AU2007331740B2 - Tube for enteral nutrition - Google Patents
Tube for enteral nutrition Download PDFInfo
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- AU2007331740B2 AU2007331740B2 AU2007331740A AU2007331740A AU2007331740B2 AU 2007331740 B2 AU2007331740 B2 AU 2007331740B2 AU 2007331740 A AU2007331740 A AU 2007331740A AU 2007331740 A AU2007331740 A AU 2007331740A AU 2007331740 B2 AU2007331740 B2 AU 2007331740B2
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- tube
- percutaneous endoscopic
- endoscopic gastrostomy
- parylene
- regions
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- 235000016709 nutrition Nutrition 0.000 title description 2
- 230000035764 nutrition Effects 0.000 title description 2
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 19
- 238000000576 coating method Methods 0.000 claims description 29
- 229920000052 poly(p-xylylene) Polymers 0.000 claims description 28
- 239000011248 coating agent Substances 0.000 claims description 27
- 150000001875 compounds Chemical class 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 12
- -1 silver ions Chemical class 0.000 claims description 12
- 229910052709 silver Inorganic materials 0.000 claims description 11
- 239000004332 silver Substances 0.000 claims description 11
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- VRBFTYUMFJWSJY-UHFFFAOYSA-N 28804-46-8 Chemical compound ClC1CC(C=C2)=CC=C2C(Cl)CC2=CC=C1C=C2 VRBFTYUMFJWSJY-UHFFFAOYSA-N 0.000 claims description 7
- 239000010936 titanium Substances 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- 239000002105 nanoparticle Substances 0.000 claims description 5
- 239000004814 polyurethane Substances 0.000 claims description 5
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004599 antimicrobial Substances 0.000 abstract description 4
- 150000003839 salts Chemical class 0.000 abstract description 2
- 210000002784 stomach Anatomy 0.000 description 9
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 8
- 208000015181 infectious disease Diseases 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 210000003815 abdominal wall Anatomy 0.000 description 5
- 230000000844 anti-bacterial effect Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- 230000000845 anti-microbial effect Effects 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000003242 anti bacterial agent Substances 0.000 description 3
- 229940088710 antibiotic agent Drugs 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 230000002421 anti-septic effect Effects 0.000 description 2
- 210000000080 chela (arthropods) Anatomy 0.000 description 2
- 239000000824 cytostatic agent Substances 0.000 description 2
- 230000001085 cytostatic effect Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000003013 cytotoxicity Effects 0.000 description 1
- 231100000135 cytotoxicity Toxicity 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 208000024386 fungal infectious disease Diseases 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 239000000017 hydrogel Substances 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 230000005660 hydrophilic surface Effects 0.000 description 1
- 229920001600 hydrophobic polymer Polymers 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000002572 peristaltic effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/34—Trocars; Puncturing needles
- A61B17/3415—Trocars; Puncturing needles for introducing tubes or catheters, e.g. gastrostomy tubes, drain catheters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/04—Macromolecular materials
- A61L29/06—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/08—Materials for coatings
- A61L29/085—Macromolecular materials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/14—Materials characterised by their function or physical properties, e.g. lubricating compositions
- A61L29/16—Biologically active materials, e.g. therapeutic substances
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00889—Material properties antimicrobial, disinfectant
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00893—Material properties pharmaceutically effective
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J15/00—Feeding-tubes for therapeutic purposes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J15/00—Feeding-tubes for therapeutic purposes
- A61J15/0026—Parts, details or accessories for feeding-tubes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/10—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing inorganic materials
- A61L2300/102—Metals or metal compounds, e.g. salts such as bicarbonates, carbonates, oxides, zeolites, silicates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/10—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing inorganic materials
- A61L2300/102—Metals or metal compounds, e.g. salts such as bicarbonates, carbonates, oxides, zeolites, silicates
- A61L2300/104—Silver, e.g. silver sulfadiazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/404—Biocides, antimicrobial agents, antiseptic agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Surgery (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Gastroenterology & Hepatology (AREA)
- Pathology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Heart & Thoracic Surgery (AREA)
- Medical Informatics (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- Materials For Medical Uses (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Media Introduction/Drainage Providing Device (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
A PEG tube comprises an antimicrobial compound of salts releasing metal ions.
