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Abstracts Book - IMRC 2018

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• SB3-P010<br />

POLY-(BUTYLENE ADIPATE-CO-TEREPHTHALATE) /<br />

POLYPYRROLE/NANO-HYDROXYAPATITE SCAFFOLDS FOR BONE<br />

TISSUE REGENERATION<br />

Conceicao de Maria Vaz Elias 1 , Antonio Luiz Martins Maia Filho 2 , Laryssa Roque Da Silva 2 ,<br />

Danniel Cabral Leão Ferreira 2 , Fernanda Roberta Marciano 1 , Anderson Oliveira Lobo 1<br />

1<br />

Universidade Brasil, Department of Biomedical Engineering, Brazil. 2 Universidade Estadual do<br />

Piauí, Department of Mutagenesis, Brazil.<br />

The combination of poly-(butylene adipate-co-terephthalate)(PBAT) with<br />

polypyrrole(PPy) and nano-hydroxyapatite(nHAp) scaffolds have emerged as an<br />

alternative for bone tissue engineering due to their excellent biodegradability,<br />

biocompatibility, bioactivity, and electric properties. Herein, we electrospun<br />

ultrathin PBAT/PPy/nHAp mats, which were then characterized. Their<br />

genotoxicity was also evaluated in vivo using a micronucleus test. For scaffold<br />

synthesis, 15g of PBAT pellets were first dissolved in 10mL of chloroform under<br />

magnetic stirrer using a closed system. After 20h, 20mg of PPy were added into<br />

2mL of DMF and sonicated for 5min. Next, both solutions were mixed and<br />

electrospun (17kV, 10cm distance, 23G needle) for 40min. The electrolyte<br />

solution used was composed of 0.042 mol L–¹ of Ca(NO3)2·4H2O + 0.025 mol L–¹<br />

of (NH4)2HPO4. The pH was adjusted to 4.7 and the temperature to 70°C. The<br />

nHAp thin films were electrodeposited using a classical three points electrode<br />

(PGSTAT 128N). The mats were coupled to a working electrode (0.25 cm²) and a<br />

platinum mesh was used as counter electrode, while Ag/AgCl (3 M KCl(aq.)) was<br />

used as the reference electrode. The nHAp crystals were produced on PBAT/PPy<br />

scaffolds by applying a constant potential of –3.8 V for 30 min. 4 groups were<br />

used: PBAT/PPy (1) with and (2) without nHAp, (3) cyclophosphamide at the dose<br />

of 50mg / kg intraperitoneally as a positive control, and (4) distilled water as a<br />

negative control. The nanocomposites were implanted into the peritoneum<br />

through a laparotomy. 20 male and adult albino Wistar rats were used (n=5 for<br />

each group). After 45 and 72 hours the animals were anesthetized with ketamine<br />

(1.0 ml/kg) and xylazine (1.1 ml/kg) intramuscularly and their blood was collected<br />

for micronucleus analysis in Polychromatic Erythrocytes (PCEs). The frequency<br />

of micronuclei in 2,000 PCE cells per animal was determined. The PBAT/PPy<br />

nanofibers had a length of 0.074 ± 0.221 um. In the micronucleous test, there<br />

was no significant difference between the membrane-exposed group with nHap<br />

and without nHap. Neither the growth nor the frequency of micronuclei in the<br />

chronic and acute periods were significant, and differences were not observed

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