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A New Carbon Nanotube-Based Breast Cancer Drug Delivery System: Preparation and In Vitro Analysis Using Paclitaxel

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Abstract

Paclitaxel (PTX) is one of the most important drugs for breast cancer; however, the drug effects are limited by its systematic toxicity and poor water solubility. Nanoparticles have been applied for delivery of cancer drugs to overcome their limitations. Toward this goal, a novel single-walled carbon nanotube (SWNT)-based drug delivery system was developed by conjugation of human serum albumin (HSA) nanoparticles for loading of antitumor agent PTX. The nanosized macromolecular SWNT-drug carrier (SWNT-HSA) was characterized by TEM, UV–Vis-NIR spectrometry, and TGA. The SWNT-based drug carrier displayed high intracellular delivery efficiency (cell uptake rate of 80 %) in breast cancer MCF-7 cells, as examined by fluorescence-labeled drug carriers, suggesting the needle-shaped SWNT-HSA drug carrier was able to transport drugs across cell membrane despite its macromolecular structure. The drug loading on SWNT-based drug carrier was through high binding affinity of PTX to HSA proteins. The PTX formulated with SWNT-HSA showed greater growth inhibition activity in MCF-7 breast cancer cells than PTX formulated with HSA nanoparticle only (cell viability of 63 vs 70 % in 48 h and 53 vs 62 % in 72 h). The increased drug efficacy could be driven by SWNT-mediated cell internalization. These data suggest that the developed SWNT-based antitumor agent is functional and effective. However, more studies for in vivo drug delivery efficacy and other properties are needed before this delivery system can be fully realized.

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References

  1. Lester, J. (2007). Breast cancer in 2007: Incidence, risk assessment, and risk reduction strategies. Clinical Journal of Oncology Nursing, 11(5), 619–622.

    Article  PubMed  Google Scholar 

  2. Rowinsky, E. K., et al. (1993). Clinical toxicities encountered with paclitaxel (Taxol). Seminars in Oncology, 20(4 Suppl 3), 1–15.

    CAS  PubMed  Google Scholar 

  3. Kavallaris, M., Verrills, N. M., & Hill, B. T. (2001). Anticancer therapy with novel tubulin-interacting drugs. Drug Resistance Updates, 4(6), 392–401.

    Article  CAS  PubMed  Google Scholar 

  4. Eniu, A., Palmieri, F. M., & Perez, E. A. (2005). Weekly administration of docetaxel and paclitaxel in metastatic or advanced breast cancer. The Oncologist, 10(9), 665–685.

    Article  CAS  PubMed  Google Scholar 

  5. Sun, M., et al. (2010). Treatment of metastatic renal cell carcinoma. Nature Reviews Urology, 7(6), 327–338.

    Article  CAS  PubMed  Google Scholar 

  6. Menard-Moyon, C., et al. (2010). Functionalized carbon nanotubes for probing and modulating molecular functions. Chemistry & Biology, 17(2), 107–115.

    Article  CAS  Google Scholar 

  7. Gardner, E. R., et al. (2008). Randomized crossover pharmacokinetic study of solvent-based paclitaxel and nab-paclitaxel. Clinical Cancer Research, 14(13), 4200–4205.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  8. Gradishar, W. J., et al. (2005). Phase III trial of nanoparticle albumin-bound paclitaxel compared with polyethylated castor oil-based paclitaxel in women with breast cancer. Journal of Clinical Oncology, 23(31), 7794–7803.

    Article  CAS  PubMed  Google Scholar 

  9. Davis, M. E., Chen, Z. G., & Shin, D. M. (2008). Nanoparticle therapeutics: an emerging treatment modality for cancer. Nature Reviews Drug Discovery, 7(9), 771–782.

    Article  CAS  PubMed  Google Scholar 

  10. Kostarelos, K., et al. (2007). Cellular uptake of functionalized carbon nanotubes is independent of functional group and cell type. Nature Nanotechnology, 2(2), 108–113.

    Article  CAS  PubMed  Google Scholar 

  11. Liu, Z., et al. (2007). In vivo biodistribution and highly efficient tumour targeting of carbon nanotubes in mice. Nature Nanotechnology, 2(1), 47–52.

