Oxygen-generating hybrid nanoparticles to enhance fluorescent/photoacoustic/ultrasound imaging guided tumor photodynamic therapy

Biomaterials

Volumn 112, Issue , 2017, Pages 324-335

  Gao, Shi ^a   Wang, Guohao ^b   Qin, Zainen ^b   Wang, Xiangyu ^b   Zhao, Guoqing ^a   Ma, Qingjie ^a   Zhu, Lei ^b,c  

^a JILIN UNIVERSITY   (China)

^b XIAMEN UNIVERSITY   (China)

^c EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Hyaluronic acid particles; Hypoxia; Image guided therapy; Manganese dioxide nanoparticles; Oxygen generating; Photodynamic therapy

Indexed keywords

CELL PROLIFERATION; DISEASES; FLUORESCENCE; HYALURONIC ACID; MANGANESE; MANGANESE OXIDE; NANOPARTICLES; ORGANIC ACIDS; OXYGEN; PHOTOACOUSTIC EFFECT; PHOTOSENSITIZERS; TUMORS; ULTRASONIC IMAGING;

HYBRID NANOPARTICLE; HYPOXIA; IMAGE GUIDED THERAPY; INTRAVENOUS ADMINISTRATION; MANGANESE DIOXIDE; PHOTO-ACOUSTIC IMAGING; PHOTOACOUSTIC SIGNALS; PHOTODYNAMIC THERAPY (PDT);

PHOTODYNAMIC THERAPY;

CASPASE 3; HEMOGLOBIN; HERMES ANTIGEN; HYALURONIC ACID; HYPOXIA INDUCIBLE FACTOR 1ALPHA; INDOCYANINE GREEN; MANGANESE DIOXIDE; NANOPARTICLE; OXYGEN; PHOTOSENSITIZING AGENT; PIMONIDAZOLE; SINGLET OXYGEN; NANOCAPSULE; NANOCONJUGATE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BIOCOMPATIBILITY; BODY WEIGHT; CANCER INHIBITION; CELL PROLIFERATION; CELL SURVIVAL; COMPARATIVE STUDY; CONTROLLED STUDY; CRYSTAL STRUCTURE; ECHOGRAPHY; FEMALE; FLUORESCENCE IMAGING; FLUORESCENCE MICROSCOPY; HYDROPHOBICITY; IN VITRO STUDY; LASER; MOUSE; NANOENCAPSULATION; NONHUMAN; PH; PHOTOACOUSTICS; PHOTODYNAMIC THERAPY; PHOTON CORRELATION SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN EXPRESSION; SIGNAL DETECTION; SYNTHESIS; TRANSMISSION ELECTRON MICROSCOPY; TUMOR ABLATION; TUMOR MICROENVIRONMENT; TUMOR VOLUME; VASCULAR TUMOR; X RAY DIFFRACTION; ANIMAL; CHEMISTRY; DIAGNOSTIC IMAGING; EXPERIMENTAL NEOPLASM; NUDE MOUSE; PHOTOCHEMOTHERAPY; PROCEDURES; THERANOSTIC NANOMEDICINE; TREATMENT OUTCOME; ULTRASTRUCTURE;

ANIMALS; FEMALE; MICE; MICE, NUDE; MICROSCOPY, FLUORESCENCE; NANOCAPSULES; NANOCONJUGATES; NEOPLASMS, EXPERIMENTAL; OXYGEN; PHOTOACOUSTIC TECHNIQUES; PHOTOCHEMOTHERAPY; PHOTOSENSITIZING AGENTS; THERANOSTIC NANOMEDICINE; TREATMENT OUTCOME; ULTRASONOGRAPHY;

EID: 84993949750     PISSN: 01429612     EISSN: 18785905     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2016.10.030     Document Type: Article

References (50)

