US20120073584A1 - Orthopaedic splinting system - Google Patents

Orthopaedic splinting system Download PDF

Info

Publication number
US20120073584A1
US20120073584A1 US13/255,936 US201013255936A US2012073584A1 US 20120073584 A1 US20120073584 A1 US 20120073584A1 US 201013255936 A US201013255936 A US 201013255936A US 2012073584 A1 US2012073584 A1 US 2012073584A1
Authority
US
United States
Prior art keywords
composite material
composite
temperature
blank
component
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
US13/255,936
Other languages
English (en)
Inventor
Antti Pärssinen
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.)
ONBONE Oy
Original Assignee
ONBONE Oy
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 ONBONE Oy filed Critical ONBONE Oy
Assigned to ONBONE OY reassignment ONBONE OY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: PARSSINEN, ANTTI
Publication of US20120073584A1 publication Critical patent/US20120073584A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • 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
    • A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices; Anti-rape devices
    • A61F5/01—Orthopaedic devices, e.g. splints, casts or braces
    • A61F5/04—Devices for stretching or reducing fractured limbs; Devices for distractions; Splints
    • A61F5/05—Devices for stretching or reducing fractured limbs; Devices for distractions; Splints for immobilising
    • A61F5/058—Splints
    • 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
    • A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
    • A61L31/12—Composite materials, i.e. containing one material dispersed in a matrix of the same or different material
    • A61L31/125—Composite materials, i.e. containing one material dispersed in a matrix of the same or different material having a macromolecular matrix
    • A—HUMAN NECESSITIES
    • A43—FOOTWEAR
    • A43B—CHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
    • A43B17/00—Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined
    • A43B17/003—Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined characterised by the material
    • 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
    • A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices; Anti-rape devices
    • A61F5/01—Orthopaedic devices, e.g. splints, casts or braces
    • A61F5/14—Special medical insertions for shoes for flat-feet, club-feet or the like
    • 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
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/07—Stiffening bandages
    • A61L15/12—Stiffening bandages containing macromolecular 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
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/07—Stiffening bandages
    • A61L15/12—Stiffening bandages containing macromolecular materials
    • A61L15/125—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
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/07—Stiffening bandages
    • A61L15/14—Use of materials characterised by their function or physical properties
    • 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
    • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/40—Composite materials, i.e. containing one material dispersed in a matrix of the same or different material
    • A61L27/44—Composite materials, i.e. containing one material dispersed in a matrix of the same or different material having a macromolecular matrix
    • 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
    • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L27/58—Materials at least partially resorbable by the body
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L97/00—Compositions of lignin-containing materials
    • C08L97/02—Lignocellulosic material, e.g. wood, straw or bagasse
    • A—HUMAN NECESSITIES
    • A63—SPORTS; GAMES; AMUSEMENTS
    • A63B—APPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B71/00—Games or sports accessories not covered in groups A63B1/00 - A63B69/00
    • A63B71/08—Body-protectors for players or sportsmen, i.e. body-protecting accessories affording protection of body parts against blows or collisions
    • A63B71/12—Body-protectors for players or sportsmen, i.e. body-protecting accessories affording protection of body parts against blows or collisions for the body or the legs, e.g. for the shoulders
    • A63B71/1225—Body-protectors for players or sportsmen, i.e. body-protecting accessories affording protection of body parts against blows or collisions for the body or the legs, e.g. for the shoulders for the legs, e.g. thighs, knees, ankles, feet
    • A63B2071/1258—Body-protectors for players or sportsmen, i.e. body-protecting accessories affording protection of body parts against blows or collisions for the body or the legs, e.g. for the shoulders for the legs, e.g. thighs, knees, ankles, feet for the shin, e.g. shin guards
    • A—HUMAN NECESSITIES
    • A63—SPORTS; GAMES; AMUSEMENTS
    • A63B—APPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2209/00—Characteristics of used materials
    • A63B2209/18—Characteristics of used materials biodegradable
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/06—Biodegradable
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00—Applications
    • C08L2203/02—Applications for biomedical use
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/249921—Web or sheet containing structurally defined element or component

