Levitation and movement of tripalmitin-based cationic lipospheres on a dielectrophoresis-based lab-on-a-chip device
Article first published online: 2 JUN 2008
DOI: 10.1002/app.28413
Copyright © 2008 Wiley Periodicals, Inc.
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How to Cite
Fabbri, E., Borgatti, M., Manaresi, N., Medoro, G., Nastruzzi, C., Di Croce, S., Tosi, A., Mazzitelli, S., Mancini, I., Guerrieri, R. and Gambari, R. (2008), Levitation and movement of tripalmitin-based cationic lipospheres on a dielectrophoresis-based lab-on-a-chip device. Journal of Applied Polymer Science, 109: 3484–3491. doi: 10.1002/app.28413
Publication History
- Issue published online: 18 JUN 2008
- Article first published online: 2 JUN 2008
- Manuscript Accepted: 10 JAN 2008
- Manuscript Received: 27 JUN 2007
Funded by
- Ministero dell' Università e della Ricerca (MIUR)-COFIN-2000 and European Union (EU) MEDICS Project. Grant Number: IST-2001-32437
- MIUR-COFIN-2002 (“Applications of a Dielectrophoresis-Based Lab-on-a-Chip)
- Fondo per gli Investimenti per la Ricerca di Base-2001 (“Development of a Lab-on-a-Chip Based on Microelectronic Technologies and Its Biotechnological Validation;”)
- Fondazione Cassa di Risparmio di Padova e Rovigo
- Fondazione Italiana Ricerca sulla Fibrosi Cistica
- Association Italiana per la Ricerca sul Cancro
- Associazione Veneta per la Lotta alla Talassemia (AVLT, Rovigo, Italy)
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- Cited By
Keywords:
- bioengineering;
- biopolymers;
- drug delivery systems
Abstract
Dielectrophoresis (DEP) is a very valuable approach for designing and developing laboratory-on-a-chip (lab-on-a-chip) devices that are able to manipulate microparticles and cells. Lab-on-a-chip technology will enable laboratory testing to move from laboratories using complex equipment to nonlaboratory settings. We used a lab-on-a-chip device, the SmartSlide, which carries 193 parallel electrodes and generates up to 50 cylinder-shaped DEP cages able to entrap microparticles and cells within DEP cages and move them along the chip. For lab-on-a-chip technology, the characterization of microparticles exhibiting a differential ability to be DEP-caged, levitated, and moved is important for the development of both diagnostic and therapeutic protocols. We determined whether the SmartSlide could be used to levitate and move tripalmitin-based lipospheres carrying increasing concentrations of dihexadecyl dimethyl ammonium bromide (DHDAB) as a cationic surfactant. The data obtained with this DEP-based platform showed that DEP caging, levitation, and movement of the cationic lipospheres depended on the percentage of DHDAB. Tripalmitin lipospheres containing 6% DHDAB could be DEP-caged and manipulated. On the contrary, lipospheres containing 12% DHDAB did not exhibit an efficient ability to be DEP-caged and moved throughout the chip. To our knowledge, this is the first report on the possible use of a DEP-based lab-on-a-chip device for guided manipulation of lipospheres. This information might be of interest in the fields of drug discovery, delivery, and diagnosis. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008

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