Description
C:\NRPortbl\DCC\TXB\3716245 1. DOC-13/07/2011 Tube for enteral nutrition The invention relates to a tube for enteral feeding, in particular a PEG tube (PEG = percutaneous endoscopic gastrostomy). Percutaneous endoscopic gastrostomy is the application of a feeding probe into 5 the stomach, through the abdominal wall, with the aid of an endoscope. A gastroscope is routinely used for this purpose, i.e. a flexible optical instrument comprising a lens and an eyepiece or an electronic image transmission device. A PEG tube (also termed PEG probe) is used for enteral feeding, i.e. feeding directly via the stomach/intestinal tract. A liquid, or food in liquid or thin-paste form, can 10 be administered via the PEG tube. The PEG tube is one of the most frequently employed means for long-term enteral feeding of patients who, owing to particular illnesses, are no longer able to take in sufficient food orally. The positioning of a PEG tube is usually effected with the aid of the so-termed is filament pull-through method. In this method, the physician pushes a gastroscope into the stomach via the mouth and the oesophagus. Air is blown into the stomach, causing it to distend, such that it is more easily examined. A hollow needle is then inserted through the abdominal wall, under endoscopic control, into the stomach through the abdominal wall. The hollow needle contains an inserted 20 small plastic tube. The hollow needle is then removed and a filament is introduced into the stomach through the small plastic tube that remains. This filament can then be gripped by means of a pincer, which the physician has introduced via the gastroscope. The filament, pincer and gastroscope are then drawn out via the oesophagus and the mouth. The PEG tube can then be connected to the end of 25 the filament protruding from the mouth and, by pulling on the other end of the filament, the probe is brought into the stomach via the mouth and oesophagus, and drawn partially through the abdominal wall. Plates on the PEG tube position it in relation to -2 the abdominal wall and the stomach. The protruding end of the PEG tube can then be connected to means for supplying food. Although percutaneous endoscopic gastrostomy has become established to a large 5 extent, nevertheless for a long time there has continued to be a considerable risk of infection, which can extend into the two-digit percentage range. Thus, a percentage rate of 5 - 15 % is still being reported in the year 2000 for peristaltic infection alone (C.H. L6ser, DMW 125, 805). In particular, necrosis and mycosis occur. lo Various attempts to prevent infections caused by PEG tubes are known in the prior art. Thus, surfaces that are as smooth as possible are used on the PEG tube, as are hydrophilic surfaces, as well as hydrogels, heparin and heparioid. Monoclonal antibodies are also used in the case of catheters. There are studies relating to the prevention of infections by means of antibiotics in the case of PEG. 15 However, antibiotics also have disadvantages; in particular, the antimicrobial effect can decline after just 24 hours, and the effect is not locally limited. In addition, the application spectrum is limited and the patient can develop resistance. Antibiotics are also disadvantageous in terms of cost. 20 US 2004/0220534 Al describes, in particular, a stomach probe having a wall made of a hydrophobic polymer, there being applied to an outer surface of the wall a hydrophilic polymer having an antimicrobial compound consisting of a phosphorus based glass in which a metal, in particular silver ions, is dispersed. Such a teaching 2s does not constitute subject-matter of the present invention. US 6,060,000 describes, in particular, catheters with the use of oligodynamic iontophoresis. For the purpose of achieving an antibacterial effect, silver ions are delivered into the surrounding fluid with the aid of an electric potential. The wall of 30 the catheter includes delimited regions, for example in the form of elongate strips, which contain electrodes for the purpose of generating the said electric potential.
