CoChat
Sign Up
Cited by 32

The DOI matches its Crossref record.

Nanoparticle Activation Methods in Cancer Treatment

White, Benjamin D, Duan, Chengchen, Townley, Helen E·2019·Biomolecules
DOI 10.3390/biom9050202PMC PMC6572460
Open this paper in CoChat — free account

Abstract

In this review, we intend to highlight the progress which has been made in recent years around different types of smart activation nanosystems for cancer treatment. Conventional treatment methods, such as chemotherapy or radiotherapy, suffer from a lack of specific targeting and consequent off-target effects. This has led to the development of smart nanosystems which can effect specific regional and temporal activation. In this review, we will discuss the different methodologies which have been designed to permit activation at the tumour site. These can be divided into mechanisms which take advantage of the differences between healthy cells and cancer cells to trigger activation, and those which activate by a mechanism extrinsic to the cell or tumour environment.

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 · 10.3390/biom9050202

Cites

Statistics

Figures

Figure 1 Graphic representation of the dissolution of dendrimer-cationized-albumin coated poly(lactic-co-glycolic-acid) (PLGA) nanoparticles. Doxorubicin (DOX) is released in the U-87 MG glioblastoma cells due to the pH of the acidic late endosomal compartment.
Figure 1 Graphic representation of the dissolution of dendrimer-cationized-albumin coated poly(lactic-co-glycolic-acid) (PLGA) nanoparticles. Doxorubicin (DOX) is released in the U-87 MG glioblastoma cells due to the pH of the acidic late endosomal compartment.CC BY · PubMed Central
Figure 2 Graphic representation of telomerase extending the 3’end aptamer which leads to the conformation change of the aptamer and release of the DOX inside tumour cells.
Figure 2 Graphic representation of telomerase extending the 3’end aptamer which leads to the conformation change of the aptamer and release of the DOX inside tumour cells.CC BY · PubMed Central
Figure 3 The singlet oxygen concentration was further enhanced by hCe6- hypoxia-activated prodrug (AQ4N)-liposome nanosystem irradiated by 660 nm laser and non-toxic AQ4N was transformed to toxic AQ4 by high concentration of singlet oxygen.
Figure 3 The singlet oxygen concentration was further enhanced by hCe6- hypoxia-activated prodrug (AQ4N)-liposome nanosystem irradiated by 660 nm laser and non-toxic AQ4N was transformed to toxic AQ4 by high concentration of singlet oxygen.CC BY · PubMed Central
Figure 4 Graphic representation of ultrasound stimulated piezoelectric stimulation of breast cancer cells. Upon ultrasound induced deformation, barium titanate nanoparticles create a potential difference that interferes with Ca2+ homeostasis and upregulates the Kir3.2 gene.
Figure 4 Graphic representation of ultrasound stimulated piezoelectric stimulation of breast cancer cells. Upon ultrasound induced deformation, barium titanate nanoparticles create a potential difference that interferes with Ca2+ homeostasis and upregulates the Kir3.2 gene.CC BY · PubMed Central
Figure 5 On-off tuneable release mechanism of chemotherapy molecules and gene therapy for DNA. The pores of the polymer reservoir are blocked by magnetic field susceptible ION nanoparticles.
Figure 5 On-off tuneable release mechanism of chemotherapy molecules and gene therapy for DNA. The pores of the polymer reservoir are blocked by magnetic field susceptible ION nanoparticles.CC BY · PubMed Central
Figure 6 Cell death mechanisms utilising different intensities of near infrared radiation (NIR) light for treating tumours at differing depths. At low penetration depths cell death is caused by reactive oxygen species (ROS) generated by Ce6 as photodynamic therapy (PDT). At high penetration depths and low light intensity cell death is caused by the release of docetaxel.
Figure 6 Cell death mechanisms utilising different intensities of near infrared radiation (NIR) light for treating tumours at differing depths. At low penetration depths cell death is caused by reactive oxygen species (ROS) generated by Ce6 as photodynamic therapy (PDT). At high penetration depths and low light intensity cell death is caused by the release of docetaxel.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

No references could be resolved yet.

