Void Content Minimization in Vacuum Infusion (VI) via Effective Degassing.

This paper addresses the major concern which component porosity represents in Vacuum Infusion (VI) manufacturing due to resin gelation at pressures close to absolute vacuum. Degassing is a fundamental step to minimize or even avoid resin outgassing and enhance dissolution of voids created during preform impregnation. The efficacy of different degassing procedures based on vacuum degassing, and assisted by adding a nucleation medium, High Speed (HS) resin stirring and/or later pressurization during different time intervals have been analyzed in terms of final void content is studied.

Tissue Compatibility of SN-38-Loaded Anticancer Nanofiber Matrices.

Delivery of chemotherapy in the surgical bed has shown preclinical activity to control cancer progression upon subtotal resection of pediatric solid tumors, but whether this new treatment is safe for tumor-adjacent healthy tissues remains unknown. Here, Wistar rats are used to study the anatomic and functional impact of electrospun nanofiber matrices eluting SN-38-a potent chemotherapeutic agent-on several body sites where pediatric tumors such as neuroblastoma, Ewing sarcoma, and rhabdomyosarcoma arise. Blank and SN-38-loaded matrices embracing the femoral neurovascular bundle or in direct contact with abdominal viscera (liver, kidney, urinary bladder, intestine, and uterus) are placed.

SN-38-loaded nanofiber matrices for local control of pediatric solid tumors after subtotal resection surgery.

In addition to surgery, local tumor control in pediatric oncology requires new treatments as an alternative to radiotherapy. SN-38 is an anticancer drug with proved activity against several pediatric solid tumors including neuroblastoma, rhabdomyosarcoma and Ewing sarcoma. Taking advantage of the extremely low aqueous solubility of SN-38, we have developed a novel drug delivery system (DDS) consisting of matrices made of poly(lactic acid) electrospun polymer nanofibers loaded with SN-38 microcrystals for local release in difficult-to-treat pediatric solid tumors.

Resolving the electrospinnability zones and diameter prediction for the electrospinning of the gelatin/water/acetic acid system.

The development of suitable biomimetic scaffolds is a fundamental requirement of tissue engineering. Although electrospinning has emerged as an effective method for producing such scaffolds of nanometer-sized fibers, the influence of solution characteristics on the morphology of the resulting nanofibers depends on each polymer solution system. In this study, gelatin nanofibers and microfibers were prepared via electrospinning using mixtures of water and acetic acid at different ratios as solvents.

Drug delivery systems using sandwich configurations of electrospun poly(lactic acid) nanofiber membranes and ibuprofen.

The primary advantages of electrospun membranes include the ability to obtain very thin fibers that are on the order of magnitude of several nanometers with a considerable superficial area and the possibility for these membranes to be manipulated and processed for many different applications. The purpose of this study is to evaluate and quantify the transport mechanisms that control the release of drugs from polymer-based sandwich membranes produced using the electrospinning processes. These electrospun membranes were composed of poly(lactic acid) (PLA) because it is one of the most promising biodegradable polymers due to its mechanical properties, thermoplastic processability and biological properties, such as its biocompatibility and biodegradability.