초록 ▼

A method and system for handling hazardous materials contained in a vial includes an isolation enclosure having an opening selectively sealable about the vial, a bag body portion, and a cap portion. A latching extraction element is attached to the cap portion and has a preceding engaging member to s

A method and system for handling hazardous materials contained in a vial includes an isolation enclosure having an opening selectively sealable about the vial, a bag body portion, and a cap portion. A latching extraction element is attached to the cap portion and has a preceding engaging member to secure the vial to the isolation enclosure, an extraction member to be inserted into the vial and remove material therefrom, and a primary engaging member to secure the vial to the extraction member. A valve is mounted outside the isolation enclosure and controls the flow of fluid from the vial. An adaptor having a reseal member permits flow when coupled to the valve and restricts flow when uncoupled from the valve. Once uncoupled, the adaptor is removably associated with a second valve located remotely from the isolation enclosure, allowing fluid to pass into the second valve.

대표청구항 ▼

We claim: 1. A method of accessing materials from a sealed vial, comprising: providing a latching extraction element comprising a body portion, an extraction member on the body portion adapted to be inserted into the vial, a preceding engaging member mounted the body portion, and a primary engaging

We claim: 1. A method of accessing materials from a sealed vial, comprising: providing a latching extraction element comprising a body portion, an extraction member on the body portion adapted to be inserted into the vial, a preceding engaging member mounted the body portion, and a primary engaging member mounted on the body portion to secure the vial to the extraction member, the preceding engaging member including a plurality of latch arms extending from the body portion in a direction common with the extraction member, the primary engaging member including a plurality of latch arms extending from the body portion in the common direction, the latch arms of the preceding engaging member extending a greater distance from the body portion in the common direction than the latch arms of the primary engaging member; placing the vial into an impermeable isolation enclosure through a selectively sealable opening thereof; securing the vial in a preceding fixed position in which the vial is secured to the latching extraction element but the extraction member is outside the vial by forcing the vial between and into engagement with the latch arms of the preceding engaging member; mounting the latching extraction element within and to the impermeable isolation enclosure; sealing closed the selectively sealable opening of the impermeable isolation enclosure; securing the vial to the latching extraction element in a primary fixed position by forcing the vial into engagement between the latch arms of the primary engaging member such that the extraction member pierces the vial; selectively accessing the contents of the vial externally from the closed impermeable isolation enclosure via a normally closed valve mounted to and outside of the impermeable isolation enclosure and in fluid communication with the extraction member of the latching extraction element; removing at least a portion of the contents of the vial through the valve and into a needleless syringe; transferring removed portion in isolation and maintaining a remaining portion of the contents in isolation within the vial while the vial remains pierced by the extraction member and in the primary fixed position; and adding a diluent to the vial via the valve while the vial is pierced and in the primary fixed position and the impermeable isolation enclosure is closed; wherein the step of adding the diluent includes venting gas from the vial through a vent channel extending through both the extraction member and the body portion to a vent port within the closed impermeable isolation enclosure. 2. The method of claim 1, wherein the latching extraction element is provided separate from the impermeable isolation enclosure and the step of securing the vial in the preceding fixed position is completed prior to the step of placing the vial into the impermeable isolation enclosure. 3. The method of claim 1, wherein the step of mounting the latching extraction element to the impermeable isolation enclosure comprises attaching the latching extraction element to an inlet port of a cap portion of the impermeable isolation enclosure. 4. The method of claim 1, wherein the step of adding a diluent comprises the substeps of: removably coupling a first end of an adaptor to a diluent-containing needleless syringe while a second end of the adaptor remains sealed by a normally closed reseal member so as to restrict diluent from leaking from the syringe; and then removably coupling the second end of the adaptor to the valve on the impermeable isolation enclosure so that the reseal member of the adaptor and the valve are opened to fluid flow. 5. The method of claim 1, wherein the step of mounting the latching extraction element to the impermeable isolation enclosure is completed prior to placing the vial into the impermeable isolation enclosure. 6. The method of claim 1, wherein the step of securing the vial in the preceding fixed position includes engaging a necked portion of the vial with the latch arms of the preceding engaging member. 7. The method of claim 6, wherein the step of securing the vial in the primary fixed position includes forcing the vial beyond the latch arms of the preceding engaging member and toward the extraction member such that the latch arms of the primary engaging member engage a necked portion of the vial. 8. The method of claim 1, wherein the step of securing the vial to the latching extraction element in the primary fixed position is accomplished by gripping the vial through a flexible portion of the impermeable isolation enclosure. 9. The method of claim 1, wherein the step of transferring the removed portion in isolation includes the substeps of: uncoupling the second end of the adaptor from the valve so as to restrict fluid flow from both the valve and the adaptor; moving the syringe to a desired destination for delivery of the removed portion; and removably coupling the second end of the adaptor to a second normally closed valve that is remote from the impermeable isolation enclosure.