Research works printed but not linked: 133

  1. Boron, 2004, Regulation of intracellular pH, Adv. Physiol. Educ., 28, 160, 10.1152/advan.00045.2004 · DOI · Paper page
  2. Kato, 2013, Acidic extracellular microenvironment and cancer, Cancer Cell Int., 13, 89, 10.1186/1475-2867-13-89 · DOI
  3. Lin, 2005, pH-sensitive polyelectrolyte complex gel microspheres composed of chitosan/sodium tripolyphosphate/dextran sulfate: Swelling kinetics and drug delivery properties, Colloids Surf. B Biointerfaces, 44, 143, 10.1016/j.colsurfb.2005.06.010 · DOI
  4. Mura, 2013, Stimuli-responsive nanocarriers for drug delivery, Nat. Mater., 12, 991, 10.1038/nmat3776 · DOI · Paper page
  5. Yang, 2011, pH-Sensitive Micelles Self-Assembled from Amphiphilic Copolymer Brush for Delivery of Poorly Water-Soluble Drugs, Biomacromolecules, 12, 116, 10.1021/bm101058w · DOI
  6. Gao, 2010, pH-Responsive Nanoparticles for Drug Delivery, Mol. Pharm., 7, 1913, 10.1021/mp100253e · DOI
  7. Bradley, 1988, Mechanism of multidrug resistance, Biochim. Biophys. Acta - Rev. Cancer, 948, 87, 10.1016/0304-419X(88)90006-6 · DOI
  8. Wang, 2018, Mechanisms of drug release in pH-sensitive micelles for tumour targeted drug delivery system: A review, Int. J. Pharm., 535, 253, 10.1016/j.ijpharm.2017.11.003 · DOI
  9. Dawidar, 2011, Biodegradable pH-responsive alginate-poly (lactic-co-glycolic acid) nano/micro hydrogel matrices for oral delivery of silymarin, Carbohydr. Polym., 83, 1345, 10.1016/j.carbpol.2010.09.055 · DOI
  10. Tian, 2017, pH-responsive poly (acrylic acid)-gated mesoporous silica and its application in oral colon targeted drug delivery for doxorubicin, Colloids Surf. B Biointerfaces, 154, 287, 10.1016/j.colsurfb.2017.03.024 · DOI
  11. Hsu, C.-H., and Cheng, A.-L. (2007). Clinical studies with Curcumin. The Molecular Targets and Therapeutic Uses of Curcumin in Health and Disease, Springer. · DOI
  12. Cui, 2009, Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems, Int. J. Pharm., 371, 148, 10.1016/j.ijpharm.2008.12.009 · DOI
  13. Raghunand, 1999, Enhancement of chemotherapy by manipulation of tumour pH, Br. J. Cancer, 80, 1005, 10.1038/sj.bjc.6690455 · DOI
  14. Peppicelli, 2017, The acidic microenvironment as a possible niche of dormant tumor cells, Cell. Mol. Life Sci., 74, 2761, 10.1007/s00018-017-2496-y · DOI
  15. Jo, 2017, In vivo quantitative imaging of tumor pH by nanosonophore assisted multispectral photoacoustic imaging, Nat. Commun., 8, 471, 10.1038/s41467-017-00598-1 · DOI
  16. Ray, 2019, PEG-b-poly (carbonate)-derived nanocarrier platform with pH-responsive properties for pancreatic cancer combination therapy, Colloids Surf. B Biointerfaces, 174, 126, 10.1016/j.colsurfb.2018.10.069 · DOI
  17. Qian, 2019, Tumor-microenvironment controlled nanomicelles with AIE property for boosting cancer therapy and apoptosis monitoring, Biomaterials, 188, 96, 10.1016/j.biomaterials.2018.10.003 · DOI
  18. Glunde, 2003, Extracellular acidification alters lysosomal trafficking in human breast cancer cells, Neoplasia, 5, 533, 10.1016/S1476-5586(03)80037-4 · DOI
  19. Griset, 2009, Expansile Nanoparticles: Synthesis, Characterization, and in Vivo Efficacy of an Acid-Responsive Polymeric Drug Delivery System, J. Am. Chem. Soc., 131, 2469, 10.1021/ja807416t · DOI
  20. Xu, 2016, Ultra-pH-Responsive and Tumor-Penetrating Nanoplatform for Targeted siRNA Delivery with Robust Anti-Cancer Efficacy, Angew. Chemie Int. Ed., 55, 7091, 10.1002/anie.201601273 · DOI
