Cited by 24Nanoplatforms for cancer theranosticsPhotodynamic Therapy Research StudiesRadiation Therapy and Dosimetry

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

MnO2 coated multi-layer nanoplatform for enhanced sonodynamic therapy and MR imaging of breast cancer

Open access
Xu, Yan, Tan, Wanlin, Chen, Mingyu, Chen, Sijie, Tang, Kui, Liao, Haiqin, Niu, Chengcheng·2022·Frontiers in Bioengineering and Biotechnology

Abstract

Sonodynamic therapy (SDT) is a promising new anti-tumor therapy that inhibits tumor growth by ultrasound activation of sonosensitizers to produce reactive oxygen species (ROS). However, the problems of hypoxia in the microenvironment within solid tumors and the effectiveness of SDT will decrease due to the little accumulation of sonosensitizers at the tumor site, as well as tumor cell tolerance, have limited the development of SDT. To overcome these problems, a core-shell structured nanoparticle (IR780/PLGA@MnO 2 NPs) loaded with IR780 and manganese dioxide (MnO 2 ) was developed as a nanocarrier to transport the sonosensitizer IR780 and the generated oxygen into the tumor tissue. The MnO 2 shell layer of IR780/PLGA@MnO 2 NPs can prevent the premature release of IR780 in the blood and also it can react with acidic and high H 2 O 2 , the generated oxygen can relieve tumor tissue hypoxia, and the generated Mn can enhance magnetic resonance imaging (MRI) signal intensity by acting as a contrast agent for MRI. More importantly, the released IR780 can produce ROS to kill tumor cells under ultrasound excitation. This PH-responsive and H 2 O 2 -triggered SDT based on the IR780/PLGA@MnO 2 NPs is an effective platform to inhibit tumor growth with negligible systemic toxicity. This work develops a multifunctional therapeutic integrated nanoplatform for breast cancer treatment, which is expected to be used in the clinic.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3389/fbioe.2022.955127

