R.
Mrówczyński
abc,
L.
Magerusan
a,
R.
Turcu
a and
J.
Liebscher
*ab
aNational Institute of Research and Development for Isotopic and Molecular Technologies (INCDTIM), Str. Donath 65-103, RO-400293 Cluj-Napoca, Romania. E-mail: liebscher@chemie.hu-berlin.de
bDepartment of Chemistry, Humboldt-University Berlin, Brook-Taylor-Str. 2, 12489 Berlin, Germany
cNanoBioMedical Centre, Adam Mickiewicz University, Umultowska 85, 61-614 Poznan, Poland
First published on 30th July 2014
The possibility of introducing azido functions onto polydopamine by diazo transfer making use of existing aminoethyl moieties was verified at polydopamine-coated magnetite nanoparticles. The resulting azido-functionalized Fe3O4@polydopamine nanoparticles serve as a magnetic nano-platform for the introduction of interesting applicatory functions by click-chemistry (CuAAC) as exemplified by linking biotin, tetraacetylglucose, dansyl and proline.
Azido groups have gained increasing interest because they can undergo copper-catalyzed azide alkyne cycloaddition (CuAAC). This reaction tolerates most functional groups and the resulting 1,2,3-triazoles are robust linkers. Thus, azido groups are powerful tools also for chemoselective20 and orthogonal functionalization of MNP.21–23
One of the methods for introducing the azido moiety onto MNP is the diazo transfer reaction to amino groups.24 This reaction was applied for membrane modification.25 It was also utilized in the preparation of trifunctional magnetic nanoparticles, one of the key synthetic steps for linking a myriad of (bio)macromolecules.20
Lately, polydopamine (PDA) has been introduced as versatile polymer coating.26,27 This nature-inspired polymer was developed by Messersmith in 2007.28 It has been shown that PDA could cover various materials like noble metals (Au, Ag, Pt, Pd), SiO2, Al2O3 and polymers (polystyrene, polyethylene, polycarbonate, polyethylene terephthalate, polytetrafluoroethylene) in basic solution resulting in strongly adherent layers. A variety of nanoparticles, including magnetic nanoparticles, have been coated with PDA. Polydopamine-coatings are considered to be non-poisonous and biocompatible and have found various biomedical applications29–35, such as in drug transport and delivery, as antibacterial coatings, in separations of biological materials or poisonous contaminants36,37 and as supports for metal29 and organocatalytic moieties.38 PDA coatings also served as media for fixing various biomolecules or enzymes.39,40 Here, the occurrence of carbonyl and Michael-acceptor moieties is exploited enabling reaction with amines or thiols as nucleophiles. In order to extend the scope of functionalization of PDA other reactive groups have to be introduced. Recently, we presented the introduction of azido groups into PDA by reaction with 4-azidobutylamine enabling CuAAC for further functionalization.38 Taking into account a recent report that PDA contains aminoethyl groups41 it appeared challenging to exploit the hitherto ignored amine reactivity rather than the carbonyl or Michel-acceptor reactivity.
Here, we disclose diazo transfer reaction performed directly at PDA coated MNP. As a result, a new magnetic azido nanoplatform with robust PDA coating is obtained. The chemical reactivity of the appearing azido functionalities was verified by subsequent CuAAC reactions with different important biological units like biotin (a recognition function), galactose (interest in cancer therapy), dansyl (fluorescent marker) and proline (organocatalyst).
FT-IR spectra were measured on a JASCO FTIR 610 spectrophotometer. The magnetic measurements were performed at room temperature using a Vibrating Sample Magnetometer, Cryogenics.
The chemical surface analysis for the functionalized magnetic nanoparticles was performed by X-ray Photoelectron Spectroscopy (XPS) using a XPS spectrometer SPECS equipped with a dual-anode X-ray source Al/Mg, a PHOIBOS 150 2D CCD hemispherical energy analyzer and a multi-channeltron detector with vacuum maintained at 1 × 10−9 torr. The AlKKα X-ray source (1486.6 eV) operated at 200 W was used for XPS investigations. The XPS survey spectra were recorded at 30 eV pass energy, 0.5 eV per step. The high resolution spectra for individual elements were recorded by accumulating 10–15 scans at 30 eV pass energy and 0.1 eV per step. The samples were applied as colloidal suspensions in methanol and dried in successive layers on an indium foil stacked on a Wolfram sample holder. The surface cleaning was performed by argon ion bombardment at 300 V for 3 minutes. Data analysis and curve fitting were performed using Casa XPS software with a Gaussian–Lorentzian product function and a non-linear Shirley background subtraction. Dynamic light scattering (DLS) measurements were carried out with a Brookhaven Instrument Corp. goniometer and a light scattering system. Acquisition time was set at 90 seconds, a laser radiation wavelength of 632.8 nm was used and the angle for data acquisition was 90°.
Magnetic nanoparticles covered with a chemisorbed oleic acid monolayer were obtained from the group of Prof. Dr Ladislau Vekas, Romanian Academy – Timisoara branch.
According to DLS-measurements the hydrodynamic diameter amounts to 340.7 nm in methanol (Fig. 6). As can be seen by the lack of a hysteresis loop in the magnetic measurement (Fig. 5) MNP 2 are superparamagnetic with a high value of saturation magnetisation Ms = 52 emu g−1.
