Industry Application, Life Sciences & Biomedical

Life Sciences &
Biomedical Devices

At Nanosystems JP Inc., we fabricate devices spanning From organ-on-chip platforms and neural recording arrays to DNA sequencing flow cells, LSPR biosensors, and implantable neural probes, Nanosystems JP Inc. provides the precision micro- and nano-fabrication services that turn biomedical device concepts into clinical-grade hardware.

Organ-on-chipMicro-electrode arraysDNA sequencing flow cellsLSPR biosensorsPDMS soft lithographyMicrofluidic chipsNeural probesFlexible biosensors
500×600mm
Max glass panel for biochips
Sub-50nm
NIL nanopores for DNA
3 days
PDMS prototype turnaround
Biocompatible
PI/Pd-Ni materials
Biomedical Device Categories
From research prototype to clinical-grade device

The biomedical device market spans three scales: nano (DNA, protein, single molecule), micro (cell, organoid, tissue), and device (implant, diagnostic instrument). Our fabrication capabilities address all three.

Microfluidic biochip - glass substrate with colored fluid channels for lab-on-chip diagnostics and cell biology applications
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Organ-on-Chip (OoC)

Multilayer PDMS chips with pneumatic Quake valves, peristaltic pumps, and thin flexible membranes replicate the microenvironment of human organs, lung, gut, kidney, brain, liver, and heart, for drug discovery and toxicity testing. PDMS soft lithography from SU-8 masters enables 3–5 day design-to-chip turnaround. COP injection-molded versions for production volumes where PDMS autofluorescence is a concern.

PDMS multilayerSU-8 masterQuake valves3–5 day prototypeCOP production version
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Micro-Electrode Arrays (MEA)

Planar and 3D MEA for extracellular neural signal recording, stimulation, and drug response monitoring. Pt or TiN electrode arrays on glass or Si substrate patterned by lift-off. SU-8 or polyimide passivation with electrode openings at recording sites. DRIE through-holes for 3D probe insertion. Biocompatible PI RDL for flexible implantable probe variants.

Pt/TiN electrodesLift-off patterningSU-8/PI passivation3D DRIE holesFlexible PI probe
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DNA Sequencing Flow Cells

Glass flow cells with NIL-defined nanopore arrays (<50nm) for nanopore sequencing, or precision microchannels for optical sequencing. Fusion or anodic bonding for hermetic glass-glass or glass-Si seals with no adhesive in the optical path. Large-format glass processing (500×600mm) enables 96-well or 384-well array formats at low cost-per-chip, critical for sequencing instrument economics.

NIL nanopores <50nmGlass fusion bonding500×600mm arraysUV-transparent glassLow cost-per-chip
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LSPR Biosensors

Localised surface plasmon resonance chips with gold nanopillar or nanohole arrays on glass, fabricated by NIL and Au lift-off. The nanostructured gold surface is functionalised with antibodies, aptamers, or nucleic acid probes for label-free detection of cancer biomarkers, pathogen proteins, and nucleic acids. Sensitivity 10–100× higher than flat Au SPR chips due to localised field enhancement.

NIL Au nanostructuresLabel-free LSPRAntibody/aptamer probeCancer biomarkers10–100× vs flat SPR
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Drug Delivery Microdevices

Ni and Pd-Ni microneedle arrays by LIGA electroforming for transdermal drug delivery and interstitial fluid (ISF) sampling. Hollow microneedles with 1µm-diameter fluid channels. Droplet microfluidic chips for monodisperse microencapsulation of drug-loaded particles (CV <2%). Pd-Ni biocompatible grade for implant-contact applications.

LIGA Pd-Ni microneedlesHollow 1µm channelDroplet microfluidicsCV <2% dropletsBiocompatible
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Implantable Neural Interfaces

Neural probes and implantable sensors using biocompatible PI RDL and Au/Pt electrodes. Hermetic AuSn sealing for implantable optical transceivers (retinal implants, deep brain stimulators). ISO 10993-assessed polyimide for electrode passivation. NDA-protected, your implant design remains confidential from first technical discussion.

