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What We Need to Know About Liposomes As Drug Nanocarriers: An Updated Review Publisher



Abbasi H1, 2 ; Kouchak M2, 3 ; Mirveis Z1, 2 ; Hajipour F1 ; Khodarahmi M1, 2 ; Rahbar N2 ; Handali S4
Authors
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Authors Affiliations
  1. 1. Department of Medicinal Chemistry, School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  2. 2. Nanotechnology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  3. 3. Department of Pharmaceutics, School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  4. 4. Medical Biomaterials Research Center (MBRC), Tehran University of Medical Sciences, Tehran, Iran

Source: Advanced Pharmaceutical Bulletin Published:2023


Abstract

Liposomes have been attracted considerable attention as phospholipid spherical vesicles, over the past 40 years. These lipid vesicles are valued in biomedical application due to their ability to carry both hydrophobic and hydrophilic agents, high biocompatibility and biodegradability. Until now, various methods have been used for the synthesis of liposomes and the numerous modifications have been performed to improve liposomes characteristics such as surface charge, size, number of their layers, and length of circulation in biological fluids. This article provides an overview of the significant advances in synthesis of liposomes via active or passive drug loading methods, as well as describes some strategies developed to fabricate their targeted formulations to overcome limitations of the “first-generation” liposomes. © 2023 The Author (s).
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