Gene Transfer into the Lung by Nanoparticle Dextran-Spermine/Plasmid DNA Complexes

Author:

Abdullah Syahril12,Wendy-Yeo Wai Yeng12,Hosseinkhani Hossein34,Hosseinkhani Mohsen5,Masrawa Ehab6,Ramasamy Rajesh17,Rosli Rozita12,Rahman Sabariah A.17,Domb Abraham J.6

Affiliation:

1. UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia

2. Medical Genetics Laboratory, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia

3. Center for Biomedical Engineering, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA

4. International Research Institute for Integrated Medical Sciences (IREIIMS), Tokyo Women’s Medical University, 8-1, Kawada-cho, Tokyo 162-8666, Japan

5. Center for Cancer Systems Biology, Caritas St. Elizabeth’s Medical Center, Tufts University School of Medicine, MA 02135, USA

6. Department of Medicinal Chemistry and Natural Products, School of Pharmacy, The Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel

7. Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia

Abstract

A novel cationic polymer, dextran-spermine (D-SPM), has been found to mediate gene expression in a wide variety of cell lines andin vivothrough systemic delivery. Here, we extended the observations by determining the optimal conditions for gene expression of D-SPM/plasmid DNA (D-SPM/pDNA) in cell lines and in the lungs of BALB/c mice via instillation delivery.In vitrostudies showed that D-SPM could partially protect pDNA from degradation by nuclease and exhibited optimal gene transfer efficiency at D-SPM to pDNA weight-mixing ratio of 12. In the lungs of mice, the levels of gene expression generated by D-SPM/pDNA are highly dependent on the weight-mixing ratio of D-SPM to pDNA, amount of pDNA in the complex, and the assay time postdelivery. Readministration of the complex at day 1 following the first dosing showed no significant effect on the retention and duration of gene expression. The study also showed that there was a clear trend of increasing size of the complexes as the amount of pDNA was increased, where the sizes of the D-SPM/pDNA complexes were within the nanometer range.

Funder

Universiti Putra Malaysia

Publisher

Hindawi Limited

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology,Molecular Medicine,General Medicine,Biotechnology

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