Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-17T17:08:29.535Z Has data issue: false hasContentIssue false

Drug Deliverable, Self-assembled Rosette Nanotubes (RNTs) for Orthopedic Applications

Published online by Cambridge University Press:  31 January 2011

Yupeng Chen
Affiliation:
[email protected], Brown University, 324 Brook Street, Providence, Rhode Island, 02912, United States
Shang Song
Affiliation:
[email protected], Brown University, Providence, Rhode Island, United States
Hicham Fenniri
Affiliation:
[email protected], University of Alberta, Edmonton, Canada
Thomas J Webster
Affiliation:
[email protected], United States
Get access

Abstract

Rosette nanotubes (RNTs) are novel, biomimetic, synthetic, self-assembled drug delivery agents. Because of base stacking and hydrophobic interactions, the RNT hollow-tube structure can be used for incorporating drugs. Another advantage of using RNTs is their ability to be injected and become solid at body temperatures for orthopedic applications without the use of any external stimuli (such as UV light or crosslinking agents). The nano-features of RNTs create a favorable, biologically-inspired, cellular environment. In this study, methods to incorporate dexamethasone (DEX, a bone growth promoting drug) into RNTs were investigated. The drug-loaded RNTs were characterized using Nuclear Magnetic Resonance (NMR), Diffusion Ordered Spectroscopy (DOSY) and Ultraviolet-visible Spectroscopy (UV-vis). Results showed that small molecular drugs with hydrophobic aromatic rings were incorporated into RNTs. Subsequent drug release experiments demonstrated that DEX was released from the RNTs and had a positive impact on osteoblast functions. Importantly, compared to other drug carriers, RNTs increased the total drug loading and was the highest when DEX was incorporated during the RNT self-assembly process. Thus, this study offered a novel drug delivery device that itself is bioactive and can be used to deliver a variety of drugs for various orthopedic applications.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1 Charnley, J. Anchorage of the fermoral head prosthesis to the shaft of the femur. Journal of bone joint surgery. 1960, 42B, 2830.Google Scholar
2 Sato, N, Kubo, K, Yamada, M, Hori, N, Suzuki, T, Maeda, H, Osteoblast, Ogawa T. mechanoresponses on Ti with different surface topographies. J Dent Res. 2009, 88(9), 812816.Google Scholar
3 GS, Shi, LF, Ren, LZ, Wang, HS, Lin, SB, Wang, YQ, Tong. H2O2/HCl and heat heat-treated Ti-6Al 6Al-4V stimulates pre pre-osteoblast proliferation and differentiation. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009, 108(3), 368375.Google Scholar
4 YC, Kuo, CF, Yeh, JT, Yang. Differentiation of bone marrow stromal cells in poly(lactide lactide-co co-glycolide)/chitosan scaffolds. Biomaterials. 2009, 30(34), 66046613.Google Scholar
5 GM, Vidigal Jr , Groisman, M, LH, Gregório, Soares Gde, A. Osseointegration of titanium alloy and HA-coated impla implants in healthy and ovariectomized animals: a histomorphometric study. Clin Oral Implants Res. 2009, 20(11), 12721277.Google Scholar
6 Balasundaram, G, TJ, Webster. Nanotechnology and biomaterials for orthopedic medical applications. Nanomed. 2006, 1(2), 169~176.Google Scholar
7 Balasundaram, G, TJ, Webster. An overview of nano ram nano-polymers for orthopedic applications. Macromol Biosci. 2007, 10, 7(5), 635~642.Google Scholar
