Abstract: The resin anchor comprises an apertured tubular envelope designed to be compressed by a traction element, characterized in that it includes, on the inside of the envelope, a resin component and a hardener component that are intended to be mixed together and to cure under the action of the compression of the envelope (1), in order to fasten the anchor, at least one of the two components being sacheted, the mix formed from the two components being expelled out of the envelope via its apertures, during its compression. The traction element may be a screw that cooperates with the end element of the bushing CD forming a nut. The anchor is fastened both mechanically and chemically, for either solid material or hollow material.

Abstract: The resin anchor comprises an apertured tubular envelope designed to be compressed by a traction element, characterized in that it includes, on the inside of the envelope, a resin component and a hardener component that are intended to be mixed together and to cure under the action of the compression of the envelope, in order to fasten the anchor. The traction element is a stud having a threaded rod part that cooperates with a tapped traction element firmly attached to the end of the bushing. The anchor is fastened both mechanically and chemically, for either solid material or hollow material.

Abstract: The resin anchor comprises an apertured tubular envelope designed to be compressed by a traction element, characterized in that it includes, on the inside of the envelope, a resin component and a hardener component that are intended to be mixed together and to cure under the action of the compression of the envelope (1), in order to fasten the anchor, at least one of the two components being sacheted, the mix formed from the two components being expelled out of the envelope via its apertures, during its compression. The traction element may be a screw that cooperates with the end element of the bushing CD forming a nut. The anchor is fastened both mechanically and chemically, for either solid material or hollow material.

Abstract: The resin anchor comprises an apertured tubular envelope designed to be compressed by a traction element, characterized in that it includes, on the inside of the envelope, a resin component and a hardener component that are intended to be mixed together and to cure under the action of the compression of the envelope, in order to fasten the anchor. The traction element is a stud having a threaded rod part that cooperates with a tapped traction element firmly attached to the end of the bushing. The anchor is fastened both mechanically and chemically, for either solid material or hollow material.

Abstract: A packaging forming a parallelepipedal display unit includes a first opening element forming a display opening disposed on a first side and a second opening element forming a second display opening disposed on a second side intersecting with the first side. The display unit is usable in one of at least two distinct positions after detaching one or the other of the first and second opening elements. An information label is disposed astride the intersection of the first and second sides and on the two adjacent sides.

Abstract: A method of enhancing the efficiency and increasing the duration of action of drugs (e.g. dihydropyridines and anti-bacterials) and particularly of nifedipine and penicillins wherein one or more hydrogen atoms are deuterated and wherein the deuterated drug has unexpectedly improved properties when used in much lower concentrations than unmodified drug. A method for determining the identity and bioequivalency of a new drug is also disclosed wherein the molecular and isotope structure of a new drug is determined by isotope ratio mass spectrometry and compared with the molecular and isotope structure of a known human drug.

Abstract: A method of enhancing the efficiency and increasing the duration of action of drugs (e.g. dihydropyridines and anti-bacterials) and particularly of nifedipine and penicillins wherein one or more hydrogen atoms are deuterated and wherein the deuterated drug has unexpectedly improved properties when used in much lower concentrations than unmodified drug. A method for determining the identity and bioequivalency of a new drug is also disclosed wherein the molecular and isotope structure of a new drug is determined by isotope ratio mass spectrometry and compared with the molecular and isotope structure of a known human drug.

Abstract: The packaging forming a parallelepipedal display unit made of cardboard or some other similar material, is characterized in that it comprises a first opening means (11, 21, 31, 41) and a second opening means (52) disposed on either side of a first edge (13), allowing use as a display unit in one of at least two distinct positions following the detachment of one or other of the said means.

Abstract: A method of enhancing the efficiency and increasing the duration of action of drugs (e.g. dihydropyridines and anti-bacterials) and particularly of nifedipine and penicillins wherein one or more hydrogen atoms are deuterated and wherein the deuterated drug has unexpectedly improved properties when used in much lower concentrations than unmodified drug. A method for determining the identity and bioequivalency of a new drug is also disclosed wherein the molecular and isotope structure of a new drug is determined by isotope ratio mass spectrometry and compared with the molecular and isotope structure of a known human drug.

Abstract: A method of enhancing the efficiency and increasing the duration of action of drugs (e.g. dihydropyridines and anti-bacterials) and particularly of nifedipine and penicillins wherein one or more hydrogen atoms are deuterated and wherein the deuterated drug has unexpectedly improved properties when used in much lower concentrations than unmodified drug. A method for determining the identity and bioequivalency of a new drug is also disclosed wherein the molecular and isotope structure of a new drug is determined by isotope ratio mass spectrometry and compared with the molecular and isotope structure of a known human drug.

Abstract: A method of enhancing the efficiency and increasing the duration of action of drugs (e.g. dihydropyridines and anti-bacterials) and particularly of nifedipine and penicillins wherein one or more hydrogen atoms are deuterated and wherein the deuterated drug has unexpectedly improved properties when used in much lower concentrations than unmodified drug. A method for determining the identity and bioequivalency of a new drug is also disclosed wherein the molecular and isotope structure of a new drug is determined by isotope ratio mass spectrometry and compared with the molecular and isotope structure of a known human drug.

Abstract: The present invention relates to an antihypertensive composition comprising N-desmethyl, deacetyl diltiazem in association with a pharmaceutically acceptable carrier.

Abstract: A machine for placing stored objects on grill stand is disclosed which has a plate carrying the grills to be filled and which successively moves them under a plurality of distributing stations. The distributing stations are continuously fed pins from bulk pin bins, and have pin transfer carriages to transfer pins between the distributing stations and grills. Individual push rod sets cooperate with the transfer carriages to make the pins go from the transfer carriages into the grills. Suitable mechanisms control the longitudinal and crosswise movement of the transfer carriages above the grills so that at each loading station, a row of the grill is filled, preferably in two passes, the pins of the row being distributed successively in alternating pockets.