Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/02—Chemical treatment or coating of shaped articles made of macromolecular substances with solvents, e.g. swelling agents
• • 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
  • A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
  • A61L29/04—Macromolecular materials
  • A61L29/06—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/12—Chemical modification
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
  • C08J2367/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds

Definitions

• PET Polyethylene terephthalate
• polyethylene terephthalate are derived from the film form. Films are prepared by any number of techniques well known to the practitioner, including extrusion. Moreover if the polyethylene terephthalate film is olecularly oriented, certain physical properties such as tensile strength, impact strength, flex life, water vapor, and organic vapor permeability and tensile modulus are enhanced.
• U.S. 2,823,421 which is incorporated by reference herein, is directed to the stretching of polyethylene terephthalate film to produce an oriented product having an outstanding combination of physical, chemical and electrical properties.
• An extruded, molten, amorphous film of polyethylene terephthalate is continuously longitudinally stretched at least at the rate of 400 percent per minute no greater than 3.25 times at a temperature of between 80-90°C.
• the longitudinally stretched film is preheated at between 90-95°C and continuously transversely stretched substantially the same amount of at least 400 percent per minute at a temperature of 90-110°C to produce a balanced film.
• the biaxially stretched film is thereafter heat-set at a temperature within the range 150-250°C.
• Oriented polyethylene terephthalate is widely used in a variety of industries including electronics (as dielectrics, coverings, and the like), the wire and cable industry (as for example filaments and protective sheaths), fibers, and polymeric articles of manufacture (such as beverage containers) , to name a few. It finds particular application in the medical device field, including medical dilatation products where strength is a critical property.
• U.S. Re 33,561 relates to balloon catheters especially useful in medical dilatation procedures, and is incorporated by reference herein. This patent provides for balloon catheters useful for the relief of arterial stenosis and other ailments requiring a surgical procedure involving insertion of an instrument into blood vessels or body cavities.
• balloons are effective in that they have thin walls which are flexible and readily collapsible and easily transportable within the body.
• Other physical properties include minimal radial expansion on inflation, and high burst strength (and rupture if at all in the axial direction to ensure against a traumatic removal) , among other attributes making these balloons effective for a number of medical procedures.
• the patent requires that the flexible balloon be made of a high molecular weight, biaxially oriented polymer having a burst pressure of at least 200 psi (1.4 MPa) and a radial expansion of less than 5 percent at 200 psi (1.4 MPa) .
• oriented polyethylene terephthalate film is that it is difficult to adhesively bond to other polymeric substrates. Such adhesion is desirable as with Re 33,561 inasmuch as the polymeric balloon must be suitably attached to other medical instruments for insertion into a vessel and surgical manipulation.
• the surface adhesion properties of oriented polyethylene terephthalate film are improved when it is subjected to a surface treatment. Such treatments include, for example, subjecting the film to any of the following: electrical stress accompanied by corona discharge; a flame; a gaseous plasma (such as oxygen, chlorine, etc.); short wave ultraviolet light; and oxidizing chemicals (sulfuric acid-dichromate, potassium permanganate, etc.).
• the treated surface is generally characterized by measuring the contact angle between a drop of liquid (usually water) and the treated surface, according to conventional techniques.
• a drop of liquid usually water
• the Sessile drop technique as reviewed by R. E. Johnson, Jr. and R. H. Dettre, "Surface and Colloid Science", Volume 2, Interscience, New York, NY, 1969 measures advancing and receding contact angles for two chemicals at a given temperature.
• High contact angle values indicate a low concentration of polar groups (or less adhesion) and low values indicate a high concentration of polar groups (or more adhesion) .
• the article of oriented polyethylene terephthalate has an initial polarity associated with it.
• the surface treatment (a) increases the polarity and further the solvent contact (b) decreases the polarity resulting from (a) .
• the net effect of steps (a) and (b) is that the polarity of the polyethylene terephthalate is increased relative to the initial polarity.
• a wide variety of articles of manufacture are contemplated for preparation according to the process of the invention. Films and tubes made be prepared by this process, with the size and shape to be selected according to the needs of the practitioner.
• medical dilatation balloons are advantageously prepared according to Re 33,561 and using oriented polyethylene terephthalate film with enhanced properties according to the presently disclosed process.
• Polyethylene terephthalate is prepared by any of a number of techniques; one such procedure is according to U.S. 2,465,319.
• the resulting product in the form of a film is next stretched in longitudinal and transverse directions in a manner such as is described in U.S.
• surface is any of the surfaces of the article for which enhanced properties according to this invention is desired. It may be one side of the article or for example the inside and outside of a dilatation balloon.
• the surface treatment may be selected from a wide variety of conventional techniques, including without limitation electrical stress accompanied by corona treatment; plasma treatment; flame treatment; ultraviolet light treatment; and chemical treatment.
