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In the last years, the development of nano-formulations for cancer treatment represents one of the major challenges of the scientific research. The prodrug strategy, that combines chemotherapeutic agents with nanocarriers such as halloysite nanotubes (HNTs), is a promising strategy both to improve the biological activity of the drug molecules and to reduce the side effects of drugs. Herein we report the synthesis and characterization of a HNTs prodrug based on 1,2,3-triazole units covalently linked to HNTs external surface, bearing different positively charged moieties, which could present interesting pharmacological activities.

LAPONITE® (Lap) clay mineral was successful functionalized by triazole groups in a two steps procedure. First, the Lap edges were modified with 3-azidopropyltrimethoxysilane by traditional heating and microwave irradiation. Microwave irradiation allowed us to obtain high loading onto the Lap edges in lower times compared to those obtained through conventional method. Afterwards, the triazole moieties were obtained by reaction between azido functionalized Lap and propargyl alcohol. The successful functionalization of Lap was proved by thermogravimetric analysis, FT-IR spectroscopy, dynamic light scattering and ζ-potential measurements. Finally, the effects of the surface modification on the gel formation ability of Lap were studied by gelation tests and the morphology of the gel phases was investigated by polarized optical microscopy measurements and diffusion experiments.

Halloysite-cyclodextrin hybrid was employed as carrier for sustained release of clotrimazole for vaginal or buccal treatment of Candidiasis. The nanocarrier was obtained by functionalization of halloysite surface with cyclodextrin moieties by means of microwave irradiation, with the final goal to obtain a scaffold for the covalent linkage of cysteamine hydrochloride. The interaction between clotrimazole and the pristine components, namely cyclodextrin and halloysite, was thoroughly investigated by several techniques such as DSC, TGA, UV–vis spectroscopy and some adsorption studies were, also, carried out. The release of the antifungine molecule was finally investigated in a medium that imitates the physiological conditions.

Clay minerals have been used for medical purposes from ancient times. Among them, the halloysite nanotube, an aluminosilicate of the kaolin group, is an emerging nanomaterial which possesses peculiar chemical characteristics. By means of suitable modifications, such as supramolecular functionalization or covalent modifications, it is possible to obtain novel nanomaterials with tunable properties for several applications. In this context the covalent grafting of suitable organic moieties on the external surface or in the halloysite lumen has been exploited to improve the loading and release of several biologically active molecules. The resulting hybrid nanomaterials have been applied as drug carrier and delivery systems, as fillers for hydrogels, in tissue regeneration and in the gene delivery field. Furthermore the loading and release of specific molecules have been also investigated for environmental purposes. This review summarizes the main developments in the halloysite modifications in the last 20 years with a particular attention to the development in the past two years.

The synthesis of photoluminescent nanomaterials based on halloysite nanotubes is described. The obtained hybrid was characterized by means of TGA, FT-IR, DLS and XPS measurements; in addition its morphology was imaged by TEM and HR-TEM. The HNT hybrid also exhibited photoluminescent properties, both in solution and in the solid state, and white-light emission (0.24, 0.36; CIE coordinates) was observed. This work could be pioneering as a new strategy for manufacturing both LEDs and fluorescent tags based on HNT nanomaterials. © 2018 The Royal Society of Chemistry.

