Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-27T22:46:01.722Z Has data issue: false hasContentIssue false
  • English
  • Français

Plasmonic Response of Light-Activated, Nano-Gold Doped Polymers

Published online by Cambridge University Press:  24 June 2019

Jessica M. Andriolo Open the ORCID record for Jessica M. Andriolo [Opens in a new window] ,
McKenzie L. Joseph ,
Molly C. Brockway  and
Jack L. Skinner
Jessica M. Andriolo*
Affiliation:
Mechanical Engineering, Montana Technological University, Butte, MT59701 Montana Tech Nanotechnology Laboratory, Butte, MT59701
McKenzie L. Joseph
Affiliation:
Mechanical Engineering, Montana Technological University, Butte, MT59701 Montana Tech Nanotechnology Laboratory, Butte, MT59701
Molly C. Brockway
Affiliation:
Montana Tech Nanotechnology Laboratory, Butte, MT59701 Materials Science Ph.D. Program, Montana Technological University, Butte, MT59701
Jack L. Skinner
Affiliation:
Mechanical Engineering, Montana Technological University, Butte, MT59701 Montana Tech Nanotechnology Laboratory, Butte, MT59701 Materials Science Ph.D. Program, Montana Technological University, Butte, MT59701
*
*(Email: Jessicamarie1304@yahoo.com)
Get access

Abstract

Incorporation of metallic nanoparticles (NPs) in polymer matrix has been used to enhance and control dissolution and release of drugs, for targeted drug delivery, as antimicrobial agents, localized heat sources, and for unique optoelectronic applications. Gold NPs in particular exhibit a plasmonic response that has been utilized for photothermal energy conversion. Because plasmonic nanoparticles typically exhibit a plasmon resonance frequency similar to the visible light spectrum, they present as good candidates for direct photothermal conversion with enhanced solar thermal efficiency in these wavelengths. In our work, we have incorporated ∼3-nm-diameter colloidal gold (Auc) NPs into electrospun polyethylene glycol (PEG) fibers to utilize the nanoparticle plasmonic response for localized heating and melting of the polymer to release medical treatment. Auc and Auc in PEG (PEG+Auc) both exhibited a minimum reflectivity at 522 nm or approximately green wavelengths of light under ultraviolet-visible (UV-Vis) spectroscopy. PEG+Auc ES fibers revealed a blue shift in minimum reflectivity at 504 nm. UV-Vis spectra were used to calculate the theoretical efficiency enhancement of PEG+Auc versus PEG alone, finding an approximate increase of 10 % under broad spectrum white light interrogation, and ∼14 % when illuminated with green light. Auc enhanced polymers were ES directly onto resistance temperature detectors and interrogated with green laser light so that temperature change could be recorded. Results showed a maximum increase of 8.9 °C. To further understand how gold nanomaterials effect the complex optical properties of our materials, spectroscopic ellipsometry was used. Using spectroscopic ellipsometry and modeling with CompleteEASE® software, the complex optical constants of our materials were determined. The complex optical constant n (index of refraction) provided us with optical density properties related to light wavelength divided by velocity, and k (extinction coefficient) was used to show the absorptive properties of the materials.

Keywords

plasmonicnanoscalepolymeropticalbiomedical
Type
Articles
Information
MRS Advances , Volume 4 , Issue 31-32: Electronics and Photonics , 2019 , pp. 1749 - 1758
Copyright
Copyright © Materials Research Society 2019 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References:

Ulbrich, K., Holá, K., Šubr, V., Badandritsos, A., Tuček, J., and Zbořil, R., Chem. Rev. 116, 5228-5431 (2016).CrossRefGoogle Scholar
Perni, S., Piccirillo, C., Pratten, J., Prokopovich, P., Chrzanowski, W., Parkin, I. P., and Wilson, M., Biomaterials 30, 89-93 (2009).CrossRefGoogle Scholar
Maity, D., Bain, AmK., Bhowmick, B., Sarker, J., Saha, S., Acharya, K., Chakraborty, M., and Chattopadhyay, D., J. Appl. Polym. Sci. 122 (4), (2011).CrossRefGoogle Scholar
Govorov, A.O. and Richardson, H.H., Nano Today 2, 30-38 (2007).CrossRefGoogle Scholar
Maity, S., Downen, L. N., Bochinski, J. R., and Clarke, L. I., Polymer 52, 1674-1685 (2011).CrossRefGoogle Scholar
Lee, J., Govorov, A.O., and Kotov, N.A., Laser Surg. Med. 37 (2), 123-129 (2005).Google Scholar
Li, S., Lin, M.M., Toprak, M.S., Kim, D.K., and Muhammed, M., Nano Rev. 1, (2010).CrossRefGoogle Scholar
Jiang, K., Smith, D.A., and Pinchuk, A., J. Phys. Chem. 117 (51), 27073-27080 (2013).Google Scholar
Bi, C., Chen, J., Chen, Y., Song, Y., Li, A., Li, S., Mao, Z., Gao, C., Wang, D., Möhwald, H., and Xia, H., Chem. Mater. 30 (8), 2709-2718 (2018).CrossRefGoogle Scholar
Huang, X., El-Sayed, I.H., Quian, W., and El-Sayed, M.A., J. Am. Chem. Soc. 128 (6), 2115-2120 (2006).CrossRefGoogle Scholar
Amendolal, V., Pilot, R., Frasconil, M., Maragò, O. M., and Iatì, M. A., J. Phys.-Condens. Mat 29 (20), (2017).Google Scholar
Skirtach, A.G., Dejugnat, C., Baaun, D., Susha, A.S., Rogach, A.L., Parak, W.J., Mɸhwald, H., and Sukhorukov, G.B., Nano Lett. 5 (7), (2005).CrossRefGoogle Scholar
Rubinstein, M. and Colby, R. H., Polymer Physics, edited by Oxford University Press (Oxford, New York, 2003), p. 5.Google Scholar