초록 ▼

Bodily fluid sample transport systems, devices, and method are provided. In at least one embodiment described herein, methods are provided for the physical transport of small volumes of bodily fluid in liquid form from one location to another location. By way of nonlimiting example, the samples are

Bodily fluid sample transport systems, devices, and method are provided. In at least one embodiment described herein, methods are provided for the physical transport of small volumes of bodily fluid in liquid form from one location to another location. By way of nonlimiting example, the samples are collected in liquid form at a collection site, transported in liquid form, and arrive at an analysis site in liquid form. In many embodiments, the liquid form during transport is not held in a porous matrix, wicking material, webbing, or similar material that prevents sample for being extracted in liquid form at the destination site. In one embodiment, small volume of sample in each sample vessel is in the range of about 1 ml to about 1 microliter.

대표청구항 ▼

1. A method comprising: collecting a bodily fluid sample on a surface of a subject, wherein collected sample is stored in one or more sample vessels;providing a transport container to house at least two or more sample vessels in a first orientation and holding the vessels in a two-dimensional, non-l

1. A method comprising: collecting a bodily fluid sample on a surface of a subject, wherein collected sample is stored in one or more sample vessels;providing a transport container to house at least two or more sample vessels in a first orientation and holding the vessels in a two-dimensional, non-linear array configuration;arranging to have the sample vessels shipped in the transport container from a first location to a second location,wherein each of the sample vessels arrives at the second location holding a majority of its bodily fluid sample in a non-wicked, non-matrixed form that is removable from the sample vessels in liquid form and wherein the amount of sample in each of the sample vessels does not exceed about 2 ml; andscanning information storage units on substantially all of the sample vessels from the transport container, wherein the scanning occurs substantially simultaneously while the samples vessels are held in the non-linear array configuration at the second location. 2. The method of claim 1 wherein the bodily fluid sample is capillary blood. 3. The method of claim 1 wherein collecting comprises making at least one puncture on the subject to release the bodily fluid, wherein the puncture is not a venipuncture. 4. The method of claim 1 wherein collecting comprises using at least one lancet to make at least one puncture on the subject. 5. The method of claim 4 the puncture is formed by pricking skin on a forearm of the subject. 6. The method of claim 1 wherein the sample vessel has an interior that is initially at sub-atmospheric pressure prior to drawing sample into the interior of the sample vessel. 7. The method of claim 6 wherein the sub-atmospheric pressure is selected to provide sufficient force to draw a desired volume of sample into the sample vessel. 8. The method of claim 1 wherein the transport container contains at least five or more sample vessels. 9. The method of claim 1 wherein the transport container is used to simultaneously ship bodily fluid samples from a plurality of different subjects. 10. The method of claim 1 wherein information associated with each of the sample vessels determines what tests will be run on the bodily fluid sample therein. 11. The method of claim 1 further comprising using a cooled tray to hold the samples vessels in a temperature controlled storage chamber prior to loading the vessels into the container and the same cooled tray is used to hold the sample vessels in the transport container, wherein the samples are placed into transport container with the cooled tray. 12. The method of claim 1 wherein sample vessels are arranged such that there are at least two vessels in each container with bodily sample fluid from the same subject, wherein at least a first sample includes a first anticoagulant and a second sample includes a second anticoagulant in the matrix. 13. The method of claim 1 the fluid sample comprises capillary blood for use in CLIA compliant laboratory testing. 14. The method of claim 1 further comprising using a housing providing a controlled thermal profile and high heat of fusion material providing at least one cooling surface facing the sample vessels. 15. The method of claim 14 wherein controlled thermal profile, high heat of fusion material is embedded in material used to form the container. 16. The method of claim 1 further comprising scanning an information storage unit on each sample at a transport container receiving site and automatically placing the container into a cartridge. 17. The method of claim 1 further comprising using the same tray to hold sample vessels in an array configuration when in a refrigeration device prior to transport and in the transport container. 18. The method of claim 17 wherein the tray comprises a plurality of slots having a shape to hold sample vessels holders in a preferential orientation, wherein the sample vessels cannot be inserted in a different orientation. 19. The method of claim 11 further comprising using a single step to load a plurality of sample vessels from cooled storage into the transport container while maintaining a desired sample-vessel-to-sample-vessel orientation during the loading step. 20. The method of claim 1 wherein the transport container has a first surface configured to define a preferential thermally conductive pathway to a controlled thermal profile, high heat of fusion material in the transport container.