CN111671982A - Medicinal coating composition and preparation method thereof - Google Patents
Medicinal coating composition and preparation method thereof Download PDFInfo
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- CN111671982A CN111671982A CN202010381154.5A CN202010381154A CN111671982A CN 111671982 A CN111671982 A CN 111671982A CN 202010381154 A CN202010381154 A CN 202010381154A CN 111671982 A CN111671982 A CN 111671982A
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- 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
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/08—Materials for coatings
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- 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
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- 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
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- 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
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/14—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L31/16—Biologically active materials, e.g. therapeutic substances
-
- 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
- A61L2300/416—Anti-neoplastic or anti-proliferative or anti-restenosis or anti-angiogenic agents, e.g. paclitaxel, sirolimus
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- 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
- A61L2300/60—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a special physical form
- A61L2300/606—Coatings
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Heart & Thoracic Surgery (AREA)
- Surgery (AREA)
- Vascular Medicine (AREA)
- Materials For Medical Uses (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention discloses a drug coating composition, which comprises a component A: a biologic agent; and (B) component: medicines for treating vascular inner wall hyperplasia; and (3) component C: a surfactant; and (3) component D: an excipient; and (3) component E: a mixed solution of the component A and the component C; and (3) component F: a mixed solution of the component B and the component C; a component G: a mixed solution of the component E and the component F; a component H: different solvents for all the above components are prepared by the following steps: sequentially preparing the solution of the component E, the solution of the component F and the solution of the component G, then adding a solvent into the component G, fully mixing the components at the concentration of 0.1-10 mg/ml, then adding 1-10 mg of the fourth component substance, uniformly stirring, and sealing to obtain the medicinal coating composition for coating the surface of the implanted or interventional medical device. The invention can prevent the loss of the medicine in the process that the device enters the blood vessel, and can also be dissolved in the blood rapidly, so that the medicine composition is directly attached to the focus of the blood vessel.
Description
Technical Field
The embodiment of the invention relates to the technical field of drug coatings, in particular to a drug coating composition for an implanted or interventional medical device and a preparation method thereof.
Background
The medicine coating stent and the saccule are both essentially catheter non-delivery devices, cell proliferation is inhibited by carrying the medicine coating, and the effect of inhibiting smooth muscle cell proliferation is achieved by different methods and time for carrying the medicine, so that the restenosis of the blood vessel is prevented.
The coating composition of the peripheral main medicine balloon company mainly at home and abroad is as follows: the components of the Cotavance drug from Bayer-Medrd corporation are: paclitaxel + iopromide; the composition of the in.pact drug from Invatec-Medtronic corporation is: paclitaxel + urea; the composition of the sequent (tm) plexase drug from braun corporation is: paclitaxel + iopromide; the constituents of the Passeo-18 Lux drug from Biotronik corporation are: paclitaxel + butyryl tri-n-ethyl citrate; the components of the Elutax medicine of Aachen-Resonance company are as follows: pure paclitaxel; the ABT drugs from abbott vascular company have the following components: zotarolimus; the composition of the advanced 18PTX drug from COOKMedical corporation is: pure paclitaxel; the components of Moxy drugs from the company Lutonix are: paclitaxel + shellac; the Clearway medicine of the Atrium company comprises the following components: paclitaxel + fatty acid; the ingredients of the whole county company canoe drug are: paclitaxel + iopromide + ethanol; the AcoArt drugs from Proreda comprise the following components: paclitaxel + magnesium stearate.
The existing medicine coating composition is uniformly mixed by an ultrasonic spraying machine and then sprayed on the outer surface of a stent or a balloon; the existing drug balloon can lose a large amount of drugs in the process of entering blood vessels, and even more, the drug coating can fall off in a large scale in the process of entering the blood vessels. In addition, the balloon medicine coating acts on the pathological changes, and the medicine cannot be quickly absorbed by blood vessel histiocyte, so that the cell proliferation cannot be well inhibited, and a good treatment effect cannot be achieved.
Disclosure of Invention
Therefore, the embodiment of the invention provides a drug coating composition and a preparation method thereof, which aim to solve the problems in the prior art.
