A resin is provided for selectively binding to perchloride and related anions (e.g., TcO.sub.4.sup.−, ReO.sub.4.sup.− and I.sup.−) in aqueous solution. The resin may take the form of microparticles or beads. The beads are prepared by cross-linking macromolecules such as hyperbranched PEI, and quaternizing the amines with hydrocarbon substituents.

Disclosed is a magnetic dendrimer compound and a method for preparing the magnetic dendrimer compound, the molecular formula of which is shown in formula (I): Γ(CH.sub.2).sub.3N.sub.(2.sup.n+1.sub.−1)R.sup.1.sub.(2.sup.n+2.sub.−2)R.sup.2.sub.(2.sup.n+1.sub.)(I). In this formula, Γ indicates magnetic particles coated with SiO.sub.2 on a surface thereof, the magnetic particles having been modified by a silane coupling agent; (CH.sub.2).sub.3N.sub.(2.sup.n+1.sub.−1)R.sup.1.sub.(2.sup.n+2.sub.−2) is a dendritic group, and R.sup.2.sub.(2.sup.n+1.sub.) is a lipophilic group, with 0≤n≤100. Further disclosed is a lubricant comprising the magnetic dendrimer compound.

An electrode for an electrochemical element with an organic electrolyte includes a polymeric material containing or composed of subunits according to general formulae (I) and/or (II):

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wherein n is an integer >2, Y represents an amide group (—NH—CO— or —CO—NH—), an ester group (—O—CO— or —CO—O—) or a urethane group (—NH—CO—O— or —O—CO—NH—), R.sub.1, R.sub.2, R.sub.3 and R.sub.4 each independently represent H, alkyl (preferably —CH.sub.3, —C.sub.2H.sub.5), Alkoxy-(preferably —OCH.sub.3, —OC.sub.2H.sub.5), -halogen or —CN, Ar.sub.1 and Ar.sub.4 independently represent a bridging aryl group, Ar.sub.e and Ar.sub.a independently represent a non-bridging aryl group, and R.sub.5 is a bridging alkyl, alkene or aryl group, wherein Ar.sub.1 and Ar.sub.4 in structures (I) and (II) independently represent a bridging aryl group.

The present invention relates to a compound having a macromolecular carrier having a plurality of terminal groups, wherein the carbonyl group of serine is linked by a peptide bond or an ester bond directly or via a linker to the terminal groups, a carrier for drug delivery composed of the compound, and a medicament for preventing or treating renal diseases, containing the carrier for drug delivery and a drug bonded to the carrier directly or via a linker or encapsulated therein. According to the present invention, a carrier for drug delivery that is selectively accumulated in kidney in vivo can be provided.

A cell culture substrate for cultivating adherent cells, including: a substrate (S), a polymer (P) comprising amino groups, which is bonded to the substrate, and a saccharide (Z) having at least two monosaccharide units for attaching the adherent cells, wherein the saccharide (Z) is covalently bonded to the polymer (P) via the amino groups.

Such a cell culture substrate is suitable for cultivating adherent cells and allows the cells to be detached from the cell culture substrate in a gentle manner by adding a saccharide.

A crosslinked resin made up of polymerized units of a linear polyamine with at least 3 primary and/or secondary amine functionalities and a bisacrylamide. The crosslinked polymers are porous spherical particles with a BET surface area in the range of 50-120 m.sup.2/g. A method of the synthesizing the crosslinked polymer is specified. A method for using the crosslinked resin as an adsorbent material in removing pollutants including organic dyes (e.g. Congo red, Rhodamine B) and heavy metals from an aqueous solution or an industrial wastewater sample is also described.

There are provided herein, inter alia, cationic amphipathic polymers, complexes, and compositions comprising same, and methods for their use including for the delivery of therapeutic, diagnostic and imaging agents, including nucleic acids, into a cell. The complexes, compositions and methods may facilitate delivery and targeted release of the therapeutic, diagnostic and imaging agents to particular cell types and tissues.

A polyamide resin with an excellent balance of mechanical characteristics such as breaking strength and breaking elongation in a solid state, a molded body containing said polyamide resin, a laminate provided with a film or a sheet containing said polyamide resin, a medical device provided with the aforementioned molded body and/or the aforementioned laminate, and a production method of the aforementioned polyamide resin are provided. A polyamide resin is used which contains: a linear aliphatic dicarbonyl unit as unit (a); a linear aliphatic diamino unit as unit (b); at least one of a unit (b) and a unit (c), each of a prescribed structure; and a trivalent unit (e).

A composition for improving softness of tissue and/or towel products includes lignocellulosic fibers; water; and a hydrophobic softener that includes the reaction product of: (1) at least one di- and/or poly-amine, (2) at least one chain extender having at least two carboxyl groups; and (3) at least one hydrophobic end-capper. The reaction product comprises a hydrophobic substitution of at least about 25 mole percent of the hydrophobic end-capper based on a total number of moles of active amine sites of the reaction product. In addition, a method of improving softness of tissue and/or towel products includes combining the lignocellulosic fibers, the water, and the hydrophobic softener; and creating the tissue and/or towel products.

A pigment dispersant can be obtained by reacting amine-rich moieties C with at least one polymer P having one or more amine reactive groups. The amine-rich moieties C have an amine density of at least 600 mg KOH/g and are obtainable from repetitive self-reaction of at least one type of substance B and/or from cross-reaction of at least one B with at least one substance A. B is an adduct of at least one substance A and at least one linker D. The amine-reactive functionality in B and D are reacted with reactive amines in B and/or A; and if B has only one amine reactive group, then additional D and/or mixture of B and A is reacted to a previously formed C, where such an additional reaction of D and/or mixture of B and A to a formed C is repeated for 1 to 10 times.