Alnis Biosciences, Inc.

University of California

Alnis, LLC

Stephen E Barry

David S Soane

Michael G Perrott

David A Offord

Rachel Decor

Andrew Goodwin

The present invention is directed to a cryoprotective system that comprises an aqueous solution containing polymeric nano- and micro-particles that exhibit a reversible temperature-dependent volume change. It is also directed to a method for providing cryoprotection to an organism or parts of an organism by pumping the cryoprotective system into the vasculature of the organism prior to exposing the organism to a lower, preferably below 0&#xb0; C., temperature.

Cryoprotective system comprising polymeric nano- or micro-particles

Synthetic polymer complements (SPCs) are provided, as well as methods for their synthesis and use. The SPCs may have surfaces that include functional groups that are complementary to surface sites of targets such as nanostructures or macromolecular targets, and may be capable of specifically interacting with such targets. The positions of the functional groups in one embodiment are stabilized by a polymer network. The SPCs are formed by contacting the target with a set of monomers which self-assemble on the target, and then are polymerized into a network to form the synthetic polymer complement. At least a portion of the surface of the resulting SPC thus may include an imprint of the target. The complex of the SPC and the target may be the desired product. Alternatively, the target is released, for example, by controllably expanding and contracting the crosslinked network. The SPC is isolated and used in many applications.

Molecular compounds having complementary surfaces to targets

Synthetic polymer complements (SPCs) are provided, as well as methods for their synthesis and use. The SPCs range in size from about 20 to about 1000 nm. The SPCs have surfaces that are complementary to surface sites of target molecules, resulting in the ability of the SPCs to selectively bind to molecular targets. The molecular recognition capability of these particles enables their use in diagnostic, therapeutic, and separation applications. The SPC is formed by contacting a target template molecule with a set of building blocks solubilized in the interior of a liposome, which building blocks are then polymerized into a network to form the synthetic polymer complement in the interior of the liposome. The target templates are removed to produce complementary sites in a SPC that map the surface of the target, resulting in a water-soluble SPC nanoparticle of similar dimensions as the interior of the liposome that originally supported it and capable of molecular recognition.

Liposome-assisted synthesis of polymeric nanoparticles

Articles exhibiting non-linear optical properties useful as electrooptic devices are prepared where the dopant moieties are aligned at relatively low temperatures. An intermediate article is formed by swelling with a diluent including a pressurized gas, such as carbon dioxide. The dopant moieties dispersed in the polymer are aligned by applying an electric field while maintaining the polymer in the swollen state caused by diluent sorption. Substantially all the diluent can then be removed without the necessity of a temperature elevation above about room temperature since the pressurized gas of the diluent can be removed by lowering the pressure to about atmospheric conditions. Polymers with high glass transition temperatures, preferably at or above about 150.degree. C., can thus be used in preparing electrooptic devices.

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Oakland, CA, United States of America

Stephen E Barry