Crafting ɣ-L-Glutamyl-l-Cysteine layered Human Serum Albumin-nanoconstructs for brain targeted delivery of ropinirole to attenuate cerebral ischemia/reperfusion injury via "3A approach".
Antioxidants
/ therapeutic use
Brain
Brain Ischemia
/ drug therapy
Cysteine
/ therapeutic use
Dopamine
/ therapeutic use
Humans
Indoles
Infarction, Middle Cerebral Artery
/ drug therapy
Ischemic Stroke
Mitochondrial Permeability Transition Pore
Neuroprotective Agents
/ pharmacology
Reperfusion Injury
/ drug therapy
Serum Albumin, Human
/ therapeutic use
Brain targeted drug delivery
Human serum albumin nanoparticles
Ischemic stroke and reperfusion injury
Mitochondria
Neuroprotection
Ropinirole hydrochloride
Journal
Biomaterials
ISSN: 1878-5905
Titre abrégé: Biomaterials
Pays: Netherlands
ID NLM: 8100316
Informations de publication
Date de publication:
10 2022
10 2022
Historique:
received:
10
03
2022
revised:
23
08
2022
accepted:
11
09
2022
pubmed:
27
9
2022
medline:
7
10
2022
entrez:
26
9
2022
Statut:
ppublish
Résumé
Treatment of Ischemic Stroke is inordinately challenging due to its complex aetiology and constraints in shuttling therapeutics across blood-brain barrier. Ropinirole hydrochloride (Rp), a propitious neuroprotectant with anti-oxidant, anti-inflammatory, and anti-apoptotic properties (3A) is repurposed for remedying ischemic stroke and reperfusion (I/R) injury. The drug's low bioavailability in brain however, limits its therapeutic efficacy. The current research work has reported sub-100 nm gamma-L-Glutamyl-L-Cysteine coated Human Serum Albumin nanoparticles encapsulating Rp (C-Rp-NPs) for active targeting in ischemic brain to encourage in situ activity and reduce unwanted toxicities. Confocal microscopy and brain distribution studies confirmed the enhanced targeting potentiality of optimized C-Rp-NPs. The pharmacokinetics elucidated that C-Rp-NPs could extend Rp retention in systemic circulation and escalate bioavailability compared with free Rp solution (Rp-S). Additionally, therapeutic assessment in transient middle cerebral occlusion (tMCAO) model suggested that C-Rp-NPs attenuated the progression of I/R injury with boosted therapeutic index at 1000 times less concentration compared to Rp-S via reinstating neurological and behavioral deficits, while reducing ischemic neuronal damage. Moreover, C-Rp-NPs blocked mitochondrial permeability transition pore (mtPTP), disrupted apoptotic mechanisms, curbed oxidative stress and neuroinflammation, and elevated dopamine levels post tMCAO. Thus, our work throws light on fabrication of rationally designed C-Rp-NPs with enormous clinical potential.
Identifiants
pubmed: 36162213
pii: S0142-9612(22)00445-8
doi: 10.1016/j.biomaterials.2022.121805
pii:
doi:
Substances chimiques
Antioxidants
0
Indoles
0
Mitochondrial Permeability Transition Pore
0
Neuroprotective Agents
0
ropinirole
030PYR8953
Cysteine
K848JZ4886
Dopamine
VTD58H1Z2X
Serum Albumin, Human
ZIF514RVZR
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
121805Informations de copyright
Copyright © 2022 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Farhan Jalees Ahmad has patent #202111059333 pending to Jamia Hamdard.