WO2011033328A1 - Dispositif de micro-perfusion à dosage d'insuline destiné au traitement du diabète - Google Patents
Dispositif de micro-perfusion à dosage d'insuline destiné au traitement du diabète Download PDFInfo
- Publication number
- WO2011033328A1 WO2011033328A1 PCT/HU2010/000098 HU2010000098W WO2011033328A1 WO 2011033328 A1 WO2011033328 A1 WO 2011033328A1 HU 2010000098 W HU2010000098 W HU 2010000098W WO 2011033328 A1 WO2011033328 A1 WO 2011033328A1
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- WO
- WIPO (PCT)
- Prior art keywords
- fibres
- micro
- infusion device
- insulin
- reservoir
- Prior art date
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- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 title claims abstract description 84
- 102000004877 Insulin Human genes 0.000 title claims abstract description 42
- 108090001061 Insulin Proteins 0.000 title claims abstract description 42
- 229940125396 insulin Drugs 0.000 title claims abstract description 42
- 238000001802 infusion Methods 0.000 title claims abstract description 31
- 206010012601 diabetes mellitus Diseases 0.000 title abstract description 4
- 239000000243 solution Substances 0.000 claims abstract description 30
- 239000004753 textile Substances 0.000 claims abstract description 29
- 238000002347 injection Methods 0.000 claims abstract description 14
- 239000007924 injection Substances 0.000 claims abstract description 14
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 239000013543 active substance Substances 0.000 claims abstract description 9
- 238000000034 method Methods 0.000 claims abstract description 6
- 238000007920 subcutaneous administration Methods 0.000 claims abstract description 6
- 230000002459 sustained effect Effects 0.000 claims abstract description 4
- 239000007787 solid Substances 0.000 claims description 19
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- 239000004033 plastic Substances 0.000 claims description 12
- 229920000742 Cotton Polymers 0.000 claims description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000004744 fabric Substances 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 7
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- 230000007935 neutral effect Effects 0.000 claims description 5
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- 229920002994 synthetic fiber Polymers 0.000 claims description 4
- 235000013311 vegetables Nutrition 0.000 claims description 4
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- 229960004418 trolamine Drugs 0.000 claims description 2
- 230000001737 promoting effect Effects 0.000 claims 1
- 210000003491 skin Anatomy 0.000 description 26
- 229940079593 drug Drugs 0.000 description 10
- 239000003814 drug Substances 0.000 description 10
- 239000000835 fiber Substances 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 6
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
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- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
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- 230000036512 infertility Effects 0.000 description 2
- 238000010254 subcutaneous injection Methods 0.000 description 2
- 239000007929 subcutaneous injection Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- -1 troiamine Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
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- 241000219146 Gossypium Species 0.000 description 1
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- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 239000004141 Sodium laurylsulphate Substances 0.000 description 1
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
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- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
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- 235000012054 meals Nutrition 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000000813 peptide hormone Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/141—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor with capillaries for restricting fluid flow
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/142—Pressure infusion, e.g. using pumps
- A61M5/14244—Pressure infusion, e.g. using pumps adapted to be carried by the patient, e.g. portable on the body
- A61M5/14248—Pressure infusion, e.g. using pumps adapted to be carried by the patient, e.g. portable on the body of the skin patch type
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/158—Needles for infusions; Accessories therefor, e.g. for inserting infusion needles, or for holding them on the body
- A61M2005/1581—Right-angle needle-type devices
Definitions
- Insulin dosing micro-infusion device useful for the treatment of diabetes
- the present invention relates to an insulin-dosing micro-infusion device useful for the treatment of diabetes, i.e. for delivering the daily need of insulin, as well as to the method for the use thereof.
- the objective of the invention was to provide a device for administering insulin that is more advantageous compared to the known solutions, which is physically more convenient and less expensive for the patients.
- the device according to the invention similarly to the known insulin pumps - there is no need for several injections a day, at the same time the costs involved are incomparably lower than in case of pumps.
- the insulin pump is very expensive, which the majority of people can hardly afford or cannot afford at all.
- Another drawback of the pumps is that in addition to their expensiveness they have to be changed every two or four years.
- the invented solution provides, by a method based on the principle of capillarity, the continuous administration of the active ingredient through a simple porous textile, e.g. cotton or cloth, and the supply thereof via a replaceable reservoir.