• Corona treatment and ultraviolet light treatment can be conducted according to the procedures set forth in Owens, D. K., "The Mechanism of Corona and Ultraviolet Light Induced Self-Adhesion of Poly(ethylene terephthalate) Film", Journal of Applied Polymer Science. Vol. 19, pp. 3315-3326 (1975). Corona treatment is also described in Owens, D. K., “Mechanism of Corona-Induced Self-Adhesion of Polyethylene Film", Journal of Applied Polymer Science. Vol. 19, pp. 265-271
• suitable solvents for contact with the surface of the polyethylene terephthalate include ketones, alcohols, and esters, each of these categories having from 3 to 12 carbon atoms (branched or linear) , amides having from 2 to 12 carbon atoms (branched or linear), chloroform, and carbon disulphide. More preferred solvents from this group are isopropanol, acetone, carbon disulphide, chloroform, cyclohexanol, and formamide. Our research indicates that acetone is the most preferred solvent.
• the biaxially oriented polyethylene terephthalate is contacted with acetone for a period of at least about 1 minute, at ambient temperature. From the moment of application of room temperature acetone through about the first 5 minutes, there is a reduction in surface blocking observable. From about 5 minutes to about 10 minutes this effect is measurable. From about 10 to about 30 minutes there is observed an increased alteration of surface polarity, and during the ensuing period from about 30 to about 60 minutes still further reduction of blocking is observable. The period of from about 60 minutes to about 120 minutes after application of the acetone is considered to achieve the maximum effective increase in surface polarity, and after this interval there is a tendency for blocking to increase.
• the solvent is removed.
• the treatment is effective with some solvent present on the article after removal, so that substantially all of the solvent is removed. Removal may be by air drying for a suitable period of time or by other methods, including partial reclamation of the solvent.
• polar and dispersive surface tensions of the article In addition to observations on polarity, another means to define the invention claimed herein is to measure polar and dispersive surface tensions of the article. This may be done by other methods readily understood by those skilled in the art. Using the surface tension approach, the process involves first forming the article of biaxially oriented polyethylene terephthalate having a ratio of the polar surface tension to the dispersive surface tension usually about 0.25. The article is next treated on a surface by exposure to an ionizing energy source (e.g., plasma) such that the ratio is greater than about 0.7. The article is then contacted with a solvent such that the ratio is decreased relative to that observed after surface treatment but increased to that observed for the untreated article. Substantially all of the solvent is then removed.
• an ionizing energy source e.g., plasma
• a biaxially oriented polyethylene terephthalate (OPET) film was prepared by extruding polyethylene terephthalate polymer having an intrinsic viscosity of about 1.0 into film having a thickness of 0.23 mm at a temperature of 280°C by conventional means and then biaxially orienting the extruded film 3 times the original length in the machine direction and 4 times the original length in the transverse direction using a T. M. Long Laboratory Film Stretcher at a temperature between 90 and 95°C.
• the OPET film was then heat set by clamping the film between frames to prevent shrinking, and then heated at 180°C for 1 minute in a hot air oven.
• the surface of the film was then plasma treated in an oxygen atmosphere for 8 minutes at 300 watts.
• a drop of deionized water was placed on the treated surface at one end of a 1 inch by 2 inch strip of film, which was then folded lengthwise so that the treated surfaces were facing each other with a layer of water between them.
• the water promotes the tendency of the material to block insofar as it accelerate hydrogen bonding at high humidity conditions.
• the folded sample was allowed to sit overnight (about 16 hours) . Attempts to separate the folded film resulted in tearing and delamination indicating severe blocking of the surfaces.
• the treated surface of the plasma treated film of Comparative Example 1 was washed with acetone and allowed to dry in air. A drop of deionized water was placed on the treated surface and then the film was folded so that the treated surfaces were facing each other with a layer of water between the surfaces. Plasma treated films that were not washed with acetone were prepared in a similar manner. After an hour of contact time the unwashed film samples had blocked surfaces while the acetone washed sample could be separated without tearing and delamination. COMPARATIVE EXAMPLE 3
• PET resin having an intrinsic viscosity of 1.05, a density of 1.41 g/cm 3 and a diethylene glycol content of 1.8 weight percent was dried to less than 0.005 weight percent water at 177°C and then processed into single lumen tubing having an outside diameter of 0.34 mm and a wall thickness of 0.0*64 mm using conventional tubing extrusion techniques.
• Biaxially oriented balloons having an outside diameter of 3 mm, a single wall thickness of 0.0076 mm and a cylindrical length of 2 cm were fabricated from the extruded tubing using the process of U.S. Patent No. Re. 33,561 and then plasma treated in an oxygen atmosphere maintained at a pressure about 33.33 Pa in a Gasonics/IPC model 4155/2 plasma treater for 16 minutes at 300 watts and 13.56 MHz.
• seven balloons were placed in a glass container containing about 80 ml of acetone having a purity of 99.9% so that all surfaces of the balloons were completely contacted with the acetone inside and outside.
• a glass cover was placed over the container. After a one minute soak time the cover was removed and the balloons were taken out individually. Excess acetone was removed from the inside surfaces by wicking followed by an argon gas purge.
• the balloons were tested for blocking by connecting the proximal end of a balloon to a Tuohy-Borst adapter and then heat sealing the distal end with an electrical heating element.
