Targeted Drug Delivery Using Niosomes: Progress, Obstacles, and Future Directions

Niosomes are carriers that contain non-ionic surfactants in a vesicular form that have been presented as an innovative drug-delivery system of significant versatility due to their structural stability, biocompatibility, and drug loading capacity with various therapeutics. When comparing niosomes to standard liposomes, niosomes exhibit an enhanced physical and chemical stability, cost-effectiveness, and facility for a large-scale manufacture to be both clinically and industrially-relevant. Recent advances in formulation techniques focused on cholesterol, charge inducers, and newer surfactant combinations have initiated new methods of modulating vesicle-size, bilayer rigidity, and loading of attachment drugs, respectively. In addition, surface modifications of niosomes with ligands such as monoclonal antibodies, peptides, aptamers and folic acid, have greatly improved the ability to actively target cellular receptors, further providing site-specific delivery with improved therapeutic efficacy and a decreased potential for systemic toxicity. The inclusion of stimuli-responsive components such as pH-sensitive polymers, redox-reactive linkers, and thermoresponsive lipids have also afforded the development of smart niosome systems to trigger drug release according to pathological indicators. These characteristics have enabled niosomal applications across diverse disease models, such as solid tumors, fungal and bacterial infections, dermatological diseases, and neurological disorders. Apart from these encouraging characteristics, various translational challenges are still present, such as instability of the vesicles during storage, quick clearance in vivo, batch-to-batch reproducibility, and regulatory ambiguities. Novel strategies like PEGylation, freeze-drying, hybridization with biodegradable polymers, and utilization of scalable processes are being explored to resolve these issues. This review provides an integrative overview of recent research directions, challenges, and prospects of niosome-based targeted delivery, highlighting technological advancement as well as translational relevance. The observations made in this review will be useful for researchers, formulation scientists, and drug developers aiming to develop next-generation, patient-specific nanocarrier systems with superior specificity, safety, and clinical relevance.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-09-26
DOI
https://doi.org/10.5281/zenodo.17205269
Primary Topic
Biodiesel Production and Applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Targeted Drug Delivery Using Niosomes: Progress, Obstacles, and Future Directions

Zenodo (CERN European Organization for Nuclear Research)
Biodiesel Production and Applications
article

Targeted Drug Delivery Using Niosomes: Progress, Obstacles, and Future Directions

article en

Abstract

Niosomes are carriers that contain non-ionic surfactants in a vesicular form that have been presented as an innovative drug-delivery system of significant versatility due to their structural stability, biocompatibility, and drug loading capacity with various therapeutics. When comparing niosomes to standard liposomes, niosomes exhibit an enhanced physical and chemical stability, cost-effectiveness, and facility for a large-scale manufacture to be both clinically and industrially-relevant. Recent advances in formulation techniques focused on cholesterol, charge inducers, and newer surfactant combinations have initiated new methods of modulating vesicle-size, bilayer rigidity, and loading of attachment drugs, respectively. In addition, surface modifications of niosomes with ligands such as monoclonal antibodies, peptides, aptamers and folic acid, have greatly improved the ability to actively target cellular receptors, further providing site-specific delivery with improved therapeutic efficacy and a decreased potential for systemic toxicity. The inclusion of stimuli-responsive components such as pH-sensitive polymers, redox-reactive linkers, and thermoresponsive lipids have also afforded the development of smart niosome systems to trigger drug release according to pathological indicators. These characteristics have enabled niosomal applications across diverse disease models, such as solid tumors, fungal and bacterial infections, dermatological diseases, and neurological disorders. Apart from these encouraging characteristics, various translational challenges are still present, such as instability of the vesicles during storage, quick clearance in vivo, batch-to-batch reproducibility, and regulatory ambiguities. Novel strategies like PEGylation, freeze-drying, hybridization with biodegradable polymers, and utilization of scalable processes are being explored to resolve these issues. This review provides an integrative overview of recent research directions, challenges, and prospects of niosome-based targeted delivery, highlighting technological advancement as well as translational relevance. The observations made in this review will be useful for researchers, formulation scientists, and drug developers aiming to develop next-generation, patient-specific nanocarrier systems with superior specificity, safety, and clinical relevance.

Zenodo (CERN European Organization for Nuclear Research)
Industry, innovation and infrastructure
Openalex Percentile: Top 52%
Biodiesel Production and Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.