Definitions

  • the present invention relates, in general, to forming a structure on or around a body part of an animal or human being. More specifically, it relates to the field of orthopedic splinting materials, methods and apparatus. Described, herein is also a method of using a novel wood-plastic composite as a splint/cast in immobilization of a fractured body part and a kit thereof.
  • a splint may be applied for supporting or immobilizing a body part.
  • Such a splint is usually wrapped with an elastic bandage and the rigid portion does not envelope the limb circumferentially.
  • Traditional splinting techniques use a variety of materials including plaster of Paris (used first time in the Crimean war 1854 in treatment of battle wounds), fiber-glass reinforced polyurethane (DE 26 51 089), alumafoam (U.S. Pat. No. 4,213,452 and U.S. Pat. No. 4,153,051; an aluminium strip padded on one side with sponge-like foam) and complex pre-formed multilayer systems containing a plurality of straps, hooks etc. (WO 2008/041215, EP 0 393 003, EP 0 407 055).
  • Fiber-glass reinforced polyurethane resin based splinting materials are considered a practical alternative for the conventional plaster of Paris casts and are currently widely used in the treatment of fractured body parts. These materials are lightweight, durable, waterproof and they tend to have a shorter setting time than traditional plaster-based materials.
  • An aspect of the present invention is to introduce a novel, innovative and ecologically friendly biodegradable wood-plastic composite which can be heat molded to the contours of an animal or human body part.
  • a further aspect of the present invention is to present a system including the novel composite material and a heating means for use in the field of orthopedics.
  • the invention is based on the concept of providing the splint material in the form of a blank which can be shaped into the desired form of a cast or splint in situ.
  • the blank for an orthopedic splint is, in particular, provided in the form of a linear structure such as a plate, a sheet, a ribbon or a tape, comprising a composite material with a first component formed by a polymer and a second component formed by a reinforcing material.
  • the polymer is a thermoplastic polymer selected from the group of biodegradable polymers and mixtures thereof, and the second component comprises a woody material derived from platy or granular wood particles.
  • the composite material is formable at least at a temperature of about 50 to 70° C., although the temperature can be as high as 120° C. without degradation of the composite taking place.
  • a particular a blank for an orthopedic splint has the form of a rectangular plate having a width of 10 to 500 mm, a length of 10 to 1000 mm and a thickness of 1.5 to 10 mm, comprising 30-90 parts by weight of a polycaprolactone homopolymer having a molecular weight of about 80,000 to 200,000 g/mol and 70 to 10 parts by weight of wood granules having an average particular size of greater than 0.6 mm and up to 3.0 mm, in particular about 1 to 2.5 mm, said granules being distributed throughout the polycaprolactone homopolymer, said composite material being formable at a temperature of 50 to 120° C., in practice typically 50 to 70° C. and preferably about 65 to 70° C., and rigid at ambient temperature.
  • the material can be used in a method of shaping a composite material to snugly fit against a part of the body of a mammal, comprising the steps of providing the composite material in the form of an essentially rectangular, planar blank, heating the blank to a temperature in the range of 50 to 120° C., in practice typically 50 to 70° C. and preferably about 65 to 70° C., to convert the material into a manually formable state, applying the material against the target part of the body to as to make the material take up the form of the target part, and cooling the material to a temperature of less than 45° C. to make the material rigid.
  • the method can comprise an embodiment for forming a removable exo-skeletal device on a portion of a body of a human or animal, the method comprising the steps of;
  • the blank according to the invention is characterized by what is stated in the characterizing part of claims 1 and 2 .
  • the composite material of the present invention provides distinct advantages over all prior art materials used for splinting or casting an injured body part.
  • the present composite material is easy to work with, has a relatively light weight while maintaining the necessary structural properties of a splint/cast. It is ecologically friendly and is reusable without substantially degrading throughout uses.
  • a further advantage of the present invention is that the splinting system is moldable at temperatures very comfortable to patient and not scorching the skin of the patient. Furthermore, the splinting system, when solidifying, forms a rigid overall structure and does not need any further reinforcement than the natural anatomic shape to build up a reliable immobilization splint for the treatment period.
  • the composite material can be easily manufactured to any shape or form during manufacture or before use. However, when the splint is applied it has a three-dimensional configuration conforming to the desired body contours without undesirable wrinkling or tearing.
  • the composite splints/casts can be cut to dimensions close to the assumed size of the treated limb from a larger blank to diminish the amount of waste material. Additionally, the leftover composite pieces as well as the abandoned and used splints/casts are fully biodegradable as their components, wood and polycaprolactone, are fully biodegradable and contain no harmful components to human or to environment.
  • linear or flat composite splints, casts and blanks can be easily packaged and stored in compact piles e.g. in emergency rooms where space is limited. When composite casts are packaged appropriately they can be easily stored for at least one year.
  • the wood like composite plate can be handled without any protection, e.g. gloves and masks, since the component materials are non-toxic.
  • the composite can then be placed in to a heating device having an adjustable thermostat system or a preprogrammed thermostat tailored to the system.
  • the cast can be heated to operating temperature of around 65° C., preferably in dry condition, in less than 10 minutes. At this temperature, the composite is soft, pliable and can be applied to the desired body part or region. Due to thermal characteristics of wood or woody components, the cast does not feel hot on a skin of operating personnel or a patient.
  • the created form closely matches the anatomical contours of the patient's body parts without undesired wrinkling or tearing.
  • the cast Due to unique properties of splinting system, the cast remains applicable for around 5-10 minutes after heating even if the surface temperature of the cast decreases close to body temperature. This unique formability and time slot is due to appropriate crystallinity of polymer matrix and wood or woody components providing thermal insulation of certain degree.
  • the cast can be easily cut with conventional scissors and reshape to accurately match an injured body part.
  • the full strength properties of the cast is achieved approximately in 20 minutes after the initial hardening; however the time may be shortened to few minutes when an external cooling system is used. In case the clinical practitioner needs to re-formulate the shape of the splint, it can be re-heated to the operating temperature.
  • the entire treatment system is water-free and during heating, applying and use there are no dust, chemicals or vapors released.
  • the casting material of an aspect of the present invention neither contains a mesh type of structure, nor layers of different materials.
  • the casting material is thoroughly uniform, homogeneous and no “weak spots” in its mechanical strength of the three-dimensional configuration are observed.
  • FIG. 4 shows in a schematic side-view the use of the present material as a cast for treating ruptures of the extensor tendon in a the first finger joint; (example 3)
  • FIG. 5 shows a schematic fashion a front-view of a reshapable wrist cast
  • FIG. 6 shows in a schematic fashion a front-view of an anatomic ankle cast according to an embodiment of the invention. (example 5)
  • FIG. 7 a shows the front and side views of an unfolded anatomic ankle cast of the kind depicted in FIG. 6
  • FIG. 7 b shows the side view of the same cast in folded position
  • FIG. 8 is a bar chart showing the results of tests carried out with a peel adhesion test method (Example 6).
  • FIG. 9 is a bar chart showing the results of a puncture test (Example 7).
  • FIG. 10 shows the cooling behavior of the composite splint when positioned onto the isolating carpet (Example 8).
  • FIG. 11 shows the cooling behavior of the composite splint when positioned onto the isolating carpet (Example 8).
  • FIG. 12 Thermal expansion behaviour of crystalline thermoplastic polymer. “Undercooling” effect is observed when the polymer is cooled down. The polymer melts at 65 deg C. and solidifies approximately at 40 degrees of Celsius.
  • FIG. 13 Mechanical strength (flexural strength) in MPa as according to ISO standard 527.
  • PCL polymers PCL-9/80 (melt flow index at 80 deg C.), PCL-40 and PCL-3.
  • An aspect of the present invention is the presentation of a novel composite material.
  • the material is novel in at least its composition and in its properties.
  • the novel composite material is presented as being formed in to a blank, to be sized prior to application, or formed in to desired specific shapes during manufacture.
  • a kit comprising at least one or more forms of the composite material and a heating means to prepare the composite material for application.
  • the composite retains its shape as it cools down. It is substantially rigid but flexible so as to be supportive and comfortable. Rigidity is generally achieved when a sample heated to the above indicated softening temperature is cooled to below 50° C., particular to less than 45° C., preferably less than 40° C. Typically, the composite is rigid at ambient temperature, a suitable temperature of use is about 20 to 50° C., in particular 22 to 40° C.
  • the material of the present invention can be simply manufactured by mixing the first component, i.e. a suitable polymer material for example in the form of pellets, with the second component i.e. wood particles or granules, by melt mixing.
  • the mixing can be carried out in any conventional apparatus designated for melt mixing or melt processing.
  • One example is a heatable vessel having a mechanical stirrer.
  • the uniformity of the composite can be increased by using an extruder, kneader or any device suitable for mixing thermoplastic polymers.
  • the desired amount of each component can be fed in to the mixing chamber of the apparatus. Then, by way of the mixing means in the mixing apparatus, there is formed a homogeneous mixture of the first and second components prior to the formation of the formation of the material.
  • One advantage to the material being formed by such a homogeneous mixture of the components is that the forces necessary to form a substantially homogeneous material are reduced. Therefore, little or no compression force is necessary to facilitate mixing of the components in a material formation step. The importance of this factor is that, by way of the homogeneous mixture, larger particles of each component can be used which would otherwise have been destroyed when subjected to high compression forces.
  • the material can be applied for use after it has been recovered from the mixing device and formed into desired shape for example into a sheet or plate or roll or any similar planar, folded, bent or tubular structure, but the material can even be formed directly on the patient.
  • the material mixed with an extruder can be shaped with appropriate nozzle to the shape of e.g. rectangular sheet or plate which can be used directly after cutting e.g. as finger splint.
  • the desired profile for the splints can be manufactured with the extruder manufactured sheet or plate with e.g. laser cutting, water jet cutting, eccentric pressing or with any tool capable for producing regular shape profiles.
  • the present material can also be process with compression moulding, injection moulding, die-casting, and pressure die-casting.
  • the sheet or plate can have a thickness of, generally about 1 to 50 mm, in particular about 1.5 to 30 mm, for example 1.5 to 20 mm. A typical thickness is about 2 to 6 mm.
  • the length and the width of the sheet or plate can vary in the range of about 1 to 150 cm (length) and 1 to 50 cm (width), a typical length being about 10 to 60 cm and a typical width being about 5 to 20 cm.
  • the proportions between the components of the material can vary in a broad range.
  • 5 to 99 wt-%, for example 40 to 99 wt-%, of the material is formed by the thermoplastic polymer component and 1 to 95 wt-%, for example 1 to 60 wt-%, by the woody material.
  • the weight ratio of polymer-to-wood can easily be modified and the weight percent of wood, based on the total weight/volume of the composition, may vary between 1 and 70% preferably however in the range of 10 to 60 weight percent, or 20 to 60 weight percent, and 15 to 50%, or 25 to 50%, by volume.
  • the second component comprises or consists essentially of a woody material having a smallest diameter of greater than 0.1 mm. As will be discussed below, there can also be other wood particles present in the second component.
  • the woody material can be granular or platy. According to one embodiment, the second component comprises a woody material derived from platy wood particles having a smallest diameter of greater than 0.1 mm.
  • the wood component can be characterized generally as being greater in size than powder.
  • the size and the shape of the wood particles may be regular or irregular.
  • the particles have an average size (of the smallest dimension) in excess of 0.1 mm, advantageously in excess of 0.5 mm, for example in excess of 0.6 mm, suitably about 1 to 40 mm, in particular about 1.2 to 20 mm, preferably about 1.5 to 10 mm, for example about 1.5 to 7 mm.
  • the length of the particles (longest dimension of the particles) can vary from a value of greater than 1 mm to value of about 1.8 to 200 mm, for example 3 to 21 mm.
  • the woody particles can be granular, platy or a mixture of both.
  • Woody particles considered to be platy means that they have generally a plate-shaped character, although particles of other firms are often included in the material.
  • the ratio of the thickness of the plate to the smaller of the width or length of the plate's edges is generally 1:1 to 1:500, in particular about 1:2 to 1:50.
  • the platy particles of the present invention generally comprise wood particles having at least two dimensions greater than 1 mm and one greater than 0.1 mm, the average volume of the wood particles being generally at least 0.1 mm 3 more specifically at least 1 mm 3 .
  • “Derived from platy wood particles” designates that the wood particles may have undergone some modification during the processing of the composition. For example, if blending of the first and second components is carried out with a mechanical melt processor, some of the original platy wood particles may be deformed to an extent.