    Article  CAS  PubMed  Google Scholar 

  12. Liu, Y., et al. (2005). Polyethylenimine-grafted multiwalled carbon nanotubes for secure noncovalent immobilization and efficient delivery of DNA. Angewandte Chemie (International ed. in English), 44(30), 4782–4785.

    Article  CAS  Google Scholar 

  13. Cheung, W., et al. (2010). DNA and carbon nanotubes as medicine. Advanced Drug Delivery Reviews, 62(6), 633–649.

    Article  CAS  PubMed  Google Scholar 

  14. Zhang, Z., et al. (2006). Delivery of telomerase reverse transcriptase small interfering RNA in complex with positively charged single-walled carbon nanotubes suppresses tumor growth. Clinical Cancer Research, 12(16), 4933–4939.

    Article  CAS  PubMed  Google Scholar 

  15. Varkouhi, A. K., et al. (2011). SiRNA delivery with functionalized carbon nanotubes. International Journal of Pharmaceutics, 416(2), 419–425.

    Article  CAS  PubMed  Google Scholar 

  16. Zhao, D., et al. (2011). Carbon nanotubes enhance CpG uptake and potentiate antiglioma immunity. Clinical Cancer Research, 17(4), 771–782.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  17. Prakash, S., et al. (2011). Polymeric nanohybrids and functionalized carbon nanotubes as drug delivery carriers for cancer therapy. Advanced Drug Delivery Reviews, 63(14–15), 1340–1351.

    Article  CAS  PubMed  Google Scholar 

  18. Hampel, S., et al. (2008). Carbon nanotubes filled with a chemotherapeutic agent: A nanocarrier mediates inhibition of tumor cell growth. Nanomedicine, 3(2), 175–182.

    Article  CAS  PubMed  Google Scholar 

  19. Liu, Z., et al. (2007). Supramolecular chemistry on water-soluble carbon nanotubes for drug loading and delivery. ACS Nano, 1(1), 50–56.

    Article  PubMed  Google Scholar 

  20. Bertucci, C., et al. (2006). Binding studies of taxanes to human serum albumin by bioaffinity chromatography and circular dichroism. Journal of Pharmaceutical and Biomedical Analysis, 42(1), 81–87.

    Article  CAS  PubMed  Google Scholar 

  21. Kratz, F. (2008). Albumin as a drug carrier: design of prodrugs, drug conjugates and nanoparticles. Journal of Controlled Release, 132(3), 171–183.

    Article  CAS  PubMed  Google Scholar 

  22. Liu, Z., et al. (2009). Preparation of carbon nanotube bioconjugates for biomedical applications. Nature Protocols, 4(9), 1372–1382.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  23. Lay, C. L., et al. (2010). Delivery of paclitaxel by physically loading onto poly(ethylene glycol) (PEG)-graft-carbon nanotubes for potent cancer therapeutics. Nanotechnology, 21(6), 065101.

    Article  PubMed  Google Scholar 

  24. Ojima, I. (2008). Guided molecular missiles for tumor-targeting chemotherapy—case studies using the second-generation taxoids as warheads. Accounts of Chemical Research, 41(1), 108–119.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This work is supported by research grant to Satya Prakash from Canadian Institutes of Health Research (CIHR) (MOP 93641). W. Shao acknowledges the Excellence Award from Biomedical Engineering Department, McGill University and the financial support from FRQS (Fonds de recherche du Québec—Santé) Doctoral award. L. Rodes acknowledges the financial support from FRQS (Fonds de recherche du Québec—Santé) Doctoral award. A. Paul acknowledges the Alexander Graham Bell Post Graduate Scholarship-Doctoral from Natural Sciences and Engineering Research Council of Canada (NSERC). The authors are grateful for the assistance provided for transmission electron microscopy imaging by Xue-Dong Liu, Department of Physics, McGill University.

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Correspondence to Satya Prakash.

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Shao, W., Paul, A., Rodes, L. et al. A New Carbon Nanotube-Based Breast Cancer Drug Delivery System: Preparation and In Vitro Analysis Using Paclitaxel. Cell Biochem Biophys 71, 1405–1414 (2015). https://doi.org/10.1007/s12013-014-0363-0

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