Exploiting the Protein Corona around Gold Nanorods for Loading and Triggered Release
Abstract
We form coronas of serum proteins on gold nanorods (NRs) coated with cetyltrimethylammonium bromide (CTAB). These coronas can be exploited for their ability to hold small molecular therapeutics at a capacity much higher (~5-10×) than what covalent conjugation strategies can achieve. Coronas are loaded with DNA oligonucleotides and Doxorubicin, showing that they can hold species of either negative or positive charge. Payload capacity varies with assembly strategy, ionic strength, and loading concentration. Payload release can be achieved by increasing the temperature or by ultrafast laser excitation of the NRs at their longitudinal surface plasmon resonance. DNA leakage from the corona is minimal within the first 3 days of preparation, although Dox leakage was more significant. The coronas also stabilize the NRs in buffer and biological media. This study demonstrates the biological utility of the protein corona around nanomaterials, contrasting the common view of the corona as an undesirable biological response.
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These strategies are still limited at conferring targeting specificity because an additional targeting ligand increases the propensity for protein corona formation to mask targeting ability and inhibit the biological effects of nanoparticles.
“these strategies are still limited at conferring targeting specificity since an additional targeting ligand increases the propensity for protein corona formation to mask the targeting ability and inhibit the biological effects of nanoparticles18–24.”
From Cloaking nanoparticles with protein corona shield for targeted drug delivery. (2018) · cites this paper as [24]
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Cloaking nanoparticles with protein corona shield for targeted drug delivery.
Oh, J. Y., Kim, H. S., Palanikumar, L., Go, E. M., Jana, B., Park, S. A., Kim, H. Y., Kim, K., Seo, J. K., Kwak, S. K., et al. (2018) · Nature communications · doi:10.1038/s41467-018-06979-4 · Cited by 409 · see citing works
How Can We Exploit The Protein Corona?
Hamad-Schifferli, K. (2013) · Nanomedicine · doi:10.2217/nnm.12.179 · Cited by 57 · see citing works
Self-citation
- Authors
- Kah, J. C. Y., Chen, J., Zubieta, A., & Hamad-Schifferli, K.
- Affiliations
- Massachusetts Institute of Technology (US)
- The University of Texas at Austin (US)
- Corresponding author
- Kah, James Chen Yong
- Venue
- ACS Nano
- Publisher
- American Chemical Society (ACS)
- Published
- 2012-07-26
- Volume
- 6
- Issue
- 8
- Pages
- 6730-6740
- ISSN
- 1936-0851 (ISSN-L)
- 1936-086X
- OpenAlex
- W2334316877
- Cited by
- 178
- References
- 0
- Citations by year
- 2025: 6 · 2024: 1 · 2023: 9 · 2022: 8 · 2021: 18 · 2020: 17 · 2019: 13 · 2018: 18 · 2017: 16 · 2016: 18 · 2015: 23 · 2014: 15 · 2013: 13 · 2012: 3
- FWCI
- 6.67
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- ACS Nano (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Materials Science › Electronic, Optical and Magnetic Materials › Gold and Silver Nanoparticles Synthesis and Applications
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- protein corona, gold nanorods, serum proteins, drug loading, triggered release, DNA oligonucleotides, doxorubicin, surface plasmon resonance, heat release, nanoparticle stability, ionic strength effects, nanoparticle assembly
- MeSH terms
- Cetrimonium, Blood Proteins, Cetrimonium Compounds, Crystallization, Delayed-Action Preparations, Diffusion, DNA, Gold, Materials Testing, Molecular Conformation, Particle Size, Surface Properties, Transfection, Nanocapsules
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