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Figures

FIGURE 1 Schematic illustration of the IR780/PLGA@MnO2 NPs used for enhance SDT and MR imaging of breast cancer.
FIGURE 1 Schematic illustration of the IR780/PLGA@MnO2 NPs used for enhance SDT and MR imaging of breast cancer.CC BY · PubMed Central
FIGURE 2 Characterization of IR780/PLGA@MnO2 NPs. (A–C) The TEM images of IR780/PLGA@MnO2 NPs (A) and IR780/PLGA NPs (B), the white arrow indicated the MnO2 on the shell of IR780/PLGA@MnO2 NPs (C). (D) The elemental mapping of Mn and O of IR780/PLGA@MnO 2. (E) Size and (F) zeta potential of IR780/PLGA NPs with and without MnO2 shell. (G) UV−vis−NIR absorption spectra of IR780/PLGA NPs, PLGA NPs, IR780/PLGA@MnO2 NPs. (H) Size distributions of IR780/PLGA@MnO2 NPs in PBS and 10% FBS for 7 days.
FIGURE 2 Characterization of IR780/PLGA@MnO2 NPs. (A–C) The TEM images of IR780/PLGA@MnO2 NPs (A) and IR780/PLGA NPs (B), the white arrow indicated the MnO2 on the shell of IR780/PLGA@MnO2 NPs (C). (D) The elemental mapping of Mn and O of IR780/PLGA@MnO 2. (E) Size and (F) zeta potential of IR780/PLGA NPs with and without MnO2 shell. (G) UV−vis−NIR absorption spectra of IR780/PLGA NPs, PLGA NPs, IR780/PLGA@MnO2 NPs. (H) Size distributions of IR780/PLGA@MnO2 NPs in PBS and 10% FBS for 7 days.CC BY · PubMed Central
FIGURE 3 (A) The IR780 release from IR780/PLGA@MnO2 NPs at pH 7.4 or 5.5 with or without H2O2. (B) Oxygen content of IR780/PLGA MnO2 NPs with H2O2. (C) Time-dependent 1O2 generation of IR780/PLGA MnO2 NPs irradiated by US (1 MHz, 1.0 W/cm2). (D) Time-dependent fluorescence increasement of SOSG with different treatments under ultrasound irradiation.
FIGURE 3 (A) The IR780 release from IR780/PLGA@MnO2 NPs at pH 7.4 or 5.5 with or without H2O2. (B) Oxygen content of IR780/PLGA MnO2 NPs with H2O2. (C) Time-dependent 1O2 generation of IR780/PLGA MnO2 NPs irradiated by US (1 MHz, 1.0 W/cm2). (D) Time-dependent fluorescence increasement of SOSG with different treatments under ultrasound irradiation.CC BY · PubMed Central
FIGURE 4 (A) Fluorescence images of 4T1 cells incubated with IR780/PLGA@MnO2 NPs for 0, 4, 12 and 24 h (scale bar: 20 μm). (B) Fluorescence microscope images of DCFH-DA stained 4T1 cells subjected to different treatments: (Hussain and Nguyen, 2014) PBS, (Wells, 2006) US, (Wu et al., 2005) IR780/PLGA NPs, (Ahmadi et al., 2020) IR780/PLGA@MnO2 NPs, (Qian et al., 2016) IR780/PLGA NPs + US, (Wood and Sehgal, 2015) IR780/PLGA@MnO2 + US (scale bar, 50 µm).
FIGURE 4 (A) Fluorescence images of 4T1 cells incubated with IR780/PLGA@MnO2 NPs for 0, 4, 12 and 24 h (scale bar: 20 μm). (B) Fluorescence microscope images of DCFH-DA stained 4T1 cells subjected to different treatments: (Hussain and Nguyen, 2014) PBS, (Wells, 2006) US, (Wu et al., 2005) IR780/PLGA NPs, (Ahmadi et al., 2020) IR780/PLGA@MnO2 NPs, (Qian et al., 2016) IR780/PLGA NPs + US, (Wood and Sehgal, 2015) IR780/PLGA@MnO2 + US (scale bar, 50 µm).CC BY · PubMed Central
FIGURE 5 (A,B) Cell viability of 4T1 and MCF-7 cells incubated with different concentrations of IR780/PLGA@MnO2 NPs under normoxia environment (A) and hypoxia environment (B). (C,D) Cell viability of 4T1 and MCF-7 cells under different treatments: (I) PBS, (II) US, (III) IR780/PLGA NPs, (IV) IR780/PLGA@MnO2, (V) IR780/PLGA NPs + US, (VI) IR780/PLGA@MnO2 + US) in normoxia environment (C) and hypoxia environment (D). (E) Fluorescence microscope images of DAPI and PI co-stained 4T1 cells after various treatments: (Hussain and Nguyen, 2014) PBS, (Wells, 2006) US only, (Wu et al., 2005) IR780/PLGA NPs, (Ahmadi et al., 2020) IR780/PLGA@MnO2 NPs, (Qian et al., 2016) IR780/PLGA NPs + US, (Wood and Sehgal, 2015) IR780/PLGA@MnO2 + US (scale bar, 100 µm). (*p < 0.05, compared with the control group).
