Abstract: The present invention relates to a determination method and system thereof. The method includes: providing or receiving a urine sample; distributing the urine sample into a first urine sample and a second urine sample; measuring a total protein concentration of the first urine sample; measuring a creatinine concentration and an albumin concentration of the second urine sample; and calculating a urine protein to creatinine ratio (UPCR) and a urine albumin to creatinine ratio (UACR), in which the UPCR is defined as a ratio of the total protein concentration to the creatinine concentration, and the UACR is defined as a ratio of the albumin concentration to the creatinine concentration.

Abstract: A centrifugal rotor includes a support disk and a centrifugal carrier. The centrifugal carrier is assembled within the support disk. The centrifugal carrier includes an arc-shaped body, a sample application chamber, a sample metering chamber, a diluent chamber, a diluent metering chamber, a metering control member and a mixing chamber. The sample metering chamber is communicated with the sample application chamber. The sample metering chamber is positioned radially outward from the sample application chamber. The diluent metering chamber is communicated with the diluent chamber. The diluent metering chamber is positioned radially outward from diluent chamber. The metering control member is slidingly connected within or detachably fixed to the sample metering, chamber or the diluent metering chamber. The mixing chamber is communicated with the diluent metering chamber and the sample metering chamber respectively.

Abstract: A centrifugal rotor includes a rotor body, a diluent container, a piercing structure and a capping film. The rotor body has a receiving cavity. The diluent container is located within the receiving cavity and has a seal film. The piercing structure is located within the receiving cavity and in contact with the seal film. The capping film is located over the diluent container and the piercing structure for securing the diluent container and the piercing structure within the receiving cavity.

Abstract: A centrifugal rotor includes a support disk and a centrifugal carrier. The centrifugal carrier is assembled within the support disk. The centrifugal carrier includes an arc-shaped body, a sample application chamber, a sample metering chamber, a diluent chamber, a diluent metering chamber, a metering control member and a mixing chamber. The sample metering chamber is communicated with the sample application chamber. The sample metering chamber is positioned radially outward from the sample application chamber. The diluent metering chamber is communicated with the diluent chamber. The diluent metering chamber is positioned radially outward from diluent chamber. The metering control member is slidingly connected within or detachably fixed to the sample metering, chamber or the diluent metering chamber. The mixing chamber is communicated with the diluent metering chamber and the sample metering chamber respectively.

Abstract: A centrifugal rotor includes a rotor body, a diluent container, a piercing structure and a capping film. The rotor body has a receiving cavity. The diluent container is located within the receiving cavity and has a seal film. The piercing structure is located within the receiving cavity and in contact with the seal film. The capping film is located over the diluent container and the piercing structure for securing the diluent container and the piercing structure within the receiving cavity.

Abstract: A body fluid absorption object wetting alarm method and an apparatus associated are revealed. A light wavelength sensor is disposed on a body fluid absorption unit for detecting wavelength of the body fluid absorption unit. After the body fluid absorption unit becoming wet, the wavelength thereof changes. Then warning signals are sent to the receiving and checking unit. Thus, a caregiver at a management end of the receiving and checking unit knows that the body fluid absorption object worn by a care recipient was already wet and there is a need to replace the wet body fluid absorption unit with a new one immediately.

Abstract: An analytical system includes a working fluid, a uniform dividing unit and a separating unit. The working fluid includes a first component and a second component with different characteristics. The uniform dividing unit is utilized to uniformly divide the working fluid and relatively rotated with respect to a reference axis. Under a capillarity force as well as the result of Coriolis force and siphon force, the first component can be separated from the second component by the separating unit.

Abstract: An analytical system includes a working fluid, a uniform dividing unit and a separating unit. The working fluid includes a first component and a second component with different characteristics. The uniform dividing unit is utilized to uniformly divide the working fluid and relatively rotated with respect to a reference axis. Under a capillarity force as well as the result of Coriolis force and siphon force, the first component can be separated from the second component by the separating unit.

Abstract: Luminescence-based compositions for measurement of aspartate aminotranserase, alanine aminotransferase, total-bilirubin, creatinine phosphokinase, or lactate dehydrogenase, wherein the chemiluminescence-based composition comprises 0.01-100 mM of luminol, 0.001-1000 U/mL of horseradish peroxidase (HRP), 0-10% of Triton X-100, 0-100 mM PIP, and 5˜500 mM of buffer at pH 6˜9, and the luminescence-base composition measures Aspartate aminotransferase (AST), alanine aminotransferase (ALT), total bilirubin, or lactate dehydrogenase (LDH).

Abstract: An immunoassay cartridge for sensing at least one analyte in a biological sample is disclosed. The immunoassay cartridge comprises a supporting plate, a reaction cavity made within the supporting plate and having at least one analyte-binding molecule immobilized therein, a sample receiving end connected to the reaction cavity to allow the biological sample to flow into the reaction cavity for forming at least one complex of the analyte and the analyte-binding molecule, a first package containing a recognizing molecule, a first channel communicating the first package and the reaction cavity to allow the recognizing molecule to flow into the reaction cavity for forming a first product of the complex and the complex-binding molecule, a second package containing a buffer solution and a second channel communicating the second package and the reaction cavity to allow the buffer solution to flow into the reaction cavity.

Abstract: Luminescence-based recipes for the measurement of creatinine, urea, uric acid, or glucose, and device using the same are provided.

Abstract: Luminescence-based recipes for the measurement of creatinine, urea, uric acid, or glucose, and device using the same are provided.

Abstract: An immunoassay cartridge for sensing at least one analyte in a biological sample is disclosed. The immunoassay cartridge comprises a supporting plate, a reaction cavity made within the supporting plate and having at least one analyte-binding molecule immobilized therein, a sample receiving end connected to the reaction cavity to allow the biological sample to flow into the reaction cavity for forming at least one complex of the analyte and the analyte-binding molecule, a first package containing a recognizing molecule, a first channel communicating the first package and the reaction cavity to allow the recognizing molecule to flow into the reaction cavity for forming a first product of the complex and the complex-binding molecule, a second package containing a buffer solution and a second channel communicating the second package and the reaction cavity to allow the buffer solution to flow into the reaction cavity.

Abstract: A device for detections of one or more analytes in one or more samples is disclosed. The device can simultaneously detect multiple analytes in a sample or an analyte in a plurality of samples. The device has a plurality of wells formed thereon. Each of the well has a respective composition loaded therein, wherein each of the composition comprising a respective catalyst is encapsulated in sol-gel. In addition, a first fluorescent dye and a second fluorescent dye are encapsulated in the sol-gel or added to the sample(s) for detection and quantitation. The catalyst(s) interacts with or reacts with the specific analyte(s) in the sample(s) and causes a change(s) in spectroscopic property. The concentration of an analyte(s) is detected by comparing the normalized spectroscopic property to a standard curve. A method is also disclosed for the detection of one or more analytes in one or more samples by using the device.