2019
DOI: 10.1039/c9ra07051f
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Therapeutic polymeric nanomedicine: GSH-responsive release promotes drug release for cancer synergistic chemotherapy

Abstract: In the GSH-responsive doxorubicin loading camptothecin prodrug nanomedicine, easy modulation of the dose ratio and controlled co-release were achieved, and the synergistic effect was significantly improved.

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Cited by 12 publications
(5 citation statements)
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“…Glutathiones is a natural compound that protects cells from oxidative damage and from the toxicity of xenobiotic electrophiles but may also enhance the intracellular reduction of Pt(IV) prodrugs into the corresponding Pt(II) active form. GSH concentrations in intracellular and extracellular environments have been found to range between 2–10 mM and 2–20 μM, respectively [ 48 , 49 , 50 ]. However, in our case, the more relevant value was that of GSH levels in the brain, reported to be 1–2 mM in normal conditions [ 51 ].…”
Section: Resultsmentioning
confidence: 99%
“…Glutathiones is a natural compound that protects cells from oxidative damage and from the toxicity of xenobiotic electrophiles but may also enhance the intracellular reduction of Pt(IV) prodrugs into the corresponding Pt(II) active form. GSH concentrations in intracellular and extracellular environments have been found to range between 2–10 mM and 2–20 μM, respectively [ 48 , 49 , 50 ]. However, in our case, the more relevant value was that of GSH levels in the brain, reported to be 1–2 mM in normal conditions [ 51 ].…”
Section: Resultsmentioning
confidence: 99%
“…For instance, Shen et al attached the disulfide-containing cleavable prodrug monomer, camptothecin (CPT), onto the methoxy poly(ethylene glycol) (mPEG)-based polymer chain by RAFT living polymerization and developed an amphiphilic copolymer. 147 Apart from the CPT, doxorubicin (DOX) was encapsulated via hydrophobic and π-π stacking interactions. In their work, the co-release of both the anticancer drugs are well controlled and demonstrated synergetic effect with enhanced anticancer efficacy, as illustrated in Figure 18.…”
Section: Disulfide Linkagementioning
confidence: 99%
“…Високі рівні глутатіону [26] спостерігаються при багатьох пухлинах, тому, враховуючи його роль в онкогенезі та запальних процесах, створено прямі підходи в терапії, направлені на регулювання синтезу GSH, який може зумовити фероптоз клітин (загибелі клітин, опосередковані перокисним окисненням ліпідів клітинних мембран) та непрямі методи, націлені на запальну реакцію або мікрооточення пухлини та імунотерапію. У процесі лікування онкохворих рівні GSH можуть бути індикатором успіху терапії [4,49,57]. Ліки на основі Lбутионін-сульфоксиміну інгібують синтез глутатіону, блокуючи активність γ-глутамілцистеїн синтетази.…”
Section: результати обговоренняunclassified