0i \exr\ nterwoven\NRPonbl\DCC\EXT\S454 E_ I. DC- 10/09/2013 -3 WO 95/04564 describes an enteral feeding probe having an outer surface coated with Parylene. US 2001/0051669 Al describes medical equipment such as, In particular, catheters or the like, having a slip layer to reduce friction. 5 The invention seeks to provide a tube for enteral feeding in which the risk of infection is reduced by simple means. For this purpose, the invention provides a tube having an antiseptic and/or antimicrobial compound, which is applied to or introduced into at least selected surface regions of the tube. 10 According to the invention, there is provided a tube for percutaneous endoscopic gastrostomy, said tube having an antiseptically or antimicrobially acting compound that releases metal ions or colloidal metal wherein said compound is in the form of nanoparticles and. is distributed homogeneously in regions of the tube, over its thickness, from the outer surface of the tube to 15 the inner surface of the tube. In some embodiments of the invention, the tube has a coating comprising Parylene or Polyparylene. In some of those embodiments, an antiseptically or antimicrobially acting compound that releases metal ions is mixed into the Parylene coating, or a layer of a material that releases metal ions is applied to 20 the Parylene coating. In one embodiment there is provided a tube for percutaneous endoscopic gastrostomy, characterized in that the compound is diffusibly distributed in the material of the tube.
-3A Metal salts, in particular silver salts, that release metal ions (silver ions) are particularly suitable as a compound for this purpose. Compounds that release colloidal silver can also be used. According to a preferred development of the invention, the compound that s releases the metal ions or colloidal metal (e.g. colloidal silver) is in the form of so-termed nanoparticles, i.e. particles having dimensions in the nano range. Embodiments of the invention may have the following advantages, in particular: a very broadband antimicrobial spectrum; a high level of activity against organisms and variants in very small colonies; a long-lasting activity 10 over weeks, months or even years; no induction of resistance; no stimulation of risk of thrombosis or cytotoxicity; no alteration of the material properties of the tube plastic; in addition, low cost. According to a preferred development, the tube is not fully provided with antiseptic and/or antimicrobial substance in all regions, but only In partial is regions. These partial regions of the tube preferably extend in striate form, in particular in the #:\dh\Ehateva\[ P~ftl\DC\ET\55465_3DOC- 10/09/201) -4 longitudin I direction of the tube, such that simple production, by means of extrusion methods, is rendered possible. A preferred development makes provision vrhereby the striate surface regions have a zigzag form or waved form. A uniform delivery and distribution of the metal ions is thereby 5 promoted, Striate regions comprising the antimicrobial compound and having a width that varies over the longitudinal extent or, also, that are arranged helically, can also be provided for this purpose. In order to enhance the possibilities for inspection, the tube can be designed, 10 preferably, to have, in part, transparent regions that extend in the longitudinal direction, for example in that its plastic material is transparent. As noted above, some embodiments of the invention provides a Parylene coating on the surface of the tube. This Parylene coating can be provided on is the outer s face and/or the inner surface of the tube. An anti-crustation layer can also be provided, in addition to or as an alternative to the Parylene coating. A further embodiment of the invention provides a tube made, for example, of 20 polyurethane or silicone, which is provided with a Parylene coating on the outer surface and/or the inner surface, a further coating, of a material that releases rmetal ions, being applied over the Parylene coating. The metal ions can be, for example, silver ions or titanium ions. A further coating, which releases c lloidal silver, can also be provided. 25 Preferably, Parylene C and/or Parylene N is/are used. It has been found that, for the application intended here, Parylene C has a particularly good chemical resistance and a slight antibacterial effect. Parylene N, on the other hand, is distinguished by a particular slipperiness. Also suitable is a mix of Parylene C -5 and Parylone N. In the case of all the exemplary embodiments described here, the layer thickness 9f the optional Parylene coating can preferably be in the pm range, 5 in particular in the range from 0.2 to 10 pm, particularly preferably in the range from I to 5 pm. In this case, a further coating, of a material that releases Ag-ions or Ti-ions or colloidal silver, can be additionally applied to the Parylene coating already io mentioned above. This applies both to the outer coating of the tube and to its inner coating. Techniques for applying such coatings are known as such from other fields, for example from the general technique of metal coatings. The concentration and/or layer thickness of the antiseptically or antimicrobially is acting substances that release metal ions or colloidal silver is/are preferably to be so dimensioned that they are active, in particular, in the first 20 days of the application for as long as the risk of infection exists. The tubes described here are preferably composed of polyurethane or 20 silicone. Multilayer tubes can also be provided, for example two-layer tubes having a somewhat thinner outer layer, in which or on which the antiseptically or antimicrgbially acting substances are arranged, while a preferably somewhat thicker inner tube layer can be free from same. Such a multilayer tube structure can be produced easily by the extrusion method. The layer 25 arrangement can also be the inverse of that described above.
