Highly efficient ablation of metastatic breast cancer using ammonium-tungsten-bronze nanocube as a novel 1064nm-laser-driven photothermal agent

Biomaterials

Volumn 52, Issue 1, 2015, Pages 407-416

  Guo, Chongshen ^a   Yu, Haijun ^b   Feng, Bing ^b   Gao, Weidong ^b   Yan, Mei ^a   Zhang, Zhiwen ^b   Li, Yaping ^b   Liu, Shaoqin ^a  

^a HARBIN INSTITUTE OF TECHNOLOGY   (China)

^b SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

Cancer; Metastasis; Photothermal ablation therapy; Tungsten bronze

Indexed keywords

ABLATION; BIOCOMPATIBILITY; BRONZE; CELL DEATH; INFRARED DEVICES; MOBILE SECURITY; MOLECULAR BIOLOGY; PATHOLOGY; TUMORS; TUNGSTEN;

CANCER; CELLULAR UPTAKE EFFICIENCY; ENDOCYTOSIS PATHWAY; HEAT CONVERSION EFFICIENCIES; METASTASIS; PHOTOTHERMAL ABLATION; PHOTOTHERMAL ABLATION THERAPY; TUNGSTEN BRONZES;

DISEASES;

AMMONIA; CYTOSKELETON PROTEIN; TUNGSTEN; AMMONIUM DERIVATIVE; BIOMATERIAL; COPPER; NANOPARTICLE;

ABLATION THERAPY; ANIMAL CELL; APOPTOSIS; AQUEOUS SOLUTION; ARTICLE; BIOCOMPATIBILITY; BREAST METASTASIS; CELL CULTURE; CELL DEATH; CELL MEMBRANE; CONTROLLED STUDY; CYTOSKELETON; CYTOTOXICITY ASSAY; DISTANT METASTASIS; ELECTRON; ENDOCYTOSIS; HYPERTHERMIA; IN VITRO STUDY; MOUSE; NONHUMAN; PARTICLE SIZE; PRIORITY JOURNAL; PROTEIN DEGRADATION; SOLID TUMOR; SURFACE CHARGE; X RAY DIFFRACTION; ANIMAL; BAGG ALBINO MOUSE; BREAST NEOPLASMS; CANCER TRANSPLANTATION; CHEMISTRY; FEMALE; LASER; LIGHT; METASTASIS; NEAR INFRARED SPECTROSCOPY; NUDE MOUSE; PATHOLOGY; PHOTOTHERAPY; PROCEDURES; TUMOR CELL LINE;

AMMONIUM COMPOUNDS; ANIMALS; BIOCOMPATIBLE MATERIALS; BREAST NEOPLASMS; CELL LINE, TUMOR; COPPER; ENDOCYTOSIS; FEMALE; LASERS; LIGHT; MICE; MICE, INBRED BALB C; MICE, NUDE; NANOPARTICLES; NEOPLASM METASTASIS; NEOPLASM TRANSPLANTATION; PHOTOTHERAPY; SPECTROSCOPY, NEAR-INFRARED; TUNGSTEN;

EID: 84932637022     PISSN: 01429612     EISSN: 18785905     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2015.02.054     Document Type: Article

References (40)