1. [1] Tang, W., Zhen, Z., Wang, M., Wang, H., CHuang, Y., Zhang, W., Wang, G., Todd, T., Cowger, T., Chen, H., Liu, L., Li, Z., Xie, J., Red blood cell-facilitated photodynamic therapy for Cancer treatment. Adv. Funct. Mater. 26 (2016), 1757–1768.
2. [2] Siegel, R.L., Miller, K.D., Jemal, A., Cancer statistics, 2015. CA Cancer J. Clin. 65 (2015), 5–29.
3. [3] Gao, Z., Zhang, L., Sun, Y., Nanotechnology applied to overcome tumor drug resistance. J. Control Release 162 (2012), 45–55.
4. [4] Lu, H.L., Syu, W.J., Nishiyama, N., Kataoka, K., Lai, P.S., Dendrimer phthalocyanine-encapsulated polymeric micelle-mediated photochemical internalization extends the efficacy of photodynamic therapy and overcomes drug-resistance in vivo. J. Control Release 155 (2011), 458–464.
5. [5] Ding, H.Y., Yu, H.J., Dong, Y., Tian, R.H., Huang, G., Boothman, D.A., et al. Photoactivation switch from type II to type I reactions by electron-rich micelles for improved photodynamic therapy of cancer cells under hypoxia. J. Control. Release 156 (2011), 276–280.
6. [6] Pineiro, M., Gonsalves, A.M.D.R., Pereira, M.M., Formosinho, S.J., Arnaut, L.G., New halogenated phenylbacteriochlorins and their efficiency in singlet-oxygen sensitization. J. Phys. Chem. A 106 (2002), 3787–3795.
7. [7] Zhang, C., Zhao, K.L., Bu, W.B., Ni, D.L., Liu, Y.Y., Feng, J.W., et al. Marriage of scintillator and semiconductor for synchronous radiotherapy and deep photodynamic therapy with diminished oxygen dependence. Angew. Chem. Int. Ed. 54 (2015), 1770–1774.
8. [8] Wang, J.J., Zhang, L.W., Chen, M.L., Gao, S., Zhu, L., Activatable ferritin nanocomplex for real-time monitoring of Caspase-3 activation during photodynamic therapy. Acs Appl. Mater. Inter. 7 (2015), 23248–23256.
9. [9] Dougherty, T.J., Gomer, C.J., Henderson, B.W., Jori, G., Kessel, D., Korbelik, M., et al. Photodynamic therapy. J. Natl. Cancer Inst. 90 (1998), 889–905.
10. [10] Huang, Z., Xu, H.P., Meyers, A.D., Musani, A.I., Wang, L.W., Tagg, R., et al. Photodynamic therapy for treatment of solid tumors - potential and technical challenges. Technol. Cancer Res. T 7 (2008), 309–320.
11. [11] Brown, J.M., Wilson, W.R., Exploiting tumour hypoxia in cancer treatment. Nat. Rev. Cancer 4 (2004), 437–447.
12. [12] Hockel, M., Vaupel, P., Tumor hypoxia: definitions and current clinical, biologic, and molecular aspects. J. Natl. Cancer I 93 (2001), 266–276.
13. [13] Vaupel, P., Mayer, A., Hypoxia in cancer: significance and impact on clinical outcome. Cancer Metast Rev. 26 (2007), 225–239.
14. [14] Henderson, B.W., Fingar, V.H., Relationship of tumor hypoxia and response to photodynamic treatment in an experimental mouse-tumor. Cancer Res. 47 (1987), 3110–3114.
15. [15] Jin, C.S., Lovell, J.F., Chen, J., Zheng, G., Ablation of hypoxic tumors with dose-equivalent photothermal, but not photodynamic, therapy using a nanostructured porphyrin assembly. Acs Nano 7 (2013), 2541–2550.
16. [16] Song, J.B., Huang, P., Duan, H.W., Chen, X.Y., Plasmonic vesicles of amphiphilic nanocrystals: optically active multifunctional platform for Cancer diagnosis and therapy. Accounts Chem. Res. 48 (2015), 2506–2515.
17. [17] Swierczewska, M., Han, H.S., Kim, K., Park, J.H., Lee, S., Polysaccharide-based nanoparticles for theranostic nanomedicine. Adv. Drug Deliv. Rev. 99 (2016), 70–84.
