;
It is available that other is surfactant-based, as:
Aminoacid is surfactant-based, as: N-lauroyl glutamic acid dibutyl amide etc.;
The high molecular surfactant class, as: natural Sodium Alginate, pectic acid sodium etc.;
Semisynthetic sodium carboxymethyl cellulose, methylcellulose, hydroxyethyl-cellulose etc.;
Synthetic polyvinylpyrrolidone, polyvinyl alcohol, polyvinylether, polyacrylamide, polyoxyethylene-polyoxypropylene etc.;
The biosurfactant class: as: tragacanth, arabic gum, gelatin, agar, sodium alginate, pectin, apricot glue, agar, lecithin etc.;
Foam substrate also can adopt higher hydrocarbon, higher fatty acids, and high fatty alcohol, higher fatty acids fat etc., amount ranges 0.000-30.000% (w/w), as:
Higher hydrocarbons, as: liquid paraffin, vaseline etc.;
The higher fatty acids class, as: myristic acid, stearic acid, Palmic acid etc.;
The high fatty alcohol class, as: octadecanol, hexadecanol etc.;
Higher fatty acids lipid, as: tristerin, Oleum Ricini, vegetable oil, isopropyl myristate, Cera Flava, lanoline etc.;
Foam stabiliser amount ranges 0.000-15.000% (w/w), as: tetrapotassium pyrophosphate, glycerol, agar, karaya, triethanolamine oleate, dioctyl sodium sulphosuccinate, Palmic acid trimethyl-ethylene amine, polyvinylpyrrolidone etc.;
Essence amount ranges 0.000-0.500% (w/w), as: all kinds of essence such as Herba Menthae essence, jasmin essence etc.;
Antiseptic amount ranges 0.000-0.200% (w/w), as: sodium benzoate, potassium sorbate, methyl hydroxybenzoate, ethyl hydroxybenzoate, propylparaben, butoben, etc.;
Antioxidant amount ranges 0.000-0.500% (w/w) as: ethylenediaminetetraacetic acid, disodium EDTA, butyl hydroxy toluene, sodium sulfite, sodium pyrosulfite, potassium metabisulfite, vitamin C, vitamin E, beta-carotene, etc.;
Solvent load 40.000-90.000% (w/w), as: distilled water, glycerol, propylene glycol, ethanol etc.;
Propellant can be one or more blended chlorofluoromethane hydrocarbons and compressibility gas etc., its amount ranges 3.000-40.000% (w/w), as:
The chlorofluoromethane hydro carbons, as: isceon, dichlorodifluoromethane, dichlorotetra-fluoroethane, chlorodifluoroethane etc., or not chloride tetrafluoroethane, Difluoroethane etc.;
Hydrocarbon, as: iso-butane, propane etc.;
The compressibility gas, as: dimethyl ether, carbon dioxide, nitrogen, carbon dioxide etc.;
Medicine of the present invention shows through Mount Taishan hospital clinical observed result: cervicitis is treated in the policresulen foam aerosol, vaginitis is better than the spray effect.Concrete clinical test results is as follows:
1. material and method
1.1 case is selected and grouping
According to the principle of clinical design, adopt the method for contrast at random to study, respectively case is divided into corresponding treatment group and matched group with table of random number.Each 50 example of cervicitis patient wherein, age 25-45 year; Each 44 example of trichomonal vaginitis, age 23-48 year, each 46 example of colpitis mycotica, age 25-47 year, each 40 example of bacterial vaginitis, age 22-50 year.
1.2 Therapeutic Method:
(1) treatment group: adopt policresulen foam aerosol of the present invention; Specification: 15% (g/g), 35g/ bottle, each administration 0.7g, twice weekly.
Matched group: adopt the self-control Policresulen spraying agent, specification: 10% (g/g), the medication number of times is with policresulen foam aerosol group.
2. result
The total effective rate of policresulen foam aerosol group is than matched group height, and difference has statistical significance (P<0.01).
Grouping Case load Case load Curative effect Cure rate
Recovery from illness Produce effects Effectively Invalid
The treatment group Cervicitis 50 40 7 2 1 80%
Trichomonal vaginitis 44 31 6 5 2 70%
Colpitis mycotica 46 39 5 2 0 85%
Bacterial vaginitis 40 32 4 3 1 80%
Matched group Cervicitis 50 20 2 22 6 40%
Trichomonal vaginitis 44 16 6 21 1 36%
Colpitis mycotica 46 19 9 16 2 41%
Bacterial vaginitis 40 22 8 8 2 55%
Conclusion: policresulen foam aerosol treatment cervicitis, various vaginitis curative effect cure rate are significantly higher than the self-control Policresulen spraying agent, may can fully contact with tract mucosa and wrinkle wall in tract with foam aerosol, and the medicinal liquid holdup time is long relevant.Product of the present invention be a kind of collect imitate excellent, effect is fast, toxic and side effects novel gynecological external use medicine little, easy to use.
Another object of the present invention has provided a kind of preparation technology of policresulen foam aerosol, and this technology comprises the following steps:
(1) the policresulen raw material stirring is dissolved in one or more mixed solvents of distilled water, glycerol, propylene glycol or ethanol;
(2) add foaming agent, foam substrate, foam stabiliser, spice, antioxidant and antiseptic, stir and make its mix homogeneously;
(3) add the pH value regulator, the pH value of regulator solution is to 4-7.
(4) check the policresulen content of preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, charge into propellant and get final product.
Perhaps:
(1) solution A: take by weighing foaming agent (particularly being insoluble in water), foam stabiliser, antiseptic, antioxidant and foam substrate and mix, water-bath or slow fire are heated to and dissolve 60-70 ℃, mix, standby;
(2) solution B: the policresulen raw material is dissolved in the water of formula ratio 80%, and slowly is heated to the temperature of solution A; And solution A slowly added in the solution B while hot, stir while adding, make into emulsion;
When (3) emulsion temperature is reduced to below 40 ℃, add essence, pH value regulator, add water to full dose, stir;
(4) check policresulen content in the preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, the propellant that charges into recipe quantity gets final product.
Policresulen foam aerosol of the present invention has overcome the defective of solid preparation such as suppository and liquid preparation, and the foam form can make medicine be evenly distributed in tract, is coated with widely, and use feeling is more comfortable than spray simultaneously, and anelasticity is stronger than spray.And the technology content of foam aerosol is than spray with high content of technology that draws medicinal liquid by valve that with water is unique solvent, and it is more accurate to measure.Aerosol and spray contrast, because used propellant, not to promote by valve, but make particle diameter have only several microns droplet to become cystose to disperse by pressure, medicine can effectively arrive rapidly and infiltrate tract mucosa wrinkle wall, medicine is that the spray of unique solvent is faster at the auxiliary absorptance down of various fat-soluble adjuvants with water, use does not have drug contamination and cross-contamination, have curative effect fully, use hygienic and convenient, safe and reliable, no foreign body sensation, the patient is easy to accept and medicine is stablized, drug dose discharges accurately, and effect duration is long.
The specific embodiment
One, contains chlorofluoromethane hydro carbons aerosol
Embodiment 1
Component: weight: (%)
Policresulen 15.000
Sodium hydroxide 0.025
Tween-40 2.000
Sodium lauryl sulphate 4.000
Dioctyl sodium sulphosuccinate 0.100
Essence 0.025
Sodium pyrosulfite 0.020
Water 68.830
Dichlorodifluoromethane 10.000
Method:
(1) solution A: take by weighing Tween-40 20g, sodium lauryl sulphate 40g, dioctyl sodium sulphosuccinate 1g, sodium pyrosulfite 0.2g mixes, and water-bath or slow fire are heated to and dissolve 60-70 ℃, mix, and is standby;
(2) solution B: policresulen raw material 150g is dissolved in the 550g water, and slowly is heated to the temperature of solution A; And solution A slowly added in the solution B while hot, stir while adding, make into emulsion;
When (3) emulsion temperature is reduced to below 40 ℃, add essence 0.25g, sodium hydroxide 0.25g, add water to full dose, stir;
(4) check policresulen content in the preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, charge into the 100g dichlorodifluoromethane and get final product.
Embodiment 2
Component: weight: (%)
Policresulen 15.000
Sodium bicarbonate 0.035
Triethanolamine 1.000
Stearic acid 3.000
Essence 0.025
Glycerol 5.000
Ethyl hydroxybenzoate 0.150
Vitamin E 0.100
Water 63.690
Dichlorotetra-fluoroethane 4.000
Dichlorodifluoromethane 8.000
Method:
(1) solution A: take by weighing triethanolamine 10g, hard ester acid 30g, glycerol 50g, ethyl hydroxybenzoate 1.5g mixes, and water-bath or slow fire are heated to and dissolve 60-70 ℃, mix, and is standby;
