Protective effect of surface-modified berberine nanoparticles against LPS-induced neurodegenerative changes: a preclinical study
Lipopolysaccharides
Male
Chitosan
0303 health sciences
Amyloid beta-Peptides
Berberine
Brain
Neurodegenerative Diseases
Glutathione
3. Good health
03 medical and health sciences
Glucose
Neuroprotective Agents
Liver
Acetylcholinesterase
Animals
Nanoparticles
Rats, Wistar
DOI:
10.1007/s13346-019-00626-1
Publication Date:
2019-03-13T11:02:20Z
AUTHORS (6)
ABSTRACT
Berberine (BBR) exerts documented protection against neurodegenerative disorders. However, data on the effect of nano-encapsulation on the neuroprotective effect of BBR are lacking. We investigated the effect of BBR loading into chitosan (CS) nanoparticles (NPs) and their surface modification with Tween 80 (T80), polyethylene glycol 4000 (PEG), and miltefosine (MFS) against lipopolysaccharide (LPS)-induced neurodegenerative changes in addition to hepatotoxicity in rats. BBR-NPs were prepared by ionic gelation and characterized for morphology by transmission electron microscopy (TEM), colloidal properties, and entrapment efficiency (EE%). The neuroprotective and hepatoprotective effects of a 14-day pretreatment with four BBR-NPs formulations (4 mg/kg BBR/day) by intraperitoneal (i.p.) injection were challenged by a single i.p. 4 mg/kg dose of LPS on the fifteenth day. Neuroprotective efficacy and potential toxicity of BBR-NPs relative to BBR solution were assessed biochemically and histopathologically. One-way ANOVA followed by Tukey's comparison test was used for statistical analysis. CS nano-encapsulation and surface modification of BBR-NPs altered the neuroprotective and hepatoprotective effects of BBR depending on the physicochemical and/or biological effects of BBR, CS, coating materials, and NP-related features. Similar to the prophylactic and treatment efficacy of NPs for brain delivery, safety of these nanostructures and their individual formulation components warrants due research attention.
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