2019
DOI: 10.1039/c9sc00375d
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NIR-II light-modulated thermosensitive hydrogel for light-triggered cisplatin release and repeatable chemo-photothermal therapy

Abstract: An injectable, NIR-II light-modulated thermosensitive hydrogel is synthesized through supramolecular self-assembly for light-triggered cisplatin release and repeated chemo-photothermal therapy.

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Cited by 104 publications
(69 citation statements)
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“…18,19 Over the past several years, uorescence based imaging in the second near-infrared channel (NIR-II, 1000-1700 nm) has gained attention for its prominent merits and surpasses the conventional visible/NIR-I channels (700-900 nm) in terms of lower tissue scattering and minimal auto-uorescence, thus leading to signicant advances in imaging qualities including image depth and spatiotemporal resolution. [20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36][37][38] More recently, based on a benzobisthiadiazole (BBTD) acceptor, a series of small molecular dyes with a donor-acceptor-donor (D-A-D) architecture have been developed. The reduced energy gap between the hybridized highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels in these molecular systems shied the uorescence emission spectrum from the NIR-I region to the NIR-II channel.…”
Section: Introductionmentioning
confidence: 99%
“…18,19 Over the past several years, uorescence based imaging in the second near-infrared channel (NIR-II, 1000-1700 nm) has gained attention for its prominent merits and surpasses the conventional visible/NIR-I channels (700-900 nm) in terms of lower tissue scattering and minimal auto-uorescence, thus leading to signicant advances in imaging qualities including image depth and spatiotemporal resolution. [20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36][37][38] More recently, based on a benzobisthiadiazole (BBTD) acceptor, a series of small molecular dyes with a donor-acceptor-donor (D-A-D) architecture have been developed. The reduced energy gap between the hybridized highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels in these molecular systems shied the uorescence emission spectrum from the NIR-I region to the NIR-II channel.…”
Section: Introductionmentioning
confidence: 99%
“…TEM images (Figure 1B) revealed that the size distribution of RuO 2 @OVA NA is suitable for further biological applications. [ 21 ] These characteristics indicate that RuO 2 @OVA NAs have the potential to be used in tumor therapy. After these characterizations, the absorption spectrum of RuO 2 @OVA NAs was determined to study their absorption behavior (Figure 1C; Figure S2, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…As a traditional treatment, chemotherapy is the most popular cooperator with NIR‐II PTT. Their combinational therapy has been achieved using 2D Nb 2 C nanosheets, ternary Janus NPs comprising MnO 2 @Au@CuS, poly( N ‐phenylglycine)–poly(ethylene glycol) (PNPG–PEG) hydrogels, and PPy‐contained alginate (PA)–Fe 3+ hydrogels . In these studies, the mesoporous structure such as the silica shell of 2D Nb 2 C nanosheet, the MnO 2 domain of Janus NP and the hydrogels served as carriers to encapsulate anticancer drugs.…”
Section: Nir‐ii Pttmentioning
confidence: 99%