Complete list of publications is available here.

As evidence of demonstrating these skills, the complete list of publications is available here. For lay summary, see My Work: Explained.
My research focuses on the chemical biology of nucleotides, exploring modifications to enhance their molecular targeting capacities and biological stability. This work is particularly relevant in advancing medical applications, as exemplified by approval of nucleic acid-based medicines such as vaccines, aptamer drugs, and nucleotide analogs.
We developed the first enzymatic method to program multiple radiometals into precise DNA positions: a step toward cancer imaging and therapy.
My first leading-author publication on positron emission tomography (PET) targeting thymidine metabolism in colorectal cancer.
Modification of nucleotide triphosphates leads to selection of DNAzymes that cleaves specific RNA sequences.
In response to the persistent public health challenge posed by cancer, our research team is developing peptide inhibitor radiopharmaceuticals by integrating diagnostic and therapeutic radioisotopes (i.e. theranostics). Building on the FDA approval of Prostate Membrane Specific Antigen (PSMA)-specific radiotracers, we aim to enhance the chemical libraries of PSMA and Fibroblast Activation Protein (FAP) inhibitors (FAPI) to optimize in vivo performance. This collaborative holds promising potential for translation to human clinical trials, such as prostate and colorectal cancer.
Careful choice of amino acid in PSMA analogs reduces salivary gland uptake in mouse model.
1 This study was conducted by an independent team; it is included for narrative completeness only.
Exploring novel tricyclic FAPI analogs (e.g. SB03178) with sustained radiotracer tumor uptake.
2 Antonio has no financial interest in this compound.
My work delves into the structural activity relationship of small molecule inhibitors, with a focus on α-amanitin, a potent neurotoxin isolated from the death cap mushroom Amanita phalloides. Leveraging the first total synthesis of amanitin, I aim to explore its close analogs to identify more potent toxins for targeted cancer therapy, tapping into the immense potential of natural products as potent drugs.
By studying the hydroxy-proline residue, novel antibody-drug conjugates (ADCs) with synthetic amanitin analogs were tested in vitro for the first time.
Novel amanitin analogs were found more potent than the naturally found α-amanitin through modification of the eastern-ring.
Complete list of publications is available here.