  21. Hwang, 2015, Functional Nanovalves on Protein-Coated Nanoparticles for In vitro and In vivo Controlled Drug Delivery, Small, 11, 319, 10.1002/smll.201400765 · DOI
  22. Muniswamy, 2019, ‘Dendrimer-Cationized-Albumin’ encrusted polymeric nanoparticle improves BBB penetration and anticancer activity of doxorubicin, Int. J. Pharm., 555, 77, 10.1016/j.ijpharm.2018.11.035 · DOI
  23. Dai, 2018, Dual-stimuli-responsive TiO x /DOX nanodrug system for lung cancer synergistic therapy, RSC Adv., 8, 21975, 10.1039/C8RA02899K · DOI
  24. Yue, 2011, Iron Oxide Nanotubes for Magnetically Guided Delivery and pH-Activated Release of Insoluble Anticancer Drugs, Adv. Funct. Mater., 21, 3446, 10.1002/adfm.201100510 · DOI
  25. Mi, 2016, A pH-activatable nanoparticle with signal-amplification capabilities for non-invasive imaging of tumour malignancy, Nat. Nanotechnol., 11, 724, 10.1038/nnano.2016.72 · DOI
  26. Dong, 2016, CaCO3 nanoparticles as an ultra-sensitive tumor-pH-responsive nanoplatform enabling real-time drug release monitoring and cancer combination therapy, Biomaterials, 110, 60, 10.1016/j.biomaterials.2016.09.025 · DOI
  27. Choi, 2016, PEGylated lipid bilayer-supported mesoporous silica nanoparticle composite for synergistic co-delivery of axitinib and celastrol in multi-targeted cancer therapy, Acta Biomater., 39, 94, 10.1016/j.actbio.2016.05.012 · DOI
  28. Schomburg, 2013, BRENDA in 2013: integrated reactions, kinetic data, enzyme function data, improved disease classification: new options and contents in BRENDA, Nucleic Acids Res., 41, D764, 10.1093/nar/gks1049 · DOI
  29. Li, 2017, Cancer-Associated, Stimuli-Driven, Turn on Theranostics for Multimodality Imaging and Therapy, Adv. Mater., 29, 1606857, 10.1002/adma.201606857 · DOI
  30. Shin, 2016, Cancer Targeted Enzymatic Theranostic Prodrug: Precise Diagnosis and Chemotherapy, Bioconjug. Chem., 27, 1419, 10.1021/acs.bioconjchem.6b00184 · DOI
  31. Tarro, 2005, Early diagnosis of lung cancer by detection of tumor liberated protein, J. Cell. Physiol., 203, 1, 10.1002/jcp.20195 · DOI
  32. Chan, 2017, Protease-activated nanomaterials for targeted cancer theranostics, Nanomedicine, 12, 2153, 10.2217/nnm-2017-0068 · DOI
  33. Han, 2017, Dual Enzymatic Reaction-Assisted Gemcitabine Delivery Systems for Programmed Pancreatic Cancer Therapy, ACS Nano, 11, 1281, 10.1021/acsnano.6b05541 · DOI
  34. Nairon, 2018, Abstract 4664: Enzymatically-responsive tumor-targeted mesoporous silica nanoparticle for identification of pancreatic cancer, Cancer Res., 78, 4664, 10.1158/1538-7445.AM2018-4664 · DOI
  35. Liu, 2018, Crosslinked self-assembled nanoparticles for chemo-sonodynamic combination therapy favoring antitumor, antimetastasis management and immune responses, J. Control. Release, 290, 150, 10.1016/j.jconrel.2018.10.007 · DOI
  36. Dzamukova, 2015, Enzyme-activated intracellular drug delivery with tubule clay nanoformulation, Sci. Rep., 5, 10560, 10.1038/srep10560 · DOI
  37. Talalay, 2010, NAD(P)H:quinone acceptor oxidoreductase 1 (NQO1), a multifunctional antioxidant enzyme and exceptionally versatile cytoprotector, Arch. Biochem. Biophys., 501, 116, 10.1016/j.abb.2010.03.019 · DOI
  38. Huang, 2014, Self-assembled hybrid nanoparticles for targeted co-delivery of two drugs into cancer cells, Chem. Commun., 50, 3103, 10.1039/c3cc49003c · DOI
  39. Shi, 2018, Molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells, Sci. Rep., 8, 16341, 10.1038/s41598-018-34670-7 · DOI
  40. Mannaris, 2018, Gas-Stabilizing Gold Nanocones for Acoustically Mediated Drug Delivery, Adv. Healthc. Mater., 7, 1800184, 10.1002/adhm.201800184 · DOI
