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Synthesis and characterization of UCNP@RB-dFer and PTP-UCNP@RB-dFer. Hydrodynamic diameter (A) (n = 3) and zeta potential (B) (n = 3) of NH 2 -UCNP, UCNP@RB, UCNP@RB-dFer and PTP-UCNP@RB-dFer; (C) Fluorescence spectroscopy of UCNP@RB and UCNP@RB-dFer (dFer was labeled with <t>FITC</t> for the synthesis of UCNP@RB-dFer); TEM images and DLS measurements of UCNP@RB-dFer (D) and PTP-UCNP@RB-dFer (E) ; (F) The hydrodynamic diameter and zeta potential stability of PTP-UCNP@RB-dFer within 7 days (n = 3); (G – K) ROS generation in different solution using DPBF as the probe; (L) The release profile of dFer from PTP-UCNP@RB-dFer with different power of NIR or without NIR (n = 3). Error bars represent the mean ± SD.
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Synthesis and characterization of UCNP@RB-dFer and PTP-UCNP@RB-dFer. Hydrodynamic diameter (A) (n = 3) and zeta potential (B) (n = 3) of NH 2 -UCNP, UCNP@RB, UCNP@RB-dFer and PTP-UCNP@RB-dFer; (C) Fluorescence spectroscopy of UCNP@RB and UCNP@RB-dFer (dFer was labeled with <t>FITC</t> for the synthesis of UCNP@RB-dFer); TEM images and DLS measurements of UCNP@RB-dFer (D) and PTP-UCNP@RB-dFer (E) ; (F) The hydrodynamic diameter and zeta potential stability of PTP-UCNP@RB-dFer within 7 days (n = 3); (G – K) ROS generation in different solution using DPBF as the probe; (L) The release profile of dFer from PTP-UCNP@RB-dFer with different power of NIR or without NIR (n = 3). Error bars represent the mean ± SD.
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Synthesis and characterization of UCNP@RB-dFer and PTP-UCNP@RB-dFer. Hydrodynamic diameter (A) (n = 3) and zeta potential (B) (n = 3) of NH 2 -UCNP, UCNP@RB, UCNP@RB-dFer and PTP-UCNP@RB-dFer; (C) Fluorescence spectroscopy of UCNP@RB and UCNP@RB-dFer (dFer was labeled with <t>FITC</t> for the synthesis of UCNP@RB-dFer); TEM images and DLS measurements of UCNP@RB-dFer (D) and PTP-UCNP@RB-dFer (E) ; (F) The hydrodynamic diameter and zeta potential stability of PTP-UCNP@RB-dFer within 7 days (n = 3); (G – K) ROS generation in different solution using DPBF as the probe; (L) The release profile of dFer from PTP-UCNP@RB-dFer with different power of NIR or without NIR (n = 3). Error bars represent the mean ± SD.
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Synthesis and characterization of UCNP@RB-dFer and PTP-UCNP@RB-dFer. Hydrodynamic diameter (A) (n = 3) and zeta potential (B) (n = 3) of NH 2 -UCNP, UCNP@RB, UCNP@RB-dFer and PTP-UCNP@RB-dFer; (C) Fluorescence spectroscopy of UCNP@RB and UCNP@RB-dFer (dFer was labeled with <t>FITC</t> for the synthesis of UCNP@RB-dFer); TEM images and DLS measurements of UCNP@RB-dFer (D) and PTP-UCNP@RB-dFer (E) ; (F) The hydrodynamic diameter and zeta potential stability of PTP-UCNP@RB-dFer within 7 days (n = 3); (G – K) ROS generation in different solution using DPBF as the probe; (L) The release profile of dFer from PTP-UCNP@RB-dFer with different power of NIR or without NIR (n = 3). Error bars represent the mean ± SD.
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Synthesis and characterization of UCNP@RB-dFer and PTP-UCNP@RB-dFer. Hydrodynamic diameter (A) (n = 3) and zeta potential (B) (n = 3) of NH 2 -UCNP, UCNP@RB, UCNP@RB-dFer and PTP-UCNP@RB-dFer; (C) Fluorescence spectroscopy of UCNP@RB and UCNP@RB-dFer (dFer was labeled with <t>FITC</t> for the synthesis of UCNP@RB-dFer); TEM images and DLS measurements of UCNP@RB-dFer (D) and PTP-UCNP@RB-dFer (E) ; (F) The hydrodynamic diameter and zeta potential stability of PTP-UCNP@RB-dFer within 7 days (n = 3); (G – K) ROS generation in different solution using DPBF as the probe; (L) The release profile of dFer from PTP-UCNP@RB-dFer with different power of NIR or without NIR (n = 3). Error bars represent the mean ± SD.
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Image Search Results


