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Fliposomes: pH-triggered conformational flip of new trans-2-aminocyclohexanol-based amphiphiles causes instant cargo release in liposomes. | LitMetric

AI Article Synopsis

  • Researchers created a new kind of pH-sensitive liposomes called fliposomes, designed to release their contents when exposed to lower pH levels.
  • These liposomes feature unique molecules called flipids that undergo a conformational change (or "flip") in response to acidic conditions, leading to membrane disruption and rapid cargo release.
  • The study demonstrated that the speed of content release can vary based on pH levels, and the design of flipids can be customized to target specific acidic environments for controlled drug delivery.

Article Abstract

A new type of pH-sensitive liposomes (fliposomes) was designed based on the amphiphiles that are able to perform a pH-triggered conformational flip (flipids). This flip disrupts the liposome membrane and causes rapid release of the liposome cargo, specifically in response to lowered pH. The flipids (1) and (2) are equipped with a trans-2-aminocyclohexanol conformational switch. pH-sensitive fliposomes containing one or both of these flipids, as well as POPC and PEG ceramide, were constructed and characterized. These compositions were stable at 4°C and pH 7.4 for several months. Fliposomes loaded with ANTS/DPX performed an unusually quick content release within a few seconds at pH below 8.5 (in case of 2) and 6.0 (in case of 1). This difference in pH sensitivity demonstrates a potential for the custom design of flipids by variation of the amino group to target areas with specific pH values. The pH titration curves for the fliposome leakage parallel the curves for the acid-induced conformational flip of 1 and 2 studied by ¹H NMR. A plausible mechanism of pH sensitivity starts with an acid-triggered conformational flip of 1 or 2, which changes the molecular size and shape, shortens the lipid tails, and perturbs the liposome membrane, resulting in the content leakage.

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Source
http://dx.doi.org/10.3109/08982104.2012.698420DOI Listing

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