  41. Decock, 2008, Cathepsin B, cathepsin H, cathepsin X and cystatin C in sera of patients with early-stage and inflammatory breast cancer, Int. J. Biol. Mark., 23, 161, 10.1177/172460080802300305 · DOI
  42. Pardo, 2018, Gold Nanorod-Based Nanohybrids for Combinatorial Therapeutics, ACS Omega, 3, 12633, 10.1021/acsomega.8b01591 · DOI
  43. Yildiz, 2018, Doxorubicin-loaded protease-activated near-infrared fluorescent polymeric nanoparticles for imaging and therapy of cancer, Int. J. Nanomed., 13, 6961, 10.2147/IJN.S174068 · DOI
  44. Coussens, 2002, Matrix metalloproteinase inhibitors and cancer: Trials and tribulations, Science, 295, 2387, 10.1126/science.1067100 · DOI · Paper page
  45. Somerville, 2003, Matrix metalloproteinases: Old dogs with new tricks, Genome Biol., 4, 216, 10.1186/gb-2003-4-6-216 · DOI
  46. Davies, 1995, Structures and mechanisms of glycosyl hydrolases, Structure, 3, 853, 10.1016/S0969-2126(01)00220-9 · DOI
  47. Shin, 2013, Oncogenic role of protein tyrosine kinase 7 in esophageal squamous cell carcinoma, Cancer Sci., 104, 1120, 10.1111/cas.12194 · DOI
  48. Yang, 2018, Stepwise Degradable Nanocarriers Enabled Cascade Delivery for Synergistic Cancer Therapy, Adv. Funct. Mater., 28, 1800706, 10.1002/adfm.201800706 · DOI
  49. Lian, 2018, Enzyme-MOF Nanoreactor Activates Nontoxic Paracetamol for Cancer Therapy, Angew. Chemie Int. Ed., 57, 5725, 10.1002/anie.201801378 · DOI
  50. Davis, 2010, Evidence of RNAi in humans from systemically administered siRNA via targeted nanoparticles, Nature, 464, 1067, 10.1038/nature08956 · DOI
  51. Wang, 2016, Self-assembled IR780-loaded transferrin nanoparticles as an imaging, targeting and PDT/PTT agent for cancer therapy, Sci. Rep., 6, 27421, 10.1038/srep27421 · DOI
  52. Dixit, 2015, Transferrin receptor-targeted theranostic gold nanoparticles for photosensitizer delivery in brain tumors, Nanoscale, 7, 1782, 10.1039/C4NR04853A · DOI
  53. Ciechanover, 1983, pH and the recycling of transferrin during receptor-mediated endocytosis, Proc. Natl. Acad. Sci. USA, 80, 2258, 10.1073/pnas.80.8.2258 · DOI
  54. Sutherland, 1981, Ubiquitous cell-surface glycoprotein on tumor cells is proliferation-associated receptor for transferrin, Proc. Natl. Acad. Sci. USA, 78, 4515, 10.1073/pnas.78.7.4515 · DOI · Paper page
  55. Zhang, Q., Wang, N., Ma, M., Luo, Y., and Chen, H. (2019). Transferrin Receptor-Mediated Sequential Intercellular Nanoparticles Relay for Tumor Deep Penetration and Sonodynamic Therapy. Adv. Ther., 1800152. · DOI
  56. Wosikowski, 1997, Altered gene expression in drug-resistant human breast cancer cells, Clin. Cancer Res., 3, 2405
  57. Akimoto, 1999, Inverse relationship between epidermal growth factor receptor expression and radiocurability of murine carcinomas, Clin. Cancer Res., 5, 2884
  58. Galizia, 2006, Prognostic Significance of Epidermal Growth Factor Receptor Expression in Colon Cancer Patients Undergoing Curative Surgery, Ann. Surg. Oncol., 13, 823, 10.1245/ASO.2006.05.052 · DOI
  59. Henriksen, L., Grandal, M.V., Knudsen, S.L.J., van Deurs, B., and Grøvdal, L.M. (2013). Internalization Mechanisms of the Epidermal Growth Factor Receptor after Activation with Different Ligands. PLoS ONE, 8. · DOI
  60. Merten, 2015, Antibody–Drug Conjugates for Tumor Targeting—Novel Conjugation Chemistries and the Promise of non-IgG Binding Proteins, Bioconjug. Chem., 26, 2176, 10.1021/acs.bioconjchem.5b00260 · DOI
