: In this paper, we critically examine the key challenges associated with the development of inorganic drugs, a field that remains underrepresented despite its significant therapeutic potential. Currently, most clinically approved pharmaceuticals are organic compounds, a trend driven by multiple interconnected factors that have historically limited the adoption and regulatory approval of metal(loid)-based entities. These challenges include issues related to stability, selectivity, pharmacokinetics, and potential toxicity, which require systematic investigation and innovative solutions. Nevertheless, the profound clinical impact of approved inorganic drugs-particularly transition metal(loid)-based agents for both therapeutic and diagnostic applications-is well-established. The success of these compounds underscores the need for expanded research efforts and optimized clinical protocols to fully harness the advantages of metal-based pharmaceuticals. In this context, we explore emerging strategies to overcome current limitations and accelerate the development of next-generation inorganic drugs. These include the rational design of metal-based therapeutics, the integration of advanced metallomics and metalloproteomics, and the application of AI-driven predictive modeling to improve drug selectivity, bioavailability, and safety. By overcoming these challenges through an interdisciplinary approach, metal-based medicine will advance significantly, expanding its impact across a wide range of therapeutic applications.

The Metal(loid)s’ Dilemma. What's the next step for a new era of inorganic molecules in medicine? / Chiaverini, Lorenzo; Di Leo, Riccardo; Famlonga, Luca; Pacini, Matteo; Baglini, Emma; Barresi, Elisabetta; Peana, Massimiliano F; Tolbatov, Iogann; Marrone, Alessandro; La Mendola, Diego; Gailer, Jürgen; Marzo, Tiziano. - In: METALLOMICS. - ISSN 1756-591X. - (2025). [10.1093/mtomcs/mfaf013]

The Metal(loid)s’ Dilemma. What's the next step for a new era of inorganic molecules in medicine?

Peana, Massimiliano F;Tolbatov, Iogann
;
2025-01-01

Abstract

: In this paper, we critically examine the key challenges associated with the development of inorganic drugs, a field that remains underrepresented despite its significant therapeutic potential. Currently, most clinically approved pharmaceuticals are organic compounds, a trend driven by multiple interconnected factors that have historically limited the adoption and regulatory approval of metal(loid)-based entities. These challenges include issues related to stability, selectivity, pharmacokinetics, and potential toxicity, which require systematic investigation and innovative solutions. Nevertheless, the profound clinical impact of approved inorganic drugs-particularly transition metal(loid)-based agents for both therapeutic and diagnostic applications-is well-established. The success of these compounds underscores the need for expanded research efforts and optimized clinical protocols to fully harness the advantages of metal-based pharmaceuticals. In this context, we explore emerging strategies to overcome current limitations and accelerate the development of next-generation inorganic drugs. These include the rational design of metal-based therapeutics, the integration of advanced metallomics and metalloproteomics, and the application of AI-driven predictive modeling to improve drug selectivity, bioavailability, and safety. By overcoming these challenges through an interdisciplinary approach, metal-based medicine will advance significantly, expanding its impact across a wide range of therapeutic applications.
2025
The Metal(loid)s’ Dilemma. What's the next step for a new era of inorganic molecules in medicine? / Chiaverini, Lorenzo; Di Leo, Riccardo; Famlonga, Luca; Pacini, Matteo; Baglini, Emma; Barresi, Elisabetta; Peana, Massimiliano F; Tolbatov, Iogann; Marrone, Alessandro; La Mendola, Diego; Gailer, Jürgen; Marzo, Tiziano. - In: METALLOMICS. - ISSN 1756-591X. - (2025). [10.1093/mtomcs/mfaf013]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/362989
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