Preparation of electrospun alginate fibers with chitosan sheath

In this study, alginate (AL) fibers were electrospun and coagulated with chitosan (ChS) and ethanol using a single spinneret. These fibers exhibited a core–sheath structure that was revealed using a confocal laser scanning microscope (CLSM) and fluorescence-labeled polymers. The resulting fibers were examined using a field emission scanning electron microscope (FESEM) for the fiber size and morphology. The average diameter of the fibers ranged from 600 to 900 nm depending on the electrospinning parameters. To mimic the stability of alginate fibers in physiological fluids, the release of alginate from these fibers in normal saline was also tested. The results demonstrated that the core–sheath structure of alginate fiber can greatly reduce the degradation by 40% for 3 d in physiological environment.     

Preparation and properties of alginate/carboxymethyl chitosan blend fibers

Alginate/carboxymethyl chitosan blend fibers, prepared by spinning their mixture solution through a viscose-type spinneret into a coagulating bath containing aqueous CaCl₂, were studied for structure and properties with the aid of infrared spectroscopy (IR), X-ray diffraction (XRD) and scanning electron micrography (SEM). The analyses indicated a good miscibility between alginate and carboxymethyl chitosan, because of the strong interaction from the intermolecular hydrogen bonds. The best values of the dry tensile strength and breaking elongation were obtained when carboxymethyl chitosan content was 30 and 10 wt%, respectively. The wet tensile strength and breaking elongation decreased with the increase of carboxymethyl chitosan content. Introduction of CM-chitosan in the blend fiber improved water-retention properties of blend fiber compared to pure alginate fiber. Antibacterial fibers, obtained by treating the fibres with aqueous solution of N-(2-hydroxy)-propyl-3-trimethylammonium chitosan chloride and silver nitrate, respectively, exhibited good antibacterial activity to Staphylococcus aureus.     

Improved delivery of biocontrolPseudomonas and their antifungal metabolites using alginate polymers

Alginate polymer was evaluated as a carrier for seed inoculation with a genetically modified strainPseudomonas fluorescens F113LacZY, which protects sugar-beet againstPythium-mediated damping-off. F113LacZY survived in alginate beads at 5 log₁₀ CFU/ bead or higher counts for 8 weeks of storage, regardless of the conditions of incubation. In plant inoculation experiments, colonisation of the growing area of the root by F113LacZY, derived from alginate beads placed in the soil next to the seed or from an alginate coating around the seeds, was improved compared with application of just free cells of the strain. F113LacZY trapped in alginate beads was an effective producer of antifungal phloroglucinols as indicated by direct HPLC quantification of phloroglucinols and in vitro inhibition of both the indicator bacteriumBacillus subtilis A1 and the pathogenic fungusPythium ultimum. Alginate polymer represents a promising carrier for the delivery of biocontrol inoculants for root colonisation and production of antifungal metabolites.     

Novel surface entrapment process for the incorporation of bioactive molecules within preformed alginate fibers

A physical entrapment technique has been developed for the surface engineering of preformed alginate fibers. Surface engineering was carried out at room temperature in aqueous solutions without additional solvent, a catalyst/initiator, a chemical cross-linking agent, or a temperature increase. Entrapment of surface-modifying molecules was achieved by exposing the alginate fibers to a Na(+)-rich NaCl/CaCl2 mixture solution, which caused the formation of a moderate dissociation layer into which the modifier could diffuse within a few seconds. The surface dissociation was then reversed by the addition of a large excess of multivalent cations, which resulted in collapse of the interface and immobilization of the modifying species. Rhodamine-tagged poly(ethylene glycol)s of different molecular weights were used as model molecules to investigate the effect of process parameters on the entrapment efficiency. It was found that the entrapment efficiency as well as the distribution of the modifier within the alginate fibers was determined by several factors, including the NaCl/CaCl2 ratio in the preswelling solution, exposure time, and concentration and molecular weight of the modifiers. The morphology of the fibers was not significantly changed in terms of shape and size after the entrapment process. By this technique, poly(L-lysine) (PLL) coupled with cell adhesion peptide sequence GRGDS (PLL-GRGDS) was entrapped within alginate fibers, and it was demonstrated that the modification promoted the attachment of mouse 3T3 fibroblasts.     

