Sealing Cap for Sealing a Sample Tube for Receiving a Liquid

Abstract

A sealing cap seals a sample tube for receiving a liquid, in particular blood. The sealing cap includes a cavity delimited by a membrane and a base having an opening that can be sealed by a non-return valve. In order to reduce the volume of liquid which, during centrifugation of the sample tube sealed by the sealing cap, flows out of the sealing cap through the then open opening into the sample tube, the cavity of the sealing cap has a separating wall that divides the cavity into a first and a second sub-area. Only the second sub-area is above the opening, also meaning that only the volume of liquid in the second sub-area can flow into the sample tube.

Claims

1.-8. (canceled)

9. A sealing cap (100) for sealing a sample tube (200) containing a liquid (300), comprising: a membrane (110) that can be pierced by a cannula (400); a base (120) arranged below the membrane, the base (120) having an opening (121); a cavity (130) formed between the membrane (110) and the base (120) for receiving the liquid (300); and a non-return valve (160) for unblocking the opening (121) in the base (120) to allow the liquid (300) to flow out of the cavity (130) into the sample tube (200) and for sealing the opening (121) to allow the liquid (300) to flow out of the sample tube (200) into the cavity (130), wherein the cavity (130) has a separating wall (150) for dividing the cavity into a first sub-area (131) and a second sub-area (132), wherein the separating wall (150) extends into the cavity (130) from the base (120) of the cavity (130), wherein the first sub-area (131) is formed above a region of the base (120) without the opening (121), wherein the second sub-area (132) is formed above the opening (121) in the base (120), and wherein the first sub-area (131) and the second sub-area (132) are in fluid communication with each other, and wherein the separating wall (150) comprises, at an end facing the membrane (110), an overflow edge (151) and/or a perforation (152), for enabling the fluid communication between the first sub-area (131) and the second sub-area (132).

10. The sealing cap (100) according to claim 9, wherein the first sub-area (131) is larger than the second sub-area (132).

11. A blood collection tube (500) comprising: a sample tube (200) for receiving a liquid (300) having a sealable end (210); and the sealing cap (100) according to claim 9 for sealing the sample tube at its sealable end (210).

12. A method for handling the blood collection tube (500) according to claim 11, comprising the steps of: sealing the sample tube (200) at its sealable end (210) with the sealing cap (100) according to 9; piercing the membrane (110) in the sealing cap (100) with one end of a cannula (400); withdrawing liquid (300) from a body with the other end of the cannula (400), wherein the liquid (300) flows through the cannula (400) and the membrane (110) into the cavity (130) of the sealing cap (100) and subsequently flows through the opening (121) in the base (120) of the sealing cap (100), which is opened in a flow direction by the non-return valve (160), into the sample tube and fills it; removing the cannula (400) from the membrane (110), whereupon the membrane (110) automatically seals again; and centrifuging the blood collection tube (500) to separate the liquid (300) into heavier and lighter components, wherein the non-return valve (160) releases the opening (121) in the base (120) of the sealing cap (100) due to a centrifugal force, such that the liquid (300) flows out of the cavity (130) into the sample tube (200); wherein, upon the withdrawal of the liquid (300), both the first sub-area (131) and the second sub-area (132) of the cavity (130), which are connected to one another in a fluid-conducting communicating manner, are filled with liquid (300); wherein during centrifugation, only liquid (300) from the second sub-area (132), in the base (120) of which the opening (121) is formed, flows into the sample tube (200); and wherein, upon withdrawing the liquid from the body, the liquid first flows into and fills the first sub-area (131) of the sealing cap (100), and then flows via an overflow (151) and/or through a perforation (152) into the second sub-area (132).

13. The method according to claim 12, wherein the sample tube (200) has been provided with a preparation for blood prior to sealing with the sealing cap (100).

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0021] FIG. 1: Illustration of the blood collection tube;

[0022] FIG. 2: Illustration of the flow-through sealing cap;

[0023] FIG. 3: Illustration of a detail from FIG. 2 showing an overflow edge or perforation, as the case may be;

[0024] FIGS. 4a-d: Illustration of the filling process of the sealing cap over time;

[0025] FIG. 5: Illustration of the sealing cap with connected sample tube; and

[0026] FIG. 6 Illustration of a cross-section through the sealing cap.

DETAILED DESCRIPTION

[0027] The invention is described in detail below with reference to the specified figures in the form of exemplary embodiments. In all figures, the same technical elements are designated with the same reference signs.

[0028] FIG. 1 depicts a blood collection tube 500 consisting of a sealing cap 100 and a sample tube 200 for receiving a fluid 300 from a human or animal body.

[0029] Preferably, the sealing cap 100 comprises a connecting part 140 for connecting the sealing cap 100 to the sample tube 200 or for sealing the sample tube 200, as the case may be. The connecting part 140 can be configured as a screw, bayonet or plug-in connection. The connection must be liquid-tight and/or air-tight according to the requirements. It may be necessary to use additional sealants for this purpose. The connecting part may also be completely dispensable, for example if the sealing cap is simply plugged onto the sample tube.

[0030] FIG. 2 shows an illustration of the sealing cap 100 through which a liquid 300 flows and which seals the sample tube 200. A cavity 130 is formed in the sealing cap 100, which is delimited by a membrane 110 and a base 120. An opening 121 is formed in the base, which can be opened or sealed by a non-return valve 160. The non-return valve 160 is configured to allow fluid 300 to flow from the cavity 130 in the sealing cap 100 into the sample tube 200, but to block the opposite direction.

