Indian Journal of Science and Technology
DOI: 10.17485/ijst/2014/v7i5.6
Year: 2014, Volume: 7, Issue: 5, Pages: 678–684
Original Article
P. Khalid1,3, M. A. Hussain2 , P. D. Rekha1 , C. Sanal4 , S. Suraj4 , M. Rajashekhar4 , V. B. Suman5 , Sangappa6 and A. B. Arun1*
1 Yenepoya Research Centre, Yenepoya University, Mangalore, 575018, India; p.khalid@live.com, rekhapd@hotmail.com, bhagwatharun@hotmail.com
2 Department of Electrical and Computer Engineering, King Abdulaziz University, Jeddah, 215895, KSA; abujuveria@gmail.com
3 Department of Biotechnology, P. A. College of Engineering, VTU, Mangalore, 574153, India; p.khalid@live.com
4 Department of Bioscience, Mangalore University, Mangalore 574199, India; sanal2019@gmail.com, surajsuvarna19@gmail.com, profmrajashekhar@yahoo.co.in
5 Kasturba Medical College, Manipal University, Mangalore 575004, India; suman.vb14@gmail.com 6 Department of Studies in Physics, Mangalore University, Mangalore 574199, India; syhalabhavi@yahoo.co.in
Hydroxyapatite (HA), as a bone mineral component, has been an attractive bioceramic for the reconstruction of hard tissues. However, its poor mechanical properties, including low fracture toughness and tensile strength, have been a significant challenge to the application of HA for the replacement of load-bearing and/or large bone defects. Hydroxyapatite (HA) composite is reinforced with high purity and well-functionalized Multiwalled Carbon Naotubes (MWCNT>98 wt%) having an average diameter of 15 nm.The cellular response of f-MWCNT, MWCNT-HA composites were examined to model gram positive and gram negative Bacteria B. subtilis, P. aeruginosa and yeast C. albicans. Ca(NO3 )2 .4H2 O and (NH4 )2 HPO4 were used to synthesize HA in situ. MWCNT were functionalized by heating at 1000 C in 3:1 ratio of H2 SO4 and HNO3 for 60 m with stirring and dispersed in Sodium Dodecyl Benzene Sulphonate (SDBS) by sonication. Hydroxy Apatite (HA) particles were produced in MWCNTs solution by adding Ca(NO3 )2 .4H2 O and (NH4 )2 HPO4 under vigorously stirring conditions. The composite were dried and washed in distilled water followed by heat treatment at 2500 C to obtain CNT-HA powder. Using FTIR, FESEM and EDS does physicochemical characterization of the composite material. The interaction of f-MWCNT and MWCNT-HA were tested on Bacillus subtilis, P. aeruginosa and C. albicans. The zone of inhibition and MIC studies were carried out with a concentration range from 62.5 – 1000 µg/ml. The test result shows no zone of inhibition and MIC > 1000 µg/ml on bacteria and yeast. This result provides further evidence that the bio-nano interface can be developed for Carbon Nanotubes reinforced Hydroxyapatite composites for load-bearing bone implants, drug delivery and diagnostic applications.
Keywords: Hydroxyapatite, MIC, MWCNTs, Nanocomposites
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