- a subcutaneous injection set is prepared, which comprises a valve/connecting means on the outer side of its part that can be stuck to the skin, and a flexible cannula to be inserted into the skin by an apparatus, e.g. by a needle on the part to be placed on the skin, and following the placement of the device the solution of the active ingredient is supplied from an outer device (syringe, infusion pump etc.) for continuous or repeated subcutaneous administration, without the need of another insertion.
- WO 03/026728 Al discloses a transcutaneous infusion device consisting of a microinjector attached to the skin and equipped with a cannula which can be inserted in a similar manner as described above and of a replaceable feeding device connectable thereto, which is operated by an external force, e.g. by spring force.
- Hungarian patent specification No. HU 222,342 Bl relates to a transcorneal drug-release system comprising an active substance reservoir and micro-pins or micro-blades placed on its side next to the skin, said micro-pins having a length corresponding at least to the thickness of the corneal layer of the skin.
- the device comprises an electronically controlled pump as well.
- US Patent Specification No. 3,964,482 describes a drug delivery system for percutaneously administering a drug, comprising a drug reservoir attachable to the skin and a plurality of tubular projections placed on its side to be attached to the skin, and the delivery of the drug is ensured by diffusion or osmotic pressure.
- this new insulin delivery system is a micro-infusion device for the subcutaneous administration of an insulin injection composition, ensuring sustained activity, comprising a fixed carrier which contains porous textile fibres, imposable on the skin surface of the body, insertable under the skin and containing an element ensuring the tightness of the fibres, and also comprising a replaceable reservoir connected to the carrier, storing the solution of the active substance and ensuring the continuous dosing thereof, wherein the fibres coming out of the reservoir are in contact with the fibres in the fixed carrier.
- the present invention offers the above benefits.
- micro-infusion device 1 according to the invention is shown in Figure 6. As it appears from the Figure, the micro-infusion device 1 consists of a replaceable reservoir 2 containing porous textile fibres 1 14 and a fixed carrier 3 or 4 also containing porous textile fibres 1 14.
- One of the main components of the invention is the mobilizable, replaceable infusion reservoir 2 containing the insulin. It can be replaced even several times a day thus permitting a dosage according to individual needs.
- the fittings are always perfect, i.e. the sealing is airtight, thereby excluding practically any infection.
- the reservoir 2 is made of a suitable synthetic material or maybe glass, with a volume capacity of 0.1 ml to 10.0 ml, preferably 0.5 ml.
- the micro-infusion device 1 is capable of subcutaneously delivering this small amount of insulin into the body continuously and evenly through a whole day.
- compositions for infusion are to be used in therapy when the amount of the solution to be administered parenterally is so high (more than 30 ml), which cannot be performed by injection. In this case the infusion, the amount of which generally exceeds 500 ml, is applied intravenously.
- the administration of micro- or milligrams of insulin is based on the theory and practice that the insulin is absorbed from the reservoir 2 through the porous textile, fabric etc., e.g. cotton or cloth fibre(s) 1 14 on the basis of the principle of capillarity and then it is delivered by diffusion, with the aid of the fixed carrier, to the blood-stream.
- the porous textile, fabric etc. e.g. cotton or cloth fibre(s) 1 14 on the basis of the principle of capillarity and then it is delivered by diffusion, with the aid of the fixed carrier, to the blood-stream.
- the other main component of the invention is therefore the fixed carrier which is to be placed on one side onto a suitable surface of the body (insert and stick) and on the other side the reservoir 2 is to be connected thereto.
- the two main components of the invention are connected by the porous textile fibres 1 14 ensuring the capillarity and constituting the essence of the invention.
- the insulin can be delivered under the skin by two variants of the fixed carrier.
- Figure 1 shows the solid insertion needle, metal lance 6 positioned in the fixed carrier comprising a plastic tube 4, which needle is provisionally positioned in the plastic tube of the fixed carrier 4.
- Figure 2 shows the solid metal lance 5 immovably positioned in the fixed carrier 3, which serves for inserting the textile fibres into the skin and keeping them tight.
- Figure 3 shows the side-view of the fixed carrier comprising the plastic tube 4.
- Figure 4 shows the fixed carrier 3 comprising the solid metal lance 5 immovably.
- the material of the solid metal lance 5 having a size and form specifically designed for this purpose as well as the material of the solid insertion needle 6 corresponds to the material of the currently used steel needles for injection and infusion.