In order to achieve the above object, an embodiment of the present invention provides the following:
in a first aspect of embodiments of the present invention, there is provided a pharmaceutical coating composition comprising the following components:
and (2) component A: a biologic agent;
and (B) component: medicines for treating vascular inner wall hyperplasia;
and (3) component C: a surfactant;
and (3) component D: an excipient;
and (3) component E: a mixed solution of the component A and the component C;
and (3) component F: a mixed solution of the component B and the component C;
a component G: a mixed solution of the component E and the component F;
a component H: different solvents for all of the above components;
in a preferred embodiment of the present invention, the biological agent is at least one of phospholipid 80h, phospholipid 90h, lipid S75, lipoid E80, lipoid EPC, lipoid E75, phosphatidylcholine, phosphatidylglycerol and phosphatidylethanolamine.
In a preferred embodiment of the present invention, the drug for treating vascular inner wall hyperplasia is one of paclitaxel, docetaxel, rapamycin, everolimus, picrolimus or bayer rolimus. (same as above 2)
As a preferable embodiment of the present invention, the surfactant is at least one of lauryl alcohol ethoxylate, tridecyl alcohol ethoxylate, cationic emulsifier, anionic emulsifier, zwitterionic emulsifier, nonionic emulsifier, tween 20, tween 60 or tween 80.
In a preferred embodiment of the present invention, the excipient is at least one of steroid, vitamin, estradiol, esterified fatty acid, non-esterified fatty acid, inositol, L-lactic acid, lipoprotein, carbohydrate, tricalcium phosphate, precipitated calcium nicotinate, glucose, d-sucrose, mannitol, magnesium stearate, and calcium stearate.
As a preferred embodiment of the present invention, the solvent in which the component a is dissolved is at least one selected from the group consisting of absolute ethanol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, chloroform, ethyl acetate, and isopropanol;
the solvent for dissolving the component B is at least one selected from absolute ethyl alcohol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, trichloromethane, ethyl acetate and isopropanol;
the solvent for dissolving the component C is at least one selected from water, absolute ethyl alcohol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, trichloromethane, ethyl acetate and isopropanol.
As a preferred aspect of the present invention, the drug coating composition for implantation or interventional medical device comprises: coronary vessel stent, coronary vessel saccule, peripheral vessel stent, peripheral vessel saccule, intracranial vessel stent, intracranial vessel saccule, urethral stent, urethral saccule, esophageal stent and esophageal saccule.
In a second aspect of embodiments of the present invention, there is provided a method of preparing a pharmaceutical coating composition, comprising the steps of:
sequentially preparing the solution of the component E, the solution of the component F and the solution of the component G, then adding a solvent into the component G, fully mixing the components at the concentration of 0.1-10 mg/ml, then adding 1-10 mg of the fourth component substance, uniformly stirring, and sealing to obtain the medicinal coating composition for coating the surface of the implanted or interventional medical device.
As a preferable scheme of the invention, the configuration method of the component E comprises the following steps:
fully mixing the component A with a solvent to prepare the mixture with the concentration of 1 mg/ml-100 g/ml; fully mixing the component C with a solvent to prepare the mixture with the concentration of 0.01 mg/ml-0.1 mg/ml; and adding the component A solution into the component C solution, and performing low-temperature ultrasonic treatment for 10 to 120 minutes to form a component D solution, wherein the ultrasonic frequency is 1 to 50 Hz.
As a preferable aspect of the present invention, the method for preparing the component F comprises:
fully mixing the component B with a solvent to prepare the mixture with the concentration of 0.1 mg/ml-10 mg/ml; fully mixing the component C with a solvent to prepare the mixture with the concentration of 0.01 mg/ml-0.1 mg/ml; and adding the component B solution into the component C solution, and performing low-temperature ultrasonic treatment for 10 to 120 minutes to form a component D solution, wherein the ultrasonic frequency is 1 to 50 Hz.
As a preferable aspect of the present invention, the method for preparing the component G comprises:
and adding 2-20 ml of the component E solution into 100ml of the component F solution, performing ultrasonic full mixing, transferring into a separating funnel, adding the solvent, shaking, standing for a period of time, taking the supernatant, and evaporating to dryness to obtain a component G substance.
