Blood Pathogen Inactivation via Sonication and Riboflavin

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Solution Overview

Problem

Current blood pathogen inactivation methods, such as methylene blue photochemical methods, face limitations due to residual toxicity and the 'window period' in nucleic acid testing, necessitating the development of novel technologies that combine sonication with antimicrobial agents, chemicals, or pressure to enhance pathogen inactivation efficiency and safety.

Innovation Solution

A blood pathogen inactivation method involving the simultaneous use of low-frequency sonication (15-500 KHz) and photochemical technology with riboflavin as a photosensitizer, applied to blood samples, including plasma, platelets, and whole blood, to enhance pathogen inactivation while reducing the dosage of photosensitizers and treatment time.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If methylene blue photochemical method is used for pathogen inactivation, then pathogen inactivation effect is improved, but residual toxicity increases

Engineering Contradiction:
Improvepathogen inactivation effectVSAvoidresidual toxicity
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent changes the chemical parameter by replacing methylene blue with riboflavin as the photosensitizer. Riboflavin is a water-soluble vitamin with no residual toxicity issues, fundamentally changing the chemical identity of the photosensitizer to eliminate the harmful residual toxicity while maintaining pathogen inactivation effectiveness

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs riboflavin which can be easily removed or metabolized, effectively treating it as a disposable photosensitizer that does not persist in the blood product. This approach eliminates long-term toxicity concerns associated with methylene blue accumulation

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

2Measurement precision

If nucleic acid testing (NAT) is used for blood screening, then detection capability is improved, but window period problem persists

Engineering Contradiction:
Improvedetection capabilityVSAvoidwindow period
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent applies pathogen inactivation treatment to the blood product itself, performing the pathogen elimination action before transfusion. This preliminary inactivation ensures that even if pathogens are present during the window period, they are destroyed before reaching the patient, effectively eliminating the window period risk

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent converts the inherent vulnerability of the window period into an opportunity by applying inactivation treatment that specifically targets and destroys pathogens regardless of their detectability by NAT. The limitation of NAT detection becomes irrelevant because the inactivation process works on all pathogens present

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

3Reliability

If low-frequency sonication is combined with photochemical method, then pathogen inactivation effectiveness is improved, but treatment time increases

Engineering Contradiction:
Improvepathogen inactivation effectivenessVSAvoidtreatment time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The patent merges two inactivation mechanisms: photochemical inactivation by riboflavin and mechanical inactivation by low-frequency sonication. The combination creates a synergistic effect where both mechanisms work simultaneously to enhance pathogen destruction, achieving better inactivation than either method alone while managing treatment time

Inventive Principle:
Principle #5Merging (Combining)

4Object-affected harmful factors

If photosensitizer dosage is reduced, then residual toxicity is reduced, but pathogen inactivation effectiveness decreases

Engineering Contradiction:
Improveresidual toxicityVSAvoidpathogen inactivation effectiveness
Core Design Contradiction:
Object-affected harmful factorsVSReliability

Solution Approach 1:

The patent changes the photosensitizer from methylene blue to riboflavin, which has fundamentally different toxicity characteristics. Riboflavin is water-soluble and readily metabolized, allowing for lower effective dosages that maintain inactivation effectiveness while minimizing residual toxicity

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite treatment system combining riboflavin photosensitizer with low-frequency sonication. This composite approach allows the mechanical sonication to enhance the chemical photochemical reaction efficiency, enabling effective pathogen inactivation at lower riboflavin concentrations

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 combination of sonication and photochemical methods significantly enhances pathogen inactivation, reduces costs, and increases the effectiveness of pathogen inactivation, making the technology more viable for market application and improving blood safety.

Implementation Method 1

adding a photosensitizer, and conducting illumination and low-frequency sonication simultaneously

Methodology Applied
Scientific EffectPhotochemical inactivation: Photo-oxidation

Implementation Method 2

low-frequency sonication is conducted at a frequency of 15-500 KHz

Methodology Applied
Scientific EffectSonication: Ultrasonic Vibration

Data Source

PatentUS20230190935A1Blood pathogen inactivation method
Publication Date: 2023.06.22 BLOOD TRASFUSION INST CHINESE ACAD OF MEDICAL SCI
  • US20230190935A1 patent drawing

AI summary

The present disclosure provides a pathogen inactivation method, which is low-frequency sonication together with illumination of a photosensitizer-containing blood sample; and the low-frequency sonication is conducted at a frequency of 15-500 KHz. Through the combination of sonication and photochemical pathogen inactivation technology that enhance and complement each other, the blood pathogen inactivation method provided by the present disclosure enhances a pathogen inactivation effect, reduces a dosage of the photosensitizer, photosensitizer-related blood quality damage, energy demand for the illumination, and pathogen inactivation treatment time, increases the blood illumination thickness for effective pathogen inactivation, saves illumination bag materials, shortens the size of illumination equipment, saves costs, and helps the pathogen inactivation technology go to the market.