The synthesis of pure fine chemicals for industrial purposes is one of the most attractive challenges of chemical research. The use of catalytic pathways mediated by palladium nanoparticles (PdNPs) for C-C bond formation is a useful way to obtain these kinds of compounds. To achieve this objective, the PdNPs can be efficiently loaded on a functionalized natural nanostructured support such as halloysite nanotubes (HNTs). Hybrid materials based on thiol functionalized halloysite nanotubes and highly cross-linked imidazolium salts were successfully developed and used for the stabilization of PdNPs. The HNT/Pd hybrids were thoroughly characterized from a physico-chemical point of view and tested as a catalyst in the Suzuki and Heck C-C coupling reactions under microwave irradiation to obtain innovative materials for fine chemicals synthesis. Catalytic tests highlighted the fact that the HNT/Pd hybrids show high performance and full recyclability (up to ten cycles) in both reactions. Regarding the Suzuki reaction, under the best experimental conditions, the remarkable values of a turnover number of 194 000 and a turnover frequency of 3 880 000 h-1 were achieved without metal contamination in the final products. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. The synthesis of pure fine chemicals for industrial purposes is one of the most attractive challenges of chemical research. The use of catalytic pathways mediated by palladium nanoparticles (PdNPs) for C–C bond formation is a useful way to obtain these kinds of compounds. To achieve this objective, the PdNPs can be efficiently loaded on a functionalized natural nanostructured support such as halloysite nanotubes (HNTs). Hybrid materials based on thiol functionalized halloysite nanotubes and highly crosslinked imidazolium salts were successfully developed and used for the stabilization of PdNPs. The HNT/Pd hybrids were thoroughly characterized from a physico-chemical point of view and tested as a catalyst in the Suzuki and Heck C–C coupling reactions under microwave irradiation to obtain innovative materials for fine chemicals synthesis. Catalytic tests highlighted the fact that the HNT/Pd hybrids show high performance and full recyclability (up to ten cycles) in both reactions. Regarding the Suzuki reaction, under the best experimental conditions, the remarkable values of a turnover number of 194 000 and a turnover frequency of 3 880 000 h1 were achieved without metal contamination in the final products.

Well designed and safe nano drug carrier systems are an important tool in biomedical applications. The combination of two or more drugs has been used in medicine both to enhance the therapeutic effect and to decrease the side effects of drugs. Biocompatible halloysite nanotubes, that possess two different surfaces, are a suitable nanomaterial for a simultaneous carrier and release of two drugs that can exert a synergistic effect against cancer cells. In this study, three curcumin derivatives and doxorubicin were loaded by supramolecular and covalent linkage at the lumen and external surface of the halloysite nanotubes. The obtained multifunctional systems were characterized by several techniques and the kinetic release of the drugs from the lumen was also investigated. Finally, the cytotoxic effects of the multifunctional carriers were evaluated on different cancer cell lines, namely breast cancer cell lines (SUM-149 and MDA-MB-231) and acute myeloid leukemia cell lines (HL60 and HL60R). The obtained results show promising cytotoxicity activity of the hybrids which is correlated to the nanoparticles size and to the release profile of the drug supramolecularly loaded on Hal surfaces.

Hybrid materials based on halloysite nanotubes (HNT) and cucurbit[8]uril (CB[8]) were prepared with the aim to obtain efficient nanosponges towards hydrocarbons both in liquid and vapor phases. The loading on both HNT surfaces and the hybrid morphology were evidenced by FTIR spectroscopy, thermogravimetric analysis and scanning electron microscopy. In order to highlight the interactions in the hybrid 13C {1H} CP-MAS NMR experiments were performed. The aqueous colloidal stability of HNT/CB[8] was highlighted through ζ potential and dynamic light scattering measurements. The HNT/CB[8] composite was employed as nanosponge to capture aromatic oils in aqueous phase as evidenced by fluorescence emission spectra of pyrene. These results were correlated with the adsorption capacity of the hybrid toward toluene in vapor phase. This paper provides an efficient way to prepare a biocompatible hybrid material that could be used as a potential multi-pockets nano-container for decontamination of polluted water and/or air.

