journal article·2010-03-12

Gold hybrid nanoparticles for targeted phototherapy and cancer imaging

Dickson K Kirui, Diego A Rey, Carl A Batt

Nanotechnology· Volume 21· Issue 10
Publisher page

Abstract

Gold and iron oxide hybrid nanoparticles (HNPs) synthesized by the thermal decomposition technique are bio-functionalized with a single chain antibody, scFv, that binds to the A33 antigen present on colorectal cancer cells. The HNP-scFv conjugates are stable in aqueous solution with a magnetization value of 44 emu g(-1) and exhibit strong optical absorbance at 800 nm. Here we test this material in targeting, imaging and selective thermal killing of colorectal cancer cells. Cellular uptake studies showed that A33-expressing cells take up the A33scFv-conjugated HNPs at a rate five times higher than cells that do not express the A33 antigen. Laser irradiation studies showed that approximately 53% of the A33-expressing cells exposed to targeted HNPs are killed after a six-minute laser treatment at 5.1 W cm(-2) using a 808 nm continuous wave laser diode while < 5% of A33-nonexpressing cells are killed. At a higher intensity, 31.5 W cm(-2), the thermal destruction increases to 99 and 40% for A33-expressing cells and A33 nonexpressing cells, respectively, after 6 min exposure. Flow cytometric analyses of the laser-irradiated A33 antigen-expressing cells show apoptosis-related cell death to be the primary mode of cell death at 5.1 W cm(-2), with increasing necrosis-related cell death at higher laser power. These results suggest that this new class of bio-conjugated hybrid nanoparticles can potentially serve as an effective antigen-targeted photothermal therapeutic agent for cancer treatment as well as a probe for magnetic resonance-based imaging.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoparticle-Based Drug Delivery · Gold and Silver Nanoparticles Synthesis and Applications · Biosensors and Analytical Detection

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (40)

Show source-provided references
1. 10.1016/j.canlet.2008.09.02410.1016/j.canlet.2008.09.024 ↗
2. 10.1002/anie.20060247110.1002/anie.200602471 ↗
3. 10.1021/nl070345g10.1021/nl070345g ↗
4. Kuo W S · Chem. Commun. · 2008 · 443010.1039/b808871c ↗
5. 10.1073/pnas.050268010210.1073/pnas.0502680102 ↗
6. 10.1016/j.canlet.2004.02.00410.1016/j.canlet.2004.02.004 ↗
7. 10.1002/ange.20080001410.1002/ange.200800014 ↗
8. 10.1002/smll.20070080710.1002/smll.200700807 ↗
9. 10.1002/anie.20080181010.1002/anie.200801810 ↗
10. 10.1039/b711962c10.1039/b711962c ↗
11. 10.1039/b719096d10.1039/b719096d ↗
12. 10.1039/b501375e10.1039/b501375e ↗
13. 10.1021/bc015555d10.1021/bc015555d ↗
14. 10.1002/ijc.2167210.1002/ijc.21672 ↗
15. 10.1021/nl050256910.1021/nl0502569 ↗
16. 10.1158/0008-5472.CAN-08-323110.1158/0008-5472.CAN-08-3231 ↗
17. 10.1039/b708156a10.1039/b708156a ↗
18. 10.1148/radiol.229302121510.1148/radiol.2293021215 ↗
19. 10.1016/S1359-6446(03)02714-410.1016/S1359-6446(03)02714-4 ↗
20. 10.1038/sj.bjc.660075110.1038/sj.bjc.6600751 ↗
21. 10.1007/s00262-007-0433-x10.1007/s00262-007-0433-x ↗
22. Daghighian F · J. Nucl. Med. · 1996 · 37 · 1052
23. 10.1016/j.pep.2004.03.01910.1016/j.pep.2004.03.019 ↗
24. 10.1002/cphc.20070059810.1002/cphc.200700598 ↗
25. Lim Y T · Chem. Commun. · 2008 · 493010.1039/b810240f ↗
26. 10.1021/nl047955q10.1021/nl047955q ↗
27. 10.1021/nl060083310.1021/nl0600833 ↗
28. 10.1002/adma.20060056410.1002/adma.200600564 ↗
29. 10.1002/anie.20070439210.1002/anie.200704392 ↗
30. 10.1117/1.312237110.1117/1.3122371 ↗
31. 10.1021/ar800035u10.1021/ar800035u ↗
32. 10.1016/j.jconrel.2006.06.01710.1016/j.jconrel.2006.06.017 ↗
33. Larson T A · Nanotechnology · 2007 · 18 · 32510110.1088/0957-4484/18/32/325101 ↗
34. 10.1021/ja026501x10.1021/ja026501x ↗
35. 10.1021/ja042215510.1021/ja0422155 ↗
36. 10.1038/nm146710.1038/nm1467 ↗
37. 10.1126/science.107719410.1126/science.1077194 ↗
38. Welt S · Clin. Cancer Res. · 2003 · 9 · 1338
39. 10.1073/pnas.223247910010.1073/pnas.2232479100 ↗
40. 10.1364/OE.16.00159010.1364/OE.16.001590 ↗