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NeuroAmph: Innovative Synergy of Polydopamine and Peptide Amphiphiles for Enhanced Cognitive Pathology Treatment
* 1, 2 , 1, 3
1  PhD Research Scholar, Institute of Pharmaceutical Research, GLA University, Mathura, India
2  Assistant Professor, Department of Pharmacy, Rakshpal Bahadur College of Pharmacy, Bareilly, India
3  Head of the Department (Academics), Department of Pharmacy, Rakshpal Bahadur College of Pharmacy, Bareilly, India
Academic Editor: Gary Bowlin

Abstract:

Introduction: The complicated nature and progressive deterioration of neural tissues make therapeutic intervention for cognitive diseases, such as Alzheimer's disease and other neurodegenerative disorders, enormously challenging. Current medications often fail to prevent the advancement of these diseases. NeuroAmph presents itself as a revolutionary therapeutic approach that combines polydopamine (PDA) and peptide amphiphiles (PAs) to overcome these barriers. PDA, which is derived from dopamine polymerization, offers strong adhesion properties and biocompatibility. On the other hand, PAs have the ability to self-assemble and deliver bioactive molecules to neural tissues with precision.

Methods: This review explores the synthesis methodologies and characterization techniques of NeuroAmph, emphasizing their seamless integration into multifunctional nanostructures tailored for neurological applications. Several studies have shown that NeuroAmph works to reduce oxidative stress markers and improve neuronal viability in disease models. This makes it even more likely that it can be used to change people's lives.

Results: NeuroAmph operates through sophisticated mechanisms tailored to combat cognitive pathologies at multiple levels. PDA facilitates the robust adhesion and stability of nanostructures that are critical for targeted drug delivery, whereas PAs self-assemble into biocompatible micelles capable of encapsulating neuroprotective agents. When administered, NeuroAmph interacts with neuronal cell membranes to help therapeutic payloads enter cells. By scavenging ROS and regulating antioxidant pathways, NeuroAmph protects neurons from oxidative stress. Additionally, the way that PDA and PAs work together allows for the long-term release of bioactive compounds, which supports neuroregenerative processes and improves synaptic plasticity.

Conclusions: NeuroAmph's integrated approach offers a promising strategy for improving treatment outcomes in cognitive pathologies by addressing key disease mechanisms. Additional research into NeuroAmph's therapeutic effectiveness and safety profiles is critical for furthering its use in clinical settings and offering novel approaches to controlling neurological disorders.

Keywords: NeuroAmph, Polydopamine (PDA), Peptide Amphiphiles (PAs), Cognitive Pathologies, Neuroprotection, Drug Delivery, Biomaterials, Neural Tissue Engineering, Oxidative Stress, Neurodegenerative Disorders.

 
 
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