(2) solution B: policresulen raw material 150g is dissolved in the 510g water, and slowly is heated to the temperature of solution A; And solution A slowly added in the solution B while hot, stir while adding, make into emulsion;
When (3) emulsion temperature is reduced to below 40 ℃, add essence 0.25g, sodium bicarbonate 0.35g, vitamin e1 .0g adds water to full dose, stirs;
(4) check policresulen content in the preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, charge into the 40g dichlorotetra-fluoroethane, the 80g dichlorodifluoromethane gets final product.
Embodiment 3
Component: weight: (%)
Policresulen 10.000
Sodium hydroxide 0.020
Palmic acid triethanolamine 3.000
Lanoline 0.200
Stearic acid 5.000
PVP 0.500
Essence 0.025
Propylparaben 0.100
Disodium EDTA 0.100
Water 69.955
Dichlorodifluoromethane 12.000
Method:
(1) solution A: take by weighing Palmic acid triethanolamine 30g, lanoline 2g, stearic acid 50g, PVP 5g, propylparaben 1g, disodium EDTA 1g mixes, and water-bath or slow fire are heated to and dissolve 60-70 ℃, mix, and is standby;
(2) solution B: policresulen raw material 100g is dissolved in the 560g water, and slowly is heated to the temperature of solution A; And solution A slowly added in the solution B while hot, stir while adding, make into emulsion;
When (3) emulsion temperature is reduced to below 40 ℃, add essence 0.25g, sodium hydroxide 0.20g, add water to full dose, stir;
(4) check policresulen content in the preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, charge into the 120g dichlorodifluoromethane and get final product.
Two, do not contain chlorofluoromethane hydro carbons aerosol
Embodiment 4
Component: weight: (%)
Policresulen 15.000
Sodium citrate 0.050
Tween-40 5.000
Arlacel-80 2.000
Dodecyl sodium sulfate 5.000
Essence 0.025
Water 44.925
Glycerol 20.000
Tetrafluoroethane 8.000
Method:
(1) solution A: take by weighing Tween-40 50g, Arlacel-80 20g, dodecyl sodium sulfate 50g, glycerol 200g mixes, and water-bath or slow fire are heated to and dissolve 60-70 ℃, mix, and is standby;
(2) solution B: policresulen raw material 150g is dissolved in the 360.25g water, and slowly is heated to the temperature of solution A; And solution A slowly added in the solution B while hot, stir while adding, make into emulsion;
When (3) emulsion temperature is reduced to below 40 ℃, add essence 0.25g, sodium citrate 0.5g, add water to full dose, stir;
(4) check policresulen content in the preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, charge into the 80g tetrafluoroethane and get final product.
Embodiment 5
Component: weight: (%)
Policresulen 15.000
Sodium hydroxide 0.025
Myij-45 4.000
Sodium lauryl sulphate 3.000
Essence 0.025
Water 59.950
Glycerol 10.000
Nitrogen 8.000
Method:
(1) solution A: take by weighing Myij-4540g, sodium lauryl sulphate 30g, glycerol 100g mixes, and water-bath or slow fire are heated to and dissolve 60-70 ℃, mix, and is standby;
(2) solution B: policresulen raw material 150g is dissolved in the 480g water, and slowly is heated to the temperature of solution A; And solution A slowly added in the solution B while hot, stir while adding, make into emulsion;
When (3) emulsion temperature is reduced to below 40 ℃, add essence 0.25g, sodium hydroxide 0.25g, add water to full dose, stir;
(4) check policresulen content in the preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, charge into 80g nitrogen and get final product.
Embodiment 6
Component: weight: (%)
Policresulen 15.000
Sodium hydroxide 0.025
Tween 80 5.000
Essence 0.025
Water 64.950
Glycerol 5.000
Propane 6.000
Iso-butane 4.000
Method:
(1) solution A: take by weighing tween 80 50g, glycerol 50g mixes, and water-bath or slow fire are heated to and dissolve 60-70 ℃, mix, and is standby;
(2) solution B: policresulen raw material 150g is dissolved in the 520g water, and slowly is heated to the temperature of solution A; And solution A slowly added in the solution B while hot, stir while adding, make into emulsion;
When (3) emulsion temperature is reduced to below 40 ℃, add essence 0.25g, sodium hydroxide 0.25g, add water to full dose, stir;
(4) check policresulen content in the preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, charge into 60g propane, the 40g iso-butane gets final product.