  61. Ducry, 2010, Antibody−Drug Conjugates: Linking Cytotoxic Payloads to Monoclonal Antibodies, Bioconjug. Chem., 21, 5, 10.1021/bc9002019 · DOI
  62. Roncato, 2018, Improvement and extension of anti-EGFR targeting in breast cancer therapy by integration with the Avidin-Nucleic-Acid-Nano-Assemblies, Nat. Commun., 9, 4070, 10.1038/s41467-018-06602-6 · DOI
  63. Zhang, 2007, Prostate-specific membrane antigen (PSMA) protein expression in normal and neoplastic tissues and its sensitivity and specificity in prostate adenocarcinoma: an immunohistochemical study using mutiple tumour tissue microarray technique, Histopathology, 50, 472, 10.1111/j.1365-2559.2007.02635.x · DOI
  64. Rauscher, 2016, 68Ga-PSMA ligand PET/CT in patients with prostate cancer: How we review and report, Cancer Imaging, 16, 14, 10.1186/s40644-016-0072-6 · DOI
  65. Liu, 1998, Constitutive and antibody-induced internalization of prostate-specific membrane antigen, Cancer Res., 58, 4055
  66. Mangadlao, 2018, Prostate-Specific Membrane Antigen Targeted Gold Nanoparticles for Theranostics of Prostate Cancer, ACS Nano, 12, 3714, 10.1021/acsnano.8b00940 · DOI
  67. Brown, 1998, The unique physiology of solid tumors: Opportunities (and problems) for cancer therapy, Cancer Res., 58, 1408
  68. Feng, 2017, Theranostic Liposomes with Hypoxia-Activated Prodrug to Effectively Destruct Hypoxic Tumors Post-Photodynamic Therapy, ACS Nano, 11, 927, 10.1021/acsnano.6b07525 · DOI
  69. Yang, 2016, Structure-Dependent and Glutathione-Responsive Biodegradable Dendritic Mesoporous Organosilica Nanoparticles for Safe Protein Delivery, Chem. Mater., 28, 9008, 10.1021/acs.chemmater.6b03896 · DOI
  70. Robinson, R.K., Batt, C.A., and Patel, P.D. (2000). Encyclopedia of Food Microbiology, Academic Press.
  71. Mullin, 2013, Nanoparticle delivery enhancement with acoustically activated microbubbles, IEEE Trans. Ultrason. Ferroelectr. Freq. Control, 60, 65, 10.1109/TUFFC.2013.2538 · DOI
  72. Deng, 2004, Ultrasound-induced cell membrane porosity, Ultrasound Med. Biol., 30, 519, 10.1016/j.ultrasmedbio.2004.01.005 · DOI
  73. Dewitte, 2011, mRNA-Lipoplex loaded microbubble contrast agents for ultrasound-assisted transfection of dendritic cells, Biomaterials, 32, 9128, 10.1016/j.biomaterials.2011.08.024 · DOI
  74. Burke, 2014, Ultrasound-activated agents comprised of 5FU-bearing nanoparticles bonded to microbubbles inhibit solid tumor growth and improve survival, Mol. Ther., 22, 321, 10.1038/mt.2013.259 · DOI
  75. Kwan, 2015, Ultrasound-Propelled Nanocups for Drug Delivery, Small, 11, 5305, 10.1002/smll.201501322 · DOI
  76. Burke, 2011, Covalently linking poly(lactic-co-glycolic acid) nanoparticles to microbubbles before intravenous injection improves their ultrasound-targeted delivery to skeletal muscle, Small, 7, 1227, 10.1002/smll.201001934 · DOI
  77. Chappell, 2008, Targeted delivery of nanoparticles bearing fibroblast growth factor-2 by ultrasonic microbubble destruction for therapeutic arteriogenesis, Small, 4, 1769, 10.1002/smll.200800806 · DOI
  78. Price, 1998, Delivery of colloidal particles and red blood cells to tissue through microvessel ruptures created by targeted microbubble destruction with ultrasound, Circulation, 98, 1264, 10.1161/01.CIR.98.13.1264 · DOI
  79. Cochran, 2011, Doxorubicin and paclitaxel loaded microbubbles for ultrasound triggered drug delivery, Int. J. Pharm., 414, 161, 10.1016/j.ijpharm.2011.05.030 · DOI
  80. Yuan, 2018, MRI tracing non-invasive TiO2-based nanoparticles activated by ultrasound for multi-mechanism therapy of prostatic cancer, Nanotechnology, 29, 125101, 10.1088/1361-6528/aaa92a · DOI
