UGC Approved Journal no 63975(19)
New UGC Peer-Reviewed Rules

ISSN: 2349-5162 | ESTD Year : 2014
Volume 13 | Issue 3 | March 2026

JETIREXPLORE- Search Thousands of research papers



WhatsApp Contact
Click Here

Published in:

Volume 12 Issue 2
February-2025
eISSN: 2349-5162

UGC and ISSN approved 7.95 impact factor UGC Approved Journal no 63975

7.95 impact factor calculated by Google scholar

Unique Identifier

Published Paper ID:
JETIR2502141


Registration ID:
554760

Page Number

b423-b447

Share This Article


Jetir RMS

Title

Recent Advances in Targeted and Stimuli-Responsive Liposomal Drug Delivery

Abstract

Phospholipids are used to make liposomes, also known as lipid vesicles. The hydrophilic interaction of polar heads with the aqueous environment and the hydrophobic interaction of phospholipid tails produces the vesicular structure of liposomes. Hydrophilic medications are easier to catch within the liposome core, whereas lipophilic drugs are easier to capture between the phospholipid layers of the liposomes. Depending on the properties of the drug and the method of manufacture, a medicine is stored into the liposomal core or in between the liposome's bilayers. Research is done on a wide range of liposome uses, such as targeted drug administration, big molecule transport, enhanced solubility, diagnostics, and medicine stability. Liposomes can be thought of as having developed from trasditional, long-circulating, immune-system-targeting liposomes to actively targeted liposomes that respond to stimuli based on their composition. Liposomes are highly biocompatible, biodegradable, and immunogenicity-free, made them most used nanocarriers for a hydrophilic and hydrophobic substances. Additionally, liposomes showed enhanced drug solubility and regulated distribution in addition to their ability to modify their surface for targeted, prolonged, and sustained release. For the treatment of a wide range of diseases, including infections by viruses, fungi, and cancer, several liposomal-based drug delivery techniques are currently clinically approved; numerous liposomes have reached the level of clinical testing.

Key Words

Revolutionary changes, Methods of drug loading, classification, Evaluations, Liposomes as a vector in pharmaceutical product, Route of BBB for liposome transport, Liposomal methods for treating savior diseases.

Cite This Article

"Recent Advances in Targeted and Stimuli-Responsive Liposomal Drug Delivery", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.12, Issue 2, page no.b423-b447, February-2025, Available :http://www.jetir.org/papers/JETIR2502141.pdf

ISSN


2349-5162 | Impact Factor 7.95 Calculate by Google Scholar

An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 7.95 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator

Cite This Article

"Recent Advances in Targeted and Stimuli-Responsive Liposomal Drug Delivery", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.12, Issue 2, page no. ppb423-b447, February-2025, Available at : http://www.jetir.org/papers/JETIR2502141.pdf

Publication Details

Published Paper ID: JETIR2502141
Registration ID: 554760
Published In: Volume 12 | Issue 2 | Year February-2025
DOI (Digital Object Identifier):
Page No: b423-b447
Country: Beed, Maharashtra , India .
Area: Pharmacy
ISSN Number: 2349-5162
Publisher: IJ Publication


Preview This Article


Downlaod

Click here for Article Preview

Download PDF

Downloads

000301

Print This Page

Current Call For Paper

Jetir RMS