2015
DOI: 10.1016/j.ijbiomac.2015.07.041
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Brain delivery of buspirone hydrochloride chitosan nanoparticles for the treatment of general anxiety disorder

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Cited by 58 publications
(37 citation statements)
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“…There are various particulate drug delivery systems either on the market or in the pipelines [ 1 ]. Different nanocarriers can be used, for example polymeric, lipid and inorganic nanoparticles [ 138 ]. Agents as chitosan, hydroxypropylcellulose, carboxymethylcellulose, and carbopol display mucoadhesive properties, but also hyaluronic acid and polyacrylic acid are well suited [ 137 ].…”
Section: Formulations Dosage Forms and Medical Devices For Intranmentioning
confidence: 99%
See 2 more Smart Citations
“…There are various particulate drug delivery systems either on the market or in the pipelines [ 1 ]. Different nanocarriers can be used, for example polymeric, lipid and inorganic nanoparticles [ 138 ]. Agents as chitosan, hydroxypropylcellulose, carboxymethylcellulose, and carbopol display mucoadhesive properties, but also hyaluronic acid and polyacrylic acid are well suited [ 137 ].…”
Section: Formulations Dosage Forms and Medical Devices For Intranmentioning
confidence: 99%
“…Agents as chitosan, hydroxypropylcellulose, carboxymethylcellulose, and carbopol display mucoadhesive properties, but also hyaluronic acid and polyacrylic acid are well suited [ 137 ]. Hassan et al showed that thiolated chitosan particles doubled the brain delivery of the anxiety disorder treatment drug buspirone hydrochloride [ 138 ]. As chitosan is a highly mucophilic agent, high concentrations can even lead to mucus gel break down what in turn leads to an easy access for the drug to epithelial cells.…”
Section: Formulations Dosage Forms and Medical Devices For Intranmentioning
confidence: 99%
See 1 more Smart Citation
“…Barthelmes nanoparticles (TCS-NPs) of buspirone hydrochloride (BUH) for delivery into the brain through the intranasal route using bovine nasal cavity tissue. It was found that TCS-NPs had 15% more binding efficiency than unmodified CS-NPs, which could be due to the low amount of CS and TCS interacting with mucin, increased particle size of BUH-loaded CS and TCS nanoparticles and absorption of drug molecules on the NP surface, leading to low NP mucosal layer penetration [27]. Improved TCS binding efficiency could be due to covalent attachment of TGA to CS generating a thiol group that interacts with mucin [37].…”
Section: Microparticles and Nanoparticlesmentioning
confidence: 99%
“…The formulation (i.e. TCS-BUH-NPs) was also tested in vivo in Wistar rats: a comparatively higher brain concentration (797.46 ± 35.76 ng/ml; tmax 120 min) was achieved after intranasal administration of TCS-NPs compared with that achieved after nasal administration of the pure drug solution (417.77 ± 19.24 ng/ml; tmax 60 min), as shown in the figure 3b [27] .…”
Section: Microparticles and Nanoparticlesmentioning
confidence: 99%