Protein release behavior from porous microparticle with lysozyme/hyaluronate ionic complex.

Eun Seong Lee; Min Jung Kwon; Kun Na; Jun Ho Bae

doi:10.1016/j.colsurfb.2006.11.024

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Protein release behavior from porous microparticle with lysozyme/hyaluronate ionic complex.

Eun Seong Lee·Min Jung Kwon·Kun Na·Jun Ho Bae

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Abstract

Porous microparticles (PMs) with a low density (<0.4 g/cm3) for pulmonary protein delivery were prepared by the water-in-oil-in-water (W1/O/W2) multi-emulsion method using a cyclodextrin derivative as a porogen. The complexation of positively charged lysozyme (Lys) and negative-charged hyaluronate (HA) was investigated for long-term protein release from PMs. The interaction of Lys and HA not only increased protein encapsulation efficiency but also stabilized Lys against a denaturing organic solvent (dichloromethane). Furthermore, PMs with Lys/HA complexes increased the Lys release period up to 7 days, as opposed to a 4h Lys release time from PMs without Lys/HA complexes. In particular, PMs containing 10mg of HA and 50mg of Lys showed almost zero-order Lys release kinetic for 7 days and preserved the bioactivity of Lys more than 98% during its entire release period. This result suggests that PMs with Lys/HA complexes may be applied in long-term pulmonary administration of protein or peptide drugs, including those that require particles to arrive at a deep lung epithelium with the help of low density (high porosity) of PMs.

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Emulsions Hyaluronic Acid Lysine Muramidase Nanoparticles Particle Size Porosity Serum Albumin, Bovine Surface Properties Time Factors Journal Article

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Eun Seong Lee, Min Jung Kwon, Kun Na, Jun Ho Bae. 2006-11-23. Protein release behavior from porous microparticle with lysozyme/hyaluronate ionic complex.. https://doi.org/10.1016/j.colsurfb.2006.11.024

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