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Lysozyme release from lipid-based implants

机译:从脂质的植入物中释放溶菌酶

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摘要

To better understand lipid-based implants applied to proteins, lysozyme was used as a model protein and was loaded into lipid-based implants in different contents. Cylindrical and spherical implants loaded with lysozyme presented a smooth surface. Protein loading efficiency decreased with increasing lysozyme loading. Lysozyme kept its activity after different implant preparation techniques. Drug release tremendously increased by increasing protein loading from 8.9 to 13.7% (w/w), for cylindrical implants. Lysozyme release was faster from cylindrical implants when compared with the spherical ones. Furthermore, by increasing the hydrophobicity of the lipid, protein release decreased. This study demonstrates the potential use of lipid-based implants for the controlled release of proteins.
机译:为了更好地了解应用于蛋白质的脂质的植入物,使用溶菌酶作为模型蛋白质,并以不同的内容物装入脂质的植入物中。装有溶菌酶的圆柱形和球形植入物呈现光滑的表面。随着溶菌酶的增加,蛋白质负载效率降低。溶菌酶在不同的植入式制备技术后保持其活性。通过增加8.9至13.7%(w / w)的蛋白质负荷,药物释放急剧增加,用于圆柱形植入物。与球面植入物相比,溶菌酶释放从圆柱形植入物更快。此外,通过增加脂质的疏水性,蛋白质释放降低。本研究表明潜在使用基于脂质的植入物用于蛋白质的受控释放。

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