FIGURE 5 (A,B) Cell viability of 4T1 and MCF-7 cells incubated with different concentrations of IR780/PLGA@MnO2 NPs under normoxia environment (A) and hypoxia environment (B). (C,D) Cell viability of 4T1 and MCF-7 cells under different treatments: (I) PBS, (II) US, (III) IR780/PLGA NPs, (IV) IR780/PLGA@MnO2, (V) IR780/PLGA NPs + US, (VI) IR780/PLGA@MnO2 + US) in normoxia environment (C) and hypoxia environment (D). (E) Fluorescence microscope images of DAPI and PI co-stained 4T1 cells after various treatments: (Hussain and Nguyen, 2014) PBS, (Wells, 2006) US only, (Wu et al., 2005) IR780/PLGA NPs, (Ahmadi et al., 2020) IR780/PLGA@MnO2 NPs, (Qian et al., 2016) IR780/PLGA NPs + US, (Wood and Sehgal, 2015) IR780/PLGA@MnO2 + US (scale bar, 100 µm). (*p < 0.05, compared with the control group).CC BY · PubMed Central
FIGURE 6 (A) Biodistribution of IR780/PLGA@MnO2 NPs in tumor-bearing mice at different time points by in vivo fluorescent imaging. (B,C) Fluorescence imaging of major organs and tumor at 8 h after injection of the IR780/PLGA@MnO2 NPs. (D) H&E-staining images of major organs collected from the IR780/PLGA@MnO2 NPs and saline groups.
FIGURE 6 (A) Biodistribution of IR780/PLGA@MnO2 NPs in tumor-bearing mice at different time points by in vivo fluorescent imaging. (B,C) Fluorescence imaging of major organs and tumor at 8 h after injection of the IR780/PLGA@MnO2 NPs. (D) H&E-staining images of major organs collected from the IR780/PLGA@MnO2 NPs and saline groups.CC BY · PubMed Central
FIGURE 7 (A) T1-weighted MR images of IR780/PLGA@MnO2 NPs suspensions at different Mn concentrations and pH values with H2O2. (B) The longitudinal (r1) relaxation rate vs. the concentration of the IR780/PLGA@MnO2 NPs (in terms of Mn). (C) In vivo MR images of mice bearing implanted 4T1 cancer before and after 24 h of the intravenous injection of IR780/PLGA@MnO2 NPs.
FIGURE 7 (A) T1-weighted MR images of IR780/PLGA@MnO2 NPs suspensions at different Mn concentrations and pH values with H2O2. (B) The longitudinal (r1) relaxation rate vs. the concentration of the IR780/PLGA@MnO2 NPs (in terms of Mn). (C) In vivo MR images of mice bearing implanted 4T1 cancer before and after 24 h of the intravenous injection of IR780/PLGA@MnO2 NPs.CC BY · PubMed Central
FIGURE 8 Representative immunofluorescence images of tumor slices stained by the HIF-1α under different treatments (scale bar, 200 µm).
FIGURE 8 Representative immunofluorescence images of tumor slices stained by the HIF-1α under different treatments (scale bar, 200 µm).CC BY · PubMed Central
FIGURE 9 (A) The relative tumor growth curves and (B) photographs of tumors during the various treatments after 14 days. (C) The weight growth curves of different groups of mice after various treatments. (D) Microscopy images of TUNEL and PCNA assays of stained tumor tissues at different treatments: (Hussain and Nguyen, 2014) Saline, (Wells, 2006) US, (Wu et al., 2005) IR780/PLGA NPs, (Ahmadi et al., 2020) IR780/PLGA@MnO2NPs, (Qian et al., 2016) IR780/PLGA NPs + US, (Wood and Sehgal, 2015) IR780/PLGA@MnO2 NPs + US (scale bar, 200 µm). (E) The relative quantification of TUNEL and (F) PCNA after different treatments. (*p < 0.05).
FIGURE 9 (A) The relative tumor growth curves and (B) photographs of tumors during the various treatments after 14 days. (C) The weight growth curves of different groups of mice after various treatments. (D) Microscopy images of TUNEL and PCNA assays of stained tumor tissues at different treatments: (Hussain and Nguyen, 2014) Saline, (Wells, 2006) US, (Wu et al., 2005) IR780/PLGA NPs, (Ahmadi et al., 2020) IR780/PLGA@MnO2NPs, (Qian et al., 2016) IR780/PLGA NPs + US, (Wood and Sehgal, 2015) IR780/PLGA@MnO2 NPs + US (scale bar, 200 µm). (E) The relative quantification of TUNEL and (F) PCNA after different treatments. (*p < 0.05).CC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 1 references

