US20100322875A1 - Silicone scar treatment preparation - Google Patents

Silicone scar treatment preparation Download PDF

Info

Publication number
US20100322875A1
US20100322875A1 US12/487,489 US48748909A US2010322875A1 US 20100322875 A1 US20100322875 A1 US 20100322875A1 US 48748909 A US48748909 A US 48748909A US 2010322875 A1 US2010322875 A1 US 2010322875A1
Authority
US
United States
Prior art keywords
volatile
preparation
coagent
active component
siloxane matrix
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.)
Abandoned
Application number
US12/487,489
Other languages
English (en)
Inventor
Paul Guilbaud
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.)
Advanced Bio Technologies Inc
Original Assignee
Advanced Bio Technologies Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43354570&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20100322875(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Advanced Bio Technologies Inc filed Critical Advanced Bio Technologies Inc
Priority to US12/487,489 priority Critical patent/US20100322875A1/en
Priority to NZ597335A priority patent/NZ597335A/en
Priority to ES10790269T priority patent/ES2781649T3/es
Priority to CN201080033062.2A priority patent/CN102802572B/zh
Priority to HRP20200560TT priority patent/HRP20200560T1/hr
Priority to KR1020127001182A priority patent/KR101543060B1/ko
Priority to AU2010263031A priority patent/AU2010263031B2/en
Priority to MX2011013965A priority patent/MX2011013965A/es
Priority to RU2011152511/15A priority patent/RU2530657C2/ru
Priority to EP10790269.4A priority patent/EP2442771B1/en
Priority to HUE10790269A priority patent/HUE048612T2/hu
Priority to CA2765964A priority patent/CA2765964C/en
Priority to SG2011093523A priority patent/SG176894A1/en
Priority to PT107902694T priority patent/PT2442771T/pt
Priority to SI201032005T priority patent/SI2442771T1/sl
Priority to PCT/US2010/039181 priority patent/WO2010148310A1/en
Priority to PL10790269T priority patent/PL2442771T3/pl
Priority to LTEP10790269.4T priority patent/LT2442771T/lt
Priority to BRPI1009689-2A priority patent/BRPI1009689B1/pt
Priority to DK10790269.4T priority patent/DK2442771T3/da
Priority to JP2012516337A priority patent/JP5740398B2/ja
Assigned to ADVANCED BIO-TECHNOLOGIES, INC. reassignment ADVANCED BIO-TECHNOLOGIES, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GUILBAUD, PAUL
Publication of US20100322875A1 publication Critical patent/US20100322875A1/en
Assigned to CLYDESDALE BANK PLC reassignment CLYDESDALE BANK PLC SECURITY AGREEMENT Assignors: ADVANCED BIO-TECHNOLOGIES, INC.
Priority to IL217056A priority patent/IL217056A/en
Priority to ZA2012/00353A priority patent/ZA201200353B/en
Priority to US13/548,899 priority patent/US8802133B2/en
Priority to US14/322,584 priority patent/US9339546B2/en
Priority to JP2015090815A priority patent/JP6016974B2/ja
Assigned to BANK OF SCOTLAND PLC reassignment BANK OF SCOTLAND PLC SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ADVANCED BIO-TECHNOLOGIES, INC.
Priority to US15/089,694 priority patent/US9795706B2/en
Priority to CY20201100176T priority patent/CY1123227T1/el
Assigned to ADVANCED BIO-TECHNOLOGIES, INC. reassignment ADVANCED BIO-TECHNOLOGIES, INC. RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: BANK OF SCOTLAND PLC
Abandoned legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/695—Silicon compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25—Silicon; Compounds thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L26/00—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0009—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form containing macromolecular materials
    • A61L26/0019—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form containing macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/12—Ketones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
    • A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/60—Salicylic acid; Derivatives thereof
    • A61K31/618—Salicylic acid; Derivatives thereof having the carboxyl group in position 1 esterified, e.g. salsalate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/24—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing atoms other than carbon, hydrogen, oxygen, halogen, nitrogen or sulfur, e.g. cyclomethicone or phospholipids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A61K8/345—Alcohols containing more than one hydroxy group
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35—Ketones, e.g. benzophenone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37—Esters of carboxylic acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585—Organosilicon compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/895—Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L26/00—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0004—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form containing inorganic materials
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L26/00—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0009—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form containing macromolecular materials
    • A61L26/0052—Mixtures of macromolecular compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L26/00—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0061—Use of materials characterised by their function or physical properties
    • A61L26/0066—Medicaments; Biocides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L26/00—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0061—Use of materials characterised by their function or physical properties
    • A61L26/008—Hydrogels or hydrocolloids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L26/00—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0095—Composite materials, i.e. containing one material dispersed in a matrix of the same or different material
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/18—Antioxidants, e.g. antiradicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59—Mixtures
    • A61K2800/592—Mixtures of compounds complementing their respective functions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59—Mixtures
    • A61K2800/594—Mixtures of polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/95—Involves in-situ formation or cross-linking of polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0014—Skin, i.e. galenical aspects of topical compositions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
    • A61L2300/41—Anti-inflammatory agents, e.g. NSAIDs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2430/00—Materials or treatment for tissue regeneration
    • A61L2430/34—Materials or treatment for tissue regeneration for soft tissue reconstruction

