36results about How to "Sufficient hydrophilicity" patented technology

A method for covering a set of open microchannel structures which are fabricated on a planar surface made of plastics and which comprise two or more part areas that have different surface characteristics. The method comprises the steps of: a) providing the surface comprising the set of microchannel structures; b) providing a lid-forming sheet having on one side an even layer of a thermoglue; c) applying the side of the sheet having the thermoglue against the surface carrying the microchannel structure; d) heating the assembly created in step (c) to selectively liquefy the hot-melt adhesive while at the same time pressing the sheet material and the planar surface of the substrate together; e) permitting the resulting laminate-covered microchannel structure to cool. An assembly comprising (a) a planar substrate, the surface of which has a set of one or more open microchannel structures each of which comprises part areas representing different functionalities, and (b) a lid-forming material covering said set of microchannel structures and having one or more openings going from a microchannel structure to ambient atmosphere. The assembly is characterized in that the joint between said surface and said sheet material is a thermoglue that possibly has been cured.

Dipeptide and tripeptide ester derivatives of acyclovir and its analogs are disclosed which are useful to treat herpes virus infections. Also disclosed is a method for preparing a therapeutic agent for targeted delivery to ocular tissue comprising linking the therapeutic agent to one or more groups of the formula —X—Y-Z_(n)-R; wherein each X, Y and Z is independently Met, Val, Thr, Tyr, Trp, Ser, Ala or Gly; each R is independently H or an amino-protecting group; and each n is independently 0 or 1.

Endblocked polysiloxanes with lateral amino functions and at least one further lateral and/or terminal functional group.

The present invention provides a hydrophilic film that has high adhesion to inorganic materials and is safer and excellent in transparency and also exhibits both very high hydrophilicity and abrasion resistance, and also provides a laminate including the hydrophilic film. The hydrophilic film is produced by applying a specific hydrophilic compound (c) having an acryloyl group and a potassium sulfonate group or the like to a surface of a layer formed from a mixture containing a silane compound (a) including one silicon atom, a mercapto group or the like, and at least one silicon-bonded group selected from the group consisting of an alkoxy group, a halogen group, and a hydroxy group, and a silane compound (b) including at least four silicon-bonded groups selected from the group consisting of an alkoxy group, a halogen group, and a hydroxy group and not including groups reactive with a carbon-carbon double bond, and allowing a reaction between at least a part of acryloyl groups contained in the hydrophilic compound (c) and at least a part of mercapto groups derived from the compound (a).

A process for producing amino-functional polysiloxanes by reacting the components A) identical or different terminally hydroxy-functional, linear or branched polysiloxanes, B) identical or different alkoxysilanes of the formula

R¹_xR²_3-xSiR³  (I)

where R¹ is identical or different alkyl radicals having 1 to 4 carbon atoms, R² is identical or different alkoxy radicals having 1 to 4 carbon atoms, R³ is an organic radical having at least one nitrogen atom, x=0 to 2, and C) water, in the presence of D) one or more phosphorus-containing, Brønsted-acidic compounds, to the correspondingly obtainable polysiloxanes containing nitrogen-containing groups, and to the use thereof are provided.

Stereochemically defined dipeptide esters of nucleoside-analogous antiviral agents including acyclovir and ganciclovir are provided. Certain of these stereochemically defined dipeptide esters are found to have unexpectedly enhanced delivery to and uptake by ocular tissues, crossing the blood-ocular barrier more effectively than other stereochemically defined dipeptide esters. For example, (L-Val)-(D-Val)-acyclovir was found to be taken up more effectively into corneal tissue than were underivatized acyclovir, monoesters (L-Val)-acyclovir or (D-Val)-acyclovir, or diester (L-Val)-(L-Val)-acyclovir.

The invention discloses an electro-Fenton cathode material based on lignin and a preparation method thereof. The preparation method includes the following steps that (1) a carbon-based material is preprocessed; (2) electrochemical polymerization deposition is carried out; and (3) an obtained conducting polymer monomer/lignin copolymerization cathode material is cleaned with deionized water and naturally dried at room temperature, and the electro-Fenton cathode material is obtained. Compared with a traditional chemical modification method, the prepared electro-Fenton cathode material is advantageous in that use of toxic reagents and complex treatment are reduced, electrode modification is achieved at one step, preparation cost is low, and electrode manufacturing industrialization is easily achieved; and modified electrodes are used for electro-Fenton systems, so that electron transfer and the oxygen reduction process of dual electrons are facilitated, the yield of hydrogen peroxide is remarkably increased, and the discoloration, degradation and mineralization degree of pollutants is further increased.

Some embodiments are directed to a support for receiving a biological sample, the support comprising at least one support member, and including graphene attached to the support member. The graphene is partially hydrogenated graphene. Some embodiments are also directed to use of a partially hydrogenated graphene surface to support a biological molecule for electron microscopy. Some other embodiments are also directed to a method for making a partially hydrogenated graphene. The method includes applying a hydrogen ion or hydrogen atom to the surface of graphene. The hydrogen ion or hydrogen atom is applied at an energy in the range 1 to 21 eV. A sensor comprising a surface capable of adsorbing a biological molecule thereto is also disclosed, wherein said surface includes partially hydrogenated graphene.

The invention is related to a dental impression composition which is curable at a temperature below about 50 C, the composition comprising: (A) a curable organopolysiloxane polymer as component (A), (B) a crosslinker compound capable of cross-linking said organopolysiloxane polymer as component (B), (C) a catalyst as component (C) capable of catalyzing a crosslinking reaction of component (A) and component (B), (D) a hydrophilizing agent as component (D), (E) a filler as component (E), (F1) a stabilizer as component (F1) selected from compounds comprising a phosphite moiety and mixtures thereof, (F2) a stabilizer as component (F2) selected from antioxidants and mixtures thereof, the composition being present in the form of a base paste and a catalyst paste physically separated from another, the base paste comprising components (A), (B), (D), (E), (F1), (F2), the catalyst paste comprising components (A), (C), (E).