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Nanoprecipitation preparation of low temperature-sensitive magnetoliposomes
[Display omitted] •Prepared hydrophobic magnetic nanoparticles-containing low temperature-sensitive liposomes using nanoprecipitation.•Developed ethanol-THF binary solvent that solubilized nanoparticle-lipids mixture, enabling magnetoliposomes self-assembly.•Confirmed drug loading capability and the...
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Published in: | Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2021-02, Vol.198, p.111453-111453, Article 111453 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Prepared hydrophobic magnetic nanoparticles-containing low temperature-sensitive liposomes using nanoprecipitation.•Developed ethanol-THF binary solvent that solubilized nanoparticle-lipids mixture, enabling magnetoliposomes self-assembly.•Confirmed drug loading capability and thermosensitivity of the magnetoliposomes prepared using nanoprecipitation.
Lysolipid-containing thermosensitive liposomes (LTSL) have gained attention for triggered release of chemotherapeutics. Superparamagnetic iron oxide nanoparticles (SPION) offers multimodal imaging and hyperthermia therapy opportunities as a promising theranostic agent. Combining LTSL with SPION may further enhance their performance and functionality of LTSL. However, a major challenge in clinical translation of nanomedicine is the poor scalability and complexity of their preparation process. Exploiting the nature of self-assembly, nanoprecipitation is a simple and scalable technique for preparing liposomes. Herein, we developed a novel SPION-incorporated lysolipid-containing thermosensitive liposome (mLTSL10) formulation using nanoprecipitation. The formulation and processing parameters were carefully designed to ensure high reproducibility and stability of mLTSL10. The effect of solvent, aqueous-to-organic volume ratio, SPION concentration on the mLTSL10 size and dispersity was investigated. mLTSL10 were successfully prepared with a small size (∼100 nm), phase transition temperature at around 42 °C, and high doxorubicin encapsulation efficiency. Indifferent from blank LTSL, we demonstrated that mLTSL10 combining the functionality of both LTSL and SPION can be successfully prepared using a scalable nanoprecipitation approach. |
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ISSN: | 0927-7765 1873-4367 |
DOI: | 10.1016/j.colsurfb.2020.111453 |