As a preferred embodiment of the present invention, the pharmaceutical coating composition has a coating density of 0.1ug/mm on the surface of the implant or interventional medical device by spray coating or dip coating2～10ug/mm2The net drug content is 0.2ug/mm2～6ug/mm2。
The embodiment of the invention has the following advantages:
the invention sticks or wraps the medicine for treating the blood vessel inner wall hyperplasia together by the biological preparation, can carry the medicine to rapidly enter the blood vessel tissue of a human body, and simultaneously, when the apparatus enters the blood vessel focus, the apparatus can prevent the medicine from losing in the process of entering the blood vessel and can be rapidly dissolved in the blood, so that the medicine composition is directly attached to the blood vessel focus.
Detailed Description
The present invention is described in terms of particular embodiments, other advantages and features of the invention will become apparent to those skilled in the art from the following disclosure, and it is to be understood that the described embodiments are merely exemplary of the invention and that it is not intended to limit the invention to the particular embodiments disclosed. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Example 1:
the present invention provides in a first aspect of embodiments of the present invention, a pharmaceutical coating composition comprising the following components:
and (2) component A: a biologic agent;
and (B) component: medicines for treating vascular inner wall hyperplasia;
and (3) component C: a surfactant;
and (3) component D: an excipient;
and (3) component E: a mixed solution of the component A and the component C;
and (3) component F: a mixed solution of the component B and the component C;
a component G: a mixed solution of the component E and the component F;
a component H: different solvents for all of the above components;
wherein the biological agent is at least one of phospholipid 80h, phospholipid 90h, lipid S75, lipoid protein E80, lipoid protein EPC, lipoid protein E75, phosphatidylcholine, phosphatidylglycerol and phosphatidylethanolamine.
The biological agent is preferably phospholipid 80h, phospholipid 90h and lipoid protein E75, and can stick or wrap the medicines for treating vascular wall hyperplasia; and can carry medicine to enter human vascular tissue quickly.
The medicine for treating vascular inner wall hyperplasia is one of paclitaxel, docetaxel, rapamycin, everolimus, Rutacrolimus or Bayer Rilimus.
The medicine for treating the vascular inner wall hyperplasia is preferably paclitaxel and rapamycin, can inhibit the regeneration of vascular smooth muscle cells and reduce vascular restenosis; and can be better adhered or wrapped by biological agents.
The surfactant is at least one of lauryl alcohol ethoxylate, tridecanol ethoxylate, cationic emulsifier, anionic emulsifier, zwitterionic emulsifier, nonionic emulsifier, Tween 20, Tween 60 or Tween 80.
The surfactant is preferably Tween 20 or Tween 80; the biological preparation and the medicines for treating the vascular inner wall hyperplasia can be promoted to be dissolved in the solvent for dissolving the component A; less solvent is used for completely dissolving the biological preparation and the medicine for treating the regeneration of the inner wall of the blood vessel.
The excipient is at least one of steroid, vitamin, estradiol, esterified fatty acid, non-esterified fatty acid, inositol, L-lactic acid, lipoprotein, carbohydrate, tricalcium phosphate, precipitated calcium nicotinate, glucose, D-sucrose, mannitol, magnesium stearate, and calcium stearate.
The excipient is preferably glucose, mannitol, or magnesium stearate; can reduce the drug loss during the process of the device entering the blood vessel; the device can be used for preventing the drug loss in the process of entering the blood vessel when entering the blood vessel focus, and can be quickly dissolved in the blood, so that the drug composition can be directly attached to the blood vessel focus.
The solvent for dissolving the component A is at least one selected from absolute ethyl alcohol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, trichloromethane, ethyl acetate and isopropanol;
the solvent for dissolving the component B is at least one selected from absolute ethyl alcohol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, trichloromethane, ethyl acetate and isopropanol;
the solvent for dissolving the component C is at least one selected from water, absolute ethyl alcohol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, trichloromethane, ethyl acetate and isopropanol.
As a preferred aspect of the present invention, the drug coating composition for implantation or interventional medical device comprises: coronary vessel stent, coronary vessel saccule, peripheral vessel stent, peripheral vessel saccule, intracranial vessel stent, intracranial vessel saccule, urethral stent, urethral saccule, esophageal stent and esophageal saccule.
Example 2:
based on the components of the composition of example 1, a method for preparing a pharmaceutical coating composition is provided, comprising the steps of:
sequentially preparing the solution of the component E, the solution of the component F and the solution of the component G, then adding a solvent into the component G, fully mixing the components at the concentration of 0.1-10 mg/ml, then adding 1-10 mg of the fourth component substance, uniformly stirring, and sealing to obtain the medicinal coating composition for coating the surface of the implanted or interventional medical device.
