Influence of polymer adjuvants on the ultrasound-mediated transfection of cells in culture
The purpose of this study was to further understand the mechanisms involved in ultrasound-mediated 25 delivery of DNA (sonoporation); in particular, to understand how a plasmid should be formulated with 26 an ultrasound contrast agent (UCA). Different polymer adjuvant–UCA combinations were formulate...
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Veröffentlicht in: | European Journal of Pharmaceutics and Biopharmaceutics 2009, Vol.72 (3), p.567-573 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The purpose of this study was to further understand the mechanisms involved in ultrasound-mediated 25 delivery of DNA (sonoporation); in particular, to understand how a plasmid should be formulated with 26 an ultrasound contrast agent (UCA). Different polymer adjuvant–UCA combinations were formulated, 27 and their impact on in vitro DNA transfection, was determined, under various experimental conditions. 28 When present in the medium surrounding a cell suspension, and in the presence of a plasmid encoding 29 for the green fluorescent protein (GFP), expression following sonoporation was increased by more than 30 1.5-fold compared to that achieved in control experiments (without the adjuvants). The effects of the 31 adjuvants were not influenced by the nature of the UCA, nor by that of the transfected cells; in contrast, 32 the adjuvant concentrations, their physico-chemical properties, and the manner in which they were 33 used, did have an impact on transfection. Close association of the adjuvants to the UCA inhibited their 34 action, suggesting that these substances must have access to the cell membrane to be effective. Indeed, 35 Pluronic F127 appeared to improve the efficacy of transfection (percentage of GFP-positive cells and 36 cell viability), via fluidization of the cell membrane, perhaps facilitating thereby the formation of tran- 37 sient pores and their re-sealing. The mechanism of action of PEG, on the other hand, remains unclear. |
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ISSN: | 0939-6411 1873-3441 |
DOI: | 10.1016/j.ejpb.2009.02.012 |