Corning Incorporated

Corning S.a.

Eurokera

Coming Incorporated

David Henry

Dana Craig Bookbinder

Corinne Walerack

Jacques Jean Vial

Yue Zhou

Martial Hervy

Anthony Glenn Frutos

Valerie Claudine Lacarriere

Andre Jean Vachet

Frederic Henri Florent

Ann MeeJin Ferrie

Ye Fang

Xavier Gerard Lafosse

Sophie Deshayes

Bertrand De Lambert

Vasiliy Nikolaevich Goral

Bruno Dufour

Mark Alan Lewis

Stephen Joseph Caracci

You-Ping Chan

Philippe Lehuede

Odessa Natalie Petzold

Maxime Moreno

Jean-Jacques B Theron

Wendy Annette Baker

John Stephen Peanasky

Qi Wu

Andrei Gennadyevich Fadeev

Shawn Michael O'Malley

Olivier Breyne

Thierry L Dannoux

Arthur Winston Martin

Jessica Jo Kelley

Marie-Maud Bear

Jerome Vivien Davidovits

Gaelle Ferriz

Kristi Lynn Simonton

Christophe Michel Remy

Eric J Firtion

Oberon Denaci Deichmann

Yves A H Brocheton

Eric Gesell

Jeffery Joseph Scibek

Sylvain M Gremetz

Michele Marie-Louise Meyer-Fredholm

Mickaël Berrebi

Michele Fredholm

Philippe Sinard

Bryan Henry Smith

Xavier LaFosse

Pierre-Jean M Laroulandie

Andre Vachet

Shreya Roy Choudhury

Remy Meyrueix

Bruno Baney

C&eacute;cile Lecrivain

Cecile Lecrivain

Thomas A Bunch

Marylène Denise Madeleine Pécheul

Melanie Emilie Celine Depardieu

Gaëlle Ferriz

Haibei Hu

Paula Jean Dolley-Sonneville

Maryléne Denise Madeleine PÉCHEUL

Jérôme Davidovits

Frédéric Florent

Odessa Petzold

Wendy A Baker

Marylène Denise Madeleine Pecheul

Bertrand Delambert

According to one or more embodiments disclosed herein, a coated pharmaceutical package may comprise a glass container comprising a first surface and a second surface opposite the first surface, wherein the first surface is an outer surface of the glass container, and wherein the glass container in an uncoated state has an average light transmittance in the UVB and UVC spectrum of at least 50% through a single wall of the coated package. The coated pharmaceutical package may further comprise a coating positioned over at least a portion of the first surface of the glass container, wherein the coated pharmaceutical package has an average light transmittance in the UVC spectrum of less than 50% through a single wall of the coated package.

Ultraviolet light-blocking coated pharmaceutical packages

A cell culture article includes a substrate having a polymer coating that is conducive to colony passaging of cells cultured on the coating. Example polymer coatings are formed from polygalacturonic acid (PGA), alginate, or combinations thereof. Cells cultured on the polymer coating can be separated from the substrate as a colony or layer of cells by exposing the polymer coating to (i) a chelating agent, (ii) a proteinase-free enzyme, or (iii) a chelating agent and a proteinase-free enzyme.

Proteinase-free coatings for colony passaging

A stable aqueous suspension includes a composition which includes nanoparticles, wherein said nanoparticles include a nucleic acid at least partially encapsulated in a matrix comprising calcium phosphate. The nanoparticle compositions and suspensions have high nucleic acid loading and high stability, and may be used for protecting crops against insects and for down-regulating expression of a target gene in an insect pest species in order to prevent and/or control pest infestation.

Alkali-resistant calcium phosphate/nucleic acids hybrid carrier for pest control and method to produce the particles

According to one or more embodiments, a pharmaceutical package may include a glass container and a coating. The glass container may include a first surface and a second surface opposite the first surface. The first surface may be an outer surface of the glass container. The coating may be positioned over at least a portion of the first surface of the glass container. The coating may include one or more polyimide compositions and one or more metal oxide compositions. The one or more polyimide compositions and the one or more metal oxide compositions may be mixed in the coating.

Glass articles with mixed polymer and metal oxide coatings

Methods for limiting bleed-through of aqueous catalyst solutions in ceramic articles are described herein. The methods include applying a hydrophobic cellulose derivative, such as ethylcellulose, to an exterior surface of a fired porous ceramic article. The aqueous catalyst solution is applied to the fired porous ceramic article, such that the hydrophobic cellulose derivative limits bleed-through of the aqueous catalyst solution through at least a portion of the ceramic article. Ceramic articles with skins that limit bleed-through of aqueous catalyst solutions are also described herein.

Ceramic articles with bleed-through barrier and methods of manufacture thereof

An aqueous cell culture medium composition includes an aqueous cell culture solution configured to support the culture of mammalian cells. The composition further includes a synthetic polymer conjugated to a polypeptide dissolved in the aqueous cell culture solution. The synthetic polymer conjugated to a polypeptide is configured to attach to the surface of a cell culture article under cell culture conditions. Incubation of the aqueous cell culture medium composition on a cell culture surface under cell culture conditions results is attachment to the surface of the synthetic polymer conjugated to the polypeptide.

Synthetic attachment medium for cell culture

As described herein, a polyimide chemical composition may be used for coating glass articles. According to embodiments, a coated glass article may include a glass container which may include a first surface and a second surface opposite the first surface, and a low-friction coating bonded to at least a portion of the first surface of the glass container. The low-friction coating may include a polyimide chemical composition. The polyimide chemical composition may be halogenated and the polyimide chemical composition may include a siloxane moiety.

Halogenated polyimide siloxane chemical compositions and glass articles with halogenated polyimide siloxane low-friction coatings

A method for preparing an article, the structure of which comprises a substrate of a glass or a glass-ceramic and a coating fixed to at least one portion of the surface of the substrate. In a characteristic way, the coating is generated from at least one loaded polysilsesquioxane resin; the at least one polysilsesquioxane resin not containing any aryl radical in its structure.

Preparation of an article of a glass or a glass-ceramic having an improved coating and that article

A method for coating a surface of a cell culture article includes dissolving a polymer having a covalently attached polypeptide in an aqueous solution to produce a polymer solution. The polymer is formed from monomers selected to form a polymer having a linear backbone, wherein the polymer is crosslink free. The weight percentage of the polypeptide relative to the polymer conjugated to the polypeptide is sufficiently high to render the polymer conjugated to the polypeptide water soluble. The aqueous solution is substantially free of organic solvents. The method further includes (i) disposing the polymer solution on the surface of the cell culture article to produce a coated article; and (ii) subjecting the coated article to sufficient heat or electromagnetic radiation to attach the polymer conjugated to a polypeptide to the surface of the cell culture article.

Synthetic coating for cell culture

A method of making a cell culture article is provided. The method includes forming a microcarrier from a microcarrier composition comprising a polygalacturonic acid compound or an alginic acid compound, infiltrating the microcarrier with a drying formulation to form an infiltrated microcarrier, and drying the infiltrated microcarrier to form a dried microcarrier, wherein the drying formulation comprises at least one of a saccharide and a monovalent cation.

Drying formulation for hydrogel microcarriers

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Morigny-Champigny, France

David Henry