Abstract: Apparatus for assessing the accuracy of a target stimulation intensity level used in transcutaneous electrical nerve stimulation to a user, the apparatus comprising: a calculation unit for calculating a set of expected values of the target stimulation intensity level for a desired sensation based on a profile of the user; a stimulation unit for electrically stimulating at least one nerve of the user at one or more stimulation levels; a discovery unit for enabling the user to indicate a target stimulation intensity level at which the electrical stimulation to the user evokes the desired sensation from the user; and an assessment unit to determine the accuracy of the indicated target stimulation intensity level based on the expected set of values of the target stimulation intensity level for the desired sensation.

Abstract: Apparatus for assessing the accuracy of a target stimulation intensity level used in transcutaneous electrical nerve stimulation to a user, the apparatus comprising: a calculation unit for calculating a set of expected values of the target stimulation intensity level for a desired sensation based on a profile of the user; a stimulation unit for electrically stimulating at least one nerve of the user at one or more stimulation levels; a discovery unit for enabling the user to indicate a target stimulation intensity level at which the electrical stimulation to the user evokes the desired sensation from the user; and an assessment unit to determine the accuracy of the indicated target stimulation intensity level based on the expected set of values of the target stimulation intensity level for the desired sensation.

Abstract: A noninvasive method for estimating a concentration of a target analyte in a sample comprises generating a first and second (reference) radiation, a principal radiation and a target analyte carrier detection radiation; directing the first, second, principal and the target analyte carrier detection radiations at the sample which includes the target analyte; and detecting a first, second, principal and target analyte carrier detection amount of the radiation that leaves the sample. The method further comprises modulating the sample thickness in order to achieve time-wise or spatial target analyte concentration variation within the sample.

Abstract: A noninvasive method for estimating a concentration of a target analyte in a sample comprises generating a first and second (reference) radiation, a principal radiation and a target analyte carrier detection radiation; directing the first, second, principal and the target analyte carrier detection radiations at the sample which includes the target analyte; and detecting a first, second, principal and target analyte carrier detection amount of the radiation that leaves the sample. The method further comprises modulating the sample thickness in order to achieve time-wise or spatial target analyte concentration variation within the sample.

Abstract: A noninvasive method for estimating a concentration of a target analyte in a sample comprises generating a first and second (reference) radiation, a principal radiation and a target analyte carrier detection radiation; directing the first, second, principal and the target analyte carrier detection radiations at the sample which includes the target analyte; and detecting a first, second, principal and target analyte carrier detection amount of the radiation that leaves the sample. The method further comprises modulating the sample thickness in order to achieve time-wise or spatial target analyte concentration variation within the sample.

Abstract: A method may include directing a radiation beam at a sample, the beam including two periods of radiation having different wavelengths, an analyte in a fluid within the sample having different absorption coefficients for the two different wavelengths, detecting the beam with a detector when the sample is in a first fluid state, the detector configured to generate an output signal proportional to an intensity of the beam at each of the two different wavelengths, detecting the beam with the detector when the sample is in a second fluid state, the sample transitioning from the first fluid state to the second fluid state by a pulsation of the sample, obtaining estimates of an amount of fluid at the first and second fluid states, and determining an analyte concentration estimate based on the output signal and the estimate of the amount of fluid at the first and second fluid states.

Abstract: An improved method for non-invasively measuring a concentration of a target analyte dissolved in a fluid flowing through a sample is presented. It includes directing a probe beam of electromagnetic radiation, having time multiplexed components of different wavelengths, where at least one of the time-multiplexed components consists of two different simultaneous wavelengths through the sample and measuring the difference of the absorption of the radiation of the time-multiplexed components at different sample states. During sample state changes, the amount of fluid containing the target analyte within the sample is changing, varying the total amount of target analyte in the sample, and the absorption properties of the sample. The sample states may be produced by compressing and uncompressing the tissue sample. The method is useful in measuring the concentration of a target analyte, such as glucose, in tissue containing blood.

Abstract: An improved method for non-invasively measuring a concentration of a target analyte dissolved in a fluid flowing through a sample is presented. It includes directing a probe beam of electromagnetic radiation, consisting of time multiplexed components of different wavelengths, where at least one of the time-multiplexed components consists of two different simultaneous wavelengths, whose intensity relation defines the effective wavelength of their combination, through the sample and measuring the difference of the absorption of the radiation of the time-multiplexed components at different sample states. During sample state changes, the amount of fluid containing the target analyte within the sample is changing, which varies the total amount of target analyte in the sample, as well as the absorption properties of the sample. The sample states are produced, for instance, by compressing and uncompressing the tissue sample.