2011
DOI: 10.1016/j.ijpharm.2011.06.014
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Solid lipid nanoparticles suspension versus commercial solutions for dermal delivery of minoxidil

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Cited by 47 publications
(53 citation statements)
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References 37 publications
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“…Vaccines, 5-fluorouracil, IL-2 and IFN-α [149][150][151] SECosomes or nanosomes Mixture of surfactant, ethanol and cholesterol siRNA [121] SLNs Produced with one single solid lipid and surfactants, with perfect crystalline lattice CoQ-10, glucocorticoids, minoxidil and oxybenzone [152][153][154][155] NLCs Produced with solid and liquid lipids and surfactants, with distorted crystalline lattice Targeted tumor delivery, phospholipase A2 inhibitors, benzocaine, lidocaine and psoriasis treatment [156][157][158][159] Polymeric nanoparticles Consist of micro-and nano-spheres or capsules developed to control the release of the entrapped drug Chlorhexidine, indomethacin, melatonin and poorly soluble drugs [160][161][162][163] ALA: Aminolevulinic acid; NLC: Nanostructured lipid carrier; SECosome: Surfactant-ethanol-cholesterol-osome; SLN: Solid lipid nanoparticle.…”
Section: Nanoemulsion or Microemulsionmentioning
confidence: 99%
“…Vaccines, 5-fluorouracil, IL-2 and IFN-α [149][150][151] SECosomes or nanosomes Mixture of surfactant, ethanol and cholesterol siRNA [121] SLNs Produced with one single solid lipid and surfactants, with perfect crystalline lattice CoQ-10, glucocorticoids, minoxidil and oxybenzone [152][153][154][155] NLCs Produced with solid and liquid lipids and surfactants, with distorted crystalline lattice Targeted tumor delivery, phospholipase A2 inhibitors, benzocaine, lidocaine and psoriasis treatment [156][157][158][159] Polymeric nanoparticles Consist of micro-and nano-spheres or capsules developed to control the release of the entrapped drug Chlorhexidine, indomethacin, melatonin and poorly soluble drugs [160][161][162][163] ALA: Aminolevulinic acid; NLC: Nanostructured lipid carrier; SECosome: Surfactant-ethanol-cholesterol-osome; SLN: Solid lipid nanoparticle.…”
Section: Nanoemulsion or Microemulsionmentioning
confidence: 99%
“…One study found that encapsulating minoxidil into solid lipid nanoparticles showed similar skin penetration to commercial solutions without the corrosive potential (i.e., dryness, irritation, burning, etc.) [47]. Finasteride, a 5-α reductase inhibitor preventing the peripheral conversion of testosterone to dihydrotestosterone, has a variety of unwanted side effects following oral administration; encapsulation of finasteride into topical liquid crystalline nanoparticles has been proposed as a viable alternative to oral administration in order to maintain high skin retention in the scalp, enable a lower dosing frequency and minimize significant side effects including mood disturbances, gynecomastia and erectile dysfunction [48].…”
Section: Hair Growth and Removalmentioning
confidence: 99%
“…After 24 hours, only a very small quantity of minoxidil crossed the skin. A previous study 1 indicated the difficulty that exists in this drug penetrating through the skin. Therefore, the results obtained in this work were not different than what was expected, according to the literature.…”
Section: In Vitro Controlled Release Studiesmentioning
confidence: 99%
“…This disease has different possible forms; androgenic alopecia (AGA) is a common form of hair loss in both men and women. 1 It affects up to half of the Caucasian male population by middle age, and almost all (95%) Caucasian men by old age (80 years). 2 This type of alopecia is progressive and related to a perturbation of the hair follicle cycle, which is caused by a shortening of the anagen stage, with the clinical consequence of increased hair loss accompanied by a transformation of terminal…”
Section: Introductionmentioning
confidence: 99%
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