18. [18] Nguyen, K.T., Zhao, Y., Engineered hybrid nanoparticles for on-demand diagnostics and therapeutics. Acc. Chem. Res. 48 (2015), 3016–3025.
19. [19] Gao, S., Zhang, L.W., Wang, G.H., Yang, K., Chen, M.L., Tian, R., et al. Hybrid graphene/Au activatable theranostic agent for multimodalities imaging guided enhanced photothermal therapy. Biomaterials 79 (2016), 36–45.
20. [20] Wang, G., Zhang, F., Tian, R., Zhang, L., Fu, G., Yang, L., et al. Nanotubes-embedded indocyanine green-hyaluronic acid nanoparticles for photoacoustic-imaging-guided phototherapy. ACS Appl. Mater. Interfaces 8 (2016), 5608–5617.
21. [21] Zhen, Z.P., Tang, W., Guo, C.L., Chen, H.M., Lin, X., Liu, G., et al. Ferritin nanocages to encapsulate and deliver photosensitizers for efficient photodynamic therapy against Cancer. Acs Nano 7 (2013), 6988–6996.
22. [22] Sheng, Z.H., Hu, D.H., Zheng, M.B., Zhao, P.F., Liu, H.L., Gao, D.Y., et al. Smart human serum albumin-indocyanine green nanoparticles generated by programmed assembly for dual-modal imaging-guided Cancer synergistic phototherapy. Acs Nano 8 (2014), 12310–12322.
23. [23] Reddy, G.R., Bhojani, M.S., McConville, P., Moody, J., Moffat, B.A., Hall, D.E., et al. Vascular targeted nanoparticles for imaging and treatment of brain tumors. Clin. Cancer Res. 12 (2006), 6677–6686.
24. [24] Ge, J., Lan, M., Zhou, B., Liu, W., Guo, L., Wang, H., et al. A graphene quantum dot photodynamic therapy agent with high singlet oxygen generation. Nat. Commun., 5, 2014, 4596.
25. [25] Zhao, J.Z., Wu, W.H., Sun, J.F., Guo, S., Triplet photosensitizers: from molecular design to applications. Chem. Soc. Rev. 42 (2013), 5323–5351.
26. [26] Sharman, W.M., Allen, C.M., van Lier, J.E., Photodynamic therapeutics: basic principles and clinical applications. Drug Discov. Today 4 (1999), 507–517.
27. [27] Chen, H.C., Tian, J.W., He, W.J., Guo, Z.J., H2O2-Activatable and O-2-Evolving nanoparticles for highly efficient and selective photodynamic therapy against hypoxic tumor cells. J. Am. Chem. Soc. 137 (2015), 1539–1547.
28. [28] Zhu, W.W., Dong, Z.L., Fu, T.T., Liu, J.J., Chen, Q., Li, Y.G., et al. Modulation of hypoxia in solid tumor microenvironment with MnO2 nanoparticles to enhance photodynamic therapy. Adv. Funct. Mater. 26 (2016), 5490–5498.
29. [29] Cheng, Y.H., Cheng, H., Jiang, C.X., Qiu, X.F., Wang, K.K., Huan, W., et al. Perfluorocarbon nanoparticles enhance reactive oxygen levels and tumour growth inhibition in photodynamic therapy. Nat. Commun. 6 (2015), 8785–8793.
30. [30] Song, X., Feng, L., Liang, C., Yang, K., Liu, Z., Ultrasound triggered tumor oxygenation with oxygen-shuttle nanoperfluorocarbon to overcome hypoxia-associated resistance in Cancer therapies. Nano Lett. 16 (2016), 6145–6153.
31. [31] Schumacker, P.T., Reactive oxygen species in cancer cells: live by the sword, die by the sword. Cancer Cell 10 (2006), 175–176.
32. [32] Szatrowski, T.P., Nathan, C.F., Production of large amounts of hydrogen-peroxide by human tumor-cells. Cancer Res. 51 (1991), 794–798.
33. [33] Prasad, P., Gordijo, C.R., Abbasi, A.Z., Maeda, A., Ip, A., Rauth, A.M., et al. Multifunctional albumin-MnO2 nanoparticles modulate solid tumor microenvironment by attenuating hypoxia, acidosis, vascular endothelial growth factor and enhance radiation response. Acs Nano 8 (2014), 3202–3212.
