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Optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion
Application of droplet microfluidics for the encapsulation of bacteria in water-in-oil-in-water (W/O/W) emulsion allows for production of monodisperse droplets with controllable size. In this study the release of bacteria from W/O/W emulsion, the effect of the double emulsion structure on bacterial...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695039/ https://www.ncbi.nlm.nih.gov/pubmed/35423274 http://dx.doi.org/10.1039/d0ra10954a |
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author | Mohd Isa, Nur Suaidah El Kadri, Hani Vigolo, Daniele Gkatzionis, Konstantinos |
author_facet | Mohd Isa, Nur Suaidah El Kadri, Hani Vigolo, Daniele Gkatzionis, Konstantinos |
author_sort | Mohd Isa, Nur Suaidah |
collection | PubMed |
description | Application of droplet microfluidics for the encapsulation of bacteria in water-in-oil-in-water (W/O/W) emulsion allows for production of monodisperse droplets with controllable size. In this study the release of bacteria from W/O/W emulsion, the effect of the double emulsion structure on bacterial growth and metabolic activity, and the stability and mechanism of bacterial release were investigated. W/O/W emulsions were formed using a double flow-focusing junction microfluidic device under controlled pressure to produce droplets of approximately 100 μm in diameter containing an inner aqueous phase (W(1)) of about 40–50 μm in diameter. GFP-labelled Escherichia coli (E. coli-GFP) bacteria were encapsulated within the W(1) droplets and the stability of emulsions was studied by monitoring droplet size and creaming behaviour. The double emulsions were stabilised using a hydrophilic (Tween 80) and a lipophilic surfactant (polyglycerol polyricinoleate) and were destabilised by altering the osmotic balance, adding NaCl either in the inner W(1) phase (hypo-osmotic) or outer W(2) phase (hyper-osmotic). The release of E. coli-GFP was monitored by plating on agar whereby the colony form unit (CFU) of the released bacteria was determined while fluorescent microscopy was employed to observe the mechanism of release from the droplets. The release of E. coli-GFP was significantly increased with higher concentrations of NaCl and lower amounts of Tween 80. Microscopic observation revealed a two-step mechanism for the release of bacteria: double W/O/W emulsion droplet splitting to release W(1) droplets forming a secondary double emulsion followed by the collapse of W(1) droplets to release E. coli-GFP into the continuous aqueous phase. |
format | Online Article Text |
id | pubmed-8695039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86950392022-04-13 Optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion Mohd Isa, Nur Suaidah El Kadri, Hani Vigolo, Daniele Gkatzionis, Konstantinos RSC Adv Chemistry Application of droplet microfluidics for the encapsulation of bacteria in water-in-oil-in-water (W/O/W) emulsion allows for production of monodisperse droplets with controllable size. In this study the release of bacteria from W/O/W emulsion, the effect of the double emulsion structure on bacterial growth and metabolic activity, and the stability and mechanism of bacterial release were investigated. W/O/W emulsions were formed using a double flow-focusing junction microfluidic device under controlled pressure to produce droplets of approximately 100 μm in diameter containing an inner aqueous phase (W(1)) of about 40–50 μm in diameter. GFP-labelled Escherichia coli (E. coli-GFP) bacteria were encapsulated within the W(1) droplets and the stability of emulsions was studied by monitoring droplet size and creaming behaviour. The double emulsions were stabilised using a hydrophilic (Tween 80) and a lipophilic surfactant (polyglycerol polyricinoleate) and were destabilised by altering the osmotic balance, adding NaCl either in the inner W(1) phase (hypo-osmotic) or outer W(2) phase (hyper-osmotic). The release of E. coli-GFP was monitored by plating on agar whereby the colony form unit (CFU) of the released bacteria was determined while fluorescent microscopy was employed to observe the mechanism of release from the droplets. The release of E. coli-GFP was significantly increased with higher concentrations of NaCl and lower amounts of Tween 80. Microscopic observation revealed a two-step mechanism for the release of bacteria: double W/O/W emulsion droplet splitting to release W(1) droplets forming a secondary double emulsion followed by the collapse of W(1) droplets to release E. coli-GFP into the continuous aqueous phase. The Royal Society of Chemistry 2021-02-17 /pmc/articles/PMC8695039/ /pubmed/35423274 http://dx.doi.org/10.1039/d0ra10954a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Mohd Isa, Nur Suaidah El Kadri, Hani Vigolo, Daniele Gkatzionis, Konstantinos Optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion |
title | Optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion |
title_full | Optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion |
title_fullStr | Optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion |
title_full_unstemmed | Optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion |
title_short | Optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion |
title_sort | optimisation of bacterial release from a stable microfluidic-generated water-in-oil-in-water emulsion |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695039/ https://www.ncbi.nlm.nih.gov/pubmed/35423274 http://dx.doi.org/10.1039/d0ra10954a |
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