CN1364493A - Nano musk joint pain stopping medicine and its preparing method - Google Patents
Nano musk joint pain stopping medicine and its preparing method Download PDFInfo
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- CN1364493A CN1364493A CN 01100267 CN01100267A CN1364493A CN 1364493 A CN1364493 A CN 1364493A CN 01100267 CN01100267 CN 01100267 CN 01100267 A CN01100267 A CN 01100267A CN 1364493 A CN1364493 A CN 1364493A
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- nanometer
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- musk
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- joint pain
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- 239000003814 drug Substances 0.000 title claims abstract description 47
- 241000402754 Erythranthe moschata Species 0.000 title claims abstract description 30
- 208000006820 Arthralgia Diseases 0.000 title claims abstract description 20
- 238000000034 method Methods 0.000 title claims description 13
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000000284 extract Substances 0.000 claims abstract description 16
- 239000012530 fluid Substances 0.000 claims abstract description 11
- 229960001047 methyl salicylate Drugs 0.000 claims abstract description 10
- 239000002994 raw material Substances 0.000 claims abstract description 7
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims abstract description 5
- 238000000605 extraction Methods 0.000 claims abstract description 5
- 238000001694 spray drying Methods 0.000 claims abstract description 5
- 229940079593 drug Drugs 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 19
- 239000000843 powder Substances 0.000 claims description 10
- 210000000582 semen Anatomy 0.000 claims description 9
- 239000002775 capsule Substances 0.000 claims description 7
- 239000008187 granular material Substances 0.000 claims description 6
- 238000002347 injection Methods 0.000 claims description 6
- 239000007924 injection Substances 0.000 claims description 6
- 239000012528 membrane Substances 0.000 claims description 6
- 239000006187 pill Substances 0.000 claims description 6
- 150000003840 hydrochlorides Chemical class 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- 229940025250 camphora Drugs 0.000 claims description 4
- 239000010238 camphora Substances 0.000 claims description 4
- 239000012141 concentrate Substances 0.000 claims description 4
- 235000008504 concentrate Nutrition 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 4
- 230000008676 import Effects 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 239000000443 aerosol Substances 0.000 claims description 3
- 239000006196 drop Substances 0.000 claims description 3
- 239000000796 flavoring agent Substances 0.000 claims description 3
- 235000019634 flavors Nutrition 0.000 claims description 3
- 239000003094 microcapsule Substances 0.000 claims description 3
- 239000002674 ointment Substances 0.000 claims description 3
- 229940100688 oral solution Drugs 0.000 claims description 3
- 239000000829 suppository Substances 0.000 claims description 3
- 239000006188 syrup Substances 0.000 claims description 3
- 235000020357 syrup Nutrition 0.000 claims description 3
- 239000003826 tablet Substances 0.000 claims description 3
- 239000003390 Chinese drug Substances 0.000 claims 2
- 230000000694 effects Effects 0.000 abstract description 10
- 238000002360 preparation method Methods 0.000 abstract description 8
- 241001106067 Atropa Species 0.000 abstract 1
- 240000004160 Capsicum annuum Species 0.000 abstract 1
- 241000723346 Cinnamomum camphora Species 0.000 abstract 1
- 229960000846 camphor Drugs 0.000 abstract 1
- 229930008380 camphor Natural products 0.000 abstract 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 abstract 1
- 229960000520 diphenhydramine Drugs 0.000 abstract 1
- 230000000704 physical effect Effects 0.000 abstract 1
- 208000002193 Pain Diseases 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000002671 adjuvant Substances 0.000 description 3
- 230000017531 blood circulation Effects 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000006071 cream Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000003203 everyday effect Effects 0.000 description 2
- 239000002086 nanomaterial Substances 0.000 description 2
- 239000011858 nanopowder Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 201000003068 rheumatic fever Diseases 0.000 description 2
- 239000007962 solid dispersion Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229940126678 chinese medicines Drugs 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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- Medicinal Preparation (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
The nano musk joint pain stopping medicine is prepared with nano musk, nano camphor, nano chilli fluid extract, nano belladonna fluid extract, nano methyl salicylate and nano diphenhydramine in certain proportion as raw material. The new medicine preparation has a grain fineness of 1200-1500 mesh, grain size of 0.1-200 nm, mostly below 100 nm, and new physical property. It is prepared through microwav extraction, decompressing concentration, spray drying in supersonic jet and other steps. it has high biological utilization and obvious treating effect.
Description
The present invention relates to the nano musk joint pain stopping medicine of a kind of expelling wind and dampness, promoting blood circulation and stopping pain, the invention still further relates to the method for this medication preparation.