- the textile fibres can be combined both in quality and quantity.
- the surface of the desired capillary is formed by using fibres of identical thickness and quality (porosity) and by fixing the fibres always at the same points.
- the textile can be vegetable, animal or synthetic fibre or any mixture thereof with arbitrary ratio and quality; the vegetable fibre can be, for example, cotton, hemp, flax, etc., and the animal fibre can be, for example, wool.
- the cotton and the retirement cloth are preferred.
- the synthetic fibre can be, for example, nylon fibre etc.
- the textile fibres 1 14 and the capillaries therein need continuity in the micro-infusion device 1. They have to be free from wrinkles and buttoning. Furthermore, a minimal space is to be provided for swelling of the fibres. When assembling the fixed carrier 3 or 4 and the replaceable reservoir 2, a continuity has to be maintained in contacting the fibres.
- the suitable space is ensured by the tubes 1 17 on the fixed carriers 3 and 4, said tubes having a length of 2 mm and intruding into the skin, as shown in Figures 3 and 4; and the thickness of the windowed, biocompatible tube 120 and the size of the windows on the fixed carrier 4 as well as the constraininjury" in the skin, caused by the 1.6 mm diameter head of the solid lance 5 intruding into the skin in case of the fixed carrier 3.
- the tightness of the fibres is guaranteed also by the windowed, biocompatible tube 120 and the lance 5.
- the textile fibres are fastened to the two opposite sides of the sphere along the line of the diameter.
- the rate of delivering the (solution of the) active substance can be controlled by adjusting the size of the capillary surface, the concentration of the solution and the composition of the solvent.
- the device 1 provides a slow, extended dissolution and effect for several hours. If the patient applies a reservoir 2 containing a daily amount of insulin, expressed in the international unit (IU), by adjusting the above parameters the patient can ensure for himself the necessary amount of insulin for 24 hours subject to having regular and conscious meals and physically training his body.
- IU international unit
- micro-infusion method is suitable for the transdermal delivery of any other drugs, the therapeutic effect of which can be achieved by a very small quantity (e.g. hormones etc.).
- Such a substance is the peptide hormone, the insulin, as used herein.
- the insulin is used in the form of a solution, because the capillary flow can occur in such a form only.
- the solution of the insulin reaches the tissue fluids under the skin, the capillaries with the required speed and in the required quantity. This can be achieved by the solvent used.
- micro-infusion device developed according to the invention consists of two main parts, components:
- the comfortably fixed carrier 3 or 4 which has to be placed on a suitable surface of the body (insert and stick).
- the reservoir 2 comprising a suitable concentration of the solution of the insulin and porous fibres 1 14, which has to be slid, positioned on the carrier.
- the placed carriers have to be placed by using thin (e.g. 0.3 mm) and short (max. 15 mm or 20 mm length) solid metal lances 5 or 6 with the aim of delivering the cotton or cloth fibres 1 14 (at 90o angle with the body surface, i.e. perpendicularly) to the bottom of the skin to a maximum depth of 10 mm, thereby ensuring the spatialtightness" of the fibres, while the whole carrier is fixed by sticking the self-adhesive surface to the skin.
- the concrettightness is provided by the plastic tube 120, thus following the setting, the insertion needle used as an aid, i.e. the lance 6, can be removed immediately, but fixing is performed by sticking in this case, too.
- the size and the structure of the solid lance 6 in figure 1 are the following: the lance, insertion needle 6 has a holder 101 of 10-20 mm (the portion 102 of the solid lance, insertion needle 6 in the carrier depends on the height of the carrier),
- the section 103 of the solid lance, insertion needle 6 in the skin is maximum 10 mm long
- the diameter of the solid lance, insertion needle 6 is 0.3 mm
- the head 105 of the solid lance, insertion needle 6 has a length of 0.5 mm.
- the lance, insertion needle is drawn out, removed from the skin.
- Figure 2 shows the fibre-holding eye 106 of the solid lance 5, having an inner width of 0.5 mm, total width of 1.1 mm, the widened part of the fibre-holding eye 106 being the head 1 12 of the solid lance, having a length of 2.0 mm and a diameter of 1.6 mm, and a 8-mm section of the handle 1 10 of the lance 5, measured from the head 1 12, being in the skin (together with the eye 106).
- the remaining part is fixed in the carrier.
