3D Molecular Imaging via Homogenized Coherent Light

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Solution Overview

Problem

Current three-dimensional imaging techniques, such as optical coherence tomography and photoacoustic tomography, are limited by shallow imaging depth, provide only morphological information, and use high-power ionizing radiation that can degrade samples and pose health risks, especially in bio-imaging.

Innovation Solution

A method and system for three-dimensional molecular imaging using homogenized monochromatic coherent light, which illuminates samples at multiple points with low power density to collect scattered light from all angles, allowing for deeper penetration and chemical information retrieval without sample degradation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Length of stationary object

If high-power light is used for irradiation of the sample, then imaging depth is improved, but sample degradation occurs due to local heating

Engineering Contradiction:
Improveimaging depthVSAvoidsample degradation
Core Design Contradiction:
Length of stationary objectVSObject-affected harmful factors

Solution Approach 1:

The imaging process is segmented into multiple low-power illumination steps rather than a single high-power exposure. The system collects scattered light at multiple angles and planes, processing each segment separately to reconstruct the final 3D image, thereby avoiding thermal damage while achieving sufficient imaging depth

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The system employs continuous low-power illumination with sequential scanning through multiple angles and planes. This continuous action at low power density maintains adequate signal collection for deep tissue imaging without causing the intermittent high-power heating that leads to sample degradation

Inventive Principle:
Principle #20Continuity of useful action

2Loss of information

If conventional optical imaging techniques are used, then morphological information is obtained, but chemical information is not provided

Engineering Contradiction:
Improvechemical informationVSAvoidimaging system complexity
Core Design Contradiction:
Loss of informationVSDevice complexity

Solution Approach 1:

The imaging system is designed to perform multiple functions: it captures both morphological information through standard scattered light detection and chemical information through Raman spectroscopy. The same optical path and detection system are used for both imaging modes, eliminating the need for separate specialized equipment

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

Solution Approach 2:

The system merges conventional optical imaging with Raman spectroscopy into a single integrated platform. By combining the scattered light collection path with Raman signal detection, the system simultaneously obtains structural and chemical information from the same sample region without requiring separate measurement systems

Inventive Principle:
Principle #5Merging (Combining)

3Measurement precision

If ionizing radiation is used for imaging, then imaging capability is improved, but health risks increase for in vivo imaging

Engineering Contradiction:
Improveimaging capabilityVSAvoidhealth risks
Core Design Contradiction:
Measurement precisionVSObject-affected harmful factors

Solution Approach 1:

The system replaces ionizing radiation (X-rays) with non-ionizing coherent light (laser) for tissue imaging. This substitution maintains the ability to obtain high-quality images through coherent scattering and Raman effects while eliminating the harmful ionizing effects that pose health risks in in vivo applications

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

4Length of stationary object

If light of high power is used, then penetration depth is improved, but local heating occurs leading to sample degradation

Engineering Contradiction:
Improvepenetration depthVSAvoidlocal heating
Core Design Contradiction:
Length of stationary objectVSTemperature

Solution Approach 1:

The system uses multiple partial illumination actions at low power density rather than a single excessive high-power exposure. By scanning through multiple angles and planes with low-power coherent light, the system accumulates sufficient signal for deep tissue imaging while keeping the power density at each location below the threshold for thermal damage

Inventive Principle:
Principle #16Partial or excessive action

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

Enables non-degradable, deep-tissue imaging that provides both morphological and chemical information, reducing sample damage and health risks, with the ability to image samples up to 60-90 mm depth, suitable for bio-applications like cancer detection and hazardous chemical identification.

Implementation Method 1

collecting the molecular scattered light from all angles and planes

Methodology Applied
Scientific EffectMolecular scattering: Scattering

Implementation Method 2

homogenizing a monochromatic coherent light source; irradiating the sample at plurality of points along all planes with the homogenized monochromatic light

Methodology Applied
Scientific EffectCoherent light propagation: Coherent Light

Data Source

PatentUS20240060900A1Three dimensional molecular imaging through homogenized coherent excitation
Publication Date: 2024.02.22 INDIAN INSTITUTE OF SCIENCE
  • US20240060900A1 patent drawing
  • US20240060900A1 patent drawing
  • US20240060900A1 patent drawing

AI summary

The method includes homogenizing a monochromatic coherent light source, irradiating the sample at plurality of points along all planes with the homogenized monochromatic light, collecting the molecular scattered light from all angles and planes to obtain a plurality of profile, resolving the plurality of profiles to obtain a molecular intensity maps, and reconstituting the intensity maps to obtain a three dimensional image of the sample. The system described is capable of obtaining molecular specific 3D morphology and profile of samples. The system described is capable of differentiating different chemicals or sample distribution throughout the 3D volume.