Amphiphilic Peptide Micelles for Soluble Antigen Nanoparticle Vaccines

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Solution Overview

Problem

Existing vaccines, particularly those targeting water-soluble antigens, face challenges in antibody production efficiency, stability, and safety, especially for viruses like dengue fever where cross-reactivity can lead to increased infection risk due to weak antibody binding.

Innovation Solution

Development of nanoparticles composed of amphiphilic peptides forming micelles that self-assemble and bind target peptides, allowing precise targeting of antigen-presenting cells without chemical modification, using small peptides to enhance antibody production and minimize side effects.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If water-soluble antigens are used as vaccines, then the vaccine can be administered easily and is safe, but antibody production efficiency is significantly lower compared to particulate antigens

Engineering Contradiction:
Improveantibody production efficiencyVSAvoidlow immunogenicity of soluble antigens
Core Design Contradiction:
ProductivityVSObject-affected harmful factors

Solution Approach 1:

The patent changes the physical state parameter of the antigen from soluble to particulate by forming micelles. The amphiphilic peptide self-assembles into micellar structures that present the water-soluble antigen in a particulate form, thereby enhancing immunogenicity and antibody production efficiency while maintaining the advantages of water-soluble antigens

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite structure where the amphiphilic peptide forms a micellar carrier that encapsulates or presents the water-soluble antigen. This composite micellar system combines the benefits of particulate antigens (high immunogenicity) with the advantages of water-soluble antigens (ease of administration and safety)

Inventive Principle:
Principle #40Composite materials

2Productivity

If traditional adjuvants are used to enhance antibody production, then immunogenicity is improved, but toxicity and safety issues arise

Engineering Contradiction:
Improveantibody production efficiencyVSAvoidtoxicity and safety of adjuvants
Core Design Contradiction:
ProductivityVSObject-affected harmful factors

Solution Approach 1:

The amphiphilic peptide micelle acts as an intermediary carrier that presents the antigen in a particulate form without requiring traditional adjuvants. The micelle structure itself provides the necessary immunogenic enhancement, eliminating the need for separate adjuvant components that would introduce toxicity and safety concerns

Inventive Principle:
Principle #24Intermediary (Mediator)

3Manufacturing precision

If haptens are used to produce antibodies, then specific antibody production is achieved, but accessibility problems and structural changes occur

Engineering Contradiction:
Improvespecific antibody productionVSAvoidchemical bond creation and structural changes
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The patent extracts the antigenic determinant from the water-soluble antigen and presents it on the surface of the amphiphilic peptide micelle. This allows the antigen to be recognized by the immune system in its native conformation without requiring chemical modification or coupling to carrier proteins, thereby avoiding accessibility problems and unwanted structural changes

Inventive Principle:
Principle #2Taking out (Extraction)

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 nanoparticles effectively induce targeted immune responses, increasing antibody production and reducing side effects by precise antigen presentation, suitable for multivalent vaccines against diseases such as dengue fever and influenza.

Implementation Method 1

an amphiphilic peptide that forms a micelle structure by self-assembly

Methodology Applied
Scientific EffectSelf-assembly: Self-Assembly

Implementation Method 2

micelle structure which is composed of an amphiphilic peptide

Methodology Applied
Scientific EffectAmphiphilic interaction: Amphiphiles

Implementation Method 3

a target peptide that electrically binds to a surface of the amphiphilic peptide

Methodology Applied
Scientific EffectElectrical binding: Ion Repulsion/Attraction

Data Source

PatentUS20260069671A1Micelle comprising amphiphilic peptide, and antigen carrier nanoparticle using same
Publication Date: 2026.03.12 RTAB CO LTD
  • US20260069671A1 patent drawing
  • US20260069671A1 patent drawing
  • US20260069671A1 patent drawing

AI summary

A nanoparticle and a preparation method therefor, the nanoparticle including an amphiphilic peptide, which forms a micelle structure through self-assembly, and a target peptide (preferably, a water-soluble antigen peptide), which electrically binds to the surface of the amphiphilic peptide. The target peptide electrically binds to the surface of the amphiphilic peptide micelle structure and becomes particulated, and thus can be effectively presented to an antigen-presenting cell, and the weight ratio of the amphiphilic peptide and the target peptide is controlled so that the size of nanoparticles is controlled and endocytosis thereof is carried out, and thus immunity by means of cytotoxic T cells can be induced. Nanoparticles exhibit use only an epitope of a more accurate region so as to be effective as a vaccine, and thus have minimal side effects. Therefore, excellent antigen-specific antibody and cell immunotherapy effects are exhibited, and thus can be used in various fields such as vaccine production.