Nanogels co-loading paclitaxel and curcumin prepared in situ through photopolymerization at 532 nm for synergistically suppressing breast tumors.
Xiaoyan SongZujian FengYuanyuan PengSiyuan YuXinjing DuPingsheng HuangWeiwei WangJinfeng XingPublished in: Journal of materials chemistry. B (2023)
Combined chemotherapy plays an increasingly important and practical role in the clinical treatment of malignant tumor. In this study, paclitaxel (PTX) and curcumin (Cur) are simultaneously encapsulated into nanogels (termed as NG-PC) in situ by microemulsion photopolymerization at 532 nm for synergistically suppressing breast tumors. NG-PC with a size of 180 nm and a low polydispersity index (PDI < 0.2) presents a controlled and cumulative release of PTX and Cur within 90 h. Moreover, NG-PC displays a remarkable killing effect against 4T1 and MCF-7 cells. In vivo antitumor evaluation on 4T1 tumor-bearing mice demonstrates that NG-PC has significantly higher ability to inhibit tumor growth, inducing necrosis, apoptosis and suppression of proliferation than that of a single drug. Our research provides a facile method to prepare a nano-drug delivery platform with excellent drug co-loading ability and synergistic antitumor effect.
Keyphrases
- cell cycle arrest
- signaling pathway
- drug delivery
- photodynamic therapy
- induced apoptosis
- oxidative stress
- endoplasmic reticulum stress
- cell death
- cancer therapy
- high throughput
- quantum dots
- breast cancer cells
- locally advanced
- radiation therapy
- chemotherapy induced
- squamous cell carcinoma
- cell proliferation
- drug induced
- highly efficient
- smoking cessation
- single cell
- wild type