Zinc(II) Complexes of Amino Acids as New Active Ingredients for Anti-Acne Dermatological Preparations

Zinc compounds have a number of beneficial properties for the skin, including antimicrobial, sebostatic and demulcent activities. The aim of the study was to develop new anti-acne preparations containing zinc–amino acid complexes as active ingredients. Firstly, the cytotoxicity of the zinc complexes was evaluated against human skin fibroblasts (1BR.3.N cell line) and human epidermal keratinocyte cell lines, and their antimicrobial activity was determined against Cutibacterium acnes. Then, zinc complexes of glycine and histidine were selected to create original gel formulations. The stability (by measuring pH, density and viscosity), microbiological purity (referring to PN-EN ISO standards) and efficacy of the preservative system (according to Ph. Eur. 10 methodology) for the preparations were evaluated. Skin tolerance was determined in a group of 25 healthy volunteers by the patch test. The preparations containing zinc(II) complexes with glycine and histidine as active substances can be topically used in the treatment of acne skin due to their high antibacterial activity against C. acnes and low cytotoxicity for the skin cells. Dermatological recipes have been appropriately composed; no irritation or allergy was observed, and the preparations showed high microbiological purity and physicochemical stability.     

Impact of the addition of dolomite to cream-firing clays on the technological and color properties of sintered ceramics

Sintered ceramics, represented by ceramic tiles or clinker bricks, are widely used in the building materials industry due to their technological properties and visual qualities. The topic of color changing of ceramic materials from cream-firing clays with the use of mineral additives has not been addressed to date. The aim of the paper was to investigate the effect of granulation of dolomite additives to ceramic masses based on cream-firing Borkowice clay on the color and properties of fired ceramic materials. The paper proposes that grain size of mineral additive affects the color of sintered ceramics. In order to confirm this hypothesis, a number of experiments were performed, consisting of determination of the color and technological properties of ceramic materials. The conducted tests showed that the color and technological properties of sintered ceramics are influenced by the grain size of the additives used.     

Transdermal Delivery Systems for Ibuprofen and Ibuprofen Modified with Amino Acids Alkyl Esters Based on Bacterial Cellulose

The potential of bacterial cellulose as a carrier for the transport of ibuprofen (a typical example of non-steroidal anti-inflammatory drugs) through the skin was investigated. Ibuprofen and its amino acid ester salts-loaded BC membranes were prepared through a simple methodology and characterized in terms of structure and morphology. Two salts of amino acid isopropyl esters were used in the research, namely L-valine isopropyl ester ibuprofenate ([ValOiPr][IBU]) and L-leucine isopropyl ester ibuprofenate ([LeuOiPr][IBU]). [LeuOiPr][IBU] is a new compound; therefore, it has been fully characterized and its identity confirmed. For all membranes obtained the surface morphology, tensile mechanical properties, active compound dissolution assays, and permeation and skin accumulation studies of API (active pharmaceutical ingredient) were determined. The obtained membranes were very homogeneous. In vitro diffusion studies with Franz cells were conducted using pig epidermal membranes, and showed that the incorporation of ibuprofen in BC membranes provided lower permeation rates to those obtained with amino acids ester salts of ibuprofen. This release profile together with the ease of application and the simple preparation and assembly of the drug-loaded membranes indicates the enormous potentialities of using BC membranes for transdermal application of ibuprofen in the form of amino acid ester salts.     

The effect of La2O3 and CeO2 modifiers on properties of Ni–Al catalysts for LNG prereforming

Ni/La–Al₂O₃ and Ni/Ce–Al₂O₃ catalysts with a small amount of promoters intended for prereforming of LNG were characterized by XRF, N₂ adsorption-desorption, XRD, H₂ chemisorption, HRTEM and XPS. The catalytic activity was evaluated in methane steam reforming both in the kinetic and diffusion regime, at temperatures characteristic of pre-reforming. Carbonaceous deposit was analysed by TPO-MS method. The nature and location of the coke were studied by HRTEM.La or Ce addition into Ni–Al system causes the increase of the active surface area of Ni by enhancing its dispersion. Studies at kinetic regime have shown that the promoted catalysts have almost twice the activity than reference Ni–Al catalyst. This effect was not confirmed by measurements in the diffusion regime on whole catalyst tablets. Almost identical textural properties of catalysts and diffusive limitations related to them but not the catalytic properties of the material itself appeared to be crucial factors. The presence of La (but not Ce) causes a significant increase in resistance to coking.     

Physicochemical and Biological Characterisation of Diclofenac Oligomeric Poly(3-hydroxyoctanoate) Hybrids as β-TCP Ceramics Modifiers for Bone Tissue Regeneration

Nowadays, regenerative medicine faces a major challenge in providing new, functional materials that will meet the characteristics desired to replenish and grow new tissue. Therefore, this study presents new ceramic-polymer composites in which the matrix consists of tricalcium phosphates covered with blends containing a chemically bounded diclofenac with the biocompatible polymer—poly(3-hydroxyoctanoate), P(3HO). Modification of P(3HO) oligomers was confirmed by NMR, IR and XPS. Moreover, obtained oligomers and their blends were subjected to an in-depth characterisation using GPC, TGA, DSC and AFM. Furthermore, we demonstrate that the hydrophobicity and surface free energy values of blends decreased with the amount of diclofenac modified oligomers. Subsequently, the designed composites were used as a substrate for growth of the pre-osteoblast cell line (MC3T3-E1). An in vitro biocompatibility study showed that the composite with the lowest concentration of the proposed drug is within the range assumed to be non-toxic (viability above 70%). Cell proliferation was visualised using the SEM method, whereas the observation of cell penetration into the scaffold was carried out by confocal microscopy. Thus, it can be an ideal new functional bone tissue substitute, allowing not only the regeneration and restoration of the defect but also inhibiting the development of chronic inflammation.     

