Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jconrel.2020.05.005
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dc.titleEnhanced penetration of pro-apoptotic and anti-angiogenic micellar nanoprobe in 3D multicellular spheroids for chemophototherapy
dc.contributor.authorMozhi, A
dc.contributor.authorSunil, V
dc.contributor.authorZhan, W
dc.contributor.authorGhode, PB
dc.contributor.authorThakor, NV
dc.contributor.authorWang, CH
dc.date.accessioned2021-04-09T06:16:10Z
dc.date.available2021-04-09T06:16:10Z
dc.date.issued2020/07/10
dc.identifier.citationMozhi, A, Sunil, V, Zhan, W, Ghode, PB, Thakor, NV, Wang, CH (2020/07/10). Enhanced penetration of pro-apoptotic and anti-angiogenic micellar nanoprobe in 3D multicellular spheroids for chemophototherapy. Journal of Controlled Release 323 : 502-518. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jconrel.2020.05.005
dc.identifier.issn01683659
dc.identifier.issn18734995
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/188980
dc.description.abstractLight irradiation is considered an ideal non-invasive stimulus that enables precise tumour treatment with flexible, facile, and spatiotemporal control. Photodynamic therapy (PDT) is an important clinically relevant therapeutic modality that has proven to compensate for the reduced therapeutic efficacy of conventional chemotherapy. However, oxygen consumption during PDT can result in an inadequate oxygen supply which reduces photodynamic efficacy. In our quest to circumvent the limitations of chemotherapy and photodynamic therapy, we have engineered a robust and smart “all-in-one” nanoparticle-based drug delivery system capable of overcoming biological barriers and leveraging on several synergistic cancer cell killing mechanisms. The fabricated Targeted Micellar Nanoprobe (TMNP) had exceptionally high encapsulation efficiencies of a hydrophobic drug simvastatin (SV) and a photosensitizer protoporphyrin IX (PpIX) due to the ℼ-ℼ stacking of the aromatic groups of SV and PpIX and strong hydrophobic interactions with the alkyl chains of the carrier. In-vitro results demonstrated that TMNP exhibited excellent colloidal stability, biocompatibility and drug retaining capability in physiological condition. Under light irradiation, TMNP causes the accelerated generation of reactive oxygen species (ROS) which subsequently damages the mitochondria. On further evaluation of the mechanisms behind the superior anti-cancer effect of TMNP, we concluded that TMNP causes synergistic apoptosis and necrosis along with cell cycle arrest at the G1-S phase and elicits anti-angiogenic effects. Taking into consideration that these promising results on 2D monolayer cell cultures might not translate into similar results in animal models, we developed 3D multicellular tumour spheroids (MCs) as an intermediate step to bridge the gap between 2-D cell experiments and in-vivo studies. TMNPs showed enhanced penetration and growth inhibition on MCs. In addition, the modelling of the transport of TMNP in the tumour exhibited the improved effective delivery volume. Overall, TMNPs could potentially be used for image-guided delivery of the therapeutic payloads for precise cancer treatment.
dc.publisherElsevier BV
dc.sourceElements
dc.typeArticle
dc.date.updated2021-04-09T04:49:26Z
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.contributor.departmentELECTRICAL AND COMPUTER ENGINEERING
dc.description.doi10.1016/j.jconrel.2020.05.005
dc.description.sourcetitleJournal of Controlled Release
dc.description.volume323
dc.description.page502-518
dc.published.statePublished
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