Evaporative Edge Lithography Lipid Microarray for Drug Screening

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for analyzing cellular migration are limited by the number and type of different compounds and dosages that can be tested in parallel, restricting the ability to effectively screen for drug efficacy and cell migration effects.

Innovation Solution

The development of lipid multilayer microarrays formed through evaporative edge lithography (EEL), which allows for the local delivery of multiple drug dosages to cells in a microarray format, enabling the measurement of cell migration and drug efficacy by patterning lipid multilayers along the edges of a stencil, facilitating high-throughput screening.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If current methods are used for analyzing cellular migration, then the process is simple, but the number and type of different compounds and dosages that can be tested in parallel is limited

Engineering Contradiction:
Improvethroughput of drug screeningVSAvoidcomplexity of microarray system
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The system segments the drug screening process into multiple parallel microarray wells, each capable of holding different compounds and dosages. This segmentation allows simultaneous testing of multiple conditions without increasing overall system complexity, as each well operates independently but can be read using a single imaging system.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The microarray system is designed to be universal, accommodating various types of compounds and dosages across multiple wells using the same hardware platform. The system can test different cell types, compounds, and concentrations simultaneously, making it multi-functional without requiring separate equipment for each assay type.

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

2Productivity

If more compounds and dosages are tested in parallel, then the drug screening throughput increases, but the complexity of the testing system increases

Engineering Contradiction:
Improvenumber of compounds and dosages testedVSAvoidcomplexity of parallel testing system
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

Multiple drug screening assays are merged into a single microarray plate, with each well containing different compounds or dosages. This combining approach allows high-throughput testing while using a single, relatively simple imaging system to read all wells, avoiding the need for multiple separate testing systems.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The microarray system is designed to be self-contained, with all necessary components (wells, compounds, cell cultures) integrated into a single plate that can be imaged and analyzed without requiring complex external equipment for each individual well. The system serves itself by using the same imaging infrastructure for all parallel assays.

Inventive Principle:
Principle #25Self-service

3Productivity

If lipid multilayer microarrays are used for local delivery of multiple drug dosages, then the throughput of cellular migration assays is enhanced, but the manufacturing complexity of lipid multilayer structures increases

Engineering Contradiction:
Improvethroughput of cellular migration assaysVSAvoidease of forming lipid multilayer structures
Core Design Contradiction:
ProductivityVSEase of manufacture

Solution Approach 1:

Lipid multilayer structures are pre-formed in each microarray well before cell seeding and drug delivery. This preliminary preparation allows the structures to be ready for immediate use, simplifying the overall manufacturing process by separating the lipid formation step from the subsequent cellular assays, and enabling batch preparation of multiple wells simultaneously.

Inventive Principle:
Principle #10Preliminary action

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

This approach enables the simultaneous testing of various compounds and dosages on the same surface, enhancing the throughput of cellular migration assays and drug screening by allowing adherent cells to take up lipophilic drugs from lipid multilayer structures, thereby inhibiting migration and assessing drug efficacy effectively.

Implementation Method 1

forming one or more arrays of lipid multilayer structures on a substrate by evaporating a solvent from each of a plurality of lipid solutions in respective spaces between pairs of barriers on a substrate

Methodology Applied
Scientific EffectEvaporation: Evaporation

Data Source

PatentUS9995732B2Evaporative edge lithography of a liposomal drug microarray for cell migration assays
Publication Date: 2018.06.12 FLORIDA STATE UNIV RES FOUND INC
  • US9995732B2 patent drawing
  • US9995732B2 patent drawing
  • US9995732B2 patent drawing

AI summary

Lipid multilayer structures are formed by evaporating a solvent from each of a plurality of lipid solutions thereby form the lipid multilayer structures. Each lipid solution comprises the solvent and one or more lipids. Each lipid multilayer structure is a microstructure comprising one or more lipids.