Early Stage In Vitro Bioprofiling of Potential Low-Molecular-Weight Organoboron Compounds for Boron Neutron Capture Therapy (BNCT)-Proposal for a Guide
- PMID: 38786022
- PMCID: PMC11119693
- DOI: 10.3390/cells13100798
Early Stage In Vitro Bioprofiling of Potential Low-Molecular-Weight Organoboron Compounds for Boron Neutron Capture Therapy (BNCT)-Proposal for a Guide
Abstract
Given the renewed interest in boron neutron capture therapy (BNCT) and the intensified search for improved boron carriers, as well as the difficulties of coherently comparing the carriers described so far, it seems necessary to define a basic set of assays and standardized methods to be used in the early stages of boron carrier development in vitro. The selection of assays and corresponding methods is based on the practical experience of the authors and is certainly not exhaustive, but open to discussion. The proposed tests/characteristics: Solubility, lipophilicity, stability, cytotoxicity, and cellular uptake apply to both low molecular weight (up to 500 Da) and high molecular weight (5000 Da and more) boron carriers. However, the specific methods have been selected primarily for low molecular weight boron carriers; in the case of high molecular weight compounds, some of the methods may need to be adapted.
Keywords: BNCT; bioprofiling; boron carriers; drug development; in vitro methods; pre-clinical testing.
Conflict of interest statement
The authors declare no conflicts of interest.
Figures
Similar articles
-
The basis and advances in clinical application of boron neutron capture therapy.Radiat Oncol. 2021 Nov 7;16(1):216. doi: 10.1186/s13014-021-01939-7. Radiat Oncol. 2021. PMID: 34743756 Free PMC article. Review.
-
Proposal of recommended experimental protocols for in vitro and in vivo evaluation methods of boron agents for neutron capture therapy.J Radiat Res. 2023 Nov 21;64(6):859-869. doi: 10.1093/jrr/rrad064. J Radiat Res. 2023. PMID: 37717596 Free PMC article.
-
In silico assessments of the small molecular boron agents to pave the way for artificial intelligence-based boron neutron capture therapy.Eur J Med Chem. 2024 Dec 5;279:116841. doi: 10.1016/j.ejmech.2024.116841. Epub 2024 Sep 6. Eur J Med Chem. 2024. PMID: 39244862 Review.
-
Hyaluronan as carrier of carboranes for tumor targeting in boron neutron capture therapy.Biomacromolecules. 2007 Feb;8(2):552-9. doi: 10.1021/bm0607426. Biomacromolecules. 2007. PMID: 17291079
-
Biocompatibility of functionalized boron phosphate (BPO4) nanoparticles for boron neutron capture therapy (BNCT) application.Nanomedicine. 2014 Apr;10(3):589-97. doi: 10.1016/j.nano.2013.10.003. Epub 2013 Oct 23. Nanomedicine. 2014. PMID: 24161383
Cited by
-
Towards New Delivery Agents for Boron Neutron Capture Therapy: Synthesis and In Vitro Evaluation of a Set of Fluorinated Carbohydrate Derivatives.Molecules. 2024 Sep 9;29(17):4263. doi: 10.3390/molecules29174263. Molecules. 2024. PMID: 39275111 Free PMC article.
-
A Novel Closo-Ortho-Carborane-Based Glucosamine Derivative as a Promising Agent for Boron Neutron Capture Therapy.Pharmaceuticals (Basel). 2025 Jun 30;18(7):986. doi: 10.3390/ph18070986. Pharmaceuticals (Basel). 2025. PMID: 40732275 Free PMC article.
References
-
- Sauerwein W. Principles and roots of neutron capture therapy. In: Sauerwein W., Wittig A., Moss R., Nakagawa Y., editors. Neutron Capture Therapy. Principles and Applications. Springer; Berlin/Heidelberg, Germany: New York, NY, USA: Dordrecht, The Netherlands: London, UK: 2012. pp. 1–16. - DOI
-
- IAEA: Advances in Boron Neutron Capture Therapy. International Atomic Energy Agency; Vienna, Austria: 2023.
-
- Kumada H., Sakae T., Sakurai H. Current development status of accelerator-based neutron source for boron neutron capture therapy. EPJ Tech. Instrum. 2023;10:18. doi: 10.1140/epjti/s40485-023-00105-5. - DOI
-
- Howell N., Middleton R.J., Sierro F., Wyatt N.A., Chacon A., HFraser B.H., Bambery K., Livio E., Dobie C., Bevitt J.J., et al. Neutron capture enhances dose and reduces cancer cell viability in and out of beam during helium and carbon ion therapy. Int. J. Radiat. Oncol. Biol. Phys. 2024 doi: 10.1016/j.ijrobp.2024.02.052. accepted . - DOI - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources