• Ketki Shyam Halnor
• Mahendra Khandare
• Dr. Gajanan Sanap

Liposomes are made of phospholipids and lipids. Liposomes are spherical or multilayered spherical vesicles with a lipid bilayer structure that form in aqueous solutions when diacyl chain phospholipids self-assemble. The number of bilayers and vesicle size both have an impact on the quantity of drug encapsulation in the liposomes, which is a key factor in determining the circulation half-life of liposomes. This method involved coating a medication and a lipid onto a soluble carrier to create a pro-liposome that was free-flowing and granular and that, when hydrated, formed an isotonic liposomal solution. The pro-liposome strategic strategy will provide motivation for mass production of liposomes containing medications that are lipophilic at low cost. Due to some special properties like increased drug solubility (amphotericin B), molecule protection (DNA, RNA), enhanced intracellular uptake (anti-cancer drugs), serving as a drug depot, and increasing the stability of the drug, these systems were successfully used for delivery of different categories of drugs such as anti-viral, anti-cancer, anti-inflammatory, antibiotics, and anti-fungal etc. Preparation and evaluation of liposomes of brimonidine tartrate as an ODDS(Occular). Development and characterization of liposomal drug delivery system for Liposomes: from a clinically Established drug delivery system to a nanoparticle platform for Theragnostic nanomedicine.

Liposomes, Drug, lipid, lymph, phospholipid

"Liposomes : Drug Delivery System", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.10, Issue 3, page no.e370-e378, March-2023, Available :http://www.jetir.org/papers/JETIR2303444.pdf

"Liposomes : Drug Delivery System", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.10, Issue 3, page no. ppe370-e378, March-2023, Available at : http://www.jetir.org/papers/JETIR2303444.pdf