Prefilled syringe and method of preparing a prefilled syringe

Patent metadata

Field	Value
Publication number	US-12296138-B2
Application number	US-201816651440-A
Country	US
Kind code	B2
Filing date	Sep 28, 2018
Priority date	Sep 29, 2017
Publication date	May 13, 2025
Grant date	May 13, 2025

Abstract

A method of preparing a prefilled syringe is disclosed that includes obtaining a syringe barrel and a needle adaptor cap assembled on the tip of the syringe barrel, wherein the needle adaptor cap has a rubber element tightly sealing the orifice of the tip of the syringe barrel and the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel is sterilized by a first sterilizing. Filling a drug substance into an interior of the syringe barrel and sealing the interior of the syringe barrel. Packaging the syringe barrel with a rubber stopper sealing the interior thereof and the needle adaptor cap assembled on the tip of the syringe barrel. Providing a second external surface sterilizing of the packaged syringe barrel with the rubber stopper sealing the interior thereof and the needle adaptor cap assembled on the tip of the syringe barrel.

First claim

The invention claimed is:

1. A method of preparing a prefilled syringe, comprising:
obtaining a syringe barrel having an open end and a tip with an orifice essentially opposite to the open end, and a needle adaptor cap assembled on the tip of the syringe barrel, wherein the needle adaptor cap has a rubber element tightly sealing the orifice of the tip of the syringe barrel and the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel is sterilized, prior to filling or sealing an interior of the syringe barrel, by performing a first sterilizing comprising a main step of exposing to the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide;
filling a drug substance through the open end of the syringe barrel or through the orifice of the syringe barrel into an interior of the syringe barrel;
sealing the interior of the syringe barrel by advancing a rubber stopper through the open end of the syringe barrel;
packaging the syringe barrel together with the rubber stopper sealing the interior of the syringe barrel and the needle adaptor cap assembled on the tip of the syringe barrel; and
performing a second external surface sterilizing of the packaged syringe barrel together with the rubber stopper sealing the interior of the syringe barrel and the needle adaptor cap assembled on the tip of the syringe barrel,
wherein the second external surface sterilizing comprises a main step of exposing to pulses of vaporized hydrogen peroxide the packaged syringe barrel together with the rubber stopper sealing the interior of the syringe barrel and the needle adaptor cap assembled on the tip of the syringe barrel to at least six pulses of vaporized hydrogen peroxide for at least about five minutes per pulse at a relative humidity of about 40% to about 100%.

2. The method of claim 1 , wherein the main step of the first sterilizing is performed in a sterilization chamber.

3. The method of claim 1 , wherein the main step of the first sterilizing comprises exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide for about 5 hours to about 60 hours at a relative humidity of about 40% to about 100% and at a temperature of about 30° C. to about 60° C.

4. The method of claim 1 , wherein the main step of the first sterilizing comprises exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide at a pressure of about 450 millibars to about 1000 millibars.

5. The method of claim 1 , wherein in the main step of the first sterilizing the ethylene oxide is provided in a concentration of about 400 milligrams per liter to about 800 milligrams per liter.

6. The method of claim 1 , wherein the main step of the first sterilizing comprises flushing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel with air, nitrogen or a combination thereof at a pressure of about 100 millibars or about 200 millibars to about 800 millibars or about 900 millibars after exposing the syringe barrel together with the needle adaptor cap to ethylene oxide.

7. The method of claim 1 , wherein the first sterilizing comprises a pre-conditioning step of exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide for about 12 hours to about 96 hours at a relative humidity of about 40% to about 100% and at a temperature of about 30° C. to about 60° C., wherein the pre-conditioning step of the first sterilizing is executed prior the main step of the first sterilization, wherein the pre-conditioning step of the first sterilizing is performed outside a sterilization chamber.

8. The method of claim 1 , wherein the first sterilizing comprises a pre-conditioning step of exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to ethylene oxide for about 10 minutes to about 2 hours at a relative humidity of about 40% to about 100% and at a temperature of about 30° C. to about 60° C., wherein the pre-conditioning step of the first sterilizing is executed prior the main step of the first sterilization, wherein the pre-conditioning step of the first sterilizing preferably is performed inside a sterilization chamber.

9. The method of claim 1 , wherein the first sterilizing comprises an aeration step of exposing the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel to an air flow for at least about 12 hours at a temperature of about 30° C. to about 60° C., wherein the aeration step of the first sterilizing is executed after the main step of the first sterilizing.

10. The method of claim 1 , wherein the second external surface sterilizing comprises a pre-conditioning step of exposing the packaged syringe barrel together with the rubber stopper sealing the interior of the syringe barrel and the needle adaptor cap assembled on the tip of the syringe barrel to about 1 to about 10 pulses of vaporized hydrogen peroxide at a temperature of about 20° C. to about 40° C. or of about 25° C. to about 35° C. or of about 27° C. to about 29° C., wherein the pre-conditioning step of the second external surface sterilizing is performed outside a sterilization chamber, and the pre-conditioning step of the second external surface sterilizing is performed at various different pressures having a low pressure of about 1 millibar to about 10 millibars and a high pressure of about 100 millibars to about 300 millibars.

11. The method of claim 1 , wherein the second external surface sterilizing comprises a post-conditioning step for removing vaporized hydrogen peroxide, wherein the post-conditioning step of the second external surface sterilizing is performed outside a sterilization chamber, wherein the post-conditioning step comprises flushing the packaged syringe barrel together with the rubber stopper sealing the interior of the syringe barrel and the needle adaptor cap assembled on the tip of the syringe barrel with air for about 10 minutes to about 1 hour at a pressure of about 300 millibars to about 1000 millibars.

12. The method of claim 1 , wherein filling the drug substance into the interior of the syringe barrel and sealing the interior of the syringe are performed in a cleanroom, wherein the second external surface sterilizing is performed outside the cleanroom.

13. The method of claim 1 , wherein, after the sealing of the open end of the syringe barrel, an auxiliary component is mounted to the syringe barrel.

14. The method of claim 1 , wherein the rubber element of the needle adaptor cap and the rubber stopper are made of a rubber material having an oxygen transmission rate at 1 atmosphere of not more than about 971 cubic centimeter per square meter and day, of not more than about 732 cubic centimeter per square meter and day, of not more than about 200 cubic centimeter per square meter and day, of not more than about 150 cubic centimeter per square meter and day, of not more than about 120 cubic centimeter per square meter and day, of between about 115 cubic centimeter per square meter and day and about 116 cubic centimeter per square meter and day, of not more than about 110 cubic centimeter per square meter and day, of not more than about 100 cubic centimeter per square meter and day, of not more than about 90 cubic centimeter per square meter and day, of not more than about 80 cubic centimeter per square meter and day, of not more than about 70 cubic centimeter per square meter and day, of not more than ab

Assignees

• Hoffmann La Roche
• Genentech Inc

Inventors

• Hemminger Markus
• Grauschopf Ulla
• Bamberg Frank
• Bowen Mayumi
• Müller Robert
• Felsovalyi Flora
• Christensen Denny

Classifications

• A61L2103/15

  Laboratory, medical or dentistry appliances, e.g. catheters or sharps · CPC title

• B65B55/02

  Sterilising, e.g. of complete packages · CPC title

• B65B3/003

  Filling medical containers such as ampoules, vials, syringes or the like · CPC title

• A61M2207/00

  Methods of manufacture, assembly or production · CPC title

• A61M5/3202

  Devices for protection of the needle before use, e.g. caps (A61M5/50 takes precedence; for infusion spikes A61M5/1626; protectors for sharps A61B50/3001) · CPC title