Hostname: page-component-8448b6f56d-c4f8m Total loading time: 0 Render date: 2024-04-16T14:32:38.097Z Has data issue: false hasContentIssue false
  • English
  • Français

Freezing Assisted Protein Delivery by Using Polymeric Cryoprotectant

Published online by Cambridge University Press:  14 January 2014

Sana AHMED  and
Kazuaki MATSUMURA
Sana AHMED
Affiliation:
School of Materials Science, Japan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi, Ishikawa 923-1292 Japan M.Tech (Chemical Synthesis and Process Technologies), Department of Chemistry, University of Delhi, Delhi-110007, India
Kazuaki MATSUMURA
Affiliation:
School of Materials Science, Japan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi, Ishikawa 923-1292 Japan
Get access

Abstract

A number of drug carrier systems such as liposomes, polymeric-nanoparticles, microparticles, polymeric micelles have been investigated for intracellular delivery. Among these liposomes are the potential drug vehicles for efficient cytosolic delivery. They have an adhesive property for cell membrane to encapsulate the drug or protein effectively and showing the enhanced absorption rate. One of the problems could be the difficulty of incorporation of the drug or protein into cell. Therefore many studies of the drug carriers have been developed to enhance the intracellular delivery of materials. Here we propose the novel method to improve the intracellular uptaking by using freeze concentration. Solutes are excluded from ice crystallization and concentrated in the remaining solution during freezing by freezing concentration. We have reported that polymeric cryoprotectant which is carboxylated poly-L-lysine was adsorbed on to the cell membrane during freezing and caused effective freeze concentration. In this study we investigated that delivery of protein effectively taking place by liposome as a carrier agent. It was successfully delivered protein to L929 cells via freeze concentration using polymeric cryoprotectant as a novel drug delivery.

Keywords

biomaterialmacromolecular structurebiomedical
Type
Articles
Information
MRS Online Proceedings Library (OPL) , Volume 1622: Symposium E – Fundamentals of Gels and Self-Assembled Polymer Systems , 2014 , pp. 123 - 127
Copyright
Copyright © Materials Research Society 2014 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Yuba, E. E, Harada, A., Sakanishi, Y., Watarai, S., Kono, K., Biomaterials 34, 3042–3052 (2013)CrossRefGoogle Scholar
Yuba, E., Harada, A., Sakanishi, Y., Kono, K., J Control Release 149, 72–80 (2011)CrossRefGoogle Scholar
Yuba, E., Kojima, C., Harada, A., Tana, , Watarai, S., Kono, K., Biomaterials 31, 943–951 (2010)CrossRefGoogle Scholar
Matsumura, K., Bae, J.Y., Hyon, S.H., Cell Transplant 19, 691–9 ( 2010)CrossRefGoogle Scholar
Matsumura, K., Hyon, S.H., Biomaterials 30, 4842–4849 (2009)CrossRefGoogle Scholar
Tolleter, D., Hincha, D., Macherel, D., Biochimica et Biophysica Acta, 1798, 1926–1933 (2010)CrossRefGoogle Scholar
Sakaguchi, N., Kojima, C., Harada, A., Koiwai, K., Emi, N., Kono, K., Bioconjugate Chem, 19, 1588–95 (2008)CrossRefGoogle Scholar
Varkouhi, A.K., Scholte, M., Storma, G., Haisma, H.J., J Control Release 151, 220–228 (2011)CrossRefGoogle Scholar
Sakaguchi, N., Kojima, C., Harada, A., and Kono, K., Bioconjugate Chem, 19, 1040–1048 (2008)CrossRefGoogle Scholar