Definitions

  • Lacerations and other wounds which compromise the integrity of the skin are common enough that most people have experienced them, from the mundane, such as a skinned knee, to the life-threatening, such as a stab wound or a serious burn. Many breaks to the skin raise the possibility of disfigurement through scarring.
  • scar tissue is a defensive response to an injury in that it repairs a breach in the skin, eliminating a site of potential infection and reinjury.
  • the rampant formation of scar tissue can result in a tough dermal surface lacking the color or consistency of the surrounding skin. Because the flexibility and elasticity of scar tissue differs from that of natural skin, scar tissue can ultimately limit the lives of those who are affected.
  • Scar tissue is generally tougher than the skin tissue in the surrounding area. This is especially true of scar tissue where the skin is subjected to deformation and elastic stresses, such as on or behind the knee or elbow. Such areas can be subject to tear at the skin/scar tissue border.
  • Scar tissue particularly new scars, covering areas having natural grooves to facilitate bending, such as the lines on the palms of the hands, are often weak at these flex lines. Stretching caused by opening and closing the hand can rupture the scar tissue at these natural grooves, resulting in an accumulation of scar tissue on either side of the groove, causing newly formed tissue in the groove even to have even greater susceptibility to tearing with hand motion.
  • the natural topography of a wound site can increase the likelihood of retearing, resulting in long healing times.
  • Some preparations for treating wounds are formulated to have a positive effect on the properties of the scar tissue formed during healing.
  • some wound dressings have functions such as reducing wound drying and preventing ultraviolet light exposure.
  • Such formulations can prevent repeated cracking and drying, resulting in, among other things, the formation of scar tissue having improved flexibility, elasticity and color characteristics relative to scar tissue formed in the absence of the formulation.
  • Gels have properties which make them suitable as wound dressings. They can cool wounds by contacting them directly, yet keep them free from contamination. Another useful property of gels is their consistency: many gels are similar to skin in elasticity and deformability, and they can bend, bunch and stretch with the skin and tissue surfaces to which they are attached without causing tearing or stress at the site of the healing wound.
  • gels can dry out rapidly with time, break down structurally and/or chemically, and they generally must be reapplied, which can be a painful process for the patient, especially if the consistency of the dressing has become stiff due to drying. Some gels can absorb moisture, developing a soft or liquid consistency. Once the gel consistency has been compromised, the potential for bacterial infection increases.
  • Siloxane gels have been found to be generally superior to other types of gel products in the treatment of wounds and scar tissue. Siloxane gels function by forming a silicone-based polymer matrix over a wound site.
  • Polymer precursors such as dimethicone, dimethicone crosspolymer, and other siloxanes, are contained in a spreadable preparation which is applied to a wound site.
  • Some polymer precursor formulations include fumed silica.
  • the preparation also contains a volatile component which begins to evaporate upon the application of the preparation to a wound site.
  • the polymer matrix begins to form upon the evaporation of volatile compounds from the spreadable preparation.
  • the preparations are, in many cases, thixotropic, particularly if the formulation contains fumed silica.
  • Thixotropic formulations change from a stiff consistency to a fluid-like consistency upon the application of stress, such as application to a wound, and revert to a stiffer, less fluid consistency once the stress is removed. This property gives siloxane gel precursor formulations the ability to spread easily into a relatively thin layer over a wound and remain in place without oozing away from the wound site, all with a minimum of stress and shear at the wound site.
  • siloxane gels Another advantage of siloxane gels is that some have been shown to have a beneficial effect on the properties of scar tissue as it is being formed, diminishing the degree of scarring and improving the texture of scar tissue that does form, such that the ultimate appearance of the healed wound is more like surrounding skin. For instance, some siloxane preparations, when applied to developing or newly formed scar tissue, have demonstrated the ability to cause excellent fading, and even near disappearance of the scar with constant application.
  • the resultant gel generally has the ability to retain its consistency over time. Furthermore, the unapplied product can be easier to store and use than other types of gels because it can be applied as siloxane polymer matrix precursors which do not “set” until after application.
  • siloxane gels have such beneficial effects upon developing scar tissue, it is desirable that such a preparation also have the ability to include additives which impart additional useful functions to the gel.
  • silicone-based formulations demonstrate superior scar reduction properties, developing scar tissue is susceptible to change in color and/or texture, as well as other types of damage, such as thermal damage, upon exposure to ultraviolet and other wavelengths of radiation. It is thus desirable to incorporate sun screening compounds into the formulation which will be retained upon matrix formation.
  • burns and other injuries which are best served by the topical application of gels can continue to be very painful, even after the wound has begun to scar over.
  • matrix forming preparations can prevent the topical application of pain relievers: unlike bandage-type coverings, most topical gels cannot be simply lifted and resituated. It can thus desirable that matrix forming preparations comprise at least one pain alleviating compound.
  • siloxane matrix precursors Unfortunately, the use of siloxane matrix precursors has severely limited the variety of additives which can be included in silicone wound dressings. Many desirable additives are not readily solvated in the mix of matrix precursors, such as dimethicone and other siloxanes which comprise the spreadable preparation. For example, many effective and commonly used sunscreen additives, such as, for example, Octocrylene, Octinoxate, Octisalate and Oxybenzone may not sufficiently dissolve in the pre-polymerized preparation. Other examples of desirable additives having poor solubility in the pre-polymerization preparation include cortisone-type compounds which reduce pain and inflammation, such as, for example, Hydrocortisone acetate.
  • the insoluble active which is insoluble in the matrix precursors without the coagent, remains incorporated within the matrix during its formation, even though the volatile coagent does not remain complexed to the active, but disjoins and is lost to evaporation.
  • the active can have mobility within the matrix resulting in the ability to migrate through the gel to the wound site, as evidenced by the effectiveness of analgesic additives.
  • the vapor pressure of the volatile coagent would be reduced upon complexing with the active, and by being incorporated, with the active, within the developing siloxane matrix. Yet it retains sufficient vapor pressure such that it can evaporate away cleanly.
  • volatile coagents such as those identified herein, permits the incorporation of diverse additive types into silicone matrix-forming formulations.
  • the present invention enables the incorporation of insoluble actives into a mixture of silicon precursors, greatly extending the usefulness of siloxane gel wound healing technology.
  • FIG. 1 Drying test results. The lowest, middle and highest curves graphically depict the drying results of the sunscreen, analgesic and control gels respectively.
  • the matrix forming composition of the present invention comprises siloxane matrix precursors, a volatile component, an active component, and a volatile coagent.
  • the volatile component and volatile coagent partially or fully evaporate from the composition once the composition is applied to a wound or scar site, leaving behind 1) components which participate in matrix formation as well as 2) one or more active components which reside in the matrix.