Claims (8)

1. policresulen foam aerosol is characterized in that this foam aerosol is made up of following component, by weight percentage:
Principal agent: policresulen 1%-40%
Pharmaceutic adjuvant: pH regulator agent 0%-5.0%, foaming agent 0.2%-30%, foam substrate 0%-30%, foam stabiliser 0%-15%, spice 0%-0.5%, solvent 40%-90%, antioxidant 0%-0.5%, antiseptic 0%-0.2%, propellant 3%-40%.
2. a kind of policresulen foam aerosol according to claim 1 is characterized in that wherein said pharmaceutic adjuvant foaming agent and foam substrate are non-ionic surface active agent, anion surfactant, cationic surfactant, amphoteric surfactant or other surfactant.
3. pharmaceutic adjuvant foaming agent in the policresulen foam aerosol according to claim 2 and foam substrate is characterized in that wherein said non-ionic surface active agent is: fatty acid esters of sorbitan: Arlacel-20, Arlacel-60, Arlacel-65, Arlacel-80 or Arlacel-85; Polyethylene glycol type: PEG-200, PEG-400, PEG-600 or PEG-1000; Polyoxyethylene sorbitan fatty acid ester: tween 20, Tween-40, Tween-60, Tween-65 or tween 80; Polyoxyethylene alkyl ether: Brij30 or polyoxyethylene stearyl alcohol ether; Polyoxyethylene fatty acid ester: Myij-45, Myij-52, Myij-53 or Myij-59; Polyol-based non-ionic surfactant: glycerol monolaurate or sorbitol lauric acid monoesters; The anion surfactant of selecting for use is: sulfuric acid: sodium lauryl sulphate, polyoxyethylene lauryl alcohol sodium sulfovinate or glycerol monolaurate sodium sulfate; Higher fatty acid salt: sodium stearate, zinc stearate, aluminium distearate, 12 imido dipropionic acids, the inferior oxygen base of Adeps Bovis seu Bubali disodium beclomethasone, sodium laurate or enuatrol; Sulfonate: dodecylbenzene sodium sulfonate or succinate sodium sulfonate; Fatty acyl-peptide condensation substance: sodium lauroyl sarcosine or oleoyl glycyl are for propylhomoserin sodium; The cationic surfactant of selecting for use is: amine salt type cationic surfactant: triethanolamine, triethanolamine stearate or Palmic acid triethanolamine; Quaternary ammonium salt cationic surfactant: dodecyl front three ammonia chloride, dodecyl dimethyl benzyl ammonia chloride or myristoyl Propylamino dimethyl benzyl ammonia chloride; The amphoteric surfactant of selecting for use is: amino acid type amphoteric surface active agent: dodecyl base sodium propionate; Betaine type amphoteric surfac-tant: dodecyl dimethyl tertiary amine; Amine oxide type amphoteric surfactant: alkyl dimethyl amine oxide or alkyl diethyl alcohol radical amine oxide; Other surfactant of selecting for use: aminoacid is surfactant: N-lauroyl glutamic acid dibutyl amide; High molecular surfactant: natural Sodium Alginate or pectic acid sodium; Semisynthetic sodium carboxymethyl cellulose, methylcellulose or hydroxyethyl-cellulose; Synthetic polyvinylpyrrolidone, polyvinyl alcohol, polyvinylether, polyacrylamide or polyoxyethylene-polyoxypropylene; Biosurfactant: tragacanth, arabic gum, gelatin, agar, sodium alginate, pectin, apricot glue, agar or lecithin; Foam substrate also can adopt higher hydrocarbon, higher fatty acids, high fatty alcohol or higher fatty acids fat, higher hydrocarbon: liquid paraffin or vaseline; Higher fatty acids: myristic acid, stearic acid or Palmic acid; High fatty alcohol: octadecanol or hexadecanol; Higher fatty acids fat: tristerin, Oleum Ricini, vegetable oil, isopropyl myristate, Cera Flava or lanoline.