-6 The invention also teaches generally the use of ionized titanium, i.e. a compound that releases titanium in ionic form, as an antiseptically or antimicrobiplly acting substance that releases metal ions. This use relates, in particular, to PEG tubes. 5 An exemplary embodiment of the invention is explained more fully in the following with reference to the non-limiting drawings. Figures 1, d and 3 each show, schematically, a portion of a PEG tube. Figure 4 shows a se tion through an exemplary embodiment of a tube for enteral feeding. 1o In the figur s, components that correspond to one another or have a similar function are denoted by the same references. Figures 1, and 3 shows a short portion of a PEG tube 10 made of PU. Silver nanoparticles 14 have been introduced into selected regions 12 of the tube. The regions 20 therebetween are free from such particles. 15 The regions 12 provided with the nanoparticles containing silver extend from the outer surface 16 of the tube 10 to the inner surface 18. The concentration of nanoparticles containing silver is such that they continually deliver antibacterially acting silver ions over relatively long periods of time, in particular periods of many days, weeks or months. 20 Figure 1 shQws an arrangement of the regions 12 having the added antibacterial compound, which extend helically (in the form of a helical line) around the longitudinal axis of the tube 10.
-7 According to Figure 2, the regions 12 having the added antibacterial compound extend in the longitudinal direction of the tube and have a zigzag form or waved form. 5 According to Figure 3, the corresponding regions 12 are so configured that their width varies in the longitudinal direction of the tube. The representations are schematic. In reality, the regions having the added antibacterial substance are geometrically so configured that the active metal ions are 1o delivered, to a very large degree, homogeneously by the tube, i.e. the regions carrying the compound are located so close to one another that no gaps remain in respect of the antimicrobial action. The tube 10 is provided with a coating that prevents the penetration of a polyvidon is iodine complex agent and/or the penetration of disinfectants into the tube material. Parylene, in particular, is suitable for this coating. Preferably by means of a coextrusion method, the inner surface 18 of the tube is provided with a layer that is resistant to cytostatics, such that the tube retains its 20 mechanical properties. Parylene, in particular, offers protection against cytostatics. In particular, Parylene or Polyparylene (trade name) is suitable as a coating material for the tube. Parylene is a polymer from the poly-p-xylylene families. 25 Figure 4 shows a section through an exemplary embodiment of a tube 10 for enteral feeding, in particular for PEG. A tube 10a made of polyurethane or silicone constitutes the supporting structure of the tube. Applied to the tube 10a, radially outwards, there is a layer 22 of Parylene, in particular Parylene C or Parylene N or a mix of Parylene C and Parylene N. Applied over the layer 22 there is a further layer 30 24, of an antimicrobially acting material that releases metal ions, the metal ions preferably being silver ions or titanium ions. A colloidal silver, or another C:\NRPortbl\DCC\TXB\3216245_1 DOC-13/07/2011 -8 antimicrobially acting layer that releases colloidal metal, can also be applied instead of the layer 24 or in addition thereto. The exemplary embodiment according to Figure 4 can be complemented by the application of an analogous coating on the inner surface 18 of the tube 10a, 5 thus there is applied to the inner surface 18, firstly, a coating (analogous to the layer 22) of Parylene C and/or Parylene N, and then, upon the latter on the inside, a further coating (analogous to the coating 24) of a material that releases metal ions and/or colloidal metal. In Figure 4, the layer thicknesses are not true to scale; rather, the outer layers 1o are shown as being thicker, for the purpose of simplified representation. In the description hereinbefore and in the claims and the drawing, tubes for enteral feeding, in particular PEG tubes, are shown in general. All described details, features and measures are suitable and applicable both for application in the case of PEG tubes and, quite generally, for application in the case of is tubes for enteral feeding. The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of 20 the common general knowledge in the field of endeavour to which this specification relates. Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer 25 or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
Claims (15)
1. Tube for percutaneous endoscopic gastrostomy, said tube having an antiseptically or antimicrobially acting compound that releases metal ions or colloidal metal wherein said compound is in the form of nanoparticles and is distributed homogeneously in regions of the tube, over its thickness, from the outer surface of the tube to the inner surface of the tube.
