Liquid Crystalline Structures Research Articles

Cubic liquid crystalline structures in diluted, concentrated and highly concentrated emulsions for topical application: Influence on drug release and human skin permeation.

Novel emulsions with a nanostructured continuous phase have been proposed as controlled drug delivery systems to enhance topical delivery of active ingredients avoiding systemic effects. In this study, oil-in-water (O/W) emulsions with two surfactant/water (S/W) weight ratios of 40:60 and 35:65, and oil concentrations of 10 wt% (diluted emulsion), 40 wt% (concentrated emulsion) and 85 wt% (highly concentrated emulsion) have been investigated to identify the presence of liquid crystalline structures and their influence on drug release and skin permeation. The emulsions have been characterized in terms of visual appearance, rheology and drug release. The presence of cubic liquid crystalline structures in emulsions with S/W 40:60 was confirmed by small angle X-ray scattering (SAXS). Rheology results showed a markedly different behaviour in emulsions with S/W 40:60 compared with nonstructured emulsions. A model drug, diclofenac sodium (DS) was successfully incorporated in the emulsions. DS release was studied with hydrophilic and lipophilic membranes, and the amount of DS in the receptor solution was significantly lower in the formulations containing cubic liquid structures. An in vitro skin permeation study with dermatomed human skin showed that emulsions with a nanostructured continuous phase are suitable formulations for topical delivery with DS retention in skin layers. The results indicate that the amount of drug retained in skin structures may be tuned by modification of liquid crystal concentration and emulsion structure.

Abstract 2171: Activatable nanodelivery of high payload gemcitabine augments therapeutic efficacy in murine breast and pancreatic cancer models

Abstract Gemcitabine (Gem) is the standard of treatment for metastatic pancreatic ductal adenocarcinoma (PDAC) and an effective anticancer drug for various solid tumors. However, clinical application of Gem chemotherapy is hampered by suboptimal delivery of the drug, mainly due to short circulation time and poor penetration of drug into the hypo-vascularized and dense fibrous stroma of PDAC. Here, we present a novel method to improve both loading and stability of Gem in temperature-sensitive liposomes (TSL). TSL have the potential to be locally activated by exposing tumor to ultrasound-mediated hyperthermia (USH) triggering release of large amounts of free drug in the tumor vasculature, which can then rapidly penetrate into the heated tumor. Gem was passively loaded into TSL composed of DPPC:DSPC:DSPE-PEG2k (80:15:5) in the presence of copper(II) gluconate and triethanolamine at final 0.12 mg-drug/mg-lipid. Formation of a CuGem complex improved drug loading and stability and reduced systemic toxicity. Mice with bilateral invasive neu deletion (NDL) tumors (4-5 mm) were treated with an i.v. administration of CuGem-TSL at 10 mg Gem/kg body weight. USH was employed to trigger the release of drug; one tumor in the bilateral tumor model was insonified with a peak ultrasound pressure of 1.1 MPa at a frequency of 1.5 MHz at 43°C for 5 min prior to and 30 min post drug injection with a variable duty cycle. We found that copper(II) gluconate possesses superior potential to solubilize Gem up to 150 mg/mL and augments passive drug loading. Upon loading Gem, formation of a complex with copper further improved drug loading and stability within TSL. By optimizing the lipid composition of the liposomal shell, we achieved high loading content of Gem at up to 12% by weight in TSL (CuGem-TSL), 4-fold greater than previously reported. Cryo electron microscopy confirmed the presence of liquid crystalline structures within CuGem-TSL, which was not observed in the absence of copper (Gem-TSL). The resulting high-content CuGem-TSL displayed a rapid release of Gem (80%) within 5 min at 42°C with only 25% release over 30 min at 37°C in the presence of serum. In vitro CuGem-TSL demonstrated equivalent toxicity to free Gem against both murine breast cancer and pancreatic cancer. One hour following intravenous administration, 75% of Gem was effectively retained in circulating TSL, whereas no drug was detected in mouse plasma with free drug administration. Three repeated administrations of CuGem-TSL combined with USH over a two-week treatment course suppressed tumor growth in NDL, model of murine breast cancer, with limited toxicity, enhancing survival when compared to treatment with free Gem alone. Additionally, in a more aggressive tumor model of murine pancreatic cancer (KrasLSL-G12D/+; Trp53LSL-R172H/+; Pdx-Cre, mT4 tumor source), CuGem-TSL with USH induced cell death and regions of apoptosis and necrosis. Citation Format: Samantha T. Tucci, Azadeh Kheirolomoom, Elizabeth S. Ingham, Lisa M. Mahakian, Sarah M. Tam, Josquin Foiret, Neil E. Hubbard, Alexander D. Borowsky, Mo Baikoghli, R. Holland Cheng, Katherine W. Ferrara. Activatable nanodelivery of high payload gemcitabine augments therapeutic efficacy in murine breast and pancreatic cancer models [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 2171.