- the solid lance 5 is fastened in the carrier 3 and it serves for delivering the textile fibres 1 14 into the skin and for keeping them tight.
- the porous textile fibres 1 14 are fastened to the inner surface of the semi- spherical carrier by the fixing element 1 13.
- the other end of the porous textile fibres 1 14 is fastened to the end of the windowed, biocompatible plastic tube 120 being in the skin.
- the spherical reservoir 2 containing the carrier 4 and the solution of the active substance as well as the identical textile fibres 1 14 are fixed by the guiding or bearing rail 1 15.
- the carrier 4 is fixed to the skin surface by a round sticker 1 16, a self-adhesive patch (0 40 mm).
- the permanent hole in the epidermis is maintained by a tube 1 17, having an inner diameter of 1.0 mm, wall thickness of 0.3 mm and a length of 2.0 mm, which can be a short, intact section of the windowed, biocompatible plastic tube 120, directly above the window, while in case of the lance the relating part 1 17 of the fixed, semi-spherical carrier 4 is extended; the height of the semi-spherical fixed carrier 4 being 6 mm; the semi- spherical fixed carrier 4 being fastened to the self-adhesive patch 1 16 by the element 1 19.
- the maximum length of the skin penetrating, partially windowed, biocompatible plastic tube 120 is 10 mm; said tube maintains the tightness of the textile fibres 1 14 in addition to serving for the penetration of the active substance.
- the porous textile fibres 1 14 are thread through the hole 106 above the lance-head 1 12 and taken back to the inside of the semi-sphere.
- the two ends of the fibres are fixed on the same place.
- the outer diameter of the semi-spherical fixed carrier 3 is 9.0 mm and the inner diameter thereof is 6.0 mm.
- the end of the solid metal lance 6 is fastened by the plastic 123 inside the semi-spherical carrier 3.
- the concentration of the insulin solution has to be adjusted prior to adding it to the reservoir.
- the concentration of the insulin is adjusted in international units (IU).
- the surface of the cotton or cloth fibre(s), i.e. the required capillary is achieved by using cotton or cloth fibre(s) of identical thickness and quality (porosity) and by fixing the fibre(s) always on the same places. In this manner the permanent length, i.e. surface of the cotton or cloth fibre(s) can be ensured.
- Figure 5 shows the sectional drawing of the replaceable reservoir 5.
- the diameter of the replaceable, spherical carrier 2 is 1 1.0 mm.
- porous textile fibres 1 14 extending from the sphere 2 are fastened by the element 125.
- the spherical reservoir 2 contains the solution of the active substance.
- FIG. 6 shows the micro-infusion device 1 of the invention, the main components of which are the following:
- the skin-penetrating section of the fixed carrier contains the windowed, biocompatible plastic tube 120 following the removal of the solid lance, insertion needle 6, said lance delivering the insulin and the textile fibres 1 14 into the skin.
- the micro-infusion device 1 of the invention can be prepared according to the drug safety requirements being well-known for the manufacture of injections, maintaining the sterility of the product.
- the fixed carrier and the reservoir are packed separately as several reservoirs can be placed or replaced on the same fixed carrier.
- the invention relates further to the use of the micro-infusion injection device 1 for the administration of insulin.
- Drugs can exert their effect only if their concentration in the blood remains within the so-called therapeutic window, i.e. it is neither too high, nor too low.
- ⁇ hydrophilic compounds e.g. dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), dimethyl acetamide (DMA) etc.
- DMSO dimethyl sulphoxide
- DMF dimethyl formamide
- DMA dimethyl acetamide
- hydrophobic compounds e.g. ethyl acetate, oleic acid etc.
- surfactants e.g. sodium lauryl sulphate, sorbitan monopalmitate, troiamine, polysorbate 20 etc.
- miscellaneous compounds e.g. urea, cineol, d-limonenon, lecithin etc.
- the pH is adjusted, by the slow addition of a solvent or a mixture of solvents and optionally surfactants, preferably of an at least 1 : 1 mixture of troiamine and DMSO to an alkaline domain near 9-10, or a permanent, nearly neutral pH is maintained under slow addition.
- the nearly neutral pH (6.5-7.0) can be achieved for example by citric acid.
- the concentration of the insulin is adjusted according to the needs of the patient, which may constitute even a tenfold difference in the case of the individual patients.
- an insulin solution of 0.45 mixed % is used.