Environmental friendly halloysite-dicationic triazolium salts (second generation) obtained by subsequent click reactions of a diyne derivative in the presence of 2-azidopropyl-modified halloysite nanotubes, were used as supports for palladium catalyst. Thanks to the high triazolium loading (25%) these materials were able to support higher amount of the metal than that on the monocationic derivative (first generation). Such materials were characterized by thermogravimetric analysis, FT-IR spectroscopy and SEM investigations. The new catalytic system was employed in the ligand free Suzuki cross-coupling under microwave irradiation. A set of solvent, time and% loading of palladium was screened. The palladium catalyst displayed good activity allowing the synthesis of several biphenyl in high yields working with only 0.1 mol% of palladium loading at 120 °C in water, for an irradiation time of 10 min. The second generation catalyst, also, showed good recyclability without any loss in activity and negligible palladium leaching that are significant improvements over the first generation triazolium catalyst.

Hypothesis: Oral insulin administration is not actually effective due to insulin rapid degradation, inactivation and digestion by proteolytic enzymes which results in low bioavailability. Moreover insulin is poorly permeable and lack of lipophilicity. These limits can be overcome by the loading of protein in some nanostructured carrier such as halloysite nanotubes (HNTs). Experiments: Herein we propose an easy strategy to obtain HNT hybrid materials for the delivery of insulin. We report a detailed description on the thermal behavior and stability of insulin loaded and released from the HNTs hybrid by the combination of several techniques. Findings: Release experiments of insulin from the HNTs revealed the efficacy of the nanocarrier. Circular Dichroism data evidenced that the released insulin exhibits its native-like secondary structure confirming the suitability of HNT/insulin as delivery system for at least three months. The loaded nanotubes were filled into chitosan matrix with the aim to prepare bionanocomposite films that can be used for transdermal delivery. This work puts forward an efficient strategy to prepare halloysite based nanocarriers containing insulin that could be employed in several biomedical applications. The detailed description of the prepared HNT/insulin hybrid represents a fundamental point for designing advanced delivery systems. © 2018 Elsevier Inc.

Halloysite nanotubes (HNTs) are clay minerals with a hollow nanotubular structure. There is growing interest in these nanomaterials, due to their biocompatibility, potential applications and availability. The surface chemistry of HNTs is versatile for the targeted chemical modification of the inner lumen and outer surface. Functionalized halloysite constitutes a valuable support for metal nanoparticles, promoting catalytic applications with tunable properties. The peculiar tubular shape of HNTs favors the dispersion and surface availability of the supported metal nanoparticles that are active in the catalytic path. Moreover, the presence of an empty lumen opens new perspectives for the production of nanoarchitectures with synergistic catalytic effects, due to the increase in local concentrations and confinement. The main focus of this review is the research on modified halloysite nanotubes for the preparation of valuable supports for metal nanoparticles and their applications in catalytic processes.

Inorganic-organic nanosponge hybrids based on halloysite clay and organic cyclodextrin derivatives (HNT-CDs) were developed by means of microwave irradiations in solvent-free conditions. The HNT-CDs nanomaterials characterized by FT-IR, TGA, BET, TEM, SEM, DLS, and zeta-potential have showed a hyper-reticulated network which possesses both HNT and cyclodextrin peculiarities. The new HNT-CDs nanosponge hybrids were employed as nanoadsorbents, first choosing Rhodamine B as the dye model, and furthermore for the removal of some cationic and anionic dyes, under different pH values (1.0, 4.54, and 7.4). The collected results showed that the pH solution as well as the electrostatic interactions affect the adsorption process. Factors controlling the adsorption process were discussed. The experimental adsorption equilibrium and kinetic data were best described by the Freundlich isotherm model. Excellent adsorption efficiency for cationic dyes were observed with respect to anionic ones. The results suggest that HNT-CDs nanosponge hybrids are a good nanoadsorbent for selective adsorption of cationic dyes with respect to the anionic ones from aqueous solutions.