  • the wood species can be freely selected from deciduous and coniferous wood species alike: beech, birch, alder, aspen, poplar, oak, cedar, Eucalyptus, mixed tropical hardwood, pine, spruce and larch tree for example.
  • woody material of the composite can also be any manufactured wood product.
  • the particles can be derived from wood raw-material typically by cutting or chipping of the raw-material. Wood chips of deciduous or coniferous wood species are preferred.
  • WO 94/03211 a composite material is described, based upon polycaprolactone, ground almond shell and wood flour.
  • the known material is impaired by several disadvantages, such as a high density of 1.1 kg/m 3 or even more, as a result of the small particle sizes of the filler material [wood, less than 600 microns (600 ⁇ m)].
  • Another disadvantage related to the use of small particle sized fillers is the poor adhesive properties of composite material. According to our experiments (cf. Example 10 below), composites consisting of 40 weight percentage of wood dust sized between 0-800 microns reveal zero adhesion toward bandage material (compression force of 0.1 bars).
  • polycaprolactone polymer presented in examples of WO 94/03211 has too low viscosity (melt flow index value of 7 g/10 minutes with 2.16 kg standard die at 160° C.) to be used at practical applying temperature of 65° C.
  • the present composite materials provide excellent properties also in this respect.
  • the present composition can contain reinforcing fibrous material, for example cellulose fibers, such as flax or seed fibers of cotton, wood skin, leaf or bark fibers of jute, hemp, soybean, banana or coconut, stalk fibers (straws) of hey, rice, barley and other crops and plants including plants having hollow stem which belong to main class of Tracheobionata and e.g. the subclass of meadow grasses (bamboo, reed, scouring rush, wild angelica and grass).
  • cellulose fibers such as flax or seed fibers of cotton, wood skin, leaf or bark fibers of jute, hemp, soybean, banana or coconut
  • stalk fibers straws of hey, rice, barley and other crops and plants including plants having hollow stem which belong to main class of Tracheobionata and e.g. the subclass of meadow grasses (bamboo, reed, scouring rush, wild angelica and grass).
  • the composition may contain particulate or powdered material, such as sawdust, typically having particles with a size of less than 0.5 mm*0.5 mm*0.5 mm.
  • Particulate or powdered material is characterised typically as material of a size in which the naked eye can no longer distinguish unique sides of the particle.
  • Platy particles are easily recognizable as one dimension is recognizable by the naked eye as being larger than another.
  • Granular particles while having substantially equal dimensions, are of such dimension that their unique sides can be determined by the naked eye and oriented.
  • particulate or powdered materials are of such a small or fine size that they cannot be easily oriented with respect to their neighbours.
  • Granular and platy particles are of such as size that their sides are recognizable and orientatable.
  • the desired composition of the second component can be achieved by sifting woody particles through one or more meshes having one or more varying qualities.
  • the desired composition can also be accomplished by other well known techniques in the art for sorting and separating particles in to desired categories.
  • the desired composition may be the resultant composition of one sifting or separating process.
  • the desired composition may also be a mixture of resultant compositions from several sifting or separation processes.
  • a particularly interesting raw-material comprises wood particles, chips or granules, of any of the above mentioned wood species having a screened size of greater than 0.6 mm and up to 3.0 mm, in particular about 1 to 2.5 mm on an average.
  • the weight ratio of fibrous material (optionally including said powdered material) to the platy material (dry weight) is about 1:100 to 100:1, preferably about 5:100 to 50:50.
  • the woody material derived from the platy wood particles forms at least 10%, preferably about 20 to 100%, in particular about 30 to 100%, of the total weight of the second component.
  • the woody material makes up at least and preferably more than 70% of the second component.
  • inorganic particulates or powdered materials such as mica, silica, silica gel, calcium carbonate and other calcium salts such as tricalcium orthophosphate, carbon, clays and kaolin may be present or added.
  • a composite useful as an orthopedic material comprises a first component formed by a polymer and a second component formed by a reinforcing material, wherein the first component comprises a thermoplastic polymer selected from the group of biodegradable polymers and mixtures thereof, and the second component comprises reinforcing fibres.
  • Such fibers can be selected from the group for example of cellulose fibers, such as flax or seed fibers of cotton, wood skin, leaf or bark fibers of jute, hemp, soybean, banana or coconut, stalk fibers (straws) of hey, rice, barley and other crops including bamboo and grass.
  • the wood filler may consist of or consist essentially of fibres of the indicated kind.
  • the polymer component can be any of the below listed polymers, caprolactone homo- or copolymers having a molecular weight of about 60000 g/mol up to 250,000 g/mol being particularly preferred.
  • thermoplastic polymer and its properties will be discussed in more detail below, but for the sake of order it is pointed out that in all of the above mentioned embodiments, wherein various fillers are used as a second and a third and even fourth component of the composition, substantial advantages with respect to biodegradability and mechanical properties have been found using caprolactone polymers, in particular homopolymers, as thermoplastics.
  • the particularly preferred polymer component is a caprolactone homopolymers having a molecular weight of above 80,000 g/mol. Specifically, caprolactone having a molecular weight of between 100,000 g/mol and 200,000 g/mol as been found to be advantageous both in terms of resultant properties and cost.
  • the woody particles Before the woody particles are mixed with the thermoplastic polymer they can be surface treated, e.g. sized, with agents which modify their properties of hydrophobicity/-hydrophobicity and surface tension. Such agents may introduce functional groups on the surface of the granules to provide for covalent bonding to the matrix. Even increased hydrogen bonding or bonding due to van der Waals forces is of interest.
  • the woody particles can also be surface treated with polymer e.g. PCL having low viscosity and molar mass values to increase holding powers between wood and PCL having high viscosity value.
  • the wood material can be also coated or treated with anti-rot compound e.g. vegetable oil to improve its properties against aging and impurities.
  • anti-rot compound e.g. vegetable oil
  • the wood material can be dehydrated to make it lighter before mixing it with polymer.
  • the mechanical and chemical properties of wood material can be improved with heat treatment, which is known to decrease e.g. swelling and shrinkage.
  • the first component (the polymer) forms the matrix of the composite, whereas the microstracture of the second component in the composition in discontinuous.
  • the particles of the second component can have random orientation or they can be arranged in a desired orientation.
  • the desired orientation may be a predetermined orientation.
  • a polycaprolactone polymer (in the following also abbreviated “PCL”) is used as a thermoplastic polymer in the first component of the composition.
  • the polycaprolactone polymer is formed by repeating units derived from epsilon caprolactone monomers.
  • the polymer may be a copolymer containing repeating units derived from other monomers, such as lactic acid, glycolic acid, but preferably the polymer contains at least 80% by volume of epsilon caprolactone monomers, in particular at least 90% by volume and in particular about 95 to 100% epsilon caprolactone monomers.
  • the thermoplastic polymer is selected from the group of epsilon-caprolactone homopolymers, blends of epsilon-caprolactone homopolymers and other biodegradable thermoplastic homopolymers, with 5-99 wt %, in particular 40 to 99 wt %, of an epsilon-caprolactone homopolymer and 1-95 wt %, in particular 1 to 60 wt %, of a biodegradable thermoplastic polymer, and copolymers or block-copolymers of epsilon-caprolactone homopolymer and any thermoplastic biodegradable polymer, with 5 to 99 wt %, in particular 40 to 99 wt % of repeating units derived from epsilon-caprolactone and 1 to 95 wt %, in particular 1 to 60 wt %, repeating units derived from other polymerizable material.
  • thermoplastic polymers examples include polylactides, poly(lactic acid), polyglycolides as well as copolymers of lactic acid and glycolic acid.
  • the first polymer component in particular the epsilon caprolactone homo- or copolymer, has an average molecular weight of 60,000 to 500,000 g/mol, for example 65,000 to 300,000/mol, in particular at least 80,000 g/mol, preferably higher than 80,000 and up to 250,000.
  • the molding properties of the present invention can be determined by the average molecular weight (M n ) of the polymer, such as epsilon caprolactone homo- or copolymer.
  • M n average molecular weight of the polymer
  • a particularly preferred molecular weight range for the M n value of PCL is from about 100,000 to about 200,000 g/mol.
  • the number average molar mass (Mn) and the weight average molar mass (Mw) as well as the polydispersity (PDI) were measured by gel permeation chromatography.
  • Samples for GPC measurements were taken directly from the polymerization reactor and dissolved in tetrahydrofuran (THF).
  • the GPC was equipped with a Waters column set styragel HR (1, 2 and 4) and a Waters 2410 Refractive Index Detector.
  • THY was used as eluent with a flow rate of 0.80 ml/min at a column temperature of 35° C.
  • a conventional polystyrene calibration was used.
  • a Metroohm 756 KF Coulometer was used.
  • the properties of mo of the present composition can also be determined by the viscosity value of the polymer.
  • epsilon caprolactone homopolymer when the inherent viscosity (IV)-value of PCL is less than 1 dl/g the composite is sticky, flows while formed and forms undesired wrinkles while cooling.
  • IV-value closer to 2 dl/g When PCL having IV-value closer to 2 dl/g is used the composite maintains its geometry during molding on the patient and it may be handled without adhesive properties.
  • IV values in excess of 1 dl/g are preferred, values in excess to 1.2 dl/g are preferred and values in excess of 1.3 dl/g are particularly suitable.
  • the values are in the range of about 1.5 to 2.5 dl/g, for example 1.6 to 2.1 dl/g.
  • Inherent Viscosity values were determined by LAUDA PVS 2.55 d rheometer at 25° C. The samples were prepared by solvating 1 mg of PCL in 1 ml chloroform (CH 3 Cl).
  • thermoplastic polymer A particularly important feature of the thermoplastic polymer is the viscosity which is relatively high, typically at least 1,800 Pas at 70° C., 1/10 s; the present examples show that the viscosity can be on the order of 8,000 to 13,000 Pas at 70° C., 1/10 s (dynamic viscosity, measured from melt phase). Below the indicated value, a reinforced material readily wrinkles during forming it on a patient.
  • the thermoplastic material is preferably a biodegradable polymer (only) but also non-biodegradable polymers may be utilized.
  • examples of such polymers include polyolefins, e.g. polyethylene, polypropylene, and polyesters, e.g. poly(ethylene terephthalate) and poly(butylenes terephthalate) and polyamides. Combinations of the above biodegradable polymers and said non-biodegradable polymers can also be used.
  • the weight ratio of biodegradable polymer to any non-biodegradable polymer is 100:1 to 1:100, preferably 50:50 to 100:1 and in particular 75:25 to 100:1.
  • the composite material has biodegradable properties greater, the material biodegrades quicker or more completely, than the thermoplastic material alone.
  • a polymer of the afore-said kind is preferably moldable at a temperature as low as +50° C., in particular at +65° C. or slightly above, and it can be mixed with wood particles or generally any porous material gaining increased rigidity of the formed composite.
  • the polymer component such as polycaprolactone homopolymer, defines the form of the splinting material against the skin.
  • the modulus (Specific Young's modulus), at ambient temperature, of the polymer component is greater than 300 MPa. By compounding the polymer with the wood component, the modulus will be improved (cf. below), typically it is about 350 to 2000 MPa for the composition.
  • the present material contains a significant portion of wood granules having a particle size greater than the micrometer range, for example a size of about 0.75 mm to 50 mm.
  • a size of about 0.75 mm to 50 mm When the material is shaped into a sheet, (at least most of) the wood granules become oriented in two dimensions within forming of the thermoplastic material into sheets.
  • the present method of producing a composite useful as an orthopedic material comprises the steps of
  • the mixing can be melt mixing carried out at a temperature sufficient for melting the thermoplastic polymer, e.g. at about 50 to 150° C.
  • the molten polymer mass containing a mixture of biopolymer and reinforcing platy or granular particles can be shaped manually or, according to a preferred embodiment by moulding in a mould.
  • the molten polymer mass can be subjected to tensile forces to achieve a desired orientation of the polymer and, in particular, the reinforcing particles.
  • the manufacturing process can, on an industrial scale, be carried out as follows:
  • wood chips or granules and plastic granules are mixed to form a uniform blend before pouring into the feed hopper of an extruder.
  • the mixing process can be carried out also by feeding of the virgin materials to the extruder directly by using separate feeding hoppers.
  • the compounding is then carried out in, e.g., an extruder, in particular a single screw extruder.
  • the screw extruder profile of the screw is preferably such that its dimensions will allow relatively large wood chips to move along the screw without crushing them.
  • the channel width and flight depth are selected so that the formation of excessive local pressure increases, potentially causing crushing of the wood particles, are avoided.
  • the temperature of the cylinder and the screw rotation speed are also selected such as to avoid decomposition of wood chip structure by excessively high pressure during extrusion.
  • a suitable barrel temperature can be in the range of about 110 to 150° C. from hopper to die, while the screw rotation speed was between 25-50 rpm.
  • the compounded composite material obtained from the melt processing/compounding step is then profiled in the tool to a homogeneous product, e.g. a sheet or plate, for example using suitable mechanical processing.
  • a homogeneous product e.g. a sheet or plate
  • suitable mechanical processing e.g. calendaring.
