Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/5052
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dc.contributor.authorPal, Santanu Kumar-
dc.date.accessioned2023-08-22T16:03:17Z-
dc.date.available2023-08-22T16:03:17Z-
dc.date.issued2022-
dc.identifier.citationJournal of Materials Chemistry B, 10(16), 3032-3038.en_US
dc.identifier.urihttps://doi.org/10.1039/d2tb00098a-
dc.identifier.urihttp://hdl.handle.net/123456789/5052-
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractNanoscale assemblies of amphiphiles have been vividly explored in pharmaceutical formulations as drug nanocarriers. Aqueous interfaces of liquid crystals (LCs) are known to direct the self-assembly of a range of amphiphiles. These amphiphile-decorated interfaces of LCs have evoked interest for applications as diverse as the detection of disease markers, screening of toxins, mimicking complex biomolecular interactions, and cell-based sensing. Aiming to explore these interfaces for encapsulation and enzyme-triggered release, we report a simple and rational design of enzyme-responsive LC interfaces programmed with a cleavable non-ionic surfactant. We encapsulated a hydrophobic dye within the surfactant micelles and investigated the enzyme-triggered dye release. Interestingly, we found that LC droplets, when decorated with the dye-loaded micelles, offer significant advantages over the conventional micellar nanocarriers. The LC droplets showed controlled release features which weren’t affected at high dilutions. Our work, although exploratory in nature, provides fresh approaches for tailoring LC interfaces as vehicles for drug delivery.en_US
dc.language.isoen_USen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectTailoring liquid crystalsen_US
dc.subjectvehicles for encapsulationen_US
dc.subjectenzyme-triggered releaseen_US
dc.titleTailoring liquid crystals as vehicles for encapsulation and enzyme- triggered release.en_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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