کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
601064 | 879930 | 2011 | 9 صفحه PDF | دانلود رایگان |

Sodium bis(2-ethylhexyl) sulfosuccinate (AOT) is well known to form nanometre sized aqueous droplets in organic solvents and used in several contemporary applications including templates of nanoparticle synthesis. However, the detailed structural characterization of AOT in aqueous media is relatively less attended. Here we have used dynamic light scattering technique for the structural characterization of AOT in aqueous solutions and found to have a monodispersed, unilamellar vesicles (∼140 nm diameter). The efficacy of the vesicle to host both charged drugs like H258 (2′-(4-hydroxyphenyl)-5-[5-(4-methylpiperazine-1-yl)-benzimidazo-2-yl-benzimidazole]), EtBr (ethidium bromide) and hydrophobic drug like DCM (4-(dicyanomethylene)-2-methyl-6-(p-dimethylamino-styryl)-4H-pyran) has also been investigated using Förster resonance energy transfer. Picosecond resolved and polarization gated spectroscopy have been used to study the solvation dynamics and microviscosity at the surface of the vesicles. We have also performed concentration and temperature dependent studies in order to confirm the stability of the vesicles in aqueous phase. The drug release profile of the vesicles has been studied through in vitro dialysis method. The non-toxic, monodispersed vesicles in aqueous media with a noteworthy stability in wide range of AOT concentration and temperature, capable of hosting drugs of various natures (both hydrophobic and charged) simultaneously for many codelivery applications with controlled drug release profile may find its applications in drug delivery.
Figure optionsDownload as PowerPoint slideHighlights
► The aggregate structure and size of AOT vesicles in dilute aqueous region has been explored.
► The size of AOT vesicles is independent of surfactant concentration indicating unilamellarity.
► The vesicles host both hydrophobic and charged model drugs simultaneously and show controlled drug release profile.
► The study explores the hydrogen bonded structure and dynamics at the interface of the AOT vesicle.
Journal: Colloids and Surfaces B: Biointerfaces - Volume 88, Issue 1, 1 November 2011, Pages 345–353