Abstract: A subject matter of the invention is a batchwise process for the manufacture of an optical fiber made of polymers, the core of the fiber being based on methyl methacrylate. This process is carried out in an in-line plant leaktight with respect to the outside ranging from a device for the purification of the starting materials to a spinning device, involving the intermediacy of an intermediate storage region. The core of the fiber is prepared from beads of a polymer based on purified methyl methacrylate obtained by aqueous suspension polymerization. Another subject matter of the invention is an in-line plant for the implementation of this process.

Abstract: A subject matter of the invention is a batchwise process for the manufacture of an optical fiber made of polymers, the core of the fiber being based on methyl methacrylate. This process is carried out in an in-line plant leaktight with respect to the outside ranging from a device for the purification of the starting materials to a spinning device, involving the intermediacy of an intermediate storage region. The core of the fiber is prepared from beads of a polymer based on purified methyl methacrylate obtained by aqueous suspension polymerization.

Abstract: Methods for the detection of a nucleotide sequence of interest comprising at least one nucleotide probe marked with a tracer. The methods include a reagent essentially comprising a linear backbone copolymer having lateral substituents, whose chain consists of a first type of repetitive unit and at least one other type of repetitive unit, in which at least one part of the units of the first type have a lateral substituent comprising a nucleotide unit, such a lateral substituent not being present on the other types of units. Each of said nucleotide units, all of which are identical, comprise at least one nucleotide sequence capable of hybridizing with said sequence of interest and nucleotide sequence capable of hybridizing with a probe, the reagent containing on average more than two of said nucleotide units, in molar equivalents, per mole of polymer. Such a reagent enables signal amplification to be obtained, and therefor lowers the sensitivity threshold.

Abstract: Device for capturing a target molecule for the purpose of detecting it and/or assaying it, including a solid support on which is immobilized a ligand, the ligand being provided in the form of a conjugate resulting from the covalent coupling of a polymer with a plurality of molecules of the ligand. The polymer is an N-vinylpyrrolidone copolymer, and the conjugate is immobilized on the solid support by adsorption.When the ligand is capable of forming a complex with the target, the device is specific for a given target. When the device comprises, in addition, a bifunctional reagent capable of forming a complex, on the one hand, with the ligand and, on the other hand, with the target, the support on which the ligand is immobilized constitutes a universal capturing system.

Abstract: Methods for the detection of a nucleotide sequence of interest comprising at least one nucleotide probe marked with a tracer. The methods comprise use of a reagent essentially comprising a linear backbone copolymer having lateral substituents, whose chain consists of a first type of repetitive unit and at least one other type of repetitive unit, in which at least one part of the units of the first type have a lateral substituent comprising a nucleotide unit, such a lateral substituent not being present on the other types of units. Each of said nucleotide units, all of which are identical, comprise at least one nucleotide sequence capable of hybridizing with said sequence of interest and nucleotide sequence capable of hybridizing with a probe, the reagent containing on average more than two of said nucleotide units, in molar equivalents, per mole of polymer. Such a reagent enables signal amplification to be obtained, and therefor lowers the sensitivity threshold.