Musk joint pain stopping cream is a kind of classical Chinese patent medicine, mainly contains effects such as expelling wind and dampness, promoting blood circulation and stopping pain, is used for the wet diseases such as other pain that cause of rheumatic arthritis and wind and cold.But traditional musk joint pain stopping cream disintegrate is slower, absorbs not exclusively, and bioavailability is not high, slow curative effect.
The object of the present invention is to provide a kind of bioavailability height, solid dispersion is good, absorbs fully the nano musk joint pain stopping medicine of increase evident in efficacy.
Another object of the present invention provides the preparation method of this nano musk joint pain stopping medicine.
To achieve these goals, the present invention takes following technical scheme:
Medicine of the present invention is to make (consumption is a weight portion) by following component:
Nano musk 3-8 part nanometer Camphora 1200-2800 part nanometer Fructus Capsici fluidextract 1000-2000 part
Nanometer Semen daturae fluid extract 400-800 part nanometer methyl salicylate 600-950 part nanometer diphhydramine hydrochloride 80-200 part
The formula optimization weight proportion scope of medicine of the present invention is:
Nano musk 4-6 part nanometer Camphora 1500-2500 part nanometer Fructus Capsici fluidextract 1200-1800 part
Nanometer Semen daturae fluid extract 500-700 part nanometer methyl salicylate 700-900 part nanometer diphhydramine hydrochloride 100-150 part
The optimum weight proportioning of medicine of the present invention is:
1500 parts of 2000 parts of nanometer Fructus Capsici fluidextracts of 5 parts of nanometer Camphoras of nano musk
130 parts of 800 parts of nanometer diphhydramine hydrochlorides of 600 parts of nanometer methyl salicylate of nanometer Semen daturae fluid extract
Technical scheme of the present invention is based on the modern material technology.One of modern material Developing Trend in Technology is to develop to the more and more littler direction of yardstick.The granule of the past composition material, its size all are at micron or more than the millimeter magnitude, and have occurred the material to the nanoscale development now.Because extremely refinement of granule, the shared percentage by volume of crystal boundary increases, and makes some performance of material that outstanding variation take place.
The property of nano material be since special construction----the material grains size of nano material less than the ultra-micro powder of 100nm, its body surface area is very big, the atom number ratio at crystal boundary place makes it to produce four big effects up to 15--50%: i.e. small-size effect, quantum effect (containing macro quanta tunnel effect), skin effect and interfacial effect.Thereby has the not available physical and chemical performance of traditional material.Nanotechnology will bring a technological revolution of the field of Chinese medicines.
One of method of above-mentioned each component being made medicine of the present invention is:
1. divide and get the Chinese crude drug of respectively distinguishing the flavor of, be processed into the common Chinese decoction pieces according to process of preparing Chinese medicine of Chinese Pharmacopoeia version in 2000.
2. divide and get the common Chinese decoction pieces of respectively distinguishing the flavor of, be processed into the nanometer prepared slices of Chinese crude drugs, its method comprises the following steps:
1. the common Chinese decoction pieces is placed extraction pot, solubilizer also imports microwave extracting, makes its speed with 20--30 hundred million times/second do the change in polarity motion, and the temperature of its microwave extracting is 30 ℃--and 60 ℃, time 1-10 hour;
2. above-mentioned extract is carried out concentrating under reduced pressure, temperature is 30 ℃--60 ℃, the time is 3-72 hour, collects volatile material in the Chinese medicine simultaneously in addition;
3. decompressed concentrate and volatile material merging are placed spray drying tower, use the supersonic jet technology, 330 meters of effluxvelocities--990 meter per seconds, at 30 ℃--60 ℃ of temperature, under 0 to the 0.05MPa pressure,, promptly make the nanometer prepared slices of Chinese crude drugs with the instantaneous drying of hypersonic velocity.
3. the nanometer prepared slices of Chinese crude drugs (powder) are prepared mixing in described ratio, according to Chinese Pharmacopoeia version two-shift system in 2000 agent standard, make pill, powder, tablet, suppository, granule, membrane, capsule, microcapsule, drop pill, aerosol, injection, unguentum, medicated wine, syrup, oral solution.
Two of medicine method for making of the present invention is:
1. be equipped with whole common Chinese decoction pieces in the proportioning ratio, place extraction pot, solubilizer also imports microwave extracting, makes its speed with 20--30 hundred million times/second do the change in polarity motion, and the temperature of its microwave extracting is 30 ℃-60 ℃, time 1-10 hour;
2. above-mentioned extract is carried out concentrating under reduced pressure, temperature is 30 ℃--60 ℃, the time is 3-72 hour, collects volatile material in the Chinese medicine simultaneously in addition;
3. decompressed concentrate and volatile material merging are placed spray drying tower, use the supersonic jet technology, 330 meters of effluxvelocities--990 meter per seconds, at 30 ℃--60 ℃ of temperature, under 0 to the 0.05MPa pressure,, get musk joint pain stopping preparation nano powder with the instantaneous drying of hypersonic velocity jet;
4. its nano powder is made aforementioned various preparation according to Chinese Pharmacopoeia version standard preparation in 2000.
