Creating permanent 3D arrangements of isolated cells using holographic optical tweezers
- 30 September 2005
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Lab on a Chip
- Vol. 5 (11) , 1224-1228
- https://doi.org/10.1039/b509218c
Abstract
We report the creation of permanent 3D configurations of cells, at predefined positions, within a gelatin matrix. The technique used holographic optical tweezers to manipulate individual E. coli within a solution comprising monomer precursors. The matrix was then set and after the laser beam was removed, we were able to demonstrate that the structures remained intact for many days. We were also able to demonstrate that, in the presence of appropriate nutrients, the E. coli survived within the gelatin matrix for several days. The technique could have a number of potential future applications, including the arrangement of a variety of different cell types in complex architectures, as motifs for promoting tissue differentiation and growth within the field of cell engineering.Keywords
This publication has 16 references indexed in Scilit:
- Assembly of 3-dimensional structures using programmable holographic optical tweezersOptics Express, 2004
- Optical trappingReview of Scientific Instruments, 2004
- Permanent 3D microstructures in a polymeric host created using holographic optical tweezersJournal of Modern Optics, 2004
- Defining the trapping limits of holographical optical tweezersJournal of Modern Optics, 2004
- A revolution in optical manipulationNature, 2003
- Dynamic holographic optical tweezersPublished by Elsevier ,2002
- Direct Observation of Transfer of Angular Momentum to Absorptive Particles from a Laser Beam with a Phase SingularityPhysical Review Letters, 1995
- Compliance of bacterial flagella measured with optical tweezersNature, 1989
- Optical trapping and manipulation of single cells using infrared laser beamsNature, 1987
- Observation of a single-beam gradient force optical trap for dielectric particlesOptics Letters, 1986