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dc.contributor.authorIlhan‐Ayisigi, Esra
dc.contributor.authorGhazal, Aghiad
dc.contributor.authorSartori, Barbara
dc.contributor.authorDimaki, Maria
dc.contributor.authorSvendsen, Winnie Edith
dc.contributor.authorYesil‐celiktas, Ozlem
dc.contributor.authorYaghmur, Anan
dc.date.accessioned2023-11-08T07:42:46Z
dc.date.available2023-11-08T07:42:46Z
dc.date.issued2021en_US
dc.identifier.citationIlhan-Ayisigi, E., Ghazal, A., Sartori, B., Dimaki, M., Svendsen, W. E., Yesil-Celiktas, O., & Yaghmur, A. (2021). Continuous microfluidic production of citrem-phosphatidylcholine nano-self-assemblies for thymoquinone delivery. Nanomaterials, 11(6), 1510.en_US
dc.identifier.issn20794991
dc.identifier.urihttps://doi.org/10.3390/nano11061510
dc.identifier.urihttps://hdl.handle.net/20.500.12513/5333
dc.description.abstractLamellar and non‐lamellar liquid crystalline nanodispersions, including liposomes, cubo-somes, and hexosomes are attractive platforms for drug delivery, bio‐imaging, and related pharmaceutical applications. As compared to liposomes, there is a modest number of reports on the continuous production of cubosomes and hexosomes. Using a binary lipid mixture of citrem and soy phosphatidylcholine (SPC), we describe the continuous production of nanocarriers for delivering thymoquinone (TQ, a substance with various therapeutic potentials) by employing a commercial microfluidic hydrodynamic flow‐focusing chip. In this study, nanoparticle tracking analysis (NTA) and synchrotron small‐angle X‐ray scattering (SAXS) were employed to characterize TQ‐free and TQ‐loaded citrem/SPC nanodispersions. Microfluidic synthesis led to formation of TQ‐free and TQ-loaded nanoparticles with mean sizes around 115 and 124 nm, and NTA findings indicated comparable nanoparticle size distributions in these nanodispersions. Despite the attractiveness of the mi-crofluidic chip for continuous production of citrem/SPC nano‐self‐assemblies, it was not efficient as comparable mean nanoparticle sizes were obtained on employing a batch (discontinuous) method based on low‐energy emulsification method. SAXS results indicated the formation of a biphasic feature of swollen lamellar (Lα) phase in coexistence with an inverse bicontinuous cubic Pn3m phase in all continuously produced TQ‐free and TQ‐loaded nanodispersions. Further, a set of SAXS experiments were conducted on samples prepared using the batch method for gaining further insight into the effects of ethanol and TQ concentration on the structural features of citrem/SPC nano‐self-assemblies. We discuss these effects and comment on the need to introduce efficient microfluidic platforms for producing nanocarriers for delivering TQ and other therapeutic agents. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.en_US
dc.language.isoengen_US
dc.publisherMDPI AGen_US
dc.relation.isversionof10.3390/nano11061510en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectInverse bicontinuous cubic Pn3m phaseen_US
dc.subjectMicrofluidicsen_US
dc.subjectNanoparticle tracking analysisen_US
dc.subjectSynchrotron small‐angle scatteringen_US
dc.subjectThymoquinoneen_US
dc.titleContinuous microfluidic production of citrem‐phosphatidylcholine nano‐self‐assemblies for thymoquinone deliveryen_US
dc.typearticleen_US
dc.relation.journalNanomaterialsen_US
dc.contributor.departmentMühendislik-Mimarlık Fakültesien_US
dc.contributor.authorIDEsra İlhan Ayışığı / 0000-0003-1880-4261en_US
dc.identifier.volume11en_US
dc.identifier.issue6en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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