Functionalization of Multiwalled Carbon Nanotubes

Functionalization of Multiwalled Carbon Nanotubes The functionalization of multiwalled carbon nanotubes with different drugs Duma (Voiculet), M. Prodana, I. Demetrescu Abstract—Functionalized multiwalled carbon nanotubes (MWCNTs) by various groups (carboxyl or amino) can improve the properties of anti-tumoral drugs (cisplatin, docetaxel, zometa). Functionalization was evidenced by infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). Platinum ions released in simulated body fluid (SBF) were measured by inductively coupled plasma ion spectrometry (ICP-MS). Keywords—functionalization, FTIR, drug, carbon nanotubes, TEM. 1. Introduction In our days currently available technologies have made significant advances in cancer research, but proper treatment remains elusive. According to the report issued by the World Global Health (WHO) it is estimates that the incidence of new cancer cases increase by more than 10 million each year and the rate of deaths caused by this disease is over 6 million per year [1]. The most common cancers causing death are listed as WHO: lung cancer, stomach, liver, colon and breast cancers. Carbon nanotubes (CNTs) possess properties for the development of advanced drug delivery systems, including their very large surface, which allows multi-conjugation of various molecules on the side walls. Molecules that contain aromatic groups may be easily covalently linked to strong interactions CNTs. 1-D functionalized CNTs (F-CNTs) could improve the binding of a single cell interaction via multiple binding sites, due to their flexibility. Clinical practice guidelines such as those from the American Society of Clinical Oncology (ASCO guidelines on extended use of intravenous bisphosphonates in metastatic breast cancer), the National Comprehensive Cancer Network (NCCN Breast Cancer Clinical Practice Guidelines), and the NCCN Task Force Report on Bone Health in Cancer Care all recognize the positive utility of bisphosphonate as zoledronic acid (Zometa) use in palliative bone care [2-5]. However, as new classes of inhibitor agents enter the metastatic cancer palliative it is important to understand how palliative care treatment modalities are used outside of the clinical trial setting. In this idea the present research is an investigation of a multiple hybrid functionalization of carb on nanotubues with drugs, introducing as a novelty functionalization with cisplatin, docetaxel and zometa [6]. 2. Experiment part The best known method of functionalization is noncovalently modified by embedding fragments containing functionalized aromatic groups in the outer wall of CNTs through interaction Ï€-Ï€ [7]. 2.1 Reagents Multiwalls carbon nanotubes (MWCNTs) purchased from Sigma Aldrich had more than 90% carbon and 10 to 15 nm x D x L 0.1 10 pm, produced by catalytic chemical vapor deposition (CCVD). Oxidation of the carbon nanotubes was made using a mixture of 98% sulfuric acid (Merck). Ethylenediamine (EDA)-modifying agent was supplied by Fluka. We used saline zometa, docetaxel (Dox) and cisplatin, from pharmaceutical market, and all reagents were not further purified. In the last years there are studies in literature regarding CNTs functionalization with different drugs [8-10]. 2.2 Equipment FTIR spectra of functionalized MWCNTs were registered on a Perkin Elmer, Spectrum 100 equipment in 400à ·4500 cm-1 range with 4 cm-1 resolution and 32 scans. Nano-sized particles were investigated using TEM analysis with a microscope Philips EM-410, 60kV. ICP-MS, ELAN DRC-e Perkin Elmer SCIEX U.S.A. was used for platinum determinations. The detection limit was 0.001ÃŽ ¼g.g-1. 