2020
DOI: 10.1016/j.ultras.2019.106033
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The use of ultrasound to increase the uptake and cytotoxicity of dual taxane and P-glycoprotein inhibitor loaded, solid core nanoparticles in drug resistant cells

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Cited by 8 publications
(4 citation statements)
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“…GC Gelatinase-stimuli di-block copolymers poly(ethylene glycol)b-poly(ε-caprolactone) (PEG-b-PCL) copolymers, MePEG114-b-PCL200 and MePEG17b-PCL5 (PCL200/PCL5) + ultrasoundIncreased accumulation of drug[132] …”
mentioning
confidence: 99%
“…GC Gelatinase-stimuli di-block copolymers poly(ethylene glycol)b-poly(ε-caprolactone) (PEG-b-PCL) copolymers, MePEG114-b-PCL200 and MePEG17b-PCL5 (PCL200/PCL5) + ultrasoundIncreased accumulation of drug[132] …”
mentioning
confidence: 99%
“…The published studies have shown that nanoparticles hold promise for a variety of biomedical applications including therapeutic and diagnostic levels [ 31 , 32 ]. Some reports also indicated that they might help to overcome resistance and sensitize cancer cells to classical chemotherapeutic agents [ 33 , 34 ]. Therefore, in the next step, we evaluated the potential of magnetic particles coated by polymeric shells containing poly(cholesteryl acrylate) to sensitize breast cancer cells to doxorubicin.…”
Section: Discussionmentioning
confidence: 99%
“…To date, numerous P-gp inhibitors have been developed 24 , 25 , 26 , 27 , such as verapamil (VPM) 28 , 29 , 30 , cyclosporine A 31 , dexverapamil 32 , valspodar 33 , tariquidar 34 , laniquidar 35 , and some of them have advanced into clinical trials 7 , 36 . Despite some P-gp inhibitors could significantly increase the efficacy of anticancer drugs in MDR cancer, none of the P-gp inhibitors have been approved for clinical use due to the drawbacks such as toxicity, interrupting drug–drug interactions, and so forth 37 . Therefore, the development of highly potent and specific P-gp inhibitors with good safety and favorable drug-like properties is still urgently needed.…”
Section: Introductionmentioning
confidence: 99%