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Mannosylated poly(acrylic acid)-coated mesoporous silica nanoparticles for anticancer therapy

Cited 14 time in Web of Science Cited 17 time in Scopus
Authors

Lee, Haesoo; Choi, Miseop; Kim, Ha-Eun; Jin, Minki; Jeon, Woo-Jin; Jung, Minwoo; Yoo, Hyelim; Won, Jong-Hee; Na, Young-Guk; Lee, Jae-Young; Seong, Hasoo; Lee, Hong-Ki; Cho, Cheong-Weon

Issue Date
2022-09
Publisher
Elsevier B.V.
Citation
Journal of Controlled Release, Vol.349, pp.241-253
Abstract
© 2022 Elsevier B.V.Although mesoporous silica nanoparticles (MSNs) are widely used as anticancer drug carriers, unmodified MSNs induce off-target effects and at high doses, there are adverse effects of hemolysis because of the interaction with the silanol group on the surface and cells. In this study, we developed doxorubicin (DOX)-loaded MSNs coated with mannose grafted poly (acrylic acid) copolymer (DOX@MSNs–man-g-PAA) to enhance the hemocompatibility and target efficacy to cancer cells. This uniform nanosized DOX@MSNs–man-g-PAA showed sustained and pH-dependent drug release with improved hemocompatibility over the bare MSNs. The uptake of the DOX@MSN–man-g-PAA in breast cancer cells was significantly improved by mannose receptor-mediated endocytosis, which showed significant increasing intracellular ROS and changes in mitochondrial membrane potential. This formulation exhibited superior tumor-suppressing activity in the MDA-MB-231 cells inoculated mice. Overall, the present study suggested the possibility of the copolymer-coated MSNs as drug carriers for cancer therapy.
ISSN
0168-3659
URI
https://hdl.handle.net/10371/199536
DOI
https://doi.org/10.1016/j.jconrel.2022.06.064
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  • College of Pharmacy
  • Department of Pharmacy
Research Area Biomaterial-based nano-platforms for cancer drug delivery and imaging, Formulation design and development, Functional protein expression and evaluation for drug delivery and therapy applications

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