Self-Assembly of Two-Dimensional Colloids in Spherical Space

Understanding the hierarchical organization of nanomaterials in different geometries is important for developing materials with new properties. It is well known that long-range ordering emerges when shape-anisotropic nanoparticles form liquid crystals; this may offer an opportunity to build large-scale ordered structures assembled by nanoparticles in a confined geometry. This study demonstrates the self-assembly of two-dimensional colloids of graphene oxide (GO) in a spherical space. The arrangements of GO nanosheets were captured by in situ photopolymerization to form microspheres, in which the nanosheets organized into lamellar liquid crystalline structures, adopting either a concentric configuration or a pseudo-concentric configuration, leaving topological defects in the central region. We also observed GO microspheres with bipolar-like configurations although they are scarce. Optical and electron microscopy observations revealed the fine structures of these topological defects caused by the frustratio...

Photoresponsive Structural Color in Liquid Crystalline Materials

AbstractPhotoresponsive liquid crystalline photonic materials are a medium in which the self‐regulation of light can occur. Liquid crystals are macroscopically self‐assembling, optically anisotropic materials capable of amplifying photochemical changes and thus are well suited to demonstrate complex light‐driven behavior. This review presents recent progress in liquid crystalline systems exhibiting photoresponsive structural color. More specifically, it surveys progress on liquid crystalline materials and structures with coloration that is the result of the constituents' spatial arrangement (not of presence of dyes or pigments) and for which this arrangement can be externally controlled by light. In cholesteric and blue‐phase liquid crystals, the structural color results from the natural self‐assembly of liquid crystal molecules in periodic structures. Several photochemically driven mechanisms can be exploited to impart color changes to these structures. Photonic liquid crystalline materials can also be generated with directed self‐assembly techniques and subsequent processes can be exploited to create photoinduced changes to their optical properties. After reviewing the recent progress in materials based on natural and directed self‐assembly, these approaches are compared and contrasted. A few interesting examples of more complex behavior are noted, including true autonomous self‐regulation of light flow in liquid crystal systems.

Tacticity Effect on Mesogen-Free Liquid Crystalline Self-assembly Induced by Strong Dipole–Dipole Interactions

Strong dipole–dipole interactions in mesogen-free aliphatic comblike polymers can induce unique liquid crystalline (LC) self-assembly. By comparing atactic and isotactic poly(oxypropylene)s with n-alkylsulfonyl side groups (aPOP-SO2Cn and iPOP-SO2Cn), the effect of main-chain tacticity on the ordered phase behavior was studied in this work. For aPOP-SO2Cn, LC self-assemblies were observed when n is ≥3. Two types of LC phases were formed depending on the side chain length n: (i) a three-dimensional (3D) high-order LC structure (possibly crystal B or E) for n = 3–5 and (ii) a smectic A (SmA) structure for n = 6–12. For iPOP-SO2Cn, crystallization was favored as a result of regular main-chain configuration. Only when n ≥ 10, the isotactic comblike polymers exhibited a monotropic phase behavior with the SmA phase appearing during cooling from the isotropic melt. Regardless of atactic or isotactic main chains, these ordered LC and crystalline phases featured a double-layer structure, which was dictated by the ...

