Deep Brain Stimulation via SERS Neurotransmitter Feedback

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Conventional deep brain stimulation systems are open loop, leading to high power consumption, frequent battery replacements, and reduced therapeutic effectiveness due to cellular encapsulation of electrodes and low sensitivity in detecting neurotransmitters, especially those with trace concentrations.

Innovation Solution

A deep brain stimulation apparatus using surface-enhanced Raman spectroscopy with plasmonic nano-particles to enhance Raman scattering, allowing for real-time monitoring of neurotransmitters and feedback-controlled electrical stimulation without high-power lasers, preventing biomolecule deformation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If continuous electrical stimulation is applied using open loop system, then therapeutic effect is maintained, but power consumption increases and battery life shortens

Engineering Contradiction:
Improvetherapeutic effectVSAvoidpower consumption
Core Design Contradiction:
ReliabilityVSUse of energy by moving object

Solution Approach 1:

The patent implements a closed-loop system where neurotransmitter concentrations are continuously monitored via SERS sensors, and stimulation parameters are adjusted in real-time based on feedback from the brain's chemical state. This allows stimulation to be applied only when and where needed, reducing overall power consumption while maintaining therapeutic effectiveness.

Inventive Principle:
Principle #23Feedback

Solution Approach 2:

The system dynamically adjusts stimulation parameters (intensity, frequency, duration) based on real-time neurotransmitter levels detected by SERS sensors. Instead of continuous fixed-parameter stimulation, the system adapts parameters according to the patient's actual brain state, reducing unnecessary energy consumption while preserving therapeutic benefits.

Inventive Principle:
Principle #15Dynamics

2Measurement precision

If measurement electrodes are inserted into brain tissue for long-term monitoring, then brain response can be measured, but electrode performance deteriorates due to cellular encapsulation

Engineering Contradiction:
Improvebrain response measurementVSAvoidelectrode performance
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

The patent replaces traditional electrical measurement electrodes with an optical detection system based on Surface-Enhanced Raman Spectroscopy (SERS). Laser light is delivered through optical fibers to excite neurotransmitters, and the resulting Raman scattered light is detected. This optical approach eliminates the problem of cellular encapsulation affecting electrical signal measurement, as optical sensors do not suffer from the same biofouling issues.

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

Solution Approach 2:

The system uses Raman scattered light as an intermediary to detect neurotransmitter concentrations. Instead of directly measuring electrical signals from the brain tissue, the system uses light scattering properties of neurotransmitters enhanced by metallic nanoparticles to obtain chemical information, bypassing the problem of electrode degradation.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Measurement precision

If high-power laser is used to enhance Raman scattering signal, then detection sensitivity improves, but biomolecule deformation occurs

Engineering Contradiction:
Improvedetection sensitivityVSAvoidbiomolecule deformation
Core Design Contradiction:
Measurement precisionVSObject-affected harmful factors

Solution Approach 1:

The patent employs metallic nanoparticles (gold, silver, or copper) with specific sizes and shapes that exhibit surface plasmon resonance at the laser wavelength. These nanoparticles are functionalized with neurotransmitter-specific receptors and attached to optical fibers. The composite structure of nanoparticle-receptor-optical fiber allows strong Raman signal enhancement at low laser powers, preventing biomolecule deformation.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The system changes the detection parameters by using Surface-Enhanced Raman Spectroscopy instead of conventional Raman spectroscopy. The electromagnetic field enhancement from metallic nanoparticles increases the Raman scattering cross-section by several orders of magnitude, allowing detection of trace neurotransmitters with low-power lasers that do not cause biomolecule deformation.

Inventive Principle:
Principle #35Parameter changes

4Device complexity

If conventional Raman spectroscopy is used without enhancement, then equipment complexity is low, but detection sensitivity for trace neurotransmitters is insufficient

Engineering Contradiction:
Improveequipment complexityVSAvoiddetection sensitivity
Core Design Contradiction:
Device complexityVSMeasurement precision

Solution Approach 1:

The patent uses composite structures consisting of metallic nanoparticles functionalized with neurotransmitter receptors attached to optical fiber surfaces. These SERS-active composite sensors provide extreme enhancement of Raman signals (10^6 to 10^8 times), enabling detection of trace neurotransmitter concentrations in the brain with equipment complexity comparable to conventional Raman systems.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The enhancement is localized to the immediate vicinity of the metallic nanoparticles on the optical fiber surface where neurotransmitters bind. This local electromagnetic field enhancement creates 'hot spots' that concentrate the Raman signal from trace amounts of neurotransmitter, providing high detection sensitivity without requiring complex instrumentation throughout the entire system.

Inventive Principle:
Principle #3Local quality

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 real-time monitoring of neurotransmitters with high sensitivity and spatial resolution, allowing for patient-customized treatment by actively controlling stimulation parameters based on changing symptoms, reducing power consumption and side effects.

Implementation Method 1

plasmonic nano-particles which allow surface-enhanced Raman scattering (SERS) by contacting a neurotransmitter

Methodology Applied
Scientific EffectSurface-enhanced Raman scattering: Scattering

Implementation Method 2

Raman spectroscopy may be used to overcome this problem. Scattering is a phenomenon in which light passes through a medium and the wavelength of the light is changed such that a portion of the light travels in a different direction away from a traveling direction

Methodology Applied
Scientific EffectLight scattering: Scattering

Data Source

PatentEP3542856B1Deep brain stimulation apparatus on basis of surface-enhanced raman spectroscopy
Publication Date: 2021.07.28 SAMSUNG LIFE PUBLIC WELFARE FOUND
  • EP3542856B1 patent drawingFigure 1
  • EP3542856B1 patent drawingFigure 2
  • EP3542856B1 patent drawingFigure 3

AI summary

A deep brain stimulation apparatus according to the present disclosure includes: a stimulator for applying electrical stimulation to a brain; a light source for providing light to the brain; plasmonic nano-particles which, when the brain releases a neurotransmitter as a result of the electrical stimulation, come into contact with the neurotransmitter to enable surface-enhanced Raman scattering (SERS); a photodetector which includes the plasmonic nano-particles and, when the light from the light source is scattered by the neurotransmitter which has come into contact with the plasmonic nano-particles, detects the scattered light; a signal processing analyzer for converting a light signal from the photodetector to an electric signal; and a controller for receiving an analysis signal from the signal processing analyzer to control the stimulator.