[0031] The membrane 110 can be pierced by a cannula 400. The cannula 400 establishes a fluid-conducting connection between the sealing cap 100 and the body from which the fluid is withdrawn, and directs the fluid 300 into the cavity 130 of the sealing cap 100. The cavity 130 is divided by a separating wall 150 into a first, preferably larger, sub-area 131 and a second, preferably smaller, sub-area 132. The larger sub-area 131 does not have an opening 121 in its base 120. The smaller sub-area 132 is formed above the opening 121 in the base 120. For example, the volume of the smaller sub-area is in a range between 0-70 μl (microliter).

[0032] The design of the separating wall 150 is such that a flow-through area is created between the two sub-areas 131, 132. The flow-through area can result from a gap between an overflow edge 151 of the separating wall 150 and the membrane 110 above it and/or a perforation 152 in the separating wall 150 (FIG. 3). The flow-through area must be large enough to ensure sufficient liquid flow during sampling. Both sub-areas 131/132 are thus connected to each other in a fluid-conducting communicating manner. The separating wall 150 preferably extends from the base 120 of the sealing cap in the direction of the membrane 110.

[0033] The vector arrows in FIG. 2 indicate a direction of flow of the fluid 300 through the two sub-areas 131/132 and the opened sealing element 161 into the sample tube 200.

[0034] The handling method in accordance with the disclosure is described below with reference to FIGS. 2 to 5. The sealing cap 100 is used to seal a sealable end 210 of the sample tube 200. Prior to sealing, a preparation can be added to the sample tube 200. The optional insertion of the preparation and/or the necessary sealing of the blood collection tube can be performed by the manufacturer. The blood collection tube 500 thus assembled can be filled with the fluid 300.

[0035] For this purpose, the body is punctured, for example with a cannula 400. One side of the cannula 400 pierces the body, and the other side pierces the membrane 110 in the sealing cap 100, see FIG. 4a.

[0036] The fluid 300 flows out of the body through the cannula 400 into the cavity 130 of the sealing cap 100, due to an existing negative pressure in the sample tube. Depending on the type of construction of the blood collection tube, the vacuum in it is already introduced there by the manufacturer. Other blood collection techniques, such as the vacuum principle or the aspiration principle, are conceivable. Interaction by the user is then required to build up pressure in the sample tube.

[0037] If a plunger or piston, as the case may be, of the sample tube is manually pulled into a rear locking position before puncturing a vein in the body, the vacuum in the blood collection tube is thereby built up only if required shortly prior to blood collection and the collection of the blood then takes place analogously to the manufacturer's pre-evacuated tube with vacuum technology (vacuum principle). We speak of aspiration technique when coupling with the vein occurs initially and blood sampling occurs in parallel with the piston stroke.

[0038] In the cavity 130 of the sealing cap 100, the large sub-area 131 is preferably filled initially, see FIG. 4b. Subsequently, the liquid 300 flows over the overflow edge 151 and/or through the perforation 152 into the small sub-area 132, see FIG. 4c. Optionally, only the smaller sub-area can be filled.

[0039] Due to an existing pressure difference between the negative pressure in the sample tube 200 and the pressure in the sealing cap 100, the non-return valve 160 opens during a blood sample collection. The liquid 300 then drains from the sealing cap 100, and in particular from its smaller sub-area, into the sample tube 200, see FIG. 4d.

[0040] Once the sample tube 200 is sufficiently filled with the fluid 300, the sampling is interrupted by cutting off the fluid line between the body and the blood collection tube. This results in a pressure equalization in the blood collection tube; in particular, it relieves the negative pressure in the sample tube. Once the pressure difference between the blood collection tube 500 and the volume 130 in the sealing cap 100 is equalized, this causes the non-return valve 160 to close again. The sample tube 200 is then sealed in a fluid-conducting manner with respect to the sealing cap.

[0041] Upon a processing of the liquid 300 in the blood collection tube 500 in a centrifuge, which follows the sampling, a force F directed towards the base of the sample tube acts on the blood collection tube 500; see the arrow in FIG. 5. This causes the heavy components to separate from the light components in the liquid 300. This force F, if sufficient, will also reopen the non-return valve 160 and the liquid 300 will flow unintentionally from the cavity of the sealing cap into the sample tube 200.

[0042] However, as shown in FIG. 5, only the volume of liquid from the second, preferably smaller, sub-area 132 flows into the sample tube 200. In contrast, the liquid 300 remains in the first, preferably larger, sub-area 131 in the sealing cap 100.

[0043] If the dimensions of the second, preferably smaller, sub-area 132 in the sealing cap 100 are sufficiently small relative to the total amount of liquid in the sample tube, the quality of the liquid required for subsequent analysis can be ensured, even if the liquid 300 flows from the smaller sub-area 132 into the sample tube 200.

[0044] FIG. 6 shows a cross-section through the sealing cap 100 in accordance with the invention. In particular, an exemplary arrangement and configuration for the separating wall 150 and for the larger sub-area 131 and the smaller sub-area 132 can be seen.

REFERENCE SIGNS

[0045] 100 Sealing cap

[0046] 110 Membrane

[0047] 120 Base

[0048] 121 Opening

[0049] 130 Cavity

[0050] 131 First, preferably larger sub-area

[0051] 132 Second, preferably smaller sub-area

[0052] 140 Connecting part

[0053] 150 Separating wall

[0054] 151 Overflow edge

[0055] 152 Perforation

[0056] 160 Non-return valve

[0057] 170 Sealing region

[0058] 200 Sample tube

[0059] 210 Sealable end

[0060] 300 Liquid

[0061] 400 Cannula

[0062] 500 Blood collection tube