  81. Lee, 2016, Theranostic gas-generating nanoparticles for targeted ultrasound imaging and treatment of neuroblastoma, J. Control. Release, 223, 197, 10.1016/j.jconrel.2015.12.051 · DOI
  82. Marshalek, 2016, Intracellular delivery and ultrasonic activation of folate receptor-targeted phase-change contrast agents in breast cancer cells in vitro, J. Control. Release, 243, 69, 10.1016/j.jconrel.2016.09.010 · DOI
  83. Wang, 2007, Direct-Current Nanogenerator Driven by Ultrasonic Waves, Science, 316, 102, 10.1126/science.1139366 · DOI
  84. Cucullo, 2005, Very low intensity alternating current decreases cell proliferation, Glia, 51, 65, 10.1002/glia.20188 · DOI
  85. Marino, 2018, Ultrasound-Activated Piezoelectric Nanoparticles Inhibit Proliferation of Breast Cancer Cells, Sci. Rep., 8, 6257, 10.1038/s41598-018-24697-1 · DOI
  86. Pearce, 2013, Magnetic Heating of Nanoparticles: The Importance of Particle Clustering to Achieve Therapeutic Temperatures, J. Nanotechnol. Eng. Med., 4, 011005, 10.1115/1.4024904 · DOI
  87. Shah, 2015, Impact of magnetic field parameters and iron oxide nanoparticle properties on heat generation for use in magnetic hyperthermia, J. Magn. Magn. Mater., 387, 96, 10.1016/j.jmmm.2015.03.085 · DOI
  88. Noto, 1989, Effects of sodium ascorbate (vitamin C) and 2-methyl-1,4-naphthoquinone (vitamin K3) treatment on human tumor cell growth in vitro. I. Synergism of combined vitamin C and K3 action, Cancer, 63, 901, 10.1002/1097-0142(19890301)63:5<901::AID-CNCR2820630518>3.0.CO;2-G · DOI
  89. Johannsen, 2005, Clinical hyperthermia of prostate cancer using magnetic nanoparticles: Presentation of a new interstitial technique, Int. J. Hyperth., 21, 637, 10.1080/02656730500158360 · DOI
  90. Teijeiro, 2013, Magnetic nanoparticle-based hyperthermia for cancer treatment, Rep. Pract. Oncol. Radiother., 18, 397, 10.1016/j.rpor.2013.09.011 · DOI
  91. Vedova, 2015, Gold Nanoparticle-Based Sensors Activated by External Radio Frequency Fields, Small, 11, 248, 10.1002/smll.201401187 · DOI
  92. Raoof, 2012, Stability of antibody-conjugated gold nanoparticles in the endolysosomal nanoenvironment: implications for noninvasive radiofrequency-based cancer therapy, Nanomed. Nanotechnol. Biol. Med., 8, 1096, 10.1016/j.nano.2012.02.001 · DOI
  93. Mironava, 2017, Gold Nanoparticles and Radio Frequency Field Interactions: Effects of Nanoparticle Size, Charge, Aggregation, Radio Frequency, and Ionic Background, Langmuir, 33, 13114, 10.1021/acs.langmuir.7b03210 · DOI
  94. Katagiri, 2011, Magnetoresponsive On-Demand Release of Hybrid Liposomes Formed from Fe3O4 Nanoparticles and Thermosensitive Block Copolymers, Small, 7, 1683, 10.1002/smll.201002180 · DOI
  95. Pradhan, 2010, Targeted temperature sensitive magnetic liposomes for thermo-chemotherapy, J. Control. Release, 142, 108, 10.1016/j.jconrel.2009.10.002 · DOI
  96. Plassat, 2011, Anti-Estrogen-Loaded Superparamagnetic Liposomes for Intracellular Magnetic Targeting and Treatment of Breast Cancer Tumors, Adv. Funct. Mater., 21, 83, 10.1002/adfm.201001450 · DOI
  97. Hu, 2012, Multifunctional Nanocapsules for Simultaneous Encapsulation of Hydrophilic and Hydrophobic Compounds and On-Demand Release, ACS Nano, 6, 2558, 10.1021/nn205023w · DOI
  98. Hua, 2011, The effectiveness of a magnetic nanoparticle-based delivery system for BCNU in the treatment of gliomas, Biomaterials, 32, 516, 10.1016/j.biomaterials.2010.09.065 · DOI
