Method for manufacturing balloons for medical devices

• US 5,223,205 A
• Filed: 10/03/1991
• Issued: 06/29/1993
• Est. Priority Date: 10/04/1988
• Status: Expired due to Term

• Current Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Original Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Inventors: Jackowski, Stefan, Pinchuk, Leonard
• Primary Examiner(s): Silbaugh, Jan H.
• Assistant Examiner(s): Timm, Catherine
• Application Number:
  US07/771,160
• Time in Patent Office: 635 Days
• Field of Search: 264/530, 264/529, 264/532, 264/521, 264/235, 264/572, 264/573, 425/529, 425/530, 425/522, 425/526, 425/532, 425/534
• US Class Current: 264/521
• CPC Class Codes: A61B 2017/00783 Valvuloplasty
• CPC Class Codes: A61M 25/1029 Production methods of the balloon members, e.g. blow-moulding, extruding, deposition or by wrapping a plurality of layers of balloon material around a mandril
• CPC Class Codes: A61M 25/1034 Joining of shaft and balloon
• CPC Class Codes: B29C 2049/465 being incompressible
• CPC Class Codes: B29C 2049/4655 water
• CPC Class Codes: B29C 2949/0715 the preform having one end closed
• CPC Class Codes: B29C 2949/08 Preforms made of several individual parts, e.g. by welding or gluing parts together
• CPC Class Codes: B29C 33/04 using liquids, gas or steam tyre moulds with incorporated heating or cooling means using liquids, gas or steam B29D30/0601
• CPC Class Codes: B29C 49/06 Injection blow-moulding
• CPC Class Codes: B29C 49/14 Clamps
• CPC Class Codes: B29C 49/18 using several blowing steps B29C49/16 takes precedence
• CPC Class Codes: B29C 49/6445 through the preform length
• CPC Class Codes: B29K 2105/258 Tubular
• CPC Class Codes: B29L 2031/7542 Catheters
• CPC Class Codes: Y10S 264/905 having plural, distinct differential fluid pressure shaping steps

Abstract

Apparatus and methods for forming dilatation balloons and catheters including same are provided. The balloons are fabricated of a material such as a nylon or a polyamide material, and they have been inflated, non-distended working profile as well as a stretched inflated profile which is achieved by applying pressure through a dilation catheter or the like that is in excess of that needed to achieve the inflated, non-distended profile and which is adequate to effect dilation or the like up to a maximum pre-bursting pressure application. The maximum pre-bursting size of the balloon can be tailored depending upon the needs of the particular balloon within a wide range of possible maximum pre-bursting sizes. The apparatus and methods facilitate fabrication of the balloons which are subjected to longitudinal elongation and radial expansion.

Claims

1. A process for fabricating medical device balloons, the process comprising:

feeding an elongated tubularly shaped parison into and through a molding apparatus including an upstream chamber and a downstream blow molding chamber until one portion of the parison is in the upstream chamber and another portion of the parison is in the downstream blow molding chamber;

axially stretching to longitudinally elongate at least the portion of the parison within the upstream chamber to provide an axially elongated parison length;

radially expanding the axially elongated parison length within the upstream chamber by infusing pressurized fluid thereinto to provide a radially expanded parison length;

axially stretching at least the portion of the radially expanded parison length until its diameter is decreased while moving the radially expanded parison length into the downstream chamber; and

blow molding the radially expanded and axially stretched parison length by infusing pressurized fluid thereinto while same is within the downstream blow molding chamber to provide a molded parison useful as a medical device balloon.

2. The balloon fabricating process according to claim 1, wherein said axially stretching steps are carried out when the chambers are at approximately room temperature.

3. The balloon fabricating process according to claim 1, wherein said radially expanding step is carried out when the upstream chamber is at an elevated temperature of between about 70°

C. and about 150°

C. or above.

4. The balloon fabricating process according to claim 1, wherein said blow molding step is carried out when the downstream blow molding chamber is at an elevated temperature of between about 70°

0 C. and about 150°

C. or above.

5. The balloon fabricating process according to claim 2, wherein said radially expanding step and said blow molding step are carried out when the chambers are at a temperature of between about 70°

C. and about 150°

C. or above.

6. The balloon fabricating process according to claim 1, wherein said feeding step feeds a parison tube of a nylon or of a polyamide, and wherein said step of axially stretching the fed parison is carried out when the upstream chamber is approximately room temperature and elongates the parison to at least twice the length of the parison prior to the axially stretching step.

7. The balloon fabricating process according to claim 3, further including thermally isolating the upstream chamber so that the elevated temperature of the radially expanding step is substantially confined to the portion of the parison to be radially expanded.

8. The balloon fabricating process according to claim 4, further including thermally isolating the blow molding chamber so that the elevated temperature of the blow molding step is substantially confined to the portion of the parison to be blow molded.

9. The balloon fabricating process according to claim 1, further including controlling the extent of radial expansion achieved by said radially expanding step by carrying out the radial expansion when the upstream chamber is at an elevated temperature and then reducing the temperature within the upstream chamber to about room temperature or lower as soon as a desired extent of radial expansion is achieved.

10. A process for fabricating medical device balloons, the process comprising:

feeding an elongated tubularly shaped parison through a molding apparatus including a free-blow chamber and a downstream blow molding chamber;

longitudinally stretching the parison within the free-blow chamber to provide an axially stretched parison length;

radially expanding the axially stretched parison length by infusing pressurized fluid thereinto while same is within the free-blow chamber to provide a radially expanded parison length;

axially stretching the radially expanded parison length;

blow molding the radially expanded and axially stretched parison length, said blow molding step including raising the temperature of the radially expanded and axially stretched parison within the downstream blow molding chamber and infusing the pressurized fluid into a portion of the elongated parison that is upstream of the free-blow chamber whereby the pressurized fluid flows through the parison within the free-blow chamber and then into the radially expanded and axially stretched parison within the downstream blow molding chamber;

closing off the parison between the free-blow chamber and the blow molding chamber to prevent passage of pressurized fluid therebetween, and radially expanding the axially stretched parison at an elevated temperature within the free-blow chamber to form another radially expanded parison length; and

axially stretching said another radially expanded parison length, following by blow molding same within the blow molding chamber at an elevated temperature to provide a molded parison useful as a medical device balloon.

11. The process according to claim 10, wherein said temperature of the blow molding step is higher than said temperature of the radially expanding steps, and wherein the pressure of the pressurized fluid of the blow molding steps is lower than the pressure of the pressurized fluid of the radially expanding steps.