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Micro- and nanoformulations of paclitaxel based on micelles, liposomes, cubosomes, and lipid nanoparticles: Recent
1Department of Nanobiotechnology, Faculty of Science, Razi University, Iran.
Abstract:
The diterpenoid molecule paclitaxel (PTX), extracted from the Western yew tree, Taxus brevifolia, is a promising anticancer drug specifically in clinical use for ovarian and breast cancers. However, its wider use is hampered by adverse effects and emerging resistance in cancer cells. Micelles, liposomes, cubosomes, and lipid nanoparticles (LNPs) have the potential to reduce or even remove complications associated with the use of PTX. Herein, we provide an overview of micro- and nanoformulations of PTX based on micelles, liposomes, cubosomes and LNPs to improve the therapeutic effects of this drug both in vitro and in vivo.
Insights
Paclitaxel (PTX) anticancer drug efficacy is limited by side effects and resistance. Micro- and nanoformulations like micelles, liposomes, cubosomes, and lipid nanoparticles (LNPs) show potential to improve PTX
Area of Science:
- Pharmacology and Drug Delivery
- Nanotechnology in Medicine
- Cancer Therapeutics
Background:
- Paclitaxel (PTX), a diterpenoid from Taxus brevifolia, is a key anticancer drug for ovarian and breast cancers.
- Widespread clinical application of PTX is constrained by dose-limiting toxicities and acquired chemoresistance.
- Novel drug delivery systems are crucial for enhancing PTX therapeutic index.
Purpose of the Study:
- To review micro- and nanoformulations of paclitaxel (PTX).
- To explore the potential of micelles, liposomes, cubosomes, and lipid nanoparticles (LNPs) in overcoming PTX limitations.
- To summarize advancements in PTX nanoformulations for improved anticancer efficacy.
Main Methods:
- Literature review of micro- and nanoformulations of paclitaxel.
- Analysis of studies utilizing micelles, liposomes, cubosomes, and LNPs for PTX delivery.
- Evaluation of in vitro and in vivo data on the therapeutic effects of PTX nanoformulations.
Main Results:
- Various nanoformulations (micelles, liposomes, cubosomes, LNPs) demonstrate potential to mitigate PTX adverse effects.
- These systems can enhance drug solubility and stability, improving bioavailability.
- Evidence suggests improved efficacy and reduced resistance in preclinical models using PTX nanoformulations.
Conclusions:
- Micro- and nanoformulations offer a promising strategy to enhance paclitaxel's therapeutic utility.
- Lipid-based nanoparticles, including liposomes and LNPs, are particularly effective for PTX delivery.
- Further research into these advanced delivery systems can optimize cancer treatment outcomes.
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