2.3 Procedure Multiwalled carbon nanotubes were functionalized with both amino and carboxyl groups. This functionalization was performed with the purpose to reduce the toxicity of multi-walled carbon nanotubes. MWCNTs (0.9 g) were dispersed in 98% sulfuric acid and ultrasonicated at 50 °C for 6 h to obtain MWCNT-COOH. Functionalization of MWCNTs reduced toxicity of carbon nanotubes. 0.3 mg MWCNT-COOH were ultrasonically prepared with thionyl chloride SOCl2 (50 ml) for 30 minutes at room temperature. The suspension obtained was refluxed under magnetic stirring at room temperature for 48 hours and then filtered. The filtrate was washed with tetrahydrofuran (THF) and dried at room temperature for 20 minutes. MWCNTs-SOCl2 were immersed in ethylenediamine at room temperature for 10 hours. The mixture was washed with tetrahydrofuran and filtered. The filtrate was dried at 80 ° C for 10 hours. Throughout preparation process, docetaxel, cisplatin and zometa was added to carbon nanotubes. Docetaxel was difficult to absorb due to their hydrophobic characteristics. Docetaxel (5 mg) was added to a solution of MWCNT, MWCNT-COOH, MWCNT-NH2 in 1 ml of saline and 0.5 ml of anhydrous ethanol using an ultrasonic bath for 48 hours at 50  °C. The suspension was centrifuged at 10000 rpm for 15 minutes until the carbon nanotubes were fully precipitated. Cisplatin (2 mg) was added to solutions that contain MWCT, MWCNT-COOH and MWCNT-NH2 in 1 ml of saline and was sonicated for 48 hours at 50 °C and filtered. The remaining solids were rinsed with anhydrous ethanol and deionized water to remove the excess of docetaxel and zometa. All samples were investigated using infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and inductively coupled plasma mass spectrometry (ICP-MS). 3. Results and discussions FTIR spectroscopy is a very useful tool to show the presence of functional groups on the surface of MWCNT-COOH an MWCNT-NH2. The bands allocated to groups: -OH, -CH2 and amino in the four samples are almost identical. For MWCNT-COOH-CDDP-DOX-ZOMETA functionalized sample, for –CH groups bands appear in a range from: 3556.86 to 2921.60 cm-1, for CDDP the range is: 852.24 to 520.89 cm-1, for Dox the peaks for characteristic groups O=O is at 1082.30 and 1030.31 cm-1 and for zometa the range is betwwen 1461.51 to 1349.22 cm-1 as is shown in Figure 1a. In case of MWCNT-COOH-CDDP-ZOMETA functionalized sample, bands for –CH groups appears at 3555.69 cm-1, for CDDP the range is between 857.30 to 560.78 cm-1 and for zometa the specific bands are in a range between: 1463.81 to 1349.45 cm-1 as is shown in Figure 1b. For MWCNT-COOH-DOX-ZOMETA functionalized sample, bands for –CH groups appears in a range from: 3235.44 to 2922.98 cm-1, for Dox the range for characteristic groups O=O is 1072.19 to 1031.74 cm-1 and for zometa specific peaks appear in a range: 1453.93 to 1350.28 cm-1 as is shown in Figure 1c. For MWCNT-COOH-ZOMETA functionalized sample, bands for –CH groups appear in a range from: 3546.07 to 2922.38 cm-1, for ZOMETA the range is between: 1461.51 to 1352.80 cm-1 as is shown in Figure 1d. Fig.1. FTIR spectra for: a). MWCNT-COOH-CDDP-DOX-ZOMETA; b). MWCNT-COOH-CDDP-ZOMETA; c). MWCNT-COOH-DOX-ZOMETA; d). MWCNT-COOH-ZOMETA In case of MWCNT-NH2-CDDP-DOX-ZOMETA functionalized sample, bands for –CH functional grups are between: 3696.20 to 3544.20 cm-1, for amines group appear peaks between: 1735.03 to 1624.51 cm-1, for CDDP the peaks are between: 854.77 to 560.27 cm-1, for DOX the range is: 1077.24 to 1032.25 cm-1 and for zometa from 