Abstract: The multichannel capillary biosensor system includes a selecting valve system for selection of the sample or a reagent. The selecting valve system is connected to a second valve system accommodating a sensing channel and a first bypass channel. The second valve system is connected to a directing valve system having at least two positions, with a first position being connected to a second bypass channel and a second position being connected to a detector for detecting the analyte. The device has a pump connected at one end to the second bypass channel and the detector and at a second end to a waste vessel. The device also has a control system for controlling the device. The analyte can be selected from the group of microorganisms, macromolecules, and small molecules.

Abstract: A method for determining a concentration of a contaminant in a first sample, the method including producing the first sample, including adding a plurality of immuno-beads to a test substance; exposing a crystal microbalance immunosensor to the first sample; determining a change in a first motional resistance of the crystal microbalance immunosensor following exposure to the first sample (?R1); and determining the concentration of the contaminant in the first sample according to ?R1.

Abstract: The multichannel capillary biosensor system includes a selecting valve system for selection of the sample or a reagent. The selecting valve system is connected to a second valve system accommodating a sensing channel and a first bypass channel. The second valve system is connected to a directing valve system having at least two positions, with a first position being connected to a second bypass channel and a second position being connected to a detector for detecting the analyte. The device has a pump connected at one end to the second bypass channel and the detector and at a second end to a waste vessel. The device also has a control system for controlling the device. The analyte can be selected from the group of microorganisms, macromolecules, and small molecules.

Abstract: A method for determining a concentration of a contaminant in a first sample, the method including producing the first sample, including adding a plurality of immuno-beads to a test substance; exposing a crystal microbalance immunosensor to the first sample; determining a change in a first motional resistance of the crystal microbalance immunosensor following exposure to the first sample (?R1); and determining the concentration of the contaminant in the first sample according to ?R1.

Abstract: Methods are provided for detecting, separating, isolating and quantifying contaminants in starting materials by separating the contaminant from the starting material using a bead coupled to an affinity moiety and quantum dot-labeling the contaminant. The contaminant is detected by the characteristic emission spectrum of the quantum dot. Also, competitive binding methods are provided wherein the starting material and a control material are contacted with a quantum dot coupled to an affinity moiety capable of binding the contaminant and a competitor complex. A decrease in the intensity of the characteristic emission spectrum of the quantum dot associated with the competitor complex from the starting material as compared to that of the control material is indicative of the presence of the contaminant in the starting material.

Abstract: A method for detecting contaminants in a solution by determining a change in resonant frequency (?F) and motional resistance (?R) of a crystal microbalance (CM) immunosensor is presented. The method includes measuring ?F and determining ?R of a CM immunosenor exposed to various samples including known concentrations and a sample including an unknown concentration of the contaminant. The unknown contaminant concentration may be determined according to ?R of the samples with the known and unknown contaminant concentrations, or ?F of the same. If ?R of the CM immunosensor exposed to the samples with the known contaminant concentrations more accurately reflects the known contaminant concentrations than ?F does, the unknown contaminant concentration may be determined according to ?R of the samples with the known contaminant concentrations and the unknown contaminant concentration. Otherwise, the unknown contaminant concentration may be determined according to ?F of the same.