  99. Yang, 2011, Self-protecting core-shell magnetic nanoparticles for targeted, traceable, long half-life delivery of BCNU to gliomas, Biomaterials, 32, 6523, 10.1016/j.biomaterials.2011.05.047 · DOI
  100. Nigam, 2017, Dendrimer-conjugated iron oxide nanoparticles as stimuli-responsive drug carriers for thermally-activated chemotherapy of cancer, Colloids Surf. B Biointerfaces, 155, 182, 10.1016/j.colsurfb.2017.04.025 · DOI
  101. Stanley, 2012, Radio-Wave Heating of Iron Oxide Nanoparticles Can Regulate Plasma Glucose in Mice, Science, 336, 604, 10.1126/science.1216753 · DOI
  102. Huang, 2012, Self-assembling PVA-F127 thermosensitive nanocarriers with highly sensitive magnetically-triggered drug release for epilepsy therapy in vivo, J. Mater. Chem., 22, 8566, 10.1039/c2jm00032f · DOI
  103. Satarkar, 2008, Hydrogel nanocomposites as remote-controlled biomaterials, Acta Biomater., 4, 11, 10.1016/j.actbio.2007.07.009 · DOI
  104. Hu, 2008, Surfactant-Free, Self-Assembled PVA-Iron Oxide/Silica Core-Shell Nanocarriers for Highly Sensitive, Magnetically Controlled Drug Release and Ultrahigh Cancer Cell Uptake Efficiency, Adv. Funct. Mater., 18, 2946, 10.1002/adfm.200800428 · DOI
  105. Hu, 2008, Core/Single-Crystal-Shell Nanospheres for Controlled Drug Release via a Magnetically Triggered Rupturing Mechanism, Adv. Mater., 20, 2690, 10.1002/adma.200800193 · DOI
  106. Bringas, 2012, Triggered release in lipid bilayer-capped mesoporous silica nanoparticles containing SPION using an alternating magnetic field, Chem. Commun., 48, 5647, 10.1039/c2cc31563g · DOI
  107. Cai, 2009, Magnetically Triggered Reversible Controlled Drug Delivery from Microfabricated Polymeric Multireservoir Devices, Adv. Mater., 21, 4045, 10.1002/adma.200900593 · DOI
  108. Thomas, 2010, Noninvasive Remote-Controlled Release of Drug Molecules in Vitro Using Magnetic Actuation of Mechanized Nanoparticles, J. Am. Chem. Soc., 132, 10623, 10.1021/ja1022267 · DOI
  109. Walker, 2017, Radio-frequency actuated polymer-based phononic meta-materials for control of ultrasonic waves, NPG Asia Mater., 9, e350, 10.1038/am.2016.209 · DOI
  110. Park, 2011, Clustered magnetite nanocrystals cross-linked with PEI for efficient siRNA delivery, Biomacromolecules, 12, 457, 10.1021/bm101244j · DOI
  111. Allison, 2010, Oncologic photodynamic therapy photosensitizers: A clinical review, Photodiagn. Photodyn. Ther., 7, 61, 10.1016/j.pdpdt.2010.02.001 · DOI
  112. Wang, 2011, Upconversion nanoparticles: Synthesis, surface modification and biological applications, Nanomedicine, 7, 710, 10.1016/j.nano.2011.02.013 · DOI
  113. Haynes, W.M. (2009). CRC Handbook of Chemistry and Physics: A Ready-Reference Book of Chemical and Physical Data, CRC Press.
  114. Meng, 2018, Light-Activated Core–Shell Nanoparticles for Spatiotemporally Specific Treatment of Metastatic Triple-Negative Breast Cancer, ACS Nano, 12, 2789, 10.1021/acsnano.7b09210 · DOI
  115. Lucky, 2015, Titania Coated Upconversion Nanoparticles for Near-Infrared Light Triggered Photodynamic Therapy, ACS Nano, 9, 191, 10.1021/nn503450t · DOI
  116. Dai, 2017, 808 nm near-infrared light controlled dual-drug release and cancer therapy in vivo by upconversion mesoporous silica nanostructures, J. Mater. Chem. B, 5, 2086, 10.1039/C7TB00224F · DOI
  117. Huang, 2016, Ultralow-Power Near Infrared Lamp Light Operable Targeted Organic Nanoparticle Photodynamic Therapy, J. Am. Chem. Soc., 138, 14586, 10.1021/jacs.6b05390 · DOI