  • the components which participate in the matrix formation are one or more siloxanes, one or more of which have organic characteristics, i.e., comprising organic components, such as bearing hydrocarbyl groups.
  • a polymer matrix can be formed with the use of other polydimethyl siloxanes instead of or in addition to dimethicone and dimethicone crosspolymer.
  • polymerization involving other polysiloxanes, and in particular, other dialkylpolysiloxanes can form a matrix exhibiting the advantages of the present invention when used with the volatile components, volatile coagents and actives listed below.
  • Such matrices are within the ambit of the present invention.
  • the fumed silica gives the prepolymerized composition a thixotropic consistency. Fumed silica also participates structurally in the gel, but its contribution to or participation in the polymerization process, if any, is unclear.
  • the matrix precursors in the preparation generally can be stored at room temperature (25 K) for extended periods of time, such as 1, 2, 4, 6, 12 months or even longer without undergoing significant polymerization. It is preferred that the matrix precursors comprise a crosspolymer component, such as dimethicone crosspolymer, as well as dimethicone.
  • the siloxane component is present in weight percentages in the range of from about 25 to 60 wt %. In preferred embodiments, the siloxane component is present in the range of from 30 to 50 wt %. In more preferred embodiments, the siloxane component is present in amounts in the range of from about 35 to 45 wt %.
  • the preferred siloxane component is dimethicone.
  • the cross polymer component is preferably present in amounts in the range of from about 0.5 to about 8 wt %, and more preferably in the range of from about 1.5 to 5 wt %.
  • the composition of the present invention comprises a volatile component (distinguished from volatile coagent, discussed below).
  • the volatile component generally begins to vaporize upon application of the composition to the wound site.
  • the formation of the siloxane matrix can begin immediately upon commencement of evaporation, proceeding with further evaporation.
  • the siloxane matrix begins to form appreciably at some time during the evaporation of the volatile component, with only negligible formation prior to the time.
  • the volatile component has limited or no participation in polymerization, but readily solvates or dissolves in the matrix precursors.
  • Preferred examples are volatile siloxane compounds which have little or no participation as reactants in siloxane polymerization.
  • cyclic siloxanes generally exhibit good solvation and volatility characteristics in siloxanes, and their participation in matrix formation is generally relatively low due to the fact that all silane oxygen atoms are unavailable for polymerization. More preferred is a cyclopentasiloxane which bears constituents comprising hydrogen or hydrocarbyl groups of less than four carbon atoms. Constituents comprising hydrogen or hydrocarbyl groups of one carbon atom are most preferred.
  • Preferred amounts of volatile component are in the range of from about 12 to about 45 wt %. More preferred are amounts in the range of from about 15 to 28 wt %, most preferred are amounts in the range of from about 20 to 25 wt %.
  • the volatile component is preferably present in amounts such that the volatile component is more than 50 percent evaporated after 15 minutes at one or more temperatures in the range of from about 30 to 40 C.
  • the volatile component functions such that upon its partial or entire evaporation, the polymer matrix begins to form.
  • the presence of the volatile can act to fully or partially inhibit the polymerization process, such that upon beginning to volatilize, the rate of polymerization increases.
  • the composition of the present invention is not limited to the compounds specifically described above, but broadly comprises compounds which can be used in relative amounts such that they fully or partially inhibit the formation of the siloxane matrix prior to wound application, but begin to evaporate upon the application of the preparation to a wound, having fully or partially evaporated by the completion of siloxane matrix formation.
  • the volatile component evaporation plateaus with time prior to complete evaporation.
  • the evaporation of the volatile component continues after the siloxane matrix is completely formed. It is preferable that the volatile component evaporate to within less than 5% of its original weight (storage concentration) within 3 hours, but in some embodiments, the volatile evaporates to within greater than 10, 20 and 30% of its original weight within 3 hours.
  • the weight percent of the volatile component concentration prior to use and during storage is in the range of from about 5 to about 40%. In other embodiments, the weight percent of the volatile component concentration prior to use and during storage is in the range of from about 15 to about 35%, In preferred embodiments, the volatile component concentration prior to use and during storage is in the range of from about 18 to about 30%.
  • the wound healing preparation of the present invention comprises a volatile coagent.
  • the volatile coagent aids in solvating the active in the matrix precursors. It has been found that certain compounds which function as volatile coagents with certain actives have the ability to volatilize appreciably despite the facts that they are chemically associated with the active which is surrounded by a growing matrix, and which itself is not ultimately volatilized.
  • the active is an ultraviolet absorbing compound comprising at least one aromatic ring.
  • the active comprises one or more Escalol compounds, available from ISP Chemicals, and the volatile coagent is an ester of 1) a linear acid having a carbon chain length in the range of from about 6 to 13 carbon atoms and 2) methanol, ethanol, or a secondary alcohol having a total carbon content in the range of from about 3 to about 8 carbon atoms.
  • the volatile coagent is a myristate ester of methanol, ethanol, or a secondary alcohol having a total carbon content in the range of from about 3 to about 8 carbon atoms, and the active is an Escalol compound.
  • the volatile coagent is isopropyl myristate
  • the active is Octocrylene (ISP Escalol 597), Octinoxate (ISP Escalol 557), Octisalate (ISP Escalol 587), or Oxybenzone (ISP Escalol 567).
  • the sunscreen active or actives present in the formulation can be present in a combined amount in the range of from about 5 to 40 wt %, with amounts in the range of from 15 to 35 wt % being more preferable. In some embodiments, the sunscreen actives are present in amounts in the range of from 25 to 30 wt %.
  • the volatile coagent preferably comprises an ester of 1) a linear acid having a carbon chain length in the range of from about 6 to 13 carbon atoms and 2) methanol, ethanol, or a secondary alcohol having a total carbon content in the range of from about 3 to about 8 carbon atoms; and more preferably isopropyl myristate; a glycol comprised of a linear chain of three or more carbons and one or more hydroxyl groups; and wherein all hydroxyl groups are on adjacent carbons including an end carbon; and more preferably pentylene glycol; or a substituted or unsubstituted isosorbide; and preferably Dimethyl isosorbide.
  • the active is a steroid compound
  • the volatile coagent is a glycol comprised of a linear chain of three or more carbons and one or more hydroxyl groups; and wherein all hydroxyl groups are on adjacent carbons including an end carbon.
  • the volatile coagent is a glycol comprised of a linear chain of from about 3 to 7 carbons and two hydroxyl groups, one attached to each terminal carbon, and the active is a steroid compound.
  • the volatile coagent is pentylene glycol, and the active is dihydrocortisone acetate.
  • the active is a steroid compound, and the volatile coagent comprises a substituted or unsubstituted isosorbide.
  • the active is a cortisone, and the volatile coagent comprises a disubstituted isosorbide.
  • the volatile coagent is dimethyl isosorbide and the active is dihydrocortisone acetate.
  • the active is a hydrocortisone compound and actives comprising both a glycol compound and an isosorbide compound are used.
  • the active is Hydrocortisone acetate.
  • the steroid compound is preferably present in an amount which is in the range of from 0.1 to 8 wt %. More preferred is an amount in the range of from about 0.5 to 3 wt %.