Heat generated during electrochemical double-layer capacitor “self-discharge”

Eight commercial 10F electrochemical double-layer capacitors (EDLCs) were connected together and placed in a container filled with mineral oil. The whole system was placed into a Dewar container. Temperature variation and heat exchanged between the test EDLC and the environment during its charging, discharging, and “self-discharge” were measured, together with voltage U changes. Charge separation during charging was equivalent to a transition into a more ordered system, which results in entropy decrease, while discharging caused entropy increase (the Peltier–Seebeck effect). Consequently, a number of charging/discharging cycles led to a corresponding series of entropy and temperature changes. The final shape of temperature versus time curve during charging/discharging cycles was due to overlapping of irreversible Joule–Lenz and reversible Peltier heats. When charged EDLC was kept under the open-circuit condition, measured heat flow was negligible in comparison to energy loss calculated from potential drop, assuming that energy E accumulated is proportional at any time to voltage to the second power (i.e., E ~ U ²). The result was interpreted assuming that the EDLC “self-discharge” phenomenon is not associated with energy loss by the device, but rather with charge redistribution between EDLC particles characterized by different time constants.     

Phase structure and thermal stability of crosslinked polyurethane elastomers based on well‐defined prepolymers

Taking advantage of the DSC method, general procedures were presented for qualitative and quantitative evaluation of the phase separation degree and the crystalline phase content in polyurethane elastomers with well‐defined structures. Those elastomers were obtained not only in a typical one‐step method but also in the prepolymer method with the use of urethane oligomers with controlled molecular weight distribution (MWD). Prepolymers with well defined chain structures and narrow distributions of their molecular weights (MWD) M _w/M _n = 1.1–1.3 were produced in a multistage method, i.e., in step‐by‐step polyaddition of 2,4‐ and 2,6‐TDI with polyoxyethylenediols or with polycaprolactonediols of varied molecular weights. Isocyanate oligomers obtained at individual stages were then crosslinked with triethanolamine, whereas hydroxyl‐terminated oligomers were crosslinked with 4,4′,4″‐triphenylmethane triisocyanate (Desmodur RE). The obtained polyurethane elastomers were found to be characterized by the presence of five phases: soft phase consisted of flexible polyol‐type segments, crystalline phase made of soft segments, crystalline and amorphous hard phase made of hard segments, and intermediate phase, which was a composition of the soft and hard segments. The polyurethanes obtained out of prepolymers with defined MWD were characterized by better phase separation of the soft segments and increased structural order inside the hard phase as well as by better thermal stability than polyurethanes obtained from the typical one‐step method. The structural effects were also discussed on the thermal properties of the synthesized elastomers as analyzed by the TG and DTA methods. © 2007 Wiley Periodicals, Inc. J Appl PolymSci 104: 1464–1474, 2007     

The HLA-G Immune Checkpoint Plays a Pivotal Role in the Regulation of Immune Response in Autoimmune Diseases

The human G-leukocyte antigen (HLA-G) molecule is a non-classical major histocompatibility complex (MHC) class I molecule. The pertinence of HLA-G has been investigated in numerous studies which have sought to elucidate the relevance of HLA-G in pathologic conditions, such as autoimmune diseases, cancers, and hematologic malignancies. One of the main goals of the current research on HLA-G is to use this molecule in clinical practice, either in diagnostics or as a therapeutic target. Since HLA-G antigens are currently considered as immunomodulatory molecules that are involved in reducing inflammatory and immune responses, in this review, we decided to focus on this group of antigens as potential determinants of progression in autoimmune diseases. This article highlights what we consider as recent pivotal findings on the immunomodulatory function of HLA-G, not only to establish the role of HLA-G in the human body, but also to explain how these proteins mediate the immune response.     

Synthesis of Dolichols in Candida albicans Is Co-Regulated with Elongation of Fatty Acids

Protein glycosylation requires dolichyl phosphate as a carbohydrate carrier. Dolichols are α-saturated polyprenols, and their saturation in S. cerevisiae is catalyzed by polyprenyl reductase Dfg10 together with some other unknown enzymes. The aim of this study was to identify such enzymes in Candida. The Dfg10 polyprenyl reductase from S. cerevisiae comprises a C-terminal 3-oxo-5-alpha-steroid 4-dehydrogenase domain. Alignment analysis revealed such a domain in two ORFs (orf19.209 and orf19.3293) from C. albicans, which were similar, respectively, to Dfg10 polyprenyl reductase and Tsc13 enoyl-transferase from S. cerevisiae. Deletion of orf19.209 in Candida impaired saturation of polyprenols. The Tsc13 homologue turned out not to be capable of saturating polyprenols, but limiting its expression reduce the cellular level of dolichols and polyprenols. This reduction was not due to a decreased expression of genes encoding cis-prenyltransferases from the dolichol branch but to a lower expression of genes encoding enzymes of the early stages of the mevalonate pathway. Despite the resulting lower consumption of acetyl-CoA, the sole precursor of the mevalonate pathway, it was not redirected towards fatty acid synthesis or elongation. Lowering the expression of TSC13 decreased the expression of the ACC1 gene encoding acetyl-CoA carboxylase, the key regulatory enzyme of fatty acid synthesis and elongation.