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Doxorubicin-Loaded PLGA Nanoparticles for Cancer Therapy: Molecular Weight Effect of PLGA in Doxorubicin Release for Controlling Immunogenic Cell Death
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Nanoparticle‐Mediated Immunogenic Cell Death Enables and Potentiates Cancer Immunotherapy
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Polyurethane/doxorubicin nanoparticles based on electrostatic interactions as pH‐sensitive drug delivery carriers
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Crosstalk between Regulatory T Cells and Tumor-Associated Dendritic Cells Negates Anti-tumor Immunity in Pancreatic Cancer
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Clinical cancer vaccine trials
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Release of chromatin protein HMGB1 by necrotic cells triggers inflammation
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Photothermal therapy with immune-adjuvant nanoparticles together with checkpoint blockade for effective cancer immunotherapy
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Antigen-capturing nanoparticles improve the abscopal effect and cancer immunotherapy
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Immunogenic cell death and DAMPs in cancer therapy
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A critical cysteine is required for HMGB1 binding to Toll-like receptor 4 and activation of macrophage cytokine release
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How subtle differences in polymer molecular weight affect doxorubicin-loaded PLGA nanoparticles degradation and drug release
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The interaction between HMGB1 and TLR4 dictates the outcome of anticancer chemotherapy and radiotherapy
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Personalized cancer vaccine effectively mobilizes antitumor T cell immunity in ovarian cancer
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Differential degradation rates in vivo and in vitro of biocompatible poly(lactic acid) and poly(glycolic acid) homo- and co-polymers for a polymeric drug-delivery microchip
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Biodegradable Microparticles Loaded with Doxorubicin and CpG ODN for In Situ Immunization Against Cancer
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PLGA-Based Nanoparticles in Cancer Treatment
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Poly Lactic-co-Glycolic Acid (PLGA) as Biodegradable Controlled Drug Delivery Carrier
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Nanoparticle-Based Vaccine Delivery for Cancer Immunotherapy
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Consensus guidelines for the detection of immunogenic cell death
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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