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Electrospinning surgical suture

Electrospun yarn as potential surgical suture

Early investigation using electrospun fibers in medical device applications is mainly as implantable scaffold. The small diameters of electrospun fibers from a few hundreds of nanometers to a few microns have been shown to facilitate cell adhesion and proliferation in numerous in vitro studies. In vivo studies have also found them to exhibit good biocompatibility. Later development in the electrospinning process has seen the construction of fibrous tubes and yarns. This expanded the potential application to sutures. There are several methods of constructing sutures from electrospinning. For finite length yarn, a rotating disk may be used to collect a bundle of fibers along the edge of the disk. Several other methods such as using water-bath as collector have been devised to collect continuous electrospun yarn. The ability to construct continuous electrospun yarn and relatively benign inflammatory response [Kashiwabuchi et al 2017] makes it an highly attractive candidate as suture.

Most electrospun sutures often includes other functional properties such as drug elution or anti-bacterial. The relative ease of loading the solution with other substances and electrospinning to form fibers make this an attractive option. Further, large surface area of small diameter electrospun fibers give greater exposure of the active substances to the surrounding. Liu et al (2010) electrospun poly(ε-caprolactone) (PCL) yarn containing ampicillin sodium salt, which is a common anti-microbial drug. The drug-loaded yarn has an initial burst release in the first hour and the release is almost completed in 96 hours. Kashiwabuchi et al (2016) constructed an electrospun poly(L-lactide) (PLLA)/ polyethylene glycol (PEG) microfibrous yarn loaded with levofloxacin targeted for ophthalmic surgery. In vitro release study showed an initial burst release for the first 48 hours followed by linear release for more than 2 months with approximately 65% cumulative release. The amount of released levofloxacin within the first 24 hrs and after 7 days were found to inhibit S. epidermidis in separate tests. In vivo tests on corneal stroma of male Sprague-Dawley rats showed no inflammation with histological results similar to that of implanted commercial nylon sutures. Weldon et al (2012) electrospun poly(lactic-co-glycolic acid) (PLGA) sutures containing anesthesia (bupivacaine HCl). With localized release of anesthesia at the operation site, it reduces postoperative discomfort and the need for other forms of anesthesia. The release of the drug in electrospun PLGA started relatively slowly and linearly for the first two days. Thereafter, the release increased rapidly from day two to day seven and all drugs were released after 12 days. Comparing the mechanical strength, electrospun drug-free PLGA suture is an order of magnitude lower than commercial PLGA suture (Vicryl, 30N).

Electrospun yarns have been tested as potential future suture material in particular, drug-loaded yarns. While the drug release performance is favourable to its intended application, more studies and modifications to the yarn is needed to improve its mechanical strength. Currently, electrospun yarns are much weaker than its commercial counterpart. Further investigations are also required to determine the benefits of having finer diameter fibers in the construction of suture over microfibers which are currently in use.

Published date: 16 May 2017
Last updated: -


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