Publications by authors named "Si-Cong Yang"

Unlabelled: Small-sized trastuzumab-targeted micelles (T-MP) were engineered using a surfactant-stripping approach that yielded concentrated phthalocyanines with strong near infrared absorption. T-MP accumulated more in the lymph node (LN) metastases of orthotopic colorectal cancer compared to the micelles conjugated with control IgG. Following surgical resection of the primary tumor, minimally invasive photothermal treatment of the metastatic LN with T-MP, but not the control micelles, extended mouse survival.

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Article Synopsis
  • Metal-phenolic networks (MPNs) are new surface modifiers that can be used in drug delivery systems.
  • The researchers developed a core-satellite nanosystem (CS-NS) combining liposomes with a metal ion chelator and mesoporous silica nanoparticles loaded with doxorubicin, which are coated with an MPN.
  • When exposed to near-infrared light, the CS-NS disassembles rapidly, enhancing drug delivery to tumors and improving survival rates in treated mice compared to controls.
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Photodynamic therapy (PDT) of cancer is limited by tumor hypoxia. Platinum nanoparticles (nano-Pt) as a catalase-like nanoenzyme can enhance PDT through catalytic oxygen supply. However, the cytotoxic activity of nano-Pt is not comprehensively considered in the existing methods to exert their multifunctional antitumor effects.

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Article Synopsis
  • Liposomal drug delivery for cancer therapy often faces challenges due to drugs leaking during circulation, which can reduce effectiveness.
  • Researchers created a new method that uses a stiff nanobowl embedded in the liposomal water cavity to enhance the stability of doxorubicin (DOX) and prevent this leakage.
  • This approach not only improves drug delivery to tumors but also boosts antitumor effects, making it a simpler and more effective solution compared to other methods that modify liposome surfaces.
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Delivery of therapeutics into the solid tumor microenvironment is a major challenge for cancer nanomedicine. Administration of certain exogenous enzymes which deplete tumor stromal components has been proposed as a method to improve drug delivery. Here we present a protein-free collagen depletion strategy for drug delivery into solid tumors, based on activating endogenous matrix metalloproteinases (MMP-1 and -2) using nitric oxide (NO).

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Brucellosis and Toxoplasmosis are important zoonotic diseases, and Neospora caninum is a parasite causing disease in cattle and other animals. Brucella spp. and N.

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Lymph node (LN) metastasis of gastric cancer (GC) is the strongest prognostic indicator for this disease; however, the majority of the LN metastasis profiles of GC remain unknown, which notably hinders the therapeutic efficacy in clinic. In the present study, an orthotopic model of human GC was established for investigation of time-dependent LN metastasis patterns in mice. Luciferase-expressing NCI-N87 human GC cells were injected into the subserosa of the gastric body, resulting in a tumor formation rate of 100%.

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Normalization of the tumor microenvironment is a promising approach to render conventional chemotherapy more effective. Although passively targeted drug nanocarriers have been investigated to this end, actively targeted tumor priming remains to be explored. In this work, we demonstrate an effective tumor priming strategy using metronomic application of nanoparticles actively targeted to tumor neovasculature.

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Tumor angiogenesis is a multistep process involved with multiple molecular events in cancer microenvironment. Several molecular-targeted agents aiming to suppress tumor angiogenesis have been successfully translated into cancer clinic. However, new strategies are still urgently desired to be excavated to overcome the poor response and resistance in some antiangiogenic therapies.

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