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Original Research

Drug-loading capacity and nuclear targeting of multiwalled carbon nanotubes grafted with anionic amphiphilic copolymers

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Pages 4427-4440 | Published online: 19 Nov 2013

Figures & data

Figure 1 Transmission electron microscopy images of multiwalled (A) oxidized, (B) heparin, and (C) polyglycolic acid (PGA) carbon nanotubes at low magnification (mag), and (D) multiwalled PGA carbon nanotubes at high magnification. The arrows in (D) denote the formation of polymeric micelles on the multiwalled carbon nanotubes (MWCNTs).

Figure 1 Transmission electron microscopy images of multiwalled (A) oxidized, (B) heparin, and (C) polyglycolic acid (PGA) carbon nanotubes at low magnification (mag), and (D) multiwalled PGA carbon nanotubes at high magnification. The arrows in (D) denote the formation of polymeric micelles on the multiwalled carbon nanotubes (MWCNTs).

Figure 2 Scanning electron microscopy images of multiwalled (A) oxidized, (B) heparin, and (C) polyglycolic acid carbon nanotubes. The blue circles in (D) denote the formation of polymeric micelles on multiwalled carbon nanotubes (MWCNTs).

Abbreviations: NTUST, National Taiwan University of Science and Technology; SEI, second electron imaging; WD, working distance.

Figure 2 Scanning electron microscopy images of multiwalled (A) oxidized, (B) heparin, and (C) polyglycolic acid carbon nanotubes. The blue circles in (D) denote the formation of polymeric micelles on multiwalled carbon nanotubes (MWCNTs).Abbreviations: NTUST, National Taiwan University of Science and Technology; SEI, second electron imaging; WD, working distance.

Figure 3 Raman spectra of multiwalled (MW) oxidized (COOH), MW heparin (Hep), and MW polyglycolic acid (PGA) carbon nanotubes.

Figure 3 Raman spectra of multiwalled (MW) oxidized (COOH), MW heparin (Hep), and MW polyglycolic acid (PGA) carbon nanotubes.

Figure 4 Particle size and distribution of multiwalled (A) oxidized, (B) heparin, and (C) polyglycolic acid carbon nanotubes analyzed by dynamic light scattering.

Abbreviation: PDI, polydispersity index; Z-average, hydrodynamic diameter.

Figure 4 Particle size and distribution of multiwalled (A) oxidized, (B) heparin, and (C) polyglycolic acid carbon nanotubes analyzed by dynamic light scattering.Abbreviation: PDI, polydispersity index; Z-average, hydrodynamic diameter.

Figure 5 Plot of the fluorescence-intensity ratio of excimer/monomer as a function of multiwalled (MW) oxidized (COOH), MW heparin, and MW polyglycolic acid (PGA) carbon nanotube concentration.

Note: I452/I380; the ration of fluorescence intensity of pyrene at 452 nm to 380 nm.

Figure 5 Plot of the fluorescence-intensity ratio of excimer/monomer as a function of multiwalled (MW) oxidized (COOH), MW heparin, and MW polyglycolic acid (PGA) carbon nanotube concentration.Note: I452/I380; the ration of fluorescence intensity of pyrene at 452 nm to 380 nm.

Table 1 Doxorubicin (Dox)-loading capacity of multiwalled oxidized (COOH), multiwalled heparin, and multiwalled polyglycolic acid (PGA) carbon nanotubes with a fixed weight of 0.162 mg

Figure 6 Zeta potentials of multiwalled (MW) oxidized (COOH), MW heparin (Hep), MW polyglycolic acid (PGA), doxorubicin (Dox)-loaded MW COOH, Dox-loaded MW Hep, and Dox-loaded MW PGA carbon nanotubes.

Figure 6 Zeta potentials of multiwalled (MW) oxidized (COOH), MW heparin (Hep), MW polyglycolic acid (PGA), doxorubicin (Dox)-loaded MW COOH, Dox-loaded MW Hep, and Dox-loaded MW PGA carbon nanotubes.

Figure 7 Drug-loading mechanism for the multiwalled polyglycolic acid (PGA) carbon nanotube (CNT) system and doxorubicin.

Figure 7 Drug-loading mechanism for the multiwalled polyglycolic acid (PGA) carbon nanotube (CNT) system and doxorubicin.

Figure 8 Cytotoxicity of multiwalled (MW) oxidized (COOH), MW heparin (Hep), MW polyglycolic acid (PGA) carbon nanotubes after incubation with HeLa cells for 24 hours at 37°C.

Figure 8 Cytotoxicity of multiwalled (MW) oxidized (COOH), MW heparin (Hep), MW polyglycolic acid (PGA) carbon nanotubes after incubation with HeLa cells for 24 hours at 37°C.

Figure 9 Confocal microscopy images of (A) free doxorubicin (Dox) and (B) multiwalled (MW) polyglycolic acid (PGA)-Dox carbon nanotubes incubated with HeLa cells for 2 hours. Red fluorescence means Dox and green fluorescence means PGA.

Figure 9 Confocal microscopy images of (A) free doxorubicin (Dox) and (B) multiwalled (MW) polyglycolic acid (PGA)-Dox carbon nanotubes incubated with HeLa cells for 2 hours. Red fluorescence means Dox and green fluorescence means PGA.

Figure 10 The cytotoxicity of free doxorubicin (Dox) and Dox-loaded multiwalled (MW) polyglycolic acid (PGA) carbon nanotubes after incubation with HeLa cells for 24 hours at 37°C

Figure 10 The cytotoxicity of free doxorubicin (Dox) and Dox-loaded multiwalled (MW) polyglycolic acid (PGA) carbon nanotubes after incubation with HeLa cells for 24 hours at 37°C

Figure S1 FTIR analysis of (A) multiwalled (MW) oxidized (COOH), heparin (Hep), MW Hep and (B) MW Hep, polyglycolic acid (PGA), and MW PGA carbon nanotubes.

Abbreviations: FTIR, Fourier-transform infrared.

Figure S1 FTIR analysis of (A) multiwalled (MW) oxidized (COOH), heparin (Hep), MW Hep and (B) MW Hep, polyglycolic acid (PGA), and MW PGA carbon nanotubes.Abbreviations: FTIR, Fourier-transform infrared.

Figure S2 Fluorescence spectra of multiwalled (MW) oxidized (COOH) carbon nanotubes, FITC, and FITC-MW-PGA solution.

Abbreviations: FITC, fluorescein isothiocyanate; PGA, polyglycolic acid.

Figure S2 Fluorescence spectra of multiwalled (MW) oxidized (COOH) carbon nanotubes, FITC, and FITC-MW-PGA solution.Abbreviations: FITC, fluorescein isothiocyanate; PGA, polyglycolic acid.

Figure S3 Release rate of doxorubicin (Dox) from diblock copolymer polyglycolic acid-co-heparin conjugated to multiwalled carbon nanotubes at 10 mM phosphate buffer solution, pH 7.4, pH 4.5, and 3 mM dithiothreitol (DTT).

Figure S3 Release rate of doxorubicin (Dox) from diblock copolymer polyglycolic acid-co-heparin conjugated to multiwalled carbon nanotubes at 10 mM phosphate buffer solution, pH 7.4, pH 4.5, and 3 mM dithiothreitol (DTT).