TY - JOUR
T1 - Influence of polymer adjuvants on the ultrasound-mediated transfection of cells in culture
AU - Mehier-Humbert, Sophie
AU - Bettinger, T
AU - Yan, F
AU - Guy, Richard H
PY - 2009
Y1 - 2009
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=67449110720&partnerID=8YFLogxK
UR - http://www.sciencedirect.com/science/journal/09396411
UR - http://dx.doi.org/10.1016/j.ejpb.2009.02.012
U2 - 10.1016/j.ejpb.2009.02.012
DO - 10.1016/j.ejpb.2009.02.012
M3 - Article
SN - 0939-6411
VL - 72
SP - 567
EP - 573
JO - European Journal of Pharmaceutics and Biopharmaceutics
JF - European Journal of Pharmaceutics and Biopharmaceutics
IS - 3
ER -