2020
DOI: 10.1002/adma.202004460
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Injectable and NIR‐Responsive DNA–Inorganic Hybrid Hydrogels with Outstanding Photothermal Therapy

Abstract: Surgical excision is one of the main treatments for malignant tumors. However, high risk of tumour recurrence is a major challenge. Near‐infrared (NIR)‐light‐induced tumor photothermal therapy has been studied, while its clinical applications are still restricted due to the limited therapeutic effects. To address this, here, a novel NIR‐light‐responsive and injectable DNA‐mediated upconversion and Au nanoparticle hybrid (DNA–UCNP‐Au) hydrogel is developed. Due to the confined and concentrated environment induc… Show more

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Cited by 131 publications
(113 citation statements)
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“…Photothermal agents can convert light energy to heat under near infrared (NIR) irradiation [ 28 , 29 ]. The target temperature of photothermal hydrogels can be adjusted by changing the concentration and proportion of photothermal agents, irradiation time, and laser intensity [ 30 ]. Mild local heat (41 °C–43 °C) can promote cell proliferation, angiogenesis, wound healing, and bone regeneration [ 31 ].…”
Section: Introductionmentioning
confidence: 99%
“…Photothermal agents can convert light energy to heat under near infrared (NIR) irradiation [ 28 , 29 ]. The target temperature of photothermal hydrogels can be adjusted by changing the concentration and proportion of photothermal agents, irradiation time, and laser intensity [ 30 ]. Mild local heat (41 °C–43 °C) can promote cell proliferation, angiogenesis, wound healing, and bone regeneration [ 31 ].…”
Section: Introductionmentioning
confidence: 99%
“…An 808 nm laser was used for this system due to the low absorption of water and a strong tissue penetration and low side effects in vivo. [27,30] To study this photothermal effect, the E 72 -Chitosan-Ag 3 AuS 2 hydrogel with different concentrations of inorganic NPs was investigated. The higher concentration of Ag 3 AuS 2 NPs in the system resulted in faster heating and higher temperature in a very short time (Figure 3A and Figure S10, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…In recent years, in order to maximize the efficiency of drug delivery, local therapy has received widespread attention. [ 12–14 ] Compared with oral administration and intravenous injection, local minimally invasive administration can directly deliver agents into the tumor site through a controlled manner, which can greatly reduce the drug dose, thus sparing the off‐target toxicity. [ 14 ] However, the clinical translation of local therapy is still impeded by many well‐known challenges: i) short retention time of therapeutic agents, [ 7 ] ii) poor uptake of anticancer therapies by drug‐resistant tumor cells, and iii) difficulty in realizing responsive multi‐modal therapy.…”
Section: Introductionmentioning
confidence: 99%