4. a kind of policresulen foam aerosol according to claim 1 is characterized in that wherein said foam stabiliser is tetrapotassium pyrophosphate, glycerol, agar, karaya, triethanolamine oleate, dioctyl sodium sulphosuccinate, Palmic acid trimethyl-ethylene amine or polyvinylpyrrolidone.
5. a kind of policresulen foam aerosol according to claim 1 is characterized in that wherein said essence is Herba Menthae essence or jasmin essence; Antiseptic is sodium benzoate, potassium sorbate, methyl hydroxybenzoate, ethyl hydroxybenzoate, propylparaben or butoben; Antioxidant is ethylenediaminetetraacetic acid, disodium EDTA, butyl hydroxy toluene, sodium sulfite, sodium pyrosulfite, potassium metabisulfite, vitamin C, vitamin E or beta-carotene; Solvent is distilled water, glycerol, propylene glycol or ethanol.
6. a kind of policresulen foam aerosol according to claim 1 is characterized in that wherein said propellant is one or more blended chlorofluoromethane hydrocarbon and compressibility gases: chlorofluoro-alkane: isceon, dichlorodifluoromethane, dichlorotetra-fluoroethane or chlorodifluoroethane; Or not chloride tetrafluoroethane or Difluoroethane; Hydrocarbon: iso-butane or propane; Compressibility gas: dimethyl ether, carbon dioxide, nitrogen or carbon dioxide.
7. the preparation technology of a policresulen foam aerosol is characterized in that this technology comprises the following steps:
(1) the policresulen raw material stirring is dissolved in one or more mixed solvents of distilled water, glycerol, propylene glycol or ethanol;
(2) add foaming agent, foam substrate, foam stabiliser, spice, antioxidant and antiseptic, stir and make its mix homogeneously;
(3) add the pH value regulator, the pH value of regulator solution is to 4-7;
(4) check the policresulen content of preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, charge into propellant and get final product.
8. the preparation technology of a policresulen foam aerosol is characterized in that this technology comprises the following steps:
(1) solution A: take by weighing foaming agent, the foaming agent, foam stabiliser, antiseptic, antioxidant and the foam substrate that particularly are insoluble in water are mixed, and water-bath or slow fire are heated to and dissolve 60-70 ℃, mix, and is standby;
(2) solution B: the policresulen raw material is dissolved in the water of formula ratio 80%, and slowly is heated to the temperature of solution A; And solution A slowly added in the solution B while hot, stir while adding, make into emulsion;
When (3) emulsion temperature is reduced to below 40 ℃, add essence, pH value regulator, add water to full dose, stir;
(4) check policresulen content in the preparating liquid, medicinal liquid is poured in the pressure vessel, add cap valve and sealing, the propellant that charges into recipe quantity gets final product.
CN 200510023561 2005-01-25 2005-01-25 Policresulen foam aerosol and its prepn process Pending CN1810256A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200510023561 CN1810256A (en) 2005-01-25 2005-01-25 Policresulen foam aerosol and its prepn process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200510023561 CN1810256A (en) 2005-01-25 2005-01-25 Policresulen foam aerosol and its prepn process

