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Drug delivery by nanoparticles - facing the obstacles

Drug delivery by nanoparticles - facing the obstacles
Drug delivery by nanoparticles - facing the obstacles
There are numerous concepts of nanoparticle mediated drug delivery. The major advantage will be the option of targeted drug delivery to specific target cells thus avoiding high systemic loads of potentially toxic chemicals. Any kind of drug delivery by nanoparticles relies on delivery of the drug into the cell. In most cases that means drug delivery into the cytoplasm, and in some instances delivery of the drug to extracellular domains of transmembrane signalling molecules. Whenever viable cells are confronted with nanoparticles these are ingested by endocytosis rather then passage through the cell plasma membrane. Once inside endosomal vesicles the nanoparticles or at least their drug payload requires release into the cytoplasm in order to exert it’s biological effect. In order to monitor whether a drug delivered by nanoparticles is biologically active a toxic model drug, disulfiram, was chosen as a payload with micelle and liposome nanoparticles. L929 mouse fibroblasts were incubated with these disulfiram loaded naoparticles and cell viability was determined by quantification of celluar reductase activity. Applied nanoparticles are toxic to the cells. However, with respect to the disulfiram payload a 100-fold higher disulfiram concentration is required in comparison to free disulfiram for a biological effect. Hence, the toxic effect is most likely not due to the disulfiram delivered by the nanoparticles but rather to the amount of free disulfiram that is present in the nanoparticle preparation. Therefore it is advised to carefully characterize the nanoparticle suspension for the amount of free payload molecules
nanoparticle, drug delivery, endocytosis, drug release, disulfiram
9783540892076
1680-0737
19
2335-2338
Springer
Löbler, Marian
2dce1fe5-4503-4fa9-8e52-55120e6dfabc
Rohm, H.W.
4e3dc08d-f7f1-4c7e-8cea-90e40cdf891f
Schmitz, K.-P.
57d0a0c2-c66b-4407-b097-55ada524d537
Johnston, A.H.
c04f2567-5945-4e08-97df-7834ce234fcd
Newman, T.A.
322290cb-2e9c-445d-a047-00b1bea39a25
Ranjan, S.
3916b9b1-7bcb-4cce-9aef-3262b419025a
Sood, R.
22e86cf1-16f9-470a-a020-e9cfa3bcd034
Kinnunen, P.K.J.
841b5744-caa3-4f2d-a4b2-dcf99aef633f
Löbler, Marian
2dce1fe5-4503-4fa9-8e52-55120e6dfabc
Rohm, H.W.
4e3dc08d-f7f1-4c7e-8cea-90e40cdf891f
Schmitz, K.-P.
57d0a0c2-c66b-4407-b097-55ada524d537
Johnston, A.H.
c04f2567-5945-4e08-97df-7834ce234fcd
Newman, T.A.
322290cb-2e9c-445d-a047-00b1bea39a25
Ranjan, S.
3916b9b1-7bcb-4cce-9aef-3262b419025a
Sood, R.
22e86cf1-16f9-470a-a020-e9cfa3bcd034
Kinnunen, P.K.J.
841b5744-caa3-4f2d-a4b2-dcf99aef633f

Löbler, Marian, Rohm, H.W., Schmitz, K.-P., Johnston, A.H., Newman, T.A., Ranjan, S., Sood, R. and Kinnunen, P.K.J. (2009) Drug delivery by nanoparticles - facing the obstacles. In 4th European Conference of the International Federation for Medical and Biological Engineering. vol. 22, Springer. pp. 2335-2338 . (doi:10.1007/978-3-540-89208-3).

Record type: Conference or Workshop Item (Paper)

Abstract

There are numerous concepts of nanoparticle mediated drug delivery. The major advantage will be the option of targeted drug delivery to specific target cells thus avoiding high systemic loads of potentially toxic chemicals. Any kind of drug delivery by nanoparticles relies on delivery of the drug into the cell. In most cases that means drug delivery into the cytoplasm, and in some instances delivery of the drug to extracellular domains of transmembrane signalling molecules. Whenever viable cells are confronted with nanoparticles these are ingested by endocytosis rather then passage through the cell plasma membrane. Once inside endosomal vesicles the nanoparticles or at least their drug payload requires release into the cytoplasm in order to exert it’s biological effect. In order to monitor whether a drug delivered by nanoparticles is biologically active a toxic model drug, disulfiram, was chosen as a payload with micelle and liposome nanoparticles. L929 mouse fibroblasts were incubated with these disulfiram loaded naoparticles and cell viability was determined by quantification of celluar reductase activity. Applied nanoparticles are toxic to the cells. However, with respect to the disulfiram payload a 100-fold higher disulfiram concentration is required in comparison to free disulfiram for a biological effect. Hence, the toxic effect is most likely not due to the disulfiram delivered by the nanoparticles but rather to the amount of free disulfiram that is present in the nanoparticle preparation. Therefore it is advised to carefully characterize the nanoparticle suspension for the amount of free payload molecules

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More information

Published date: 4 February 2009
Venue - Dates: 4th European Conference of the International Federation for Medical and Biological Engineering, Antwerp, Belgium, 2008-11-23 - 2008-11-27
Keywords: nanoparticle, drug delivery, endocytosis, drug release, disulfiram

Identifiers

Local EPrints ID: 73045
URI: http://eprints.soton.ac.uk/id/eprint/73045
ISBN: 9783540892076
ISSN: 1680-0737
PURE UUID: 7f562f2b-ecf3-41ee-9c6c-bffd006c5be6
ORCID for T.A. Newman: ORCID iD orcid.org/0000-0002-3727-9258

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Date deposited: 26 Feb 2010
Last modified: 14 Mar 2024 02:39

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Contributors

Author: Marian Löbler
Author: H.W. Rohm
Author: K.-P. Schmitz
Author: A.H. Johnston
Author: T.A. Newman ORCID iD
Author: S. Ranjan
Author: R. Sood
Author: P.K.J. Kinnunen

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