Microfluidic Viscous Shearing for Vesicle Control

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Solution Overview

Problem

Current methods for producing micro-sized droplets lack control over both droplet generation speed and size, and fail to enable precise formation of multilamellar or asymmetric vesicles, which is crucial for applications like drug delivery and biochemical assays.

Innovation Solution

Microfluidic devices with tunable viscous shear forces and pressure gradients are used to control droplet formation, allowing for programmable control of droplet size, composition, and post-processing operations like splitting, fusing, and sorting, enabling the creation of amphiphilic vesicles with precise dimensions and properties.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If droplets are generated from capillary tip or stream breakup, then droplet formation is achieved, but control over both droplet generation speed and size is not possible

Engineering Contradiction:
Improvedroplet size controlVSAvoiddroplet generation speed control
Core Design Contradiction:
Manufacturing precisionVSProductivity

Solution Approach 1:

A third immiscible fluid (intermediate fluid) is introduced as a mediator between the aqueous phase and organic phase. This intermediate fluid enables independent control of droplet size (through its flow rate) and generation speed (through the aqueous phase flow rate), resolving the contradiction by adding a controlling intermediary element to the system.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The invention changes the flow rate parameters of multiple immiscible fluids independently to control different aspects of droplet formation. By adjusting the flow rates of the aqueous phase, organic phase, and intermediate fluid separately, both droplet size and generation speed can be precisely controlled without compromising either parameter.

Inventive Principle:
Principle #35Parameter changes

2Manufacturing precision

If droplets are extruded through microporous membranes or microchannels for size control, then droplet size is controlled, but size is limited to channel or pore diameter

Engineering Contradiction:
Improvedroplet size controlVSAvoiddroplet size range
Core Design Contradiction:
Manufacturing precisionVSAdaptability or versatility

Solution Approach 1:

The intermediate fluid acts as a mediator that enables droplet size control through flow rate adjustment rather than physical constriction. This allows droplets of varying sizes to be generated by changing the flow rate ratio between the aqueous phase and intermediate fluid, providing versatility without being limited by fixed channel or pore dimensions.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The invention replaces static size control (fixed channel/pore diameter) with dynamic size control through adjustable flow rates. The droplet size can be dynamically changed by varying the flow rate parameters during operation, enabling a wide range of sizes to be produced from the same device.

Inventive Principle:
Principle #15Dynamics

3Stability of the object's composition

If bulk mixing processes are used, then mixing is achieved, but individual control of droplet composition for precise multilamellar or asymmetric vesicles is not possible

Engineering Contradiction:
Improvedroplet composition controlVSAvoidvesicle structure precision
Core Design Contradiction:
Stability of the object's compositionVSManufacturing precision

Solution Approach 1:

The continuous bulk mixing process is segmented into discrete, sequential droplet formation events. Each droplet is formed individually with controlled composition through the sequential introduction of immiscible phases, enabling precise control over multilamellar and asymmetric structures while maintaining compositional stability.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The composition of each droplet is predetermined by the flow rate ratios and sequence of phase introduction before the droplet forms. This preliminary control of composition parameters enables precise fabrication of specific vesicle structures (multilamellar or asymmetric) with controlled reagent distribution.

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 allows for reproducible and efficient production of vesicles with controlled size and composition, enabling 100% encapsulation of reagents, precise drug delivery, and versatile applications in medicine and biology.

Implementation Method 1

microfluidic devices for controlled viscous shearing of oil-water emulsions

Methodology Applied
Scientific EffectViscous shear: Shear Stress

Implementation Method 2

pressure gradient design advantageously generates favorable conditions for high speed droplet formation

Methodology Applied
Scientific EffectPressure gradient: Pressure Gradient

Implementation Method 3

controlled assembly of multi-lamellar vesicles

Methodology Applied
Scientific EffectSelf-assembly: Self-Assembly

Implementation Method 4

formation of amphiphilic vesicles such as liposomes, polymer vesicles, micelles

Methodology Applied
Scientific EffectAmphiphilic: Amphiphiles

Data Source

PatentUS7595195B2Microfluidic devices for controlled viscous shearing and formation of amphiphilic vesicles
Publication Date: 2009.09.29 RGT UNIV OF CALIFORNIA
  • US7595195B2 patent drawing
  • US7595195B2 patent drawing
  • US7595195B2 patent drawing

AI summary

Systems and methods that control the size and composition of emulsified droplets, multi-lamellar and asymmetric vesicles, encapsulation of reagents, membrane proteins, and sorting of vesicles/droplets. More particularly, microfluidic devices for controlled viscous shearing of oil-water emulsions of micro- and nano-scale droplets, the subsequent formation of amphiphilic vesicles such as liposomes, polymer vesicles, micelles, and the like, the post-assembly and post-processing of the droplets including splitting, fusing, sorting and the like, polymer emulsions, and the integration of amphiphilic vesicle production-line on a single microfluidic chip. Preferably, the microfluidic device enables oil-water co-flows with tunable viscous shear forces higher than the immiscible interfacial tension forces that generate favorable conditions for droplet formation.