L’allosite (HNT) è un interessante materiale argilloso allumino-silicato naturale, non tossico e biocompatibile, con la caratteristica forma tubolare cava dotata di parziale carica positiva interna e negativa esterna.Combinando le peculiarità di un composto organico con le proprietà di un materiale inorganico, è possibile ottenere sistemi ibridi organici–inorganici con interessanti proprietà e vasti campi di applicazione. Sono un esempio delle “nanospugne” capaci di adsorbire efficacemente potenziali inquinanti. In questo contesto sono stati preparati, dei materiali ibridi “spugna” costituiti da unità ciclodestriniche e allosite e ancora un sistema ibrido HNT-Cucurbit[8]uril. Il primo possiede una struttura altamente ramificata e mostra interessanti capacità di assorbimento di coloranti organici con proprietà modulabili in funzione di pH e temperatura, il secondo è stato dimostrato possedere una spiccata attività di adsorbimento di toluene e pirene.

Multicavity halloysite nanotube materials were employed as simultaneous carriers for two different natural drugs, silibinin and quercetin, at 6.1% and 2.2% drug loadings, respectively. The materials were obtained by grafting functionalized amphiphilic cyclodextrin onto the HNT external surface. The new materials were characterized by FT-IR spectroscopy, SEM, thermogravimetry, turbidimetry, dynamic light scattering and ζ-potential techniques. The interaction of the two molecules with the carrier was studied by HPLC measurements and fluorescence spectroscopy, respectively. The release of the drugs from HNT-amphiphilic cyclodextrin, at two different pH values, was also investigated by means of UV-vis spectroscopy. Biological assays showed that the new complex exhibits anti-proliferative activity against human anaplastic thyroid cancer cell lines 8505C. Furthermore, fluorescence microscopy was used to evaluate whether the carrier was uptaken into 8505C thyroid cancer cell lines. The successful results revealed that the synthesized multicavity system is a material of suitable size to transport drugs into living cells.

Halloysite nanoclays (HNTs) are promising nanomaterials because of their versatile properties, such as hollow tubular morphology and tunable surface chemistry. HNTs are biocompatible, no toxic and abundantly available at low cost. Due to these characteristics HNTs are suitable for development of hybrid sustainable materials, which are perspective for wastewater remediation, green packaging and drug delivery. HNTs are quite polydisperse in size with a length of ca. 1 m, while the external diameter and the lumen range between 50-80 nm and 10-15 nm, respectively. Chemically, halloysite is composed of gibbsite octahedral sheet (Al-OH) groups on the inner surface and siloxane (Si−O−Si) groups on the external surface. This different chemistry allows the selective modification of HNTs surfaces. We performed several chemical functionalization of HNTs materials to confer properties valuable in specific applications. The HNTs inner lumen was modified to generate an hydrophobic microenvironment for the solubilization of compounds sparingly soluble in water (aromatic and aliphatic oils). Oppositely, the outer surface hydrophobization was employed to create reverse inorganic micelles to be used as dispersant for hydrophilic compounds (such as CuSO4·5H2O) in a confined environment within an organic solvent. Grafting chemically modified cyclodextrin units onto the nanotube surface endowed to obtain a singular nanoparticle with double cavity (HNTs and cyclodextrin lumen). The obtained materials were characterized to investigate the structure and colloidal stability in aqueous dispersions. The grafted cyclodextrins were modified with thiosaccharide pendants, to mimic the binding of sugars to proteins and the glyco-cluster effect for cellular recognition events. Drug-loading and delivery abilities were tested by using curcumin, a common naturally occurring anticancer agent.

Halloysite nanotubes were explored as drug carrier for cardanol, which is considered as a promising natural anticancer active species. To this aim, besides the pristine nanoclay, a chemical modification of the nanocarrier was performed by attaching triazolium salts with different hydrophobicity at the outer surface of the hollow nanotubes. The interaction between cardanol and nanotubes was highlighted in solution by HPLC. This method proved the loading of the drug into the nanotubes. The solid dried complexes formed by pristine and modified halloysite with the cardanol were characterized by IR spectroscopy, thermogravimetric analysis as well as water contact angle to evidence the structure, thermal properties and wettability of the obtained materials. The kinetics of cardanol release as well as cell viability experiments provided promising results that put forward a new strategy for potential applications of cardanol as active antiproliferative molecule and clay nanotubes as drug carrier.

