Dextran

Periodate oxidized dextran has been widely studied in a broad range of biotechnological applications, regardless of this, usually little attention is paid to the oxidation extension consequences on the properties of the final modified dextran. Based on a bidimensional NMR analysis, we suggest that the two aldehydes groups, resulting from the periodate oxidation, are not fully reactive with N-nucleophiles, under certain pH conditions. The aldehyde group bonded to C3 appeared to be the only prone to react. The other aldehyde might be arrested in more stable hemiacetal structures. The hemiacetals are also responsible for oxidized dextran crosslinking, interfering in simple processing steps, such as dissolution and solubility, as well as increasing the viscosity of the solutions. The molecular weight variation on the oxidized samples can be followed by dynamic mechanical thermal analysis in consequence of the variation of glass transition temperature with the molecular weight, which was corroborated by the onset temperature of the thermal degradation.

Initiator-free injectable hydrogels are very interesting for drug and/or cell delivery applications, since they can be administered in a minimally invasive way, and avoid the use of potentially harmful chemical initiators. In the current work, oxidized dextran crosslinked with adipic acid dihydrazide hydrogels were further characterized and tuned to produce formulations, with the aim of producing an injectable formulation for the possible treatment of posterior eye diseases. The gelation rate and the hydrogel dissolution profile were shown to be dependent on the balance between the degree of dextran oxidation, and the concentration of both components. For the in vitro studies, rabbit corneal endothelial cells were seeded on the hydrogels to assess cytotoxicity. Hydrogels prepared with low oxidized dextrans were able to promote cell adhesion and proliferation to confluence in just 24 h, while more highly oxidized samples promoted cell adhesion and proliferation, but without achieving confluence. Cell viability studies were performed using MTS assays to verify the non-cytotoxicity of hydrogels and their degradation byproducts, rendering these formulations attractive for further in vivo studies.

Plants gums are complex mixtures of different polysaccharides with a variety of biological activities and pharmaceutical applications. Few studies have focused on physicochemical and biological properties of gums obtained from different plants. This study was designed to determine potential pharmaceutical and pharmacological values of the gum exudates and its isolated biopolymers obtained from Astragalus myriacanthus Boiss [syn. Astracantha myriacantha (Boiss.) Podlech] (Fabaceae). The physicochemical, rheological, and mucoadhesion properties of the gum and its fractions was measured at 7, 27, and 37 °C with and without the presence of NaCl (1%). Also, the structural and immunomodulatory properties of several water soluble biopolymers isolated using ion exchange and size exclusion chromatographic methods were investigated on Jurkat cells at concentrations of 31.25, 62.5, 125, 250, 500 and 1000 μg/mL. The consistency and shear-thinning property of the gum and its fractions decreased as temperature increased. In the presence of NaCl, the consistency increased but no regular pattern was observed regarding to shear-thinning behavior. The mucoadhesion strength was 40.66 ± 2.08 g/cm 2 which is suitable for use as a formulary mucoadhesive polymer. The isolated biopolymers had proteo-arabinoglycan structure. Their molecular weight was calculated to be 1.67-667 kDa. One biopolymer had a proliferative effect and others had dose dependent cytotoxic/proliferative properties. The crude gum and its insoluble fraction showed suitable mucoadhesion, swellability and rheological properties which makes them suitable for designing drug delivery systems. The gum proteo-arabinoglycans with different molecular weight and structures had different immunomodulatory properties.

Injectable and degradable hydrogels are very interesting networks for drug delivery and cell transplantation applications since they can be administered in the human body in a minimally invasive way. In most cases, the crosslinking reaction occurs by photopolymerisation or free radical polymerisation; however, the use of chemical initiators may promote cell death. In the current work, injectable and degradable dextran-based hydrogels were prepared without the use of initiators. Dextran, a natural glucose-containing polysaccharide, was oxidized with sodium periodate (dexOx) and the derivatives characterized by NMR and FTIR spectroscopy's as well as by colorimetric techniques. The oxidized derivatives were crosslinked with adipic acid dihydrazide (AAD), forming a gel within 2–4 min. The obtained hydrogels were characterized by their mechanical properties, swelling and degradation behavior under physiologic conditions. In addition, the hydrogel interior morphology as well as porous structure was evaluated by scanning electron microscopy (SEM) and mercury intrusion porosimetry (MIP). MIP analysis showed that dexOx hydrogels crosslinked with 10% of AAD were macroporous with pore sizes ranging from 0.32 to 0.08 μm. As expected, the average pore size increased during hydrogel degradation as confirmed by SEM and MIP studies.