Research works printed but not linked: 34

  1. Ahmadi, 2020, Recent advances in ultrasound-triggered drug delivery through lipid-based nanomaterials, Drug Discov. Today, 25, 2182, 10.1016/j.drudis.2020.09.026 · DOI
  2. Chen, 2020, Mitochondria-targeting oxygen-sufficient perfluorocarbon nanoparticles for imaging-guided tumor phototherapy, Int. J. Nanomedicine, 15, 8641, 10.2147/IJN.S281649 · DOI
  3. Chu, 2017, Tumor microenvironment-triggered supramolecular system as an in situ nanotheranostic generator for cancer phototherapy, Adv. Mat., 29, 1605928, 10.1002/adma.201605928 · DOI
  4. Costley, 2015, Treating cancer with sonodynamic therapy: A review, Int. J. Hyperth., 31, 107, 10.3109/02656736.2014.992484 · DOI
  5. Ding, 2020, Manganese oxide nanomaterials: Synthesis, properties, and theranostic applications, Adv. Mat., 32, e1905823, 10.1002/adma.201905823 · DOI
  6. Dong, 2021, Inorganic chemoreactive nanosonosensitzers with unique physiochemical properties and structural features for versatile sonodynamic nanotherapies, Biomed. Mat., 16, 032006, 10.1088/1748-605X/abef58 · DOI
  7. Fu, 2019, Targeted magnetic resonance imaging and modulation of hypoxia with multifunctional hyaluronic acid-MnO2 nanoparticles in glioma, Adv. Healthc. Mat., 8, e1900047, 10.1002/adhm.201900047 · DOI
  8. Gordijo, 2015, Design of hybrid MnO2-polymer-lipid nanoparticles with tunable oxygen generation rates and tumor accumulation for cancer treatment, Adv. Funct. Mat., 25, 1858, 10.1002/adfm.201404511 · DOI
  9. Hockel, 2001, Tumor hypoxia: Definitions and current clinical, biologic, and molecular aspects, JNCI J. Natl. Cancer Inst., 93, 266, 10.1093/jnci/93.4.266 · DOI · Paper page
  10. Huang, 2020, Oxygen-sufficient nanoplatform for chemo-sonodynamic therapy of hypoxic tumors, Front. Chem., 8, 358, 10.3389/fchem.2020.00358 · DOI
  11. Huang, 2017, Metalloporphyrin-encapsulated biodegradable nanosystems for highly efficient magnetic resonance imaging-guided sonodynamic cancer therapy, J. Am. Chem. Soc., 139, 1275, 10.1021/jacs.6b11846 · DOI
  12. Hussain, 2014, Molecular imaging for cancer diagnosis and surgery, Adv. Drug Deliv. Rev., 66, 90, 10.1016/j.addr.2013.09.007 · DOI
  13. Liu, 2021, Enzymatically synthesised MnO2 nanoparticles for efficient near-infrared photothermal therapy and dual-responsive magnetic resonance imaging, Nanoscale, 13, 11093, 10.1039/d1nr02400k · DOI
  14. Liu, 2018, Theranostic 2D ultrathin MnO2 nanosheets with fast responsibility to endogenous tumor microenvironment and exogenous NIR irradiation, Biomaterials, 155, 54, 10.1016/j.biomaterials.2017.11.015 · DOI
  15. Ma, 2017, MnO2Gatekeeper: An intelligent and O2-evolving shell for preventing premature release of high cargo payload core, overcoming tumor hypoxia, and acidic H2O2-sensitive MRI, Adv. Funct. Mat., 27, 1604258, 10.1002/adfm.201604258 · DOI
  16. Niu, 2017, Near-infrared induced phase-shifted ICG/Fe3O4 loaded PLGA nanoparticles for photothermal tumor ablation, Sci. Rep., 7, 5490, 10.1038/s41598-017-06122-1 · DOI
  17. Pei, 2020, Platelet-Mimicking drug delivery nanoparticles for enhanced chemo-photothermal therapy of breast cancer , Int. J. Nanomedicine, 15, 10151, 10.2147/IJN.S285952 · DOI
  18. Qian, 2016, Micro/nanoparticle-augmented sonodynamic therapy (SDT): Breaking the depth shallow of photoactivation, Adv. Mat., 28, 8097, 10.1002/adma.201602012 · DOI
  19. Rosenthal, 2004, Sonodynamic therapy--a review of the synergistic effects of drugs and ultrasound, Ultrason. Sonochem., 11, 349, 10.1016/j.ultsonch.2004.03.004 · DOI
  20. Song, 2016, Perfluorocarbon-loaded hollow Bi2Se3 nanoparticles for timely supply of oxygen under near-infrared light to enhance the radiotherapy of cancer, Adv. Mat., 28, 2716, 10.1002/adma.201504617 · DOI
  21. Song, 2016, Ultrasound triggered tumor oxygenation with oxygen-shuttle nanoperfluorocarbon to overcome hypoxia-associated resistance in cancer therapies, Nano Lett., 16, 6145, 10.1021/acs.nanolett.6b02365 · DOI
  22. Sun, 2021, MnO2 nanoflowers as a multifunctional nano-platform for enhanced photothermal/photodynamic therapy and MR imaging, Biomater. Sci., 9, 3662, 10.1039/d1bm00033k · DOI
  23. Wan, 2016, Recent advances of sonodynamic therapy in cancer treatment, Cancer Biol. Med., 13, 325, 10.20892/j.issn.2095-3941.2016.0068 · DOI
  24. Wang, 2018, Triple-modal imaging-guided chemo-photothermal synergistic therapy for breast cancer with magnetically targeted phase-shifted nanoparticles, ACS Appl. Mat. Interfaces, 10, 42102, 10.1021/acsami.8b16323 · DOI
  25. Wang, 2020, Newly developed strategies for improving sonodynamic therapy, Mat. Horiz., 7, 2028, 10.1039/d0mh00613k · DOI
  26. Wells, 2006, Ultrasound imaging, Phys. Med. Biol., 51, R83, 10.1088/0031-9155/51/13/R06 · DOI
  27. Wood, 2015, A review of low-intensity ultrasound for cancer therapy, Ultrasound Med. Biol., 41, 905, 10.1016/j.ultrasmedbio.2014.11.019 · DOI
  28. Wu, 2005, Feasibility of US-guided high-intensity focused ultrasound treatment in patients with advanced pancreatic cancer: Initial experience, Radiology, 236, 1034, 10.1148/radiol.2362041105 · DOI
  29. Xu, 2020, Near-Infrared responsive phase-shifted nanoparticles for magnetically targeted MR/US imaging and photothermal therapy of cancer, Front. Bioeng. Biotechnol., 8, 599107, 10.3389/fbioe.2020.599107 · DOI
  30. Yang, 2019, Biomimetic hybrid nanozymes with self-supplied H(+) and accelerated O2 generation for enhanced starvation and photodynamic therapy against hypoxic tumors, Nano Lett., 19, 4334, 10.1021/acs.nanolett.9b00934 · DOI
  31. Zhang, 2019, Mitochondria-targeted and ultrasound-activated nanodroplets for enhanced deep-penetration sonodynamic cancer therapy, ACS Appl. Mat. Interfaces, 11, 9355, 10.1021/acsami.8b21968 · DOI
  32. Zhang, 2020, Hollow magnetic nanosystem-boosting synergistic effect between magnetic hyperthermia and sonodynamic therapy via modulating reactive oxygen species and heat shock proteins, Chem. Eng. J., 390, 124521, 10.1016/j.cej.2020.124521 · DOI
  33. Zhang, 2020, Nanostructured manganese dioxide for anticancer applications: Preparation, diagnosis, and therapy, Nanoscale, 12, 17982, 10.1039/d0nr04067c · DOI
  34. Zhu, 2018, Nanoenzyme-augmented cancer sonodynamic therapy by catalytic tumor oxygenation, ACS Nano, 12, 3780, 10.1021/acsnano.8b00999 · DOI

