Title of article :
The cellular uptake of antisense oligonucleotid of E6 mRNA into cervical
Author/Authors :
Saffarzadeh، Negin نويسنده Department of Medical Genetic, Shahid Sadoughi University of Medical Sciences, Yazd, Iran , , Kalantar، Seyed Mehdi نويسنده , , Jebali، Ali نويسنده Department of Medical Nanotechnology, Pajoohesh Lab, Yazd, Iran. , , Hekmatimoghaddam، Seyed Hossein نويسنده Department of Laboratory Sciences, Faculty of Paramedicine, Shahid Sadoughi University of Medical Sciences, , , Sheikhha، Mohammad Hassan نويسنده , , Ghasemi، Nasrin نويسنده , , Farashahi، Ehsan نويسنده Research and Clinical Centre for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran ,
Issue Information :
دوفصلنامه با شماره پیاپی 5 سال 2014
Pages :
6
From page :
292
To page :
297
Abstract :
Objective(s): Although several chemical and physical methods for gene delivery have been introduced, their cytotoxicity, non-specific immune responses and the lack of biodegradability remain the main issues. In this study, hydroxyapatite nanoparticles (NPs) and 1,2-dioleoyl-snglycero- 3-phosphoethanolamine (DOPE)-modified hydroxyapatite NPs was coated with antisense oligonucleotide of E6 mRNA, and their uptakes into the cervical cancer cell line were evaluated. Materials and Methods: Calcium nitrate and diammonium phosphate were used for the synthesis of the hydroxyapatite nanoparticle. Thus, they were coated with polyethylene glycol (PEG), DOPE and antisense oligonucleotide of E6 mRNA using a cross-linker. Then, hydroxyapatite NPs and DOPE-modified hydroxyapatite NPs were incubated 48 hours with cervical cancer cells and their uptakes were evaluated by fluorescent microscopy. Results: The hydroxyapatite NPs had different shapes and some agglomeration with average size of 100 nm. The results showed DOPE-modified hydroxyapatite NPs had higher uptake than hydroxyapatite NPs (P < 0.05). Conclusions: Hydroxyapatite NPs conjugated with DOPE are a good choice for gene delivery and silencing of viral genes in cervical cancer cells, but their efficacy should be addressed more in future studies.
Journal title :
Nanomedicine Journal
Serial Year :
2014
Journal title :
Nanomedicine Journal
Record number :
1371012
Link To Document :
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