Device Overview and Working Principle
This device is engineered for the quantitative estimation of nitric oxide (NO) concentration in blood samples. Its operation is based on the specific fluorescence response of a proprietary fluorescent protein upon binding with NO molecules.
Core Components:
- Optical Detection Module: A high-sensitivity camera serves as the primary sensor. It is equipped with a dedicated optical filter to precisely capture the fluorescence emission from the sample while completely blocking the scattered excitation light.
- Excitation Source: An ultraviolet (UV) lamp module is designed to emit light at two distinct, precise wavelengths. This dual-wavelength excitation is crucial for ratiometric measurement, which enhances accuracy by compensating for potential sample variability.
- Sample Presentation Unit: A specialized glass slide ensures optimal presentation of the prepared sample. The slide is crafted from materials with low fluorescence background and high UV transmission to maximize signal-to-noise ratio.
Operational Workflow
The device follows a systematic four-step process to accurately quantify nitric oxide concentration in blood samples:
- Sample Preparation: The blood sample is pre-mixed with the specific fluorescent protein marker, which selectively binds to NO molecules present in the sample.
- Loading: The prepared mixture is placed onto the designated glass slide and carefully inserted into the device's sample compartment, ensuring proper positioning for optimal optical detection.
- Excitation & Data Acquisition: The UV lamp sequentially illuminates the sample at the two predefined wavelengths. For each wavelength, the high-sensitivity camera captures the corresponding fluorescence intensity, creating a pair of measurements for ratiometric analysis.
- Signal Processing & Analysis: The device's integrated processor calculates the ratio of the two fluorescence intensities. This ratio is then correlated to the NO concentration through a pre-calibrated algorithm, yielding a final estimated value that is displayed to the user.
The design and workflow of this device fully embody the three core principles of our solution: The fully automated four-step detection process with integrated intelligent algorithms delivers true Intelligent Detection; its compact modular design and universal consumables ensure Universal Accessibility, enabling deployment across diverse settings from tertiary hospitals to primary care clinics; the simplified operational steps and intuitive result output perfectly demonstrate User-Centric Design, allowing even non-specialists to perform accurate testing with ease.