Lipid-Based Nanoparticle Compositions for Therapeutic Delivery

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Solution Overview

Problem

Current delivery systems for therapeutic agents like CBD, hemp extracts, and mushroom extracts face challenges with stability, bioavailability, and consistency due to impurities and variable purity profiles, leading to unpredictable delivery and side effects.

Innovation Solution

A lipid-based particle composition comprising nanoparticles or liposomes with high-purity therapeutic agents, such as CBD, hemp, and mushroom extracts, formulated with phosphatidylcholine, sterols, and medium chain triglycerides, which enhances solubility and stability, allowing for reproducible and effective delivery.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If conventional delivery systems (oils, capsules, sprays) are used for therapeutic agents, then ease of administration is improved, but stability and bioavailability deteriorate due to impurities and variable purity profiles

Engineering Contradiction:
Improveease of administrationVSAvoidstability and bioavailability
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The patent transforms the physical and chemical parameters of therapeutic agents by converting them into lipid-based particle formulations. This changes the delivery system from conventional oils and capsules to standardized particles with controlled size, composition, and surface properties, thereby improving stability and bioavailability while maintaining ease of administration

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates composite lipid-based particle systems that combine therapeutic agents with lipid materials (phospholipids, triglycerides, sterols). This composite structure provides both the stability of lipid materials and the therapeutic efficacy of the active agents, resolving the contradiction between reliability and ease of operation

Inventive Principle:
Principle #40Composite materials

2Reliability

If high-purity therapeutic agents are used, then reliability of delivery is improved, but manufacturing complexity increases due to purification requirements

Engineering Contradiction:
Improveconsistency of deliveryVSAvoidmanufacturing complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent segments the manufacturing process into distinct stages: first incorporating therapeutic agents into lipid particles, then purifying the particles separately. This segmentation allows purification to occur at a stage where particles are already formed, simplifying the overall process compared to purifying crude extracts before formulation

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The lipid-based particles serve as an intermediary carrier that facilitates the separation and purification of therapeutic agents. The particles act as a medium through which impurities can be removed while maintaining the integrity and concentration of the active therapeutic compounds, thereby achieving high purity without excessive manufacturing complexity

Inventive Principle:
Principle #24Intermediary (Mediator)

3Reliability

If lipid-based particle compositions are formulated, then bioavailability and stability are improved, but device complexity increases due to formulation requirements

Engineering Contradiction:
Improvebioavailability and stabilityVSAvoidformulation complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent develops universal lipid-based particle formulations that can accommodate multiple different therapeutic agents (cannabinoids, terpenes, flavonoids, peptides, proteins) within a single platform. This multi-functional approach reduces formulation complexity by providing a standardized system that works across different drug types, rather than requiring separate formulations for each agent

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

Solution Approach 2:

The patent controls and standardizes key parameters of the lipid particles (size, composition, surface charge) to create a reproducible formulation system. By fixing these critical parameters within specific ranges, the formulation process becomes more predictable and less complex, while still achieving improved bioavailability and stability

Inventive Principle:
Principle #35Parameter changes

4Ease of manufacture

If conventional extraction methods are used, then ease of manufacture is improved, but purity and consistency deteriorate due to impurities

Engineering Contradiction:
Improveease of extractionVSAvoidpurity and consistency
Core Design Contradiction:
Ease of manufactureVSManufacturing precision

Solution Approach 1:

The patent selectively extracts therapeutic agents from plant material using lipid-based solvents and particle formation processes. This extraction method specifically isolates the desired compounds (cannabinoids, terpenes, flavonoids) while leaving behind unwanted impurities (chlorophyll, waxes, plant debris), thereby achieving high purity and consistency while maintaining manufacturing efficiency

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent uses composite lipid extraction systems that combine multiple lipid materials (phospholipids, triglycerides, sterols) to enhance the selectivity and efficiency of the extraction process. This composite approach improves both the ease of manufacture and the purity of the extracted therapeutic agents by leveraging the complementary properties of different lipid materials

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 lipid-based particle composition improves bioavailability, stability, and consistency of therapeutic agents, reducing side effects and enhancing efficacy by providing a stable and predictable delivery system for hydrophobic and hydrophilic agents.

Implementation Method 1

formulated with phosphatidylcholine, sterols, and medium chain triglycerides, which enhances solubility

Methodology Applied
Scientific EffectSolvation: Solvation

Implementation Method 2

A lipid-based particle composition comprising nanoparticles or liposomes with high-purity therapeutic agents

Methodology Applied
Scientific EffectPhysical containment: Physical Containment

Data Source

PatentUS20230233466A1Compositions for supplementing products with therapeutic agents and methods of use thereof
Publication Date: 2023.07.27 CORENHANCED TECHNOLOGIES LLC
  • US20230233466A1 patent drawing
  • US20230233466A1 patent drawing
  • US20230233466A1 patent drawing

AI summary

Some embodiments pertain to nanoparticle-based compositions and their use in methods for the delivery of therapeutic ingredients to subjects. In some embodiments, the compositions are stable for prolonged periods of time and provide enhanced bioavailability.