Patterned Electrode Assisted One-Step Fabrication of Biomimetic Morphing Hydrogels with Sophisticated Anisotropic Structures.

Anisotropic structures are ubiquitous in nature, affording fascinating morphing behaviors. Biomimetic morphing materials can be developed by spatially controlling the orientations of molecules or nanofillers that produce anisotropic responses and internal stresses under external stimuli. However, it remains a serious challenge to fabricate materials with sophisticated anisotropic architectures. Here, a facile strategy to fabricate morphing hydrogels with elaborately ordered structures of nanosheets, which are oriented under distributed electric field and immobilized by polymerization to form a poly(N-isopropylacrylamide) matrix, is proposed. Diverse sophisticated anisotropic structures are obtained by engineering the electric field through the patterns and relative locations of the electrodes. Upon heating, the monolithic hydrogels with through-thickness and/or in-plane gradients in orientation of the nanosheets deform into various three-dimensional configurations. After incorporating gold nanoparticles, the hydrogels become photoresponsive and capable of programmable motions, for example, dynamic twisting and flipping under spatiotemporal stimuli. Such a strategy of using patterned electrodes to generate distributed electric field should be applicable to systems of liquid crystals or charged particles/molecules to direct orientation or electrophoresis and form functional structures. The biomimetically architectured hydrogels would be ideal materials to develop artificial muscles, soft actuators/robots, and biomedical devices with versatile applications.

Biomimetic amphiphiles: properties and potential use.

Surfactants are the amphiphilic molecules that tend to alter the interfacial and surface tension. The fundamental property related to the structure of surfactant molecules is their self-aggregation resulting in the formation of association colloids. Apart from the packing of these molecules into closed structures, the structural network also results in formation of extended bilayers, which are thermodynamically stable and lead to existence of biological membranes and vesicles. From biological point of view the development of new knowledge and techniques in the area of vesicles, bilayers and multiplayer membranes and their polymerizable analogue provide new opportunities for research in the respective area. 'Green Surfactants' or the biologically compatible surfactants are in demand to replace some of the existing surfactants and thereby reduce the environmental impact, in general caused by classic surfactants. In this context, the term 'natural surfactants or biosurfactants' is often used to indicate the natural origin of the surfactant molecules. Most important aspect of biosurfactants is their environmental acceptability, because they are readily biodegradable and have low toxicity than synthetic surfactants. Some of the major applications of biosurfactants in pollution and environmental control are microbial enhanced oil recovery, hydrocarbon degradation, hexa-chloro cyclohexane (HCH) degradation and heavy-metal removal from contaminated soil. In this chapter, we tried to make a hierarchy from vital surfactant molecules toward understanding their behavioral aspects and application potential thereby ending into the higher class of broad spectrum 'biosurfactants'. Pertaining to the budding promise offered by these molecules, the selection of the type and size of each structural moiety enables a delicate balance between surface activity and biological function and this represents the most effective approach of harnessing the power of molecular self-assembly.

Utilization of 3'-carboxy-containing tyrosine derivatives as a new class of phosphotyrosyl mimetics in the preparation of novel non-phosphorylated cyclic peptide inhibitors of the Grb2-SH2 domain.

A new class of phosphotyrosyl (pTyr) mimetics, distinct from the conventional pTyr mimetic design of adding non-hydrolyzable acidic functionalities to the 4'-position of phenylalanine, was created by introducing carboxy-containing groups to the 3'-position of tyrosine. The effect of the chain length of the carboxy substituent was examined. Reported herein is the chiral pool synthesis of the new pTyr mimetics, and their first use in a novel non-phosphorylated Grb2-SH2 domain binding motif with the 5-amino-acid sequence Xx1-Leu-(3'-substituted-Tyr)-Ac6c-Asn. The highest affinity was exhibited by the 3-L-(2-carboxyethyl)tyrosine-containing sulfoxide-cyclized peptide , with an IC50 = 1.1 microM, providing a promising new template for further development of potent Grb2-SH2 domain inhibitors with reduced charge and peptidic nature, but improved selectivity and bioavailability.

Biomimetics--using nature to inspire human innovation.

Evolution has resolved many of nature's challenges leading to lasting solutions. Nature has always inspired human achievements and has led to effective materials, structures, tools, mechanisms, processes, algorithms, methods, systems, and many other benefits (Bar-Cohen Y (ed) 2005 Biomimetics-Biologically Inspired Technologies (Boca Raton, FL: CRC Press) pp 1-552). This field, which is known as biomimetics, offers enormous potential for inspiring new capabilities for exciting future technologies. There are numerous examples of biomimetic successes that involve making simple copies, such as the use of fins for swimming. Others examples involved greater mimicking complexity including the mastery of flying that became possible only after the principles of aerodynamics were better understood. Some commercial implementations of biomimetics, including robotic toys and movie subjects, are increasingly appearing and behaving like living creatures. More substantial benefits of biomimetics include the development of prosthetics that closely mimic real limbs and sensory-enhancing microchips that are interfaced with the brain to assist in hearing, seeing and controlling instruments. A review is given of selected areas that were inspired by nature, and an outlook for potential development in biomimetics is presented.

1-Pentyl-3-phenylacetylindoles, a new class of cannabimimetic indoles.

A new class of cannabimimetic indoles, with 3-phenylacetyl or substituted 3-phenylacetyl substituents, has been prepared and their affinities for the cannabinoid CB1 and CB2 receptors have been determined. In general those compounds with a 2-substituted phenylacetyl group have good affinity for both receptors. The 4-substituted analogs have little affinity for either receptor, while the 3-substituted compounds are intermediate in their affinities. Two of these compounds, 1-pentyl-3-(2-methylphenylacetyl)indole (JWH-251) and 1-pentyl-3-(3-methoxyphenylacetyl)indole (JWH-302), have 5-fold selectivity for the CB1 receptor with modest affinity for the CB2 receptor. GTPgammaS determinations indicate that both compounds are highly efficacious agonists at the CB1 receptor and partial agonists at the CB2 receptor.

Emerging technologies in biocompatible surface modifying additives: quest for physiologic cardiopulmonary bypass.

Modification of polymer surfaces to achieve a surface with enhanced compatibility is an important means of obtaining improved biomaterials. The molecular design of the novel technologies is carried out with attention to create a biomembrane-mimicking surface on medical devices. This review focuses on the comparison of the chemical composition of recent novel surface modifying additives and coating technologies, their biomaterial evaluation and clinical efficacy under the scope of our previous studies and current literature.