Amino Acid-Based Boron Carriers in Boron Neutron Capture Therapy (BNCT).

BNCT LAT1 amino acids boron carriers boron neutron capture therapy glioma tumor targeting

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
23 Nov 2023
Historique:
received: 22 10 2023
revised: 18 11 2023
accepted: 21 11 2023
medline: 23 12 2023
pubmed: 23 12 2023
entrez: 23 12 2023
Statut: epublish

Résumé

Interest in the design of boronated amino acids has emerged, partly due to the utilization of boronophenylalanine (BPA), one of the two agents employed in clinical Boron Neutron Capture Therapy (BNCT). The boronated amino acids synthesized thus far for BNCT investigations can be classified into two categories based on the source of boron: boronic acids or carboranes. Amino acid-based boron carriers, employed in the context of BNCT treatment, demonstrate significant potential in the treatment of challenging tumors, such as those located in the brain. This review aims to shed light on the developmental journey and challenges encountered over the years in the field of amino acid-based boron delivery compound development. The primary focus centers on the utilization of the large amino acid transporter 1 (LAT1) as a target for boron carriers in BNCT. The development of efficient carriers remains a critical objective, addressing challenges related to tumor specificity, effective boron delivery, and rapid clearance from normal tissue and blood. LAT1 presents an intriguing and promising target for boron delivery, given its numerous characteristics that make it well suited for drug delivery into tumor tissues, particularly in the case of brain tumors.

Identifiants

pubmed: 38140004
pii: pharmaceutics15122663
doi: 10.3390/pharmaceutics15122663
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Finnish Cultural Foundation
ID : 00211097
Organisme : Olvi Säätiö
ID : 201920713
Organisme : Orion Research Foundation
ID : N.A
Organisme : The Finnish Pharmaceutical Society
ID : N.A.
Organisme : Emil Aaltonen Foundation
ID : N.A.

Auteurs

Juulia Järvinen (J)

School of Pharmacy, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.

Herkko Pulkkinen (H)

Department of Technical Physics, Faculty of Science, Forestry and Technology, University of Eastern Finland, 70211 Kuopio, Finland.

Jarkko Rautio (J)

School of Pharmacy, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.

Juri M Timonen (JM)

School of Pharmacy, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.
Drug Research Program, Division of Pharmaceutical Chemistry and Technology, Faculty of Pharmacy, University of Helsinki, Viikinkaari 5E, P.O. Box 56, 00014 Helsinki, Finland.

Classifications MeSH