2. Tube for percutaneous endoscopic gastrostomy according to claim 1, characterized in that the compound is diffusibly distributed in the material of the tube.
3. Tube for percutaneous endoscopic gastrostomy according to claim 1 or 2, characterized in that the tube has a Parylene coating.
4. Tube for percutaneous endoscopic gastrostomy as claimed in claim 3, wherein the Parylene coating comprises Parylene N and/or Parylene C.
5. Tube for percutaneous endoscopic gastrostomy according to claim 3 or 4, characterized in that an antimicrobially acting compound that releases metal ions is mixed into the Parylene coating, or a layer of a material that releases metal ions is applied to the Parylene coating.
6. Tube for percutaneous endoscopic gastrostomy according to claim 5, wherein the released metal ions are silver ions or titanium ions.
7. Tube for percutaneous endoscopic gastrostomy according to any one of claims 3 to 6, characterized by the Parylene coating being on the outer surface and/or inner surface of the tube. - 10
8. Tube for percutaneous endoscopic gastrostomy according to any one of the preceding claims, characterized in that the regions extend in striate form in the longitudinal direction of the tube.
9. Tube for percutaneous endoscopic gastrostomy according to claim 8, characterized in that the striate regions have a zigzag form, waved form or helical form.
10. Tube for percutaneous endoscopic gastrostomy according to claim 8 or 9, characterized in that the striate regions have a varying width.
11. Tube for percutaneous endoscopic gastrostomy according to any one of the preceding claims, characterized In that the tube is at least partially transparent.
12. Tube for percutaneous endoscopic gastrostomy according to any one of the preceding claims, characterized in that the tube is at least partially opaque.
13. Tube for percutaneous endoscopic gastrostomy according to any one of the preceding claims, made of polyurethane or silicone.
14. Tube for percutaneous endoscopic gastrostomy according to any one of the preceding claims, wherein the metal ions released from the antiseptically or antimicrobially acting compound distributed homogeneously in the regions of the tube are silver ions or titanium ions.
15. Tube according to claim 1 and substantially as hereinbefore described with reference to the drawings.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06025588.2 | 2006-12-11 | ||
EP06025588.2A EP1935355B1 (en) | 2006-12-11 | 2006-12-11 | Tube for enteral nutrition |
PCT/EP2007/010582 WO2008071330A2 (en) | 2006-12-11 | 2007-12-05 | Tube for enteral nutrition |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2007331740A1 AU2007331740A1 (en) | 2008-06-19 |
AU2007331740B2 true AU2007331740B2 (en) | 2013-10-17 |
Family
ID=38337886
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2007331740A Active AU2007331740B2 (en) | 2006-12-11 | 2007-12-05 | Tube for enteral nutrition |
Country Status (6)
Country | Link |
---|---|
EP (2) | EP1935355B1 (en) |
AU (1) | AU2007331740B2 (en) |
NZ (1) | NZ578314A (en) |
PL (2) | PL1935355T3 (en) |
RU (1) | RU2463009C2 (en) |
WO (1) | WO2008071330A2 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2729194B1 (en) * | 2011-07-08 | 2021-06-02 | Specialty Coating Systems, Inc. | Antimicrobial parylene coatings and methods of depositing same |
US9210933B2 (en) | 2011-07-08 | 2015-12-15 | Specialty Coating Systems, Inc. | Antimicrobial parylene coatings and methods of depositing same |
US8936564B2 (en) * | 2011-08-26 | 2015-01-20 | Marshall Kerr | Bio-compatible catheter |
US9033930B2 (en) * | 2011-12-22 | 2015-05-19 | Avent, Inc. | Base for an enteral feeding device |
WO2013138534A1 (en) * | 2012-03-13 | 2013-09-19 | Pfm Medical, Inc. | Catheter having antimicrobial coating |
CN107743404A (en) | 2015-06-18 | 2018-02-27 | 心脏起搏器股份公司 | The polymeric cover and its production method comprising biologically absorbable polymer and antimicrobial for implantable medical device |
CN107735115B (en) | 2015-07-11 | 2020-12-22 | 心脏起搏器股份公司 | Polymeric coating with antimicrobial material and method of making the same |
US11524098B2 (en) * | 2018-09-14 | 2022-12-13 | Avent, Inc. | Systems and methods for biofilm inoculation |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995004564A1 (en) * | 1993-08-05 | 1995-02-16 | Abbott Laboratories | Enteral feeding device |
US6530951B1 (en) * | 1996-10-24 | 2003-03-11 | Cook Incorporated | Silver implantable medical device |
US20040220534A1 (en) * | 2003-04-29 | 2004-11-04 | Martens Paul W. | Medical device with antimicrobial layer |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3070132A (en) * | 1960-04-06 | 1962-12-25 | David S Sheridan | Non-sparking medico-surgical tubes |
US4027659A (en) * | 1975-11-21 | 1977-06-07 | Krandex Corporation | Radiographic opaque and conductive stripped medical tubes |
GEP20002074B (en) * | 1992-05-19 | 2000-05-10 | Westaim Tech Inc Ca | Modified Material and Method for its Production |
US6060000A (en) * | 1992-11-12 | 2000-05-09 | Implemed, Inc. | Iontophoretic material containing carbon and metal granules |
US6645483B2 (en) | 1998-10-07 | 2003-11-11 | Sherwood Services Ag | Lubricious coating |
RU18229U1 (en) * | 1999-07-23 | 2001-06-10 | Благитко Евгений Михайлович | ANTISEPTIC DEVICE FOR DRAINING CAVITIES AND RAS |
US6977138B2 (en) * | 2001-07-24 | 2005-12-20 | Massachusetts Institute Of Technology | Reactive polymer coatings |
-
2006
- 2006-12-11 EP EP06025588.2A patent/EP1935355B1/en active Active
- 2006-12-11 PL PL06025588T patent/PL1935355T3/en unknown
-
2007
- 2007-12-05 NZ NZ578314A patent/NZ578314A/en unknown
- 2007-12-05 EP EP07847010.1A patent/EP2099370B1/en active Active
- 2007-12-05 RU RU2009125467/14A patent/RU2463009C2/en active
- 2007-12-05 PL PL07847010T patent/PL2099370T3/en unknown
- 2007-12-05 WO PCT/EP2007/010582 patent/WO2008071330A2/en active Application Filing
- 2007-12-05 AU AU2007331740A patent/AU2007331740B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995004564A1 (en) * | 1993-08-05 | 1995-02-16 | Abbott Laboratories | Enteral feeding device |
US6530951B1 (en) * | 1996-10-24 | 2003-03-11 | Cook Incorporated | Silver implantable medical device |
US20040220534A1 (en) * | 2003-04-29 | 2004-11-04 | Martens Paul W. | Medical device with antimicrobial layer |
Also Published As
Publication number | Publication date |
---|---|
EP2099370B1 (en) | 2019-02-20 |
PL2099370T3 (en) | 2019-06-28 |
PL1935355T3 (en) | 2016-03-31 |
RU2463009C2 (en) | 2012-10-10 |
WO2008071330A2 (en) | 2008-06-19 |
RU2009125467A (en) | 2011-01-20 |
AU2007331740A1 (en) | 2008-06-19 |
NZ578314A (en) | 2012-03-30 |
WO2008071330A3 (en) | 2008-11-13 |
EP1935355B1 (en) | 2015-12-02 |
EP2099370A2 (en) | 2009-09-16 |
EP1935355A1 (en) | 2008-06-25 |
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