Boron Nitride Nanotubes for Biomedical Applications: Challenges Ahead

Editorial

Austin J Nanomed Nanotechnol. 2015; 3(1): 1040.

Boron Nitride Nanotubes for Biomedical Applications: Challenges Ahead

Soodeh Baghaee-Ravari, Mahdi Ghazizadeh and Ajit D Kelkar*

Joint School of Nanoscience and Nanoengineering, North Carolina A&T State University, USA

*Corresponding author: Ajit D Kelkar, Department of Nanoengineering, Joint School of Nanoscience and Nanoengineering, North Carolina, USA

Venkat Reddy B.Ch, Department of Biotechnology, Sri Indu Engineering College, Jawaharlal Nehru Technological University, Hyderabad, India

Received: July 01, 2015; Accepted: September 01, 2015; Published: September 10, 2015

Editorial

Introduction of nanomaterials in different areas of biology has resulted into addressing several challenging problems. While the use of nanomaterials has improved the efficiency and effectiveness of traditional drug delivery approaches, their introduction also has led into discovery of the fast and accurate imaging processes. The high surface ratio of these materials increases the interaction with their surrounding environment and improves their effectiveness in such applications. Carbon Nano Tubes (CNTs) are one of the most used nanomaterials in different bio applications including but not limited to drug delivery and transportation devices, cancer and gene therapy, tissue engineering, bio sensing and detection [1-5]. The unique combination of strength and high surface area alongside their thermal, chemical and optical properties has made CNTs to be investigated extensively for different bio applications [6].

After introduction of CNTs in 1991 by Iijima using arc discharge between two graphite electrodes [7], the search for new nanotubes has increased in order to find materials that one or more aspect of their characteristics can be enhanced for specific applications. One of such effort led to prediction of Boron Nitride Nanotubes (BNNTs) by rolling up a hexagonal BN nanosheet in 1994 [8] followed by its synthesis in 1995 using are-discharge process [9]. While both nanotubes possess comparable properties due to the similarity in their chemical structure (in BNNT, boron and nitrogen atoms substituting alternating carbon atoms in CNT), there are some differences caused by the nature of chemical bonds forming the structure of the two nanotubes (ionic bond between B and N in BNNT and covalent bond between C atoms in CNT) which makes each to be a better choice for specific application [10]. Unlike CNTs which can be semi-conductor or metallic depending on chirality and geometry of the tube, BNNTs are insulator. In terms of mechanical properties, BNNTs possess slightly lower Young`s modulus while they offer better structural flexibility and resilience under cyclic loads. BNNTs possess better chemical and thermals stability, better oxidation resistance and more importantly, better solubility. BNNTs are not only proved to be non-toxic, it is shown that the addition of these nanotubes into the Polylactide–Polycaprolactone Copolymer (PLC) as a scaffold for orthopedic applications improves both mechanical properties and cell viabilities as compared with bare PLC [11]. Due to above- mentioned properties, BNNTs can be used in many applications in biomedical fields including the one that CNTs already proven to be effective [12-14].

The unique properties of BNNTs have made them a promising material for revolutionizing different industries; however, there are few challenges that need to be addressed before any interesting results in research laboratories can be translated into commercial products for curing different diseases in human.

One of the toughest challenges ahead is finding a manufacturing method which is able to produce high quality (in terms of purity and homogeneity) BNNTs in large scale with affordable price. Currently, different techniques are being used to produce BNNTs with acceptable quality but the low production rate, high manufacturing cost, impurities and inconsistency in the product have made it difficult to rely on these methods especially for biomedical applications. Different fabrication methods have been studied by researchers for production of BNNTs including but not limited to chemical vapor deposition [15], laser ablation [16], are discharge [17], ball milling [18] and copyrolysis [13]. The majority of these procedures are based on incorporating a Boron precursor and heating at elevated temperature in presence of a certain gas as Nitrogen source. While the type of precursor and the required temperature can be altered by introducing a catalyst gas but there is still no reliable manufacturing method which is capable of producing large quantity, high quality BNNTs consistently.

