Metal-Complex Nucleic Acid Adjuvant Composition for Vaccine Stability

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Solution Overview

Problem

Current adjuvants used in vaccines, such as aluminum salts and TLR agonists, primarily induce humoral immune responses but are inadequate for cell-mediated immune responses, and nucleic acids like RNA and CpG motifs face stability issues due to rapid degradation in the body.

Innovation Solution

A pharmaceutical composition comprising a nucleic acid molecule stabilized by a metal complex with a specific structure, potentially including an immunogen, to enhance both humoral and cell-mediated immune responses while maintaining stability.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If nucleic acid adjuvants (RNA, CpG motifs) are used to enhance immune responses, then both humoral and cell-mediated immune responses are improved, but the nucleic acid molecules are rapidly degraded in the body, reducing their stability and duration of action

Engineering Contradiction:
Improveimmune response effectivenessVSAvoidnucleic acid stability
Core Design Contradiction:
ReliabilityVSStability of the object's composition

Solution Approach 1:

The patent introduces a metal complex as an intermediary substance that binds to nucleic acid adjuvants (RNA, CpG motifs) and prevents their degradation by nucleases in the body. This metal complex acts as a protective mediator that stabilizes the nucleic acid molecules while allowing them to maintain their immune-stimulating function, thus resolving the contradiction between effectiveness and stability.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent creates a composite formulation combining metal complexes with nucleic acid adjuvants. This composite structure provides both the immune-stimulating properties of the nucleic acid and the stabilizing properties of the metal complex, achieving both improved reliability and enhanced stability simultaneously.

Inventive Principle:
Principle #40Composite materials

2Reliability

If conventional adjuvants (alum, oil in water emulsion) are used to induce humoral immune responses, then antibody production is improved, but cell-mediated immune responses are insufficient

Engineering Contradiction:
Improvehumoral immune responseVSAvoidimmune response type
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent changes the chemical and molecular parameters of the adjuvant by using nucleic acid molecules (RNA, CpG motifs) instead of conventional alum or oil-based adjuvants. This parameter change enables the adjuvant to stimulate both humoral and cell-mediated immune responses, achieving versatility while maintaining effectiveness.

Inventive Principle:
Principle #35Parameter changes

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 composition effectively stabilizes nucleic acid adjuvants, enhancing both types of immune responses and providing a stable platform for vaccine development.

Implementation Method 1

a metal complex stabilizing the nucleic acid molecule and having the following structure of Formula 1

Methodology Applied
Scientific EffectCoordination bonding: Chemical Bonding

Data Source

PatentUS12465644B2Pharmaceutical composition containing stabilized nucleic acid adjuvant
Publication Date: 2025.11.11 SML BIOPHARM CO LTD
  • US12465644B2 patent drawing
  • US12465644B2 patent drawing
  • US12465644B2 patent drawing

AI summary

The present disclosure relates to a pharmaceutical composition comprising a nucleic acid molecule of an adjuvant, a metal complex stabilizing the nucleic acid molecule, and optionally an immunogen that may be a peptide or a protein, or a composition of stabilizing the nucleic acid molecule of the adjuvant comprising the metal complex. The metal complex interacts with the nucleic acid molecule of the adjuvant and/or the immunogen so as to stabilize such pharmaceutically active ingredients, and induces continuous effectiveness of the active ingredients without degradation.