Vancomycin ocular delivery systems based on glycerol monooleate reversed hexagonal and reversed cubic liquid crystalline phases

Lyotropic bulk reversed hexagonal and reversed cubic liquid crystalline phases (hexagonal and cubic phases) composed of glycerol monooleate (GM) were used to design the vancomycin hydrochloride’s (VHCl) delivery systems aiming to maintain VHCl’s therapeutic concentration during 24 h in the eye, locally (as an insert) and/or intravitreally (as a bulk phase injection).Bulk VHCl’s hexagonal and cubic phases were successfully prepared by melted homogenization and solvent evaporation method, and then an insert was prepared.The structural characteristics of liquid crystalline phases were studied using cross polarized light microscopy and small angle X-ray scattering technique. The presence of VHCl (1–9.5% w/w VHCl solution) did not exhibit any change in the liquid crystalline phase’s structure to another liquid crystalline phase, and showed little effect on the lattice parameter of the existing liquid crystalline phase structure.In order to relate the liquid crystalline phase structure to VHCl’s release rate locally into the eye, in-vitro release test of an implant has been done using a simulated tear fluid. VHCl’s release in the simulated tear fluid from the cubic phase obeyed Higuchi kinetics, with linear VHCl’s release versus the square root of time. The hexagonal phase released VHCl in simulated tear fluid significantly slower than the cubic phase. In order to relate the liquid phase structure to VHCl’s diffusion intravitreally, in vitro release test by the Sirius‘ Subcutaneous Injection Site Simulator (Scissor) has been performed. Comparing the release properties by a Scissor, the VHCl’s cubic phase demonstrated slower permeation through extra-cellular matrix than the VHCl solution.To evaluate the efficacy of the system investigated, the release properties of VHCl’s cubic phase were compared with literature data indicating that the cubic phase could be a potential matrix system in the delivery of VHCl intravitreally during 24 h after intravitreal injection. The release data in the simulated tear fluid indicated that the cubic phase should be further optimized to achieve a therapeutic VHCl concentration locally in the eye during 24 h.

Benzoxazine-epoxy thermosets with smectic phase structures for high thermal conductive materials

ABSTRACTTo further increase the intrinsic thermal conductivity (TC) of polybenzoxazine, a series of benzoxazine-epoxy thermosets (s-PBEI) were obtained through the sequential curing of a smectic phase epoxy monomer (s-EP) and a bifunctional benzoxazine monomer (BZ) in the presence of imidazole. The results show that s-PBEI exhibits a smectic mesophase. The formation mechanism of the smectic phase is reaction-induced phase separation caused by the preferential curing of s-EP. Owing to the increment of the liquid crystalline structure content, the TC of s-PBEI increases with increasing s-EP content. The TC of s-PBEI55 containing equal weight of BZ and s-EP reaches 0.30 W m−1 K−1, which is higher than that of n-PBEI55, a benzoxazine-epoxy thermoset with nematic phase structures. Additionally, the TC, glass transition temperature, and 10% weight loss temperature of s-PBEI64 containing 60 wt% BZ and 40 wt% s-EP are 0.28 W m−1 K−1, 216°C, and 334°C, respectively, indicating its potential applications in electronic packaging, LED lighting, and other fields requiring a high TC resin matrix.

Experimental Conditions for the Stabilization of the Lyotropic Biaxial Nematic Mesophase

Nematic phases are some of the most common phases among the lyotropic liquid crystalline structures. They have been widely investigated during last decades. In early studies, two uniaxial nematic phases (discotic, ND, and calamitic, NC) were identified. After the discovery of the third one, named biaxial nematic phase (NB) in 1980, however, some controversies in the stability of biaxial nematic phases began and still continue in the literature. From the theoretical point of view, the existence of a biaxial nematic phase is well established. This review aims to bring information about the historical development of those phases considering the early studies and then summarize the recent studies on how to stabilize different nematic phases from the experimental conditions, especially, choosing the suitable constituents of lyotropic mixtures.

