Influence of surfactant on glass transition temperature of poly(lactic--glycolic acid) nanoparticles.

Poly(D,L-lactic--glycolic acid) (PLGA) is one of the most commonly used drug carriers in nanomedicines because of its biodegradability, biocompatibility and low toxicity. However, the physico-chemical characterization and study of drug release are often lacking the investigation of the glass transition temperature (), which is an excellent indicator of drug release behavior. In addition, the residual surfactant used during the synthesis of nanoparticles will change the glass transition temperature.

Glass Transition Temperature of PLGA Particles and the Influence on Drug Delivery Applications.

Over recent decades, poly(lactic-co-glycolic acid) (PLGA) based nano- and micro- drug delivery vehicles have been rapidly developed since PLGA was approved by the Food and Drug Administration (FDA). Common factors that influence PLGA particle properties have been extensively studied by researchers, such as particle size, polydispersity index (PDI), surface morphology, zeta potential, and drug loading efficiency. These properties have all been found to be key factors for determining the drug release kinetics of the drug delivery particles.

Single and Multiple Stimuli-Responsive Polymer Particles for Controlled Drug Delivery.

Polymers that can change their properties in response to an external or internal stimulus have become an interesting platform for drug delivery systems. Polymeric nanoparticles can be used to decrease the toxicity of drugs, improve the circulation of hydrophobic drugs, and increase a drug's efficacy. Furthermore, polymers that are sensitive to specific stimuli can be used to achieve controlled release of drugs into specific areas of the body.

Solid particles adsorbed on capillary-bridge-shaped fluid polystyrene surfaces.

Particles adsorbed on microscopic polystyrene (PS) capillary bridge surfaces were observed to investigate their motion under capillary forces arising from a nonuniform shape. Capillary bridges were created by placing thin PS films, heated above the glass transition temperature (Tg), between two electrodes with an air gap between the surface of the PS and the upper electrode. Silica particles, 100 nm in diameter, were placed on the surface of the PS capillary bridges, and the sample was heated above the Tg of PS to enable particle motion.

Density fluctuations and phase transitions of ferroelectric polymer nanowires.

Phase transitions of polymeric materials are accompanied by changes in density as a function of temperature. Being able to measure these changes in polymeric systems in one, two or three dimensions on the nanoscopic length-scale is a challenge, but it would provide a simple route to assess phase transitions in nanoscopically confined systems. It is shown that the measurement of the dielectric permittivity in the high frequency limit (in spectral regions not affected by dielectric dispersions) offers an effective and very sensitive means to assess density fluctuations, and hence phase transitions, in nanoscopic systems.

Elastomeric flexible free-standing hydrogen-bonded nanoscale assemblies.

Poly(ethylene oxide) (PEO) is a key material in solid polymer electrolytes, biomaterials, drug delivery devices, and sensors. Through the use of hydrogen bonds, layer-by-layer (LBL) assemblies allow for the incorporation of PEO in a controllable tunable thin film, but little is known about the bulk properties of LBL thin films because they are often tightly bound to the substrate of assembly. The construction technique involves alternately exposing a substrate to a hydrogen-bond-donating polymer (poly(acrylic acid)) and a hydrogen-bond-accepting polymer (PEO) in solution, producing mechanically stable interdigitated layers of PEO and poly(acrylic acid) (PAA).