34. [34] Gordijo, C.R., Abbasi, A.Z., Amini, M.A., Lip, H.Y., Maeda, A., Cai, P., et al. Design of hybrid MnO2-polymer-lipid nanoparticles with tunable oxygen generation rates and tumor accumulation for Cancer treatment. Adv. Funct. Mater. 25 (2015), 1858–1872.
35. [35] Misra, S., Heldin, P., Hascall, V.C., Karamanos, N.K., Skandalis, S.S., Markwald, R.R., et al. Hyaluronan-CD44 interactions as potential targets for cancer therapy. Febs J. 278 (2011), 1429–1443.
36. [36] Jiang, H., Peterson, R.S., Wang, W.H., Bartnik, E., Knudson, C.B., Knudson, W., A requirement for the CD44 cytoplasmic domain for hyaluronan binding, pericellular matrix assembly, and receptor-mediated endocytosis in COS-7 cells. J. Biol. Chem. 277 (2002), 10531–10538.
37. [37] Huang, R.P., Peng, A., Hossain, M.Z., Fan, Y., Jagdale, A., Boynton, A.L., Tumor promotion by hydrogen peroxide in rat liver epithelial cells. Carcinogenesis 20 (1999), 485–492.
38. 2 and CdO nanoparticles. Adv. Sci. Lett. 5 (2012), 1–4.
39. [39] Zhu, J.Y., He, J.H., Facile synthesis of graphene-wrapped honeycomb MnO2 nanospheres and their application in supercapacitors. Acs Appl. Mater. Inter. 4 (2012), 1770–1776.
40. [40] Zhang, L.W., Gao, S., Zhang, F., Yang, K., Ma, Q.J., Zhu, L., Activatable hyaluronic acid nanoparticle as a theranostic agent for optical/photoacoustic image-guided photothermal therapy. Acs Nano 8 (2014), 12250–12258.
41. [41] Luo, Y.L., Preparation of MnO2 nanoparticles by directly mixing potassium permanganate and polyelectrolyte aqueous solutions. Mater. Lett. 61 (2007), 1893–1895.
42. [42] Kato, Y., Ozawa, S., Miyamoto, C., Maehata, Y., Suzuki, A., Maeda, T., et al. Acidic extracellular microenvironment and cancer. Cancer Cell Int. 13 (2013), 89–97.
43. [43] Rofstad, E.K., Mathiesen, B., Kindem, K., Galappathi, K., Acidic extracellular pH promotes experimental metastasis of human melanoma cells in athymic nude mice. Cancer Res. 66 (2006), 6699–6707.
44. [44] Choi, K.Y., Min, K.H., Yoon, H.Y., Kim, K., Park, J.H., Kwon, I.C., et al. PEGylation of hyaluronic acid nanoparticles improves tumor targetability in vivo. Biomaterials 32 (2011), 1880–1889.
45. [45] Dolmans, D.E.J.G.J., Fukumura, D., Jain, R.K., Photodynamic therapy for cancer. Nat. Rev. Cancer 3 (2003), 380–387.
46. [46] Milanesio, M.E., Alvarez, M.G., Rivarola, V., Silber, J.J., Durantini, E.N., Porphyrin-fullerene C-60 dyads with high ability to form photoinduced charge-separated state as novel sensitizers for photodynamic therapy. Photochem. Photobiol. 81 (2005), 891–897.
47. [47] Pineiro, M., Pereira, M.M., Gonsalves, A.M.D.R., Arnaut, L.G., Formosinho, S.J., Singlet oxygen quantum yields from halogenated chlorins: potential new photodynamic therapy agents. J. Photochem. Photobiol. A 138 (2001), 147–157.
48. [48] Carter, W.O., Narayanan, P.K., Robinson, J.P., Intracellular hydrogen peroxide and superoxide anion detection in endothelial cells. J. Leukoc. Biol. 55 (1994), 253–258.
49. [49] Choi, K.Y., Chung, H., Min, K.H., Yoon, H.Y., Kim, K., Park, J.H., et al. Self-assembled hyaluronic acid nanoparticles for active tumor targeting. Biomaterials 31 (2010), 106–114.
50. [50] Song, M.L., Liu, T., Shi, C.R., Zhang, X.Z., Chen, X.Y., Bioconjugated manganese dioxide nanoparticles enhance chemotherapy response by priming tumor-associated tL.A macrophages toward m1-like phenotype and 11 attenuating tumor hypoxia (vol 10, pg 633, 2016). Acs Nano, 10, 2016 3872-3872.