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Intrauterine delivery system for contraception

a delivery system and intrauterine technology, applied in the field of intrauterine delivery system for contraception, can solve the problems of reducing the success rate of medical treatment, reluctance to prescribe the required high oral dosage, and general lack of evidence-based approaches, and achieves stable amenorrhea, low side effects or related complications, and high success rate.

Inactive Publication Date: 2011-06-23
BAYER OY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0021]The object is particularly to provide an intrauterine system having a high success rate at providing earlier onset of reliably stable amenorrhea and having minimal to no side-effects or related complications.
[0022]In general, the present invention contemplates an intrauterine delivery system providing a method which not only enhances the anti-fertility action of the system but also provides reduction or elimination of abnormal or excessive bleeding, such as spotting or menorrhagia, for an extended period of time as well as reduces menstrual complaints, such as dysmenorrhea and premenstrual symptoms. Avoiding undesired menstrual bleeding always means also avoiding symptoms associated with menstrual bleeding such as dysmenorrhea and premenstrual symptoms. Some of the proposed compounds can also reduce bleeding problems in women with van Willebrand disease.
[0023]By using the intrauterine delivery system an anti-proteolytic action and a decrease of the prostaglandin activity in the endometrium and / or muscle wall of the uterus can reduce the risk of expulsion.
[0024]The therapeutically active substance capable of preventing or suppressing abnormal and / or irregular endometrial bleeding can be used in dosages that are much lower compared to the systemic treatment yet without loosing its efficacy. Since synergistic effects between progestogens and these additional compounds can be assumed, further dose reductions are possible. Therefore, the risk of undesired systemic effects would be extremely low. An atrophic endometrium could further increase the contraceptive reliability.

Problems solved by technology

Despite the availability of a number of drugs, there is a general lack of an evidence-based approach, marked variation in practice and continuing uncertainty regarding the most appropriate therapy.
Adverse effects and problems with compliance also undermine the success of medical treatment.
There has been a reluctance to prescribe the required high oral dosages of tranexamic acid due to possible side effects of the drugs such as an increased risk of thrombogenic disease (deep venous thrombosis).
The oral use of danazol may be limited by its side effect profile, its acceptability to women and the need for continuing treatment.
As a group, NSAIDs have shown to be less effective than either tranexamic acid or danazol.
However, the application does not describe any practical examples of using these intrauterine devices to introduce the compounds.
The distortion of the endometrial vasculature by the presence of an intrauterine system can be explained by the direct effect of the device on the superficial vessels causing abrasions and erosions with possible irregular bleeding and / or the pressure distortion of the device, probably transmitted through endometrial tissue and resulting in endothelian injuries with the formation of fragile and dysfunctional blood vessels in the functional zone of the endometrium.
Complete amenorrhea is achieved only in part of the users even after long-term usage, and users often report about occasional bleedings, that are irregular and not predictable.
Irregular bleeding is a common initial complaint among the users and long-term bleedings are often a reason for discontinuing the use of the system.

Method used

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  • Intrauterine delivery system for contraception
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  • Intrauterine delivery system for contraception

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0089]Core Preparation

[0090]45 parts by weight of levonorgestrel, 10 parts by weight of tranexamic acid and 50 parts by weight of poly(dimethylsiloxane-co-vinylmethylsiloxane) and 1.2 parts by weight of dichlorobenzoylperoxide-polydimethylsiloxane paste (50% of dichlorobenzoylperoxide) were mixed with a 2-roll mill. The mixture was extruded to a tube-like form with a wall thickness of 0.8 mm and outer diameter of 2.8 mm and cured by heat at +150° C. for 15 minutes, during which crosslinking took place. The crosslinked core was cut into 24 mm length.

