摘要:
A medical apparatus for the extracorporeal treatment of blood or plasma comprises a semi-permeable membrane consisting of at least one electronegative polymer, such that the surface of the semi-permeable membrane has negative electric charges. Before the sterilization of the apparatus, and before or after the formation of the membrane, at least one cationic and anti-protease agent is incorporated in at least one part of the membrane, this agent undergoing bulk adsorption or semi-bulk adsorption in the membrane and/or being bound by an ionic interaction with the electronegative sites of the membrane.
摘要:
The invention relates to the use of a neutral or cationic polymer for preventing activation of the contact phase of blood or plasma which comes into contact with a semi-permeable membrane based on polyacrylonitrile bearing fixed negative charges, which is fitted in apparatus for the treatment of blood or plasma by extra-corporal circulation, by combination of the neutral or cationic polymer, before or after formation of the membrane and before its sterilization, so as to modify the electrical properties of the membrane, the Zeta potential “Z” and the electrical resistivity “R” in order to obtain: either an electrokinetic index “I” of less than or equal to 0.8, “I” corresponding to Log10 (|Z|/R), or a positive Zeta potential “Z” of between 0 and 15 mV (limits not included).
摘要翻译:本发明涉及中性或阳离子聚合物用于防止与基于聚丙烯腈的半透膜接触的血液或血浆的接触相活化的固定负电荷的用途,所述聚乙烯腈装在用于治疗 通过体外循环的血液或血浆,通过中性或阳离子聚合物的组合,在膜的形成之前和之后并在其灭菌之前,以改变膜的电性能,Zeta电位“Z”和电 电阻率“R”,以获得小于或等于0.8的电动指数“I”,对应于Log10(| Z | / R)的“I”或0和15之间的正Zeta电位“Z” mV(不包括限制)。
摘要:
A method for preventing activation of the contact phase of blood or plasma which comes into contact with a semi-permeable membrane based on polyacrylonitrile bearing fixed negative charges, which is fitted in apparatus for the treatment of blood or plasma, by extra-corporal circulation, said method comprising contacting blood or plasma with said semi-permeable membrane, wherein: a neutral or cationic polymer is combined with said semi-permeable membrane before or after formation of the membrane, and before sterilization of the membrane; the overall ionic capacity of the semi-permeable membrane, based on polyacrylonitrile bearing fixed negative charges and containing a neutral or cationic polymer, is negative; the overall ionic capacity of the semi-permeable membrane, based on polyacrylonitrile bearing fixed negative charges and containing a neutral or cationic polymer, is, as an absolute value, not more than 10% less than the overall ionic capacity of the same semi-permeable membrane without a neutral or cationic polymer, at least one of said polymer being present at the surface of the membrane; the semi-permeable membrane based on polyacrylonitrile bearing fixed negative charges and containing a neutral or cationic polymer complies, before sterilization, with the following two electrical characteristic: the electrokinetic index “I” is less than or equal to 0.8, “I” being equal to the logarithm, in base 10, of the ratio |Z|/R, where “Z” is the Zeta potential, as an absolute value, expressed in microvolts, of the surface of the membrane intended to come into contact with blood or plasma, and where “R” is the electrical resistivity of the membrane, expressed in ohm.centimeters, and the Zeta potential “Z” is negative.
摘要:
A coupling is connectable to an access of a blood compartment. The compartment has at least one inner surface intended to be coated with at least one molecular layer of a substance soluble in an aqueous solution and capable of increasing biocompatibility. A determined quantity of the substance is deposited inside the coupling in a form such that the substance is capable of undergoing, substantially without deterioration, an irradiation capable of sterilizing the coupling.
摘要:
An apparatus for the treatment of blood or plasma by extracorporeal circulation includes a compartment for the circulation of blood. The compartment is provided with two accesses and has at least one inner surface intended to be coated, after sterilization, with at least one molecular layer of a substance soluble in an aqueous solution. The aqueous solution is capable of increasing the bicompatibility of the inner surface of the compartment. A determined quantity of the substance is deposited inside the blood compartment, at one of the accesses, in a form such that the substance is capable of undergoing, substantially without deterioration, an irradiation capable of sterilizing the apparatus. The quantity of substance is determined such that the circulation of a determined volume of aqueous solution through the blood compartment, starting from the access where the substance has been deposited, should result in the formation, by durable bonding, of at least one molecular layer of the substance on the inner surface of the blood compartment to be treated.