Another important challenge for using BNNTs in biomedical application is their solubility in aqueousmedia. The solubility in water, homogeneity (size distribution of nanotubes) and stability of solution are some important factors which need to be considered for a given application [13]. While the solubility of nanotubes is very decisive step during their preparation for most biomedical application, making sure that they maintain their initial state in terms of solubility and even distribution is as important. The interaction between nanotubes due to vanderwal forces leads to agglomeration of tubes which in terms result in decrease in cellular up-take of BNNTs. Therefore it is absolutely essential to produce BNNTs with high solubility and stability for duration of its mission whether its drug delivery or sensing. In order to achieve this goal some avenues can be explored including use of surface modifiers through non-covalent bonding, polymer wrapping and pi-pi interactions [19,20].

Although many researchers have been conducted to investigate the different toxicity aspects of BNNTs (cyto and geno) and the results are promising compared to CNTs [20-22], it is widely believed that extensive laboratory and clinical experimentations is needed to be able to use these materials for full scale commercial applications [1]. One of the challenges in investigating BNNTs toxicity behavior is the lack of unanimity in literature where controversial results (sometimes contradicting with each other) are reported for these nanomaterials. Many of these inconsistencies are due to dependency of BNNTs toxicity behavior to factors such as nanotubes type, size, structure (presence of defects), preparation process and surface modification which shows the difficulty in finding a solid reliable approach for evaluating their toxicity [23-25].

