Platinum complexes are among the most commonly used drugs against cancer.

They are successful, but have severe side effects.

An international research team led by Dr Johannes Karges from the Faculty of Chemistry and Biochemistry at Ruhr University Bochum, Germany, has developed a complex that accumulates in tumour tissue and is activated there by ultrasound waves.

Its cell-damaging effect thus only unfolds where it is actually wanted.

“Where previous studies relied on light activations that can only penetrate a few millimetres deep into the tissue, we have now developed a treatment method with ultrasound activation that penetrates several centimetres deep into the body,” says Karges.

This could make treatment with few side effects possible even for large and deep-seated tumours.

The researchers published their results in the journal Angewandte Chemie International Edition of 24 March 2023.

The platinum(II) complexes cisplatin, oxaliplatin and carboplatin are among the most commonly used cancer drugs.

Their clinical success is offset by severe side effects, such as nausea, vomiting, kidney damage and bone marrow suppression.

To overcome these limitations, major research efforts have been invested in the development of so-called platinum (IV) complex prodrugs over the past decades.

“These prodrugs are stable and inactive, so they are completely harmless,” explains Johannes Karges.

“In healthy tissue, they are supposed to stay that way. In cancer tissue, however, they should be rapidly converted into the therapeutically active platinum (II) complexes.”

Energy is required for the reduction of the metal complex.

Previous studies reported activation with ultraviolet, blue or red light.

“The problem is that light can only penetrate less than a centimetre deep into the body and thus does not reach many tumours,” explains Johannes Karges.

To overcome this limitation, his team has for the first time combined platinum (IV) complex prodrugs with sonosensitizers that can be selectively activated with ultrasound irradiation.

To develop a therapeutically effective complex, the researchers encapsulated the platinum (IV) complex prodrugs and the sonosensitizers together in haemoglobin to form nanoparticles.

“We were able to observe that the nanoparticles selectively accumulated in a mouse intestinal tumour after injection into the bloodstream, thus supporting targeted treatment,” reports Johannes Karges.

“After irradiation with ultrasound, the platinum (IV) prodrug was activated at the tumour site, triggering the release of cisplatin, which is toxic to cells, and almost completely eradicating the tumour.”

These results could pave the way for the development of novel techniques and agents for the treatment of very large or deep-seated tumours.

Ultrasound can penetrate more than an order of magnitude deeper into tissue than near-infrared light.

In addition, ultrasound treatments are generally considered to be less invasive and easy to use.

Another advantage is that hospitals are usually already equipped with the necessary equipment.

“Our work is still fundamental research,” Johannes Karges emphasises.

“Whether and when treatments based on this can be offered in clinical practice is not yet foreseeable.”

Article: Reduction of platinum (IV) prodrug haemoglobin nanoparticles with deeply-penetrating ultrasound radiation for tumour-targeted therapeutically enhanced anticancer therapy

Source: Ruhr-University Bochum