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从普罗布考/聚乙烯吡咯烷酮/十二烷基硫酸钠三元研磨混合物中获得的胶体纳米颗粒的形成机制。

Formation mechanism of colloidal nanoparticles obtained from probucol/PVP/SDS ternary ground mixture.

作者信息

Pongpeerapat Adchara, Wanawongthai Chalermphon, Tozuka Yuichi, Moribe Kunikazu, Yamamoto Keiji

机构信息

Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.

出版信息

Int J Pharm. 2008 Mar 20;352(1-2):309-16. doi: 10.1016/j.ijpharm.2007.10.052. Epub 2007 Nov 9.

Abstract

The purpose of this study was to investigate the formation mechanism of colloidal nanoparticles after dispersion of probucol/polyvinylpyrrolidone (PVP)/sodium dodecyl sulphate (SDS) ternary ground mixture (GM) into water. Probucol, PVP and SDS were mixed at a weight ratio of 1:3:1 and ground for 30 min with a vibrational rod mill. The morphology and physicochemical properties were investigated through high resolution scanning electron microscopy (SEM), environmental SEM, dynamic light scattering, (13)C NMR and zeta potential measurements. SEM images confirmed the presence of 20 nm size primary particles in the GM powder of probucol/PVP K17/SDS. Spherical nanoparticles with a size of around 100 nm, formed after dispersion of the GM into water, suggested an agglomeration of the primary particles. A further agglomeration of around 160 nm was observed with the stability experiment. Zeta potential and particle size measurements using latex beads revealed that PVPK 17/SDS complex was adsorbed on the probucol particle surface forming a layered structure. A similar agglomeration behavior was observed using the GM of probucol/PVP K12/SDS, though the molecular state of the PVPK 12/SDS complex at the particle surface was different from that of the PVPK 17/SDS complex. (13)C NMR results suggested that intermolecular interactions between PVP K12 and SDS did not reach the same level as the interactions between PVP K17 and SDS. This study proposed a formation mechanism of colloidal nanoparticles.

摘要

本研究的目的是探究普罗布考/聚乙烯吡咯烷酮(PVP)/十二烷基硫酸钠(SDS)三元研磨混合物(GM)分散于水中后胶体纳米颗粒的形成机制。将普罗布考、PVP和SDS按重量比1:3:1混合,并用振动棒磨机研磨30分钟。通过高分辨率扫描电子显微镜(SEM)、环境扫描电子显微镜、动态光散射、(13)C核磁共振和zeta电位测量对其形态和理化性质进行了研究。SEM图像证实普罗布考/PVP K17/SDS的GM粉末中存在尺寸为20 nm的初级颗粒。GM分散于水中后形成的尺寸约为100 nm的球形纳米颗粒表明初级颗粒发生了团聚。稳定性实验观察到进一步团聚至约160 nm。使用乳胶珠进行的zeta电位和粒径测量表明,PVPK 17/SDS复合物吸附在普罗布考颗粒表面形成层状结构。使用普罗布考/PVP K12/SDS的GM也观察到类似的团聚行为,尽管颗粒表面PVPK 12/SDS复合物的分子状态与PVPK 17/SDS复合物不同。(13)C核磁共振结果表明,PVP K12与SDS之间的分子间相互作用未达到PVP K17与SDS之间相互作用的水平。本研究提出了一种胶体纳米颗粒的形成机制。

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