A novel drug delivery nanosystem was here designed, linking thiahelicenes to halloysite nanotubes. Tetrathia[7]helicenes are very promising DNA intercalators, whose usage in biomedical field has been so far limited by their poor bioavailability. The study of appropriate drug delivery systems is needed to exploit helicenes as therapeutics. In this work, imine chemistry was adopted to covalently attach the bioactive compound and release it in acidic environments such as those surrounding tumour cells. To this aim, halloysite nanotubes were functionalized with (3-aminopropyl)triethoxysilane. The latter acted as linker providing NH2 groups to react with the formyl moiety of the thiahelicene derivative. The nanoconstruct preparation was studied in depth by surface-sensitive spectroscopies and angle-resolved X-ray absorption, to investigate the attachment mode, surface coverage and molecular orientation of the thiahelicene units. Release tests were carried out also in vitro on two tumour cell lines with different extracellular pH values. Mildly acidic pH conditions catalyzed the hydrolysis of the imine bond and promoted the cytotoxic compound release, which proved selective to slight pH differences, confirming the potential of this novel nanoconstruct.

Thiahelicene-grafted halloysite nanotubes: Characterization, biological studies and pH triggered release / T. Taroni, S. Cauteruccio, R. Vago, S. Franchi, N. Barbero, E. Licandro, S. Ardizzone, D. Meroni. - In: APPLIED SURFACE SCIENCE. - ISSN 0169-4332. - 520(2020 Aug 01).

Thiahelicene-grafted halloysite nanotubes: Characterization, biological studies and pH triggered release

T. Taroni
Primo
;
S. Cauteruccio
Secondo
;
E. Licandro;S. Ardizzone
Penultimo
;
D. Meroni
Ultimo
2020-08-01

Abstract

A novel drug delivery nanosystem was here designed, linking thiahelicenes to halloysite nanotubes. Tetrathia[7]helicenes are very promising DNA intercalators, whose usage in biomedical field has been so far limited by their poor bioavailability. The study of appropriate drug delivery systems is needed to exploit helicenes as therapeutics. In this work, imine chemistry was adopted to covalently attach the bioactive compound and release it in acidic environments such as those surrounding tumour cells. To this aim, halloysite nanotubes were functionalized with (3-aminopropyl)triethoxysilane. The latter acted as linker providing NH2 groups to react with the formyl moiety of the thiahelicene derivative. The nanoconstruct preparation was studied in depth by surface-sensitive spectroscopies and angle-resolved X-ray absorption, to investigate the attachment mode, surface coverage and molecular orientation of the thiahelicene units. Release tests were carried out also in vitro on two tumour cell lines with different extracellular pH values. Mildly acidic pH conditions catalyzed the hydrolysis of the imine bond and promoted the cytotoxic compound release, which proved selective to slight pH differences, confirming the potential of this novel nanoconstruct.
Halloysite nanotubes; Helicene; Nanocarrier; NEXAFS; Triggered release;
Settore CHIM/02 - Chimica Fisica
18-apr-2020
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/731116
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