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- Health & Medical Sciences (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Anesthesiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Fluid Mechanics (AREA)
- Dermatology (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- External Artificial Organs (AREA)
Abstract
La présente invention concerne un dispositif de micro-perfusion à dosage d'insuline (1) destiné au traitement du diabète, c'est-à-dire permettant l'administration de la dose quotidienne d'insuline requise, ainsi que la méthode d'utilisation de ce dispositif. Un dispositif de micro-perfusion pour l'administration sous-cutanée d'une composition d'injection d'insuline, assurant une activité prolongée, se caractérise en ce qu'il comprend un support fixe (3, 4) ou contenant des fibres textiles poreuses (114), pouvant être posé sur la surface cutanée du corps, pouvant être inséré sous la peau, et comportant un élément assurant le maintien des fibres à l'état serré. Il comprend en outre un réservoir remplaçable (2) contenant des fibres textiles identiques, relié au support, et assurant le stockage de la solution de la substance active ainsi que son dosage continu. Les fibres sortant du réservoir sont en contact avec les fibres situées dans le support fixe.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU0900596A HU227748B1 (en) | 2009-09-21 | 2009-09-21 | Microinfusion device for dosing insuline in the treatment of diabetes |
HUP0900596 | 2009-09-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011033328A1 true WO2011033328A1 (fr) | 2011-03-24 |
Family
ID=89989259
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/HU2010/000098 WO2011033328A1 (fr) | 2009-09-21 | 2010-09-15 | Dispositif de micro-perfusion à dosage d'insuline destiné au traitement du diabète |
Country Status (2)
Country | Link |
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HU (1) | HU227748B1 (fr) |
WO (1) | WO2011033328A1 (fr) |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3964482A (en) | 1971-05-17 | 1976-06-22 | Alza Corporation | Drug delivery device |
US4159720A (en) * | 1977-11-28 | 1979-07-03 | Burton Andrew F | Infusion of liquids into tissue |
EP0239244A1 (fr) | 1986-02-25 | 1987-09-30 | Pacesetter Infusion Ltd. | Trousse d'injection sous-cutanée |
WO2003026728A1 (fr) | 2001-09-27 | 2003-04-03 | Unomedical A/S | Dispositif d'injection destine a placer un equipement de perfusion sous-cutanee |
HU222342B1 (hu) | 1995-07-14 | 2003-06-28 | Boehringer Ingelheim Kg | Transzkorneális hatóanyag-leadó rendszer |
WO2006127905A2 (fr) * | 2005-05-24 | 2006-11-30 | Chrono Therapeutics, Inc. | Dispositif d'apport de medicament portatif comprenant un element de dosage et d'administration detachable et remplaçable |
WO2009015389A2 (fr) | 2007-07-26 | 2009-01-29 | Entra Pharmaceuticals Inc. | Systèmes et procédés pour administrer des médicaments |
-
2009
- 2009-09-21 HU HU0900596A patent/HU227748B1/hu not_active IP Right Cessation
-
2010
- 2010-09-15 WO PCT/HU2010/000098 patent/WO2011033328A1/fr active Application Filing
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3964482A (en) | 1971-05-17 | 1976-06-22 | Alza Corporation | Drug delivery device |
US4159720A (en) * | 1977-11-28 | 1979-07-03 | Burton Andrew F | Infusion of liquids into tissue |
EP0239244A1 (fr) | 1986-02-25 | 1987-09-30 | Pacesetter Infusion Ltd. | Trousse d'injection sous-cutanée |
HU222342B1 (hu) | 1995-07-14 | 2003-06-28 | Boehringer Ingelheim Kg | Transzkorneális hatóanyag-leadó rendszer |
WO2003026728A1 (fr) | 2001-09-27 | 2003-04-03 | Unomedical A/S | Dispositif d'injection destine a placer un equipement de perfusion sous-cutanee |
WO2006127905A2 (fr) * | 2005-05-24 | 2006-11-30 | Chrono Therapeutics, Inc. | Dispositif d'apport de medicament portatif comprenant un element de dosage et d'administration detachable et remplaçable |
WO2009015389A2 (fr) | 2007-07-26 | 2009-01-29 | Entra Pharmaceuticals Inc. | Systèmes et procédés pour administrer des médicaments |
Also Published As
Publication number | Publication date |
---|---|
HU227748B1 (en) | 2012-02-28 |
HUP0900596A2 (en) | 2011-05-30 |
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