Development and preclinical evaluation of microneedle-assisted resveratrol loaded nanostructured lipid carriers for localized delivery to breast cancer therapy

dc.contributor.authorGadag, S.
dc.contributor.authorNarayan, R.
dc.contributor.authorNayak, A.S.
dc.contributor.authorCatalina Ardila, D.
dc.contributor.authorSant, S.
dc.contributor.authorYogendra, Y.
dc.contributor.authorGarg, S.
dc.contributor.authorNayak, U.Y.
dc.date.accessioned2026-02-05T09:26:44Z
dc.date.issued2021
dc.description.abstractResveratrol (RVT) is one of the potent anticancer phytochemicals which has shown promising potential for breast cancer therapy. However, its short half-life and low bioavailability is a major hurdle in its effective use. In this study, we have developed nanostructured lipid carriers (NLCs) of RVT to enable localized delivery of the drug to the breast tissues using microneedle arrays to improve effectiveness. The NLCs were optimized using the Design of Experiments approach and characterized for their particle size, polydispersity index, zeta potential and entrapment efficiency. The RVT-NLCs delivered using microneedle array 1200 showed a higher permeation of RVT across the skin with lower skin retention compared to pure RVT. Further, RVT-NLCs showed higher anticancer activity on MDA-MB-231 breast cancer cell lines and enhanced internalization compared to pure RVT. Moreover, the RVT-NLCs were found to inhibit the migration of MDA-MB-231 breast cancer cell lines. Preclinical studies in rats showed that RVT-NLCs delivered via microneedles demonstrated a remarkable increase in the C<inf>max</inf>, T<inf>max</inf> and AUC<inf>0-inf</inf>, and a higher localization in breast tissue compared to pure RVT administered orally. These results suggests that the RVT-NLCs administered by microneedle array system is an effective strategy for the local delivery of RVT for breast cancer therapy. © 2021 Elsevier B.V.
dc.identifier.citationInternational Journal of Pharmaceutics, 2021, 606, , pp. -
dc.identifier.issn3785173
dc.identifier.urihttps://doi.org/10.1016/j.ijpharm.2021.120877
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/23082
dc.publisherElsevier B.V.
dc.subjectlipid nanoparticle
dc.subjectresveratrol
dc.subjectdrug carrier
dc.subjectlipid
dc.subjectnanomaterial
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantineoplastic activity
dc.subjectarea under the curve
dc.subjectArticle
dc.subjectbreast cancer
dc.subjectbreast tissue
dc.subjectcancer therapy
dc.subjectcontrolled study
dc.subjectdispersity
dc.subjectdrug blood level
dc.subjectdrug delivery system
dc.subjectdrug dosage form comparison
dc.subjectdrug half life
dc.subjectdrug retention
dc.subjectelimination rate constant
dc.subjectfemale
dc.subjectIC50
dc.subjectin vitro study
dc.subjectinternalization (cell)
dc.subjectmaximum concentration
dc.subjectMDA-MB-231 cell line
dc.subjectmean residence time
dc.subjectmigration inhibition
dc.subjectnonhuman
dc.subjectparticle size
dc.subjectplasma concentration-time curve
dc.subjectpreclinical study
dc.subjectrat
dc.subjecttime to maximum plasma concentration
dc.subjecttissue distribution
dc.subjectzeta potential
dc.subjectanimal
dc.subjectneoplasm
dc.subjectAnimals
dc.subjectDrug Carriers
dc.subjectDrug Delivery Systems
dc.subjectLipids
dc.subjectNanostructures
dc.subjectNeoplasms
dc.subjectParticle Size
dc.subjectRats
dc.subjectResveratrol
dc.titleDevelopment and preclinical evaluation of microneedle-assisted resveratrol loaded nanostructured lipid carriers for localized delivery to breast cancer therapy

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