8. The method for preparing the pharmaceutical coating composition according to claim 6, wherein the method for preparing the component E comprises the following steps:
fully mixing the component A with a solvent to prepare the mixture with the concentration of 1 mg/ml-100 g/ml; fully mixing the component C with a solvent to prepare the mixture with the concentration of 0.01 mg/ml-0.1 mg/ml; and adding the component A solution into the component C solution, and performing low-temperature ultrasonic treatment for 10 to 120 minutes to form a component D solution, wherein the ultrasonic frequency is 1 to 50 Hz.
As a preferable aspect of the present invention, the method for preparing the component F comprises:
fully mixing the component B with a solvent to prepare the mixture with the concentration of 0.1 mg/ml-10 mg/ml; fully mixing the component C with a solvent to prepare the mixture with the concentration of 0.01 mg/ml-0.1 mg/ml; and adding the component B solution into the component C solution, and performing low-temperature ultrasonic treatment for 10 to 120 minutes to form a component D solution, wherein the ultrasonic frequency is 1 to 50 Hz.
As a preferable aspect of the present invention, the method for preparing the component G comprises:
and adding 2-20 ml of the component E solution into 100ml of the component F solution, performing ultrasonic full mixing, transferring into a separating funnel, adding the solvent, shaking, standing for a period of time, taking the supernatant, and evaporating to dryness to obtain a component G substance.
As a preferred embodiment of the present invention, the pharmaceutical coating composition has a coating density of 0.1ug/mm on the surface of the implant or interventional medical device by spray coating or dip coating2～10ug/mm2The net drug content is 0.2ug/mm2～6ug/mm2。
The invention sticks or wraps the medicine for treating the blood vessel inner wall hyperplasia together by the biological preparation, can carry the medicine to rapidly enter the blood vessel tissue of a human body, and simultaneously, when the apparatus enters the blood vessel focus, the apparatus can prevent the medicine from losing in the process of entering the blood vessel and can be rapidly dissolved in the blood, so that the medicine composition is directly attached to the blood vessel focus.
Although the invention has been described in detail above with reference to a general description and specific examples, it will be apparent to one skilled in the art that modifications or improvements may be made thereto based on the invention. Accordingly, such modifications and improvements are intended to be within the scope of the invention as claimed.
Claims (12)
1. A pharmaceutical coating composition comprising the following components:
and (2) component A: a biologic agent;
and (B) component: medicines for treating vascular inner wall hyperplasia;
and (3) component C: a surfactant;
and (3) component D: an excipient;
and (3) component E: a mixed solution of the component A and the component C;
and (3) component F: a mixed solution of the component B and the component C;
a component G: a mixed solution of the component E and the component F;
a component H: different solvents for all the above components.
2. The pharmaceutical coating composition of claim 1,
the biological agent is at least one of phospholipid 80h, phospholipid 90h, lipid S75, lipoid protein E80, lipoid protein EPC, lipoid protein E75, phosphatidylcholine, phosphatidylglycerol and phosphatidylethanolamine.
3. The pharmaceutical coating composition of claim 1,
the medicine for treating vascular inner wall hyperplasia is one of paclitaxel, docetaxel, rapamycin, everolimus, Rutacrolimus or Bayer Rilimus.
4. The pharmaceutical coating composition of claim 1,
the surfactant is at least one of lauryl alcohol ethoxylate, tridecanol ethoxylate, cationic emulsifier, anionic emulsifier, zwitterionic emulsifier, nonionic emulsifier, Tween 20, Tween 60 or Tween 80.
5. The pharmaceutical coating composition of claim 1,
the excipient is at least one of steroid, vitamin, estradiol, esterified fatty acid, non-esterified fatty acid, inositol, L-lactic acid, lipoprotein, carbohydrate, tricalcium phosphate, precipitated calcium nicotinate, glucose, D-sucrose, mannitol, magnesium stearate and calcium stearate.
6. The pharmaceutical coating composition of claim 1, wherein the solvent in which component a is dissolved is at least one selected from the group consisting of absolute ethanol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, chloroform, ethyl acetate, and isopropanol;
the solvent for dissolving the component B is at least one selected from absolute ethyl alcohol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, trichloromethane, ethyl acetate and isopropanol;
the solvent for dissolving the component C is at least one selected from water, absolute ethyl alcohol, methanol, ethanol, tetrahydrofuran, acetone, glacial acetic acid, dichloromethane, trichloromethane, ethyl acetate and isopropanol.