The pharmacological effect that above-mentioned two kinds of methods are made nano musk joint pain stopping medicine is identical.
A kind of important feature of the present invention is: the made drug material of the present invention has reached nanoscale, common musk joint pain stopping paste formulation material is micron or the above particle diameter of millimeter, can only cross the 80-120 mesh sieve, the drug material that the present invention is made, particle diameter is at 0.1--200nm, the overwhelming majority can be crossed the 1200--1500 mesh sieve less than 100nm.
Another important feature of the present invention is: solid preparation of the present invention disintegrate rapidly, and solid dispersion is good in water, absorb fully, the bioavailability height, the pharmacological action effect that mainly contains effective constituent is significantly higher than conventional formulation.
The pharmaceutical preparation that the present invention is made does not need to add any adjuvant, and is more favourable to human body.
The present invention has also created the new drug formulation that pill, powder, tablet, suppository, granule, membrane, capsule, microcapsule, drop pill, aerosol, injection, unguentum, medicated wine, syrup, oral solution of nano musk joint pain stopping medicine etc. had no precedent in the past.
Pharmaceutical preparation of the present invention can be used for effects such as expelling wind and dampness, promoting blood circulation and stopping pain, is used for the wet treatment of conditions such as other pain that cause of rheumatic arthritis and wind and cold, and clinical efficacy significantly is better than traditional musk joint pain stopping cream.
The present invention's added solvent in microwave extracting is water or ethanol.
The present invention carries out in the concentrating under reduced pressure step at extract, and its concentrating under reduced pressure is conventional scheme.
Embodiment 1:
Prepare nano raw material by preceding method:
1500 parts of 2000 parts of nanometer Fructus Capsici fluidextracts of 5 parts of nanometer Camphoras of nano musk
130 parts of 800 parts of nanometer diphhydramine hydrochlorides of 600 parts of nanometer methyl salicylate of nanometer Semen daturae fluid extract
Production method is as follows:
In the GMP cleaning shop, after the above-mentioned nanometer prepared slices of Chinese crude drugs or powder prepared mixing in described ratio, according to Chinese Pharmacopoeia version two-shift system in 2000 agent capsules agent standard, do not add adjuvant, do not granulate, directly divide encapsulated with the fully-automatic capsule racking machine, make capsule, every capsules content of dispersion is the 0.1--0.6 gram, and the patient takes the 1-5 grain at every turn, and take 1-4 every day.
Embodiment 2:
Prepare nano raw material by preceding method:
1500 parts of 2000 parts of nanometer Fructus Capsici fluidextracts of 5 parts of nanometer Camphoras of nano musk
130 parts of 800 parts of nanometer diphhydramine hydrochlorides of 600 parts of nanometer methyl salicylate of nanometer Semen daturae fluid extract
Production method is as follows:
In the GMP cleaning shop, with the above-mentioned nanometer prepared slices of Chinese crude drugs or the described mixed of powder good after, according to 2000 editions two-shift system agent of Chinese Pharmacopoeia powder needle injection standard, do not add any adjuvant, make the nano musk joint pain stopping powder needle injection, every injection content is the 5-20 milligram, each consumption is that 1-2 props up, and use 1-3 every day.
Embodiment 3:
Prepare nano raw material by preceding method:
1500 parts of 2000 parts of nanometer Fructus Capsici fluidextracts of 5 parts of nanometer Camphoras of nano musk
130 parts of 800 parts of nanometer diphhydramine hydrochlorides of 600 parts of nanometer methyl salicylate of nanometer Semen daturae fluid extract
Production method is as follows:
In the GMP cleaning shop, with the above-mentioned nanometer prepared slices of Chinese crude drugs or powder by described mixed good after, according to 2000 editions two-shift system agent of Chinese Pharmacopoeia membrane standard, filmogen adopts polyvinyl alcohol, make the nano musk joint pain stopping membrane, every membrane area size is the 2-100 square centimeter, and content of dispersion is the 1-50 gram, every medicine film pasted 1-7 days, pasted the medicine position: the affected part.
