2001
DOI: 10.1016/s0378-5173(01)00671-8
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Topical transport of hydrophilic compounds using water-in-oil nanoemulsions

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Cited by 162 publications
(85 citation statements)
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“…Droplet size is typically in the range of 10-100 nm. [22][23][24] They are typically composed of an aqueous phase, oil phase, surfactant, and cosurfactant. Microemulsions can be prepared by spontaneous emulsification, which offers several advantages over other drug vehicles, such as liposome and polymeric nanoparticles, including lower preparation costs, high drug loading, no need for an organic solvent, and a long shelf-life for both hydrophilic and lipophilic therapeutic agents.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Droplet size is typically in the range of 10-100 nm. [22][23][24] They are typically composed of an aqueous phase, oil phase, surfactant, and cosurfactant. Microemulsions can be prepared by spontaneous emulsification, which offers several advantages over other drug vehicles, such as liposome and polymeric nanoparticles, including lower preparation costs, high drug loading, no need for an organic solvent, and a long shelf-life for both hydrophilic and lipophilic therapeutic agents.…”
Section: Introductionmentioning
confidence: 99%
“…Microemulsions can be prepared by spontaneous emulsification, which offers several advantages over other drug vehicles, such as liposome and polymeric nanoparticles, including lower preparation costs, high drug loading, no need for an organic solvent, and a long shelf-life for both hydrophilic and lipophilic therapeutic agents. [16][17][18][19][20][21][22][23][24][25] Numerous studies have demonstrated that microemulsions can improve drug transport through the skin compared with conventional topical preparations, such as gels, creams, and ointments. [26][27][28][29] Hence, microemulsions were used as the vehicle for transdermal delivery of citalopram in the present study.…”
Section: Introductionmentioning
confidence: 99%
“…As a result of the sampling, the receptor compartment concentration of alaptide was corrected for sample removal and replenishment using equation: C' n = C n (V t /V t -V s ) (C' n-1 /C n-1 ); where C' n = corrected drug concentration in the n th sample, C n = measured drug concentration in the n th sample, C' n-1 = corrected drug concentration in the (n-1) th sample, C n-1 = measured drug concentration in the (n-1) th sample, V t = total volume of receptor solution, V s = volume of the sample, and C' 1 = C 1 [28]. The corrected data were expressed as the cumulative drug permeation (Q t ) per unit of skin surface area using equation: Q t = C' n /A; where A = 0.6359 cm 2 in our experiment.…”
Section: In Vitro Transdermal Permeation Experimentsmentioning
confidence: 99%
“…They are independent of molecular size of the hydrophilic solute and the nature of the aqueous phase. In addition, nanoemulsions delivery system was independent of animal skin characteristics such as the stratum corneum thickness and the follicle-type (Wu et al 2001). Thus, nanoemulsions due to their extremely small size are suitable to be used as delivery system in cosmeceuticals.…”
Section: Fabrication Rheology and Antioxidant Activity Of Palm Estermentioning
confidence: 99%