Luxendo Light-Sheet Microscopes

Papilio5D

Multi-sample and dual-view light-sheet microscope ideal for organoids and 3D cell cultures

Papilio5D

The Bruker Papilio5D light-sheet microscope delivers high-sensitivity imaging for organoids and 3D cell cultures with a high degree of flexibility, enabling researchers to adapt the system to specific sample types, study conditions, and experimental designs.

The system’s horizontal lens geometry with dual-view detection and a choice of Gaussian or Bessel beam illumination, combined with support for simultaneous multi-sample and multi-condition imaging, make Papilio5D a flexible solution for achieving deep and high-resolution imaging while maintaining sample integrity — even on challenging samples and in complex, multi-sample, and multi-condition experiments.

To learn more, continue reading, contact us, or download the brochure.

Unprecedented
photon efficiency
With dual-sided detection and modular illumination beams.
Fast
dual-view acquisition and fusion
For highest-quality, high-resolution images.
Delicate & simultaneous
light-sheet imaging
For diverse samples under different experimental conditions.
Features

Fast and Photo-Efficient for the Highest Quality Images

Papilio5D is photo-efficient for the most delicate samples, using a horizontal geometry with two views/dual-sided detection and a perpendicular light-sheet. This setup is capable of capturing twice as many photons as single-objective detection setups and enables a more comprehensive 3D view of samples.

Fast dual-view acquisition and fusion deliver high-resolution images. Water-dipping high-NA lenses ensure the light sheet is ultra-thin. Area- and line-mode detection also allow data acquisition specialized for different sample requirements.

Together, these features deliver:

  • A high signal-to-noise ratio
  • An impressive z resolution
  • Optimized depth penetration

Papilio5D can also reach Nyquist sampling, which improves subsequent image processing and enables state-of-the-art deconvolution. Destriping further enhances image quality.

Papilio5D uses horizontal lenses, dual-view detection, and Bessel or Gaussian illumination. This setup enables optimized depth penetration and provides a large and evenly illuminated field of view with four different optical magnifications.

Customizable for Complex Experimental Design

Papilio5D was designed with maximum flexibility in mind. This includes multi-beam and multi-acquisition modes, as well as multi-sample mounting and multi-condition comparison. 

Modular illumination beam options

Papilio5D users get to choose the best light beam for their experiment. The choice of Gaussian or Bessel beam illumination, both with a beam width below one micrometer, ensures outstanding image quality and great depth-penetration for a wide variety of objects, including dense organoids or zebrafish larvae and fish.

  • Gaussian beams are ideal for small, light-sensitive samples, such as early mouse embryology studies.
  • Bessel beams provide multi-direction illumination from a 360° angular range for robust imaging of even optically dense objects.

Multi-acquisition modes

These beams are complemented by two modes of acquisition: area or line mode.

  • In area mode, the camera captures the entire field of view at once, making it fast and efficient.
  • In line mode, the camera uses a confocal slit-like rolling shutter that synchronizes with the scanned light-sheet. This effectively rejects out-of-focus and scattered light, improving contrast in thick or scattering samples (e.g., organoids). 


     

Mouse embryo with and without Line Mode.

Multi-sample and multi-condition configurations

The Papilio5D has a generous sample holder that can hold up to three dishes with two separate chambers each, enabling a total of six experimental conditions to be tested at once. Sample health and integrity are further maintained with environmental control that supports long-term imaging (hours to days). Papilio5D provides control over temperature (20 to 37°C), gas concentration (CO₂ and O₂), and humidity. 

Configuration options

Illumination ModesGaussian BeamBessel Beam
Beam Waist Thickness [µm]1 bis 61 (main lobe)
Beam Length [µm]20350
Pivot Scan
Confocal Line Mode
Acquisition Options

- Gaussian beam

- Gaussian with line mode

- Gaussian with line mode and pivot scan

- Bessel beam

- Bessel beam with line mode

- Bessel beam with line mode and pivot scan

Illumination Optics20x 0.6NA
Detection OpticsDual 25x 1.1NA / 16x 0.8NA
Multi-Sample/Multi-Condition Experiments6 seperate compartments
Magnification Changer4 seperate steps
Data processingContent based dual view registration & fusion
PhotomanipulationCW or pulsed, VIS to NIR
Applications

Optimized for Different Applications

Papilio5D supports a wide range of biological imaging applications, from deep imaging of complex 3D organoids to long-term in vivo studies. Its dual-view detection and multi-sample mounting enable comparative experiments, such as tracking regenerative processes in zebrafish under different treatment conditions.

TO DISCUSS YOUR SPECIFIC APPLICATION, CONTACT US.

Case Study 1

In Vivo Time-Lapse After Photomanipulation in Zebrafish

Time-lapse imaging of zebrafish distal tubules after localized photodamaging can provide novel insights into understanding wound healing processes over time. The design of Papilio5D sample mounting within separate chambers enables imaging under different treatment conditions to be studied at the same time. This allows comparative insights into how pharmaceutical components might impact wound healing.

In this example, regeneration of the distal tubule is studied in the embryonic zebrafish kidney using the cdh17:egfp transgenic line after photodamaging with a photomanipulation module.

