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牛血清白蛋白-烷基磺酸钠生物缀合物作为药物传递系统。

Bovine serum albumin-sodium alkyl sulfates bioconjugates as drug delivery systems.

机构信息

MTA-SZTE Supramolecular and Nanostructured Materials Research Group, University of Szeged, H-6720 Dóm tér. 8, Szeged, Hungary.

Department of Physical Chemistry and Materials Science, Faculty of Science and Informatics, University of Szeged, H-6720 Aradi vt. 1, Szeged, Hungary.

出版信息

Colloids Surf B Biointerfaces. 2015 Jun 1;130:126-32. doi: 10.1016/j.colsurfb.2015.04.018. Epub 2015 Apr 17.

Abstract

Precipitation of bovine serum albumin (BSA) by anionic surfactants with alkyl chains of increasing lengths (octyl, decyl, dodecyl sulfates) was studied at room temperature, at pH 3.0, in isotonic sodium chloride solution. The particle size of albumin, the zeta potential, the surface charge and fluorescent properties of BSA-surfactant composites were investigated concerning addition of increasing amount of surfactant. The thermal stability of the systems was monitored by calorimetric analysis (DSC). The formation of the well-ordered structure in the self-assembly process in liquid phase was studied by XRD measurement. The structure of the precipitated BSA-surfactant nanocomposites was characterized by small-angle X-ray scattering (SAXS). Finally, ibuprofen (IBU) molecules were enclosed in BSA-surfactant bioconjugate systems and the release properties of the drug were investigated. It has been found out that, as a consequence to the increasing number of carbon atoms in the alkyl chains of the surfactant, the structure and the fluorescent properties of the aggregates formed can be controlled due to the increase in the hydrophobicity of BSA-surfactant composites. The bioconjugates are well applicable as carrier to realize controlled release of drug molecules.

摘要

在室温下、pH 值为 3.0 且在等渗氯化钠溶液中,研究了带不同链长(辛基、癸基、十二烷基硫酸盐)的阴离子表面活性剂对牛血清白蛋白(BSA)的沉淀作用。考察了外加不同量表面活性剂时 BSA-表面活性剂复合物的粒径、Zeta 电位、表面电荷和荧光性质。通过量热分析(DSC)监测了体系的热稳定性。通过 X 射线衍射(XRD)测量研究了在液相自组装过程中形成的有序结构。通过小角 X 射线散射(SAXS)对沉淀的 BSA-表面活性剂纳米复合物的结构进行了表征。最后,将布洛芬(IBU)分子包封在 BSA-表面活性剂生物缀合物系统中,并研究了药物的释放性能。结果表明,由于表面活性剂烷基链中的碳原子数增加,BSA-表面活性剂复合物的疏水性增加,因此可以控制所形成的聚集体的结构和荧光性质。这些生物缀合物可用作载体以实现药物分子的控制释放。

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