2019
DOI: 10.1016/j.colsurfb.2019.110427
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Polydopamine coated hollow mesoporous silica nanoparticles as pH-sensitive nanocarriers for overcoming multidrug resistance

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Cited by 66 publications
(30 citation statements)
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“…The platform fulfills innovative ideas for targeting cancer and improving therapy. In another attempt, polydopaminecoated hollow MSNs combining Dox hydrochloride with quercetin efficiently overcame multidrug resistance in taxol and Dox double-resistant human colorectal cancer cells (HCT-8/TAX cells) [371]. Fang et al [262] developed a hyaluronic acid-modified MSNs that co-deliver quercetin and Dox to enhance the efficacy of chemotherapy for gastric carcinoma.…”
Section: Quercetinmentioning
confidence: 99%
“…The platform fulfills innovative ideas for targeting cancer and improving therapy. In another attempt, polydopaminecoated hollow MSNs combining Dox hydrochloride with quercetin efficiently overcame multidrug resistance in taxol and Dox double-resistant human colorectal cancer cells (HCT-8/TAX cells) [371]. Fang et al [262] developed a hyaluronic acid-modified MSNs that co-deliver quercetin and Dox to enhance the efficacy of chemotherapy for gastric carcinoma.…”
Section: Quercetinmentioning
confidence: 99%
“…have developed hybrid lipid‐capped MSNs as promising vehicles for doxorubicin (DOX) delivery to realize controlled drug release and overcome MDR 29 . Polydopamine‐coated hollow MSNs have also been explored as pH‐sensitive nanocarriers to reverse MDR and improve anticancer effects on taxol and DOX double‐resistant human colorectal cancer cells 30 . Recently, our research group and others have developed several controlled release formulations (CRFs) of pesticides using versatile MSNs as scaffolds 31–36 .…”
Section: Introductionmentioning
confidence: 99%
“…Specifically, the drug delivery system can control the drug release pattern and improve the accumulation of the drugs at targeting sites [ 71 , 73 ]. In this context, nanocarriers can achieve synergistic therapeutic effects and prove to have a stronger killing effect on cancer cells [ 74 ]. This can be seen in Alvandifar et al (2018), in a study that constructed poly-lactid-co-glycolide (PLGA) carriers using SN38, an active metabolite of irinotecan, and verapamil, a MDR1 reversal agent, and they obtained a good result in cellular uptake and reduction of cell viability on MDA-MB-231 breast cancer cell line [ 71 ].…”
Section: Resistance Of Nanocarriersmentioning
confidence: 99%