Leana Travaglini
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Leana Travaglini has a total of 65 co-authors. Here are the top co-authors by number of shared publications:
- Luciano Galantini
Department of Chemistry, Sapienza University of Rome, P.le A. Moro 5, Rome 00185, Italy
14 shared publications - Nicolae Viorel Pavel
Department of Chemistry, Sapienza University of Rome , P. le A. Moro 5, 00185 Rome, Italy
13 shared publications Marta Gubitosi
Department of Chemistry, Sapienza University of Rome, P. le A. Moro 5, 00185 Rome, Italy
9 shared publicationsMaria Chiara di Gregorio
Department of Organic Chemistry , Weizmann Institute of Science , 7610001 Rehovot , Israel
8 shared publications- Karin Schillén
Division of Physical Chemistry, Department of Chemistry, Lund University, P.O. Box 124, SE-22100 Lund, Sweden
7 shared publications - Luisa De Cola
Dipartimento di Scienze Farmaceutiche Università degli Studi di Milano Milano Italy
6 shared publications
Latest Publications
- 12 January 2024
- Published by Wiley in ChemSystemsChem
- Vol. 6 (1)
Time to Celebrate: 5 Years of ChemSystemsChem
- 12 January 2024
- Published by Wiley in ChemSystemsChem
- Vol. 6 (1)
Time to Celebrate: 5 Years of ChemSystemsChem
- Open Access
- 22 December 2021
- Published by Wiley in ChemSystemsChem
- Vol. 4 (1) , e202100046
A New Systems Year
- 22 December 2021
- Published by Wiley in ChemSystemsChem
- Vol. 4 (1) , e202100046
Open AccessA New Systems Year
- 2 December 2019
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 32 (1) , 392-399
Breaking with Light: Stimuli-Responsive Mesoporous Organosilica Particles
- 2 December 2019
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 32 (1) , 392-399
Breaking with Light: Stimuli-Responsive Mesoporous Organosilica Particles
- 1 October 2019
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 554, 453-462
Deoxycholic acid and l-Phenylalanine enrich their hydrogel properties when combined in a zwitterionic derivative
- 1 October 2019
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 554, 453-462
Deoxycholic acid and l-Phenylalanine enrich their hydrogel properties when combined in a zwitterionic derivative
- 1 May 2019
- Published by Elsevier in Microporous and Mesoporous Materials
- Vol. 279, 423-431
Tuning and controlling the shape of mesoporous silica particles with CTAB/sodium deoxycholate catanionic mixtures
- 1 May 2019
- Published by Elsevier in Microporous and Mesoporous Materials
- Vol. 279, 423-431
Tuning and controlling the shape of mesoporous silica particles with CTAB/sodium deoxycholate catanionic mixtures
- 31 October 2018
- Published by Royal Society of Chemistry (RSC) in Materials Chemistry Frontiers
- Vol. 3 (1) , 111-119
Highly degradable imine-doped mesoporous silica particles
The degradation of mesoporous silica particles (MSPs) in water is a key aspect that boosts their use especially in bio-related fields. Although MSP degradation in aqueous media has been proven, big efforts have been devoted to tuning silica dissolution in order to obtain functional materials whose degradation can be finely controlled and enhanced, to tackle the issue of bioaccumulation. In particular, the introduction of stimuli-responsive functional groups into the silica framework was proven to be a successful strategy. Yet, the fast dissolution of silica particles in aqueous media in the absence of external stimuli has to be fully addressed. In this context, we reported herein the preparation and thorough characterisation of MSPs containing imine groups embedded within the silica framework (Im-MSPs). Particles with different contents of imine groups have been investigated in order to assess the effect on the physicochemical properties and the Im-MSPs showed fast degradation in both acidic and neutral aqueous solutions, at a rate that depended on the pH value. Of special interest is their fast degradation at acidic pH, where instead MSPs are normally more stable. The described results unveil the potential of these particles in applications that require a fast degradation in aqueous media.
