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Stability of Drugs and Dosage Forms Sumie Yoshioka

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198 Chapter 5 • <strong>Stability</strong> <strong>of</strong> Peptide <strong>and</strong> Protein Pharmaceuticals<br />

Figure 206. First-order plots <strong>of</strong> the degradation <strong>of</strong> an LH-RH antagonist in aqueous solution at varying pH values<br />

(80°C). (Reproduced from Ref. 802 with permission.)<br />

decay, apparent first-order kinetics (Fig. 208). 879 Apparent inactivation <strong>of</strong> kallikrein was<br />

described according to a kinetic model representing a reversible <strong>and</strong> an irreversible reaction<br />

(Eq. 5.1) or an alternative model representing independent irreversible inactivation <strong>of</strong> two<br />

isoenzymes (Eq. 5.2). 879 (5.1)<br />

Figure 207. First-order plots <strong>of</strong> the deamidation <strong>of</strong> calcitonin in aqueous solution at varying pH values (70°C).<br />

(Reproduced from Ref. 876 with permission.)

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