Reagent cartridge for an assembly for selectively performing a clincial chemical test or an elisa test, use of said reagent cartridge and assembly

a technology for clincial chemical tests and assembly, which is applied in the field of assembly assembly assembly assembly assembly assembly assembly assembly assembly, can solve the problems of falsifying analysis, affecting the accuracy of clincial chemical tests, and reagents in other cavities may spill out of the cavities, so as to achieve the effect of enhancing binding of the desired antigen and huge cost savings

Inactive Publication Date: 2012-10-04
DRG INSTR
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  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

[0016]It is another advantage of the invention that the solid phase is made of a different material than the housing. For example, the solid phase can be made of polystyrene. This plastic primarily enhances binding of the desired antigen or antibody to the solid phase. At the same time however, it is not particularly resistant to many reagents needed for performing clinical chemical tests. One can see the benefit gained if the housing consists of another material as mentioned above. For example, it is conceivable that the housing is made of polypropylene, a much more resistant material. It is also ensured in this way that the antigen or the antibody will be coupled to the solid phase safely and lastingly while the reagents for performing clinical chemical tests can still be well stored in the reagent cartridge.
[0017]It is therefore advantageous if a reagent is pre-filled in at least one of the cavities while the solid phase is either charged with antibody, or is empty, or is used as diluting cavity.
[0018]The invention also relates to the use of a reagent cartridge according to the invention for analyzing a clinical chemical parameter in a sample, the use of a reagent cartridge according to the invention for analyzing a immunodiagnostic parameter in a sample, the use of a reagent cartridge according to the invention as a diluting device, and the use of a reagent cartridge according to the invention for providing additional reagents.
[0025]f) Removal of used reagent cartridges and sample containers.
[0026]It is apparent that, in this way, both clinical chemical parameters and immunodiagnostic components of a sample can be determined in one and the same procedure. First

Problems solved by technology

There is a risk that the reagents in the other cavities may spill out of the cavities when the user has to apply an adequate compressive force to press the well safely into the analytical insert.
There is another risk that the well in the end may not be correctly positioned in the analytical device, which may result in undesirable light refraction and deflection of the sample beam of the photometric device and falsify the analysis.
In addition, the analytical insert is very fragile, and just the rem

Method used

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  • Reagent cartridge for an assembly for selectively performing a clincial chemical test or an elisa test, use of said reagent cartridge and assembly
  • Reagent cartridge for an assembly for selectively performing a clincial chemical test or an elisa test, use of said reagent cartridge and assembly
  • Reagent cartridge for an assembly for selectively performing a clincial chemical test or an elisa test, use of said reagent cartridge and assembly

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Embodiment Construction

[0057]The reagent cartridge 10 shown in FIGS. 1, 2, and 3 consists of a housing 11 in which three cavities 12, 13, 14 are formed. The housing 11 also comprises a recess 15 into which a solid phase 20 can be inserted. The solid phase 20 has the form of a single well from a microtiter plate and is preferably made of polystyrene while the housing 11 and the cavities 12, 13, 14 are made of a resistant material matched to the reagents of the clinical chemical test, such as polypropylene.

[0058]The housing 11 has a main level 16 with a front end 161 and a rear end 162. When the reagent cartridge 10 is inserted into the analytical device, the bottom sides of its front and rear ends 161, 162 rest on the analytical device and thus secure it in its position (see also FIG. 5). It can be seen that the upper openings of the cavities 12, 13, 14 are located in the upper level 16. The recess 15 that is to accommodate the solid phase 20 is formed at a deeper level 18.

[0059]The solid phase 20 has been...

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Abstract

The invention relates to a reagent cartridge 10 for an assembly for selectively performing a clinical chemical test or an ELISA assay comprising a housing 11 having at least one cavity 12, 13, 14 that contains a reaction or diluting component and having a recess 15 in which a solid phase 20 to which an antigen or antibody can be coupled is inserted into the recess 15 of the housing 11. It is particularly advantageous if the reagent cartridge 10 comprises three cavities 12, 13, 14 and the reagent cartridge 10 can be used for analyzing clinical chemical parameters, for analyzing immunodiagnostic parameters, for providing additional reagents, and as a diluting cartridge.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application claims priority to PCT patent application PCT / EP / 2010 / 063732 filed on Oct. 17, 2010; and German patent application DE 051428.7 filed on Oct. 30, 2009, the contents of which are incorporated by reference.FIELD OF INVENTION[0002]The invention relates to a reagent cartridge for an assembly for selectively performing a clinical-chemical test or an ELISA test according to the preamble of claim 1, use of the reagent cartridge according to claims 11 to 15, and an assembly according to the preamble of claim 16.BACKGROUND OF THE INVENTION[0003]Among experts skilled in the art, analytical devices are known for the automatic determination of clinical chemical as well as immunodiagnostic parameters. The devices for determining clinical chemical parameters must meet different requirements than devices for determining immunological parameters.[0004]Clinical chemical parameters are typically determined in the liquid phase of a sample. A...

Claims

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Application Information

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IPC IPC(8): C12M1/40B01L3/00
CPCB01L2300/0609B01L2200/16B01L3/508G01N33/54386
Inventor JANETZKO, ALFREDSANGER, WILHELMGEACINTOV, CYRIL E.
Owner DRG INSTR
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