  • Another suitable process is by pressing.
  • the composite material can be subjected to gentle folded between the processing steps.
  • the mechanical processing is carried out at a temperature well above the glass transition/melting point of the polymer.
  • the density of composite manufactured typically lies in the range of about 600 to 850 kg/m 3 , depending on the weight percent of wood in material.
  • the reinforced, material typically exhibits properties selected from one or several of the following:
  • the splinting material can be manipulated and manually shaped for up to 10 minutes and it is typically pliable for 3-10 minutes after the finishing of heating, depending of the size of splint.
  • the material hardens entirely in one hour.
  • Operation time of the melt material can be expanded by heating the material close to +100° C. which is the temperature limit for the material to be handled without protective gloves.
  • the material can be heated to +150° C. and held there for several hours without changes in the material properties.
  • a cooling spray or a cooling gel or wrap can be used.
  • the present composition can be used as a composite material according to any of the preceding claims for use as an orthopedic material.
  • Such materials are exemplified by finger splints, wrist casts and ankle casts.
  • the platy particles form about 30 to 70%, preferably in excess of 40 up to about 60%, of the total weight of the composition, for finger splints and for ankle casts about 20 to 60%, preferably about 30 to 50% of the total weight of the composition.
  • There is typically a greater portion of the larger particles present in the larger casts which will reduce the total weight of the cast without impairing the strength properties thereof.
  • the composite cast/splint is very user-friendly. There is no unpleasant odor from volatile chemicals, quite the opposite; there is only mild odor of virgin wood e.g. spruce and aspen. Also the appearance of the casting material is trustworthy. The polymer material is not visible and the whole look is based on small wood particles.
  • the cooling of the composite when placed onto the platform having low thermal conductivity represents the situation when the splint has long time to reach equilibrium temperature at RT. Based on the results the cooling process can be divided into three phases. 1) Rapid cooling phase when the temperature of test sample decreases from starting temperature of ⁇ 65° C. to 38° C. during 5 minutes. 2) Steady state phase during the temperature of test specimen remains at 38° C. for 5 minutes. 3) Slow cooling phase during the temperature of the test specimen slowly approaches the equilibrium temperature of surroundings during 50 minutes.
  • the cooling of the composite when placed directly onto the skin of the thigh represents the situation when the splint has shortest possible time to reach equilibrium temperature at limb temperature of ⁇ 31° C. when no additional cooling is utilized (e.g. cooling spray).
  • the temperature behavior of the test specimen is similar with data presented in the previous experiment. The differences in cooling process are at the Rapid cooling phase and at the Slow cooling phase. The temperature of the test specimen decreases from ⁇ 67° C. to 38° C. during 3 minutes at the first phase. 2) Steady state phase at 39° C. lasts for 5 minutes. 3) Slow cooling phase during the temperature of the test specimen slowly approaches the equilibrium temperature of surroundings during 30 minutes.
  • the pliability of the test specimen was tested manually by lifting one side of sample and allowing it to settle down. After the settling procedure of the sample plate was not anymore complete the pliability is lost. The time to reach this level was marked. After this point, the shaping capability of the composite was limited.
  • the self-supporting test was carried out at two different temperature surroundings (skin and ambient as presented in surface temperature test.
  • the composite having surface temperature of ⁇ 65° C. neither caused any unpleasant feeling for the patient nor caused any skin changes (itching burns etc).
  • the splinting material can be manipulated and manually shaped for up to 10 minutes and it is typically pliable for 3-10 minutes after the finishing of heating, depending of the size of splint.
  • the material hardens entirely in one hour.
  • Operation time of the melt material can be expanded by heating the material close to +100° C., which is the temperature limit for the material to be handled without protective gloves. Due to good insulation property of the splinting system, which is based on unique wood-thermoplastic composite, the surface of the splint does not feel burning hot even close to 100° C.
  • the material can be heated up to +150° C. and held there for several hours without changes in the material properties.
  • the surface temperature of splinting system decreases rapidly below its physical hardening temperature of ⁇ 55° C. (in less than a minute) and the splinting material still remains pliable down to temperature of 40° C. Cooling time to solidification temperature typically takes 3-5 minutes. This is obviously an advantageous phenomenon when high temperatures close to skin must be avoided during the application.
  • a cooling spray or a cooling gel or wrap can be used.
  • our composite cast can be reheated and reshaped and even cut to match new anatomical contour of the fractured limb.
  • the composite material of the present invention has specific properties which are not present in the existing materials.
  • the uniqueness of the material is based both on the utilized polycaprolactone polymer and the specific sized wood chips.
  • MFI Melt Flow Index
  • the properties of compounded polymer at molten stage are more relevant than the flexural strength of pure polymer at room temperature.
  • a punctuation test was carried out and the results are shown in FIG. 9 .
  • the goal of punctuation test is to gain information about compressive strength of the molten WPC-splint at applicable temperature.
  • the uniqueness of the contouring possibilities of the herein introduced WPC-material can be adequately demonstrated by measuring viscosity of WPC-material at the applicable temperature of ⁇ 65° C. with universal penetrometer which is routinely used in determinations of consistency of semi-solid to solid materials such as greases, waxes, cosmetics etc.
  • the measurements were carried out according to the modified standard D 1321, D 1988 or EN-1426 (Standard Test Method for needle penetration of petroleum waxes and bitumen). At 65° C. carried out measurements reveal useful information about compression strength of the polycaprolactone homopolymer as well as from WPC-material in molten state. The penetration depth of the 100 g needle assembly reflects well on the behavior of the WPC splint during application.
  • the composites based on PCL having MFI value of 40 are typically very sticky and they do not tolerate any compression without strong rupturing at temperature of 65° C. These composites are not suitable to be used as splints in fracture fixation.
  • the composite based on PCL having MFI value of 7 (CAPA 656) is only slightly sticky, as presented in patent application IE 050593, but during applying it onto limb it does not tolerate strong bending or strong compression without tearing or forming of a dent.
  • PCL-7 possesses no resistance against needle assembly penetration. Even at temperature of 58° C., the needle assembly penetration depth during one second is out of scale (needle reach the bottom of foil cup). Estimated penetration value for PCL-40 was over 1000.
  • PCL-7 and PCL-3 having MFI value of 7 and 3 respectively are more viscous polymers and their penetrations depths were measured in standard circumstances.
  • the penetration value for PCL-7 was 240 and for PCL-3 the corresponding value was 103 as seen in the FIG. 9 .
  • Materials having a penetration value of 100 reflects well on the material which can be easily mounted onto the fractured limb, but does not tolerate any compression during installation without creeping or wrinkle formation.
  • the composites consisting of polycaprolactone PCL-7, PCL-35 and PCL-40 have MFI values of seven or above, revealed average penetration values between 56 and 88.
  • commercial splinting material Aquaplast® (respecta blue) revealed penetration value of 55.
  • These composites tolerate moderate compression and could be, in theory, used in splinting applications. Unfortunately the risk of tearing and dent formation under pressure or during bending is too high for medical applications. In addition, the stickiness of these composites may cause undesired fastening to the materials used in fracture fixation operation rooms.
  • the composite materials of our invention reveal average penetration values between 15 and 50. The value is depending on the wood weight percentage in the composite. The more there is wood the less is the value. When the wood content in the composite is kept between 15 and 50 weight percentage, composites tolerate appropriate compression during mounting and tearing and dent formation during applying can be avoided. Worth of mentioning is that by placing the needle assembly directly onto the wood chip surface, lower penetration value than expected is achieved.
  • the adhesive properties of composite can be varied by introducing different proportion of wood into the material. This phenomenon can be exploited in production of different kind of splinting applications. Reasonable adhesion is required in all casting/splinting applications.
  • the adhesion forces of the herein introduced composites were tested in a peel adhesion test. The goal of the peel adhesion test is to find appropriate composition for the wood-plastic composite featuring elevated adhesive forces when applied with various gauze bandages. Appropriate adhesion between the splint and the bandage improves the stability of the fracture fixation system.
  • the peeling force should be at such a level that gauze bandage is easy-to-peel with bare hands and without causing unnecessary pain to the patient.
  • the adhesive/tape is rolled with 2 kg cylinder shaped roller on substrate.
  • roller can't be used due it can form irregularities on the surface of the substrate. Therefore roller was replaced with rectangular shaped steel slab weighting 3.3 kg. By this way the reproducibility of the test reproducibility improved remarkably.
  • the steel slab addresses pressure of 0.09 bars to the gauze which correspond to a gentle press with palm.
  • the PCL-3 revealed only insignificant deformation during the pressing process and the test was possible to carry out without problems.
  • the average peeling force value of 19 N was achieved.
  • Self-adhesive forces are usually needed in casting/splinting applications. For example immobilization of fractured foot can be nicely carried out with splint having strongly self-adhesive straps which decrease the possibility of failure of the splint assembly. In some cases when fractured limb is immobilized with circumferentially casting applications it is beneficial if the support can be taken off easily and set again. With our material both the weak and the strong adhesion can be achieved.
  • the former having adhesion forces above 100 N can be considered to be “everlasting” bond which can't be broken without casting saw.
  • the latter composites having adhesion forces less than 10 N can be easily separated apart by hands.
  • the novel composite material of the present invention has a composition and properties that are substantially well suited for use in orthopedic situations.
  • the composite material can be used to form an exo-skeletal device on a portion of an animals or human beings body or body part.
  • the exo-skeletal device can be used as a shin-pad, wrist guard or even a foot bed for footwear. However, it is especially well suited as a splint or cast structure to immobilize, or partially immobilize a portion of an animals or humans body or body part.
  • the composite material of the present invention is manufactured in to either a blank or in to a desired, specific shape or form.
  • the blanks and forms are linear, two dimensional and easily stackable.
  • the blanks can be either substantially lamer than the intended size to be applied to the animal or human being, herein referred to as the patient, or of substantially similar size.
  • the blank can be cut with normal scissors or other conventional cutting means before application.
  • a large blank is preferable in the sense that one blank may be cut in to several splints at various times according to the size required by each. Therefore, it is not necessary to store many different shapes and sizes of the material, which take up room and may be rarely used. Additionally, multiple splints may be cut from one blank in such a way as to maximize the material used and not produce a large amount of waste product.
  • the material is then heated to the desired operating temperature by a heating means.
  • a heating means Numerous heating means are known in the art, but it is preferable to uniformly heat the material to a specific desired temperature. If the temperature is too high then there is risk of discomfort or harm to the patient's skin. If the temperature is not high enough then the material will not be able to properly conform to the patient's body.
  • the composite materials are provided along with a heater which is specifically tailored to the application of the composite materials.
  • the heater may have an adjustable thermostat or may be preprogrammed to heat automatically to the desired temperature.
  • the heater will have a heating element capable of heating an entire blank or form of the composite material evenly and completely.
  • the size of the heater should be sufficient enough to handle the size of the composite materials to be used.
  • the heater may be given complimentary along with complementary or paid composite material blanks or forms to entice people to use the system and material.
  • the heating element is other than one specifically tailored to the present composite material it can be selected from the range of known heating elements including contact heaters, convection heaters, chemical heating and the like.
  • the material can be placed on the patient in the desired location to form the exo-skeletal device.
  • the advantage of the present material is that it can be handled by hand without any protective requirement such as gloves. Equally important is that the material can be formed directly against the patient's skin. However, it can be advantageous to have some material, such as gauze or other cloth/cloth like material, directly in contact with the patients skin and to form the composite material over that material.
  • the composite material With the composite material still pliable and moldable, it can be tit to contour the patient's body, part nearly or exactly. Additionally, if the initial placement is not desirable, the material can be moved while still moldable to a more desirable location. If the material has lost its desired moldability, then it can be reheated and likewise moved to the new location.
  • One of the particular advantages of the present material is that it can be heated and cooled many times without degrading its mechanical properties.
