Glucose dextran

Parenteral preparations are regularly prepared aseptically a short time or immediately prior to administration. Compounds susceptible to hydrolysis or oxidative decomposition in solution are preferentially stored as dry powders, concentrates under an inert atmosphere, or in combination with stabilizers. Concentrates for injections or infusions (European Pharmacopoeia, 2002) are diluted prior to administration, usually with sterilized Water for injection (European Pharmacopoeia, 2002) or sterile, isotonic solutions of sodium chloride, glucose, dextran, or buffer (see Table 14.3). Powders for injections or infusions (European Pharmacopoeia, 2002) are dissolved or suspended in the same media. Vitamins are aseptically added ex tempore to TPN preparations due to poor stability and the risk of precipitation (Hutchinson, 1998), as are trace metals that may influence the stability of the TPN formulation. A limited number of drugs may also be dissolved in the TPN infusion prior to administration (Hutchinson, 1998). 

Much of the degraded plant polysaccharide is converted into bacterial biomass. Radiolabelled glucose, dextran and plant tissues have been added to soils to determine the fate of plant polysaccharides. Appreciable amounts of radiolabel become localised in bacterial exopolysaccharides. 

Polarimetric determination of the sucrose concentration of a solution is vaUd when sucrose is the only optically active constituent of the sample. In practice, sugar solutions are almost never pure, but contain other optically active substances, most notably the products of sucrose inversion, fmctose and glucose, and sometimes also the microbial polysaccharide dextran, which is dextrorotatory. Corrections can be made for the presence of impurities, such as invert, moisture, and ash. The advantage of polarization is that it is rapid, easy, and very reproducible, having a precision of 0.001°. 

Glucose A 6-carbon sugar molecule, which is the building block of natural substances like cellulose, starch, dextrans, xanthan, and some other biopolymers and used as a basic energy source by the cells of most organisms. 

FIGURE 16.5 Broad standard calibration (linear mode) of a semipreparative Sephacryl S-IOOO system (95 x 1.6 cm) with an aqueous mixture of Blue Dextran, Dextran T-SOO, and glucose eluent 0.005 M NaOH V, i = 75 ml. = 162 ml. 

The selective separation range of the S-500/S 1000-system for glucans is shown for hybrid starch Triticale T22. This mixture of scb and nb/lcb glucans contains components in the range between approximately dp 50-300,000 glucose monomers (Fig. 16.11). The degree of polymerization distribution obtained from dextran-based calibration was computed as well in terms of... 

FIGURE 16.13 Degree of polymerization distribution (m dpD d) for synthesized amylose -type nb/lcb glucans calculated from dextran-calibrated — amylose-converted calibration of S-SOO/S-IOOO dp. = SSI [glucose units]. 

Briefly summarized, S-1000 shows better resolution in the high dp range, whereas the CL 2B system resolves low dp components better. Due to these differences in separation performance, the degree of polymerization distribution and degree of polymerization average values for the same sample obtained from broad scb— nb/lcb-transformed dextran calibration yielded dp = 29,900 glucose units for the S-1000 system and dp = 21,100 glucose units for the CL 2B system (Fig. 16.18). 

Homopolysaccharides are synthesised by relatively few spedfic enzymes and are not constructed from subunits. The commerdally important homo polymer dextran is synthesised extracellularly by the enzyme dextransucrase. In Leuconostoc mesenteroides the enzyme is induced by the substrate sucrose. This is deaved to release free fructose and link the glucose to the redudng end of the acceptor dextran chain, which is bound to the enzyme. The product from this bacterium is composed almost exdusively of... 

There are two types of stationary phases commonly used in exclusion chromatography silica gel and micro-reticulated cross-linked polystyrene gels. A third type of exclusion media is comprised of the Dextran gels. Dextran gels are produced by the action of certain bacteria on a sucrose substrate. They consist of framework of glucose units that can form a gel in aqueous solvents that have size exclusion properties. Unfortunately the gels are mechanically weak and thus, cannot tolerate the high pressures necessary for HPLC and, as a consequence, are of very limited use to the analyst. 

A prehminary study of the use of larch AGs in aqueous two-phase systems [394] revealed that this polysaccharide provides a low-cost alternative to fractionated dextrans for use in aqueous two-phase, two-polymer systems with polyethylene glycol (PEG). The narrow molecular-weight distribution (Mw/Mn of 1-2) and low viscosity at high concentration of AG can be exploited for reproducible separations of proteins under a variety of conditions. The AG/PEG systems were used with success for batch extractive bioconversions of cornstarch to cyclodextrin and glucose. 

Some antigens, such as type 3 pneumococcal polysaccharide, EPS and other polymeric substances such as dextrans (poly-D-glucose) and levan (poly-D-fructose) can induce antibody synthesis without the assistance of TH cells. These are known as T-independent (Ti) antigens. Only one class of immunoglobulin (IgM) is synthesized and there is a weak memory response. 

Other important examples are blood and blood products, which are collected and processed in sterile containers, and plasma substitutes, for example dextrans and degraded gelatin. Dextrans, glucose polymers consisting essentially of (1 - 6) a-links, are produced as a result of the biochemical activities of certain bacteria of the genus Leuconostoc, e.g. L. mesenteroides (see Chapter 25). 

A summary of the properties of the different types of dextrans available is presented in Table 25.1. Dextrans for clinical use as plasma expanders must have moleeular weights between 40000 (= 220 glucose units) and 300000. Polymers below the minimum are excreted too rapidly fiom the kidneys, whilst those above the maximum are potentially dangerous because of retention in the body. In practice, infusions containing dextrans of average molecular weights of40000,70000 and 110000 are commonly encountered. 

Dextran 40 40000 10% w/v in 5% w/v glucose injection or 0.9% w/v sodium chloride injection Autoclave IV infusion improves blood flow and tissue function in burns and conditions associated with local ischaemia... 

Solubility generally decreases with increase in chain size and extent of branching. The solubility of dextran can be divided into four groups — those that are readily soluble at room temperature in water, IMF, DMSO and dilute base those that have difficulty dissolving in water those that are soluble in aqueous solution only in the presence of base and, those that are soluble only under pressure, at high temperatures (> 100°C) and in the presence of base. Dextran B-512 readily dissolves in water and 6M, 2M glycine and 50% glucose aqueous solutions. 

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