With these novel magnetic nanoplatforms 2 in hand we checked their versatility to attach bio-entities via CuAAC reaction in some selected examples. CuAAC was performed with propargyl derivatives of biotin 3a, tetraacetylgalactose 3b, dansyl 3c and proline 3d (Scheme 1) in MeOH using CuSO4–Na-ascorbate as the catalytic system. FTIR spectra of the resulting MNP 4 revealed a decrease of the intensity of the azide peak as compared with the precursors 2 confirming a successful transformation of azido moieties into triazoles as a result of the CuAAC. Obviously, some of the azido groups of MNP 2 were not accessible by the CuAAC explaining the fact that the azido IR-band did not fully disappear. A similar effect was observed in CuAAC reactions of PDA-coated MNP.38 Anyway, the remaining azido groups in MNP 4 do not create problems because they are hardly accessible and chemically inert in most other applications. In the galactose–tetraacetate containing MNP 4b a CO stretching vibration at 1757 cm−1 and a C–O–C valence band at 1236 cm−1 was observed in the FTIR spectrum, while MNP 4c exhibit an IR-band at 1370 cm−1 due to the stretching vibration of the sulfonamide group found in dansyl.
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Scheme 1 Diazo transfer at PDA-coated magnetite NP 1 and CuAAC at the resulting azido-functionalized MNP 2 for the introduction of bio-entities and dansyl. |
TGA of the MNP 2 and 4b revealed an increase in organic material after the CuAAC which is in agreement with the increase in molecular weight of 4b (see ESI†).
The successful introduction of bio-entities was further proved by XPS measurements. Thus the deconvoluted S 2p spectrum of 4a (Fig. 3) proved the presence of sulphur. It contains a doublet S 2p3/2 –162.9 eV and S 2p1/2 164.5 eV in the ratio 2:
1 corresponding to the C–S–C moiety of biotin. In addition, another doublet S 2p3/2 –167.8 eV, S 2p1/2 169.4 eV is found, which can be explained by a –C–SO2–C– moiety obviously derived from oxidized biotin. It is well known that the oxidation of the biotin moiety occurs easily with different oxidizing reagents such as peroxides under mild conditions and is also observed in biological metabolism of biotin.43
The C 1s spectrum can be deconvoluted into three peaks corresponding to carbon atoms from different groups. The higher binding energy component centered at 289.2 eV corresponds to carbon atoms from the O–CNH/C
O groups, the intense component peak located at 286.5 eV is ascribed to carbon atoms from the C–S/C–N/C–O groups, while the component at 285.3 eV corresponds to C–C/CHn groups.
The O 1s spectrum exhibits three components assigned to the oxygen atoms of the CO/O
C–NH group (534.4 eV), C–O groups (531.7 eV) and to metal oxides, magnetite and oxidized indium support, respectively Fe–O/In–O (529.9 eV). The N 1s core-level spectrum shows three components in agreement with the functionalization with biotin and the presence of unmodified azido groups: (i) the component at 399.9 eV corresponds to –NH; (ii) the component located at 401.1 eV is ascribed to the negatively charged terminal nitrogen atom of the azido group (–N
N+
N−); (iii) the high binding energy component located at 402.1 eV corresponds to a positively charged central nitrogen atom of the azido group (–N
N+
N−).
The SO2N moiety of the dansyl functionalized MNP 4c is confirmed by the presence of two components at 2p3/2 (168.4 eV) and 2p1/2 (169.3 eV) in a ratio of 2:
1 in the S 2p core-level XPS spectrum (Fig. 4). Again, residual azido groups are found at 399.5 eV and 401.4 eV. The best approximations of the C 1s and O 1s spectra were obtained with three components described by a Gaussian–Lorentzian product function, with full-width at half maximum (FWHM) smaller than 3.1 eV. C 1s consists of the following peaks: C–C/CHn at 284.3 eV, an intense component corresponding to C–O/C–N/C–S at 285.2 eV and the component located in the high binding energy region of the spectra, at 288.1 eV, corresponding to the carbon atoms of C
O groups. O 1s was deconvoluted in FeO/In–O (529.6 eV), C–O (531.5 eV) and O
C/S
O (532.9 eV). The spin–orbit coupling gives rise to a doublet of lines in the Fe 2p high resolution spectrum: Fe 2p3/2 (710.4 eV) and Fe 2p1/2 (723.7 eV).
The PDA-coated NP maintained their superparamagnetic properties during the transformation from 2 to 4 as can be seen by the magnetic measurements (Fig. 5). The slight decrease in the saturation magnetization values is attributed to the increase in weight as a result of the CuAAC. But they are still high (4a: 45 emu g−1, 4b: 39 emu g−1, 4c: 45 emu g−1, 4d: 49 emu g−1) making the MNP 4 attractive for applications in biology or medicine where localization is necessary under the influence of an external magnetic field.
The functionalized MNP 4 form colloidal suspensions in water where they showed narrow size distributions (Fig. 6). Interestingly, their hydrodynamic diameters (4a: Dh = 194.6 nm, 4b: Dh = 114.1 nm, 4c: Dh = 186.2 nm, 4d: Dh = 219.5 nm) were smaller than that of their precursor 2 (Dh = 340.7 nm). The phenomenon might be caused by partial reduction of the polydopamine under the reaction conditions (formation of H-bond forming phenolic OH groups from o-quinone units) of the CuAAC (Na-ascorbate as the reducing reagent).
Footnote |
† Electronic supplementary information (ESI) available: TGA of MNP 2 and 4b. See DOI: 10.1039/c4py00670d |
This journal is © The Royal Society of Chemistry 2014 |