Fabrication of artificial endothelialized tubes with predetermined three-dimensional configuration from flexible cell-enclosing alginate fibers

One possible strategy for creating three-dimensional (3D) tissue-engineered organs in vitro is to develop a vasculature for sufficient transport of oxygen and nutrients within these constructs. Here, we describe a novel technique to fabricate endothelialized tubes with predetermined 3D configuration, as a starting point for self-developing capillary-like networks in vitro. Calcium-alginate hydrogel fibers of ca. 250 and 500 mum in diameter, enclosing bovine carotid artery vascular endothelial cells (BECs), were used as templates for endothelialized tubes. Fibers were prepared by extruding a 2% (w/v) sodium alginate solution containing BECs into a 100 mM calcium chloride solution flowing in the same direction. Fibers were embedded in type I collagen gels and enzymatically degraded by alginate lyase, resulting in channels with predetermined 3D configuration filled with a BEC suspension. Cells attached to and covered the surfaces of the channels. Exposing the cells to medium containing basic fibroblast growth factor resulted in their migration into the ambient collagen gel and self-assembly into capillary-like structures. These results demonstrate that using artificial endothelialized tubes with predetermined 3D configuration, as a starting point for a self-developing capillary-like network, could be potentially useful for constructing 3D tissue-engineered organs.     

聚羟基脂肪酸酯(PHA)及其共混纤维研究进展

聚羟基脂肪酸酯(PHA)是代表性的生物基可降解高分子,其种类超过150种,性能多样、可调。文中综述了PHA的研究概况及潜在应用,介绍了四代商业化PHA的性质及其与其他生物基可降解材料形成共混纤维的研究进展。     

Square arrays and their role in ridge formation in human lens fibers

Square arrays in human lens fibers were studied with freeze-fracture and thin-section TEM. In superficial fibers a number of patches of square array particles in the P face and pits in the E face are found in the smooth membrane. In the deeper cortex and the nucleus, fiber cells have undulating membranes and many ridges. Numerous patches of the particles (P face) are distributed in the concave regions, and the pits (E face) in the convex areas of the bumpy membrane. In most ridges, patches of the particles occur at regular intervals in the "valley" portion, while the pits are on the "crest" portion of ridges. Also, continuous square arrays having the same "valley" location as the regularly arranged patches are found in areas with extensive ridge patterns. The overlapping of the outer portions of two adjacent square arrays is found on the sides between the "crest" and the "valley" of the ridges. Structurally, square arrays are located in a nonjunctional part of the membrane; in an orthogonal crystalline arrangement; and with a particle size of about 6 nm and center-center spacing about 6.4 nm. They are structurally different from gap junctions found in the lens fibers. Thin-section studies reveal two types of cellular contacts: thin pentalamellar structures (about 12-13 nm in overall thickness) associated with the ridge patterns are believed to be square arrays; thick heptalamellar structures (about 16-17 nm in overall thickness) with a narrow gap in between the two central laminae are believed to be gap junctions. This study strongly suggests that square arrays are specifically involved in ridge formation in human lens fibers.     

紫花苜蓿的传粉昆虫种类及其访花行为

紫花苜蓿(Medicago sativa)属典型的异花授粉植物,其种子生产主要依靠蜜蜂等传粉昆虫.本文对河西地区张掖实验站紫花苜蓿传粉昆虫种类及其访花行为进行了调查.结果表明:苜蓿访花昆虫共计22种,分别属于4个目,11个科,根据弹花效率初步确定鳞地蜂、黑颚条蜂、净切叶蜂、细切叶蜂和紫木蜂为河西地区主要传粉昆虫;主要传粉昆虫的日活动规律出现单峰型和双峰型2种,净切叶蜂、细切叶蜂和紫木蜂属于前者,只在11:30-15:30出现一个活动高峰,而鳞地蜂与黑颚条蜂则为双峰型,在9:30-11:30和16:30-18:30分别出现访花高峰,不同的传粉昆虫之间存在互补关系;主要传粉昆虫的弹花频率和小花停留时间存在显著差异,且访花行为与野生蜂体型紧密相关.     

Injection of foreign particles and their intracellular translocation in living phloem fibers

Summary Droplets of castor oil 5–10 in diameter were injected into individual cells of living differentiated phloem fibers. The droplets retained their integrity and their movement was recorded on 16-mm movie film. These foreign particles were translocated, along with indigenous particles, by the rotational cytoplasmic currents of the fibers.     

Elastic fibers: building bridges between cells and their matrix

Extracellular elastic fibers confer resilience and flexibility to tissues. Recent studies have identified a protein, fibulin-5, that connects these fibers to cells and regulates their assembly and organization.     

Afferent proprioreceptive fibers in the rat and their distribution in the dorsal roots

