Fluid connectors

4022205
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Inventors

Tenczar, Francis J.

Application #

412553

Filed

Nov-5-1973

Published

May-10-1977

Current US Class

029/432
138/109
222/80
285/21.2
285/3
285/423
285/901
285/915
604/411
604/905

International Classes

A61M 005/00; F16L 047/00

Field of Search

285/3 285/4 285/2 285/21 285/DIG. 21/54 83/171 128/272 128/214

Examiners

Callaghan; Thomas F.

Attorney, Agent or Firm

Dominik, Knechtel, Godula & Demeur

Referenced by:

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Citation

Cite This Patent

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Abstract
A connector means for conveying fluid from a supply source to a delivery location, said connectors having one conduit extending to the supply source and another conduit extending to the delivery location. Each terminal part has a cylindrical housing with a closed end to which the conduit is joined, and having an opposite operable end which is closed by a penetrable barrier. The barrier and closed end of the housing define an interior environment safe from external contaminants. A male tubular coupler is in one housing, a female tubular coupler is in the other housing, and a penetrator element is disposed around one of the tubular connectors. The penetrable barriers have a film of covered adhesive. The exposed adhesive films are placed in face to face contact to coaxially align the housing parts and bond the barrier membranes to exclude the environment. The penetrator element pierces the adhering barriers by either moving the penetrator element from one housing into the coaxially aligned housing, or by telescoping the housing cylinders so that the adhering barriers are contacted by the fixed penetrator element. The male tubular connector then engages the female tubular connector within a protected environment to effect connection between the supply source and the delivery location.
 
Claims
What is claimed is:

1. A connector assembly to prevent entry of contaminants, such as microorganisms, gases and particulates, including,

a pair of terminal connectors each terminal connector having a housing, a conduit extending from one end of the housing and communicating with the interior of the housing, an openable end of each housing closed by a penetratable barrier, a film of adhesive substantially covering the area of at least one of the barriers,

coupling means within each housing communicating with the conduit,

a penetrator element associated with one of the coupling means so that said barriers may be adhesively joined to immobilize any present environmental contaminants and to exclude contact with the environment at an area of adhesion and relative movement between the adhesively joined barriers and the penetrator element results in penetration of the barriers within the area of adhesion and communication between the terminal connectors so that fluid may move from a supply source to a delivery location through the conduits of the terminal connectors.



Description
This invention relates to an improved connector assembly, and particularly relates to a sterile connector assembly for blood bags or the like.

Connectors have been provided in the art for moving fluid under sterile conditions from a source to a delivered location, such as plastic blood bags. Such connectors are conventionally sterilized with a protective cover in place. When this cover is removed, the connector itself is exposed to the possibility of environmental (usually atmospheric) contamination in the time before the actual connection is frequently made with plastic bags for blood infusion and/or component preparation. Multiple transfers involving several bags and many different solutions increase the problem in procedures such as glyceralization, deglyceralization, and washing in the preparation of frozen red cells. Each manipulation of an exposed connector increases the likelihood of microbiological contamination. A connector that is manipulated while exposed to atmospheric contamination presents a serious problem to the practitioner and recipient. Although such exposed connectors may be rapidly connected to reduce the hazard of possible contamination such components have only a short useful time (now 24 hours) because of this danger of contamination. It will be appreciated that it is highly desirable to obtain a connection which can be made without loss of sterility. Reliably sterile connections would reduce wasteage of blood and components by increasing the safe time for use (expiration date) and encouraging component preparation.
 
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