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Covalent immobilization of liposomes on plasma functionalized metallic surfaces

机译:将脂质体共价固定在血浆功能化金属表面上

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摘要

A method was developed to functionalize biomedical metals with liposomes. The novelty of the method includes the plasma-functionalization of the metal surface with proper chemical groups to be used as anchor sites for the covalent immobilization of the liposomes. Stainless steel (SS-316) disks were processed in radiofrequency glow discharges fed with vapors of acrylic acid to coat them with thin adherent films characterized by surface carboxylic groups, where liposomes were covalently bound through the formation of amide bonds. For this, liposomes decorated with polyethylene glycol molecules bearing terminal amine-groups were prepared. After ensuring that the liposomes remain intact, under the conditions applying for immobilization; different attachment conditions were evaluated (incubation time, concentration of liposome dispersion) for optimization of the technique. Immobilization of calcein-entrapping liposomes was evaluated by monitoring the percent of calcein attached on the surfaces. Best results were obtained when liposome dispersions with 5. mg/ml (liposomal lipid) concentration were incubated on each disk for 24. h at 37°C. The method is proposed for developing drug-eluting biomedical materials or devices by using liposomes that have appropriate membrane compositions and are loaded with drugs or other bioactive agents.
机译:开发了一种用脂质体功能化生物医学金属的方法。该方法的新颖性包括用适当的化学基团对金属表面进行等离子体官能化,以用作脂质体共价固定的锚定位点。不锈钢(SS-316)圆盘在射频辉光放电中进行了处理,该放电中注入了丙烯酸蒸气,从而在其上覆盖了以表面羧基为特征的薄粘附膜,其中脂质体通过形成酰胺键共价键合。为此,制备了用带有末端胺基的聚乙二醇分子修饰的脂质体。在确保脂质体完好无损之后,在申请固定化的条件下;评估了不同的附着条件(孵育时间,脂质体分散液的浓度)以优化技术。通过监测附着在表面上的钙黄绿素的百分比来评估钙黄绿素截留脂质体的固定化。当将浓度为5. mg / ml(脂质体脂质)的脂质体分散液在每个圆盘上于37°C孵育24小时时,可获得最佳结果。提出了通过使用具有合适的膜组成并且负载有药物或其他生物活性剂的脂质体来开发药物洗脱生物医学材料或装置的方法。

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