Time-lapse imaging of the zebrafish distal tubule after PM.

Samples provided by Leon Rapp (Westhoff lab). The experiment is part of the INFLANET project (Sankeert Satheesan / Jochen Gehrig, Luxendo) in collaboration with Prof. Jens Westhoff (Children’s University Hospital Heidelberg). Acquisition details: 25x 1.1 NA, 242 slices at 1μm, every 10 min for 10 hours, Gauss 1.6μm, 2x1 tiling, Fused view.

Specifications

Select Papilio5D Technical Specifications

Dual Sided Detection with 2x ObjectivesTube LensMagnificationPixel Size [nm] Orca FlashFOV [µm]Pixel Size [nm] Orca FireFOV [µm] Orca Fire
Detection 2x Nikon CFI APO LWD 25x 1.10 NA10012.5x5201065370876
 20025x260532184436
 30037.5x173353123290
 40050x13026692* (Nyquist sampling)218
Detection 2x Nikon CFI APO LWD 16x 0.8 NA1008x81316645751362
 20016x406832288681
 30024x271555192454
 40032x203416144340
DOWNLOAD THE BROCHURE TO LEARN MORE

System Comparison
* COMPATIBLE MODULE

 

MuVi SPIM

The perfect allrounder - multi-view imaging for diverse samples (live and cleared option)

Papilio5D

Multi-sample and dual view flexibility for highly sensitive imaging, ideal for organoids and 3D cell cultures

TruLive3D Imager

In vivo multi-sample and multi-condition imaging, ideal for drug treatment comparison

LCS SPIM

Perfection for cleared samples prepared by any type of clearing protocol

InVi SPIM Lattice Pro

High-end imaging with various beam patterns from single cells to 3D cell cultures

GeometryHorizontal with multiviewHorizontal with dual viewInverted with dual illuminationInverted dual illumination with moving opticsInverted geometry at 360°
Beam TypeGaussianGaussian and BesselGaussianGaussianAdvanced Illumination Module (AIM)
Application Examples

- Long-term imaging of Drosophila development

- Photomanipulation studies in zebrafish embryos

- Cleared and stained samples up to mouse brain size

- High-resolution full 3D imaging of multiple organoids over time

- Long-term imaging of highly light-sensitive samples

- Comparing the pharmacological impact in zebrafish wound healing after PM

- Time-lapse imaging of multiple pancreatic spheres

- Studying pharmacological impact on zebrafish development

- Comparing genetically altered organoids

- Pharmacokinetics in mouse brain

- Multi-stained rat brain

- Whole mouse imaging

- Fast imaging of photo-sensitive 2D cell culture

- Lattice imaging for enhanced resolution in 3D cell cultures

- FCS and FLIM in cell culture

User LevelBeginner friendlyBeginner friendlyBeginner friendlyIntermediateAdvanced
# Lenses

4 lenses (2 IO, 2 DO)3 lenses (1 IO, 2 DO)3 lenses (2 IO, 1 DO)3 lenses (2 IO, 1 DO)2 lenses (1 IO, 1 DO)
Multi-View
   
Live/Fixed Samples
 
Cleared Samples
   
Expanded Samples
Best Embedding
Capillary/FEP tube w/ agarose 3D stageCustom-solution and FEP foilTruLive3D dishes and FEP foilQuartz-crystal cuvetteFEP foil; glass slides
Photomanipulation*
 
Environmental Control* 
Destriping/Uniform Illumination*✓ (w/ Advanced Illumination Module)
Benchtop Design
Software

All-in-One LuxBundle Software

Intuitive design

Bruker's LuxBundle software saves time and enhances productivity by providing:

  • All-in-one, easy-to-use interface for acquisition, viewing, and post-processing
  • Fully scriptable microscope control and post-processing via open interface (e.g., Python or any other language), ready for custom "smart" microscopy
  • High reproducibility of experiments: all parameters are saved in the metadata and configurations can be saved for future experiments
  • Data formats (.tiff, .hdf5, .ims) compatible with common image processing software: Imaris, Aivia, BigDataViewer, Arivis, Fiji, Python, Matlab, Napari


Impressive Image Post Processor

Our dual-view light-sheet microscopes record a sample from different angles/views and generate images composed of multiple tiles. The LuxBundle software ensures high-quality, 360° crisp images of the sample that compensate for absorption and scattering. Features include:

  • Multi-color alignment
  • Tile stitching of hundreds of tiles for large samples
  • Multi-view image fusion and deconvolution


3D Data Viewer

LuxBundle's integrated 3D data viewer allows researchers to inspect the entire dataset directly after acquisition. This gives users control over their data with key capabilities, including:

  • The ability to turn tile stitching on or off
  • Both raw and post-processed images
  • Fast viewing of multi-terabyte data sets
  • Flexible options to draw and annotate regions and landmarks
Cleared mouse embryo labeled with methylene blue (cyan) and showing autofluorescence (magenta). Image composed of 12 tiles and 920 planes, all processed and stitched with LuxBundle (Image courtesy of Montserrat Coll Lladó, European Molecular Biology Laboratory, Barcelona, Spain)
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