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Photonic crystals in biology

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Poster Session, Tuesday, June 15<br />

Theme A1 - B702<br />

Preparat ion of Ag doped HAP/PHBV Nanocompos ite Fibers via Electrosp<strong>in</strong>n<strong>in</strong>g Technique<br />

Aslihan Suslu 1 *, Ayl<strong>in</strong> Ziylan Albayrak 1 and Umit Cocen 1<br />

1 Department of Metallurgical and Materials Eng<strong>in</strong>eer<strong>in</strong>g, Dokuz Eylul University, 35160, Izmir, Turkey<br />

Abstract- Silver doped hydroxyapatites were produced by coprecipitation method and Ag doped HAP-PHBV nanocomposite suspensions<br />

were prepared with the aid of the surfactant, 12-hydroxysteric acid (HSA). Nanocomposite fibers prepared from Ag doped HAP-PHBV<br />

suspensions were produced via electrosp<strong>in</strong>n<strong>in</strong>g. Surface morphology of the fibers analyzed by SEM and HAP dispersion on the fiber surface<br />

was <strong>in</strong>vestigated by EDS analysis via Ca, P and Ag quantity determ<strong>in</strong>ation. XRD was used <strong>in</strong> order to see whether the crystal structure of<br />

HAP is ma<strong>in</strong>ta<strong>in</strong>ed or not.<br />

An ideal tissue scaffold should be mechanically stable,<br />

bio-compatible and capable of function<strong>in</strong>g biologically <strong>in</strong><br />

the implant site. Biologic function<strong>in</strong>g is regulated by<br />

biologic signals from growth factors, extracellular matrix<br />

(ECM), and the surround<strong>in</strong>g cells. ECM molecules<br />

surround cells to provide mechanical support and regulate<br />

cell activities [1].To mimic natural ECM, many research<br />

groups have tried to produce nanofibrous tissue scaffolds<br />

us<strong>in</strong>g electro-sp<strong>in</strong>n<strong>in</strong>g method [2]. Electrosp<strong>in</strong>n<strong>in</strong>g is an<br />

actively <strong>in</strong>vestigated technique recently, as well as the<br />

simplicity of the process; it offers ultraf<strong>in</strong>e polymer fibers,<br />

high specific surface area, highly porous structure and the<br />

possibility of various modifications [3-5]. In tissue<br />

eng<strong>in</strong>eer<strong>in</strong>g applications <strong>in</strong> particular, ultraf<strong>in</strong>e nanofibers<br />

have been fabricated from biodegradable and<br />

biocompatible natural or synthetic polymers such as<br />

collagen, fibr<strong>in</strong>ogen, poly(glycolic acid) (PGA), poly(L-<br />

Lactic acid) (PLA), poly(lactic acid-co-glycolic acid)<br />

(PLGA), poly(3-hydroxybutyrate-co-3-hydroxyvalerate)<br />

(PHBV) [6].<br />

The target of our study is to produce polymer based<br />

tissue scaffold that can be used <strong>in</strong> the field of tissue<br />

eng<strong>in</strong>eer<strong>in</strong>g. As the ma<strong>in</strong> matrix, PHBV as a<br />

biodegradable and a biocompatible polymer was chosen.<br />

Together with the cheapness, PHBV has longer<br />

degradation time than PLA and PLGA polymers, which<br />

means that the scaffold can ma<strong>in</strong>ta<strong>in</strong> its mechanical<br />

<strong>in</strong>tegrity until there is sufficient tissue formation [6]. To<br />

<strong>in</strong>crease the mechanical strength of the ma<strong>in</strong> matrix and<br />

also to improve cell adhesion hydroxyapatite (HAP) is<br />

used. In addition, as the cation exchange rate of HAP is<br />

very high, HAP is doped with m<strong>in</strong>or amount of Ag ions <strong>in</strong><br />

this way tissue scaffold will ga<strong>in</strong> antibacterial function as<br />

well as the osteoconductive function. [7-9]. Due to its<br />

nontoxic and cell-friendly nature HSA is a safely used<br />

chemical <strong>in</strong> biomedical applications as a surfactant [10]. In<br />