1. DeSantis C., Ma J.L., Bryan L., Jemal A. Breast cancer statistics. CA Cancer J Clin 2013, 2014(64):52-62.
2. Weigelt B., Peterse J.L., Veer L.J. Breast cancer metastasis: markers and models. Nat Rev Cancer 2005, 5:591-602.
3. Gonzalez-Angulo A.M., Morales-Vasquez F., Hortobagyi G.N. Overview of resistance to systemic therapy in patients with breast cancer. Adv Exp Med Biol 2007, 608:1-22.
4. Becker S., Solomayer E., Becker-Pergola G., Wallwiener D., Fehm T. Primary systemic therapy does not eradicate disseminated tumor cells in breast cancer patients. Breast Cancer Res Treat 2007, 106:239-242.
5. Szakacs G., Paterson J.K., Ludwig J.A., Booth-Genthe C., Gottesman M.M. Targeting multidrug resistance in cancer. Nat Rev Drug Discov 2006, 5:219-234.
6. Moon H.K., Lee S.H., Choi H.C. Invivo near-infrared mediated tumor destruction by photothermal effect of carbon nanotubes. ACS Nano 2009, 3:3707-3713.
7. Choi W., Kim J., Kang C., Byeon C.C., Kim Y.H., Gi Tae Tumor regression invivo by photothermal therapy based on gold-nanorod-loaded, functional nanocarriers. ACS Nano 2011, 5:1995-2003.
8. Chen J., Wang D., Xi J., Au L., Siekkinen A., Warsen A., et al. Immuno gold nanocages with tailored optical properties for targeted photothermal destruction of cancer cells. Nano Lett 2007, 7:1318-1322.
9. Huang X.H., El-Sayed I.H., Qian W., El-Sayed M.A. Cancer cell imaging and photothermal therapy in the near-infrared region by using gold nanorods. JAm Chem Soc 2006, 128:2115-2120.
10. Lal S., Clare S.E., Halas N.J. Nanoshell-enabled photothermal cancer therapy: impending clinical impact. Acc Chem Res 2008, 41:1842-1851.
11. Rai P., Mallidi S., Zheng X., Rahmanzadeh R., Mir Y., Elrington S., et al. Development and applications of photo-triggered theranostic agents. Adv Drug Deliv Rev 2010, 62:1094-1124.
12. Lu W., Melancon M.P., Xiong C.Y., Huang Q., Elliott A., Song S.L., et al. Effects of photoacoustic imaging and photothermal ablation therapy mediated by targeted hollow gold nanospheres in an orthotopic mouse xenograft model of glioma. Cancer Res 2011, 71:6116-6121.
13. Hu K.W., Liu T.M., Chung K.Y., Huang K.S., Hsieh C.T., Sun C.K., et al. Efficient near-IR hyperthermia and intense nonlinear optical imaging contrast on the gold nanorod-in-shell nanostructures. JAm Chem Soc 2009, 131:14186-14187.
14. Jang B., Park J.Y., Tung C.H., Kim I.H., Choi Y. Gold nanorod-photosensitizer complex for near-infrared fluorescence imaging and photodynamic/photothermal therapy invivo. ACS Nano 2011, 5:1086-1094.
15. Huang H.C., Rege K., Heys J.J. Spatiotemporal temperature distribution and cancer cell death in response to extracellular hyperthermia induced by gold nanorods. ACS Nano 2010, 4:2892-2900.
16. Zhang Z.J., Wang L.M., Wang J., Jiang X.M., Li X.H., Hu Z.J., et al. Mesoporous silica-coated gold nanorods as a light-mediated multifunctional theranostic platform for cancer treatment. Adv Mater 2012, 24:1418-1423.
17. Hirsch L.R., Stafford R.J., Bankson J.A., Sershen S.R., Rivera B., Price R.E., et al. Nanoshell-mediated near-infrared thermal therapy of tumors under magnetic resonance guidance. Proc Natl Acad Sci U S A 2003, 100:13549-13554.
18. Huang Y., Sefah K., Bamrungsap S., Chang H., Tan W. Selective photothermal therapy for mixed cancer cells using aptamer-conjugated nanorods. Langmuir 2008, 24:11860-11865.
19. Wu M.C., Deokar A.R., Liao J.H., Shih P.Y., Ling Y.C. Graphene-based photothermal agent for rapid and effective killing of bacteria. ACS Nano 2013, 7:1281-1290.
20. Zhou M., Zhang R., Huang M.A., Lu W., Song S.L., Melancon M.P., et al. Achelator-free multifunctional [Cu-64]CuS nanoparticle platform for simultaneous micro-PET/CT imaging and photothermal ablation therapy. JAm Chem Soc 2010, 132:15351-15358.
21. Tian Q., Jiang F., Zou R., Liu Q., Chen Z., Zhu M., et al. Hydrophilic Cu9S5 nanocrystals: a photothermal agent with a 25.7% heat conversion efficiency for photothermal ablation of cancer cells invivo. ACS Nano 2011, 5:9761-9771.
