2018
DOI: 10.1016/j.nano.2018.08.004
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Pharmacokinetics and pharmacodynamics of intranasally administered selegiline nanoparticles with improved brain delivery in Parkinson's disease

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Cited by 92 publications
(29 citation statements)
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“…The treatment of Parkinson’s disease through the administration of polymeric nanocarriers has also been studied. Thus, administering chitosan nanoparticles through the intranasal route for the delivery of selegiline [110] and pramipexole [111] increases the brain targeting efficiency and the amount of drug reaching the brain by decreasing the pre-systemic metabolism. Moreover, the in vitro and in vivo studies on the delivery of apolipoprotein E and α-mangostin by using phosphatidic acid-conjugated liposomes [112] and transferrin-modified liposomes [113], respectively, confirmed the potential for an enhanced BBB permeation and efficient drug delivery.…”
Section: Nanomedicine In Central Nervous System Disordersmentioning
confidence: 99%
“…The treatment of Parkinson’s disease through the administration of polymeric nanocarriers has also been studied. Thus, administering chitosan nanoparticles through the intranasal route for the delivery of selegiline [110] and pramipexole [111] increases the brain targeting efficiency and the amount of drug reaching the brain by decreasing the pre-systemic metabolism. Moreover, the in vitro and in vivo studies on the delivery of apolipoprotein E and α-mangostin by using phosphatidic acid-conjugated liposomes [112] and transferrin-modified liposomes [113], respectively, confirmed the potential for an enhanced BBB permeation and efficient drug delivery.…”
Section: Nanomedicine In Central Nervous System Disordersmentioning
confidence: 99%
“…For the treatment of Parkinson’s disease, which is associated with motor features, such as rest tremor, bradykinesia, rigidity and postural instability, olfactory dysfunction, cognitive impairment, psychiatric symptoms, and autonomic dysfunction [59], various types of nanoparticles have been studied. Some of these studies reported ex vivo of chitosan nanoparticles for the delivery of Selegiline, a well-known anti-Parkinson agent [60], and Pramipexole [61], a non-ergot based dopamine that effectively counters Parkinson’s diseases progression [62]. Additionally, the use of cerium oxide nanoparticles, which protect neurons against reactive oxygen species-induced damage, has resulted in the improvement of motor dysfunctions and decreased apoptosis [63].…”
Section: The Use Of Nanoparticles For the Diagnosis And Treatment mentioning
confidence: 99%
“…Likewise, metformin-loaded polydopamine NPs promote anti-inflammatory, antiapoptotic, and antioxidative properties associated with the proteolytic degradation of phosphorylated serine 129 of α-synuclein protein induced by targeting a histone-lysine N-methyltransferase enzyme known as the enhancer of zeste homolog 2 (Sardoiwala et al, 2020). Other NPs and nanodrugs that have been reported to have significant potential in the treatment of PD by regulating oxidative stress and inflammation including vitamin E-loaded naringenin nanoemulsions (Gaba et al, 2019), selegiline CS NPs (Sridhar et al, 2018), borneol and lactoferrin comodified NPs (Tang et al, 2019), resveratrol NPs (Palle and Neerati, 2018), and Cerium NPs (Hegazy et al, 2017). In summary, NPs and nanodrugs have great potential in treatment of PD because of their role in the regulation of inflammation, oxidative stress, apoptosis, α-synuclein activities, and the downstream effects in motor and non-motor dysfunctions.…”
Section: Pdmentioning
confidence: 99%