Notes

Cobalt as well as steer amounts in cosmetics marketed from local marketplaces in Saudi Arabia.
Microencapsulation of polysaccharidic nanoparticles is met with nanoscale and biological performance changes. This study designs soft agglomerates as nanoparticle vehicle without nanoparticles undergoing physical processes that alter their geometry. The nanoparticles were made of high molecular weight chitosan/pectin with covalent 5-fluorouracil/folate. Nanoparticle aggregation vehicle was prepared from low molecular weight chitosan. The nanoparticles and aggregation vehicle were blended in specific weight ratios to produce soft agglomerates. Nanoparticles alone are unable to agglomerate. Adding aggregation vehicle ( less then 2 μm) promoted soft agglomeration with nanoparticles deposited onto its surfaces with minimal binary coalescence. selleck The large and rough-surfaced aggregation vehicle promoted nanoparticles deposition and agglomeration. A rounder vehicle allowed assembly of nanoparticles-on-aggregation vehicle into agglomerates through interspersing smaller between larger populations. Soft agglomeration reduced early drug release, and was responsive to intracapsular sodium alginate coat to further sustain drug release. The soft agglomerates can serve as a primary oral colon-specific vehicle.Nanocomposites as "stevedores" for co-delivery of multidrugs hold great promise in addressing the drawbacks of traditional cancer chemotherapy. In this work, our strategy presents a new avenue for the stepwise release of two co-delivered agents into the tumor cells. The hybrid nanocomposite consists of a pH-responsive chitosan (CS), a thermosensitive poly(N-vinylcaprolactam) (PNVCL) and a functionalized cell-penetrating peptide (H6R6). Doxorubicin (DOX) and oleanolic acid (OA) are loaded into the nanocomposite (H6R6-CS-g-PNVCL). The system displayed a suitable size (∼190 nm), a high DOX loading (13.2 %) and OA loading efficiency (7.3 %). The tumor microenvironment triggered the nanocomposite to be selectively retained in tumor cells, then releasing the drugs. Both in vitro and in vivo studies showed a significant enhancement in antitumor activity of the co-delivered system in comparison to mono-delivery. This approach which relies on redox, pH and temperature effects utilizing co-delivery nanosystems may be beneficial for future applications in cancer chemotherapy.Heparin was immobilized on magnetic chitosan particles to be used as a tool for human plasma protein identification. Chitosan was magnetized by co-precipitation with Fe2+/Fe3+ (MAG-CH). Heparin was functionalized with carbodiimide and N-hydroxysuccinimide and covalently linked to MAG-CH (MAG-CH-hep). X-ray diffraction confirmed the presence of chitosan and Fe3O4 in MAG-CH. This particle exhibited superparamagnetism and size between 100-300 μm. Human plasma diluted with 10 mM phosphate buffer (pH 5.5) or 50 mM Tris-HCl buffer (pH 8.5) was incubated with MAG-CH-hep, and the proteins fixed were eluted with the same buffers containing increasing concentrations of NaCl. The proteins obtained were investigated by SDS-PAGE, LC/MS, and biological activity tests (PT, aPTT, and enzymatic chromogenic assay). Inhibitors of the serpin family, prothrombin, and human albumin were identified in this study. Therefore, MAG-CH-hep can be used to purify these proteins and presents the following advantages low-cost synthesis, magnetic separation, ion-exchange purification, and reusability.With the growing interest in food safety and in environmental protection, it is more attractive to develop novel biodegradable packaging films. In this regard, one new blending film was prepared with curdlan (CD)/polyvinyl alcohol (PVA)/thyme essential oil. Our results demonstrated that the mechanical properties of the blending film were the best when the ratio of the CD and PVA was 41. Further, the barrier properties of the film were optimized by incorporating with thyme essential oil. It was proved that not only water vapor permeability was lower, but also the elongation at break was improved, when 2% (w/w) thyme essential oil used. The potential interactions of the film matrix were analyzed by FTIR, XRD and Cryo-scanning electron microscopy. Importantly, both the antioxidant activity and antibacterial activity were improved. Finally, the blending film was employed for the preservation of chilled meat, while the shelf life was extended up to 10 days.A quick control of heavy hemorrhaging is critical to save the life of injured person. Herein we developed a hemostat of chitosan@calcium alginate microspheres through combination of microemulsion, polyelectrolyte complexation coating, and thermally induced phase separation. The alginate coated microspheres featured a structure of a porous chitosan core and a compact calcium alginate shell layer. Their in vitro and in vivo hemostatic properties were evaluated by the whole blood clotting kinetics, and rat tail amputation and liver laceration models. Compared to the porous chitosan microspheres, the alginate coated microspheres showed much enhanced hemostatic efficiency. The latter formed bigger blood clots; its hemostatic time on the liver laceration was substantially shortened to 53 ± 10 s from 107 ± 9 s of the former. It was shown that calcium ions released from the calcium alginate layer may accelerate the formation of blood clots. Such a biocompatible microsphere is a promising quick hemostat for controlling traumatic bleeding.Cellulose limited by fusibility and solubility is impossible to be directly thermoformed, of which the existing progress crucially relies on larger liquids, making it hard to achieve a direct all-green manufacture. Here, we propose an innovative strategy that the surface molecular chains of cellulose nanospheres are activated at 100 °C and intertwined under 500 MPa because