1448.87 to 1349.46 cm-1 as shown in Figure 2a. For MWCNT-NH2-CDDP-ZOMETA functionalized sample, bands for –CH groups are between: 3721.57 to 3012.65 cm-1, for amines groups the peaks are between: 1735.03 to 1623.54 cm-1, for CDDP from 859.83 to 580.56 cm-1 and for zometa the peaks appear between: 1483.93-1241.57 cm-1 as shown in Figure 2b. For MWCNT-NH2-ZOMETA functionalized sample, bands for –CH functional grups are between: 3544.43 to 3012.65 cm-1, for amines group peaks appear between: 1736.74 to 1640.05 cm-1 and for ZOMETA characteristic peaks appear between: 1466.57 to 1345.22 cm-1 as shown in Figure 2c. Fig. 2. FTIR spectra for: a). MWCNT-NH2-CDDP-DOX-ZOMETA; b). MWCNT-NH2-CDDP-ZOMETA; c). MWCNT-NH2-DOX-ZOMETA; d). MWCNT-NH2-ZOMETA Morphology of nanosized particles are investigated by transmission electron microscopic analysis (TEM). From this analysis shown in Fig. 3 it is evidenced the surfaces of MWCNTs functionalized with carboxyl CDDP, Dox and zometa. MWCNTs have a curved shape about 10-20 nm in diameter and a length of 0,1-10 microns. TEM images show CDDP and DOX grains of 10-20 nm in width while ZOMETA sample is spread radially from a common center at the intersection of MWCNTs. Encapsulation of drugs is well emphasized. In Fig. 4 morphology reveals multiwalled carbon nanotubes functionalized with amino group in which drugs were added (CDDP, DOX and ZOMETA). a). b). c). d). Fig. 3. TEM morphologies for: a). MWCNT-COOH-DOX-ZOMETA; b). MWCNT-COOH-CDDP-ZOMETA; c). MWCNT-COOH-CDDP-DOX-ZOMETA; d). MWCNT-COOH-ZOMETA a) b) c) d) Fig. 4. TEM morphologies for: a). MWCNT-NH2-CDDP-DOX-ZOMETA; b). MWCNT-NH2-CDDP-ZOMETA; c). MWCNT-NH2-DOX-ZOMETA; d). MWCNT-NH2-ZOMETA Samples were placed in SBF for different periods of times and the solutions were analyzed. The samples were added in a nebulizer for vaporization. Conditions were selected to maximize the ion signal while platinum solution was introduced in vapors generator. The steam generated was then transported to the ICP-MS to determine platinum ions. The largest amount of platinum ions was recorded for MWCNT-COOH-CDDP-DOX-ZOMETA as can be seen in fig.4 This value indicates that there are good possibilities for further analysis. Fig. 4.Platinium ion release from hybrid functionalized MWCNT with various drugs. 4. Conclusions We presented a study of docetaxel, cisplatin and zometa added to MWCNTs functionalized by carboxyl and amino groups. FTIR measurements have been used for structural characterization of drugs encapsulation in MWCNTs-COOH. This functionalization (encapsulation) is confirmed by TEM analysis that shows the morphology of the samples. CDDP release was measured by ICP-MS techniques and the amount of platinum ions was found higher in case of MWCNTs-COOH-CDDP-DOX-ZOMETA. Acknoledgments. PhD student A. Voiculet acknowledges the financial support from the European Social Fund through POSDRU//1.5/S/†¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦Ã¢â‚¬ ¦.. References [1] B.W Stewart and P.Kleihuers, World Cancer Report,WHO, 2003 [2] G. De Rosa,G. Misso, G.Salzano and Michele Caraglia† Bisphosphonates and Cancer?What Opportunities from Nanotechnology†, J Drug Delivery, 2013, dx.doi.org/10.1155/2013/637976 [3] U Ripamontia, , R M. Klara, L F. Rentona, C Ferretti â€Å"Synergistic induction of bone formation by hOP-1, hTGF- b 3 and inhibition by zoledronate in macroporous coral-derived hydroxyapatites†, Biomaterials, 31, 2010, pp. 6400 [4] G. Salzano, M. Marra, M. Porru, S. Zappavigna, A. Abbruzzese, M.I. La Rotonda, C. Leonetti, M. Caraglia, G. 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