  • the composite material When the composite material is located properly and molded to the desired form, then it can be allowed to cool to a temperature where it can be removed but maintain its shape.
  • the cooling may be accomplished by allowing the ambient conditions to reduce the temperature of the material or the cooling may be aided by spraying the material with water or another chemical to speed up the cooling. Additionally, solid cooling means can be used to cool the material such as a cold pack or ice place directly against the composite material.
  • a fastening means can be employed to attach the device to the body part.
  • gauze can be wrapped around the splint and body part. The adhesive properties of the not yet cooled composite material will hold the gauze in place, therefore facilitating the immobilization of the intended body part.
  • Other fastening means apart from gauze may also be attached as desirable or necessary.
  • the device Once the device is cooled to or near room temperature, with or without the fastening means, then it will remain substantially rigid until the time at which it is reheated.
  • the device In the case of a splint or cast, the device need not be removed for medical imaging such as x-rays. However, if the splint or cast was originally place while there was swelling present, it can be easily heated and reformed to better fit the unswelled shape of the body part. In this sense, less material is wasted since in previous splinting devices a completely new splint/cast would be required.
  • the device When the device is no longer needed for its previous purpose it can be reheated, removed if necessary, and either flattened or stored as is until the next time when it is required.
  • the resultant material has the same mechanical properties in subsequent uses as in previous uses and is therefore not degraded through multiple uses. However, when the composite material is desired to be discarded, it is biodegradable and therefore ecologically friendly.
  • the present composition can be used as a composite material for use as an orthopedic material.
  • Such materials are exemplified by finger splints, shown in FIG. 4 , wrist casts, shown in FIGS. 5-7 , and ankle casts.
  • the platy particles form about 30 to 70%, preferably in excess of 40 up to about 60%, of the total weight of the composition, for finger splints and for ankle casts about 20 to 60%, preferably about 30 to 50% of the total weight of the composition.
  • There is typically a greater portion of the larger particles present in the larger casts which will reduce the total weight of the cast without impairing the strength properties thereof.
  • the polycaprolactone polymer used was a commercially available PCL homopolymer supplied under the tradename CAPA 6800 by Perstorp Ltd. Sweden).
  • the polycaprolactone has a melt flow rate of about 3 g/10 min (measured at 150° C. and with a weight of 2.16 kg) and referred to as “PCL-3”.
  • PCL-7 another caprolactone homopolymer also used had a significantly higher melt flow rate of about 7 g/10 min (referred to as “PCL-7”).
  • the wood material if not separately indicated, was conventional spruce chips produced at a Finnish saw mill. In some of the examples wood particles of other wood species were used.
  • the influence of the reinforcing component on mechanical properties was studied with the 3-point bending test.
  • the flexural strengths and modulus of the composites were measured with universal testing machine Instron 4411. A neat PCL, without any reinforcement, was used as control.
  • test samples (dimensions 55 ⁇ 10.5 ⁇ 5.5 mm) were prepared by mixing constant ratio of different size wood chips (30 weight %) and epsilon-polycaprolactone homopolymer (70 weight %) and pressed into a Teflon mould. The melting and shaping of samples until a homogenous distribution of components was achieved. The samples were tested by constant cross head speed of 10 mm/min. The 3-point bending forces are presented graphically in FIG. 1 and Specific Young's modulus of elasticity in FIG. 2 .
  • FIG. 1 the reinforcing effect of wood particles to the flexural strength of composites can be clearly observed.
  • the stress at yield is 19 MPa but after incorporating 30 weight-% of different sized wood particles to the polymer stress values increased over 20% reaching value of ⁇ 27 MPa at the best.
  • the difference in specific modulus values of pure PCL and herein introduced composites were even greater ( FIG. 2 ).
  • Pure PCL revealed specific modulus value of ⁇ 400 MPa and corresponding value with the composite reinforced with wood, particles having average volume of 10 mm 3 , was slightly over 1500 MPa. In the worst case when composite was reinforced with small wood particles modulus values were still two times greater than with pure PCL homopolymer.
  • the densities of the samples prepared in Example 1 for mechanical testing were measured by determining the dimensions of the regular size samples and weighting them.
  • the densities of the composites are graphically presented in FIG. 3 .
  • composites according to the present invention have a considerably smaller density than polycaprolactone as such and are therefore suitable for light-weight splinting applications.
  • WO 94/03211 a composite material is described, based upon polycaprolactone, ground almond shell and wood flour.
  • the known material is impaired by several disadvantages, such as a high density of 1.1 kg/dm 3 or even more, as a result of the small particle sizes of the filler material [wood, less than 600 microns (600 ⁇ m)].
  • the composite material prepared in the Example 3 was tooled into a plate suitable for making a splint cast to support finger (a “finger splint”).
  • FIG. 4 shows the use of the finger splint.
  • the upper drawing illustrates an injured (mallet) index finger 2 which has a rupture of the extensor cordon.
  • the composite plate 1 can be applied directly on the dorsal side of the mallet finger 2 .
  • the composite plate can shaped to contour the finger so that the palmar side of finger is left open.
  • Upon cooling the composite splint solidifies. Cooling was accelerated with a wet tissue. After cooling, ordinary bandage (strips 3 a and 3 b ) can be added to immobilize the treated finger.
  • This example describes the production of a re-shapable wrist cast 1 having the general shape shown in FIG. 5 .
  • Example 1 Approximately 100 grams of composite material prepared in Example 1 was cast onto a metal plate and release paper at 100° C. and allowed to cool down. The composite was re-heated up to 70° C. and when still warm and moldable the cast composite was manipulated to form of a thick plate, thickness approximately 6 mm. Excess of materials was cut away with scissors when still warm. The cut edges were gently contoured by hand in order to soften the sharp edges. The size of received composite plate was 12 ⁇ 25 cm.
  • the composite plate was applied directly on repositioned wrist.
  • the composite plate was left open on medial side of wrist.
  • the wrist was kept repositioned until the cast had solidified.
  • the semi-open wrist cast can be easily removed and re-shaped if after imaging the clinician need to the repair the resulted repositioning of wrist bones.
  • the wrist cast may be re-softened at the oven heated to 70° C. or in water bath and replaced in the corrected position on the wrist.
  • This example illustrates the preparation of an anatomic ankle cast and the application thereof.
  • Example 2 200 grams of composite material manufactured in the Example 2 was cast on release paper at 100° C. and allowed to cool down. The composite was re-heated up to 70° C. in heat oven to resemble a thick plate, thickness approximately 8 mm. The received composite plate, dimensions 15 ⁇ 40 cm was cut to anatomical shape with scissors when it was still warm. Especially area that is needed for the medical personnel to hold the leg when repositioning the ankle was cut slightly open. Also, extra strips were cut to be later attached on the anterior side of the cast. The cut edges were gently contoured by hand in order to soften the sharp edges.
  • FIG. 6 shows the general form of the produced cast plate.
  • Reference numeral 21 refers to the cast plate and numerals 22 to 24 to foldable flaps.
  • FIGS. 7 a and 7 b show how the composite plate 21 can be reshaped when applied directly on the leg during repositioning of the ankle after an injury.
  • the leg is kept repositioned until the cast has solidified.
  • the cut flaps 22 and 23 are folded along folding lines 25 and 26 and compressed gently on the anterior side of the composite cast.
  • the cut flap 24 can in a similar fashion be bent and shaped by folding its side portions along folding lines 27 and 28 .
  • the material is non-tack but it grips well with itself when it is still moldable, i.e. above 65° C.
  • This example illustrates how a test according to the peel adhesion test method shows the relative bond strength of a given tape/bandage to surface (material and texture) of composite splint.
  • a molten WPC-material can be considered to be a pressure sensitive adhesive.
  • gauze bandage is pressed with steel slab surface of molten composite for 30 seconds and allowed to cool to RT. After hardening of the composite gauze is peeled off at a 180° angle from substrate at a constant peel rate by using Instron mechanical testing device. The measurements were carried out according to the modified standard SFS-EN 1939 (Standard Test Method for Peel Adhesion of Pressure-Sensitive Tape).
  • the loose end of the strip was connected to the peel arm and the composite plate was mounted horizontally onto a stage allowing ⁇ 180° angle to be maintained as the tape was pulled from the surface of the composite ( FIG. 8 ).
  • the rate of peeling was kept constant at 50 mm/min.
  • the peeling force as a function of distance was collected. The peeling is ended before the last 20 mm of the test specimen is achieved.
  • the composite manufactured of PCL-7 and small wood particles in weight ratio of 60:40 revealed zero adhesive force (material has similar properties with the material presented in patent WO 94/03211).
  • an adhesion force in the range of 1 to 50 N was detected. This force is sufficient for adhering the bandages to the surface to avoid sliding of them when applying the splint on a patient.
  • the large wood particles were combined with high molar mass polycaprolactone in weight ratio of 70:30 adhesion force of 23 N was achieved.
  • the size of the wood particles in the composites containing over 40 weight-% of wood has dramatic influence to the adhering properties of the composite.
  • composite consisting of 40 weight-% of wood dust and 60 weight-% of CAPA 6500 possesses extremely smooth surface, chipboard-like, without any adhering properties. After changing the wood particles with larger ones minor adhesion was observed being enough for holding the bandage material stationary during the circumferential casting procedure.
  • PCL-7 as such had an adhesive force of 197 N.
  • the adhesion is very strong and the gauge bandage cannot be anymore removed by hands from the polymer sample.
  • a volume of material is softened to operating temperature of 65° C. in foil container beaker (depth of at least 15 mm in excess of the expected penetration).
  • the beaker is placed on the stand of the penetration apparatus ( FIG. 9 ) “remove” and the needle is adjusted to make contact with the surface of the sample.
  • the dial reading is adjusted to zero and the needle is released for exactly 5 seconds.
  • the dial reading is recorded. The procedure is repeated three times.
  • Penetration is read from indicator dial of 0-400 divisions each representing 0.1 mm of penetration.
  • FIG. 9 shows the needle penetration depths into PCL homopolymers and wood-plastic composites. Experiments are carried out with the universal manual penetrometer.
  • the composite materials of our invention reveal average penetration values between 15 and 50. The value is depending on the wood weight percentage in the composite. The more there is wood the less is the value. When the wood content in the composite is kept between 15 and 50 weight percentage, composites tolerate appropriate compression during mounting and tearing and dent formation during applying can be avoided.
  • the composite test specimen (10 cm*40 cm*4 mm) was placed into in-house developed heating device and heated to 65° C. After heating procedure sample was removed from the oven and positioned either onto the skin of the thigh or onto the carpet (Astro Turf®) covered with baking paper. The temperature of the cooling composite splint surface was followed with IR thermometer pistol (Tamo Distance Thermo).
  • the cooling of the present composite splint when placed onto the carpet having low thermal conductivity represents the situation when the splint has longest possible time to reach equilibrium temperature at RT. Based on the results the cooling process can be divided into three phases. 1) Rapid cooling phase when the temperature of test sample decreases from starting temperature of ⁇ 65° C. to 38° C. during 5 minutes. 2) Steady state phase during the temperature of test specimen remains at 38° C. for 5 minutes. 3) Slow cooling phase during the temperature of the test specimen slowly approaches the equilibrium temperature of surroundings within 50 minutes.
  • the cooling of the present composite splint when placed directly onto the skin of the thigh represents the situation when the splint has shortest possible time to reach equilibrium temperature at limb temperature of ⁇ 31° C. when no additional cooling is utilized (e.g. cooling spray).
  • the temperature behavior of the test specimen was similar with data presented in the previous experiment. The only differences being the faster rapid cooling phase and Slow cooling phase.
  • the temperature of the test specimen decreases from ⁇ 67° C. to 38° C. during 3 minutes. 2) Steady state phase at 39° C. lasts for 5 minutes. 3) Slow cooling phase during the temperature of the test specimen slowly approaches the equilibrium temperature of surroundings during 30 minutes.
  • Self-supporting/full hardening test reveals information of the changes in pliability of the composite test specimen while cooling it down from 65° C. to the equilibrium temperature.
  • the pliability of the test specimen was tested manually by lifting one side of sample and allowing it to settle down. After the settling procedure of the sample plate is not anymore complete the pliability is lost. The time to reach this level will be marked. After this point, the shaping capability of the composite will be limited.
  • the self-supporting test will be carried out at two different temperature surroundings (skin and ambient) as presented in surface temperature test. In the isolated test setup (carpet), the pliability was lost after 5 minutes. After this point the test specimen remained partly flexible for 5 minutes followed by final hardening during one hour.
US13/255,936 2009-03-11 2010-03-11 Orthopaedic splinting system Abandoned US20120073584A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FI20095251 2009-03-11
FI20095251A FI125448B (fi) 2009-03-11 2009-03-11 Uudet materiaalit
PCT/FI2010/050186 WO2010103187A2 (en) 2009-03-11 2010-03-11 Orthopaedic splinting system