PI RDL biocompatibleAu/Pt electrodesAuSn hermetic sealISO 10993 PIRetinal · DBS
Building the Biochip: From Substrate to Sensing Layer - exploded 4-layer diagram showing microfluidic interface, active circuitry and electrodes, vias and interconnects, and base substrate
Key Processes for Biomedical
The fabrication technologies behind biomedical devices
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PDMS Soft Lithography

SU-8 master on Si wafer → PDMS cast and cure → O₂ plasma bond to glass or PDMS. The fastest route from biochip design to working prototype. 3–5 days from GDS to first functional chip. Multilayer for Quake valves and 3D channel networks.

3–5 day turnaroundSU-8 masterO₂ plasma bond
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NIL Nanopores & LSPR

E-beam master + UV/thermal NIL for sub-50nm nanopores and Au nanostructure arrays. All : master fabrication, NIL, dry etch transfer, and Au lift-off on the same substrate.

Sub-50nm poresAu LSPR arraysNIL master fabrication
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Thin Film Deposition Bioelectrodes

Au, Pt, ITO, and TiN electrode deposition by PVD sputtering and evaporation. Lift-off patterning for electrode arrays with sub-5µm features. ITO for transparent electrodes in optogenetics and fluorescence biochips.

Au · Pt · ITO · TiNLift-offSub-5µm features
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Glass Bonding

Anodic bonding (glass-Si, hermetic) and fusion bonding (glass-glass, UV-transparent) for biochip sealing. C-SAM inspection on every bond. Large-format to 500×600mm.

Anodic · FusionHermetic seal500×600mm glass
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Injection Molding (COP/PC)

PC and COP chip production via injection molding, from SU-8/PDMS prototype to mass-produced polymer chip. Mold tooling fabricated . COP for low autofluorescence fluorescence assays.

COP · PC injection moldLow autofluorescenceMold tooling available
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LIGA Microneedles

Ni and Pd-Ni microneedle arrays by X-ray LIGA electroforming. 1µm hollow channel diameter. Biocompatible Pd-Ni for ISF sampling and drug delivery applications.

LIGA Pd-Ni1µm channelBiocompatible
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Why Nanosystems JP Inc. for Life Sciences
Nano to micro, one coordinated process flow, fast turnaround
01

500×600mm glass for low chip cost

Panel-scale glass biochip processing produces 5–10× more chips per run versus wafer-format foundries, dramatically reducing cost-per-chip for array biosensors and diagnostic plates.

02

PDMS prototype in 3–5 days

From SU-8 master fabrication to first functional PDMS chip in 3–5 days. Iterate channel geometry, valve placement, or electrode layout rapidly without waiting for minimum lot commitments.

03

Sub-50nm nanopores

NIL nanopore arrays for DNA sequencing, nanofluidic confinement, and molecular sieving, with master mold fabrication and pattern transfer done . No separate nanofab vendor.

04

Biocompatible materials, PI and Pd-Ni

ISO 10993-assessed polyimide for electrode passivation in implantable devices. Pd-Ni electroforming for biocompatible microneedles and microstructures in direct contact with biological tissue.

05

PDMS to production, same design

Prototype in PDMS, then transition to injection-molded COP with the same channel design. Mold tooling . No redesign for a different foundry process.

06

NDA available on request

Biomedical device designs, assay protocols, and surface chemistry specifications are among the most sensitive in any industry. An NDA can be arranged before any design files or technical details are shared - just mention it in your first message. Initial inquiries and quotes can proceed without one.

PROCESSES FOR LIFE SCIENCES Fabrication flow for microfluidics & biomedical devices

Start your project.
Response within 1 business day.

Share your process requirements, substrate, and production volume, A Nanosystems JP Inc. engineer will respond within 1 business day. Full quote typically within 7–10 business days, subject to project complexity and NDA requirements.

[email protected] · +81-3-5288-5569 · NDA available

Technical AI — Nanosystems JP Inc.
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