References

  1. 1. He H, Pham-Huy LA, Dramou P, Xiao D, Zuo P, Pham-Huy C. Carbon Nanotubes: Applications in Pharmacy and Medicine. BioMed Research International. 2013; 1-12.
  2. 2. Lacerda L, Bianco A, Prato M, Kostarelos K. Carbon nanotubes as nanomedicines: from toxicology to pharmacology. Adv Drug Deliv Rev. 2006; 58: 1460-1470.
  3. 3. Bekyarova E, Ni Y, Malarkey EB, Montana V, McWilliams JL, Haddon RC, et al. Applications of carbon nanotubes in biotechnology and biomedicine. Journal of Biomedical Nanotechnology. 2005; 1: 3-17.
  4. 4. Singh BGP, Baburao C, Pispati V, Pathipati H, Muthy N, Prassana SRV, et al. Carbon nanotubes - A novel drug delivery system. International Journal of Research in Pharmacy and Chemistry. 2012; 523-532.
  5. 5. Zhang W, Zhang Z, Zhang Y. The application of carbonnanotubes in target drug delivery systems for cancer therapies. Nanoscale Research Letters. 2011; 6: 555-577.
  6. 6. Vardharajula S, Ali SKZ, Tiwarim PM, Eroglu E, Vig K, Dennis VA, et al. Functionalized carbon nanotubes: biomedical applications. International Journal of Nanomedicine. 2012; 7: 5361-5374.
  7. 7. Iijima S. Helical microtubules of graphitic carbon. Nature. 1991; 354: 56-58.
  8. 8. Angel Rubio, Jennifer L Corkill, Marvin L Cohen. Theory of graphitic boron nitride nanotubes.Phys Rev B. 1994; 49: 5081-5084.
  9. 9. Dolati S, Fereidoon A, Kashyzadeh KR. A Comparison Study between Boron nitride Nanotubes and Carbon Nanotubes. International Journal of Emerging Technology and Advanced Engineering. 2012; 2: 470-474.
  10. 10. Zhi C, Bando Y, Tang C, Golberg D. Boron nitride nanotubes. Mat Sci Eng R. 2010; 70: 92-111.
  11. 11. Lahiri D, Rouzaud F, Richard T, Keshri AK, Bakshi SR, Kos L, et al. Boron nitride nanotube reinforced polylactide–polycaprolactone copolymercomposite: Mechanical properties and cytocompatibility with osteoblasts and macrophages in vitro. Acta Biomaterialia. 2010; 6: 3524-3533.
  12. 12. Chen H, Chen Y, Li CP, Zhang H, Williams JS, Liu Y, et al. Eu-doped Boron Nitride Nanotubes as a Nanometer-Sized Visible-Light Source. Adv Mater. 2007; 19: 1845-1848.
  13. 13. Ciofani G, Danti S, Ricotti L, D’Alessandro D, Moscato S, Berrettini S, et al. Boron Nitride Nanotubes: Production, Properties, Biological Interactions and Potential Applications as Therapeutic Agents in Brain Diseases. Current Nanoscience. 2011; 7: 94-109.
  14. 14. Ciofani G, Raffa V, Menciassi A, Cuschieri A. Boron nitride nanotubes: An innovative tool for nanomedicine. Nano Today. 2009; 4: 8-10.
  15. 15. Tang CC, Bando Y, Sato T, Kurashima K. A novel precursor for synthesis of pure BN nanotubes. Chem Comm. 2002; 12: 1290-1291.
  16. 16. Lee RS, Gavillet J, Lamy de la Chapelle M, Loiseau A. Catalyst-free synthesis of boron nitride single-wall nanotubes with a preferred zig-zag configuration. Phys Rev B. 2001; 65: 121405-121408.
  17. 17. Cumings J, Zettl A. Mass-production of boron nitride double-wall nanotubes and nanococoons. Chem Phys Lett. 2000; 316: 211-216.
  18. 18. Chen Y, Fitz Gerald J, Williams JS, Bulcock S. Synthesis of boron nitride nanotubes at low temperatures using reactive ball milling. Chem Phys Lett. 1999; 299: 260-264.
  19. 19. Ciofani G,Danti S, D’Alessandro D,Moscato S, Menciassi A. Assessing cytotoxicity of boron nitride nanotubes: Interference with the MTT assay. Biochem Biophys Res. Commun. 2010; 394: 405-411.
  20. 20. Ciofani G,Ricotti L,Danti S,Moscato S,Nesti C, D’Alessandro D, et al. Investigation of interactions between poly-l-lysine-coated boron nitride nanotubesand C2C12 cells: up-take, cytocompatibility, and differentiation. Int J Nanomed. 2010; 5: 285-298.
  21. 21. Digge MS, Moon RS, Gattani SG. Applications of carbon nanotubes in drug delivery: a review. International Journal of Pharm Tech Research. 2012; 4: 839–847.
  22. 22. Yang W, Thordarson P, Gooding JJ, Ringer SP, Braet F. Carbon nanotubes for biological and biomedical applications. Nanotechnology. 2007; 18: 12.
  23. 23. Ciofani G, Raffa V, Menciassi A, Cuschieri A. Cytocompatibility, interactions and uptake of polyethyleneimine-coated boron nitride nanotubes by living cells: confirmation of their potential for biomedical applications. Biotechnol Bioeng. 2008; 101: 850-858.
  24. 24. Chen X, Wu P, Rousseas M, Okawa D, Gartner Z, Zettl A, et al. Boron nitride nanotubes are noncytotoxic and can be functionalized for interaction with proteins and cells. J Am Chem Soc. 2009; 131: 890-891.
  25. 25. Lahiri D, Rouzaud F, Richard T, Keshri AK, Bakshi SR, Kos L, et al. Boron nitride nanotube reinforced polylactide-polycaprolactone copolymer composite: mechanical properties and cytocompatibility with osteoblasts and macrophages in vitro. Act Biomater. 2010; 6: 3524-3533.

Download PDF

Citation: Baghaee-Ravari S, Ghazizadeh M and Kelkar AD. Boron Nitride Nanotubes for Biomedical Applications: Challenges Ahead. Austin J Nanomed Nanotechnol. 2015; 3(1): 1040. ISSN:2381-8956

Home
Journal Scope
Online First
Current Issue
Editorial Board
Instruction for Authors
Submit Your Article
Contact Us