Positively charged halloysite nanotubes functionalized with triazolium salts (f-HNT) were employed as a carrier for curcumin molecules delivery. The synthesis of these f-HNT new materials is described. Their interaction with curcumin was evaluated by means dynamic light scattering (DLS) and UV–vis spectroscopy in comparison with pristine unmodified HNT (p-HNT). The curcumin load into HNT was estimated by thermogravimetric analysis (TGA) measurements, while the morphology was investigated by scanning electron microscopy (SEM) techniques. Release of curcumin from f-HNT, at three different pH values, by means of UV–vis spectroscopy was also studied. Furthermore, different cancer cell lines were used to evaluate the potential cytotoxic effect of HNT at different concentrations and culture times. The results indicated that the f-HNT drug carrier system improves the solubility of curcumin in water, and that the drug-loaded f-HNT exerted cytotoxic effects against different cell lines.

In the last years SILLP (supported ionic liquid-like phase)-based materials prepared by covalent attachment have been synthesized [1]. Recently, we have synthesized a palladium-based catalytic system using halloysite nanotubes modified with octylimidazolium moieties and we have tested it in the Suzuki cross-coupling reaction under traditional heating, microwave irradiation and a very small amount of Pd catalyst [2,3]. It is known that support based on triazole motif showed superior activity to the analogous imidazole molecules [4] so, we have focused our attention to develop a new SILLP system with triazolium moiety. Herein we report the synthesis of an original Pd-dicationic triazolium support based on halloysite nanotubes (HNT-triazo/Pd). The new HNT/Pd catalyst was used as catalyst in the Suzuki reaction under microwave irradiation. The best experimental conditions were obtained when the reactions were carried out for 10 minutes in water at 120 °C in presence of K2CO3 as base using 0.1 mol% of catalyst. Good recyclability was observed too.

Phenolic compound originated from one of the main class of secondary metabolites, as curcumin and its derivatives have been studied and their biological and pharmacological activities have been evaluated, too [1,2]. Unfortunately, curcumin exhibits poor bioavailability after oral or topic administration [3]. Therefore a carefully designed carrier could significantly facilitate curcumin delivery and broaden the range of its possible pharmaceutical applications. Halloysite was found to be a viable and inexpensive nanoscale container for the encapsulation of biological active molecules [4]. In this communication we report data about a new potential curcumin carrier based on positively charged functionalized halloysite nanotubes with triazolium salts (f-HNT). The interaction between curcumin and f-HNT was investigated by classical techniques as well as the release. Furthermore different cancer cell lines were used to evaluate the potential cytotoxic effect of the drug-carrier system.

Halloysite nanotubes modified with triazolium salts (f-HNT) were found to be promising drug carriers for biological molecules [1 ]. In this work we report data about f-HNT as carrier for cardanol, a molecule with interesting biological activity [2]. The interactio n between cardanol and f- HNT was highlighted by HPLC, FTIR spectroscopy, TGA , water contact angle measurements and SEM investigations. Release of cardanol from the system and cytotoxic e ffect of the complex f- HNT/Card on hepatocarcinoma cell lines were, also, evaluated. The obtained results put forward the use of halloysite as drug c arrier

Da precedenti studi è stato valutato che i nanotubi di allosite modificati con sali triazolici (f-HNT), sono dei promettenti sistemi carrier per molecole biologiche1. In questo lavoro si riportano i risultati ottenuti studiando gli f-HNT come carrier per il cardanolo, molecola con interessanti attività biologiche. L’interazione fra il cardanolo e gli f-HNT è stata valutata tramite HPLC, spettroscopia FTIR, analisi termogravimentrica, misure di angolo di contatto e microscopia a scansione elettronica. Infine sono stati studiati sia il rilascio del cardanolo dal sistema che gli effetti citotossici del complesso f-HNT/Cardanolo verso linee cellulari di epatocarcinoma. I dati sperimentali ottenuti mostrano che l’allosite risulta un promettente sistema atto al drug carrier.