Cited by

Sorted by citations

See all 24

Metadata

Authors
Xu, Y., Tan, W., Chen, M., Chen, S., Tang, K., Liao, H., & Niu, C.
Affiliations
Central South University (CN)
Corresponding author
Niu, Chengcheng
Venue
Frontiers in Bioengineering and Biotechnology
Published
2022-10-19
Volume
10
Pages
955127-955127
ISSN
2296-4185 (ISSN-L)
OpenAlex
W4306842424
Cited by
24
References
1
Citations by year
2026: 11 · 2025: 5 · 2024: 5 · 2023: 3
FWCI
0.94
Type
journal article
Language
en
Open access
Locations
  • Frontiers in Bioengineering and Biotechnology (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • National Natural Science Foundation of China
  • Science and Technology Program of Hunan Province
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › Nanoplatforms for cancer theranostics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Photodynamic Therapy Research Studies
  • Physical Sciences › Physics and Astronomy › Radiation › Radiation Therapy and Dosimetry
Keywords
sonodynamic therapy, breast cancer, IR780, manganese dioxide, PLGA nanoparticles, core-shell nanoparticles, tumor hypoxia, reactive oxygen species, pH-responsive drug release, MRI contrast agents

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: MnO2 coated multi-layer nanoplatform for enhanced sonodynamic therapy and MR imaging of breast cancer. https://app.cochat.ai/papers/10.3389/fbioe.2022.955127
The paper
Xu, Y., Tan, W., Chen, M., Chen, S., Tang, K., Liao, H., & Niu, C. (2022). MnO2 coated multi-layer nanoplatform for enhanced sonodynamic therapy and MR imaging of breast cancer. Frontiers in Bioengineering and Biotechnology. https://doi.org/10.3389/fbioe.2022.955127