Synthesis and characterization of UCNP@RB-dFer and PTP-UCNP@RB-dFer. Hydrodynamic diameter (A) (n = 3) and zeta potential (B) (n = 3) of NH 2 -UCNP, UCNP@RB, UCNP@RB-dFer and PTP-UCNP@RB-dFer; (C) Fluorescence spectroscopy of UCNP@RB and UCNP@RB-dFer (dFer was labeled with FITC for the synthesis of UCNP@RB-dFer); TEM images and DLS measurements of UCNP@RB-dFer (D) and PTP-UCNP@RB-dFer (E) ; (F) The hydrodynamic diameter and zeta potential stability of PTP-UCNP@RB-dFer within 7 days (n = 3); (G – K) ROS generation in different solution using DPBF as the probe; (L) The release profile of dFer from PTP-UCNP@RB-dFer with different power of NIR or without NIR (n = 3). Error bars represent the mean ± SD.

Journal: Materials Today Bio

Article Title: Spatiotemporally controlled ferritin-targeting PROTAC nanoplatform for visualized manipulation of endogenous “Iron pool” in pancreatic cancer therapy

doi: 10.1016/j.mtbio.2025.102661

Figure Lengend Snippet: Synthesis and characterization of UCNP@RB-dFer and PTP-UCNP@RB-dFer. Hydrodynamic diameter (A) (n = 3) and zeta potential (B) (n = 3) of NH 2 -UCNP, UCNP@RB, UCNP@RB-dFer and PTP-UCNP@RB-dFer; (C) Fluorescence spectroscopy of UCNP@RB and UCNP@RB-dFer (dFer was labeled with FITC for the synthesis of UCNP@RB-dFer); TEM images and DLS measurements of UCNP@RB-dFer (D) and PTP-UCNP@RB-dFer (E) ; (F) The hydrodynamic diameter and zeta potential stability of PTP-UCNP@RB-dFer within 7 days (n = 3); (G – K) ROS generation in different solution using DPBF as the probe; (L) The release profile of dFer from PTP-UCNP@RB-dFer with different power of NIR or without NIR (n = 3). Error bars represent the mean ± SD.

Article Snippet: Fluorescamine, H 2 N-PEG 2 -CH 2 COOH, (S,R,S)-AHPC-Me hydrochloride (VHL ligand), fluorescein isothiocyanate (FITC), 1,3-diphenylisobenzofuran (DPBF), BODIPY581/591-C11, FerroOrange, MG132 and Protein A/G IP Magnetic Beads were purchased from MedChemExpress LLC (Shanghai, China).

Techniques: Zeta Potential Analyzer, Fluorescence, Spectroscopy, Labeling

Cellular uptake, ferritin degradation and mobilization of the “Iron Pool&”. (A) CLSM images of PANC1 cells after incubation with FITC-labeled dFer, UCNP@RB-dFer, PTP-UCNP@RB-dFer and PTP-UCNP@RB-dFer + (PTP) for 4 and 12 h; (B) FCM analysis of the cellular uptake of dFer, UCNP@RB-dFer, PTP-UCNP@RB-dFer and PTP-UCNP@RB-dFer + (PTP); (C) Bio-TEM image of PANC1 cells’ internalization of UCNP@RB-dFer and PTP-UCNP@RB-dFer; Western blotting (D) and quantitative analysis (E) (n = 3) of the expression levels of ferritin in PANC1 cells with different treatment; Western blotting (F) and quantitative analysis (G) (n = 3) of the expression levels of ferritin in PANC1 cells treated with VHL ligand, HKN 15 , VHL ligand + HKN 15 , PTP-UCNP@RB-dFer and PTP-UCNP@RB-dFer + NIR; (H) Mechanism of ferritin degradation mediated by PTP-UCNP@RB-dFer and inhibition mechanism of MLN4924 and Epoxomicin; Western blotting (I) and quantitative analysis (J) (n = 3) of the expression levels of ferritin in PANC1 cells treated with MLN4924, epoxomicin and PTP-UCNP@RB-dFer + NIR; (K) Co-IP analysis of ferritin ubiquitination levels under different treatments; (L) CLSM images of FerroOrange stained PANC1 cells after different treatments. Error bars represent the mean ± SD.