- 31 October 2018
- Published by Royal Society of Chemistry (RSC) in Materials Chemistry Frontiers
- Vol. 3 (1) , 111-119
Highly degradable imine-doped mesoporous silica particles
The degradation of mesoporous silica particles (MSPs) in water is a key aspect that boosts their use especially in bio-related fields. Although MSP degradation in aqueous media has been proven, big efforts have been devoted to tuning silica dissolution in order to obtain functional materials whose degradation can be finely controlled and enhanced, to tackle the issue of bioaccumulation. In particular, the introduction of stimuli-responsive functional groups into the silica framework was proven to be a successful strategy. Yet, the fast dissolution of silica particles in aqueous media in the absence of external stimuli has to be fully addressed. In this context, we reported herein the preparation and thorough characterisation of MSPs containing imine groups embedded within the silica framework (Im-MSPs). Particles with different contents of imine groups have been investigated in order to assess the effect on the physicochemical properties and the Im-MSPs showed fast degradation in both acidic and neutral aqueous solutions, at a rate that depended on the pH value. Of special interest is their fast degradation at acidic pH, where instead MSPs are normally more stable. The described results unveil the potential of these particles in applications that require a fast degradation in aqueous media.
- 20 September 2018
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 35 (21) , 6803-6821
Bile Salts: Natural Surfactants and Precursors of a Broad Family of Complex Amphiphiles
Bile salts (BSs) are naturally occurring rigid surfactants with a steroidal skeleton and specific self-assembly and interface behaviors. Using bile salts as precursors, derivatives can be synthesized to obtain molecules with specific functionalities and amphiphilic structure. Modifications on single molecules are normally performed by substituting the least-hindered hydroxyl group on carbon C-3 of the steroidal A ring or at the end of the lateral chain. This leads to monosteroidal rigid building blocks that are often able to self-organize into 1D structures such as tubules, twisted ribbons, and fibrils with helical supramolecular packing. Tubular aggregates are of particular interest, and they are characterized by cross-section inner diameters spanning a wide range of values (3–500 nm). They can form through appealing pH- or temperature-responsive aggregation and in mixtures of bile salt derivatives to provide mixed tubules with tunable charge and size. Other derivatives can be prepared by covalently linking two or more bile salt molecules to provide complex systems such as oligomers, dendrimers, and polymeric materials. The unconventional amphiphilic molecular structure imparts specific features to BSs and derivatives that can be exploited in the formulation of capsules, drug carriers, dispersants, and templates for the synthesis of nanomaterials.
- 20 September 2018
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 35 (21) , 6803-6821
Bile Salts: Natural Surfactants and Precursors of a Broad Family of Complex Amphiphiles
Bile salts (BSs) are naturally occurring rigid surfactants with a steroidal skeleton and specific self-assembly and interface behaviors. Using bile salts as precursors, derivatives can be synthesized to obtain molecules with specific functionalities and amphiphilic structure. Modifications on single molecules are normally performed by substituting the least-hindered hydroxyl group on carbon C-3 of the steroidal A ring or at the end of the lateral chain. This leads to monosteroidal rigid building blocks that are often able to self-organize into 1D structures such as tubules, twisted ribbons, and fibrils with helical supramolecular packing. Tubular aggregates are of particular interest, and they are characterized by cross-section inner diameters spanning a wide range of values (3–500 nm). They can form through appealing pH- or temperature-responsive aggregation and in mixtures of bile salt derivatives to provide mixed tubules with tunable charge and size. Other derivatives can be prepared by covalently linking two or more bile salt molecules to provide complex systems such as oligomers, dendrimers, and polymeric materials. The unconventional amphiphilic molecular structure imparts specific features to BSs and derivatives that can be exploited in the formulation of capsules, drug carriers, dispersants, and templates for the synthesis of nanomaterials.
- 26 June 2018
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 20 (28) , 18957-18968
Bile acid derivative-based catanionic mixtures: versatile tools for superficial charge modulation of supramolecular lamellae and nanotubes
Self-assembly in mixtures of cationic and anionic derivatives of a bile acid provides supramolecular lamellae and nanotubes with different charge.
- 26 June 2018
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 20 (28) , 18957-18968
Bile acid derivative-based catanionic mixtures: versatile tools for superficial charge modulation of supramolecular lamellae and nanotubes
Self-assembly in mixtures of cationic and anionic derivatives of a bile acid provides supramolecular lamellae and nanotubes with different charge.
- 30 May 2018
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 30 (12) , 4168-4175
Morphology Control of Mesoporous Silica Particles Using Bile Acids as Cosurfactants
- 30 May 2018
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 30 (12) , 4168-4175
Morphology Control of Mesoporous Silica Particles Using Bile Acids as Cosurfactants