7. The drug coating composition of claim 1, wherein the drug coating composition is for implantation or interventional medical devices comprising: coronary vessel stent, coronary vessel saccule, peripheral vessel stent, peripheral vessel saccule, intracranial vessel stent, intracranial vessel saccule, urethral stent, urethral saccule, esophageal stent and esophageal saccule.
8. A method for preparing a pharmaceutical coating composition, comprising the steps of:
sequentially preparing the solution of the component E, the solution of the component F and the solution of the component G, then adding a solvent into the component G, fully mixing the components at the concentration of 0.1-10 mg/ml, then adding 1-10 mg of the fourth component substance, uniformly stirring, and sealing to obtain the medicinal coating composition for coating the surface of the implanted or interventional medical device.
9. The method of claim 8, wherein the step of formulating component E comprises:
fully mixing the component A with a solvent to prepare the mixture with the concentration of 1 mg/ml-100 g/ml; fully mixing the component C with a solvent to prepare the mixture with the concentration of 0.01 mg/ml-0.1 mg/ml; and adding the component A solution into the component C solution, and performing low-temperature ultrasonic treatment for 10 to 120 minutes to form a component D solution, wherein the ultrasonic frequency is 1 to 50 Hz.
10. The method of claim 8, wherein the component F is formulated by a method comprising:
fully mixing the component B with a solvent to prepare the mixture with the concentration of 0.1 mg/ml-10 mg/ml; fully mixing the component C with a solvent to prepare the mixture with the concentration of 0.01 mg/ml-0.1 mg/ml; and adding the component B solution into the component C solution, and performing low-temperature ultrasonic treatment for 10 to 120 minutes to form a component D solution, wherein the ultrasonic frequency is 1 to 50 Hz.
11. The method of claim 8, wherein the component G is formulated by a method comprising:
and adding 2-20 ml of the component E solution into 100ml of the component F solution, performing ultrasonic full mixing, transferring into a separating funnel, adding the solvent, shaking, standing for a period of time, taking the supernatant, and evaporating to dryness to obtain a component G substance.
12. The method of claim 8, wherein the drug coating composition is applied by spraying or dipping to the surface of the implant or interventional medical device at a coating density of 0.1ug/mm2～10ug/mm2The net drug content is 0.2ug/mm2～6ug/mm2。
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Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080255509A1 (en) * | 2006-11-20 | 2008-10-16 | Lutonix, Inc. | Medical device rapid drug releasing coatings comprising oils, fatty acids, and/or lipids |
| US20110054396A1 (en) * | 2009-08-27 | 2011-03-03 | Boston Scientific Scimed, Inc. | Balloon Catheter Devices With Drug-Coated Sheath |
| CN102188379A (en) * | 2010-03-18 | 2011-09-21 | 鲁翠涛 | Preparation method of drug-carrying liposome |
| US20120065584A1 (en) * | 2009-06-02 | 2012-03-15 | Concept Medical Research Private Limited | Rejuvenating coronary artery by improving blood flow with the help of insertion of nano-balls (encapsulated nanoparticles) containing therapeutic agents by non implantable device for tissues and thereby providing in tissue release to address the required cell cycle |
| CN102470196A (en) * | 2009-08-27 | 2012-05-23 | 泰尔茂株式会社 | Medical device for drug delivery |
| US20120321670A1 (en) * | 2010-01-18 | 2012-12-20 | Envision Scientific Private Limited | Formulations of nano-carriers and methods of preparing the same |
| US20130189329A1 (en) * | 2006-11-20 | 2013-07-25 | Lutonix, Inc. | Drug releasing coatings for medical devices |
| CN104174074A (en) * | 2013-11-27 | 2014-12-03 | 浙江归创医疗器械有限公司 | Medicine coating composition as well as preparation method thereof and an implanting or intervention medical apparatus made thereof |
