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dc.contributor.authorChitkara, Deepak-
dc.contributor.authorMittal, Anupama-
dc.date.accessioned2024-01-03T10:43:31Z-
dc.date.available2024-01-03T10:43:31Z-
dc.date.issued2018-05-
dc.identifier.urihttps://pubs.acs.org/doi/full/10.1021/acs.molpharmaceut.8b00228-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13653-
dc.description.abstractmiR-34a is a master tumor suppressor playing a key role in the several signaling mechanisms involved in cancer. However, its delivery to the cancer cells is the bottleneck in its clinical translation. Herein we report cationic amphiphilic copolymers grafted with cholesterol (chol), N,N-dimethyldipropylenetriamine (cation chain) and 4-(2-aminoethyl)morpholine (morph) for miR-34a delivery. The copolymer interacts with miR-34a at low N/P ratios (∼2/1) to form nanoplexes of size ∼108 nm and a zeta potential ∼ +39 mV. In vitro studies in 4T1 and MCF-7 cells indicated efficient transfection efficiency. The intracellular colocalization suggested that the copolymer effectively transported the FAM labeled siRNA into the cytoplasm within 2 h and escaped from the endo-/lysosomal environment. The developed miR-34a nanoplexes inhibited the breast cancer cell growth as confirmed by MTT assay wherein 28% and 34% cancer cell viability was observed in 4T1 and MCF-7 cells, respectively. Further, miR-34a nanoplexes possess immense potential to induce apoptosis in both cell lines.en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectPharmacyen_US
dc.subjectNanoplexesen_US
dc.subjectmiR-34aen_US
dc.subjectAmphiphilic cationic polymeren_US
dc.subjectAnticancer therapyen_US
dc.titleCholesterol and Morpholine Grafted Cationic Amphiphilic Copolymers for miRNA-34a Deliveryen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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