Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 683, P. 552 - 563
Published: Dec. 11, 2024
Language: Английский
Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 683, P. 552 - 563
Published: Dec. 11, 2024
Language: Английский
Bioactive Materials, Journal Year: 2024, Volume and Issue: 39, P. 191 - 205
Published: May 21, 2024
Unnecessary exposure to ionizing radiation (IR) often causes acute and chronic oxidative damages normal cells organs, leading serious physiological even life-threatening consequences. Amifostine (AMF) is a validated radioprotectant extensively applied in chemotherapy medicine, but the short half-life limits its bioavailability clinical applications, remaining as great challenge be addressed. DNA-assembled nanostructures especially tetrahedral framework nucleic acids (tFNAs) are promising nanocarriers with preeminent biosafety, low biotoxicity, high transport efficiency. The tFNAs also have relative long-term maintenance for structural stability excellent endocytosis capacity. We therefore synthesized tFNA-based delivery system of AMF multi-organ radioprotection (tFNAs@AMF, termed nanosuit). By establishing mice models accidental total body irradiation (TBI) radiotherapy model Lewis lung cancer, we demonstrated that nanosuit could shield from IR-induced DNA damage by regulating molecular biomarkers anti-apoptosis anti-oxidative stress. In model, pretreated exhibited satisfactory alteration superoxide dismutase (SOD) activities malondialdehyde (MDA) contents, functional recovery hematopoietic system, reducing pathological safeguarding lethal radiation. More importantly, showed selective organs without interferences tumor control cancer. Based on conveniently available tetrahedron-based nanocarrier, this work presents high-efficiency prolonged enhanced multi-organs. Such pioneers strategy translation potential radioactivity protection.
Language: Английский
Citations
21Science Bulletin, Journal Year: 2024, Volume and Issue: unknown
Published: Oct. 1, 2024
Language: Английский
Citations
13ACS Applied Nano Materials, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 28, 2025
Language: Английский
Citations
0Advanced Materials, Journal Year: 2025, Volume and Issue: unknown
Published: May 2, 2025
Abstract Various biomaterials have been developed to address challenging critical‐sized bone defects. However, most of them focus on intramembranous ossification (IMO) rather than endochondral (ECO), often resulting in suboptimal therapeutic outcomes. Drawing inspiration from the functionality greenhouse ecosystem, herein a bionic niche is innovatively crafted recapitulate ECO process. This consists three hierarchical components: an embedded microchannel network that facilitates cell infiltration and matter exchange, polydopamine surface modification layer with immunomodulatory functions, ECO‐targeted delivery system based mesoporous silica nanoparticles. Through spatiotemporally programming microenvironment, effectively recapitulates key stages ECO. Notably, even rat calvaria, region well‐known for IMO, capable initiating ECO, evident by cartilage template formation, leading efficient regeneration. Taken together, this study introduces prospective concepts designing next‐generation ECO‐driven tissue engineering.
Language: Английский
Citations
0Science China Materials, Journal Year: 2025, Volume and Issue: unknown
Published: May 7, 2025
Language: Английский
Citations
0Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 683, P. 398 - 407
Published: Dec. 14, 2024
Language: Английский
Citations
3Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 495, P. 153249 - 153249
Published: June 19, 2024
Language: Английский
Citations
1ACS Applied Nano Materials, Journal Year: 2024, Volume and Issue: 7(22), P. 25447 - 25458
Published: Nov. 8, 2024
Studies on immunogenic cell death of tumor cells have confirmed that some chemotherapy drugs can induce antitumor immune response. This response is caused by the antigens released dead cells. However, these and damage-associated molecular patterns (DAMPs) be degraded autophagy pathway, which highly upregulated in shown inhibition increase accumulation autophagosomes, reduce degradation major histocompatibility complex (MHC) class I molecules, maintain or even enhance responses. In order to chemotherapy-induced through regulation autophagy, this project intends create a nanoplatform for codelivery chemotherapeutics inhibitors. Phospholipid-modified inhibitor DSPE-BiQ drug DSPE-OXA-PEG were synthesized, respectively, generated system OXA/BiQ-Lip could achieve efficient delivery release EPR effect stimulation from intracellular pH gradient/reduced glutathione concentration changing. The strategy inhibitors not only overcome oxaliplatin resistance but also promote intact autophagosomes containing multiple DAMPs, antigen presentation infiltration, improve triggered chemotherapy.
Language: Английский
Citations
1Colloids and Surfaces B Biointerfaces, Journal Year: 2024, Volume and Issue: 242, P. 114109 - 114109
Published: July 18, 2024
Language: Английский
Citations
0Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 500, P. 157141 - 157141
Published: Oct. 28, 2024
Language: Английский
Citations
0