Braccia, Simone (2025) Design of smart peptide-based nanoplatforms for precision medicine. [Tesi di dottorato]

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Tipologia del documento: Tesi di dottorato
Lingua: English
Titolo: Design of smart peptide-based nanoplatforms for precision medicine
Autori:
Autore
Email
Braccia, Simone
simone.braccia@unina.it
Data: 9 Dicembre 2025
Numero di pagine: 219
Istituzione: Università degli Studi di Napoli Federico II
Dipartimento: Farmacia
Dottorato: Scienza del farmaco
Ciclo di dottorato: 38
Coordinatore del Corso di dottorato:
nome
email
Meli, Rosaria
rosaria.meli@unina.it
Tutor:
nome
email
Galdiero, Stefania
[non definito]
D'Auria, Gabriella
[non definito]
Data: 9 Dicembre 2025
Numero di pagine: 219
Parole chiave: Peptide, drug delivery systems, cell penetrating peptide
Settori scientifico-disciplinari del MIUR: Area 03 - Scienze chimiche > CHIM/03 - Chimica generale e inorganica
Informazioni aggiuntive: 38 ciclo
Depositato il: 22 Dic 2025 10:19
Ultima modifica: 12 Ago 2026 05:37
URI: https://www.fedoa.unina.it/id/eprint/16089

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Abstract

The World Health Organization recognizes cancer as one of the leading causes of mortality worldwide. Conventional therapies, although characterized by high therapeutic efficacy, are often associated with severe side effects that significantly impair patients’ quality of life. Therefore, current research is increasingly focused on the development of precision medicine approaches based on targeted drug delivery systems, capable of improving selectivity and therapeutic outcomes while minimizing systemic toxicity. In this context, the present research focused on the design and optimization of innovative drug delivery systems aimed at overcoming the major limitations of conventional treatments. An anticancer delivery platform entirely composed of EPA, an omega-3 fatty acid, was developed and optimized to achieve controlled and site-specific drug release. This system was functionalized with peptide sequences designed to recognize overexpressed receptors on tumor cells and enable the selective release of Doxorubicin and Pemetrexed, in addition we added a cell penetrating peptide, namely gH625, to enhance intracellular uptake. In parallel, a cationic liposomal formulation was optimized for gene therapy applications, while a self-assembling amphiphilic peptide nanofiber nanosystem was engineered for the treatment of glioblastoma and for efficient gene delivery in TNBC treatment. The same nanofiber nanoplatform was further adapted for the treatment of fungal infections in the agri-food sector, with potential implications for preventing opportunistic infections in immuno-compromised patients. The integration of distinct components and functional peptide sequences enabled the development of smart, controlled-release nanoplatforms, representing a concrete step toward the realization of personalized precision medicine, tailored to the individual patient and guided by the synergy between multidisciplinary research and clinical needs.

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