Claims (6)
1, a kind of nano musk joint pain stopping medicine is characterized in that it is the medicament that the nano raw material of following weight proportioning is made:
Nano musk 3-8 part nanometer Camphora 1200-2800 part nanometer Fructus Capsici fluidextract 1000-2000 part
Nanometer Semen daturae fluid extract 400-800 part nanometer methyl salicylate 600-950 part nanometer diphhydramine hydrochloride 80-200 part
And adopt following method to make: to select the formula Chinese drug material to concoct and be processed into the prepared slices of Chinese crude drugs; Place extraction pot, solubilizer also imports microwave extracting, makes it do the change in polarity motion with hundred million times/second speed of 20--30, and the temperature of its microwave extracting is 30--60 ℃, time 1-10 hour; Above-mentioned extract is carried out concentrating under reduced pressure, and temperature is 30--60 ℃, and the time is 3-72 hour, collects volatile material in the Chinese medicine simultaneously in addition; Decompressed concentrate and volatile material merging are placed spray drying tower, use the Supersonic fluidics, 30--60 ℃ of temperature, under 0 to the 0.05MPa pressure, with hypersonic velocity instantaneous jet drying, wherein supersonic jet speed is 330 meters-990 meter per seconds, promptly makes the nanometer prepared slices of Chinese crude drugs.
2, nano musk joint pain stopping medicine according to claim 1, wherein the weight proportion of each nano raw material is:
Nano musk 4-6 part nanometer Camphora 1500-2500 part nanometer Fructus Capsici fluidextract 1200-1800 part
Nanometer Semen daturae fluid extract 500-700 part nanometer methyl salicylate 700-900 part nanometer diphhydramine hydrochloride 100-150 part
3, nano musk joint pain stopping medicine according to claim 1, wherein the weight proportion of each nano raw material is:
1500 parts of 2000 parts of nanometer Fructus Capsici fluidextracts of 5 parts of nanometer Camphoras of nano musk
130 parts of 800 parts of nanometer diphhydramine hydrochlorides of 600 parts of nanometer methyl salicylate of nanometer Semen daturae fluid extract
4,, it is characterized in that said medicine is pill, powder, tablet, suppository, granule, membrane, capsule, microcapsule, drop pill, aerosol, injection, unguentum, medicated wine, syrup, oral solution according to claim 1 or 2 or 3 described nano musk joint pain stopping medicines.
5,, it is characterized in that this method comprises the steps: to select the formula Chinese drug material to concoct and is processed into the prepared slices of Chinese crude drugs according to the pharmaceutical methods of claim 1 or 2 or 3 described nano musk joint pain stopping medicines; Place extraction pot, solubilizer also imports microwave extracting, makes it do the change in polarity motion with hundred million times/second speed of 20--30, and the temperature of its microwave extracting is 30--60 ℃, time 1-10 hour; Above-mentioned extract is carried out concentrating under reduced pressure, and temperature is 30--60 ℃, and the time is 3-72 hour, collects volatile material in the Chinese medicine simultaneously in addition; Decompressed concentrate and volatile material merging are placed spray drying tower, use the Supersonic fluidics, 30--60 ℃ of temperature, under 0 to the 0.05MPa pressure, with hypersonic velocity instantaneous jet drying, wherein supersonic jet speed is 330 meters-990 meter per seconds, promptly makes the nanometer prepared slices of Chinese crude drugs.
6, wherein respectively distinguish the flavor of Chinese medicine in the ratio of prescription or Chinese crude drug concoct be processed into the prepared slices of Chinese crude drugs after mixing, or after making the nanometer prepared slices of Chinese crude drugs mixing.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 01100267 CN1364493A (en) | 2001-01-12 | 2001-01-12 | Nano musk joint pain stopping medicine and its preparing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 01100267 CN1364493A (en) | 2001-01-12 | 2001-01-12 | Nano musk joint pain stopping medicine and its preparing method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1364493A true CN1364493A (en) | 2002-08-21 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 01100267 Pending CN1364493A (en) | 2001-01-12 | 2001-01-12 | Nano musk joint pain stopping medicine and its preparing method |
Country Status (1)
| Country | Link |
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| CN (1) | CN1364493A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106680387A (en) * | 2016-12-09 | 2017-05-17 | 山东明人福瑞达卫生材料有限公司 | Content detection method of musk bone strengthening medicine composition |
| CN107432895A (en) * | 2017-08-17 | 2017-12-05 | 杭州仁德医药有限公司 | A kind of external plaster for expel endogenous wind to relieve convulsion |
-
2001
- 2001-01-12 CN CN 01100267 patent/CN1364493A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106680387A (en) * | 2016-12-09 | 2017-05-17 | 山东明人福瑞达卫生材料有限公司 | Content detection method of musk bone strengthening medicine composition |
| CN107432895A (en) * | 2017-08-17 | 2017-12-05 | 杭州仁德医药有限公司 | A kind of external plaster for expel endogenous wind to relieve convulsion |
| CN107432895B (en) * | 2017-08-17 | 2021-05-25 | 杭州仁德医药有限公司 | External plaster for eliminating dampness and relieving pain |
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| PB01 | Publication | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |