DOI: https://doi.org/10.63345/ijrmp.v14.i5.2
Shruti Rao
Independent Researcher
Jayanagar, Karnataka, India
Abstract
Self-assembling nanoparticles have emerged as a promising strategy to overcome the challenges associated with oral drug delivery. Their unique ability to spontaneously form nanostructured assemblies offers improved solubility, enhanced permeability, and protection from the harsh gastrointestinal environment, thereby increasing the bioavailability of drugs that traditionally suffer from low absorption rates. This study reviews the recent literature (up to 2020) on self-assembling nanoparticle systems, investigates their physicochemical characteristics, and assesses their efficacy in improving oral bioavailability through statistical analysis. The experimental methodology was designed to compare key pharmacokinetic parameters of drugs encapsulated in self-assembling nanoparticles versus conventional formulations. The results indicate significant improvements in absorption and bioavailability, suggesting that self-assembling nanoparticles represent a viable approach for the oral delivery of poorly soluble drugs. The findings underscore the potential of nanotechnology in pharmaceutical development and invite further exploration of nanoparticle-based drug delivery systems.
Keywords
Self-assembling nanoparticles; oral drug delivery; bioavailability; nanotechnology; pharmacokinetics
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