  • the glycol and the isosorbide are present in amounts in the range of from 5 to 40 wt % percent (combined weight, if both are present). In preferred embodiments, both are present, each in amounts in the range of from 5 to 50 wt %. In other embodiments, the glycol and the isosorbide are present in amounts in the range of from 0 to 15 wt %, with a total weight % in the range of from 10 to 25.
  • glycol and isosorbide components can be used with sunscreen actives instead of isopropyl myristate if a deeper penetration is desired.
  • the composition of the present invention can be prepared by mixing together the matrix precursors such as, for example, fumed silica, dimethicone and dimethicone cross polymer; and the volatile component, such as, for example, cyclopentasiloxane.
  • the foregoing compounds can be mixed together to form a siloxane base.
  • the active component is generally mixed with the volatile coagent to form a mixture which is added to the siloxane base before introducing it into the balance of the composition.
  • the base contains only cyclopentasiloxane and dimethicone crosspolymer.
  • the mixture is then combined with the base.
  • Fumed silica was added next to the overall mixture using a high-shear mixing process (an eductor). The dimethicone is added last, and the mixture is mixed until homogeneous, resulting in a viscous, opaque gel, with no lumps or visible separation.
  • the formulation has an SPF rating of 30 or higher.
  • a drying test was performed (time take to reach a constant weight) (see FIG. 1 ), and the formulation dried in essentially the same amount of time as the formulation in the absence of the Octocrylene, Octinoxate, Octisalate, Oxybenzone and isopropyl myristate (control formulation). The addition of the sunscreen additives does not appreciably slow the drying of the formulation.
  • the “1% Hydrocortisone Acetate Silicone Scar Gel,” described in Example 2, above, contains the ingredients of the Control Formula Scar Gel” with the addition of 1% w/w of Hydrocortisone Acetate, an FDA approved anti-inflammatory agent. Also, 5.0% of Propylene Glycol (a humectant and skin conditioning agent) and 10.0% of Dimethyl Isosorbide, a solvent which is a dimethyl ether of an anhydride of an isomer of sorbitol, used for better skin penetration of the Hydrocortisone Acetate.
  • n is the weight recorded at times of 5, 10, 40, 60, 180, 240, 300 and 1440 minutes.
  • the Percent Weight Loss values were averaged for each of the three products at the appropriate time interval (5, 10, 40, 60, 180, 240, 300 and 1440) and displayed in graphically, see FIG. 1 .
  • the test product had an expected SPF of 30 and the HMS standard sunscreen had an expected SPF of 4.
  • UV doses ranging from 0.76 to 1.32 times the product of the MED and 30 were administered to the test sunscreen-protected area.
  • UV doses ranging from 0.64 to 1.56 times the product of the MED and 4 were administered to the HMS standard sunscreen-protected area.
  • a series of UV doses were also administered to a second unprotected site.
  • the MED was determined for the sunscreen-protected sites and the unprotected site.
  • the SPF of each sunscreen was calculated as the ratio of the MED for each sunscreen-protected site to the final MED.
  • t upper 5% of student's t distribution
  • s Standard Deviation
  • n Number of Subjects
  • the SPF of the HMS standard sunscreen must fall within the standard deviation range of the expected SPF (i.e. 4.47 ⁇ 1.279) and the 95% confidence interval for the mean SPF of the HMS standard sunscreen must contain the value 4.
  • Protocol Deviations were reported for Subject 04. The Repeat MED and Final SPF evaluations were performed outside of the 22 to 24 hour time frame (21:50 and 21:54 respectively). This Protocol Deviation did not affect study results.
  • Subject 03 was disqualified during Day 1 procedures for a prohibited medication and Subjects 05 and 06 were disqualified due to procedural error. Data for these subjects were not included in this report.
  • test product Reference Test Formulation
  • test product would be likely to meet the FDA Final Monograph requirements for labeling as Static SPF 30+. 1
  • the FDA Final Monograph1 describes the procedures for determining the Static sun protection factor.
  • the Static SPF is defined by the ratio of the minimal erythema dose of ultraviolet radiation for sunscreen-protected skin to that for unprotected skin.
  • the minimal erythema dose (MED) is the dose of ultraviolet (UV) radiation that produces mild erythema (sunburn) with clearly defined borders, 22 to 24 hours after administration.
  • Timed UV radiation doses were administered using a xenon arc lamp that simulated solar radiation.
  • the technician monitored the output of the solar simulator using a calibrated radiometer to insure that the erythemally effective irradiance was constant. Readings of erythemally effective irradiance were recorded.
  • the objective of this test was to measure the Static SPF of an over-the-counter (OTC) sunscreen-containing formula according to the FDA Final Monograph 1 .
  • OTC over-the-counter
  • UV doses A timed series of 5 UV doses, increasing in 25 percent increments, were administered to the mid-back, just below the shoulder blades and above the belt-line. UV doses for the MED, the time doses were completed and lamp readings were recorded on the MED form.
  • UV exposure Subjects were instructed to avoid UV exposure, photosensitizers, analgesics, antihistamines and anti-inflammatory medications and to return to the testing laboratory 22 to 24 hours after completion of UV doses.
  • the MED was determined as the first exposure site in the series that produces an erythema grade of at least 2 (Mild erythema with clearly defined borders). The progression of erythema grades was to be consistent with the UV doses administered.
  • the subject was to be considered likely Type IV and not qualified for the study. In this case the subject was to be dropped from the study and replaced. Grades for each UV-exposed site, any comments and the evaluation time were recorded.
  • the study technician drew 50 cm 2 rectangles in the designated locations on the subject's back between the belt-line and shoulder blades using a template and an indelible marker. The technician then applied 100 mg of test product in its designated rectangle and 100 mg of the HMS standard in an adjacent rectangle.
  • the sunscreens were applied by “spotting” the material across the area and gently spreading, using a finger cot, until a uniform film is applied to the entire area.
  • the technician administered a series of 7 progressively increasing, timed UV doses to the sites treated with the test products.
  • the dose series was determined by the product of the expected SPF of each test product, the subject's MED and the following number:
  • the technician administered 7 progressively increasing timed UV doses to the HMS standard site.
  • the dose series was determined by the product of the HMS standard SPF (4), the subject MED and the following numbers:
  • the technician administered a timed series of 5 UV doses, increasing by 25 percent increments, to an unprotected area of the mid-back.
  • the series of 5 doses included the original MED in the center as follows:
  • UV doses for the repeat MED, time completed and the lamp effective irradiance were recorded.
  • the technician instructed subjects to return to the testing laboratory for evaluation within 22 to 24 hours after completion of the UV doses for the static SPF, HMS standard SPF and the repeat MED.
  • the technician determined the repeat MED as above and computed the SPF values for each subject.
  • the final MED was to be the repeat MED, unless the repeat MED could not be determined. In that case the initial MED would be used as the final MED.
  • SPF values were calculated as the ratio of the MED for sunscreen-protected sites to the final MED.
  • the labeled SPF were calculated as follows, based on 20 subjects:
  • the SPF of the HMS standard sunscreen must fall within the standard deviation range of the expected SPF (i.e. 4.47 ⁇ 1.279) and the 95% confidence interval for the mean SPF of the HMS standard sunscreen must contain the value 4.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Birds (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Biochemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Composite Materials (AREA)
  • Dispersion Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Silicon Polymers (AREA)
  • Cosmetics (AREA)
  • Materials For Medical Uses (AREA)
US12/487,489 2009-06-18 2009-06-18 Silicone scar treatment preparation Abandoned US20100322875A1 (en)