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/FI2010/050186 A-371-Of-International WO2010103187A2 (en) 2009-03-11 2010-03-11 Orthopaedic splinting system

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US14/106,973 Division US9803080B2 (en) 2009-03-11 2013-12-16 Orthopaedic splinting system

Publications (1)

Publication Number Publication Date
US20120073584A1 true US20120073584A1 (en) 2012-03-29

Family

ID=40510249

Family Applications (5)

Application Number Title Priority Date Filing Date
US13/255,942 Abandoned US20120090759A1 (en) 2009-03-11 2010-03-11 Method of producing composite materials
US13/255,936 Abandoned US20120073584A1 (en) 2009-03-11 2010-03-11 Orthopaedic splinting system
US13/255,930 Active US10336900B2 (en) 2009-03-11 2010-03-11 Composite materials comprising a thermoplastic matrix polymer and wood particles
US14/106,973 Active 2030-10-10 US9803080B2 (en) 2009-03-11 2013-12-16 Orthopaedic splinting system
US15/347,280 Abandoned US20170058120A1 (en) 2009-03-11 2016-11-09 Novel composite materials comprising a thermoplastic matrix polymer and wood particles

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US13/255,942 Abandoned US20120090759A1 (en) 2009-03-11 2010-03-11 Method of producing composite materials

Family Applications After (3)

Application Number Title Priority Date Filing Date
US13/255,930 Active US10336900B2 (en) 2009-03-11 2010-03-11 Composite materials comprising a thermoplastic matrix polymer and wood particles
US14/106,973 Active 2030-10-10 US9803080B2 (en) 2009-03-11 2013-12-16 Orthopaedic splinting system
US15/347,280 Abandoned US20170058120A1 (en) 2009-03-11 2016-11-09 Novel composite materials comprising a thermoplastic matrix polymer and wood particles

Country Status (16)

Country Link
US (5) US20120090759A1 (fi)
EP (4) EP2405951B1 (fi)
JP (2) JP5761719B2 (fi)
KR (2) KR101756305B1 (fi)
CN (2) CN102405062B (fi)
AU (2) AU2010222771B2 (fi)
BR (1) BRPI1008947A2 (fi)
CA (2) CA2755126C (fi)
EA (2) EA023530B1 (fi)
ES (2) ES2835653T3 (fi)
FI (1) FI125448B (fi)
HR (2) HRP20201963T1 (fi)
NZ (2) NZ595696A (fi)
PL (1) PL2405949T3 (fi)
WO (3) WO2010103188A2 (fi)
ZA (2) ZA201107117B (fi)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160068682A1 (en) * 2013-06-21 2016-03-10 Lg Hausys, Ltd. Board comprising biodegradable resin and wooden flour and method of manufacturing the same
US20170354861A1 (en) * 2016-06-10 2017-12-14 Onbone Sports Limited Sports protection device
WO2018104940A1 (en) * 2016-12-05 2018-06-14 CASSIT ORTHOPEDICS Ltd. Thermoplastic orthopedic devices
US10285844B2 (en) 2013-10-07 2019-05-14 Wichita State University Rapid setting composite article

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI125448B (fi) * 2009-03-11 2015-10-15 Onbone Oy Uudet materiaalit
FI123137B (fi) 2010-09-11 2012-11-30 Onbone Oy Kipsausmateriaalit
CN102120870A (zh) * 2011-02-28 2011-07-13 殷正福 一种可降解塑料及其生产方法
BE1019852A3 (nl) * 2011-02-28 2013-01-08 Orfit Ind Gebruik van een velvormig koolstof nanobuis-polymeer composiet materiaal.
WO2013107866A1 (en) * 2012-01-18 2013-07-25 Novortex Ab Splint
GB2513536A (en) * 2012-12-19 2014-11-05 Ronald Vincent Taylor Orthopaedic cast replacement
CN103330959B (zh) * 2013-06-04 2014-12-17 东南大学 预应力增强的轻质高强可控降解医用复合材料及制备方法
FI126725B (fi) 2013-10-21 2017-04-28 Onbone Oy Hengittävät materiaalit
FI20136038L (fi) 2013-10-21 2015-04-22 Onbone Oy Uudet materiaalit
BR102013029084B1 (pt) * 2013-11-12 2021-11-30 Cleber Pereira Gama Processo de obtenção de composto plástico a base de material vegetal fibroso, composto plástico a base de material vegetal fibroso obtido e equipamento para extrusão de composto plástico a base de material vegetal fibroso
CN103736155B (zh) * 2014-01-07 2015-04-01 东南大学 载铈功能化可吸收骨科器械材料及其制备方法
US9642736B2 (en) 2014-03-12 2017-05-09 Rechargeable Battery Corporation Thermoformable splint structure with integrally associated oxygen activated heater and method of manufacturing same
US9872795B2 (en) * 2014-03-12 2018-01-23 Rechargeable Battery Corporation Thermoformable medical member with heater and method of manufacturing same
JP2017055884A (ja) * 2015-09-15 2017-03-23 東洋アルミエコープロダクツ株式会社 医療用固定材および医療用固定具
CN105546230B (zh) * 2016-02-02 2018-05-15 浙江鑫宙竹基复合材料科技有限公司 一种秸秆竹缠绕复合管及其制备方法
GB2551329A (en) * 2016-06-10 2017-12-20 Onbone Oy Personal protection device
FR3052780B1 (fr) * 2016-06-16 2018-09-21 Greenpile Bmh - bio-materiau hybride
WO2018012548A1 (ja) * 2016-07-12 2018-01-18 国立大学法人大阪大学 身体ホルダー、及びその使用方法
AU2017305190B2 (en) * 2016-08-02 2019-10-03 Vinventions Usa, Llc Closure for a product-retaining container
US20200085142A1 (en) * 2016-12-15 2020-03-19 Edensoles Ltd. Reusable custom insoles
FI127576B (fi) * 2017-03-02 2018-09-14 Sulapac Oy Uudet pakkausmateriaalit
CN107126308A (zh) * 2017-03-17 2017-09-05 南京天朗制药有限公司 形状记忆分趾器及分趾袜及其使用方法
EP3420830A1 (en) * 2017-06-28 2019-01-02 Liiteguard ApS A knitted protective sock
GB201717223D0 (en) * 2017-10-20 2017-12-06 Onbone Oy Cast
TWI655941B (zh) * 2017-11-07 2019-04-11 遠東科技大學 副木及其製作方法
US20190308086A1 (en) * 2018-04-05 2019-10-10 Sport Maska Inc. Hockey goalkeeper leg pad
WO2019201872A1 (en) 2018-04-17 2019-10-24 Mp Lumber D.O.O. A kit for in situ immobilization with antifungal and antimicrobial effects
RU182764U1 (ru) * 2018-06-06 2018-08-30 Роман Юрьевич Бартош Композитный функциональный материал
FI130445B (fi) * 2018-09-01 2023-09-01 Sulapac Oy Kompostoituva puukomposiittimateriaali
EP3639998A1 (en) * 2018-10-15 2020-04-22 FCA Italy S.p.A. Forming process to manufacture a finishing/covering element for a component in a vehicle passenger compartment, and finishing/covering element manufactured by means of said process
FI20186033A1 (fi) * 2018-12-02 2020-06-03 Sulapac Oy Kompostoituva puukomposiittimateriaali ohutseinämäisille tuotteille
JP7045025B2 (ja) * 2020-09-23 2022-03-31 東洋アルミエコープロダクツ株式会社 医療用固定材および医療用固定具
RU2750712C1 (ru) * 2020-11-24 2021-07-01 федеральное государственное бюджетное образовательное учреждение высшего образования "Казанский национальный исследовательский технологический университет" (ФГБОУ ВО "КНИТУ") Способ получения биоразлагаемой полимерной композиции