this study, HSA was used to disperse Ag doped HAP <strong>in</strong><br />

the PHBV matrix <strong>in</strong> a homogenous manner. Also,<br />

organosoluble salt benzyl triethylammonium chloride<br />

(BTEAC) was used to <strong>in</strong>crease the conductivity of solution<br />

and to obta<strong>in</strong> uniform fibers.<br />

Ag doped (2 wt %) hydroxyapatite powder was<br />

produced by coprecipitation method us<strong>in</strong>g AgNO 3 , H 3 PO 4<br />

and Ca(OH) 2 as start<strong>in</strong>g materials. Ag doped HAP<br />

powders were characterized by XRD and SEM/EDS. As<br />

the Ag content of the powders was very low, no difference<br />

between the XRD patterns of HAP and Ag dopped HAP<br />

was observed. Nanocomposite fibers were successfully<br />

fabricated by us<strong>in</strong>g the Ag doped HAP-PHBV suspensions<br />

via electrosp<strong>in</strong>n<strong>in</strong>g. Optimum parameters were def<strong>in</strong>ed as<br />

follows: Voltage supply, 20 kV; distance between the<br />

needle and the collector, 15 cm; flow rate, 0,3 ml/h. SEM<br />

and EDS analyses showed Ag doped HAP was<br />

successfully <strong>in</strong>corporated and homogenously dispersed on<br />

the PHBV fibers. In order to reduce the fiber diameter and<br />

get better sp<strong>in</strong>ability BTEA C salt (2-5 wt %) was used.<br />

In conclusion Ag doped HAP powder was synthesized<br />

successfully by coprecipitation method. Ag doped HAP-<br />

PHBV nanocomposite suspensions prepared. The <strong>in</strong>nate<br />

dispersion and agglomerate problems associated with<strong>in</strong><br />

hydrophilic bioceramic powder with<strong>in</strong> hydrophobic<br />

biopolymers were solved by us<strong>in</strong>g a surfactant.<br />

Nanocomposite fibers successfully produced from the<br />

prepared Ag doped HAP-PHBV suspensions via<br />

electrosp<strong>in</strong>n<strong>in</strong>g technique. Author A.S acknowledges the<br />

support from TUBITAK, <strong>in</strong> the framework of the National<br />

Scholarship Programmes for PhD Students.<br />

* Correspond<strong>in</strong>g author: 0Taslihan.suslu@deu.edu.tr<br />

[1] W. J. Li, C. T. Laurenc<strong>in</strong>, E. J. Caterson, R. S. Tuan, F. K.<br />

Ko, Journal of Biomedical Materials Research, 60, 613-621,<br />

(2002).<br />

[2] Y., Ito, H., Hasuda, M. Kamitakahara, C. Ohtsuki, M.<br />

Tanihara, I. K. Kang, O. H. Kwon, Journal of Bioscience and<br />

Bioeng<strong>in</strong>eer<strong>in</strong>g, 100, 1, 43-49.,(2005).<br />

[3] D. Li , Y. Xia, Advanced Materials, 16, 1151-1170, (2004).<br />

[4]. M. Sawickak, P. Gouma, Journal of Nanoparticle Research,<br />

8, 769-781, (2006).<br />

[5] O. H .Kwon, I. K. Lee, Y. G. Ko, W. Meng, K. H. Jung, I. K.<br />

Kang, Y. , Biomedical Materials, 2, S52-S58, (2007).<br />

[6] N. Sultana, M. Wang, J. Mater Sci: Mater Med, 19, 2555-256<br />

(2008).<br />

[7] N. Sanpo , M. L. Tan, P. Cheang, K. A. Khor,, Journal of<br />

Thermal Spray Technology, 18, 1, 10-15, (2009).<br />

[8] N. Rameshbabu, T.S. Sampath Kumar, T.G. Prabhakar, V.S.<br />

Sastry, K.V.G.K. Murty, K. Prasad Rao, , Journal of Biomedical<br />

Materials Research Part A, 581-591, ( 2006).<br />

[9] W. Chen, Y. Liu, H. S. Courtney, M. Bettenga, C. M.<br />

Agrawal, J. D. Bumgardner, J. L. Ong, Biomaterials, 27, 5512-<br />

5517, (2006).<br />

[10] H. W. Kim, H. H. Lee, J. C. Knowles, J. Biomed Mater<br />

Res, 79A, 643-649, (2006).<br />

6th Nanoscience and Nanotechnology Conference, zmir, 2010 375

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