Enhanced oral bioavailability and hepatoprotective activity of thymoquinone in the form of phospholipidic nano-constructs
dc.contributor.author | Rathore, C. | |
dc.contributor.author | Upadhyay, N. | |
dc.contributor.author | Kaundal, R. | |
dc.contributor.author | Dwivedi, R. P. | |
dc.contributor.author | Rahatekar, Sameer S. | |
dc.contributor.author | John, A. | |
dc.contributor.author | Dua, K | |
dc.contributor.author | Tambuwala, M. M. | |
dc.contributor.author | Jain, S. | |
dc.contributor.author | Chaudari, D. | |
dc.contributor.author | Negi, P. | |
dc.date.accessioned | 2020-04-29T10:10:41Z | |
dc.date.available | 2020-04-29T10:10:41Z | |
dc.date.issued | 2020-01-31 | |
dc.description.abstract | Background: The poor biopharmaceutical properties of thymoquinone (TQ) obstruct its development as a hepatoprotective agent. To surmount the delivery challenges of TQ, phospholipid nanoconstructs (PNCs) were constructed. Method: PNCs were constructed employing microemulsification technique and systematic optimization by three-factor three level Box-Behnken design. Result: Optimized PNC composition exhibited nano size (<100 nm), spherical morphology, within acceptable range of polydispersity index (0.55), high drug entrapment efficiency (>90%), controlled drug release pattern, and neutral surface charge (zeta potential of −0.65 mV). After oral administration of a single dose of PNC, it showed a relative bioavailability of 386.03% vis-à-vis plain TQ suspension. Further, TQ-loaded PNC demonstrated significant enhanced hepato-protective effect vis-à-vis pure TQ suspension and silymarin, as evidenced by reduction in the ALP, ALT, AST, bilirubin, and albumin level and ratified by histopathological analysis. Conclusion: TQ-loaded PNCs can be efficient nano-platforms for the management of hepatic disorders and promising drug delivery systems to enhance oral bioavailability of this hydrophobic molecule. | en_UK |
dc.identifier.citation | Rathore C, Upadhyay N, Kaundal R, et al., (2020) Enhanced oral bioavailability and hepatoprotective activity of thymoquinone in the form of phospholipidic nano-constructs. Expert Opinion on Drug Delivery, Volume 17, Issue 2, 2020, pp. 237-253 | en_UK |
dc.identifier.issn | 1742-5247 | |
dc.identifier.uri | https://doi.org/10.1080/17425247.2020.1716728 | |
dc.identifier.uri | https://dspace.lib.cranfield.ac.uk/handle/1826/15416 | |
dc.language.iso | en | en_UK |
dc.publisher | Taylor and Francis | en_UK |
dc.rights | Attribution-NonCommercial 4.0 International | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | * |
dc.subject | Thymoquinone | en_UK |
dc.subject | box-Behnken design | en_UK |
dc.subject | lipid carriers | en_UK |
dc.subject | microemulsifcation | en_UK |
dc.subject | hepatotoxicity | en_UK |
dc.subject | pharmacokinetics | en_UK |
dc.title | Enhanced oral bioavailability and hepatoprotective activity of thymoquinone in the form of phospholipidic nano-constructs | en_UK |
dc.type | Article | en_UK |