Glass manufacturing – Processes – Forming product or preform from molten glass
Reexamination Certificate
2000-11-01
2002-07-09
Colaianni, Michael (Department: 1731)
Glass manufacturing
Processes
Forming product or preform from molten glass
C065S036000, C065S056000, C065S057000, C065S102000, C065S112000, C065S105000, C065S108000, C065S109000, C065S166000, C065S177000, C065S292000, C065S296000, C425S392000, C425S393000, C264S154000, C264S238000, C264S255000, C264S259000, C264S267000, C264S319000, C264S299000, C264S325000
Reexamination Certificate
active
06415631
ABSTRACT:
FIELD OF THE INVENTION
The invention is in the field of needleless injectors which use a capsule for containing a liquid drug to be injected, and needle-type hypodermic syringe bodies.
BACKGROUND OF THE INVENTION
Needleless injectors are used as an alternative to conventional hypodermic injectors to deliver medicaments through the patient's skin into the underlying tissues. Such injectors use a high pressure piston pump to dispense a jet of liquid drug with sufficient force to penetrate the skin, and thereafter deposit the drug into the dermal. subcutaneous or muscular tissues.
The drug is dispensed from a cylindrical chamber, having a fine orifice at one end through which the drug is discharged. A piston is slidingly and sealingly located in the chamber, and the drug is contained within the space between the orifice and piston. To make an injection, the orifice is placed on the skin, and by operating a release mechanism, the piston is acted upon by a force which may be derived from a spring, pressurised gas or chemical reaction.
The capsule may be filled by the user, or may be prefilled and pre-assembled to an actuator. In the latter case particularly, the materials from which the capsule and piston are constructed must be inert to the drug—i.e. they must not react with the drug chemically, nor physically, and must not contain harmful extractives that might contaminate the drug. The choice of materials is small: borosilicate glass is the most favoured capsule material when drugs must be stored for more than a few hours. If an alternative material is selected for the capsule, years of testing must be done to validate that material, whereas borosilicate glass has a known compatibility with most drugs.
During the injection, the pressure generated in the capsule is at least 100 bars, and it is preferable, in order to avoid leakage during injection, that the orifice is integral with the cylindrical chamber. Furthermore, the form and dimension of the orifice is critical to the injection performance, and for repeatable results these features should be made to close tolerances. However, glass is a difficult material to mould and maintain such close tolerances over many millions of components. One traditional method is to work the heated and softened end of a glass tube on a lathe, and by applying a shaping wheel or paddle, to close up one end onto a mandrel to form the orifice. This is a relatively crude method, and the only parameters that may be controlled accurately are the orifice diameter and the diameter of the surrounding glass: the length and entry profile of the orifice are left to chance because the process shapes only the outside of the tube and the orifice diameter. An alternative process is moulding, whereby a hot “gob” of molten glass is moulded in a die. This process is suitable for large components, but needleless injector capsules are seldom larger than 1 ml capacity, and such a small gob of glass loses its heat rapidly and is difficult to mould. Also the surface finish inside a moulded tube is not smooth enough for this application, nor is the bore parallel. Drawn tubing, which has an excellent surface finish and form, is the preferred starting material, but current working methods, as described, do not provide control of both inside and outside dimensions.
Conventional glass hypodermic syringes are made on automatic lathes from glass by working heat-softened tube, as previously described. Low cost disposable glass syringes are generally made with the hollow needle glued into a precisely formed hole in one end of the syringe body. The manufacturing process is relatively primitive, with low production rates and high reject rates.
OBJECT OF THE INVENTION
The present invention seeks to overcome the drawbacks of current glass tube forming methods by providing a means of forming the orifice, and the inside and outside profiles of a needleless injector capsule or hypodermic syringe body, which means has excellent repeatability and is capable of high speed production.
SUMMARY OF THE INVENTION
According to the invention there is provided a method of making an article from a formable material, the article having a cavity communicating with the exterior via an orifice, wherein a blank having an open end is mounted on a first forming tool, and the open end is engaged by a second forming tool while an end region of the blank adjacent the said open end is in a condition to permit it to be formed, one of the said tools having a pin extending therefrom, and the said one tool and the other of said tools are brought together to form the said end region into a desired shape, with the pin defining the said orifice.
The invention further provides an apparatus for making an article from a formable material, the article having a cavity communicating with the exterior via an orifice, comprising a first forming tool for receiving an open-ended blank, and a second forming tool for engaging an end region of the blank adjacent the open end thereof to form the same, one of the said tools having a pin extending therefrom, the tools being so arranged that when they are brought together to form the said end region into a desired shape the pin defines the said orifice.
The pin can be on either of the forming tools, though in the embodiments described below it is preferably on the first forming tool.
In a preferred embodiment of the invention, a glass tube, cut to length, is placed onto a mandrel having a profile to which the glass may be formed. The mandrel has a pin at its extreme for forming the orifice. The glass is rotated and heated on the end to be formed. When it is at the optimum forming consistency, a form tool having a profile to which the outside of the tube is to be formed, is applied to the exterior of the glass tube and presses the softened glass onto the mandrel and pin. Immediately before forming, the rotation of the glass tube is stopped; alternatively the external forming tool is rotated at the same speed as the tube, so that there is no relative movement between the tube and external form tool.
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Briggs Christopher John
Weston Terence Edward
Colaianni Michael
Darby & Darby
Weston Medical Limited
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