The distribution in the dorsal roots of proprioceptive afferent fibres from tibialis anterior (TA) and extensor digitorum longus (EDL) muscles of the rat and the physiological characteristics of the related nervous endings have been investigated. Axons of proprioceptive endings from TA and EDL were found mainly in L4, only a few in L5. Afferent proprioceptive fibres from posterior superficial crural muscles (gastrocnemius, soleus, plantaris) pass mainly through root L5; axons of extrafusal motor units are distributed in a similar way. Sensory endings in TA and EDL were examined, after identification, by means of their static threshold to passive stretch. Almost all steady-state responses to passive stretch, within the physiological extension range, came from muscle spindles. 1-2 to 20 g loads were necessary to obtain steady-state discharges from these receptors. Spindle endings were classified as primary or secondary by measuring the conduction velocity of the afferent fibres, and according to the features of their passive behaviour. Threshold difference cannot be regarded as a fundamental characteristic, because of the considerable overlapping of the values obtained from the two types of endings. Conduction velocities of 50 to 80 m/sec for primary and of 20 to 40 m/sec for secondary afferent fibres were observed. Afferent fibres conducting at intermediate velocity often behave like primary ones. As a rule, tendon organs showed a higher static threshold to passive stretch; the loads employed only rarely elicited a steady-state response. As for these receptors, which usually showed marked adaptation characteristics, passive force is a less effective stimulus than active contraction. The conduction velocity range of afferent fibres from tendon organs is the same as that of primary afferents. The results are discussed.     

Chitosan staple fibers and their chemical modification with some aldehydes

Nine wet-spinning conditions were examined for the preparation of chitosan staple fibers, and novel five N-alkylidene and N-arylidene-chitosan staple fibers were obtained by the post-treatment of the chitosan fibers with aldehydes including vanillin. The tenacity and elongation values of the chitosan filaments were almost unchanged by their post-treatment with monoaldehydes except that with formaldehyde and glyoxal. However, these values decreased significantly in the partially N-modified filaments, which were obtained by the pre-treatment with vanillin. The chitosan filaments (31–79 μm in diameter) had a scaly structure on the filament surface as examined by SEM observation.     

畜禽养殖过程中雌激素的排放及其环境行为

由于存在广泛和较强的内分泌干扰性,环境雌激素越来越受到关注,其中人与动物排放的天然类固醇雌激素(雌酮、雌二醇和雌三醇)具有最强的干扰性。综述了畜禽养殖过程中天然雌激素的排放、危害以及其物化性质,并结合国内外近期研究阐明了天然雌激素的吸附、降解和迁移转化等环境行为。在目前雌激素研究现状的基础上,对未来的研究方向及目标提出了建议。     

Studies on the characteristics of alginate gels in relation to their use in separation and immobilized applications

Studies on diffusion of NAD and hemoglobin from calcium and barium gels are reported where alginate grade, concentration, and gel dimensions were varied. These show that NAD diffusion characteristics are unaffected by alginate and ion concentrations; however, hemoglobin diffusion is affected by alginate concentration. Both hemoglobin and NAD diffusion patterns were shown to be affected by alginate gel dimensions. Studies are reported that show that polymannuronic alginate gels posses good porosity characteristics while polyguluronic alginates from gels with lower porosity, specifically with respect to high-molecular-weight compounds. These findings are discussed with the view to the use of alginate gels for immobilization, solids separation, and diffusion chromatography techniques.     

Diacetyl production by co-immobilized citrate-positiveLactococcus lactis subsp.lactis 3022 and homogenized bovin liver in alginate fibers with double gel layers

Summary Diacetyl production by (Citr⁺)Lactococcus lactis subsp.lactis 3022 cells immobilized in Ca-alginate fine fibers with single layer in the presence of catalase was three times higher than that in the absence of catalase. A co-immobilized culture system of the lactic acid bacterial cells (outer) and the homogenized bovine liver (inner layer) in Ca-alginate fibers with double gel layers was developed. The culture system gave high diacetyl productivity (30 mg/l) for ten repeated batch cultures.     

Creatine kinase reaction in skinned rat psoas muscle fibers and their myofibrils.

The aim of this study was to evaluate myofibrillar creatine kinase (EC 2.7.3.2) activity on the background of the effect of substrate channeling by myosin ATPase and to compare it with creatine kinase (CK) activity of whole skinned fibers. In order to assess CK activity, skinned fibers were prepared from the rat psoas major muscles defined by light microscopy. The activity in permeabilized fibers after treatment with saponin, Triton X-100 and Ca(2+)-free medium reached 2.80, 6.97 and 3.32 micromol ATP min(-1) mg(-1) protein, respectively, when a coupled enzyme assay system with external hexokinase and glucose-6-phosphate dehydrogenase was used. Transmission electron microscopy (TEM) revealed a possible interference among activities of sarcolemmal, sarcoplasmic, myofibrillar and mitochondrial CK from persisting structures. For evaluation of the myofibrillar CK itself, a pure myofibrillar fraction was prepared. Fraction purity was confirmed by TEM and by enzymatic assays for marker enzymes. Two procedures, i.e. the coupled enzyme assay and the evaluation of phosphocreatine (PCr) concentration before and after the CK reaction, were used for measurement of CK activity in this fraction. The procedures resulted in 3.2 nmol ATP min(-1) mg(-1) protein and 7.6 nmol PCr min(-1) mg(-1) protein, respectively. These alternative approaches revealed a discrepancy between the reacting portions of PCr by more than 50 %, which provides information about the size of the effect, generally described as substrate channeling.