Solvophobic Linker Compounds for Medical Device Surface Activation

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Solution Overview

Problem

The development of medical devices with bioactive agents bound directly to the device for localized treatment is complex, often limited by reaction schemes and by-products upon device degradation in the body.

Innovation Solution

Compounds with solvophilic and solvophobic portions, where the solvophobic portion is functionalized with reactive members, allowing for the simple combination and blending to create an activated medical device capable of attaching bioactive agents without complex cross-linking reactions, using a solvent matrix that positions the reactive members at the device surface.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If complex reaction schemes and cross-linking reactions are used to bind bioactive agents to medical devices, then the binding strength and reliability are improved, but the device complexity and manufacturing difficulty increase

Engineering Contradiction:
Improvebinding strengthVSAvoidreaction scheme complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The compound is divided into distinct functional segments: a solvophilic portion that interacts with the solvent matrix and a solvophobic portion that presents reactive members at the surface. This segmentation allows each portion to perform its specific function independently, simplifying the overall binding process while maintaining reliability

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The solvophobic portion acts as an intermediary between the solvent matrix and bioactive agents. It presents reactive members that can directly interact with bioactive agents without requiring complex cross-linking chemistry, thus simplifying the binding mechanism while ensuring reliable attachment

Inventive Principle:
Principle #24Intermediary (Mediator)

2Adaptability or versatility

If complex cross-linking reactions are used to activate medical devices, then the reactivity and bioactive agent attachment capability are improved, but the manufacturing simplicity is reduced

Engineering Contradiction:
Improvebioactive agent attachment capabilityVSAvoidproduction process simplicity
Core Design Contradiction:
Adaptability or versatilityVSEase of manufacture

Solution Approach 1:

The reactive members are pre-positioned on the solvophobic portion during compound synthesis, before the medical device is activated or used. This preliminary preparation eliminates the need for complex activation procedures later, allowing simple blending with the solvent matrix to create the activated device

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

When the compound is blended with the solvent matrix, the solvophobic portion automatically migrates to the surface and self-organizes to present reactive members. This self-service behavior eliminates the need for complex external activation processes, simplifying manufacturing while maintaining high attachment capability

Inventive Principle:
Principle #25Self-service

3Quantity of substance

If reactive members are positioned throughout the bulk of the device, then the total number of reactive sites is increased, but the surface reactivity and localized attachment efficiency are reduced

Engineering Contradiction:
Improvetotal reactive membersVSAvoidsurface reactive member positioning
Core Design Contradiction:
Quantity of substanceVSManufacturing precision

Solution Approach 1:

The solvophobic portion is designed with local quality that causes it to preferentially locate at the device surface when blended with the solvent matrix. This ensures reactive members are concentrated where they are most needed for bioactive agent attachment, improving surface reactivity and localized efficiency

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The reactive members are distributed throughout the bulk in three dimensions during mixing, but the solvophobic portion's amphiphilic nature causes them to self-organize into a two-dimensional surface layer. This dimensional transition concentrates reactive members at the surface without requiring precise positioning during manufacturing

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

4Adaptability or versatility

If bioactive agents are delivered systemically through intravenous means, then the treatment coverage is improved, but the localization precision to the disease site is reduced

Engineering Contradiction:
Improvetreatment coverageVSAvoidlocalization precision
Core Design Contradiction:
Adaptability or versatilityVSMeasurement precision

Solution Approach 1:

The invention extracts the bioactive agent delivery from the bloodstream and relocates it to the implant site. By binding agents directly to the medical device, the treatment is localized precisely where the device is implanted, eliminating systemic distribution while maintaining effective treatment coverage at the target site

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

Enables the easy attachment of bioactive agents to the medical device surface, simplifying the production process and potentially improving the localized delivery of therapeutic agents while minimizing adverse reactions and by-products during device degradation.

Implementation Method 1

a solvophobic portion that is relatively incompatible with the solvent matrix and therefore remains at or near the surface of the device

Methodology Applied
Scientific EffectSolvophobic interaction: Hydrophobe

Data Source

PatentUS10632207B2Compounds and medical devices activated with solvophobic linkers
Publication Date: 2020.04.28 SOFRADIM PRODUCTION SAS
  • US10632207B2 patent drawing
  • US10632207B2 patent drawing
  • US10632207B2 patent drawing

AI summary

The present disclosure relates to compounds and medical devices activated with a solvophobic material functionalized with a first reactive member and methods of making such compounds and devices.