Priority Applications (28)

Application Number Priority Date Filing Date Title
US12/487,489 US20100322875A1 (en) 2009-06-18 2009-06-18 Silicone scar treatment preparation
JP2012516337A JP5740398B2 (ja) 2009-06-18 2010-06-18 瘢痕治療用シリコーン製剤
PL10790269T PL2442771T3 (pl) 2009-06-18 2010-06-18 Silikonowy preparat do leczenia blizn
LTEP10790269.4T LT2442771T (lt) 2009-06-18 2010-06-18 Silikoninis randų gydymo preparatas
CN201080033062.2A CN102802572B (zh) 2009-06-18 2010-06-18 硅氧烷瘢痕治疗制剂
HRP20200560TT HRP20200560T1 (hr) 2009-06-18 2010-06-18 Pripravak za liječenje ožiljaka silikonom
KR1020127001182A KR101543060B1 (ko) 2009-06-18 2010-06-18 실리콘 반흔 치료 제제
AU2010263031A AU2010263031B2 (en) 2009-06-18 2010-06-18 Silicone scar treatment preparation
MX2011013965A MX2011013965A (es) 2009-06-18 2010-06-18 Preparacion para tratamiento de cicatrices con silicona.
RU2011152511/15A RU2530657C2 (ru) 2009-06-18 2010-06-18 Силиконовый препарат для лечения рубцов
EP10790269.4A EP2442771B1 (en) 2009-06-18 2010-06-18 Silicone scar treatment preparation
HUE10790269A HUE048612T2 (hu) 2009-06-18 2010-06-18 Hegkezelõ szilikon preparátum
CA2765964A CA2765964C (en) 2009-06-18 2010-06-18 Silicone scar treatment preparation
SG2011093523A SG176894A1 (en) 2009-06-18 2010-06-18 Silicone scar treatment preparation
PT107902694T PT2442771T (pt) 2009-06-18 2010-06-18 Preparação para tratamento de cicatrizes com silicone
SI201032005T SI2442771T1 (sl) 2009-06-18 2010-06-18 Silikonski pripravek za zdravljenje brazgotin
PCT/US2010/039181 WO2010148310A1 (en) 2009-06-18 2010-06-18 Silicone scar treatment preparation
NZ597335A NZ597335A (en) 2009-06-18 2010-06-18 Silicone scar treatment preparation
DK10790269.4T DK2442771T3 (da) 2009-06-18 2010-06-18 Silikone-arbehandlingspræparat
ES10790269T ES2781649T3 (es) 2009-06-18 2010-06-18 Preparación de tratamiento de cicatrices con silicona
BRPI1009689-2A BRPI1009689B1 (pt) 2009-06-18 2010-06-18 preparação espalhável para auxiliar na cicatrização de feridas e melhorar as características do tecido pós epitelialmente desenvolvido no local da ferida e método para a obtenção de uma preparação espalhável para auxiliar na cicatrização de feridas e no desenvolvimento de tecido de cicatriz
IL217056A IL217056A (en) 2009-06-18 2011-12-18 Silicone preparation for scar treatment
ZA2012/00353A ZA201200353B (en) 2009-06-18 2012-01-17 Silicone scar treatment preparation
US13/548,899 US8802133B2 (en) 2009-06-18 2012-07-13 Silicone scar treatment preparation
US14/322,584 US9339546B2 (en) 2009-06-18 2014-07-02 Silicone scar treatment preparation
JP2015090815A JP6016974B2 (ja) 2009-06-18 2015-04-27 瘢痕治療用シリコーン製剤
US15/089,694 US9795706B2 (en) 2009-06-18 2016-04-04 Silicone scar treatment preparation
CY20201100176T CY1123227T1 (el) 2009-06-18 2020-02-26 Παρασκευασμα θεραπειας ουλης με σιλικονη

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US12/487,489 US20100322875A1 (en) 2009-06-18 2009-06-18 Silicone scar treatment preparation

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/548,899 Continuation US8802133B2 (en) 2009-06-18 2012-07-13 Silicone scar treatment preparation

Publications (1)

