From in vitro to ex vivo: subcellular localization and uptake of graphene quantum dots into solid tumors
Creators
- Kersting, David1
- Fasbender, Stefan1
- Pilch, Rabea1
- Kurth, Jennifer1
- Heinzel, Thomas1
- Franken, André2
- Ludescher, Marina2
- Naskou, Johanna2
- Fehm, Tanja2
- Niederacher, Dieter2
- Neubauer, Hans2
- Hallenberger, Angelika3
- Gall, Charlotte von3
- Mohr, Corinna J4
- Lukowski, Robert4
- Raba, Katharina5
- Fischer, Johannes C5
- Jaschinski, Sandra6
- Esposito, Irene6
- 1. Condensed Matter Physics Laboratory, Heinrich-Heine-University, D-40204 Düsseldorf (Germany)
- 2. Department of Obstetrics and Gynecology, University Hospital and Medical Faculty, Heinrich-Heine-University, D-40204 Düsseldorf (Germany)
- 3. Institute for Anatomy II, Medical Faculty, Heinrich-Heine-University, D-40204 Düsseldorf (Germany)
- 4. Institute of Pharmacy, Department of Pharmacology, Toxicology and Clinical Pharmacy, University of Tübingen, D-72076 Tübingen (Germany)
- 5. Institute for Transplantation Diagnostics and Cell Therapeutics, Heinrich-Heine-University, D-40204 Düsseldorf (Germany)
- 6. Institute of Pathology, University Hospital and Medical Faculty, Heinrich-Heine-University, D-40204 Düsseldorf (Germany)
Description
Among various nanoparticles tested for pharmacological applications over the recent years, graphene quantum dots (GQDs) seem to be promising candidates for the construction of drug delivery systems due to their superior biophysical and biochemical properties. The subcellular fate of incorporated nanomaterial is decisive for transporting pharmaceuticals into target cells. Therefore a detailed characterization of the uptake of GQDs into different breast cancer models was performed. The demonstrated accumulation inside the endolysosomal system might be the reason for the particles' low toxicity, but has to be overcome for cytosolic or nuclear drug delivery. Furthermore, the penetration of GQDs into precision-cut mammary tumor slices was studied. These constitute a far closer to reality model system than monoclonal cell lines. The constant uptake into the depth of the tissue slices underlines the systems' potential for drug delivery into solid tumors. (paper)
Availability note (English)
Available from http://dx.doi.org/10.1088/1361-6528/ab2cb4Additional details
Identifiers
Publishing Information
- Journal Title
- Nanotechnology (Print)
- Journal Volume
- 30
- Journal Issue
- 39
- Journal Page Range
- [10 p.]
- ISSN
- 0957-4484
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 51054219
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- ACCURACY; ANIMAL TISSUES; DRUG DELIVERY; GRAPHENE; IN VITRO; MAMMARY GLANDS; NANOMATERIALS; NANOPARTICLES; NEOPLASMS; QUANTUM DOTS; TOXICITY
- Descriptors DEC
- BODY; CARBON; DISEASES; ELEMENTS; GLANDS; MATERIALS; NANOSTRUCTURES; NONMETALS; ORGANS; PARTICLES