Industrial and Medical Material Applications of a Mega-polysaccharide Derived from Cyanobacteria

Polysaccharides (PS) are one form of biomass occurring in great abundance on earth and are promising organic material alternatives to petroleum-based ones. We have focused on PS produced by cyanobacteria. Aphanothece sacrum, which is a freshwater unicellular cyanobacterium, produces large amounts PS as a main component of the extracellular matrix. We successfully extracted the PS sacran from A. sacrum biomaterials and demonstrated that sacran contains carboxyls and sulfate groups. Furthermore, the constituent sugars of the sacran extracted were determined to be fucose, rhamnose, xylose, arabinose, mannose, glucose, galactose, glucuronic acid, galacturonic acid, and galactosamine. The sequence of sacran is still under investigation. In addition, we confirmed that the sacran was a supergiant with a high absolute molecular weight of 2.35×107 g/mol. Sacran shows a self-orienting behavior in dilute solution at a concentration range over 0.25 wt% to form a liquid crystalline structure. Using this property, it is possible to prepare a sacran cast film with an orientation structure, especially swelling in the thickness direction, to form anisotropic hydrogels. The anisotropy and degree of swelling of the hydrogels could be controlled by varying the heating temperature of the sacran cast file. Furthermore, sacran could be combined successfully with rayon as new fiber materials, and the sacran-rayon complex materials showed increased water absorption compared with the original rayon. This article introduces various applications of sacran in the industrial and medical fields.

Curcumin- and Fish Oil-Loaded Spongosome and Cubosome Nanoparticles with Neuroprotective Potential against H2O2-Induced Oxidative Stress in Differentiated Human SH-SY5Y Cells

Many phytochemical antioxidant compounds, including curcumin (CU), are water-insoluble and thus require delivery carriers in order to increase their bioavailability for in vivo applications. Oxidative stress-related apoptosis is a common cause for the neuronal loss in the progression of neurodegenerative diseases. Lipid nanoparticles (NPs) with internal self-assembled liquid crystalline structures present strong interest as safe drug delivery systems for neuronal regeneration through combination therapies. Here, we report spongosome and cubosome lipid NPs, which co-encapsulate CU and fish oil (FO), rich in ω-3 polyunsaturated fatty acids. The performed structural investigation by synchrotron small-angle X-ray scattering evidenced the liquid crystalline organization of the self-assembled NPs. The encapsulation efficiency for CU in the lipid nanocarriers was found to be higher as compared to that reported for polymer-based carriers. The cytotoxicity of the blank and antioxidant-loaded nanocarriers was negli...

Synthesis and supramolecular liquid crystalline structure modulation of side-chain polynorbornenes with asymmetrical substituent mesogenic groups

The substituent position and number have an important effect on the supramolecular liquid crystalline structure evolution in side-chain polymers.

Synthesis of novel thermotropic liquid crystalline polymers by a reactive extrusion process.

The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step via a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion.

Cubosomes for topical delivery of the antimicrobial peptide LL-37

In this study, the use of cubosomes for topical delivery of the antimicrobial peptide (AMP) LL-37 was investigated. Topical delivery of AMPs is of great interest for treatment of skin infections caused by bacteria, such as Staphylococcus aureus. AMP containing cubosomes were produced by three different preparation protocols and compared: (i) pre-loading, where LL-37 was incorporated into a liquid crystalline gel, which thereafter was dispersed into nanoparticles, (ii) post-loading, where LL-37 was let to adsorb onto pre-formed cubosomes, and (iii) hydrotrope-loading, where LL-37 was incorporated during the spontaneously formed cubosomes in an ethanol/glycerol monooleate mixture. Particle size and size distribution were analyzed using dynamic light scattering (DLS), liquid crystalline structure by small angle x-ray scattering (SAXS) and release of LL-37 by a fluorescamine assay. Proteolytic protection of LL-37 as well as bactericidal effect after enzyme exposure was investigated. The skin irritation potential of cubosomes was examined by an in vitro epidermis model. Finally, the bacterial killing property of the cubosomes was examined by an ex vivo pig skin wound infection model with Staphylococcus aureus. Data showed that a high loading of LL-37 induced formation of vesicles in case of cubosomes prepared by sonication (pre-loading). No release of LL-37 was observed from the cubosomes, indicating strong association of the peptide to the particles. Proteolysis studies showed that LL-37 was fully protected against enzymatic attacks while associated with the cubosomes, also denoting strong association of the peptide to the particles. As a consequence, bactericidal effect after enzyme exposure remained, compared to pure LL-37 which was subjected to proteolysis. No skin irritation potential of the cubosomes was found, thus enabling for topical administration. The ex vivo wound infection model showed that LL-37 in pre-loaded cubosomes killed bacteria most efficient.

