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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Barua, Sutapa Rege, Kaushal |
| Description | Country affiliation: United States Author Affiliation: Barua S ( Department of Chemical Engineering, Arizona State University, Tempe, AZ 85287-6006, USA.) |
| Abstract | A diverse array of nanoparticles, including quantum dots (QDs), metals, polymers, liposomes, and dendrimers, are being investigated as therapeutics and imaging agents in cancer diseases. However, the role of the cancer-cell phenotype on the uptake and intracellular fate of nanoparticles in cancer cells remains poorly understood. Reported here is that differences in cancer-cell phenotypes can lead to significant differences in intracellular sorting, trafficking, and localization of nanoparticles. Unconjugated anionic QDs demonstrate dramatically different intracellular profiles in three closely related human-prostate-cancer cells used in the investigation: PC3, PC3-flu, and PC3-PSMA. QDs demonstrate punctated intracellular localization throughout the cytoplasm in PC3 cells. In contrast, the nanoparticles localize mainly at a single juxtanuclear location ('dot-of-dots') inside the perinuclear recycling compartment in PC3-PSMA cells, where they co-localize with transferrin and the prostate-specific membrane antigen. The results indicate that nanoparticle sorting and transport is influenced by changes in cancer-cell phenotype and can have significant implications in the design and engineering of nanoscale drug delivery and imaging systems for advanced tumors. |
| File Format | HTM / HTML |
| ISSN | 16136810 |
| e-ISSN | 16136829 |
| DOI | 10.1002/smll.200800972 |
| Journal | Small |
| Issue Number | 3 |
| Volume Number | 5 |
| Language | English |
| Publisher | Wiley-VCH |
| Publisher Date | 2009-03-01 |
| Publisher Place | Germany |
| Access Restriction | Open |
| Subject Keyword | Discipline Nanotechnology Prostatic Neoplasms Metabolism Quantum Dots Biological Transport Cell Line, Tumor Clathrin Drug Delivery Systems Microscopy, Confocal Microscopy, Fluorescence Phenotype Research Support, N.i.h., Extramural Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry Nanoscience and Nanotechnology Medicine Biomaterials Engineering Biotechnology |
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