The study aimed to evaluate the safety and function of poly(lactic-acid-co-ε-caprolactone) (PLCL)/fibrinogen nanofibers (P/F-Ns), and provide theoretical basis for the clinical application. The surface morphology, mechanical properties, the hydrophilicity and the fibrinogen content of P/F-Ns were tested by scanning electron microscope, the material testing machine, the contact angle meter and the microplate reader, respectively. The cell adhesion, proliferation and ligament remodeling genes expression of Hig-82 cells on P/F-Ns were conducted through cell counting kit-8 (CCK-8) and real-time quantitative PCR analyses, respectively. The results showed that with the increase of the fibrinogen content, the pore sizes and hydrophilicity of three P/F-Ns increased, but the mechanical properties decreased. Cell adhesion and proliferation tests showed that P/F-N-2 held the best ability to promote cell adhesion and proliferation. The ligament remodeling genes expressions of Hig-82 cells on P/F-N-1, P/F-N-2 and P/F-N-3 were all up-regulated compared to P/F-N-0 on days 3 and 7. All the three P/F-Ns containing fibrinogen (P/F-N-1, P/F-N-2 and P/F-N-3) had better biocompatibility compared to P/F-N-0, and could be efficiently applied to the reconstruction of anterior cruciate ligament.
A drug vaccarin loaded polymer poly (vinyl alcohol) (PVA)-stilbazole quaternized (SbQ)/Zein was prepared in this study, using co-electrospun method. Then the morphologies and structures of PVA-SbQ/Zein composite nanofibers were observed by scanning electron microscope (SEM) and Fourier transform infrared spectrum (FTIR), respectively. Finally, biocompatibility of PVA-SbQ/Zein nanofibers with drug and without drug was evaluated. Results showed that vaccarin-loaded PVA-SbQ/Zein nanofibers had smooth surface and showed non-toxic to L929 cells. Drug vaccarin could promote cells attachment on nanofibers. The wound healing performance was examined in vivo by rat skin models and histological observations, and PVA-SbQ/Zein/vaccarin nanofibers showed better wound healing performance than petrolatum gauze group.
Drug-eluting stents used to inhibit granulation tissue hyperplasia after tracheal stent implantation rely on passive drug release mechanisms, which make precise controlled release difficult and may lead to either insufficient efficacy or toxic side effects. This study aims to design a piezoelectric effect-based adaptive drug-releasing film for tracheal stents, capable of self-regulating the release of anti-inflammatory drugs according to the mechanical changes in the pathological environment within the patient’s airway. First, a polyvinylidene fluoride piezoelectric film was prepared on a metal stent surface via electrospinning. Curcumin-loaded poly(3,4-ethylenedioxythiophene) conductive nanoparticles were dispersed in a polyvinyl alcohol hydrogel and adhered to the upper and lower edges of the stent (prone to hyperplasia areas). Experiments showed uniform nanoparticle morphology with a curcumin loading rate of (12.6 ± 1.80)%. Electrochemical tests indicated that the curcumin release rate was highest (approximately 90%) at a reduction potential of –1.5 V, and “on/off” controlled release could be achieved through intermittent electrical stimulation. When periodic pressure was applied to the film, its output voltage increased with loading speed (up to –8 V). Furthermore, the curcumin release rate was positively correlated with the pressure speed, reaching a cumulative release of about 15% within 48 h at a loading speed of 2.5 m/min. The drug-loaded piezoelectric film-covered stent developed in this study successfully achieves mechanically controlled release of the anti-inflammatory drug curcumin under intermittent cyclic pressure, providing an effective strategy for developing intelligent tracheal stents with adaptive and controllable drug release.