Plasma Synthesis of Carbon-Based Nanocarriers for Linker-Free Immobilization of Bioactive Cargo

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Plasma Synthesis of Carbon-Based Nanocarriers for Linker-Free Immobilization of Bioactive Cargo. / Santos, Miguel; Michael, Praveesuda L.; Filipe, Elysse C.; Chan, Alex H. P.; Hung, Juichien; Tan, Richard P.; Lee, Bob S. L.; Minh Huynh; Hawkins, Clare; Waterhouse, Anna; Bilek, Marcela M. M.; Wise, Steven G.

In: ACS Applied Nano Materials, Vol. 1, No. 2, 2018, p. 580-594.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Santos, M, Michael, PL, Filipe, EC, Chan, AHP, Hung, J, Tan, RP, Lee, BSL, Minh Huynh, Hawkins, C, Waterhouse, A, Bilek, MMM & Wise, SG 2018, 'Plasma Synthesis of Carbon-Based Nanocarriers for Linker-Free Immobilization of Bioactive Cargo', ACS Applied Nano Materials, vol. 1, no. 2, pp. 580-594. https://doi.org/10.1021/acsanm.7b00086

APA

Santos, M., Michael, P. L., Filipe, E. C., Chan, A. H. P., Hung, J., Tan, R. P., Lee, B. S. L., Minh Huynh, Hawkins, C., Waterhouse, A., Bilek, M. M. M., & Wise, S. G. (2018). Plasma Synthesis of Carbon-Based Nanocarriers for Linker-Free Immobilization of Bioactive Cargo. ACS Applied Nano Materials, 1(2), 580-594. https://doi.org/10.1021/acsanm.7b00086

Vancouver

Santos M, Michael PL, Filipe EC, Chan AHP, Hung J, Tan RP et al. Plasma Synthesis of Carbon-Based Nanocarriers for Linker-Free Immobilization of Bioactive Cargo. ACS Applied Nano Materials. 2018;1(2):580-594. https://doi.org/10.1021/acsanm.7b00086

Author

Santos, Miguel ; Michael, Praveesuda L. ; Filipe, Elysse C. ; Chan, Alex H. P. ; Hung, Juichien ; Tan, Richard P. ; Lee, Bob S. L. ; Minh Huynh ; Hawkins, Clare ; Waterhouse, Anna ; Bilek, Marcela M. M. ; Wise, Steven G. / Plasma Synthesis of Carbon-Based Nanocarriers for Linker-Free Immobilization of Bioactive Cargo. In: ACS Applied Nano Materials. 2018 ; Vol. 1, No. 2. pp. 580-594.

Bibtex

@article{f5bc678930a64520b0745937f5063ffd,
title = "Plasma Synthesis of Carbon-Based Nanocarriers for Linker-Free Immobilization of Bioactive Cargo",
abstract = "Multifunctional nanoparticles are increasingly employed to improve biological efficiency in medical imaging, diagnostics, and treatment applications. However, even the most well-established nanoparticle platforms rely on multiple-step wet-chemistry approaches for functionalization often with linkers, substantially increasing complexity and cost, while limiting efficacy. Plasma dust nanoparticles are ubiquitous in space, commonly observed in reactive plasmas, and long regarded as detrimental to many manufacturing processes. As the bulk of research to date has sought to eliminate plasma nanoparticles, their potential in theranostics has been overlooked. Here we show that carbon-activated plasma-polymerized nanoparticles (nanoP(3)) can be synthesized in dusty plasmas with tailored properties, in a process that is compatible with scale up to high throughput, low-cost commercial production. We demonstrate that nanoP(3) have a long active shelf life, containing a reservoir of long-lived radicals embedded during their synthesis that facilitate attachment of molecules upon contact with the nanoparticle surface. Following synthesis, nanoP(3) are transferred to the bench, where simple one-step incubation in aqueous solution, without the need for intermediate chemical linkers or purification steps, immobilizes multiple cargo that retain biological activity. Bare nanoP(3) readily enter multiple cell types and do not inhibit cell proliferation. Following functionalization with multiple fluorescently labeled cargo, nanoP(3) retain their ability to cross the cell membrane. This paper shows the unanticipated potential of carbonaceous plasma dust for theranostics, facilitating simultaneous imaging and cargo delivery on an easily customizable, functionalizable, cost-effective, and scalable nanoparticle platform.",
keywords = "dusty plasmas, plasma polymerization, carbon, functionalization, multifunctional nanoparticles, nanotechnology, theranostics",
author = "Miguel Santos and Michael, {Praveesuda L.} and Filipe, {Elysse C.} and Chan, {Alex H. P.} and Juichien Hung and Tan, {Richard P.} and Lee, {Bob S. L.} and {Minh Huynh} and Clare Hawkins and Anna Waterhouse and Bilek, {Marcela M. M.} and Wise, {Steven G.}",
year = "2018",
doi = "10.1021/acsanm.7b00086",
language = "English",
volume = "1",
pages = "580--594",
journal = "ACS Applied Nano Materials",
issn = "2574-0970",
publisher = "American Chemical Society",
number = "2",

}

RIS

TY - JOUR

T1 - Plasma Synthesis of Carbon-Based Nanocarriers for Linker-Free Immobilization of Bioactive Cargo

AU - Santos, Miguel

AU - Michael, Praveesuda L.

