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1 sing, biological imaging, drug delivery, and photothermal therapy.
2 is completely eliminated with combined chemo-photothermal therapy.
3 ic resonance (MR) imaging, gene-delivery and photothermal therapy.
4 veloped with limited success for tumor chemo-photothermal therapy.
5 ell to enable both photoacoustic imaging and photothermal therapy.
6 erved, which allowed for efficient plasmonic photothermal therapy.
7 under preclinical settings, and as a type of photothermal therapy.
8 f SERS agents for targeted drug delivery and photothermal therapy.
9 bsorbance and biocompatibility for potential photothermal therapy.
10 animal levels compared with chemotherapy or photothermal therapy alone, indicating the PEG-OJNP-LA c
11 chemotherapy and enables the combination of photothermal therapy and chemotherapy to receive superio
12 synergistic interaction between CuS-mediated photothermal therapy and porphyrin-mediated photodynamic
13 d nanostructure based in vivo bioimaging and photothermal therapy and their loading capacity for both
14 hotothermal multimodal-imaging-guided cancer photothermal therapy and UV and gamma-irradiation protec
15 owerful potential tools for in vivo imaging, photothermal therapy, and drug delivery thanks to plasmo
16 ts in various bioimaging modalities, near-IR photothermal therapy, and for light-triggered therapeuti
17 induced via gold nanorod mediated plasmonic photothermal therapy, and intravenous administration of
18 roscopy, superresolution optical microscopy, photothermal therapy, and long-distance telecommunicatio
20 herapeutic approaches (i.e. drug delivery or photothermal therapy), are also included in this overvie
21 heat upon irradiation are being explored for photothermal therapy as a minimally invasive approach to
22 Gold nanorods (AuNRs)-assisted plasmonic photothermal therapy (AuNRs-PPTT) is a promising strateg
23 frared (NIR) light-assisted nanoparticles in photothermal therapy, chemotherapy, and photodynamic the
24 ed to investigate the prostate tumor uptake, photothermal therapy mediated macromolecular delivery, a
25 For cancer therapy in mice, tumor PS and photothermal therapy of anti-CD11b Abs-linked gold nanor
27 ional ~150nm silica core gold nanoshells for photothermal therapy of triple negative breast cancer.
28 red and photoacoustic imaging and synergetic photothermal therapy/photodynamic therapy derived from t
29 oparticles have great potential in plasmonic photothermal therapy (photothermolysis), but their intra
31 n that gold nanorod (GNR) mediated plasmonic photothermal therapy (PPTT) is capable of increasing the
33 ar-infrared (NIR) light to generate heat for photothermal therapy (PPTT), where the temperature was a
38 e-enabled fluorescence-guided transbronchial photothermal therapy (PTT) of peripheral lung cancer was
40 tly convert light to heat inside tumours for photothermal therapy (PTT), and light to singlet oxygen
42 been widely studied in cancer detection and photothermal therapy (PTT), while it remains a great cha
46 ation has potential in photodynamic therapy, photothermal therapy, radiotherapy, protected delivery o
47 rate information needed for optimization of photothermal therapy that invokes infrared irradiation t
48 n and plasmonic gold nanostar (GNS)-mediated photothermal therapy, we were able to achieve complete e
49 s reduced tumor burden in a single course of photothermal therapy while coupling three complementary
50 vehicles are constructed for combined chemo-photothermal therapy with pinpointed drug delivery and r
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