Release of liposome-encapsulated calcein from liposome entrapping gelatin-carboxymethylcellulose films: a presentation of different possibilities

Liposome entrapment in films consisting of gelatin (GEL) or GEL/sodium carboxymethylcellulose (NaCMC) mixtures, as a method to alter drug release kinetics from polymeric films and/or incorporate sensitive bioactive molecules in solid films, was investigated. Bulk or thin complex (liposome trapping) films were formed by crosslinking (with glutaraldehyde) solutions of GEL or GEL/NaCMC in presence of calcein-encapsulating or rhodamine-labeled liposomes (Rho-Lip). Rho-Lip were observed by confocal microscopy to be homogenously distributed in the films. Calcein release from films was evaluated for periods up to 25 d, and it was found that several possibilities, concerning the release of the liposome-encapsulated molecule from the films, are offered; (i) Release can be sustained, if large liposomes are entrapped in the films. In this case the liposome-encapsulated molecules are released from the films only after they have been released from the vesicles, and the release can be controlled by modifying the film composition, the network density and/or the film geometry. (ii) Intact small unilamellar liposomes (SUV) can be released from the polymeric films depending on their swelling degree. The later can be controlled by modulating the film composition and amount of crosslinker. Film composition also affects the integrity of the film-entrapped liposomes during the crosslinking process, possibly due its effect on the density of the polymeric network of the film.     

Protective coatings on extensible biofibres

Formulating effective coatings for use in nano- and biotechnology poses considerable technical challenges. If they are to provide abrasion resistance, coatings must be hard and adhere well to the underlying substrate. High hardness, however, comes at the expense of extensibility. This property trade-off makes the design of coatings for even moderately compliant substrates problematic, because substrate deformation easily exceeds the strain limit of the coating. Although the highest strain capacity of synthetic fibre coatings is less than 10%, deformable coatings are ubiquitous in biological systems. With an eye to heeding the lessons of nature, the cuticular coatings of byssal threads from two species of marine mussels, Mytilus galloprovincialis and Perna canaliculus, have been investigated. Consistent with their function to protect collagenous fibres in the byssal-thread core, these coatings show hardness and stiffness comparable to those of engineering plastics and yet are surprisingly extensible; the tensile failure strain of P. canaliculus cuticle is about 30% and that of M. galloprovincialis is a remarkable 70%. The difference in extensibility is attributable to the presence of deformable microphase-separated granules within the cuticle of M. galloprovincialis. The results have important implications in the design of bio-inspired extensible coatings.     

Liking of food textures and its relationship with oral physiological parameters and mouth-behavior groups

Researchers have categorized people into four “mouth-behavior” groups based on their oral processing preferences, and claimed that members of those mouth-behavior groups differ in their food texture preferences. If people could be classified into groups based on their liking of different textures, food products could be targeted to specific subgroups, potentially enhancing consumer acceptability. In the first part of our study, we grouped people based on their liking ratings of a wide variety of food textures by asking 288 participants to rate their liking of 106 food texture attributes in an online survey. In the second part of our study, we further examined relationships among individuals' food texture liking ratings, mouth-behavior group membership, and measurements of four oral physiological parameters (saliva flow rate, chewing efficiency, biting force, and particle size sensitivity). One-hundred participants completed the online survey on food texture liking, classified themselves into one of four mouth-behavior groups (Chewers, Crunchers, Smooshers, and Suckers), and were measured for four oral physiological parameters. We refuted the idea that large texture-liking subgroups exist. Although our participants self-categorized themselves into the four mouth-behavior groups similarly to previous researchers, our texture liking measurements did not support the presumed preferences of those mouth-behavior groups. Clustering of participants on their oral physiological measurements produced a “low particle-size sensitivity” cluster, a “high biting force” cluster, a “high saliva flow rate” cluster, and a “low saliva flow and low chewing efficiency” cluster. Neither our texture liking nor our oral physiological measurements predicted membership in the four mouth-behavior groups.     