  118. Vankayala, 2015, Nucleus-Targeting Gold Nanoclusters for Simultaneous In Vivo Fluorescence Imaging, Gene Delivery, and NIR-Light Activated Photodynamic Therapy, Adv. Funct. Mater., 25, 5934, 10.1002/adfm.201502650 · DOI
  119. Qiu, 2018, Novel concept of the smart NIR-light-controlled drug release of black phosphorus nanostructure for cancer therapy, Proc. Natl. Acad. Sci. USA, 115, 501, 10.1073/pnas.1714421115 · DOI
  120. Liu, 2015, Gold Nanorods Coated with Mesoporous Silica Shell as Drug Delivery System for Remote Near Infrared Light-Activated Release and Potential Phototherapy, Small, 11, 2323, 10.1002/smll.201402145 · DOI
  121. He, 2015, Self-Assembled Core–Shell Nanoparticles for Combined Chemotherapy and Photodynamic Therapy of Resistant Head and Neck Cancers, ACS Nano, 9, 991, 10.1021/nn506963h · DOI
  122. Qian, 2016, Light-Activated Hypoxia-Responsive Nanocarriers for Enhanced Anticancer Therapy, Adv. Mater., 28, 3313, 10.1002/adma.201505869 · DOI
  123. Guan, 2015, Multifunctional upconversion–nanoparticles–trismethylpyridylporphyrin–fullerene nanocomposite: A near-infrared light-triggered theranostic platform for imaging-guided photodynamic therapy, NPG Asia Mater., 7, e205, 10.1038/am.2015.82 · DOI
  124. Yue, 2016, ROS-Responsive Mitochondria-Targeting Blended Nanoparticles: Chemo- and Photodynamic Synergistic Therapy for Lung Cancer with On-Demand Drug Release upon Irradiation with a Single Light Source, Theranostics, 6, 2352, 10.7150/thno.15433 · DOI
  125. Lu, 2015, A Chlorin-Based Nanoscale Metal–Organic Framework for Photodynamic Therapy of Colon Cancers, J. Am. Chem. Soc., 137, 7600, 10.1021/jacs.5b04069 · DOI
  126. Solís-López, M., and Ramírez-Zamora, R.M. (2019, January 24). Fenton Reaction—An Overview | ScienceDirect Topics. Available online: https://www.sciencedirect.com/topics/chemistry/fenton-reaction.
  127. Kim, 2017, Continuous O2-Evolving MnFe2O4 Nanoparticle-Anchored Mesoporous Silica Nanoparticles for Efficient Photodynamic Therapy in Hypoxic Cancer, J. Am. Chem. Soc., 139, 10992, 10.1021/jacs.7b05559 · DOI
  128. Espinosa, 2016, Duality of Iron Oxide Nanoparticles in Cancer Therapy: Amplification of Heating Efficiency by Magnetic Hyperthermia and Photothermal Bimodal Treatment, ACS Nano, 10, 2436, 10.1021/acsnano.5b07249 · DOI
  129. Goodman, 2017, Near-infrared remotely triggered drug-release strategies for cancer treatment, Proc. Natl. Acad. Sci. USA, 114, 12419, 10.1073/pnas.1713137114 · DOI
  130. Yang, 2016, Near-infrared light-activated cancer cell targeting and drug delivery with aptamer-modified nanostructures, Nano Res., 9, 139, 10.1007/s12274-015-0898-4 · DOI
  131. Chen, 2015, Nanoscintillator-Mediated X-ray Inducible Photodynamic Therapy for In Vivo Cancer Treatment, Nano Lett., 15, 2249, 10.1021/nl504044p · DOI
  132. Kotagiri, 2018, Radionuclides transform chemotherapeutics into phototherapeutics for precise treatment of disseminated cancer, Nat. Commun., 9, 275, 10.1038/s41467-017-02758-9 · DOI
  133. Stolik, 2000, Measurement of the penetration depths of red and near infrared light in human “ex vivo” tissues, J. Photochem. Photobiol. B Biol., 57, 90, 10.1016/S1011-1344(00)00082-8 · DOI

Cited by

Sorted by citations

Metadata

Authors
White, B. D., Duan, C., & Townley, H. E.
Venue
Biomolecules
Publisher
MDPI AG
Published
2019-05-24
Volume
9
Issue
5
Pages
202
ISSN
2218-273X
DOI
10.3390/biom9050202
PMC
PMC6572460
Cited by
32
References
0
Language
en
Licence
creativecommons.org/licenses/by/4.0/ (vor)

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