2014
DOI: 10.1016/j.ejpb.2014.05.004
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Solid lipid nanoparticles as vehicles of drugs to the brain: Current state of the art

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Cited by 188 publications
(98 citation statements)
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“…In this dual-drug delivery system, SLNs itself can cross the BBB and deliver the drug molecular to a specific brain site; Myrj52 and HU-211 can be used to modify SLNs and enhance this ability, mainly because Myrj52 can inhibit the function of P-gp and because HU-211 is highly lipophilic. [51][52][53] To confirm the successful fabrication of Cur/SLNs-HU-211, many physicochemical characterizations were performed. Transmission electron microscopy results showed that Cur/SLNs-HU-211 was uniform, which may contribute to better solubility in water and bioavailability in biological system.…”
Section: Discussionmentioning
confidence: 99%
“…In this dual-drug delivery system, SLNs itself can cross the BBB and deliver the drug molecular to a specific brain site; Myrj52 and HU-211 can be used to modify SLNs and enhance this ability, mainly because Myrj52 can inhibit the function of P-gp and because HU-211 is highly lipophilic. [51][52][53] To confirm the successful fabrication of Cur/SLNs-HU-211, many physicochemical characterizations were performed. Transmission electron microscopy results showed that Cur/SLNs-HU-211 was uniform, which may contribute to better solubility in water and bioavailability in biological system.…”
Section: Discussionmentioning
confidence: 99%
“…Therapeutic nanocarriers can range in size from 1 to 1000 nm and be generated from a wide variety of substances, both biodegradable and non-biodegradable, including polymers, lipids, carbon nanotubes and ceramics (Kreuter 2014, Patel et al 2012, Gastaldi et al 2014). Nanoparticles are especially important for therapeutic delivery to areas that are otherwise difficult to access, such as the central nervous system and areas beyond the blood-brain barrier.…”
Section: Nanoparticlesmentioning
confidence: 99%
“…While this therapeutic approach has been successfully applied in vitro , preclinical validation is needed to address potential concerns regarding overexpression of the target protein above endogenous levels as well as safety and efficacy of viral delivery. A novel approach to overcome potential off-target toxicity using viral delivery methods is the use of lipid nanoparticles [171,172], which have been shown recently to efficiently deliver siRNAs into the brain with little apparent toxicity [173]. …”
Section: Potential Therapies Targeting Aberrant Rna Homeostasismentioning
confidence: 99%