Interference of phosphatidylcholines with in-vitro cell proliferation - no flock without black sheep.
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Summary
Unlike the non-toxic PCs usually used for liposomal drug delivery, the elucidated diacyl-PCs may be worthy of further examination to eventually construct a toxic shell for toxic drugs, thereby enhancing anticancer drug delivery via lipid particles.
- Type
- article
- Published
- 2015-07-01
- Cited by
- 11
- References
- 41
- OpenAlex
- https://openalex.org/W25911997
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:43280403
Keywords
Art
References
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- Acetate-encapsulated Linolenic Acid Liposomes Reduce SARS-CoV-2 and RSV Infection
- Fusogenic liposome-coated nanoparticles for rapid internalization into donor corneal endothelial tissue to enable prophylaxis before transplantation
- Functional, transcriptomic, and lipidomic studies of the choC gene encoding a phospholipid methyltransferase in Aspergillus fumigatus
- Phospholipids with two polyunsaturated fatty acyl tails promote ferroptosis
- Host sphingolipids support Plasmodium berghei liver stage development
- Self-assembly of lipid corona on biocompatible gold nanoparticle suprastructures with plasmonic and theranostic functions.
- Enhancement of tobramycin and amikacin activities by co-encapsulation in liposomal-thymoquinone formulation: antibacterial, antibiofilm, and cytocompatibility study
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