Publication Number Publication Date
US20100322875A1 true US20100322875A1 (en) 2010-12-23

Family

ID=43354570

Family Applications (4)

Application Number Title Priority Date Filing Date
US12/487,489 Abandoned US20100322875A1 (en) 2009-06-18 2009-06-18 Silicone scar treatment preparation
US13/548,899 Active 2030-01-17 US8802133B2 (en) 2009-06-18 2012-07-13 Silicone scar treatment preparation
US14/322,584 Active 2029-07-26 US9339546B2 (en) 2009-06-18 2014-07-02 Silicone scar treatment preparation
US15/089,694 Active US9795706B2 (en) 2009-06-18 2016-04-04 Silicone scar treatment preparation

Family Applications After (3)

Application Number Title Priority Date Filing Date
US13/548,899 Active 2030-01-17 US8802133B2 (en) 2009-06-18 2012-07-13 Silicone scar treatment preparation
US14/322,584 Active 2029-07-26 US9339546B2 (en) 2009-06-18 2014-07-02 Silicone scar treatment preparation
US15/089,694 Active US9795706B2 (en) 2009-06-18 2016-04-04 Silicone scar treatment preparation

Country Status (24)

Country Link
US (4) US20100322875A1 (enExample)
EP (1) EP2442771B1 (enExample)
JP (2) JP5740398B2 (enExample)
KR (1) KR101543060B1 (enExample)
CN (1) CN102802572B (enExample)
AU (1) AU2010263031B2 (enExample)
BR (1) BRPI1009689B1 (enExample)
CA (1) CA2765964C (enExample)
CY (1) CY1123227T1 (enExample)
DK (1) DK2442771T3 (enExample)
ES (1) ES2781649T3 (enExample)
HR (1) HRP20200560T1 (enExample)
HU (1) HUE048612T2 (enExample)
IL (1) IL217056A (enExample)
LT (1) LT2442771T (enExample)
MX (1) MX2011013965A (enExample)
NZ (1) NZ597335A (enExample)
PL (1) PL2442771T3 (enExample)
PT (1) PT2442771T (enExample)
RU (1) RU2530657C2 (enExample)
SG (1) SG176894A1 (enExample)
SI (1) SI2442771T1 (enExample)
WO (1) WO2010148310A1 (enExample)
ZA (1) ZA201200353B (enExample)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9271989B2 (en) 2011-12-27 2016-03-01 Cmpd Licensing, Llc Silicone-based composition for skin treatment
WO2016145233A1 (en) * 2015-03-12 2016-09-15 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
WO2020178005A1 (en) * 2019-03-01 2020-09-10 Wasserman Medic AB Novel compositions and use thereof
US20210379023A1 (en) * 2013-05-20 2021-12-09 Zoetis Services Llc Long-acting spiro-isoxazoline antiparasitic compositions
US12396946B1 (en) 2024-12-30 2025-08-26 Cristcot Llc Methods of treating gastrointestinal diseases and disorders

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100322875A1 (en) * 2009-06-18 2010-12-23 Advanced Bio-Technologies, Inc. Silicone scar treatment preparation
US9499678B2 (en) * 2012-02-24 2016-11-22 Daikin Industries, Ltd. Fluororubber composition
US9511034B1 (en) 2013-12-09 2016-12-06 Bio-Silicote, Inc. Method for applying a skin treatment
US9226890B1 (en) 2013-12-10 2016-01-05 Englewood Lab, Llc Polysilicone base for scar treatment
TWI559923B (en) * 2015-03-16 2016-12-01 Amed Co Ltd A composition of silicone gel for wound dressing
CN104814886A (zh) * 2015-04-10 2015-08-05 浙江省诸暨市珠力神医用品有限公司 一种硅凝胶组合物
CN104784066A (zh) * 2015-04-10 2015-07-22 浙江省诸暨市珠力神医用品有限公司 一种抗紫外线的硅凝胶组合物
CA3037582A1 (en) 2016-09-21 2018-03-29 Avexxin As Pharmaceutical composition
GB201616088D0 (en) * 2016-09-21 2016-11-02 Avexxin As Pharmaceutical composition
KR101921727B1 (ko) * 2016-12-28 2018-11-23 주식회사 제네웰 실리콘 수지 조성물, 이의 제조방법 및 이를 포함하는 흉터 치료제
WO2020141986A1 (en) * 2018-12-30 2020-07-09 Jamjoom Pharmaceuticals Factory Company Limited Silicone gel composition containing hyaluronic acid and/or its salt for prevention and repair of skin scars
CN110200988A (zh) * 2019-06-17 2019-09-06 瑞希(重庆)生物科技有限公司 一种疤痕修复剂及其制备方法
IT202000001831A1 (it) * 2020-01-30 2021-07-30 Caprika Srl Composizione per applicazione rettale a base di sale di acido butirrico per il trattamento delle patologie proctologiche

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US175414A (en) * 1876-03-28 Improvement in compensating-journals for machinery
US5292530A (en) * 1991-06-02 1994-03-08 Helene Curtis, Inc. Stable anhydrous topically-active composition and suspending agent therefor
US5389092A (en) * 1991-07-03 1995-02-14 Laboratoires D'hygiene Et De Dietetique (L.H.D.) Non-adhesive healing dressing
US5556699A (en) * 1987-06-30 1996-09-17 Shingawa Fuel Co. Ltd. Antibiotic zeolite-containing film
US5741509A (en) * 1996-08-26 1998-04-21 Alvin S. Berlat Silicone wound dressing
US5833998A (en) * 1995-11-06 1998-11-10 The Procter & Gamble Company Topical compositions for regulating the oily/shiny appearance of skin
US5972320A (en) * 1996-07-26 1999-10-26 The Gillette Company Antiperspirant or deodorant composition with silicone latex
US6155265A (en) * 1997-12-17 2000-12-05 Hemodynamics, Inc. Controlled viscosity dermal adhesive
US6183766B1 (en) * 1999-02-12 2001-02-06 The Procter & Gamble Company Skin sanitizing compositions
US6827929B1 (en) * 1999-09-27 2004-12-07 Dow Corning France S.A. Scar treatment composition
US20060110415A1 (en) * 2004-11-22 2006-05-25 Bioderm Research Topical Delivery System for Cosmetic and Pharmaceutical Agents
US20080292560A1 (en) * 2007-01-12 2008-11-27 Dov Tamarkin Silicone in glycol pharmaceutical and cosmetic compositions with accommodating agent
US20080299220A1 (en) * 2003-08-04 2008-12-04 Dov Tamarkin Hydrophilic, non-aqueous pharmaceutical carriers and compositions and uses
US20090143333A1 (en) * 2007-09-30 2009-06-04 Irwin Palefsky Silicone gel-based compositions for wound healing and scar reduction
US20100092409A1 (en) * 2008-10-15 2010-04-15 Amin Neelam S Personal care compositions comprising modified variant bowman birk protease inhibitors