AU - Filipe, Elysse C.

AU - Chan, Alex H. P.

AU - Hung, Juichien

AU - Tan, Richard P.

AU - Lee, Bob S. L.

AU - Minh Huynh, null

AU - Hawkins, Clare

AU - Waterhouse, Anna

AU - Bilek, Marcela M. M.

AU - Wise, Steven G.

PY - 2018

Y1 - 2018

N2 - Multifunctional nanoparticles are increasingly employed to improve biological efficiency in medical imaging, diagnostics, and treatment applications. However, even the most well-established nanoparticle platforms rely on multiple-step wet-chemistry approaches for functionalization often with linkers, substantially increasing complexity and cost, while limiting efficacy. Plasma dust nanoparticles are ubiquitous in space, commonly observed in reactive plasmas, and long regarded as detrimental to many manufacturing processes. As the bulk of research to date has sought to eliminate plasma nanoparticles, their potential in theranostics has been overlooked. Here we show that carbon-activated plasma-polymerized nanoparticles (nanoP(3)) can be synthesized in dusty plasmas with tailored properties, in a process that is compatible with scale up to high throughput, low-cost commercial production. We demonstrate that nanoP(3) have a long active shelf life, containing a reservoir of long-lived radicals embedded during their synthesis that facilitate attachment of molecules upon contact with the nanoparticle surface. Following synthesis, nanoP(3) are transferred to the bench, where simple one-step incubation in aqueous solution, without the need for intermediate chemical linkers or purification steps, immobilizes multiple cargo that retain biological activity. Bare nanoP(3) readily enter multiple cell types and do not inhibit cell proliferation. Following functionalization with multiple fluorescently labeled cargo, nanoP(3) retain their ability to cross the cell membrane. This paper shows the unanticipated potential of carbonaceous plasma dust for theranostics, facilitating simultaneous imaging and cargo delivery on an easily customizable, functionalizable, cost-effective, and scalable nanoparticle platform.

AB - Multifunctional nanoparticles are increasingly employed to improve biological efficiency in medical imaging, diagnostics, and treatment applications. However, even the most well-established nanoparticle platforms rely on multiple-step wet-chemistry approaches for functionalization often with linkers, substantially increasing complexity and cost, while limiting efficacy. Plasma dust nanoparticles are ubiquitous in space, commonly observed in reactive plasmas, and long regarded as detrimental to many manufacturing processes. As the bulk of research to date has sought to eliminate plasma nanoparticles, their potential in theranostics has been overlooked. Here we show that carbon-activated plasma-polymerized nanoparticles (nanoP(3)) can be synthesized in dusty plasmas with tailored properties, in a process that is compatible with scale up to high throughput, low-cost commercial production. We demonstrate that nanoP(3) have a long active shelf life, containing a reservoir of long-lived radicals embedded during their synthesis that facilitate attachment of molecules upon contact with the nanoparticle surface. Following synthesis, nanoP(3) are transferred to the bench, where simple one-step incubation in aqueous solution, without the need for intermediate chemical linkers or purification steps, immobilizes multiple cargo that retain biological activity. Bare nanoP(3) readily enter multiple cell types and do not inhibit cell proliferation. Following functionalization with multiple fluorescently labeled cargo, nanoP(3) retain their ability to cross the cell membrane. This paper shows the unanticipated potential of carbonaceous plasma dust for theranostics, facilitating simultaneous imaging and cargo delivery on an easily customizable, functionalizable, cost-effective, and scalable nanoparticle platform.

KW - dusty plasmas

KW - plasma polymerization

KW - carbon

KW - functionalization

KW - multifunctional nanoparticles

KW - nanotechnology

KW - theranostics

U2 - 10.1021/acsanm.7b00086

DO - 10.1021/acsanm.7b00086

M3 - Journal article

VL - 1

SP - 580

EP - 594

JO - ACS Applied Nano Materials

JF - ACS Applied Nano Materials

SN - 2574-0970

IS - 2

ER -

ID: 216164119