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2023
DOI: 10.1016/j.jconrel.2023.08.019
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Polysaccharide-based tumor microenvironment-responsive drug delivery systems for cancer therapy

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Cited by 24 publications
(17 citation statements)
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“…1,2 Among these examples, polysaccharides such as HA, dextran, pullulan, and heparin are responsible to improve the solubility, dispersibility, and biocompatibility of nanohybrids. 3 Moreover, cationic polysaccharide CS can be used to deliver genes. 4 To realize biocompatibility and active targeting, we utilized HA to construct polysaccharide−inorganic nanohybrids.…”
Section: Nanohybrids Fabricated By Surface Modificationmentioning
confidence: 99%
See 3 more Smart Citations
“…1,2 Among these examples, polysaccharides such as HA, dextran, pullulan, and heparin are responsible to improve the solubility, dispersibility, and biocompatibility of nanohybrids. 3 Moreover, cationic polysaccharide CS can be used to deliver genes. 4 To realize biocompatibility and active targeting, we utilized HA to construct polysaccharide−inorganic nanohybrids.…”
Section: Nanohybrids Fabricated By Surface Modificationmentioning
confidence: 99%
“…Polysaccharides can be modified on the surface of the as-synthesized inorganic nanoparticles through chemical bonding or self-assembly strategy to construct nanohybrids. , Among these examples, polysaccharides such as HA, dextran, pullulan, and heparin are responsible to improve the solubility, dispersibility, and biocompatibility of nanohybrids . Moreover, cationic polysaccharide CS can be used to deliver genes .…”
Section: Nanohybrids Fabricated By Surface Modificationmentioning
confidence: 99%
See 2 more Smart Citations
“…The vacuoles that originated persist, grow, and eventually explode in the tissue, producing localized thermal and cytotoxic effects, including hyperoxidative cellular structural damage and acoustodynamic effects such as shearing stress and shock waves. At the same time, the bursting of the vacuole causes cell membrane disruption, allowing drugs and other substances to enter the cell passively. , However, a single SDT has limited effect on tumor inhibition. , Relevant studies have revealed that ultrasound can be used to increase the chemotherapeutic drug uptake by cancer cells, thus reducing the poisonous side effects on healthy cells and organizations. , Despite the anticipated favorable therapeutic effect of combining chemotherapy and SDT, the efficacy of treatment is compromised primarily due to tumor hypoxia resulting from aberrant cancer cell proliferation and distorted tumor vasculatures. , SDT works by turning oxygen into deadly singlet oxygen ( 1 O 2 ) causing cells; thus, the hypoxic environment of the tumor greatly limited oxygen utilization and reduced the efficiency of SDT. , In addition, the hypoxia condition in the tumor will trigger the hypoxia-inducible factor α (HIF-1α) and subsequently increase the expression of P-glycoprotein (P-gp), thereby inducing the transportation of chemotherapeutic drugs outside the cancer cells and leading to drug resistance. Therefore, tumor hypoxia is of paramount importance in furthering the therapeutic effect of SDT. Recent studies have revealed that manganese oxide (MnO 2 ) can produce oxygen by reacting with extra hydrogen dioxide in the microenvironment of tumor to alleviate hypoxia. For efficient SDT and chemotherapy, the fabrication of nanocarriers with a high drug loading capacity is crucial.…”
Section: Introductionmentioning
confidence: 99%