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2622955B2 (ja) * 1986-07-29 1997-06-25 エイボン プロダクツ インコ−ポレイテツド 無水化粧品
JPH049327A (ja) 1990-04-04 1992-01-14 Kootec Kk 創傷被覆材
US5380527A (en) * 1991-08-26 1995-01-10 Dow Corning Corporation Alkylmethylsiloxane mixtures for skin care
US5456906B1 (en) * 1993-11-17 2000-12-05 Gen Electric Antiperspirant compositions
WO1997003710A1 (en) 1995-07-19 1997-02-06 Innovative Technologies Limited Wound treatment composition
JPH09194350A (ja) 1996-01-19 1997-07-29 Morishita Jintan Kk 創傷被覆材
US5750123A (en) * 1996-06-28 1998-05-12 Chesebrough-Pond's Co., Division Of Conopco, Inc. Vitamin C delivery system
JPH10265324A (ja) * 1997-03-25 1998-10-06 Noevir Co Ltd 油性化粧料
JP2002536397A (ja) 1999-02-12 2002-10-29 ザ、プロクター、エンド、ギャンブル、カンパニー 皮膚消毒剤組成物
MXPA02011440A (es) * 2000-05-23 2003-04-25 Unilever Nv Composiciones desodorantes y/o antitranspirantes.
DK1409034T3 (da) * 2001-07-24 2006-10-30 Advanced Biotechnologies Topisk farmaceutisk formulering
JP4071030B2 (ja) * 2002-04-11 2008-04-02 花王株式会社 表面疎水化吸水性ポリマー粒子
GB0216427D0 (en) * 2002-07-16 2002-08-21 Advanced Biotechnologies Inter Wound dressing
WO2004039347A1 (ja) * 2002-11-01 2004-05-13 Kao Corporation 液状皮膚保護剤組成物
US20050142079A1 (en) * 2003-12-26 2005-06-30 Garrison Mark S. Oil in silicone emulsion and compositions containing same
FR2879931B1 (fr) * 2004-12-24 2007-03-30 Rhodia Chimie Sa Materiau silicone pour la liberation d'une molecule active
FR2887150B1 (fr) * 2005-06-17 2007-08-03 Galderma Res & Dev Composition pharmaceutique comprenant un elastomere organopolysiloxane et un principe actif solubilise
JP4993983B2 (ja) * 2005-09-28 2012-08-08 信越化学工業株式会社 オルガノポリシロキサン表面処理剤系及び該処理剤系で表面処理された粉体、並びに該粉体を含有する化粧料
EP2407148B1 (en) * 2006-05-11 2018-02-21 Evonik Degussa GmbH Personal care compositions containing functionalized polymers
MX2009009557A (es) 2007-03-08 2010-08-10 Crescendo Therapeutics Llc Formulaciones de aposito para prevenir o reducir la cicatrizacion.
JP2009132638A (ja) * 2007-11-29 2009-06-18 Shin Etsu Chem Co Ltd 化粧料
US20100322875A1 (en) * 2009-06-18 2010-12-23 Advanced Bio-Technologies, Inc. Silicone scar treatment preparation
AU2010271205A1 (en) 2009-07-09 2012-02-09 Moko Therapeutics Llc. Method of wound healing and scar modulation

Patent Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US175414A (en) * 1876-03-28 Improvement in compensating-journals for machinery
US5556699A (en) * 1987-06-30 1996-09-17 Shingawa Fuel Co. Ltd. Antibiotic zeolite-containing film
US5292530A (en) * 1991-06-02 1994-03-08 Helene Curtis, Inc. Stable anhydrous topically-active composition and suspending agent therefor
US5389092A (en) * 1991-07-03 1995-02-14 Laboratoires D'hygiene Et De Dietetique (L.H.D.) Non-adhesive healing dressing
US5833998A (en) * 1995-11-06 1998-11-10 The Procter & Gamble Company Topical compositions for regulating the oily/shiny appearance of skin
US5972320A (en) * 1996-07-26 1999-10-26 The Gillette Company Antiperspirant or deodorant composition with silicone latex
US5741509A (en) * 1996-08-26 1998-04-21 Alvin S. Berlat Silicone wound dressing
US6155265A (en) * 1997-12-17 2000-12-05 Hemodynamics, Inc. Controlled viscosity dermal adhesive
US6183766B1 (en) * 1999-02-12 2001-02-06 The Procter & Gamble Company Skin sanitizing compositions
US6827929B1 (en) * 1999-09-27 2004-12-07 Dow Corning France S.A. Scar treatment composition
US20080299220A1 (en) * 2003-08-04 2008-12-04 Dov Tamarkin Hydrophilic, non-aqueous pharmaceutical carriers and compositions and uses
US20060110415A1 (en) * 2004-11-22 2006-05-25 Bioderm Research Topical Delivery System for Cosmetic and Pharmaceutical Agents
US20080292560A1 (en) * 2007-01-12 2008-11-27 Dov Tamarkin Silicone in glycol pharmaceutical and cosmetic compositions with accommodating agent
US20090143333A1 (en) * 2007-09-30 2009-06-04 Irwin Palefsky Silicone gel-based compositions for wound healing and scar reduction
US20100092409A1 (en) * 2008-10-15 2010-04-15 Amin Neelam S Personal care compositions comprising modified variant bowman birk protease inhibitors