| US20150079160A1 (en) * | 2009-06-02 | 2015-03-19 | Concept Medical Research Private Limited | Non-implantable medical device coated with nano-carriers for delivering one or more drugs to a body site |
| CN106237395A (en) * | 2016-09-30 | 2016-12-21 | 鼎科医疗技术（苏州）有限公司 | A kind of medicine-coated balloon and preparation method thereof |
| US20170224878A1 (en) * | 2014-08-07 | 2017-08-10 | Cook Medical Technologies Llc | Encapsulated drug compositions and methods of use thereof |
| WO2018093329A1 (en) * | 2016-11-17 | 2018-05-24 | Vascuros Medical Pte Ltd | Drug eluting balloon |
| CN110201243A (en) * | 2019-07-09 | 2019-09-06 | 科睿驰（深圳）医疗科技发展有限公司 | A kind of combination drug coating foley's tube and preparation method thereof |
| CN110292701A (en) * | 2019-06-27 | 2019-10-01 | 山东瑞安泰医疗技术有限公司 | A kind of medicine eluting balloon catheter and preparation method thereof |
-
2020
- 2020-05-08 CN CN202010381154.5A patent/CN111671982A/en active Pending
Patent Citations (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080255509A1 (en) * | 2006-11-20 | 2008-10-16 | Lutonix, Inc. | Medical device rapid drug releasing coatings comprising oils, fatty acids, and/or lipids |
| US20160263076A1 (en) * | 2006-11-20 | 2016-09-15 | Lutonix, Inc. | Medical device rapid drug releasing coatings comprising oils, fatty acids and/or lipids |
| US20130197435A1 (en) * | 2006-11-20 | 2013-08-01 | Lutonix, Inc. | Medical device rapid drug releasing coatings comprising oils, fatty acids, and/or lipids |
| US20130189329A1 (en) * | 2006-11-20 | 2013-07-25 | Lutonix, Inc. | Drug releasing coatings for medical devices |
| CN102458555A (en) * | 2009-06-02 | 2012-05-16 | 概念医疗股份有限公司 | Rejuvenating coronary artery by improving blood flow with the help of insertion of nano-balls (encapsulated nanoparticles) containing therapeutic agents by non implantable device for tissues and thereby providing in tissue release to address the requ |
| US20120065584A1 (en) * | 2009-06-02 | 2012-03-15 | Concept Medical Research Private Limited | Rejuvenating coronary artery by improving blood flow with the help of insertion of nano-balls (encapsulated nanoparticles) containing therapeutic agents by non implantable device for tissues and thereby providing in tissue release to address the required cell cycle |
| US20150079160A1 (en) * | 2009-06-02 | 2015-03-19 | Concept Medical Research Private Limited | Non-implantable medical device coated with nano-carriers for delivering one or more drugs to a body site |
| CN102470196A (en) * | 2009-08-27 | 2012-05-23 | 泰尔茂株式会社 | Medical device for drug delivery |
| US20110054396A1 (en) * | 2009-08-27 | 2011-03-03 | Boston Scientific Scimed, Inc. | Balloon Catheter Devices With Drug-Coated Sheath |
| US20120321670A1 (en) * | 2010-01-18 | 2012-12-20 | Envision Scientific Private Limited | Formulations of nano-carriers and methods of preparing the same |
| CN102188379A (en) * | 2010-03-18 | 2011-09-21 | 鲁翠涛 | Preparation method of drug-carrying liposome |
| CN104174074A (en) * | 2013-11-27 | 2014-12-03 | 浙江归创医疗器械有限公司 | Medicine coating composition as well as preparation method thereof and an implanting or intervention medical apparatus made thereof |
| US20170224878A1 (en) * | 2014-08-07 | 2017-08-10 | Cook Medical Technologies Llc | Encapsulated drug compositions and methods of use thereof |
| CN106237395A (en) * | 2016-09-30 | 2016-12-21 | 鼎科医疗技术（苏州）有限公司 | A kind of medicine-coated balloon and preparation method thereof |
| WO2018093329A1 (en) * | 2016-11-17 | 2018-05-24 | Vascuros Medical Pte Ltd | Drug eluting balloon |
| CN110292701A (en) * | 2019-06-27 | 2019-10-01 | 山东瑞安泰医疗技术有限公司 | A kind of medicine eluting balloon catheter and preparation method thereof |
| CN110201243A (en) * | 2019-07-09 | 2019-09-06 | 科睿驰（深圳）医疗科技发展有限公司 | A kind of combination drug coating foley's tube and preparation method thereof |
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