Carefusion 2200, Inc.

Satish Degala

Kenneth Bruce Thurmond, Ii

Kenneth Bruce Thurmond

Christopher Matthew McGinley

Christopher Matthew Mcginley

Benjamin Thomas Krupp

Andre M Rustad

David Andrew Parrott

Louis P Mingione

Michael McMahon

Charlie Beuchat

Angel Magallon

Kenneth Michael Dokken

Maya Prakash Singh

Christopher Mcginley

Taryn Bagby

Aishwarya Vaidyanathan

Michael Mcmahon

Maya P Singh

Benjamin T Krupp

An antiseptic polymeric material, wherein an antimicrobial compound is covalently bonded to the material, and the material is used for contacting with a luer lock. The antiseptic polymeric material may help disinfect or prevent any further microbial contamination to the luer lock, wherein the use of a covalently bound antimicrobial compound may also reduce any risk of having the antimicrobial compound entering the intravenous line and being exposed to the patient bloodstream. Preferably, the antiseptic polymeric material may be used in the healthcare industry for disinfection, the suppression of, reduction in and/or maintenance of the microbial load on a surface of the luer lock.

Inclusion of bound antiseptic in a luer lock

A method for sterilizing an antiseptic solution includes providing a container containing the antiseptic solution, the antiseptic solution having an initial purity, selecting a sterilization temperature from about 85&#xb0; C. to about 135&#xb0; C. and an sterilization time from about 1 minute to about 19 hours, heating the antiseptic solution to the selected sterilization temperature, maintaining the temperature for the selected sterilization time, and terminating the heating of the antiseptic solution when the sterilization time expires. After terminating the heating, the antiseptic solution has a post-sterilization purity. The sterilization temperature and the sterilization time are selected such that after terminating the heating, the antiseptic solution is sterile and has a post-sterilization purity of at least about 92% and the percentage point change in purity from the initial purity to the post-sterilization purity is at most about 5%.

Systems, methods, and devices for sterilizing antiseptic solutions

An applicator assembly includes at least one ampoule formed of a frangible material and containing liquid to be applied, a body having a proximal end, a distal end, and an interior portion defining a chamber adapted to receive the at least one ampoule, an application member attached to the distal end of the body, an actuator projecting from the body operable to fracture the at least one ampoule, a trench formed in a surface of the body, and a vent disposed through a surface of the trench.

Antiseptic applicator

A method for sterilizing an aqueous antiseptic solution, the method comprising providing a container containing the aqueous antiseptic solution, the aqueous antiseptic solution comprising a bis-(dihydropyridinyl)-decane derivative or a biguanide, heating the aqueous antiseptic solution to a predetermined temperature, maintaining the aqueous antiseptic solution at the predetermined temperature for a predetermined time, and terminating the heating of the aqueous antiseptic solution when the predetermined time expires. The predetermined temperature and the predetermined time are selected such that after terminating the heating, the aqueous antiseptic solution is sterile.

An applicator assembly may include a body having a proximal end portion and a distal end portion, an actuator operatively coupled to the body, a container disposed within the body, an application member attached to the distal end portion, and a valve disposed between the container and the application member. Actuation of the actuator opens the valve and places the interior of the container in fluid communication with the application member by way of a compressive force applied to the body. A method of applying a solution to a surface may include actuating the actuator, wherein actuation of the actuator applies a compressive force to the body that opens the valve and places the interior of the container in fluid communication with the application member, and contacting the application member to the surface, thereby applying the solution to the surface.

A method for sterilizing an antiseptic solution includes providing a plurality of containers containing the antiseptic solution, the antiseptic solution having an initial purity, selecting a sterilization temperature from about 85&#xb0; C. to about 135&#xb0; C. and an sterilization time from about 1 minute to about 19 hours, heating the antiseptic solution in the plurality of containers to the selected sterilization temperature, maintaining the temperature for the selected sterilization time, and terminating the heating of the antiseptic solution when the sterilization time expires. After terminating the heating, the antiseptic solution in the plurality of containers has a post-sterilization purity. The sterilization temperature and the sterilization time are selected such that after terminating the heating, the antiseptic solution is sterile and have a post-sterilization purity of at least about 92% and the percentage point change in purity from the initial purity to the post-sterilization purity is at most about 5%.

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Arlington Heights, IL, United States of America

Satish Degala