Programming Drug Delivery Kinetics for Active Burst Release with DNA Toehold Switches.
Mingshu XiaoWei LaiFei WangLi LiChun-Hai FanHao PeiPublished in: Journal of the American Chemical Society (2019)
Despite smart drug delivery systems (DDSs) with high delivery efficiency and improved efficacy for chemotherapy, precise drug release in targeted tumor cells in a controllable way is still challenging. In this work, we develop DNA toehold switch-engineered spherical nucleic acid-templated hydrogel (SNAgel) for on-site active burst release of chemotherapeutic (tumor-killing) drugs in target cancer cells. By designing ligand-specific toehold sequences on hybridization chain reaction (HCR)-generated SNAgel, we realize burst release of payloads with a wide range of t1/2 ranging from 60.52 to 5.49 min by active dynamic control of the kinetics. The camouflage of SNAgels with compact DNA shell enables elongated/prolonged blood circulation and targeted accumulation, cell entry, and apoptosis induction in vivo. The enhanced anticancer activity of SNAgels was substantiated in both cancer cell lines and xenografted tumor-bearing mice. This DNA-engineered kinetic control approach sheds new light on developing paradigm-shifting DDSs for cancer therapeutics.
Keyphrases
- nucleic acid
- drug delivery
- circulating tumor
- drug release
- single molecule
- cell free
- cancer therapy
- papillary thyroid
- high frequency
- oxidative stress
- endoplasmic reticulum stress
- squamous cell carcinoma
- lymph node metastasis
- circulating tumor cells
- cell therapy
- bone marrow
- mesenchymal stem cells
- childhood cancer
- adipose tissue
- drug induced
- rectal cancer