Acetalated Dextran (Ac-Dex) is a promising pH-sensitive biocompatible and biodegradable polymer for nanomedicine applications. In this work, Ac-Dex nanoparticles were synthesized by two different solvent evaporation methods, the single nanoemulsion and the double nanoemulsion. The Ac-Dex particles were characterized by Scanning Electron Microscopy and the synthesis of highly homogeneous spherical particles was verified. Then, an optical fiber sensor based on quasi-elastic light scattering and comprised of only single-mode optical fibers and standard telecommunication devices showed sensitivity regarding the nanoparticles concentrations and was used for monitoring their degradation over 12 h under pH and temperature conditions of cancerous tissues. The results revealed a well-controlled degradation pattern, corroborating the suitability of the modified polymer to the release of active compounds in a sustainable manner and also demonstrating the applicability of the sensor for the in-situ evaluation of the degradation.

In this study, we aimed to determine the in vitro activity of Leuconostoc mesenteroides var. mesenteroides isolatedfrom sugar-industry effluents to produce a dextran bioflocculant from sucrose as a low-cost substrate.L. mesenteroides strains present in residual cane juice from a sugar factory were isolated and biochemicallyidentified using Mayeux, Sandine, and Elliker agar (MSE) as a selective medium. The strain number 3 (LM03) wasbiochemically identified as L. mesenteroides var. mesenteroides, which was used for this study. The concentrationof dextran was quantified by dry weight, the morphology and purity were evaluated using Fourier-transforminfrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy(EDS). Flocculation was evaluated via turbidimetric assays in different pH ranges from sugar-industry effluentsand doses of dextran.To evaluate the flocculant activity according to the effect of pH, a jar test kit from Phipps and Bird, US...

The cellular environment is crowded by macromolecules of various sizes, shapes, and charges, which modulate protein structure, function and dynamics. Herein, we contemplated the effect of three different macromolecular crowders: dextran-40, ficoll-70 and PEG-35 on the structure, active-site conformational dynamics, function and relative domain movement of multi-domain human serum albumin (HSA). All the crowders used in this study have zero charges and similar sizes (at least in the dilute region) but different shapes and compositions. Some observations follow the traditional crowding theory. For example, all the crowders increased the α-helicity of HSA and hindered the conformational fluctuation dynamics. However, some observations are not in line with the expectations, as an increase in the size of HSA with PEG-35 and uncorrelated domain movement of HSA with ficoll-70 and PEG-35. The relative domain movement is correlated with the activity, suggesting that such moves are essential for protein function. The interaction between HSA and ficoll-70 is proposed to be hydrophobic in nature. Overall, our results provide a somewhat systematic study of the shape-dependent macromolecular crowding effect on various protein properties and present a possible new insight into the mechanism of macromolecular crowding

The bio-compatible magnetic nanoparticles of maghemite were prepared by a chemical co-precipitation method and dextran was selected as the surfactant to suspend them. By transmission electron microscopy (TEM), the iron oxide nanoparticles appeared nearly spherical with an average diameter of about 8.0 ±1 nm. SAED pattern of iron oxide nanoparticles is indexed by a cubic γ-Fe 2 O 3 , the diffraction rings are attributed to the (220), (311), (400), (422), (511) and (440) planes, respectively. Regular fringes are clearly observed in the nanoparticle with a spacing of 0.24 nm , whigh is the (311) interplanar distance of the cubic maghemite. This is in perfect agreement with the X-Ray Diffraction (XRD) results, indicating that the nanoparticles are well crystallyzed in spite of their ultrafine sized. The attachment of the dextran on the particle surface was confirmed by Fourier Transform Infrared (FTIR) Spectroscopy. The biocompatibility of maghemite nanoparticles covered by dextran with...

The industrial Leuconostoc strain B/110-1-2 producing dextran and dextran derivatives was taxonomically identified by 16S rRNA as L. citreum. Its dextransucrase enzymes were characterized according to their cellular location and reaction specificity. In the presence of sucrose, the strain B/110-1-2 produced two cell-associated dextransucrases (31.54% of the total glucosyltransferase activity) with molecular weights of 160 and 240 kDa and a soluble dextransucrase (68.46%) at 160–180 kDa. Two open reading frames (ORF) coding for L. citreum strain B/110-1-2 dextransucrases were identified. One of them shared a 52% identity with the alternansucrase ASR of L. citreum NRRL B-1355 and with a putative annotated alternansucrase sequence found in the genome of L. citreum KM20. The structural analysis (HPAEC-PAD, HPSEC, and 13C-NMR) of the polymer and oligodextrans produced by the B/110-1-2 dextransucrases suggest this novel glucansucrase has specificity similar to a dextransucrase but not to an alternansucrase, producing a soluble linear dextran with glucose molecules linked mainly in α-1,6 and α-1,3 with α-1,4 branches. These results enhance the understanding of this industrially significant strain and will aid in distinguishing between physiologically similar Leuconostoc spp. strains.