Device and method for sample collection
The present disclosure provides devices, methods and kits for collecting a sample of a subject for nucleic acid amplification. The device may comprise: a collection vessel that can include reagents necessary for nucleic acid amplification, wherein the collection vessel may be adapted to accept at least one swab containing a sample; a cap integrated with the collection vessel and having a channel extending therethrough to permit the at least one swab to be deposited in the collection vessel, wherein the channel is closable upon rotation of the cap; and at least one cutting member that severs a longitudinal portion of a stem of the swab extending through said channel upon rotation of the cap.
1. A device for collecting a sample from a subject for nucleic acid amplification, comprising:
a collection vessel that includes reagents necessary for nucleic acid amplification, wherein said collection vessel is adapted to accept at least one swab containing said sample;
a cap integrated with said collection vessel and having a channel extending therethrough to permit said at least one swab to be deposited in said collection vessel, wherein said channel is closable upon rotation of said cap; and
at least one cutting member that severs a longitudinal portion of a stem of said at least one swab extending through said channel upon rotation of said cap,
wherein said collection vessel and/or said cap are dimensioned such that upon depositing said at least one swab in said collection vessel, said stem of said at least one swab extends through said channel, and
wherein upon rotation of said cap, said at least one cutting member severs a longitudinal portion of said stem of said at least one swab extending through said channel to provide said at least one swab sealed in said collection vessel and in contact with said reagents necessary for nucleic acid amplification.
2. The device of claim 1 , wherein rotation of said cap provides a hermetic seal to said collection vessel.
3. The device of claim 1 , wherein said at least one cutting member is integrated with said cap.
4. The device of claim 1 , wherein said stem of said at least one swab includes a collar capable of engaging with said channel to provide said stem extending through said channel when said at least one swab is deposited in said collection vessel.
5. The device of claim 1 , wherein said cap includes a gasket that provides a seal to said collection vessel upon rotation of said cap.
6. The device of claim 1 , wherein said at least one cutting member includes at least one blade.
7. The device of claim 6 , wherein said at least one cutting member is in said channel.
8. The device of claim 6 , wherein said at least one blade is rotatable with respect to a circumference of said channel.
9. The device of claim 6 , wherein said at least one blade includes at least two blades.
10. The device of claim 1 , wherein said at least one swab includes at least two swabs.
11. The device of claim 10 , wherein said at least one swab includes at least five swabs.
12. The device of claim 10 , wherein said at least two swabs are integrated with said stem.
13. The device of claim 1 , wherein rotation of said cap seals said channel.
14. The device of claim 13 , wherein upon rotation of said cap to seal said channel, said cap moves towards said collection vessel.
15. The device of claim 1 , wherein said collection vessel includes identifying information of said subject.
16. The device of claim 15 , wherein said identifying information is encoded in a barcode.
17. The device of claim 15 , wherein said identifying information is encoded in a radio-frequency identification (RFID) tag.
18. The device of claim 1 , wherein said collection vessel includes identifying information that anonymously identifies said bodily fluid sample from said subject.
19. The device of claim 1 , wherein said reagents include one or more primers and a polymerizing enzyme.
20. The device of claim 19 , wherein said reagents include magnesium (Mg) or manganese (Mn) ions.
21. The device of claim 19 , wherein said one or more primers have sequences that are configured to assay for a presence of an infectious disease in said subject.
22. A method for collecting a biological sample from a subject for nucleic acid amplification, comprising:
(a) providing a collection device comprising (i) a collection vessel that includes reagents necessary for nucleic acid amplification, wherein said collection vessel is adapted to accept at least one swab containing said biological sample, (ii) a cap integrated with said collection vessel and having a channel extending therethrough to permit said at least one swab to be deposited in said collection vessel, wherein said channel is closable upon rotation of said cap, and (iii) at least one cutting member that severs a longitudinal portion of a stem of said at least one swab extending through said channel upon rotation of said cap, wherein said collection vessel and/or said cap are dimensioned such that upon depositing said at least one swab in said collection vessel, said stem of said at least one swab extends through said channel;
(b) depositing said at least one swab having said biological sample from said subject in said collection vessel, and
(c) rotating said cap, wherein upon rotation of said cap, said at least one cutting member severs a longitudinal portion of said stem of said at least one swab extending through said channel to provide said at least one swab sealed in said collection vessel and in contact with said reagents necessary for nucleic acid amplification.
23. A kit for nucleic acid amplification, comprising:
a collection device comprising (i) a collection vessel that includes reagents necessary for nucleic acid amplification, wherein said collection vessel is adapted to accept at least one swab, (ii) a cap integrated with said collection vessel and having a channel extending therethrough to permit said at least one swab to be deposited in said collection vessel, wherein said channel is closable upon rotation of said cap, and (iii) at least one cutting member that severs a longitudinal portion of a stem of said at least one swab extending through said channel upon rotation of said cap, wherein said collection vessel and/or said cap are dimensioned such that upon depositing said at least one swab in said collection vessel, said stem of said at least one swab extends through said channel; and
instructions that permit a user to (a) collect a biological sample from a source of said sample using said at least one swab, and (b) deposit said at least one swab having said biological sample into said collection vessel to provide a reaction mixture comprising said biological sample and said reagents necessary for nucleic acid amplification.