Tapered fiber liquid crystal hybrid broad band device

This paper presents the results of design, manufacturing and characterization of a hybrid broad band filter based on taper technology and liquid crystalline structure using a standard single mode fiber. A liquid crystal mixture, denoted 1550*, was designed for the electrically driven modulation of an electromagnetic wave at visible range. The main reason for using a biconical optical fiber taper as a core is surrounding it by a liquid crystalline medium providing the possibility to control an effective refractive index of fiber cladding. Two kinds of rubbing, orientation parallel and orthogonal to the taper axis, were applied. The performance of a tuned cladding was studied at electric field and temperature domains. The induced reorientation of liquid crystal molecules was measured at a broad wavelength range, between 500 and 1200 nm. All fabricated tunable broad band filter devices exhibit internal losses lower than 0.5 dB.

Large Hexosomes from Emulsion Droplets: Particle Shape and Mesostructure Control.

Soft, rotationally symmetric particles of dispersed hexagonal liquid crystalline phase are produced using a method previously developed for cubosome microparticle production. The technique forms hexosome particles via removal of ethanol from emulsion droplets containing monoolein, water, and one of the various hydrophobic molecules: vitamin E, hexadecane, oleic acid, cyclohexane, or divinylbenzene. The unique rotational symmetry of the particles is characterized by optical microscopy and small-angle X-ray scattering to link particle phase, shape, and structure to composition. Rheology of the soft particles can be varied independently of shape, enabling control of transport, deformation, and biological response by controlling composition and molecular structure of the additives. The direct observations of formation, and the resultant hexosome shapes, link the particle-scale and mesoscale properties of these novel self-assembled particles and broaden their applications. The micron-scale hexosomes provide a route to understanding the effects of particle size, crystallization rate, and rheology on the production of soft particles with liquid crystalline structure and unique shape and symmetry.

Phase Transitions of Branched Fatty‐Acid Calcium Salt/Water Systems

AbstractCalcium (Ca) salts of fatty acids are powder materials, which exhibit lubricant, hydrophobic, and bactericidal properties. These physical and biological properties depend on the chemical structure of the alkyl chain of the fatty acids. In this study, the phase behavior of iso‐stearic acid Ca salt/water binary systems was studied, and the effect of the branched structure in the alkyl chain was analyzed. Herein, calcium chloride is added to the iso‐stearic acid aqueous solution. The state of the binary systems changed with the molar ratio (R) of [Ca2+]/[iso‐stearic acid]. Precipitation occurred when R was more than 0.05, whereas the mixture changed from a micelle phase (Wm) to an oil phase (O) through a liquid crystalline phase (LC) when R was less than 0.01. The polarized microscopy images and small‐angle X‐ray scattering profiles showed that the LC is in a lamellar liquid crystalline state. In addition, we evaluated the crystal structure of the precipitated material. These results showed that the iso‐stearic acid Ca salt was in the amorphous state. In contrast, the n‐stearic acid Ca salt formed only the Wm and gel phases. These findings suggest that the branched structure of fatty acids induces loose intermolecular packing of liquid crystalline structures.

In situ phase transition of microemulsions for parenteral injection yielding lyotropic liquid crystalline carriers of the antitumor drug bufalin.

