Spatially and optically tailored 3D printing for highly miniaturized and integrated microfluidics
Supplemental record retained to make the downloaded paper corpus fully navigable.
- Year
- —
- Skill
- medium
- Docs
- moderate
- Rubric
- 3.5 / 5
Implementation assessment
Scoring by criterion
Scores describe accessibility and implementation characteristics reported in the reviewed source. They are not a measure of scientific quality.
Resolution
Smallest feature/positioning evidence about 7.6 um.
Scalability/Throughput
Throughput not explicit; assigned moderate default.
Build and Part Sourcing Complexity
Mix of common parts and custom/printed components.
Skill Complexity
Multiple advanced technical skills appear required.
Equipment/Cosumable/Facility Requirement Accessibility
Requires specialized facilities, equipment, or consumables.
Application Level
Presented as modular or usable across multiple workflows.
Accessibility to documentation
Some open documentation or files are available.
Validation/Troubleshooting Complexity
Validation includes standards, benchmarking, replicates, or multi-condition tests.
Speed/Cycle Time
Speed evidence suggests rapid, real-time, or automated operation.
Build Time
Build/setup evidence indicates same-day or <4 h setup.
Record metadata
Publication data
Crossref and OpenAlex
Publication record
Abstract
Traditional 3D printing based on Digital Light Processing Stereolithography (DLP-SL) is unnecessarily limiting as applied to microfluidic device fabrication, especially for high-resolution features. This limitation is due primarily to inherent tradeoffs between layer thickness, exposure time, material strength, and optical penetration that can be impossible to satisfy for microfluidic features. We introduce a generalized 3D printing process that significantly expands the accessible spatially distributed optical dose parameter space to enable the fabrication of much higher resolution 3D components without increasing the resolution of the 3D printer. Here we demonstrate component miniaturization in conjunction with a high degree of integration, including 15 μm × 15 μm valves and a 2.2 mm × 1.1 mm 10-stage 2-fold serial diluter. These results illustrate our approach's promise to enable highly functional and compact microfluidic devices for a wide variety of biomolecular applications.
Bibliographic details
Access and metrics
Topics and keywords
Funding
- U.S. Department of Health & Human Services | National Institutes of Health · R01EB027096
- U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences · R15GM123405-02
Perspective and practical signals
Why it matters
Supplemental record retained to make the downloaded paper corpus fully navigable.
Limitations
Metadata is limited to the download manifest and title-derived mapping.