Halloysite nanotubes (HNTs) are a natural, biocompatible, environmental friendly and cheap double-layered aluminosilicate mineral that has a predominantly hollow tubular structure. The general stoichiometry of halloysite is Al2Si2O5·4(H2O). The layer units consist of a tetrahedral SiOH sheet stacked with an edge shared octahedral AlO6 sheet with an internal aluminol group AlOH. A water layer exists between the adjacent two layers. Thanks to their structural features, HNTs are suitable for a potential application as support for catalytic composites. Recently, we reported the synthesis of novel palladium-based catalytic systems using halloysite nanotubes modified with imidazolium or triazolium moieties as supports for PdNPs and we successfully employed these supported catalysts in the Suzuki reaction under microwave irradiation. Herein we report an efficient strategy to prepare HNTs-based catalyst through direct chemical grafting with stimuli-responsive polymer (PNIPAAM) coordinating PdNPs. The HNT-PNIPAAM/PdNPs was tested as catalyst in the Suzuki reaction under microwave irradiation.

Halloysite (HNT) is a natural clay that, in the last years, has shown an important increasing on various applications in different field of interesting. Chemically similar to kaolin, it shows the predominately rolled shape, to form multilayers tubes of nanometric dimensions. The different chemical composition of the inside lumen (Al-OH) surface and outside (Si-O) give to the tubes a partial negative charge outside and positive inside. In this way, it is possible to get different interactions of different molecules or systems selectivity on one or another surface. The selective functionalization, covalent or not, of the HNT lumen or outer surface, gives the possibility to the nanotubes to further expand and modulate their properties, increasing the potential efficacy and the application fields. Recently some studies are, also, focused on the edges and interlayer properties and potentials. Among the countless applications of halloysite, is central the nanotube ability to interact with metals. Metals ions are one of the worst pollutants in the environmental contest. Halloysite has shown interesting properties as starting point to make environmental recovery system. Another important application of the ability of HNT of interaction with metals is catalysis. Catalyst immobilization is a good opportunity to obtain materials that can be recovered and reused for several cycles with low leaching. Several studies have been carried out on the use of ionic liquids as reaction media and as stabilizers for metal nanoparticles. In particular, great attention has been devoted to the use of supported ionic liquid phase (SILP)-based materials as heterogeneous recyclable palladium catalyst. Herein are reported some recent developments about immobilization of metal nanoparticles on halloysite nanotubes and studies about the materials and applications.

I composti fenolici fanno parte dei metaboliti secondari delle piante e tra questi la curcumina è stata ampiamente studiata per le sue intrinseche proprietà farmacologiche.1-4 La curcumina [bis(4-idrossi-3-metossi-fenil)-1,6-eptadiene-3,5-dione] isolata sotto forma di pigmento giallo dal rizoma secco della curcuma longa è stata utilizzata in presenza di sistemi delivery per applicazioni farmaceutiche.5 Uno degli svantaggi della curcumina è la sua scarsa biodisponibilità in ambiente acquoso;6 problema che può essere risolto incapsulandola in nanocontenitori. Tra i sistemi nanodelivery naturali che non presentano citotossicità vi sono i nanotubi di allosite. I nanotubi di allosite sono stati utilizzati da Price e Lvov come molecole in grado di incapsulare farmaci.7 Inoltre tale capacità può essere migliorata attraverso la funzionalizzazione sia della superfice interna che esterna dei nanotubi stessi. In questa comunicazione riportiamo dei dati preliminari sull’incapsulamento della curcumina in nanotubi di allosite modificati e non, con lo scopo futuro di provare tali sistemi in vitro su cellule tumorali mammarie