Niosomes: A promising approach for targeted drug delivery

Niosomes, also known as nonionic surfactant vesicles, are small lamellar structures that are created by combining nonionic surfactants from the alkyl or dialkyl polyglycerol ether category with cholesterol, and then hydrating them in water-based solutions. These are vesicle systems resembling liposomes that can be utilized as carriers for drugs that are both amphiphilic and lipophilic. The production process of niosomes is derived from liposome technology. The fundamental manufacturing method remains unchanged, wherein the lipid phase is hydrated by the aqueous phase. The lipid phase can consist of either a pure surfactant or a combination of surfactant and cholesterol. Niosomes effectively tackle the challenges associated with medication insolubility, instability, inadequate bioavailability, and fast degradation. The amphiphilic character of niosomes, which combines both hydrophilic and lipophilic properties, enhances their capacity to encapsulate medicines that are either hydrophilic or lipophilic. Cholesterol is frequently utilized as one of the ingredients. Preserving the stiffness of the niosome structure. The present article discusses the essential elements of niosomes, including their structural constituents, methods of manufacturing, and their uses in different disorders.

Authors

Institutions

Publication Details

Journal
GSC Biological and Pharmaceutical Sciences
Published
2024-10-22
DOI
https://doi.org/10.30574/gscbps.2024.29.1.0341
Citations
7
Primary Topic
Advancements in Transdermal Drug Delivery
Type
article
Field-Weighted Citation Impact
1.46
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Niosomes: A promising approach for targeted drug delivery

Jitendra A. Kubde, Disha A. Deulkar, Pooja R. Hatwar, Ravindra L. Bakal et al.
7 citations
GSC Biological and Pharmaceutical Sciences
Advancements in Transdermal Drug Delivery
1.46
article

Niosomes: A promising approach for targeted drug delivery

Jitendra A. Kubde, Disha A. Deulkar, Pooja R. Hatwar, Ravindra L. Bakal, Anjali N. Motwani
article en
7 citations

Abstract

Niosomes, also known as nonionic surfactant vesicles, are small lamellar structures that are created by combining nonionic surfactants from the alkyl or dialkyl polyglycerol ether category with cholesterol, and then hydrating them in water-based solutions. These are vesicle systems resembling liposomes that can be utilized as carriers for drugs that are both amphiphilic and lipophilic. The production process of niosomes is derived from liposome technology. The fundamental manufacturing method remains unchanged, wherein the lipid phase is hydrated by the aqueous phase. The lipid phase can consist of either a pure surfactant or a combination of surfactant and cholesterol. Niosomes effectively tackle the challenges associated with medication insolubility, instability, inadequate bioavailability, and fast degradation. The amphiphilic character of niosomes, which combines both hydrophilic and lipophilic properties, enhances their capacity to encapsulate medicines that are either hydrophilic or lipophilic. Cholesterol is frequently utilized as one of the ingredients. Preserving the stiffness of the niosome structure. The present article discusses the essential elements of niosomes, including their structural constituents, methods of manufacturing, and their uses in different disorders.

GSC Biological and Pharmaceutical SciencesVol. 29(1)
Shri Vile Parle Kelavani Mandal (IN)
Openalex Percentile: Top 20%
Advancements in Transdermal Drug Delivery
1.46
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.