• the Tuohy-Borst adapter with the sealed balloon attached was then connected to a "PRESTO" inflation device of C. R. Bard, Inc. (USCI Division), that had been deaerated as much as possible and contained 4 cm 3 of distilled water.
• the plunger was pulled to its limit to remove the air from the balloon while evacuating the balloon to a pressure of about 16 KPa. With the air out of the balloon the screw plunger was pushed and rotated to achieve a pressure of 1300 KPa.
• This pressure was held for one minute while the balloon was checked for leaks. If no leaks were found, the plunger was pulled to its limit, again with the pressure device pointing down, to achieve a balloon pressure of about 16 KPa. While ensuring that the balloon had been completely deflated, this pressure was held for 20 minutes. The balloon was then inflated to a pressure of 1200 KPa as quickly as possible and maintained at that pressure for one minute while the balloon was checked for leaks. The balloon pressure was returned to atmospheric and the Tuohy-Borst adapter and balloon were disconnected from the inflation device. The balloon inside surface was then examined for delamination caused by blocking using a stereo polarizing microscope. Changes in balloon wall thickness as a result of delamination were evident as localized differences in retardation colors when viewed between crossed polaroids.
• the Tuohy-Borst adapter with balloon was reattached to the inflation device and the vacuum - pressure - vacuum cycle was repeated except that the final vacuum was held for 40 minutes.
• the balloon was again checked for leaks at 1200 KPa and reinspected for delamination using the stereo polarizing microscope.
• the vacuum - pressure - vacuum cycle was repeated again except that the final vacuum was held for 140 minutes. Checks for leaks and delamination were repeated.
• Example 2 Four balloons were plasma treated and submerged in acetone as were described ' in Example 2 but processed in the following manner:
• Table 1 shows acetone washing has little or no effect on the polar surface tension of the inner surface of non-plasma treated balloons and a significant effect (reduction) on the polar surface tension of plasma treated balloons.
• EXAMPLE 4 The inside surfaces of the four balloons processed in the same manner as Example 3 were analyzed for surface element content using a Perkin Elmer PHI 5000 Electron Spectrometer for Chemical Analysis (ESCA) instrument. The results (Table 2) show that plasma treatment increases the polar group concentration on the surface and that plasma treatment followed by an acetone wash removes some of the polar groups, but not to the level of the untreated surface. The remaining polar groups on the inside surface of Type D balloons are sufficient to provide good adhesive strength, but do not contribute to blocking.
• EXAMPLE 4 The inside surfaces of the four balloons processed in the same manner as Example 3 were analyzed for surface element content using a Perkin Elmer PHI 5000 Electron Spectrometer for Chemical Analysis (ESCA) instrument. The results (Table 2) show that plasma treatment increases the polar group concentration on the surface and that plasma treatment followed by an acetone wash removes some of the polar groups, but not to the level of the untreated surface. The remaining polar groups on the inside surface of Type D balloons are
• Example 2 Five balloons were fabricated, plasma treated, and acetone washed as in Example 2, except that the acetone soak time was 5 minutes. Three of the balloons did not leak or show evidence of delamination after the described 140 minute period. The remaining two balloons leaked and showed evidence of delamination after the 140 minute period; this is probably due to variability in wall thickness and/or surface characteristics of these samples.
• Example 8 Five balloons were fabricated and plasma treated as in Example 2, but not subjected to acetone washing. Four of these balloons leaked and showed evidence of delamination after the first 20 minute cycle test procedure. One balloon did not leak or delaminate until the 140 minute test procedure; this is probably due to variability in wall thickness and/or surface characteristics of this sample. EXAMPLE 8
• the solvent contact times were 30, 90 and 270 minutes and the solvent temperatures were 24, 38 and 51°C.
• the ratio of the polar surface tension (PST) to dispersive surface tension (DST) of the inside surfaces of the balloons were measured as also described in Example 3.
• the experimental design runs and PST/DST ratios are given in Table 4.
• Example 5 The balloons were prepared as described in Example 3 (B) and the solvents and plasma treatment levels were also the same as in Example 8.
• the balloons were tested for blocking using the method described in Example 2.
• a blocking tendency value was determined for each run by assigning a value of 20 to balloons that failed after 20 minutes, 10 to balloons that failed after 40 minutes, 2 to balloons that failed after 140 minutes and 0 to balloons that did not fail after 140 minutes.
• the blocking tendency for a given run was the sum of the blocking tendency of the 5 replicates in the run.
• the experimental design runs and the blocking tendency values are given in Table 5.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Polymers & Plastics (AREA)
• Medicinal Chemistry (AREA)
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• Public Health (AREA)
• Veterinary Medicine (AREA)
• General Chemical & Material Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Life Sciences & Earth Sciences (AREA)
• Epidemiology (AREA)
• Treatments Of Macromolecular Shaped Articles (AREA)

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• 1993
  • 1993-08-20 WO PCT/US1993/007761 patent/WO1994004601A1/en not_active Application Discontinuation
  • 1993-08-20 EP EP93920162A patent/EP0656918A1/de not_active Withdrawn
  • 1993-08-20 JP JP6506504A patent/JPH08502767A/ja active Pending

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