Journal: Materials Today Bio

Article Title: Spatiotemporally controlled ferritin-targeting PROTAC nanoplatform for visualized manipulation of endogenous “Iron pool” in pancreatic cancer therapy

doi: 10.1016/j.mtbio.2025.102661

Figure Lengend Snippet: Cellular uptake, ferritin degradation and mobilization of the “Iron Pool&”. (A) CLSM images of PANC1 cells after incubation with FITC-labeled dFer, UCNP@RB-dFer, PTP-UCNP@RB-dFer and PTP-UCNP@RB-dFer + (PTP) for 4 and 12 h; (B) FCM analysis of the cellular uptake of dFer, UCNP@RB-dFer, PTP-UCNP@RB-dFer and PTP-UCNP@RB-dFer + (PTP); (C) Bio-TEM image of PANC1 cells’ internalization of UCNP@RB-dFer and PTP-UCNP@RB-dFer; Western blotting (D) and quantitative analysis (E) (n = 3) of the expression levels of ferritin in PANC1 cells with different treatment; Western blotting (F) and quantitative analysis (G) (n = 3) of the expression levels of ferritin in PANC1 cells treated with VHL ligand, HKN 15 , VHL ligand + HKN 15 , PTP-UCNP@RB-dFer and PTP-UCNP@RB-dFer + NIR; (H) Mechanism of ferritin degradation mediated by PTP-UCNP@RB-dFer and inhibition mechanism of MLN4924 and Epoxomicin; Western blotting (I) and quantitative analysis (J) (n = 3) of the expression levels of ferritin in PANC1 cells treated with MLN4924, epoxomicin and PTP-UCNP@RB-dFer + NIR; (K) Co-IP analysis of ferritin ubiquitination levels under different treatments; (L) CLSM images of FerroOrange stained PANC1 cells after different treatments. Error bars represent the mean ± SD.

Article Snippet: Fluorescamine, H 2 N-PEG 2 -CH 2 COOH, (S,R,S)-AHPC-Me hydrochloride (VHL ligand), fluorescein isothiocyanate (FITC), 1,3-diphenylisobenzofuran (DPBF), BODIPY581/591-C11, FerroOrange, MG132 and Protein A/G IP Magnetic Beads were purchased from MedChemExpress LLC (Shanghai, China).

Techniques: Incubation, Labeling, Western Blot, Expressing, Inhibition, Co-Immunoprecipitation Assay, Ubiquitin Proteomics, Staining

Therapeutic effects of endogenous iron-mediated ferroptosis in combination with PDT in vitro . (A) CCK8 assay of PANC1 cells treated with PBS, UCNP@RB, UCNP@RB-dFer, PTP-UCNP@RB-dFer, dFer, UCNP@RB + NIR, UCNP@RB-dFer + NIR and PTP-UCNP@RB-dFer + NIR (n = 6); CCK8 assay of PANC1 cells treated with PTP-UCNP@RB + NIR (B) (n = 6) or PTP-UCNP@RB-dFer + NIR (C) (n = 6) in the presence of different inhibitors (DFO, Fer-1, GSH and VE); Live/dead staining assay (D) and Annexin V-FITC/PI double staining (E) of PANC1 cells with different treatments. Error bars represent the mean ± SD.

Journal: Materials Today Bio

Article Title: Spatiotemporally controlled ferritin-targeting PROTAC nanoplatform for visualized manipulation of endogenous “Iron pool” in pancreatic cancer therapy

doi: 10.1016/j.mtbio.2025.102661

Figure Lengend Snippet: Therapeutic effects of endogenous iron-mediated ferroptosis in combination with PDT in vitro . (A) CCK8 assay of PANC1 cells treated with PBS, UCNP@RB, UCNP@RB-dFer, PTP-UCNP@RB-dFer, dFer, UCNP@RB + NIR, UCNP@RB-dFer + NIR and PTP-UCNP@RB-dFer + NIR (n = 6); CCK8 assay of PANC1 cells treated with PTP-UCNP@RB + NIR (B) (n = 6) or PTP-UCNP@RB-dFer + NIR (C) (n = 6) in the presence of different inhibitors (DFO, Fer-1, GSH and VE); Live/dead staining assay (D) and Annexin V-FITC/PI double staining (E) of PANC1 cells with different treatments. Error bars represent the mean ± SD.

Article Snippet: Fluorescamine, H 2 N-PEG 2 -CH 2 COOH, (S,R,S)-AHPC-Me hydrochloride (VHL ligand), fluorescein isothiocyanate (FITC), 1,3-diphenylisobenzofuran (DPBF), BODIPY581/591-C11, FerroOrange, MG132 and Protein A/G IP Magnetic Beads were purchased from MedChemExpress LLC (Shanghai, China).

Techniques: In Vitro, CCK-8 Assay, Staining, Double Staining