Poly (∊-caprolactone), (PCL) or simply polycaprolactone as it is usually referred to, is a synthetic biodegradable aliphatic polyester which has attracted considerable attention in recent years, notably in the biomedical areas of controlled-release drug delivery systems, absorbable surgical sutures, nerve guides, and three-dimensional (3-D) scaffolds, for use in tissue engineering. Various polymeric devices like microspheres, microcapsules, nanoparticles, pellets, implants, and films have been fabricated using this polymer. It can be transformed by spinning into filaments for subsequent fabrication of desirable textile structures. Spinning may be accomplished by various approaches. The fibers may be fabricated into various forms and can be used for implants and other surgical applications such as sutures. Although numerous studies have investigated different properties and applications of PCL, there is no comprehensive study investigating different fabrication methods of PCL fibers and their biomedical applications. The present article presents a review on the production of PCL fiber via various methods, along with correlations between structure and properties of the fibers. The applications of these fibers in biomedical domains are also discussed.

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An index Xh21 with numerator calculated solely from solubility parameters and denominator measured by on-line viscosity of the fiber precursor in coagulation medium was defined as an indicator of the fiber structure and tensile properties. The Xh 21 values of wet-spun and wound polyacrylonitrile fibers from their dimethylformamide solutions with different polymer concentrations (series A) or nonsolvent concentrations in 10 vol % polymer solutions (series B) into water with draw ratio of one were determined and compared with the corresponding fiber structure and tensile properties. The Xh 21 value of about 0.8 3 10 6 s 21 led to finger-like structure with overall fiber porosity of 82 vol %. By reducing Xh 21 through dope polymer concentration enhancement to 20 vol %, overall fiber porosity decreased to 62 vol % via substitution of some micrometer voids with dense polymer ligament. Accordingly, strong fiber modulus and elongation at break enhancement were observed due to structural defect reduction and cohesive energy density increment. On the other hand, dope nonsolvent concentration increment from 0 to 5 vol % at 10 vol % polymer concentration showed minute overall fiber porosity decrement via Xh 21 increment through micrometer void substitution with nanometer ones (nuclei). Therefore, mild fiber modulus and elongation at break improvements were detected due to defect size reduction which magnifies mechanical properties improvements. Curve fitting of the Wang's second order modulus-porosity correlation to the as-spun fibers modulusporosity data verified the solid-liquid phase separation through nuclei growth-resistance as the main governing morphological evolution mechanism.

Co-polymers of lactide and glycolide, referred to as PLGA, have generated tremendous interest because of their excellent biocompatibility, biodegradability and mechanical strength. Various polymeric devices like microspheres, microcapsules, nanoparticles, pellets, implants, and films have been fabricated using these polymers. They can be transformed by spinning into filaments for subsequent fabrication of desirable textile structures. Spinning may be accomplished by various routes. The fibers may be fabricated into various forms and may be used for implants and other surgical applications such as sutures. They are also easy to formulate into various delivery systems for carrying a variety of drug classes. The present article presents a review on the production of PLGA fiber by various methods, along with correlations between structure and properties of the fibers. The applications of these fibers in biomedical domains are also discussed.

Wet spinning of polyacrylonitrile/carbon nanotubes (PAN/CNT) composite fibers was studied and the effect of spinning conditions on structure and properties of as-spun fibers influenced by the presence of CNTs investigated. Unlike PAN fibers, shear force had a larger effect on crystalline structure and physical and mechanical properties of PAN/CNT composite fibers compared to the elongational force inside a coagulation bath. Under shear force CNTs induced nucleation of new crystals, whereas under elongational force nucleation of new crystals were hindered but the already formed crystals grew bigger. To our knowledge, this key effect has not been reported elsewhere. At different shear rates, strength, Young’s modulus and strain at break of PAN/CNT as-spun fibers were improved up to 20% compared to PAN fibers. Application of jet stretch had less influence on physical and mechanical properties of PAN/CNT fibers compared to PAN fibers. However, the improvement of interphase between polymer chains and CNTs as a result of chain orientation may have contributed to enhancement of Young’s modulus of jet stretched composite fibers.

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Using different indices calculated from Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), and Differential Scanning Calorimetry (DSC) spectra, progress in stabilization reactions of three different commercial grade polyacrylonitrile (PAN) fibers is calculated. From each analysis technique quantitative indices are computed which could assess in some particular reactions. Combination of these indices gives further information about the progress of stabilization reactions which cannot be concluded from single indices. The results show that different indices are not fully consistent with each other, depending on the analysis technique and the changes they assess. The advantages and disadvantages of each index are investigated and practical indices are identified which can be used to design the optimum stabilization process. In addition, by combination of some indices it is possible to separate the temperature ranges in which reactions occur in amorphous or crystalline regions. This approach can be used to design appropriate stretching process during stabilization.