22. Yang J., Choi J., Bang D., Kim E., Lim E.K., Park H., et al. Convertible organic nanoparticles for near-infrared photothermal ablation of cancer cells. Angew Chem Int Ed 2011, 50:441-444.
23. Lovell J.F., Jin C.S., Huynh E., Jin H., Kim C., Rubinstein J.L., et al. Porphysome nanovesicles generated by porphyrin bilayers for use as multimodal biophotonic contrast agents. Nat Mater 2011, 10:324-332.
24. Cheng L., Yang K., Chen Q., Liu Z. Organic stealth nanoparticles for highly effective invivo near-infrared photothermal therapy of cancer. ACS Nano 2012, 6:5605-5613.
25. Yang K., Xu H., Cheng L., Sun C., Wang J., Liu Z. Invitro and invivo near-infrared photothermal therapy of cancer using polypyrrole organic nanoparticles. Adv Mater 2012, 24:5586-5592.
26. Smith A.M., Mancini M.C., Nie SBIOIMAGING. Second window for invivo imaging. Nat Nanotechnol 2009, 4:710-711.
27. Tsai M., Chang S.G., Cheng F., Shanmugam V., Cheng Y., Su C., et al. Au nanorod design as light-absorber in the first and second biological near-infrared windows for invivo photothermal therapy. ACS Nano 2013, 7:5330-5342.
28. Chen Z., Wang Q., Wang H., Zhang L., Song G., Song L., et al. Ultrathin PEGylated W18O49 nanowires as a new 980 nm-laser-driven photothermal agent for efficient ablation of cancer cells invivo. Adv Mater 2013, 25:2095-2100.
29. Kalluru P., Vankayala R., Chiang C., Hwang K.C. Photosensitization of singlet oxygen and invivo photodynamic therapeutic effects mediated by PEGylated W18O49 nanowires. Angew Chem Int Ed 2013, 52:12332-12336.
30. Guo C.S., Yin S., Yu H., Liu S.Q., Dong Q., Goto T., et al. Photothermal ablation cancer therapy using homogeneous CsxWO3 nanorods with broad near-infrared absorption. Nanoscale 2013, 5:6469-6478.
31. Guo C.S., Yin S., Yan M., Sato T. Facile synthesis of homogeneous CsxWO3 nanorods with excellent low-emissivity and NIR shielding property by a water controlled-release process. JMater Chem 2011, 21:5099-5105.
32. Guo C.S., Yin S., Zhang P.L., Yan M., Adachi K., Chonan T., et al. Novel synthesis of homogenous CsxWO3 nanorods with excellent NIR shielding properties by a water controlled-release solvothermal process. JMater Chem 2010, 20:8227-8229.
33. Guo C.S., Yin S., Yan M., Kobayashi M., Kakihana M., Sato T. Morphology-controlled synthesis of W18O49 nanostructures and their near-infrared absorption properties. Inorg Chem 2012, 51:4763-4771.
34. Guo C.S., Yin S., Huang L.J., Yang L., Sato T. Discovery of an excellent IR absorbent with a broad working waveband: CsxWO3 nanorods. Chem Commun 2011, 47:8853-8855.
35. Hussain A., Kihlborg L., Klug A. The transformation between hexagonal potassium tungsten bronze and polytungstateOriginal. JSolid State Chem 1978, 25:189-195.
36. Lynch Y.D.W., Rosei R., Weaver J.H., Olson C.G. The optical properties of some alkali metal tungsten bronzes from 0.1 to 38eV. JSolid State Chem 1973, 8:242-252.
37. Manthiram K., Alivisatos A.P. Tunable localized surface plasmon resonances in tungsten oxide nanocrystals. JAm Chem Soc 2012, 134:3995-3998.
38. Liu X.J., Li B., Fu F.F., Xu K.B., Zou R.J., Wang Q., et al. Facile synthesis of biocompatible cysteine-coated CuS nanoparticles with high photothermal conversion efficiency for cancer therapy. Dalton Trans 2014, 43:11709-11715.
39. Zhan Q.Q., Qian J., Liang H.J., Somesfalean G., Wang D., He S.L., et al. Using 915nm laser excited Tm3+/Er3+/Ho3+-Doped NaYbF4 Upconversion nanoparticles for invitro and deeper invivo bioimaging without overheating irradiation. ACS Nano 2011, 5:3744-3757.
40. Zurgil N., Shafran Y., Afrimzon E., Fixler D., Shainberg A., Deutsch M. Concomitant real-time monitoring of intracellular reactive oxygen species and mitochondrial membrane potential in individual living promonocytic cells. JImmunol Methods 2006, 316:27-41.