In this work, we used the small angle X-ray scattering (SAXS) method for controlled preparation of in situ forming sustained-release carriers for the antitumor drug bufalin (BUF), which has very poor solubility and a considerable cardiotoxicity in a non-encapsulated state. To that aim, we exploited the pseudo-ternary phase diagram of an oil(O)/surfactant(S)/water(W) system containing medium chain capric/caprylic triglycerides (MCT) and a co-surfactant blend of Macrogol (15)-hydroxystearate (Solutol HS 15) and sorbitan monooleate (Span 80). Two compositions with different oil contents (sample B and C) were selected from the microemulsion region of the phase diagram in order to study the effect of the aqueous environment on their structural behavior. A phase transition from a microemulsion (ME) to a liquid crystalline phase (LC) was established by SAXS upon progressive dilution. The drug bufalin (BUF) was encapsulated in the microemulsions with low viscosity, whereas the release of the drug occurred from the in situ generated lamellar liquid crystalline structures. The formulations were characterized by SAXS, dynamic light scattering (DLS), cryogenic transmission electron microscopy (Cryo-TEM), rheology, drug loading and encapsulation efficiency, and in vitro release profiles. A correlation was suggested between the structures of the in situ phase-transition formed LCME formulations, the differences in their viscosities and drug release profiles. The performed cytotoxicity, cell apoptosis and pharmacokinetic experiments showed an enhanced bioavailability of BUF after encapsulation. These results suggest potential clinical applications for the obtained safe in situ phase-transition sustained-release formulations of BUF.

Deuterated phytantriol – A versatile compound for probing material distribution in liquid crystalline lipid phases using neutron scattering

Phytantriol is an interfacially-active lipid that is chemically robust, non-digestible and forms particles with internal bicontinuous cubic phase structures (cubosomes) when dispersed with non-ionic surfactants at ambient and physiological temperatures. The liquid crystalline internal structure of phytantriol-based cubosomes can be changed to alter the interfacial contact area/topology with the aqueous dispersant to trigger bioactive payload release or to alter the local membrane curvature around bound or embedded proteins. To enable the study of payload distribution, structure and transformation kinetics within phytantriol particles by neutron scattering techniques it is desirable to have access to a deuterated version of this molecule but to date a synthetic route has not been available. The first successful synthesis of phytantriol-d39 is presented here alongside a preliminary physical characterisation of related particle structures when phytantriol-d39 is dispersed using two non-ionic surfactants, Tween® 80 and Pluronic® F127. Synchrotron small angle X-ray scattering (SAXS) was used to confirm that phytantriol-d39-based nanoparticles in D2O form similar liquid crystalline structures to those of their natural isotopic abundance (phytantriol/H2O) counterparts as a function of temperature. Finally, small angle neutron scattering (SANS) with solvent contrast to match out the phytantriol-d39 structuring was used to show that the spatial correlations between the Tween® and Pluronic® non-ionic surfactant molecules are different within dispersed phytantriol-d39 particles with different liquid crystalline structures in D2O. The surfactant molecules in phytantriol-d39/Tween® 80 particles with Im3m cubic structures were found to follow a self-avoiding walk, whereas in phytantriol-d39/Pluronic® F127 particles with Pn3m cubic structures they were found to follow a more rod-like packing arrangement.

Azodendrimers as a photoactive interface for liquid crystals

ABSTRACTDendrimers with azo moieties in their peripherals (azodendrimers), which we developed, are useful as a photoactive interface for liquid crystal (LC) systems. The azodendrimer spontaneously adsorbs on a variety of interfaces, so that we can obtain photoactive surfaces without pretreatment only by introducing a small amount of the azodendrimers in LCs. We first describe our previous studies applied for a variety of LC systems such as sandwich cells, LC droplets and shells in a solvent and microparticles in LCs. Some unpublished results on nematic droplets of bent-shaped molecules demonstrate current developments in the research of the interactions between the photoswitchable dendrimer and complex liquid crystalline structures.

Discotic liquid crystals of cucurbit[7]uril (CB[7])-functionalised Laponite clays

ABSTRACTHere we demonstrate that in the presence of the small, barrel-shaped molecule cucurbit[7]uril (CB[7]) Laponite clay particles undergo a phase transition into a birefringent gel with lamellar structure and a fluid, Laponite-poor aqueous solution. We employ various characterisation methods and polarised light microscopy to study this transition and the system's structural and optical properties. Furthermore, when dried completely we obtain a layered, transparent composite film, still retaining some liquid-crystalline structure that can be rehydrated reversibly. We argue that this new system may be a model system for anisotropic patchy particles.