of the high molecular activity on the surface of nanospheres and the reduction of activation energy after ball-milling. It is confirmed that only physical changes are involved, according to infrared spectrum. Results show that applicable mechanical properties (hardness and modulus reach 0.44 and 9.66 GPa, respectively) are successfully obtained. Simultaneously, the optimum optical performance of all-cellulose substrate reaches more than 80 % at visible light. Combined with their intrinsic properties, these cellulose-based products could be potentially utilized as biomass substrates. Therefore, our innovative strategy opens up a door for the direct thermoforming of cellulose.Maize starches of different amylose contents were co-gelatinized with caffeic acid (CA), quercetin (Qu) and epigallocatechin gallate (EGCG), respectively. The decomposition temperature of waxy maize starch (WS)-CA blends was increased compared to WS, while that of normal maize starch (MS) and high amylose starch (HS) was decreased. The more complex of the phenolic compounds, the lower the decomposition temperature of the MS. The results of Fourier-transform infrared spectroscopy suggested that CA increased short range ordered structure of gelatinized WS but decreased that of gelatinized MS and HS. Hydrogen bonds associated with CA and starch led to the arrangement of ordered structures in different starch. Nuclear magnetic resonance (NMR) indicated that all hydroxyl groups of CA and EGCG formed hydrogen bonds, while hydroxyl group at C-4' of quercetin had priority to form hydrogen bonds. During co-gelatinization process, more single helixes were induced in MS by CA than Qu or EGCG did.The present study reports on the comprehensive physico-mechanical evaluation of 3D printable alginate-methylcellulose hydrogels with bioactive components (Manuka honey, aloe vera gel, eucalyptus essential oil) using a combined experimental-numerical approach. The 3D printable carbohydrate inks demonstrated good swelling properties under moist conditions and adequate antimicrobial and antibiofilm efficacy against both Gram positive and negative bacteria. The effect of the bioactive compounds on the viscosity and mechanical properties of the 3D printable hydrogels was assessed with rheological, nanoindentation and shear test measurements. All hydrogel compositions showed good biocompatibility on human dermal fibroblasts, stimulating cell growth as confirmed by an in vitro wound healing assay. Finite element analysis simulation was employed to further advance the calculation accuracy of the nanoindentation tests, concluding that combination of an experimental and a numerical technique may constitute a useful method to characterize the mechanical behavior of composite hydrogel films for use in wound healing applications.Accumulation of protein-bound uremic toxins (PBUTs) has a high incidence in the blood of hemodialysis-treated patients with chronic kidney disease. Development of adsorbent for the high-efficient, selective, and removal of various PBUTs is still challenging because of their strong interactions to the corresponding binding proteins and the complex blood background. Herein, we reported poly-cyclodextrins adsorbents with multi adsorption-sites for PBUTs removal from plasma. Compared to poly-α-cyclodextrin and poly-γ-cyclodextrin, poly-β-cyclodextrin (PβCD) showed the best adsorption capability and the maximum p-cresol sulfate (PCS, a model PBUT) binding capacity of PβCD (263 mg g-1). Combining with hemodialysis, PβCD adsorbents added into the dialysate can remove 96 % PCS in the plasma via adsorbent once-through mode. Additionally, various PBUTs co-exsiting in the plasma could be effectively removed, exhibiting high-concentrition PBUT adsorption property of PβCD. We expect that the PCD adsorbents combining with hemodialysis therapy may become a promising potential for clinical PBUT removal.Nanocelluloses, both cellulose nanofibrils and cellulose nanocrystals, are gaining research traction due to their viability as key components in commercial applications and industrial processes. Significant efforts have been made to understand both the potential of assembling nanocelluloses, and the limits and prospectives of the resulting structures. This Review focuses on bottom-up techniques used to prepare nanocellulose-only structures, and details the intermolecular and surface forces driving their assembly. Additionally, the interactions that contribute to their structural integrity are discussed along with alternate pathways and suggestions for improved properties. Six categories of nanocellulose structures are presented (1) powders, beads, and droplets; (2) capsules; (3) continuous fibres; (4) films; (5) hydrogels; and (6) aerogels and dried foams. Although research on nanocellulose assembly often focuses on fundamental science, this Review also provides insight on the potential utilization of such structures in a wide array of applications.Although core-shell structure is favored by many applications, preparing it with green way is rarely been reported. Herein, a core-shell structured Cu@Pd-CS nanocomposite is greenly fabricated utilizing a natural chitosan and applied to glucose detection. As-obtained Cu@Pd-CS nanoparticles were characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and powder X-ray diffraction (XRD). When applied to glucose detection, the Cu@Pd-CS exhibits good stability, sensitivity and anti-interference. Moreover, it has a good linear relationship in glucose concentrations range of 0.1-1 mM with the sensitivity of 1.53 μA mM-1 cm-2 and 1-10 mM with the sensitivity of 23.00 μA mM-1 cm-2. This work proves the practicability of building metal-based core-shell structure nanoparticles with green resources and glucose detection application.
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