Designing implants with good antibacterial activity and simultaneously providing a platform for osteoblast adhesion is a challenge for researchers. All metallic implants, currently in use, are biocompatible but bioinert. This may lead to a weak interface with the bone and cause asceptic loosening. The aim of the present study is designing an implant with good antibacterial activity and simultaneously providing a platform for osteoblast adhesion. This is achieved by surface engineering of the currently used metallic implants without affecting their mechanical properties. The FDA approved plasma spraying technique is utilized to synthesize interconnected microporous bioactive hydroxyapatite (HA) coating on the Ti-6Al-4 V implant surface. The modified implant surface is impregnated with drug (gentamicin) loaded biodegradable polymer (chitosan) through a customized vacuum impregnation process. During impregnation, drug loaded polymer filled the pores of coating while leaving the rest of the HA surface exposed to promote osteoconductivity. The hardness and elastic modulus of the HA coating showed insignificant changes after impregnation with the drug loaded polymer, while the fracture toughness is improved by ∼42%. In vitro drug release studies have revealed a sustained release up to 180 h, with an ideal initial burst release. The drug loaded surfaces have also shown very efficient antibacterial activity against S. aureus, even after 5 days of incubation. Further, the modified surfaces have shown excellent osteocompatibility, due to the presence of the exposed HA coated surface. Thus, the surface modified implants, with a unique combination of antibacterial activity, osteocompatibility, and improved fracture toughness, have promising potential applications in orthopedics.
Nanometer-
and submicrometer-sized fiber have been used
as scaffolds
for tissue engineering, because of their fundamental load-bearing
properties in synergy with mechano-transduction. This study investigates
a single biodegradable poly(lactic-co-glycolic acid)
(PLGA) fiber’s load–displacement behavior utilizing
the nanoindentation technique coupled with a high-resolution in situ
imaging system. It is demonstrated that a maximum force of ∼3
μN in the radial direction and displacement of at least 150%
of fiber diameter should be applied to acquire the fiber’s
macroscopic mechanical properties for tissue engineering. The adhesion
behavior of a single fiber is captured using a high-resolution camera.
The digital image correlation (DIC) technique is adopted to quantify
the adhesion force (∼25 μN) between the fiber and the
tip. Adhesion force has also been quantified for the fiber after immersing
in phosphate-buffered saline (PBS) to mimic the bioenvironment. A
4-fold increase in adhesion force after PBS treatment was observed
due to water penetration and hydrolysis on the fiber’s surface.
A high similarity between mechanical properties of a single fiber
and native tissues (elastic modulus of 10–25 kPa) and superior
adhesion force (25–107.25 μN) was observed, which is
excellent for promoting cell-matrix communication. Overall, this study
examines the mechanics of a single fiber using innovative indentation
and imaging processing techniques, disclosing its profound and striking
roles in tissue engineering.
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