The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.
Ligand modified nanoparticles increases cell uptake, alters endocytosis and elevates glioma distribution and internalization
Open accessAbstract
Nanoparticles (NPs) were widely used in drugs/probes delivery for improved disease diagnosis and/or treatment. Targeted delivery to cancer cells is a highly attractive application of NPs. However, few studies have been performed on the targeting mechanisms of these ligand-modified delivery systems. Additional studies are needed to understand the transport of nanoparticles in the cancer site, the interactions between nanoparticles and cancer cells, the intracellular trafficking of nanoparticles within the cancer cells and the subcellular destiny and potential toxicity. Interleukin 13 (IL-13) peptide can specifically bind IL-13Rα2, a receptor that is highly expressed on glioma cells but is expressed at low levels on other normal cells. It was shown that the nanoparticels modification with the IL-13 peptide could improve glioma treatment by selectively increasing cellular uptake, facilitating cell internalization, altering the uptake pathway and increasing glioma localization.
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Nanoparticle-Based Immunotherapy for Cancer
Shao, K., Singha, S., Clemente-Casares, X., Tsai, S., Yang, Y., & Santamaria, P. (2015) · ACS Nano · doi:10.1021/nn5062029 · Cited by 470
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Metadata
- Authors
- Gao, H., Yang, Z., Zhang, S., Cao, S., Shen, S., Pang, Z., & Jiang, X.
- Venue
- Scientific Reports
- Published
- 2013-08-28
- Volume
- 3
- Issue
- 1
- Pages
- 2534-2534
- ISSN
- 2045-2322 (ISSN-L)
- OpenAlex
- W1964429118
- Cited by
- 306
- References
- 40
- FWCI
- 13.06
- Type
- journal article
- Language
- en
- Open access
- gold
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- Gao, H., Yang, Z., Zhang, S., Cao, S., Shen, S., Pang, Z., & Jiang, X. (2013). Ligand modified nanoparticles increases cell uptake, alters endocytosis and elevates glioma distribution and internalization. Scientific Reports. https://doi.org/10.1038/srep02534
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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