Multi-Signal Fluorescent Probe for Tumor Biomarker Detection

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Solution Overview

Problem

Existing fluorescent probes cannot simultaneously detect and discriminate between peroxynitrite (ONOO−) and sodium disulfide (Na2S2), limiting their application in dual-channel ratiometric fluorescence imaging for early tumor diagnosis.

Innovation Solution

A multi-signal fluorescent probe is developed, synthesized through specific chemical reactions involving 2-methoxyphenothiazine, ethyl iodide, boron tribromide, malonic acid, zinc chloride, and phosphorus oxychloride, which emits distinct fluorescence signals under different excitation wavelengths when reacting with ONOO− and Na2S2, enabling simultaneous detection.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If existing fluorescent probes are used, then detection of single analyte is achieved, but simultaneous discrimination and detection of ONOO− and Na2S2 cannot be performed

Engineering Contradiction:
Improvedetection capabilityVSAvoiddiscrimination accuracy
Core Design Contradiction:
Adaptability or versatilityVSLoss of information

Solution Approach 1:

The probe is designed with distinct detection channels (dual-channel ratiometric fluorescence imaging) that segment the detection process into separate pathways for ONOO− and Na2S2, allowing simultaneous discrimination while maintaining high detection capability for each analyte

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The fluorescent probe exhibits multi-functionality by being capable of detecting multiple analytes (ONOO− and Na2S2) simultaneously through different fluorescence channels, transforming a single-function probe into a universal detection tool that maintains high adaptability and discrimination accuracy

Inventive Principle:
Principle #6Universality (Multi-functionality)

2Measurement precision

If conventional detection methods are used, then simple detection is achieved, but early diagnosis of tumors requiring simultaneous detection of multiple biomarkers is limited

Engineering Contradiction:
Improvedetection sensitivityVSAvoidprobe structure
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The fluorescent probe employs a composite molecular structure that integrates multiple detection functionalities into a single probe entity, achieving high measurement precision for simultaneous detection of ONOO− and Na2S2 while managing the inherent complexity through rational molecular design rather than multiple separate probes

Inventive Principle:
Principle #40Composite materials

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The probe allows for the simultaneous ratiometric discrimination and detection of ONOO− and Na2S2, facilitating early medical diagnosis by emitting specific fluorescence signals under different excitation wavelengths, with a limit of detection of 42.12 nM for ONOO− and 38.45 nM for Na2S2.

Implementation Method 1

the small-molecule fluorescent probe-based fluorescence imaging technology has become an effective strategy for visualizing the spatio-temporal distribution of biomolecules in biological samples

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentUS11857644B2Multi-signal fluorescent probe for early diagnosis of tumors, and preparation and use thereof
Publication Date: 2024.01.02 HUNAN PROVINCIAL TUMOR HOSPITAL
  • US11857644B2 patent drawing
  • US11857644B2 patent drawing
  • US11857644B2 patent drawing

AI summary

A multi-signal fluorescent probe, represented by:A method for preparing the multi-signal fluorescent probe includes: (a) adding 2-methoxyphenothiazine and ethyl iodide into a mixture of dichloromethane (DCM) and acetonitrile followed by a first reaction and a first post-treatment to obtain 10-ethyl-2-methoxy-10H-phenothiazine; (b) adding boron tribromide into the 10-ethyl-2-methoxy-10H-phenothiazine under an inert gas followed by a second reaction under an ice bath and a second post-treatment to obtain 10-ethyl-10H-phenothiazin-2-ol; and (c) mixing the 10-ethyl-10H-phenothiazin-2-ol, malonic acid, zinc chloride and phosphorus oxychloride followed by a third reaction and a third post-treatment to obtain the multi-signal fluorescent probe. A use of the multi-signal fluorescent probe in the detection of intracellular ONOO− and Na2S2 is also provided.