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Poly-L-Lysine coated fluorescent upconversion nanoparticles for siRNA delivery and tracking

Published online by Cambridge University Press:  07 January 2014

Akshaya Bansal
Affiliation:
NUS Graduate School for Integrative Sciences & Engineering, Singapore
Muthu Kumara Gnanasammandhan
Affiliation:
Department of Biomedical Engineering, National University of Singapore, Singapore
Zhang Yong
Affiliation:
Department of Biomedical Engineering, National University of Singapore, Singapore NUS Graduate School for Integrative Sciences & Engineering, Singapore
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Abstract

Nanoparticle-based vectors are fast becoming the main choice for nucleic acid delivery. Fluorescent nanoparticles have the added advantage of tracking the delivery process and also of tracking cells transfected with nucleic acids for cell therapy. Fluorescent upconversion nanoparticles (UCNs) are ideal candidates for tracking since they are excited by NIR light and hence have very low phototoxicity, high signal-to-noise ratio and enable imaging in deep tissues. UCNs coated with a layer of silica and adsorbed with siRNA or siRNA loaded into the mesoporous silica coating on the UCNs have been used for siRNA delivery. However the loading of siRNA is very poor since the silica coating is negatively charged and it repels the negatively charged siRNA limiting the amount of siRNA that can be adsorbed on the surface of nanoparticles. Here we report the use of a layer-by-layer approach to coat the UCNs with Poly-L-Lysine (PLL) and use it for delivery. Highly monodispersed UCNs were synthesized with an average size of 50 nm. They were then modified with PLL and STAT-3 siRNA was adsorbed on to the surface of the modified UCNs. The loading of the siRNA was found to be 60 % more efficient by this approach as compared to silica coated UCNs alone. The PLL-coated UCNs also were minimally cytotoxic as shown by MTS assay. The siRNA coated UCNs also efficiently transfected B16F0 cells and knocked down STAT3 significantly and also enabled cell imaging. Thus, This method shows good promise for siRNA delivery and tracking and this could also be extended to in-vivo transfection and tracking.

Type
Articles
Copyright
Copyright © Materials Research Society 2014 

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References

REFERENCES

Davis, M. E., “The first targeted delivery of siRNA in humans via a self-assembling, cyclodextrin polymer-based nanoparticle: from concept to clinic,” Molecular pharmaceutics, vol. 6, pp. 659668, 2009.CrossRefGoogle Scholar
Lee, S. K., Han, M. S., Asokan, S., and Tung, C. H., “Effective Gene Silencing by Multilayered siRNA‐Coated Gold Nanoparticles,” Small, vol. 7, pp. 364370, 2011.CrossRefGoogle ScholarPubMed
Endoh, T. and Ohtsuki, T., “Cellular siRNA delivery using cell-penetrating peptides modified for endosomal escape,” Advanced drug delivery reviews, vol. 61, pp. 704709, 2009.CrossRefGoogle ScholarPubMed
Wang, F., Banerjee, D., Liu, Y., Chen, X., and Liu, X., “Upconversion nanoparticles in biological labeling, imaging, and therapy,” Analyst, vol. 135, pp. 1839–54, Aug 2010.CrossRefGoogle Scholar
Chatterjee, D. K., Gnanasammandhan, M. K., and Zhang, Y., “Small upconverting fluorescent nanoparticles for biomedical applications,” Small, vol. 6, pp. 2781–95, Dec 20 2010.CrossRefGoogle ScholarPubMed
Zhao, L., Peng, J., Huang, Q., Li, C., Chen, M., Sun, Y., et al. ., “Near‐Infrared Photoregulated Drug Release in Living Tumor Tissue via Yolk‐Shell Upconversion Nanocages,” Advanced Functional Materials, 2013.Google Scholar
Yang, Y., Qu, Y., Zhao, J., Zeng, Q., Ran, Y., Zhang, Q., et al. ., “Fabrication of and drug delivery by an upconversion emission nanocomposite with monodisperse LaF3: Yb, Er core/mesoporous silica shell structure,” European Journal of Inorganic Chemistry, vol. 2010, pp. 51955199, 2010.CrossRefGoogle Scholar
Qian, H. S., Guo, H. C., Ho, P. C. L., Mahendran, R., and Zhang, Y., “Mesoporous‐Silica‐coated up‐conversion fluorescent nanoparticles for photodynamic therapy,” Small, vol. 5, pp. 22852290, 2009.CrossRefGoogle ScholarPubMed
Jayakumar, M. K., Idris, N. M., and Zhang, Y., “Remote activation of biomolecules in deep tissues using near-infrared-to-UV upconversion nanotransducers,” Proc Natl Acad Sci U S A, vol. 109, pp. 8483–8, May 29 2012.CrossRefGoogle ScholarPubMed