journal article·2025-06-20

Halloysite Nanotubes Functionalized with Naphthalene Diimide and Peptide Nucleic Acid Derivatives: Toward Multifunctional Nanomaterials

Francesca Cardano, Marina Massaro, Federica Leone, Giuseppe Cinà, Nicola Borbone, Andrea P. Falanga, Giorgia Oliviero, Angelo Nicosia, Martina Fresia, Andrea Fin, Vittorio Scardaci, Raquel de Melo Barbosa, Serena Riela

ACS Applied Nano Materials· Volume 8· Issue 24
Publisher page

Abstract

The development of multifunctional nanomaterials is an area of growing interest, particularly for systems that integrate optical and molecular recognition capabilities. Halloysite nanotubes (HNTs) provide a versatile platform for functionalization owing to their unique tubular structure and distinct inner and outer surface chemistry. In this study, we report the synthesis and characterization of HNTs-based nanomaterials functionalized with naphthalene diimide derivatives (NDIs) and peptide nucleic acid (PNA). NDIs were covalently anchored onto the external surface of HNTs to enhance their solubility and photophysical properties, while a model PNA sequence was incorporated to explore the suitability of NDI-functionalized HNTs as an efficient platform for the delivery of molecular probes. The synthesized nanomaterial was thoroughly characterized through morphological (HAADF/STEM), spectroscopic (UV–vis, fluorescence, FT-IR), and thermal (TGA) analyses. The results confirm the successful functionalization of HNTs, demonstrating the tunability of their optical properties and the effective integration of the PNA. This study provides insights into the engineering of hybrid nanomaterials with potential applications in molecular recognition, sensing, and advanced material design.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Clay minerals and soil interactions · Iron oxide chemistry and applications · Chemical Synthesis and Characterization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Dipartimento di Chimica, Università di Torino, Via Pietro Giuria 7, Torino 10125, Italy

Dipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), Università di Palermo, Viale delle Scienze, Parco d’Orleans II, Ed. 16-17 90128 Palermo, Italy

Dipartimento di Farmacia, Università degli Studi di Napoli Federico II, Via Domenico Montesano 49, 80131 Napoli, Italy

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Via Sergio Pansini 5, 80131 Napoli, Italy

Dipartimento di Scienze Chimiche (DSC), Università di Catania, Viale Andrea Doria 6, 95125 Catania, Italy

Department of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University of Seville, C/Professor García González 2, 41012 Sevilla, Spain

Funding

Junta de Andaluc?a · Ministero dell'Universit? e della Ricerca · NextGenerationEU

References (36)

Show source-provided references
1. 10.1021/acsnano.4c0437210.1021/acsnano.4c04372 ↗
2. 10.1002/aoc.466510.1002/aoc.4665 ↗
3. 10.1016/j.snb.2023.13417610.1016/j.snb.2023.134176 ↗
4. 10.1021/acsami.8b1753310.1021/acsami.8b17533 ↗
5. 10.3390/ijms2510537010.3390/ijms25105370 ↗
6. 10.1016/j.jcis.2024.02.13610.1016/j.jcis.2024.02.136 ↗
7. 10.1016/j.ccr.2021.21395610.1016/j.ccr.2021.213956 ↗
8. 10.3390/antibiotics1112176110.3390/antibiotics11121761 ↗
9. 10.1016/j.clay.2019.10537110.1016/j.clay.2019.105371 ↗
10. 10.1039/C4CC08265F10.1039/C4CC08265F ↗
11. 10.1021/jm901131m10.1021/jm901131m ↗
12. 10.1021/jo401347z10.1021/jo401347z ↗
13. 10.1039/c1ob05702b10.1039/c1ob05702b ↗
14. 10.1039/B615857A10.1039/B615857A ↗
15. 10.3390/nano1011223310.3390/nano10112233 ↗
16. 10.15171/apb.2018.06410.15171/apb.2018.064 ↗
17. 10.1021/acs.bioconjchem.8b0067410.1021/acs.bioconjchem.8b00674 ↗
18. 10.1021/bc100444v10.1021/bc100444v ↗
19. 10.1016/j.heliyon.2024.e2459910.1016/j.heliyon.2024.e24599 ↗
20. 10.1038/s41598-021-85549-z10.1038/s41598-021-85549-z ↗
21. 10.1002/smll.20220473210.1002/smll.202204732 ↗
22. 10.1039/C3MD00257H10.1039/C3MD00257H ↗
23. 10.1155/2014/61071810.1155/2014/610718 ↗
24. 10.1021/acs.orglett.5b0054310.1021/acs.orglett.5b00543 ↗
25. 10.1021/jo702392q10.1021/jo702392q ↗
26. 10.1016/j.clay.2019.10540010.1016/j.clay.2019.105400 ↗
27. 10.1039/C4RA02717E10.1039/C4RA02717E ↗
28. 10.1002/chem.20210002010.1002/chem.202100020 ↗
29. 10.1016/j.dyepig.2014.08.02010.1016/j.dyepig.2014.08.020 ↗
30. 10.1016/j.clay.2021.10631010.1016/j.clay.2021.106310 ↗
31. 10.1021/acsomega.7b0181310.1021/acsomega.7b01813 ↗
32. 10.1039/D2PY01593E10.1039/D2PY01593E ↗
33. 10.3390/pharmaceutics1611142810.3390/pharmaceutics16111428 ↗
34. 10.1039/C6OB00987E10.1039/C6OB00987E ↗
35. 10.1039/D3TB00637A10.1039/D3TB00637A ↗
36. 10.1021/acsbiomaterials.1c0043110.1021/acsbiomaterials.1c00431 ↗