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Perivascular wraps

A biological, polymer technology, applied in the direction of blood vessels, cardiovascular system diseases, fabrics, etc.

Inactive Publication Date: 2005-10-19
ANGIOTECH INT AG (CH)
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Local drug delivery methods to the inside of blood vessels have also failed to produce clinical efficacy

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0182] Synthesis of Polymer MEPEG750-PDLLA-2080 Polymer

[0183] To synthesize the MePEG750-PDLLA-2080 polymer, weigh 40 g of MePEG (molecular weight = 750; Sigma-Aldrich, St. Louis, MO) in a 500RB flask, and 160 g of D,L-lactide (PURASORB  , PURAC, Lincolnshire, IL). Both reagents were dried under vacuum overnight at room temperature. 600 mg of stannous 2-ethyl-hexanoate catalyst (Sigma) was then added to the RB flask containing MePEG and a magnetic stir bar. Flask with N 2 Purge (without oxygen) for 5 minutes, cover with a glass stopper, place in an oil bath (maintained at 135°C), and gradually adjust the magnetic stirrer to setting 6 (Corning). After 30 minutes, the flask was removed from the oil bath and cooled to room temperature in a water bath. Add D,L-lactide to the flask, and then 2After purging for 15 minutes, the flask was capped and placed in an oil bath (135° C.) again. Adjust the magnetic stirrer to setting 3 and allow the polymerization to continue for at...

Embodiment 2

[0185] Purification of MEPEG750-PDLLA-2080

[0186] MePEG750-PDLLA-2080 was prepared as outlined in the example, then 75 g of MePEG750-PDLLA-2080 was dissolved in 100 ml of ethyl acetate (Fisher, HPLC grade) in a 250 ml Erlenmeyer flask. The polymer was precipitated by slowly adding the solution to 900 ml of isopropanol (Caledon, HPLC grade) in a 2L Erlenmeyer flask with stirring. The solution was stirred for 30 minutes and the suspension was cooled to 5°C using a cooling system. The supernatant was separated and the pellet was transferred to a 400ml beaker. The polymer was first pre-dried in a forced air oven at 50°C for 24 hours to remove most of the solvent. The pre-dried polymer was then transferred to a vacuum oven (50°C) and further dried for 24 hours until residual solvent was below acceptable levels. Store the purified polymer at 2-8°C.

Embodiment 3

[0188] Coat MEPEG750-PDLLA-2080 on PLGA (10:90) mesh

[0189] Wash with isopropanol (Caledon, HPLC) and measure 3 x 6 cm 2 PLGA (10:90) mesh and dried in a forced air oven at 50°C. 3 g of MePEG750-PDLLA-2080 were then dissolved in 15 ml of ethyl acetate (20% solution; Fisher HPLC grade) in a 20 mL glass scintillation vial. Paclitaxel (10.13 mg) was added to the polymer solution and paclitaxel was completely dissolved by using a vortex mixer. The meshes were coated with the polymer / paclitaxel solution by dipping into the solution. Excess solution was then removed and the coated mesh was dried using an electric fan for 2-3 minutes. The coated mesh was placed in a PTFE petri dish and dried further in a fume hood using an electric fan for 60 minutes. The coated mesh was then transferred to a vacuum oven and dried overnight at room temperature under vacuum. The dry coated mesh was packed between two pieces of release-liner (Rexam A10) and sealed in the pouch.

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Abstract

The present invention provides compositions, devices, and methods for maintaining or improving the integrity of body passageways following surgery, such as at a graft site, or injury. Delivery devices including one or more therapeutic agents and a mesh are described. Representative examples of therapeutic agents include microtubule stabilizing agents, anti-angiogenic factors, inhibitors of smooth muscle cell growth or proliferation, non-steroidal anti-inflammatory drugs, and other factors useful preventing and / or reducing a proliferative biological response that may obstruct or hinder the optimal functioning of the passageway or cavity.

Description

technical field [0001] The present invention relates generally to compositions and methods for improving and maintaining the integrity of a bodily passage or cavity following surgery or injury, and more particularly to compositions comprising therapeutic agents that can be delivered to a bodily passage or cavity to facilitate Inhibition and / or reduction of proliferative biological responses that may interfere with or prevent optimal function of the channel or lumen. Background technique [0002] Every year, tens of thousands of people lose the ability to deliver enough blood to all parts of the body. When blood vessels fail, natural or artificial grafts can be used to restore blood vessel function. For example, patients who must have chronic injections or have their blood vessels punctured may end up damaging the vessels to death (eg, patients suffering from end-stage renal failure requiring hemodialysis and multiple injections or punctures). Many artificial grafts, such a...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61F2/00A61F2/06A61F2/90A61L27/14A61L27/54A61L27/58A61L31/06A61L31/10A61L31/16
CPCA61L2300/406A61L31/06A61L2300/404A61L2300/43A61L2300/416A61F2/90A61L31/10A61L27/14A61L31/16A61F2250/0067A61L2300/41Y10T442/2525A61L27/54A61F2/06A61L27/58A61P21/00A61P29/00A61P31/04A61P31/10A61P31/12A61P37/06A61P41/00A61P43/00A61P5/30A61P7/02A61P9/00A61P9/10C08L67/04A61F2/04
Inventor D·M·格雷维特P·M·托莱克斯关德池P·E·西尼奥雷T·S·斯班瑟W·L·亨特王凯越
Owner ANGIOTECH INT AG (CH)