The Neuropeptide Y Receptor Ligand-Modified Cell Membrane Promotes Targeted Photodynamic Therapy of Zeolitic Imidazolate Frameworks for Breast Cancer.

J Phys Chem Lett

Cixi Institute of Biomedical Engineering, International Cooperation Base of Biomedical Materials Technology and Application, CAS Key Laboratory of Magnetic Materials and Devices, Zhejiang Engineering Research Center for Biomedical Materials, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, China.

Published: November 2021

Zeolitic imidazolate frameworks (ZIFs), widely regarded as promising materials for application in catalysis and separation, hold an increasingly significant position in drug delivery systems for their high drug loading capacity. Focused specifically on the rational design of targeting and bioresponsive nanovehicles, a neuropeptide Y receptor ligand (YL)-modified cell membrane camouflaged bioresponsive ZIF system (YL-RBC@ZIF-90@Ce6) was constructed for targeted photodynamic therapy of breast cancer. The biomimetic ZIF-based nanocarrier enhanced tumor accumulation by both neuropeptide Y receptor-targeted guidance and long-term stability. YL served as a good ligand-mediated selective targeting molecule for breast cancer, and red blood cell membrane-camouflaged nanocomposites displayed favorable biocompatibility. With the dual response of the ZIF to pH and adenosine triphosphate, the stimulus responsive photosensitizer Chlorin e6 delivery system effectively suppressed tumors . This work offers a platform for developing much safer and more efficient photodynamic therapy for the treatment of YR-overexpressed breast cancer.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.jpclett.1c03562DOI Listing

Publication Analysis

Top Keywords

breast cancer
16
photodynamic therapy
12
neuropeptide receptor
8
cell membrane
8
targeted photodynamic
8
zeolitic imidazolate
8
imidazolate frameworks
8
receptor ligand-modified
4
ligand-modified cell
4
membrane promotes
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!