Curcumin to Promote the Synthesis of Silver NPs and their Self-Assembly with a Thermoresponsive Polymer in Core-Shell Nanohybrids
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Curcumin to Promote the Synthesis
of Silver NPs and their SelfAssembly with a Thermoresponsive
Polymer in Core-Shell Nanohybrids
Albanelly Soto-Quintero, Nekane Guarrotxena*, Olga García & Isabel Quijada-Garrido
*
This work presents a simple one-pot protocol to achieve core-doped shell nanohybrids comprising
silver nanoparticles, curcumin and thermoresponsive polymeric shell taking advantage of the
reducing properties of phenolic curcumin substance and its ability to decorate metallic surfaces.
Silver nanoparticles were synthesized, via sodium citrate and silver nitrate addition into a boiling
aqueous solution of curcumin, monomers and surfactant. Curcumin and sodium citrate promoted silver
nucleation, acting as reducing and stabilizing agents. These curcumin-capped AgNPs enabled, after
adding the radical polymerization initiator, the assembling of the growing polymer chains around the
hydrophobic AgNP surface. The resultant core-doped shell nanohybrids exhibit plasmonic, luminescent
and volume thermoresponsive properties, with improved possibilities to be used as successful
therapeutic platforms. In fact, the possibility to nanoconfine the synergistic antioxidant, antiviral,
antibacterial features of silver and curcumin in one bioavailable hybrid paves the way to promising
applications in the biomedical field.
The exciting electronic, optical, catalytic and antimicrobial properties of metal NPs can be stymied by their
tendency to aggregate. To overcome this issue and provide metallic nanoparticles with additional features, the
hybridization with polymeric materials is a successful strategy. In this regard, polymer micro/nanogels exhibit
high colloidal stability, great versatility in their chemical and topological composition, drug loading and functionalization capabilities1 that make them unique vehicles and reservoirs for metal nanoparticles2,3. Additionally, the
permeability of the gel-system coating allows a controlled loading and release of bioactive molecules and drugs.
Furthermore, polymer microgels are frequently used as nanoreactors for the in situ synthesis of metallic NPs4,
and small particles decorating the microgel are successfully formed5. However, the control over the metallic NP
structure and distribution is rather difficult.
Core-shell hybrid nanogels usually face metal@polymer nanohybrid synthesis from a different point of view;
and the most reported protocols are based on the polymer self-assembling around a preformed metal NP. The
ligand exchange using polymers with functional groups able to attach the metal NP is a successful approach
to attain thin polymer shells6. However to achieve polymer coating with tunable thickness, polymerization in
heterogeneous media, as free radical precipitation polymerization (FRPP) is the most widely choice7,8. Since this
technique relies on the precipitation of water insoluble growing polymer chain, a previous surface preparation of
metal NP is required. Note that the organic polymer is not compatible with the anionic citrate ligand, commonly
used to synthesize metal NPs, in aqueous medium9,10. Therefore a variety of strategies can be found in the literature, mainly for gold7,8,11–15, whereas works focused on achieving silver@polymer core-shell nanogels are scarce;
despite the reliable properties of silver NPs in applications as ultrasensitive analysis of molecules through Surface
Enhanced Raman Spectroscopy (SERS)2,16, catalysis17, cancer cell imaging16,18 and other applications related to
their antimicrobial properties19.
Recently, we developed one-step protocol supporting core-shell hybrid nanogel synthesis, regardless of the
monomer polarity. The strategy was based on the use of hydrophobic thiolated methacrylate monomer as compatible bridge between the as-synthesized Au@citrate surface and the growing polymer chains14. The modification
Instituto de Ciencia y Tecnología de Polímeros. Consejo Superior de Investigaciones Científicas (ICTP-CSIC) c/Juan de
la Cierva, 3 E-28006, Madrid, Spain. *email: ;
Scientific Reports |
(2019) 9:18187 | https://doi.org/10.1038/s41598-019-54752-4
1
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Figure 1. Schematic representation of the one-pot two-step chemical route to synthesize Ag@cur-P(MEO2MA)
core-doped shell hybrid NPs. (A) Mixture at room temperature of curcumin, MEO2MA monomer, crosslinker
and surfactant. (B) First step of AgNO3 reduction and Ag@cur NPs formation. (C) Free radical precipitation
polymerization of MEO2MA and crosslinker encapsulating AgNPs forming Ag@cur-P(MEO2MA) NPs.
of the metal surface with the hydrophobic compound led to effective polymer self-assembling around the inorganic core.
Thus, we envisioned, in this work, that hydrophobic molecules as curcumin (Fig. 1A), having a two-fold function, as reducing agent in silver NP synthesis as well as diminishing the interfacial energy between the growing
polymer chain and the metallic surface, might trigger the core-shell hybrid NP assembly. Previous backgrounds
evidenced the curcumin ability to reduce Ag+ and Au3+ ions to silver20–22 and gold23 nanoparticles, without any
other additional reductant or in the presence of citrate and CTBA to modulate NP shape24. Thus, Kundu and
Nithiyanantham20, in a pioneer work, were able to synthesize different shapes of AgNP (spheres, nanowires and
anisotropic nanoflakes) by tuning the molar ratio of curcumin to AgNO3. Nevertheless, even though the reductant ability of curcumin has been already reported, it should be noted that, as far as we know, none has postulated that hydrophobic curcumin presence nearby metal surface may facilitate polymer self-assembling during
post-crosslinking polymerization. In addition, by considering the antioxidant properties of this natural phenolic
compound, our curcumin-promoted Ag@nanogel hybrid system will state a double benefit arising from the biomedical properties of curcumin itself, as antibacterial, self-healing25,26, antiviral27 and anti-inflammatory28; and
from the antibacterial19 synergistic effect and remarkable antiviral29 activity of particles comprising silver nanoparticles and curcumin in one hybrid. Moreover, encapsulation of curcumin in the hydrophobic polymer shell
will increase curcumin bioavailability protecting curcumin from hydrolytic degradation30, since this is the main
limitation for its therapeutic applications.
Experimental
Materials. The monomer 2-(2-methoxyethoxy)ethyl methacrylate (MEO2MA) (Aldrich 95%) was purified by
passing through a neutral alumina column. Tetraethylene glycol dimethacrylate (TEGDMA) (≥90%), trisodium
citrate dihydrate (≥98%) and silver nitrate (AgNO3) (99.99%) were purchased from Aldrich. Sodium dodecyl
sulfate (SDS) (≥97%) and ammonium persulfate (APS) (>98%), were purchased from Fluka. Curcumin (≥98%)
was obtained from Acros Organics. All chemical reagents were employed as received. The solvents used, ethanol
and water (...truncated)