2013
DOI: 10.7439/ijbr.v4i10.398
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Development, characterization & in vitro skin permeation of rutin ethosomes as a novel vesicular carrier

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Cited by 6 publications
(4 citation statements)
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“…Based on the physicochemical properties of the drug(s), it may be dissolved either in an aqueous or inorganic phase [83]. The organic phase is added drop by drop to the aqueous medium with continuous stirring to obtain the vesicles [84].…”
Section: Methods Of Preparationmentioning
confidence: 99%
See 1 more Smart Citation
“…Based on the physicochemical properties of the drug(s), it may be dissolved either in an aqueous or inorganic phase [83]. The organic phase is added drop by drop to the aqueous medium with continuous stirring to obtain the vesicles [84].…”
Section: Methods Of Preparationmentioning
confidence: 99%
“…In the hot process, phospholipids dispersed in purified water are added to the organic phase containing ethanol, cholesterol, and an edge activator or permeation enhancer (deformable vesicles) at 40 °C. The vesicular size is reduced by sonication or the high-pressure extrusion method [84,85]. In the ethanol injection method, drops of ethanol are added to the aqueous phase with constant stirring.…”
Section: Methods Of Preparationmentioning
confidence: 99%
“…Rutin, in its free state, is unstable when exposed to UV rays and cannot permeate through the stratum corneum (Bakowska et al 2003). A growing body of research has confirmed better photostability and permeability of rutin in nanosystem forms (e.g., nanoparticle, nanoemulsion, liposome-in-hydrogel) (Das and Kalita 2014;Dhiman and Singh 2015;Park et al 2014) compared with free rutin. Attempting to improve its photostability profile and antioxidant effects, Oliveira et al strategically formulated rutin nanoparticles with SPF enhancing property.…”
Section: Flavonolmentioning
confidence: 99%
“…For the studies at 25 C ± 2 C/60 ± 5% RH and 40 C ± 2 C/70 ± 5% RH, patches were stored in a stability chamber (Model NEC2355; Nutronics India, New Delhi, India). Sampling was done on 0, 15, 30, 45, 60, 90, 120 and 180 days [45,46]. Drug content (%) was evaluated at the end of the specified period [47].…”
Section: Stability Studymentioning
confidence: 99%