[0091]Preparation of the Delivery System

[0092]The core was swollen in cyclohexane and pulled over the IUS body. Cyclohexane was allowed to evaporate.

example 2

[0093]Core Preparation

[0094]50 parts by weight of levonorgestrel, 50 parts by weight of poly(dimethylsiloxane-co-vinylmethylsiloxane) and 1.2 parts by weight of dichlorobenzoylperoxide-polydimethylsiloxane paste (50% of dichlorobenzoylperoxide) were mixed with a 2-roll mill. The mixture was extruded to a tube-like form with a wall thickness of 0.8 mm and outer diameter of 2.8 mm and cured by heat at +150° C. for 15 minutes, during which crosslinking took place. The crosslinked core was cut into 15 mm length.

[0095]Second core was prepared in a similar manner by using 10 parts by weight of danazol in place of levonorgestrel. The crosslinked core was cut into 8 mm length.

[0096]Membrane Preparation

[0097]99 parts of silica-filled poly(dimethylsiloxane-co-vinylmethylsiloxane), 10 ppm Pt-catalyst (of the reaction species) and 0.03 parts of inhibitor (ethynyl cyclohexanol) and approximately 0.6 parts of poly(hydrogenmethylsiloxane-co-dimethylsiloxane) crosslinker were mixed in a 2-roll mill...

example 3

[0098]Core Preparation

[0099]54 parts of commercial poly(dimethylsiloxane-co-vinylmethylsiloxane), 45.5 parts by weight of levonorgestrel, 0.4 parts of poly(hydrogenmethylsiloxane-co-dimethylsiloxane) crosslinker, 0.02 parts of ethynyl cyclohexanol inhibitor and 10 ppm of Pt-catalyst (of the reaction species) in vinyl-methyl-siloxane were mixed in a kneating mill. The mixture was extruded to a tube-like form with a wall thickness of 0.7 mm and cured by heat at +115° C. for 30 minutes and cooled.

[0100]Second core was prepared in a similar manner by using 79.5 parts of commercial poly(dimethylsiloxane-co-vinylmethylsiloxane) and in place of levonorgestrel 20 parts by weight of mefenamic acid.

[0101]Membrane Preparation

[0102]9 parts of α,ω-divinylether terminated poly(ethylene oxide)-b-poly(dimethylsiloxane) multiblock copolymer (PEO-b-PDMS), 89 parts of silica-filled poly(dimethylsiloxane-co-vinylmethylsiloxane), 10 ppm Pt-catalyst (of the reaction species), 0.03 parts inhibitor (ethyny...

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Abstract

The invention relates to a method for contraception and for reducing menstrual problems and inducing amenorrhea, wherein an intrauterine delivery device is used for the controlled release of a combination of progestogen or a drug having a progestogenic activity and at least one therapeutically active substance capable of preventing or suppressing abnormal and / or irregular endometrial bleeding over a prolonged period of time.

Description

[0001]The present invention is related to an improved method of contraception, for preventing or suppressing abnormal and / or irregular endometrial bleeding and achieving a rapid induction of amenorrhea by using an intrauterine delivery system comprising progestogen, or a drug having a progestogenic activity, for the controlled release over a prolonged period of time and at a therapeutic level required for contraception, and a sufficient amount of one or more therapeutically active substances capable of suppressing abnormal and / or irregular endometrial bleeding.[0002]The intrauterine delivery system comprises a body construction and at least one reservoir comprising a core and optionally a membrane encasing the core, the core and membrane essentially consisting of a same or different polymer composition, wherein said at least one reservoir comprises a progestogen, or a drug having a progestogenic activity, and one or more therapeutically active substances capable of suppressing abnor...

Claims

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Application Information

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IPC IPC(8): A61F6/14A61K31/56
CPCA61K9/0039A61K31/195A61K31/196A61K31/565A61K31/567A61K31/569A61K31/58A61K45/06A61K31/57A61K2300/00A61P15/00A61P15/18A61P43/00A61P7/00A61P7/04
Inventor DUESTERBERG, BERNDAHOLA, MANJAPIHLAJA, JYRKILYYTIKAINEN, HEIKKIJUKARAINEN, HARRIKLEEMOLA, SATUPARKATTI, TERO
Owner BAYER OY
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