New-Concept Chemotherapy by Nanoparticles of Biodegradable Polymers: Where Are We Now?
Open accessAbstract
Among several promising new drug-delivery systems, liposomes represent an advanced technology to deliver active molecules to the site of action, and at present several formulations are in clinical use. Research on liposome technology has progressed from conventional vesicles ("first-generation liposomes") to "second-generation liposomes", in which long-circulating liposomes are obtained by modulating the lipid composition, size, and charge of the vesicle. Liposomes with modified surfaces have also been developed using several molecules, such as glycolipids or sialic acid. A significant step in the development of long-circulating liposomes came with inclusion of the synthetic polymer poly-(ethylene glycol) (PEG) in liposome composition. The presence of PEG on the surface of the liposomal carrier has been shown to extend blood-circulation time while reducing mononuclear phagocyte system uptake (stealth liposomes). This technology has resulted in a large number of liposome formulations encapsulating active molecules, with high target efficiency and activity. Further, by synthetic modification of the terminal PEG molecule, stealth liposomes can be actively targeted with monoclonal antibodies or ligands. This review focuses on stealth technology and summarizes pre-clinical and clinical data relating to the principal liposome formulations; it also discusses emerging trends of this promising technology.
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Liposomes have been widely used in medical diagnostics and drug delivery, but their use as boundary lubricants on solid surfaces has only very recently been explored.
“Liposomes have been widely used in medical diagnostics and for drug delivery [97, 98], but their use as boundary lubricants on solid surfaces has only very recently been explored.”
From Hydration lubrication (2013) · cites this paper as [97]
Stealth liposomes have been used successfully in delivery of doxorubicin for treatment of solid tumors and are marketed as Doxil or Caelyx.
“Stealth liposomes have been used successfully in the delivery of doxorubicin for the treatment of solid tumors and are presently marketed as ‘Doxil’ or ‘Caelyx’.54”
From Targeted therapy in chronic diseases using nanomaterial-based drug delivery vehicles (2019) · cites this paper as [54]
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- Authors
- Feng, S.-S.
- Affiliations
- National University of Singapore (SG)
- Corresponding author
- Feng, Si-Shen
- Venue
- Nanomedicine
- Publisher
- Informa UK Limited
- Published
- 2006-10
- Volume
- 1
- Issue
- 3
- Pages
- 297-309
- ISSN
- 1743-5889 (ISSN-L)
- 1748-6963
- PMC
- PMC2426795
- OpenAlex
- W1585705786
- Cited by
- 1,951
- References
- 223
- Citations by year
- 2026: 25 · 2025: 36 · 2024: 57 · 2023: 78 · 2022: 94 · 2021: 136 · 2020: 135 · 2019: 145 · 2018: 128 · 2017: 174 · 2016: 164 · 2015: 144 · 2014: 178 · 2013: 148 · 2012: 93
- FWCI
- 1.54
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nanomedicine (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
- Funders
- University of Texas MD Anderson Cancer Center
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- liposomes, PEGylated liposomes, long-circulating liposomes, biodegradable polymers, nanoparticle drug delivery, active targeting, monoclonal antibody targeting, sialic acid, glycolipids, chemotherapy, liposomal formulation
- MeSH terms
- Animals, Biocompatible Materials, Pharmaceutical Preparations, Humans, Neoplasms, Polymers, Drug Delivery Systems, Nanomedicine, Nanoparticles
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