Use of protease inhibitors in composite polyelectrolyte microparticles in order to increase the bioavailability of perorally administered encapsulated proteins

Pechenkin, M.A.; Balabushevich, N.G.; Zorov, I.N.; Izumrudov, V.A.; Klyachko, N.L.; Kabanov, A.V.; Larionova, N.I.

Авторы: Pechenkin M.A., Balabushevich N.G., Zorov I.N., Izumrudov V.A., Klyachko N.L., Kabanov A.V., Larionova N.I.
Журнал: Pharmaceutical Chemistry Journal
Том: 47
Номер: 1
Год издания: 2013
Издательство: Kluwer Academic/Plenum Publishers
Местоположение издательства: United States
Первая страница: 62
Последняя страница: 69
DOI: 10.1007/s11094-013-0898-1
Аннотация: Protein protease inhibitors (aprotinin, soybean Bowman–Birk inhibitor, and Kunitz soybean trypsin inhibitor) possessing different specificity with respect to trypsin, chymotrypsin, and elastase were encapsulated together with a cargo protein in polyelectrolyte microparticles using layer-by-layer (LbL) deposition techniques. The most efficient inclusion of the inhibitors occurred at the formation stage of the insoluble protein complex with the polyanion. Simultaneous immobilization of the inhibitor and protein did not influence the physicochemical properties of the microparticles, specifically their pH-sensitive behavior under conditions modeling the passage through various parts of the human gastrointestinal tract after peroral administration. The most effective protection against the action of proteolytic enzymes of pancreatic juice and the small intestine was achieved for simultaneous release of cargo protein and inhibitor from the microparticles. Soybean Bowman–Birk inhibitor, which is most similar to insulin with respect to physicochemical properties, in addition to the soybean extract enriched with protease inhibitors were the most suitable agents for protection of human insulin or its rapidly acting analogs (lispro and aspart). These findings suggested that simultaneous microencapsulation of both protein and protein protease inhibitor was a promising way to increase the protein bioavailability upon peroral administration of polyelectrolyte microparticles.
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Use of protease inhibitors in composite polyelectrolyte microparticles in order to increase the bioavailability of perorally administered encapsulated proteinsстатья

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