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Updated: Aug 5, 2026

Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
Published on: August 28, 2015
Self-assembled paclitaxel-loaded spermidine-geranic acid ionic liquid nanoaggregates: preparation, enhanced cellular
1Laboratory of Pharmaceutical Crystal Engineering & Technology, State Key Laboratory of Bioreactor Engineering, Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Engineering Research Centre of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, No. 130 Meilong Road, Shanghai 200237, China.
Abstract:
Paclitaxel (PTX) is a potent anticancer drug whose efficacy is limited by poor solubility and severe side effects. This study developed a self-assembled nanoaggregate system based on a novel spermidine-geranic acid ionic liquid ([Spd][Ger] IL) for PTX delivery. The synthesized [Spd][Ger] IL exhibited a low apparent critical aggregation concentration (0.33 mg/mL), and molecular dynamics simulation confirmed its spontaneous self-assembly in water. PTX was efficiently incorporated into [Spd][Ger] nanoaggregates, affording a stable formulation with an encapsulation efficiency of 89.6%, a drug loading of 8.3%, and an average particle size of 171.8 nm. PTX@[Spd][Ger] showed sustained and pH-responsive release, with cumulative PTX release of 73.66% at pH 6.5 and 61.60% at pH 7.4 after 72 h. In vitro, PTX@[Spd][Ger] reduced the IC50 from 2.25 to 0.60 μg/mL in MCF-7 cells and from 4.33 to 1.24 μg/mL in 4 T1 cells after incubation for 24 h, which was attributed to the higher cellular uptake of [Spd][Ger] nanoaggregates. In a 4 T1 orthotopic mouse model, PTX@[Spd][Ger] produced tumor suppression comparable to Taxol® with markedly improved systemic tolerability. These results indicate that [Spd][Ger]-based nanoaggregates provide an effective and safer platform for water-insoluble drug delivery such as PTX.
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