8 KJ, Bozic, SM, Kurtz, Lau, E, et al. The epidemiology of revision total hip arthroplasty in the United States. J Bone Joint Surg (Am). 2009, 91: 128133.Google Scholar
9 CK, Chan, TS, Kumar, Liao, S, Murugan, R, Ngiam, M, Ramakrishnan, S. Biomimetic nanocomposites for bone graft applications. Nanomed. 2006, 1(2): 177188.Google Scholar
10 Balasundaram, G, TJ, Webster. An overview of nano nano-polymers for orthopedic applications. Macromol Biosci. 2007, 10;7(5): 635642.Google Scholar
11 AL, Chun, JG, Moralez, Fenniri, H, TJ, Webster. Helical rosette nanotubes: a biomimetic coating for orthopedics? Biomaterials 2005; 26: 73047309.Google Scholar
12 AL, Chun, JG, Moralez, Fenniri, H, TJ, Webster. Helical rosette nanotubes: A more ef effective. orthopaedic implant material. Nanotechnology 2004; 15: s234–s239.Google Scholar
13 Fenniri, H, mathivanan, P, KL, Vidale, DM, Sherman, Hallenga, K, KV, wood and JG, Stowell. Helical rosette nanotubes: design, self self-assembly and characterization. J. Am. Chem. Soc. 2001, 123, 38543855.Google Scholar
14 Zhang, L, Chen, Y, Rodriguez, J, Fenniri, H, TJ, Webster. Biomimetic helical rosette nanotubes and nanocrystalline hydroxyapatite coatings on titanium for improving orthopedic implants. Int J Nanomedicine. 2008, 3(3): 323333.Google Scholar
15 Zhang, L, Rakotondradany, F, AJ, Myles, Fenniri, H, TJ, Webster. Arginine ny Arginine-glycine glycine-aspartic acid modified rosette nanotube nanotube-hydrogel composites for bone tissue engineering. Biomaterials. 2009, 30(7): 1309~1320.Google Scholar
16 Guzmán-Morales, J, El-Gabalawy, H, MH, Pham, Tran-Khanh, N, MD, McKee, Wu, W, Ce Centola, M, CD, Hoemann. Effect of chitosan particles and DEXamethasone on human amethasone bone marrow stromal cell osteogenesis and angiogenic factor secretion. Bone. 2009, 45(4): 617626.Google Scholar
17 AG, Beule, Steinmeier, E, Kaftan, H, KE, Biebler, Göpferich, A, Wolf, E, Hosemann, W. Effects of a DEXamethasone amethasone-releasing stent on osteoneogenesis in a rabbit model. Am J Rhinol Allergy. 2009, 23(4): 433436.Google Scholar
18 Yang, L, Tao, T, Wang, X, Du, N, Chen, W, Tao, S, Wang, Z, Wu, L. Effects of DEXamethasone on proliferation, differentiation and apoptosi amethasone apoptosis of adult human osteoblasts in vitro. Chin Med J (Engl). 2003, 116(9): 1357–60.Google Scholar
19 IV, Arutyunyan, AA, Rzhaninova, AV, Volkov, DV, Goldstein. Effect of DEXamethasone amethasone on differentiation of multipotent stromal cells from human adipose tissue. Bull Exp Biol Med. 2009, 147(4): 503508.Google Scholar
20 Yang, L, TJ, Webster. Nanotechnology controlled drug delivery for treating bone diseases. Expert Opin Drug Deliv. 2009, 6(8): 851864.Google Scholar
21 ME, Gindy, RK, Prud'homme. Multifunctional nanoparticles for imaging, delivery and targeting in cancer ther therapy. Expert Opin Drug Deliv. 2009, 6(8): 865878.Google Scholar
22 WS, Cho, Cho, M, SR, Kim, Choi, M, JY, Lee, BS, Han, SN, Park, MK, Yu, Jon, S, Jeong, J. Pulmonary toxicity and kinetic study of Cy5.5-conjugated superparamagnetic iron oxide nanoparticles by optical imaging. Toxicol Appl Pharmacol. 2009; 239(1): 106115.Google Scholar
23 Yang, Z, Zhang, Y, Yang, Y, Sun, L, Han, D, Li, H, Wang, C. Pharmacological and toxicological target organelles and safe use of single single-walled carbon nanotubes as drug carriers in treating Alzheimer disease. Nanomedicine. 2010 (Epub).Google Scholar
24 Prakash, S, AG, Kulamarva. Recent advances in drug delivery: potential and limitations of carbon nanotubes. Recent Pat Drug Deliv Formul. 2007;1(3): 214221.Google Scholar