Peptide-conjugated nanoparticles for targeted photodynamic therapy

Author:

Dhaini Batoul12,Kenzhebayeva Bibigul34ORCID,Ben-Mihoub Amina3,Gries Mickaël5,Acherar Samir3,Baros Francis1,Thomas Noémie5,Daouk Joël5,Schohn Hervé5,Hamieh Tayssir26,Frochot Céline1ORCID

Affiliation:

1. Reactions and Chemical Engineering Laboratory , Université de Lorraine, LRGP-CNRS , F-54000 , Nancy , France

2. Laboratory of Materials , Catalysis , Environment and Analytical Methods Laboratory (MCEMA) , Faculty of Sciences , Lebanese University , Hadath , Lebanon

3. Laboratory of Macromolecular Physical Chemistry , Université de Lorraine, LCPM-CNRS , F-54000 , Nancy , France

4. The Department of Chemical and Biochemical Engineering , University of Satbayev , Almaty , Kasakhstan

5. Department of Biology, Signals and Systems in Cancer and Neuroscience , Université de Lorraine, CRAN-CNRS , F-54000 Nancy , France

6. Faculty of Science and Engineering , Maastricht University , , 6200 MD Maastricht , The Netherlands

Abstract

Abstract Cancer is the second leading cause of death worldwide after cardiovascular disease. Depending on the type and the location of the tumor, several cancer treatments are implemented. Among these, the three most conventional therapies are surgery, radiotherapy and chemotherapy. However, there are other therapeutic approaches such as photodynamic therapy (PDT). PDT relies on the combined action of light, a photoactivable molecule called photosensitizer (PS) and molecular oxygen. Most of the PSs used for clinical applications are not cancer-cell specific. One of the solutions to overcome this problem is the use of nanoparticles (NPs) to induce a passive targeting. It is also possible to graft a vector onto the NPs to specifically target membrane receptors overexpressed in the tumor cells or neovessels surrounding the tumor. In this review, we focus on the NPs loaded with PSs and coupled to peptides for targeted PDT. We described nanosystems that targeted Neuropilin-1 (NRP-1), αvβ3 integrins, nucleolin membrane receptor, epidermal growth factor (EGF) receptor, protein-glutamine-gamma-glutamyltransferase (TGM2), p32, transferrin, PD-1, and mitochondrial membrane. The use of a cell absorbing-peptide is also described.

Publisher

Walter de Gruyter GmbH

Subject

Electrical and Electronic Engineering,Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials,Biotechnology

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