This invention relates to the measurement of hemoglobin in the blood. Previously, chemical interference from medications, other blood components, and incomplete reagent rehydration can impact the accuracy and prolong the reaction time required to determine total hemoglobin in blood. Embodiments of the present invention use a disposable body is housed within the capillary channel and adapted to receive a flow of blood from the entrance such that air in the disposable body is pushed out through a vent. A measurement system is configured to measure a property of the flow of blood. That property can be correlated to total hemoglobin count.

A method and system for early detection of Bovine Mastitis (BM) uses enhanced chemiluminescence (CL) to determine Haptoglobin (Hp) levels in highly diluted milk samples. The samples are placed in the wells of one or more bio-functionalized Hemoglobin (Hb) modified CL assay plates. Hp-Hb binding occurs in those samples containing Hp. After a first pre-determined time duration, the wells are treated with a CL solution containing luminol and peroxide, and a colloidal suspension of crosslinked nanoparticles. After a second pre-determined time duration, the CL intensity approaches a steady state value. A processor analyzes CL images provided by a camera in order to measure CL intensity and to determine an estimate of Hp level in each well, based on a pre-determined regression curve. The processor then forms a BM clinical diagnosis by combining the estimated HP levels from wells with different milk sample dilutions.

A method for determining the amount of glycated haemoglobin (HbA1c), in whichif requiredthe erythrocytes in a sample are haemolysed, the haemoglobin that is then releasedif requiredis contacted with a proteolytic agent and the glycated haemoglobin degradation products obtained in this way or otherwise are quantified is disclosed. In order to provide such a process and reagents employable therein that has/have the property of sufficient stability of the chemical compounds that are essential to the reaction, the provision of the requisite proteolytic agent in the form of an inactivated protease is proposed, which is then only reactivated in situ. For the stabilization of the haemoglobin, which is unfolded at a very low pH in the range from 1 to 3, at least one suitable stabilizer should be present in the haemolysis solution, and, where a leuco dye is used in connection with the determination of the amount of HbA1c, it is proposed that the latter be stabilized with particular phosphine compounds and/or thio compounds.

In one aspect, the inventive concepts disclosed herein are directed to a chromatographic assay device for detecting the presence of free hemoglobin in a whole blood sample. The device comprising a chromatographic detection pad with a sample application site and a detection side. The chromatographic detection pad defines a path for capillary fluid flow. The chromatographic detection pad has a pore size. The sample application site on the chromatographic detection pad is for application of a portion of the whole blood sample. The detection site on the chromatographic detection pad is spaced apart from the application site and is downstream of the sample application site. The chromatographic detection pad is devoid of a compound located downstream of the application site that is reactive to the whole blood sample.

A method for determining the amount of glycated haemoglobin (HbA1c), in whichif requiredthe erythrocytes in a sample are haemolysed, the haemoglobin that is then releasedif requiredis contacted with a proteolytic agent and the glycated haemoglobin degradation products obtained in this way or otherwise are quantified is disclosed. In order to provide such a process and reagents employable therein that has/have the property of sufficient stability of the chemical compounds that are essential to the reaction, for the stabilization of the haemoglobin which is unfolded at a very low pH in the range from 1 to 3, at least one suitable stabilizer is present in the haemolysis solution. Where a leuco dye is used in connection with the determination of the amount of HbA1c, it is proposed that the latter be stabilized with particular phosphine compounds and/or thio compounds, and, in particular embodiments, the requisite proteolytic agent is to be provided in the form of an inactivated protease which is then only reactivated in situ.

Provided in the present application are a composition for detecting occult blood in excreta, and a preparation method therefor and the use thereof. The composition comprises, in parts by weight, 20-80 parts of organic solvent, 0.01-50 parts of thickener, 0.01-2 parts of benzidine, 0.01-5 parts of peroxide, 0.001-0.5 parts of EDTA-2Na and 10-80 parts of water. The composition provided in the present application can quickly and effectively detect the occult blood condition of excreta, has fast color change, long color retention time and high sensitivity.