摘要:
The present invention relates to an applicator device for applying a product of the fluid or pasty type to keratin fibres, comprising a central core (1) having an elongate shape which extends along a longitudinal axis XX, at least one row of elongate spikes (2) comprising a first end (20) embedded in the core and a second, free end (21). According to the invention, at least one of the spikes (2) is delimited by a first flat face (200) that is coincident with a longitudinal plane, known as the reference plane P, and by a second flat face (210) that forms an angle of between 10 and 180° with said first flat face, said at least one spike comprising a first region (22) that is embedded in the core (1) and has a substantially constant cross section in the form of a portion of a circle, and a second region (23) having a variable cross section that is situated substantially in the longitudinal continuation of said first region (22).
摘要:
The present invention relates to an applicator device for a fluid or paste-like make-up and/or care product across a complex surface of the human body, having an elongated general outer shape axisymmetric about an XX axis; wherein the general outer shape thereof comprises a first rounded volume (1) connected to a second rounded volume (2) by an area (3) with a cross section smaller than the largest cross section of the first and the second volumes: where said device comprises at least one flexible longitudinal arch (10, 11) embedded in at least one point of a core (15) extending along the XX axis, where said at least one arch is suitable for defining with the core a product reservoir having a variable volume, resulting in the pumping of the product.
摘要:
A device that is connectable to a phototherapy apparatus for applying targeted phototherapy to an area of skin to place a skin condition into remission and a method of determining a maximum tolerable dose of phototherapy applied to a treatment area to determine an optimum therapeutic dose to quickly place a skin condition into remission. The dosimetry device can include a housing and an optical matrix arranged within the housing. The optical matrix includes a plurality of at least one of absorptive, reflective and/or partially transmissive regions that each permits a different percentage of light to be delivered to an individual's skin. An assessment can then be made as to the maximum tolerable dose of phototherapy that can be applied to the individual's skin in order to place a skin condition into remission.
摘要:
The invention concerns an apparatus for cleaning delicate textiles, comprising a motorized and rotating drum (1) housed in a fluid tight basket (2), at least a water inlet (20) and a fluid outlet (11), at least a first container (5) for a first chemical composition, and a heating means (4). According to the invention, the first container is appropriate to contain a warm mixture of water and the said first chemical composition, the apparatus comprises at least a conduit (51, 52; 53, 54) cooperating with a circulating means (6; 61, 62) for mixing and circulating the said warm mixture between said first container (5) and said circulating means, a means (7; 8,9) for injecting or spraying said mixture into said drum (1) and over dry textiles, said circulating means (6; 61,62) having an inlet for said warm mixture and at least an outlet cooperating with at least a first end of a conduit (71, 72) opening at its second end into the drum (1). The invention further relates to a method implemented by such an apparatus.
摘要:
The invention relates to a method for the detection of heparin-dependent antibodies and the diagnosis of immune or autoimmune pathologies potentiated by a heparin substance, such as thrombocytopenia induced by heparin (HIT type II) as inducer drug. The invention is characterized in that said method comprises the steps consisting in: 1) reacting: at least one substance with high affinity for a heparin substance (SFA), consisting of any molecule or complex having a high affinity for a heparin substance, with at least one heparin substance (SH) so as to form a substance with high affinity for heparin-heparin substance (SFA-SH) complex, wherein the heparin substance is in slight or large excess, so as to be able to bind other substances with affinity for heparin; then with at least one potential antigenic substance capable of reacting with the heparin substance, thus forming a complex (Ag-SH); and, finally, with the plasma or the serum of a patient to be tested (preferably diluted to a dilution of the order of 1:100) potentially containing: an anti(Ag-SH) antibody material generated in the organism after administration of a heparin substance, and/or at least one immune complex consisting of an Ag-SH/anti(Ag-SH) antibody complex present in the plasma or serum of the patient capable of reacting with the substance with high affinity for the heparin substance-heparin substance (SFA-SH) complex, and then, 2) revealing the resulting (Ag-SH)-anti(Ag-SH) complex produced.