Salt-Sensitive Hypertension in GR+/− Rats Is Accompanied with Dysregulation in Adrenal Soluble Epoxide Hydrolase and Polyunsaturated Fatty Acid Pathways

Mutations within the glucocorticoid receptor (GR) gene locus lead to glucocorticoid resistance which is characterized by several clinical symptoms such as adrenal gland hyperplasia and salt-sensitive hypertension, although the underlying mechanisms are still unknown. We studied GR haploinsufficient (GR^+/−) Sprague Dawley rats which, on a standard diet, showed significantly increased plasma aldosterone and corticosterone levels and an adrenocortex hyperplasia accompanied by a normal systolic blood pressure. Following a high salt diet, these rats developed salt-sensitive hypertension and maintained elevated enzyme-soluble epoxide hydrolase (sEH) in adrenal glands, while sEH was significantly decreased in wild-type rats. Furthermore, GR^+/− rats showed dysregulation of the equilibrated linoleic and arachidonic acid pathways, with a significant increase of less active metabolites such as 8,9-DiHETrE. In Sprague Dawley rats, GR haploinsufficiency induced steroid disturbances, which provoked hypertension only in combination with high salt intake, which was accompanied by disturbances in sEH and fatty acid metabolism. Our results suggest that sEH inhibition could be a potential target to treat hypertension in patients with GR haploinsufficiency.     

PPAR-Gamma Activation May Inhibit the In Vivo Degeneration of Bioprosthetic Aortic and Aortic Valve Grafts under Diabetic Conditions

Background: We aimed to examine the anti-calcification and anti-inflammatory effects of pioglitazone as a PPAR-gamma agonist on bioprosthetic-valve-bearing aortic grafts in a rat model of diabetes mellitus (DM). Methods: DM was induced in male Wistar rats by high-fat diet with an intraperitoneal streptozotocin (STZ) injection. The experimental group received additional pioglitazone, and controls received normal chow without STZ (n = 20 each group). Cryopreserved aortic donor grafts including the aortic valve were analyzed after 4 weeks and 12 weeks in vivo for analysis of calcific bioprosthetic degeneration. Results: DM led to a significant media proliferation at 4 weeks. The additional administration of pioglitazone significantly increased circulating adiponectin levels and significantly reduced media thickness at 4 and 12 weeks, respectively (p = 0.0002 and p = 0.0107, respectively). Graft media calcification was highly significantly inhibited by pioglitazone after 12 weeks (p = 0.0079). Gene-expression analysis revealed a significant reduction in relevant chondro-osteogenic markers osteopontin and RUNX-2 by pioglitazone at 4 weeks. Conclusions: Under diabetic conditions, pioglitazone leads to elevated circulating levels of adiponectin and to an inhibition of bioprosthetic graft degeneration, including lower expression of chondro-osteogenic genes, decreased media proliferation, and inhibited graft calcification in a small-animal model of DM.     

Localisation of Amylose and Amylopectin in Starch Granules Using Enzyme-Gold Labelling

The independent localisation of amylose and amylopectin in a range of dry and hydrated native starch granules with varying amylose content (0—70 %) has been indirectly visualised using enzyme-gold cytochemical markers. Increasing amylose content was clearly demonstrated to result in distinct changes in granule architecture. In the absence of amylose (waxy maize starch) a framework of closely packed concentric layers of amylopectin exists in the granules. Low amylose content (potato starch) results in alternating layers of densely packed amylopectin and amylose molecules. High amylose content (amylomaize starch) granules were shown to possess an amylopectin centre surrounded by an amylose periphery encapsulated by an amylopectin surface. Elongated granules without the amylopectin centre were also observed in high amylose starches suggesting a relationship between amylopectin, amylose and granule shape. A model of starch granule architecture is proposed where increased compartmentalisation of amylose and amylopectin is observed in granules containing increasing levels of amylose.     

