Dextran amine derivatives

Figure 25.14 An amine derivative of dextran may be prepared through a two-step process involving the reac-tion of chloroacetic acid with the hydroxyl groups of the polymer to create carboxylates. Next, ethylene diamine is coupled in excess using a carbodiimide-mediated reaction to give the primary amine functional groups.

To make an amine derivative of dextran, dissolve ethylene diamine (or another suitable diamine) in 0.1 M sodium phosphate, 0.15 M NaCl, pH 7.2, at a concentration of 3 M. Note Use of the hydrochloride form of ethylene diamine is more convenient, since it avoids having to adjust the pH of the highly alkaline free-base form of the molecule. Alternatively, to prepare a hydrazide-dextran derivative, dissolve adipic acid dihydrazide (Chapter 4, Section 8.1) in the coupling buffer at a concentration of 30 mg/ml (heating under a hot water tap may be necessary to completely dissolve the hydrazide compound). Adjust the pH to 7.2 with HC1 and cool to room temperature. 

Figure 25.18 An amine-derivative of dextran may be coupled with iodoacetic acid using a carbodiimide reaction to produce a sulfhydryl-reactive iodoacetamide polymer.

Dextran carbamate derivatives. Activation of dextran with 4-nitro-phenyl chloroformate and subsequent reaction with amines leads to the formation of the corresponding carbamate derivatives 2-Hydroxypro-pylamine was selected as a model for amine type drugs. 

Dextran derivatives containing carboxyl- or amine-terminal spacer arms may be prepared by a number of techniques. These derivatives are useful for coupling amine- or carboxylate-containing molecules through a carbodiimide-mediated reaction to form an amide bond (Chapter 3, Section 1). Amine-terminal spacers also can be used to create secondary reactive groups by modification with a heterobifunctional crosslinking agent (Chapter 5). 

This type of modification process has been used to form sulfhydryl-reactive dextran polymers by coupling amine spacers with crosslinkers containing an amine reactive end and a thiol-reactive end (Brunswick et al., 1988 Noguchi et al., 1992). The result was a multivalent sulfhydryl-reactive dextran derivative that could couple numerous sulfhydryl-containing molecules per polymer chain. 

Another approach uses reactive alkyl halogen compounds containing a terminal carboxylate group on the other end to form spacer arms off the dextran polymer from each available hydroxyl. In this manner, Brunswick et al. (1988) used chloroacetic acid to modify the hydroxyl groups to form the carboxymethyl derivative. The carboxylates then were aminated with ethylene diamine to create an amine-terminal derivative (Inman, 1985). Finally, the amines were modified with iodoacetate to form a sulfhydryl-reactive polymer (Figure 25.14). 

In a somewhat similar scheme, Noguchi et al. (1992) prepared a carboxylate spacer arm by reacting 6-bromohexanoic acid with a dextran polymer. The carboxylate then was aminated with ethylene diamine to form an amine-terminal spacer (Figure 25.15). This dextran derivative finally was reacted with N-Succinimidyl 3-(2-pyridyldithio)propionate (SPDP) (Chapter 5, Section 1.1) to create the desired sulfhydryl-reactive polymer (Section 2.4, this chapter). The SPDP-activated polymer then could be used to prepare an immunoconjugate composed of an antibody against human colon cancer conjugated with the drug mitomycin-C. 

The following protocols may be used to create carboxyl-, amine-, or hydrazide-containing derivatives of dextran. 

The ethylene diamine-dextran derivative may be used for the coupling of carboxylate-contain-ing molecules by the carbodiimide reaction, for the coupling of amine-reactive probes, or to modify further using heterobifunctional crosslinkers. The hydrazide-dextran derivative may be used to crosslink aldehyde-containing molecules, such as oxidized carbohydrates or glycoproteins. 

The carboxymethyl-dextran derivative may be used to couple amine-containing molecules by the carbodiimide reaction. Heindel et al. (1994) prepared the lactone derivative of carboxymethyl-dextran by refluxing for 5 hours in toluene or other anhydrous solvents. The lactone derivative is highly reactive toward amine-containing molecules, thus creating a preactivated polymer for conjugation purposes. 

Figure 25.17 An amine-functionalized dextran derivative may be further reacted with SPDP to create a sulfhydryl-reactive product.

Several chemical approaches may be used to form the amine- or carboxyl-terminal dextran derivative. The simplest procedure may be to prepare polyaldehyde dextran according to the procedure of Section 2.1, and then make the spacer arm derivative by reductively animating an amine-containing organic compound onto it. For instance, short diamine compounds such as ethylene diamine or diaminodipropylamine (3,3 -iminotepropylamine) can be coupled in excess to polyaldehyde dextran to create an amine-terminal derivative. Carboxyl-terminal derivatives may be prepared similarly by coupling molecules such as 6-aminocaproic acid or p-alanine to polyaldehyde... 

Noguchi et al. (1992) used an amine-terminal spacer arm derivative of dextran to react with SPDP (Chapter 5, Section 1.1) in the creation of a pyridyldisulfide-activated polymer (Fig. 391). Brunswick etal. (1988) used a different amine-terminal spacer arm derivative of dextran and subsequently coupled iodoacetate to form a sulfhydryl-reactive polymer (Fig. 392). Heindel et al. (1991) used a unique approach. They... 

CMD and mixed derivatives based on CMD may be used for the fixation of antibiotics and enzymes on a polysaccharide matrix. A procedure was developed for amidation of CMD and its ethyl ester (CMDEE) with various aromatic amines in dioxane (100 °C), ethanol (78 °C), n-propanol (97 °C) and 2-propanol (82 °C) in the presence of a small amount of water [301]. CMDEE reacts with aliphatic and aromatic amines but in the case of amino acids the degree of amidation depends on the position of the amino moieties in the acids [302,303]. The DS decreases from S-, y-, /3, to a-amino acids. For the reaction with a-amino acids, carboxymethyl and carboxyethyl dextran azides are used [304],... 

This method was reported before as a convenient way to couple drugs to dextran and starch (7). For the attachment of alcohols this method is obviously only practical when using the tri-ester derivatives in order to avoid intra- or inter-molecular reactions during the subsequent coupling procedures. However also with amine type drugs similar competitive side reaction may occur as will be illustrated. 

Polysaccharides can be derivatized by reductive amination at the reducing end group. With highly fluorescing labels like 2-aminoanthracene (2-AA), dex-trans up to a molecular mass of 20 kDa can be visualized and hence analyzed by CE [35]. The separation of the AA derivative (only one chromophore introduced) of a synthetic dextran (4-6 kDa) is shown in Fig. 15. This opens new possibilities in the characterization of polysaccharides. 

Chloro-2-hydroxypropyl derivatives of such polysaccharides as cellulose and cross-linked dextran (Sephadex) may be prepared by treatment with epichlorohydrin in boron trifluoride etherate. These 3-chloro-2-hydroxypropylated polysaccharides may, in turn, react with ammonia, or primary, secondary, or tertiary amines, and the resultant derivatives of cellulose and Sephadex LH-20, particularly an 0-[3-(di-butylamino)-2-hydroxypropyl] derivative of the latter, are useful anion-exchangers. In the amination procedure, between 50 and 100% of the chlorine atoms are utilized, except in the reaction with tertiary... 

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