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4240415A (en) * 1978-12-18 1980-12-23 WFR/Aquaplast Corp. Orthopedic cast
US4661535A (en) * 1984-07-13 1987-04-28 Johnson & Johnson Thermoplastic composition
WO2006027763A2 (en) * 2004-09-09 2006-03-16 Fastform Research Limited Geometrically apertured protective and/or splint device comprising a re-mouldable thermoplastic material
US20060065993A1 (en) * 1998-04-03 2006-03-30 Certainteed Corporation Foamed polymer-fiber composite
US7323253B2 (en) * 2002-05-08 2008-01-29 Inter Ikea Systems B.V. Chip board and a process for the preparation thereof
WO2008041215A1 (en) * 2006-10-03 2008-04-10 Fastform Research Limited Orthopaedic devices
WO2008124035A2 (en) * 2007-04-09 2008-10-16 University Of Connecticut Ring-opening polymerization of cyclic esters, polyesters formed thereby, and articles comprising the polyesters
US20120071590A1 (en) * 2009-03-11 2012-03-22 Onbone Oy Novel composite materials comprising a thermoplastic matrix polymer and wood particles

Family Cites Families (80)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT298391B (de) 1967-11-23 1972-04-15 Turcksin C Verfahren zur herstellung von sowohl in lang-richtung als auch in querrichtung elastischen gewebebahnen sowie elastische gewebebahn
US4021388A (en) * 1972-05-18 1977-05-03 Coloroll Limited Synthetic resin sheet material
US3921333A (en) * 1972-07-28 1975-11-25 Union Carbide Corp Transplanter containers made from biodegradable-environmentally degradable blends
US4019505A (en) 1974-09-30 1977-04-26 Norman S. Blodgett Method of forming an orthopedic cast
DE2651089C3 (de) 1976-11-09 1980-06-12 Bayer Ag, 5090 Leverkusen Selbsthältendes Material für Stutzverbände
US4153051A (en) 1977-07-08 1979-05-08 Shippert Ronald D Compound splint and kit
US4273115A (en) 1979-03-12 1981-06-16 Hexcel Corporation Moldable plastic orthopedic cast
US4213452A (en) 1979-05-03 1980-07-22 The Denver Splint Company Compound splint and kit
JPS56148355A (en) 1980-04-17 1981-11-17 Daicel Ltd Fixing bandage material
JPS5819253A (ja) * 1981-07-28 1983-02-04 藤倉ゴム工業株式会社 外科医療用保護材料用組成物
JPS59194746A (ja) 1983-04-19 1984-11-05 テルモ株式会社 医療用具
US4473671A (en) 1983-09-01 1984-09-25 Johnson & Johnson Products, Inc. Formable orthopedic casts and splints
US4784123A (en) 1986-01-03 1988-11-15 Union Carbide Corporation Orthopedic/orthotic splint materials
EP0393003B1 (en) 1986-10-08 1993-05-26 Tom Paul Marthe Ghislain Ponnet Composite material for medical or paramedical, particularly orthopaedic use
JP2733610B2 (ja) * 1989-01-25 1998-03-30 ダイセル化学工業株式会社 医療用固定材
US5273802A (en) 1989-07-07 1993-12-28 Minnesota Mining And Manufacturing Company Orthopedic casting materials having superior lamination characteristics due to napped surface
GB9216775D0 (en) * 1992-08-07 1992-09-23 British United Shoe Machinery Orthopaedic splinting/casting material
JPH06118460A (ja) 1992-09-30 1994-04-28 Nippon Telegr & Teleph Corp <Ntt> 光位相変調回路
CA2158344A1 (en) 1993-04-16 1994-10-27 Matthew T. Scholz Orthopedic casting materials
US5417904A (en) * 1993-05-05 1995-05-23 Razi; Parviz S. Thermoplastic polymer composites and their manufacture
JPH07328058A (ja) * 1994-06-09 1995-12-19 Mitsubishi Rayon Co Ltd 整形外科用ギプス内装材
US5681649A (en) * 1994-07-29 1997-10-28 Bridgestone Corporation Footwear member
US5863480A (en) 1994-08-29 1999-01-26 Srp Industries Ltd. Process for making a filler reinforced thermoplastic composites having biaxially oriented components
JP2810864B2 (ja) 1995-06-15 1998-10-15 株式会社モルテン シンガード
US6071984A (en) * 1995-09-26 2000-06-06 Bayer Aktiengesellschaft Biodegradable plastics filled with reinforcing materials
EP0765911A3 (de) 1995-09-26 1998-05-20 Bayer Ag Mit Verstärkungsstoffen gefüllte biologisch abbaubare Kunststoffe
US5801224A (en) * 1996-04-26 1998-09-01 Board Of Trustees Operating Michigan State University Bulk reactive extrusion polymerization process producing aliphatic ester polymer compositions
DE19705280C1 (de) * 1997-02-12 1998-03-05 Daimler Benz Ag Faserverstärktes Kunststoff-Formteil und Verfahren zu dessen Herstellung
US6124384A (en) 1997-08-19 2000-09-26 Mitsui Chemicals, Inc. Composite resin composition
US6143811A (en) 1998-08-14 2000-11-07 The Japan Steel Works, Ltd. Method of producing compound pellets containing wood flour
WO2000035501A1 (en) 1998-12-16 2000-06-22 Smith & Nephew, Plc Casting material
DE19860836C1 (de) * 1998-12-30 2000-05-18 Haller Formholz Verfahren und Vorrichtung zum kontinuierlichen Herstellen von Formkörpern
EP1118636A1 (fr) 2000-01-20 2001-07-25 SOLVAY (Société Anonyme) Compositions à base de polymère de l'caprolactone chargées, procédé pour leur préparation et articles à base de ces compositions
FI108403B (fi) 2000-02-25 2002-01-31 Yli Urpo Antti Yksil÷n kudosrekonstruktioon soveltuva materiaali
DE10010414A1 (de) 2000-03-03 2001-09-06 Trespa Int Bv Verfahren zur Herstellung eines mattenförmigen Vorprodukts, Vorprodukt und Verwendung eines Vorprodukts
AUPQ880500A0 (en) 2000-07-14 2000-08-10 Bio-Deg. Mouldings Pty. Ltd. Biodegradable composition and products prepared therefrom
US20020128420A1 (en) * 2000-12-27 2002-09-12 Simpson Scott S. Polyurethane elastomers and method of manufacture thereof
US6482167B2 (en) 2001-03-29 2002-11-19 Royce Medical Product Sealed edge orthopaedic casting technique
US6617376B2 (en) 2001-03-30 2003-09-09 Crane Plastics Company Llc Flexible wood composition
JP4081579B2 (ja) * 2001-09-14 2008-04-30 愛知県 リグノセルロース系材料及びその利用
US6780359B1 (en) * 2002-01-29 2004-08-24 Crane Plastics Company Llc Synthetic wood composite material and method for molding
FR2852599B1 (fr) 2003-03-17 2007-08-10 Odil Materiau a biodegradabilite ajustable notamment pour contenant d'horticulture et suremballage de contenants
US20050137304A1 (en) * 2003-12-18 2005-06-23 Strand Marc A. Process for calendering of polyesters
JP4498783B2 (ja) 2004-03-17 2010-07-07 トヨタ紡織株式会社 木質成形体の製造方法
ATE439394T1 (de) 2004-05-25 2009-08-15 Novamont Spa Verwendung von perforierten biologisch abbaubaren folien und daraus erhaltene hygieneprodukte
JP2006016461A (ja) * 2004-06-30 2006-01-19 Fa M Inc 天然系充填材を含有する樹脂組成物の製造方法およびそれにより製造された樹脂組成物
IE20050593A1 (en) 2004-09-09 2006-03-22 Fastform Res Ltd Geometrically apertured protective and/or splint device comprising a re-mouldable thermoplastic material
WO2006076932A1 (en) 2005-01-24 2006-07-27 T Tape Company Bv Orthosis and method for manufacture thereof
JP5181413B2 (ja) 2005-09-13 2013-04-10 日立電線株式会社 電気化学装置用電極、固体電解質／電極接合体及びその製造方法
US7659330B2 (en) 2005-09-16 2010-02-09 University Of Maine System Board Of Trustees Thermoplastic composites containing lignocellulosic materials and methods of making same
WO2007035875A2 (en) * 2005-09-21 2007-03-29 Qfix Systems, Llc Reinforced low temperature thermoplastic material
US7601282B2 (en) 2005-10-24 2009-10-13 Johns Manville Processes for forming a fiber-reinforced product
US20070132133A1 (en) 2005-12-07 2007-06-14 Katuyuki Hasegawa Method for manufacturing resin composite formed product
BRPI0600787A (pt) * 2006-02-24 2007-11-20 Phb Ind Sa composição polimérica ambientalmente degradável e seu método de obtenção
BRPI0600683A (pt) * 2006-02-24 2007-11-20 Phb Ind Sa composição polimérica ambientalmente degradável e seu processo de obtenção
US7524554B2 (en) 2006-04-14 2009-04-28 Mitsubishi Jidosha Kogyo Kabushiki Kaisha Synthetic board and method of producing the same
US20070259584A1 (en) * 2006-05-04 2007-11-08 Ronald Whitehouse Biodegradable polymer composites and related methods
US20100240806A1 (en) 2006-05-23 2010-09-23 Tetsuo Kondo Materials containing polyactic acid and cellulose fibers
US20070287795A1 (en) 2006-06-08 2007-12-13 Board Of Trustees Of Michigan State University Composite materials from corncob granules and process for preparation
US20080015285A1 (en) 2006-07-14 2008-01-17 Steven Richard Oriani Process aid for extruded wood composites
JP2008030380A (ja) 2006-07-31 2008-02-14 Mitsubishi Motors Corp 合成板
CN101172164A (zh) * 2006-11-03 2008-05-07 中国科学院化学研究所 可生物降解及吸收的生物高分子纳米纤维膜材料及其制法和用途
CA2667114C (en) * 2006-11-15 2014-10-07 Entex Rust & Mitschke Gmbh Blend of plastics with wood particles
KR100816679B1 (ko) * 2006-12-13 2008-03-27 제일모직주식회사 천연섬유 강화 폴리유산 수지 조성물
TWM321371U (en) 2006-12-22 2007-11-01 Chun-Chih Lai Flaky texture for polylactic acid and thin wood sheet
WO2008116025A2 (en) * 2007-03-19 2008-09-25 Qfix Systems, Llc Direct contact moldable low temperature thermoplastic prosthetic devices and method of making same
US7846991B2 (en) 2007-04-19 2010-12-07 Gaia Basis Co., Ltd. Biodegradable resin composition and method for producing the same
US7942837B2 (en) 2007-04-21 2011-05-17 Prosthotics Functional Systems, Llc Composite moldable splint and method of forming same
CN101678564A (zh) 2007-05-01 2010-03-24 上越农业未来株式会社 高分子复合材料、其制造装置及其制造方法
US8303527B2 (en) 2007-06-20 2012-11-06 Exos Corporation Orthopedic system for immobilizing and supporting body parts
JP5337363B2 (ja) 2007-10-11 2013-11-06 出光興産株式会社 芳香族ポリカーボネート樹脂組成物及びその成形品
KR20110081235A (ko) 2008-09-29 2011-07-13 바스프 에스이 생분해성 중합체 혼합물
WO2010053167A1 (ja) * 2008-11-05 2010-05-14 帝人化成株式会社 ポリ乳酸組成物およびその成形品
KR101182149B1 (ko) 2009-09-24 2012-09-12 (주)엘지하우시스 수축성을 가진 타카 시공용 판재
FI123137B (fi) 2010-09-11 2012-11-30 Onbone Oy Kipsausmateriaalit
US20120090068A1 (en) 2010-09-16 2012-04-19 Nistevo Sport Manufacturing Corporation User-moldable sports equipment using heated water bath
CN102120870A (zh) 2011-02-28 2011-07-13 殷正福 一种可降解塑料及其生产方法
BE1020363A3 (nl) 2011-12-23 2013-08-06 Orfit Ind Werkwijze voor het vervaardigen van een polymeer vel voor gebruik als immobilisatie element.
US9198471B2 (en) 2013-03-14 2015-12-01 Nike, Inc. Articulated protective apparatus
FI126725B (fi) 2013-10-21 2017-04-28 Onbone Oy Hengittävät materiaalit