Arsonoliposomes: novel nanosized arsenic-containing vesicles for drug delivery

Natural and synthetic arsenolipids, have been discovered, synthesized, and evaluated for their biological activity. Arsonolipids, are analogs of phosphonolipids, in which P has been replaced by As. The synthesis of arsonolipids has been explored and a simple one-pot method with high yield is currently available for their preparation. However, although arsonolipids posses interesting biophysical and biochemical properties their anticancer or antiparasitic activity is not considered adequate for therapeutic applications. But when arsonolipids are incorporated in liposomes, the vesicles formulated have interesting possibilities, as seen in a number of studies. In cell culture studies, nanosized arsonolipid-containing liposomes or else arsonoliposomes, showed increased toxicity against cancer cells (compared to that of arsenic trioxide) but at the same time were less toxic than arsenic trioxide for normal cells. Furthermore, arsonoliposomes also demonstrate antiparasitic activity in vitro. Nevertheless, As is rapidly cleared from blood after in vivo administration of arsonoliposomes, and this will highly limit possible therapeutic applications. In addition, the fact that arsonoliposomes were observed to aggregate and subsequently fuse into larger particles in presence of cations, may also be considered as a problem. Thereby, methods to modulate the stability of arsonoliposomes and, perhaps, their in vivo distribution (as surface property modification) are currently being investigated. In very recent experiments it has been shown that arsonoliposome pegylation results in the formation of liposomes with very high membrane integrity. In addition, pegylation results in increased physical stability of arsonoliposomes and abolishment of cation-induced aggregation and fusion. Nevertheless, further in vivo studies are required in order to prove if pegylation alters arsonoliposome in vivo kinetics in a positive way, without affecting their activity. From studies performed thus far it is concluded that arsonoliposomes are nanosized-vesicles with interesting properties that justify further exploitation towards the development of therapeutic systems for cancer or parasitic diseases.     

Boride coatings obtained by pack cementation deposited on powder metallurgy and wrought Ti and Ti-6Al-4V

Wear resistance of Ti alloys needs to be improved, and an effective way to achieve this is through surface treatment. Boronizing is a surface treatment in which boron diffuses into the surface of Ti leading to the formation of hard and wear-resistant Ti borides. Boronizing of wrought and/or cast Ti alloys by pack cementation has been studied, while similar coatings on Ti alloys produced by powder metallurgy (PM) have not been reported. Also critical process parameters for boronizing Ti alloys, such as pack cementation powder composition and the process temperature have not been systematically studied and analysed. The present work reports on the surface modification of PM Ti and PM Ti-6Al-4V by boronizing, and presents some important thermodynamic aspects of the process comparing it with similar coatings applied to wrought Ti-6Al-4V. The coatings were characterised using scanning electron microscopy and X-ray diffraction. For both Ti and Ti-6Al-4V alloys the use of amorphous B as a B element supplier in the boriding powder pack led to the formation of a uniform external boride layer, while the use of B₄C as a B element supplier in the pack and under the same boronizing conditions, led to the formation of an external TiN layer and an internal layer containing B. The thermodynamic calculations performed proved successful in determining the appropriate conditions for boride coating deposition and estimating the phases likely to be formed. Finally the effect of surface roughness on the coating quality is discussed.     

Effect of V on Hot Deformation Characteristics of TWIP Steels

Twinning induced plasticity (TWIP) steels, which rely on high Mn contents to promote twinning as the deformation mechanism, exhibit high ultimate strengths together with outstanding combinations of ultimate strength and ductility. In terms of mechanical properties, one of the most important microstructural features is grain size. The knowledge of the kinetics of recrystallization mechanisms, i.e., dynamic recrystallization (DRX) and static recrystallization (SRX), can be used in order to control the grain size of the final product by a proper rolling schedule design. The focus of this work is the characterization of the DRX kinetics of two TWIP steels. The basic composition of the steels is Fe–21Mn–0.4C–1.5Al–1.5Si, and one of them is further alloyed with 0.12% V. With this objective, compression tests were carried out at 900, 1000, and 1100°C and strain rates ranging from 1 × 10^?1 s^?1 to 1 × 10^?4 s^?1. Furthermore, metallographic observation by optical microscopy (OM) was done to assess the evolution of grain size for the different deformation conditions. According to the results, the existence of V in the composition does not affect the hot flow behavior of the steel, although recrystallization fraction and recrystallized grain size decrease for the V‐containing steel.