Simultaneous Application of Photothermal Therapy and an Anti-inflammatory Prodrug using Pyrene-Aspirin-Loaded Gold Nanorod Graphitic Nanocapsules.
Qian DongXuewei WangXiaoxiao HuLangqiu XiaoLiang ZhangLijuan SongMinglu XuYuxiu ZouLong ChenZhuo ChenWeihong TanPublished in: Angewandte Chemie (International ed. in English) (2017)
Photothermal therapy (PTT) has been extensively developed as an effective approach against cancer. However, PTT can trigger inflammatory responses, in turn simulating tumor regeneration and hindering subsequent therapy. A therapeutic strategy was developed to deliver enhanced PTT and simultaneously inhibit PTT-induced inflammatory response. 1-Pyrene methanol was utilize to synthesize the anti-inflammatory prodrug pyrene-aspirin (P-aspirin) with a cleavable ester bond and also facilitate loading the prodrug on gold nanorod (AuNR)-encapsulated graphitic nanocapsule (AuNR@G), a photothermal agent, through π-π interactions. Such AuNR@G-P-aspirin complexes were used for near-infrared laser-triggered photothermal ablation of solid tumor and simultaneous inhibition of PTT-induced inflammation through the release of aspirin in tumor milieu. This strategy showed excellent effects in vitro and in vivo.
Keyphrases
- low dose
- cancer therapy
- cardiovascular events
- antiplatelet therapy
- anti inflammatory
- drug release
- drug delivery
- inflammatory response
- high glucose
- diabetic rats
- stem cells
- photodynamic therapy
- anti inflammatory drugs
- acute coronary syndrome
- oxidative stress
- multidrug resistant
- percutaneous coronary intervention
- squamous cell carcinoma
- lipopolysaccharide induced
- squamous cell
- type diabetes
- wound healing
- young adults
- silver nanoparticles
- atrial fibrillation