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2016
DOI: 10.1016/j.colsurfb.2016.08.059
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Transferrin functionalized chitosan-PEG nanoparticles for targeted delivery of paclitaxel to cancer cells

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Cited by 99 publications
(41 citation statements)
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“…This chitosan nanoparticle system carrying DNA not only improved the water solubility upon PEG addition, but also showed low cytotoxicity towards normal HEK 293 (Human embryonic kidney cells 293) cells. A recent study demonstrated the use of transferrin (Tf)-functionalized chitosan nanoparticles, where PEG was used to conjugate Tf onto chitosan [52]. Thus, PEG modification is an important step in designing water-soluble, long-circulating, and target-specific nanoparticles.…”
Section: Chitosan As Gene Delivery Vehicle For Cancer Therapymentioning
confidence: 99%
“…This chitosan nanoparticle system carrying DNA not only improved the water solubility upon PEG addition, but also showed low cytotoxicity towards normal HEK 293 (Human embryonic kidney cells 293) cells. A recent study demonstrated the use of transferrin (Tf)-functionalized chitosan nanoparticles, where PEG was used to conjugate Tf onto chitosan [52]. Thus, PEG modification is an important step in designing water-soluble, long-circulating, and target-specific nanoparticles.…”
Section: Chitosan As Gene Delivery Vehicle For Cancer Therapymentioning
confidence: 99%
“…Pure paclitaxel with a concentration of 0.28 ug / ml reduce cell viability CT26-CEA; while paclitaxel was released by nano-polyelectrolyte-PEG reduce cell viability CT26-CEA at a concentration of 0.014 µg / ml. This indicates that the nano-encapsulation paclitaxel-PEG Nanomaterial is used for encapsulation paclitaxel to speed up the release of the drug brush [25]. Within the duration of 24 hours, at pH of 5.6 about 11.2% from 13.1% paclitaxel that was delivered by nano-PEG-folic acid has reached the target cell.…”
Section: Cell Viabilitymentioning
confidence: 98%
“…The results showed that the uptake of transferrin‐modified nanoparticles was higher than nontargeted nanoparticles. Moreover, the modified nanoparticles exhibited higher cytotoxicity against human nonsmall cell lung cancer cell lines and lower hemolytic toxicity than the free drug form (Nag, Gajbhiye, Kesharwani, & Jain, ). More significantly, it has also been reported that transferrin receptor‐targeted nanotherapeutics enable the transport of cargoes across the blood–brain barrier for the treatment of brain cancer (Clark & Davis, ; Ulbrich, Hekmatara, Herbert, & Kreuter, ).…”
Section: Two Targeting Strategies Are Used For In Vivo Drug Deliverymentioning
confidence: 99%