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4240415A (en) * 1978-12-18 1980-12-23 WFR/Aquaplast Corp. Orthopedic cast
US4661535A (en) * 1984-07-13 1987-04-28 Johnson & Johnson Thermoplastic composition
US20060065993A1 (en) * 1998-04-03 2006-03-30 Certainteed Corporation Foamed polymer-fiber composite
US7323253B2 (en) * 2002-05-08 2008-01-29 Inter Ikea Systems B.V. Chip board and a process for the preparation thereof
WO2006027763A2 (en) * 2004-09-09 2006-03-16 Fastform Research Limited Geometrically apertured protective and/or splint device comprising a re-mouldable thermoplastic material
WO2008041215A1 (en) * 2006-10-03 2008-04-10 Fastform Research Limited Orthopaedic devices
WO2008124035A2 (en) * 2007-04-09 2008-10-16 University Of Connecticut Ring-opening polymerization of cyclic esters, polyesters formed thereby, and articles comprising the polyesters
US20120071590A1 (en) * 2009-03-11 2012-03-22 Onbone Oy Novel composite materials comprising a thermoplastic matrix polymer and wood particles
US20120090759A1 (en) * 2009-03-11 2012-04-19 Onbone Oy Method of producing composite materials

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
"CAPA for bioplastics," Informational Slides from PERSTORP, 2015, 22 pages. *
Elias, H.-G., "Plastics, General Survey," Ullmann's Encyclopedia of Industrial Chemistry, published online 2000, Vol 28, pages 35-154. *
Material safety data sheet for CAPA polycaprolactones. Perstorp. 2007. *
Particle Size Conversion Table. Downloaded from the aldrich website on January 22, 2014. Two pages. *
Trademark registration record for "Lignocel." Registration date of September 8, 1987. Downloaded from the USPTO website on January 23, 2014. *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160068682A1 (en) * 2013-06-21 2016-03-10 Lg Hausys, Ltd. Board comprising biodegradable resin and wooden flour and method of manufacturing the same
US10285844B2 (en) 2013-10-07 2019-05-14 Wichita State University Rapid setting composite article
US11278442B2 (en) 2013-10-07 2022-03-22 Wichita State University Rapid setting composite article
US11865025B2 (en) 2013-10-07 2024-01-09 Wichita State University Rapid setting composite article
US20170354861A1 (en) * 2016-06-10 2017-12-14 Onbone Sports Limited Sports protection device
WO2018104940A1 (en) * 2016-12-05 2018-06-14 CASSIT ORTHOPEDICS Ltd. Thermoplastic orthopedic devices
EP3547972A4 (en) * 2016-12-05 2020-10-28 Cassit Orthopedics Ltd. THERMOPLASTIC ORTHOPEDIC DEVICES

Also Published As

Publication number Publication date
JP5761719B2 (ja) 2015-08-12
EP2405951A2 (en) 2012-01-18
EP2405949B1 (en) 2020-09-16
WO2010103188A2 (en) 2010-09-16
EA201190165A1 (ru) 2012-03-30
AU2010222771B2 (en) 2015-02-26
CA2755128C (en) 2019-01-08
FI20095251A (fi) 2010-09-12
WO2010103188A3 (en) 2010-12-29
EP2405950B1 (en) 2020-09-16
US20120071590A1 (en) 2012-03-22
US9803080B2 (en) 2017-10-31
WO2010103186A3 (en) 2011-01-06
CA2755126A1 (en) 2010-09-16
KR101706662B1 (ko) 2017-02-14
NZ595557A (en) 2015-01-30
EA201190164A1 (ru) 2013-01-30
ZA201107118B (en) 2012-06-27
JP5670361B2 (ja) 2015-02-18
KR101756305B1 (ko) 2017-07-10
US20170058120A1 (en) 2017-03-02
KR20120026033A (ko) 2012-03-16
EP3106180A3 (en) 2017-02-22
WO2010103187A3 (en) 2011-01-06
AU2010222771A1 (en) 2011-11-03
EA023530B1 (ru) 2016-06-30
CA2755126C (en) 2019-03-05
EP2405950A2 (en) 2012-01-18
NZ595696A (en) 2014-03-28
HRP20201963T1 (hr) 2021-02-05
EP2405951B1 (en) 2017-11-22
CN102387818B (zh) 2014-10-22
WO2010103186A2 (en) 2010-09-16
AU2010222772A1 (en) 2011-10-27
FI20095251A0 (fi) 2009-03-11
EP2405949A2 (en) 2012-01-18
BRPI1008947A2 (pt) 2016-08-16
FI125448B (fi) 2015-10-15
CN102387818A (zh) 2012-03-21
EP2405949B8 (en) 2020-11-18
US20120090759A1 (en) 2012-04-19
PL2405949T3 (pl) 2021-04-19
JP2012520099A (ja) 2012-09-06
CN102405062B (zh) 2014-12-17
EP2405950B8 (en) 2020-11-18
HRP20201971T1 (hr) 2021-02-05
AU2010222772B2 (en) 2014-10-23
ES2836949T3 (es) 2021-06-28
CN102405062A (zh) 2012-04-04
CA2755128A1 (en) 2010-09-16
KR20120044921A (ko) 2012-05-08
JP2012520368A (ja) 2012-09-06
EA022386B1 (ru) 2015-12-30
EP3106180A2 (en) 2016-12-21
ES2835653T3 (es) 2021-06-22
WO2010103187A2 (en) 2010-09-16
US10336900B2 (en) 2019-07-02
US20140188021A1 (en) 2014-07-03
ZA201107117B (en) 2012-06-27

Similar Documents

Publication Publication Date Title
US9803080B2 (en) Orthopaedic splinting system
US9226846B2 (en) Bandaging material
FI126725B (fi) Hengittävät materiaalit
US20160250063A1 (en) Novel materials

Legal Events

Date Code Title Description
AS Assignment

Owner name: ONBONE OY, FINLAND

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:PARSSINEN, ANTTI;REEL/FRAME:027304/0321

Effective date: 20110923

STCB Information on status: application discontinuation

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