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9271989B2 (en) 2011-12-27 2016-03-01 Cmpd Licensing, Llc Silicone-based composition for skin treatment
US9592241B2 (en) 2011-12-27 2017-03-14 Cmpd Licensing, Llc Silicone-based composition for skin treatment
US10064949B2 (en) 2011-12-27 2018-09-04 Cmpd Licensing, Llc Silicone-based composition for skin treatment
US20210379023A1 (en) * 2013-05-20 2021-12-09 Zoetis Services Llc Long-acting spiro-isoxazoline antiparasitic compositions
US12115253B2 (en) 2015-03-12 2024-10-15 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
US10653623B2 (en) * 2015-03-12 2020-05-19 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
US11376217B2 (en) 2015-03-12 2022-07-05 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
US12090226B2 (en) 2015-03-12 2024-09-17 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
US12097288B2 (en) 2015-03-12 2024-09-24 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
US12109306B2 (en) 2015-03-12 2024-10-08 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
WO2016145233A1 (en) * 2015-03-12 2016-09-15 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
US12115251B2 (en) 2015-03-12 2024-10-15 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
US12115252B2 (en) 2015-03-12 2024-10-15 Cristcot Llc Hydrocortisone acetate suppository formulation for treatment of disease
WO2020178005A1 (en) * 2019-03-01 2020-09-10 Wasserman Medic AB Novel compositions and use thereof
US11759410B2 (en) 2019-03-01 2023-09-19 Wasserman Medic AB Silicone composition and uses thereof
US12396946B1 (en) 2024-12-30 2025-08-26 Cristcot Llc Methods of treating gastrointestinal diseases and disorders

Also Published As

Publication number Publication date
JP2015166362A (ja) 2015-09-24
EP2442771A1 (en) 2012-04-25
JP2012530719A (ja) 2012-12-06
HRP20200560T1 (hr) 2020-07-10
ZA201200353B (en) 2013-07-31
BRPI1009689B1 (pt) 2019-11-12
BRPI1009689A2 (pt) 2016-03-15
ES2781649T3 (es) 2020-09-04
KR20120062678A (ko) 2012-06-14
IL217056A (en) 2013-12-31
AU2010263031B2 (en) 2014-05-01
MX2011013965A (es) 2012-04-19
CA2765964C (en) 2017-05-23
US20130183256A1 (en) 2013-07-18
US20160213810A1 (en) 2016-07-28
PT2442771T (pt) 2020-04-07
AU2010263031A1 (en) 2012-01-19
US9795706B2 (en) 2017-10-24
JP6016974B2 (ja) 2016-10-26
EP2442771B1 (en) 2020-02-05
PL2442771T3 (pl) 2020-07-13
US9339546B2 (en) 2016-05-17
NZ597335A (en) 2014-02-28
HUE048612T2 (hu) 2020-08-28
EP2442771A4 (en) 2013-01-09
US20140314695A1 (en) 2014-10-23
KR101543060B1 (ko) 2015-08-07
SG176894A1 (en) 2012-01-30
US8802133B2 (en) 2014-08-12
SI2442771T1 (sl) 2020-07-31
CA2765964A1 (en) 2010-12-23
WO2010148310A1 (en) 2010-12-23
CY1123227T1 (el) 2021-10-29
IL217056A0 (en) 2012-02-29
LT2442771T (lt) 2020-05-25
CN102802572B (zh) 2015-12-02
DK2442771T3 (da) 2020-04-27
RU2530657C2 (ru) 2014-10-10
JP5740398B2 (ja) 2015-06-24
RU2011152511A (ru) 2013-07-27
CN102802572A (zh) 2012-11-28

Similar Documents

Publication Publication Date Title
US9795706B2 (en) Silicone scar treatment preparation
US4806344A (en) Sun protectant composition and method
JPH02121915A (ja) 耐水性クリーム・コンディショナー
KR20130092172A (ko) 폴리올 및 유화제를 포함하는 저 자극 및 고 보습성 수중유형 화장료 조성물 및 그 제조방법
US20100112103A1 (en) Burn treatment composition and method
JPH09110680A (ja) 皮膚炎治療貼付剤
ES2730885T3 (es) Composición para cubrir y proteger cicatrices
JPS58140013A (ja) 外用剤
KR20150106244A (ko) 자외선 차단 및 보습용 화장품 조성물
HK1164105B (en) Silicone scar treatment preparation
HK1164105A (en) Silicone scar treatment preparation
CN117357411A (zh) 一种天然温和的儿童植物防晒乳制备工艺
EP2618892B1 (en) High protection uva/uvb composition and topical cosmetic composition
EP2618804B1 (en) High protection uva/uvb composition, its preparation process and topical cosmetic composition
EP4635522A1 (en) Pharmaceutical composition for preventing of abnormal scars growth and treatment of scars
ES2660978T3 (es) Método y composiciones para el tratamiento de la psoriasis
BR102021004476A2 (pt) Formulação tópica em gel de poloxamer adicionado de hesperidina metil chalcona para tratamento de queimaduras térmicas
BR102021004443A2 (pt) Gel termossensível adicionado de naringenina para tratamento de queimadura térmica
BR102023001180A2 (pt) Cosmético natural com propriedades multifuncionais para uniformidade e integridade da pele

Legal Events

Date Code Title Description
AS Assignment

Owner name: ADVANCED BIO-TECHNOLOGIES, INC., GEORGIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:GUILBAUD, PAUL;REEL/FRAME:024700/0651

Effective date: 20100630

AS Assignment

Owner name: CLYDESDALE BANK PLC, UNITED KINGDOM

Free format text: SECURITY AGREEMENT;ASSIGNOR:ADVANCED BIO-TECHNOLOGIES, INC.;REEL/FRAME:027389/0115

Effective date: 20111215

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

AS Assignment

Owner name: BANK OF SCOTLAND PLC, UNITED KINGDOM

Free format text: SECURITY INTEREST;ASSIGNOR:ADVANCED BIO-TECHNOLOGIES, INC.;REEL/FRAME:037894/0237

Effective date: 20160229

AS Assignment

Owner name: ADVANCED BIO-TECHNOLOGIES, INC., NORTH CAROLINA

Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:BANK OF SCOTLAND PLC;REEL/FRAME:071374/0859

Effective date: 20250520