Authors :
Sushmita P. Sawant; Madan D. Pomaje; Dr. Ashwini Patil
Volume/Issue :
Volume 10 - 2025, Issue 11 - November
Google Scholar :
https://tinyurl.com/4ps3jmjh
Scribd :
https://tinyurl.com/54s4ptmz
DOI :
https://doi.org/10.38124/ijisrt/25nov1105
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Note : Google Scholar may take 30 to 40 days to display the article.
Abstract :
Conventional drug delivery systems such as tablets, capsules, and injections often suffer from limitations
including poor solubility, low bioavailability, rapid clearance, and lack of site-specific targeting, which reduce therapeutic
efficiency and increase systemic side effects. In recent years, nanotechnology has become a promising strategy for
addressing these issues. Nanoparticles generally measure between 10 and 1000 nm, exhibit distinctive physicochemical
properties, such as a large surface area and adjustable surface features, allowing for enhanced drug solubility, controlled
release, and precise delivery. Nanoparticulate drug delivery systems (NDDS) offer several advantages, including enhanced
bioavailability, reduced dosing frequency, and the ability to cross biological barriers like the blood–brain barrier. Several
nanoparticle-based formulations, such as Doxil® and Abraxane®, have already received regulatory approval, highlighting
their clinical potential. This review aims to provide an overview of nanoparticulate drug delivery systems, with an
emphasis on the types of nanoparticles, methods of preparation, characterization, applications, regulatory considerations,
and future perspectives.
Keywords :
Nanoparticles, Drug Delivery, Targeted Delivery, Nanotechnology, Bioavailability.
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Conventional drug delivery systems such as tablets, capsules, and injections often suffer from limitations
including poor solubility, low bioavailability, rapid clearance, and lack of site-specific targeting, which reduce therapeutic
efficiency and increase systemic side effects. In recent years, nanotechnology has become a promising strategy for
addressing these issues. Nanoparticles generally measure between 10 and 1000 nm, exhibit distinctive physicochemical
properties, such as a large surface area and adjustable surface features, allowing for enhanced drug solubility, controlled
release, and precise delivery. Nanoparticulate drug delivery systems (NDDS) offer several advantages, including enhanced
bioavailability, reduced dosing frequency, and the ability to cross biological barriers like the blood–brain barrier. Several
nanoparticle-based formulations, such as Doxil® and Abraxane®, have already received regulatory approval, highlighting
their clinical potential. This review aims to provide an overview of nanoparticulate drug delivery systems, with an
emphasis on the types of nanoparticles, methods of preparation, characterization, applications, regulatory considerations,
and future perspectives.
Keywords :
Nanoparticles, Drug Delivery, Targeted Delivery, Nanotechnology, Bioavailability.