Publications (1)

Publication Number Publication Date
CN1810256A true CN1810256A (en) 2006-08-02

Family

ID=36843469

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200510023561 Pending CN1810256A (en) 2005-01-25 2005-01-25 Policresulen foam aerosol and its prepn process

Country Status (1)

Country Link
CN (1) CN1810256A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100396290C (en) * 2006-11-03 2008-06-25 段炬红 External use anti-bacteria foaming agent for gynecology
CN102018973A (en) * 2010-11-23 2011-04-20 大连三达奥克化学股份有限公司 Sterilizing odor-absorbing deodorant and preparation method
CN108888553A (en) * 2018-07-24 2018-11-27 上海韵宜生物科技有限公司 A kind of perfume atmosphere is spraying and preparation method thereof
CN108938674A (en) * 2017-05-27 2018-12-07 福建省山河药业有限公司 Purposes of the Lyopgized Nocardia rubra-cell Wall Skeleton in preparation treatment cutaneous lesions drug
CN109310633A (en) * 2016-06-16 2019-02-05 宝丽制药股份有限公司 Foam, the composition and its evaluation method for sieving infusion

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100396290C (en) * 2006-11-03 2008-06-25 段炬红 External use anti-bacteria foaming agent for gynecology
CN102018973A (en) * 2010-11-23 2011-04-20 大连三达奥克化学股份有限公司 Sterilizing odor-absorbing deodorant and preparation method
CN102018973B (en) * 2010-11-23 2013-10-30 大连三达奥克化学股份有限公司 Sterilizing odor-absorbing deodorant and preparation method
CN109310633A (en) * 2016-06-16 2019-02-05 宝丽制药股份有限公司 Foam, the composition and its evaluation method for sieving infusion
CN109310633B (en) * 2016-06-16 2021-10-22 宝丽制药股份有限公司 Composition for foam and foam screening agent and evaluation method thereof
CN108938674A (en) * 2017-05-27 2018-12-07 福建省山河药业有限公司 Purposes of the Lyopgized Nocardia rubra-cell Wall Skeleton in preparation treatment cutaneous lesions drug
CN108888553A (en) * 2018-07-24 2018-11-27 上海韵宜生物科技有限公司 A kind of perfume atmosphere is spraying and preparation method thereof

Similar Documents

Publication Publication Date Title
CN1050514C (en) Antiallergic composition for ophthalmic or nasal use
CN1262274C (en) Complexes of phosphate derivatives
KR20200039677A (en) Topical formulations comprising a combination with montelukast and mussel adhesion proteins
CN1810256A (en) Policresulen foam aerosol and its prepn process
WO2019228307A1 (en) New pharmaceutical use
CN1173868A (en) Thienopyrimidine derivatives, their production and use
CN1709445A (en) Tibetan medicine for major functions of acute-chronic sprain-contusion, rheumatism, rheumatoid diseases, and its preparing method
CN101066260A (en) Coenzyme Q10 emulsion and its freeze dried prepn and their prepn process
CN102379879B (en) Liranaftate and mometasone furoate containing locally applied compound pharmaceutical composition
CN1308033C (en) Medicine for decreasing vagina acidity and treating vaginitis, use thereof
CN1555252A (en) Topical composition for follicular delivery of an ornithine decarboxylase inhibitor
CN1224424C (en) Thermosetting medical carrier composition with mucosa adsorption
CN1899600A (en) Antibiotic peptide spray film forming agent and its preparing method
CN1438886A (en) Ophthalmic solution
CN1660343A (en) Combination of medication of containing eucalyptol, limonene and alpha pinene and application
EP3908284A1 (en) New formulations containing leukotriene receptor antagonists
CN1813724A (en) Liranaftate paste and its preparing method
CN1803185A (en) Compound zedoary turmeric oil gelata and its preparing method
CN1850086A (en) Use of levo morpholine nidazole for preparing medicine for antiparasitic infection
CN1284864A (en) Novel formulation for use in pain management
CN1399542A (en) Pharmaceutical carrier formulation
CN1210034C (en) Medicinal composition for treating psoriasis
CN100341495C (en) Solid dispersion and preoral combination of glibenclamide and preparation method
CN1398182A (en) Dual inhibitors of cholestery lester and wax ester synthesis for sebaceous gland disorders
CN1166353C (en) Amphoteric lipids dispersion body

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication