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2.1.8.2. Absorbency Under Load (AUL) - BADA

2.1.8.2. Absorbency Under Load (AUL) - BADA

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All the nucleophilic groups in proteins are sensitive to acylating. Tyrosine phenolic groups against<br />

nucleophilic reactions are usually less reactive than linear amino groups partly because of their<br />

higher pKa and partly because they are normally shielded in proteins structure. Another important<br />

difference is instability of acylated tyrosine due to acylation of tyrosine residues may easily<br />

reversible.<br />

Comparable case of reversibility of acylated products of other nucleophiles, such as imidazolyl,<br />

carboxyl and sulfhydryl are more selective than amino groups, hence EDTAD or succinic<br />

anhydride has been utilized to convert amino groups to carboxylic acid [22] (Fig. 7).<br />

1.7. Crosslinking<br />

Figure 7. Conversion of an amine to carboxylic acid with succinic anhydride<br />

The most common method for decreasing molecular freedom is crosslinking which joins the<br />

polymer chains together through covalent or ionic bonds to form a network (Fig.8). Frequently the<br />

term curing is used to indicate crosslinking.<br />

The crosslinking may possibly contain the same structural features as the main chains, or they may<br />

have a completely different structure. In the presence of solvent, a crosslinked polymer swells for<br />

the reason that solvent molecules penetrate into the network. The degree of swelling depends on<br />

the affinity of solvent and polymer for one another, as well as the level of crosslinking, protein<br />

concentration during the crosslinking step, gel particle size, and environmental condition, such as<br />

temperature, pH, and ionic strength [17] .<br />

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