Photoswitchable Carbamazepine Analogs for Non‐Invasive Neuroinhibition In Vivo

Author:

Camerin Luisa123ORCID,Maleeva Galyna12,Gomila Alexandre M. J.12,Suárez‐Pereira Irene456,Matera Carlo127,Prischich Davia128,Opar Ekin12,Riefolo Fabio129,Berrocoso Esther456,Gorostiza Pau1210ORCID

Affiliation:

1. Institute for Bioengineering of Catalonia (IBEC) The Barcelona Institute for Science and Technology Barcelona 08028 Spain

2. Networking Biomedical Center in Bioengineering, Biomaterials, and Nanomedicine (CIBER-BBN) ISCIII Madrid 28029 Spain

3. Doctorate program in organic chemistry University of Barcelona Barcelona 08028 Spain

4. Neuropsychopharmacology & Psychobiology Research Group, Department of Neuroscience University of Cádiz Cádiz 11003 Spain

5. Networking Biomedical Center in Mental Health (CIBER-SAM) ISCIII Madrid 28029 Spain

6. Institute for Research and Innovation in Biomedical Sciences of Cádiz, INiBICA University Hospital Puerta del Mar Cádiz 11009 Spain

7. Department of Pharmaceutical Sciences University of Milan Milan 20133 Italy

8. Current address: Department of Chemistry, Molecular Sciences Research Hub, Imperial College London London SW120BZ United Kingdom

9. Current address: Teamit Institute, Partnerships Barcelona Health Hub Barcelona 08025 Spain

10. Catalan Institution of Research and Advanced Studies (ICREA) Barcelona 08010 Spain

Abstract

AbstractA problem of systemic pharmacotherapy is off‐target activity, which causes adverse effects. Outstanding examples include neuroinhibitory medications like antiseizure drugs, which are used against epilepsy and neuropathic pain but cause systemic side effects. There is a need of drugs that inhibit nerve signals locally and on‐demand without affecting other regions of the body. Photopharmacology aims to address this problem with light‐activated drugs and localized illumination in the target organ. Here, we have developed photoswitchable derivatives of the widely prescribed antiseizure drug carbamazepine. For that purpose, we expanded our method of ortho azologization of tricyclic drugs to meta/para and to N‐bridged diazocine. Our results validate the concept of ortho cryptoazologs (uniquely exemplified by Carbazopine‐1) and bring to light Carbadiazocine (8), which can be photoswitched between 400–590 nm light (using violet LEDs and halogen lamps) and shows good drug‐likeness and predicted safety. Both compounds display photoswitchable activity in vitro and in translucent zebrafish larvae. Carbadiazocine (8) also offers in vivo analgesic efficacy (mechanical and thermal stimuli) in a rat model of neuropathic pain and a simple and compelling treatment demonstration with non‐invasive illumination.

Funder

H2020 LEIT Information and Communication Technologies

Agencia Estatal de Investigación

Publisher

Wiley

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