Rifampicin-Loaded Nanoparticles for Targeted Tuberculosis Therapy: Enhancing Delivery and Efficacy
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Abstract
Tuberculosis (TB) remains a major global health challenge, with limitations in the present drug regimens, including
poor bioavailability, systemic side effects, and the emergence of multidrug resistance. Rifampicin (RMP), a firstline anti-TB drug, suffers from rapid metabolism, limited tissue penetration, and poor targeting, necessitating
frequent dosing. Nanoparticle-based drug delivery systems offer a promising strategy to address these challenges
by enhancing targeted delivery, reducing toxicity, and improving therapeutic efficacy. A disruptive solution
to these challenges is presented by nanotechnology-based drug delivery systems. In this review, we examine
various studies on RMP-loaded nanoparticles, including polymeric nanoparticles, lipid-based nanocarriers (such
as liposomes and solid lipid nanoparticles), metallic nanoparticles, dendrimers, and micelles. These carriers
enhance the stability of the drug, facilitate its controlled release, and target its delivery to TB-infected tissues and
macrophages. Nanocarriers loaded with RMP have a high potential for transforming TB treatment because they
are more effective, have fewer systemic adverse effects, and are part of combating TB drug resistance on a global
scale.
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