CN114533805B - External prescription for cervical vertebra and lumbar vertebra diseases - Google Patents

External prescription for cervical vertebra and lumbar vertebra diseases Download PDF

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CN114533805B
CN114533805B CN202210271512.6A CN202210271512A CN114533805B CN 114533805 B CN114533805 B CN 114533805B CN 202210271512 A CN202210271512 A CN 202210271512A CN 114533805 B CN114533805 B CN 114533805B
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fine powder
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external prescription
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CN114533805A (en
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刘韦淞
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Nandao Nanyao Health Industry Investment Hainan Co ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/60Moraceae (Mulberry family), e.g. breadfruit or fig
    • A61K36/605Morus (mulberry)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/28Asteraceae or Compositae (Aster or Sunflower family), e.g. chamomile, feverfew, yarrow or echinacea
    • A61K36/282Artemisia, e.g. wormwood or sagebrush
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/70Polygonaceae (Buckwheat family), e.g. spineflower or dock
    • A61K36/704Polygonum, e.g. knotweed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/74Rubiaceae (Madder family)
    • A61K36/746Morinda
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/88Liliopsida (monocotyledons)
    • A61K36/889Arecaceae, Palmae or Palmaceae (Palm family), e.g. date or coconut palm or palmetto
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/70Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
    • A61K9/7023Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
    • A61K9/703Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
    • A61K9/7038Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer
    • A61K9/7046Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds
    • A61K9/7053Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds, e.g. polyvinyl, polyisobutylene, polystyrene
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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Abstract

The invention discloses an external prescription for cervical spondylosis and lumbar spondylosis, which relates to the technical field of external traditional Chinese medicine products and comprises the following raw materials in parts by weight: 0.5 to 2.0 parts of carbomer, 8.0 to 10.0 parts of NP-700, 0.3 to 0.8 part of aluminum glycyrrhizate, 30 to 60 parts of glycerin, 0.01 to 0.07 part of EDTA, 0.05 to 0.3 part of citric acid, 35 to 50 parts of compound fine powder and 80 to 100 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 5.0 to 7.0 parts of mulberry twig, 5.0 to 6.0 parts of wormwood, 1.0 to 2.0 parts of coconut shell, 1.0 to 2.0 parts of morinda officinalis and 1.0 to 2.0 parts of prepared fleece-flower root. The external prescription for cervical spondylosis and lumbar spondylosis has the advantages that mulberry twig, wormwood, coconut shell, morinda officinalis and prepared fleece-flower root are taken as raw materials, the raw materials are combined, the synergistic effect is obvious, and the external prescription has the effects of dispelling wind and removing dampness, relaxing tendons and activating collaterals, dispelling cold and relieving pain, so that the external prescription can play a relatively obvious role in relieving neck and shoulder discomfort and waist and leg ache caused by damp-cold wind evil in the cervical vertebra and lumbar vertebra.

Description

External prescription for cervical vertebra and lumbar vertebra diseases
Technical Field
The invention relates to the technical field of traditional Chinese medicine external products, in particular to an external prescription for cervical spondylosis and lumbar spondylosis.
Background
Cervical and lumbar vertebra diseases refer to the corresponding symptoms and signs of spinal cord, nerve and vascular damage caused by cervical and lumbar disc degeneration and secondary intervertebral joint degeneration. Is one of common diseases of the elderly. However, with the change of life and work habits of modern people, the chances of strain in a single posture are increased, the incidence rate of cervical and lumbar diseases is on an ascending trend, and the age of patients tends to be younger. Although the treatment methods of the diseases are many, the diseases can really and rapidly and effectively relieve less pains of patients, namely' lumbago of patients and headache of doctors
The plaster in the external prescription on the market at present is a plaster preparation with longer use history, but has more defects, such as the black plaster adopts lead ions as a matrix, is harmful to human bodies after long-term use, is processed under high temperature condition, is not beneficial to the protection of active ingredients, has pain when being torn off, and the like; the preparation of the rubber paste requires a large amount of gasoline, has potential safety hazard and is not beneficial to environmental protection.
Disclosure of Invention
The invention mainly aims to provide an external prescription for cervical spondylosis and lumbar spondylosis, which can effectively solve the problems that the black plaster in the background technology takes lead ions as a matrix, is harmful to human bodies after long-term use, and is prepared under high temperature conditions, is not beneficial to the protection of active ingredients, and is painful when torn off; the preparation of the rubber paste requires a large amount of gasoline, has potential safety hazard and is not beneficial to environmental protection.
In order to achieve the above purpose, the technical scheme adopted by the invention is as follows: an external prescription for cervical vertebra and lumbar vertebra diseases comprises the following raw materials in parts by weight: 0.5 to 2.0 parts of carbomer, 8.0 to 10.0 parts of NP-700, 0.3 to 0.8 part of aluminum glycyrrhizate, 30 to 60 parts of glycerin, 0.01 to 0.07 part of EDTA, 0.05 to 0.3 part of citric acid, 35 to 50 parts of compound fine powder and 80 to 100 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 5.0 to 7.0 parts of mulberry twig, 5.0 to 6.0 parts of wormwood, 1.0 to 2.0 parts of coconut shell, 1.0 to 2.0 parts of morinda officinalis and 1.0 to 2.0 parts of prepared fleece-flower root.
Preferably, the method comprises the following steps:
s1, weighing certain parts by weight of mulberry twig, wormwood, coconut shell, morinda officinalis and prepared fleece-flower root according to the formula, respectively processing the mulberry twig, wormwood, coconut shell, morinda officinalis and prepared fleece-flower root into powder by a superfine pulverizer, screening the powder by a filter screen, drying the powder, and fully mixing the powder;
s2, placing the mixed finished product into a non-woven fabric bag with the size of about 11cm multiplied by 8cm, and sealing the bag;
s3, adding purified water into a carbomer container with a certain amount, soaking for 12 hours, adding EDTA into the soaked carbomer solution, stirring uniformly to obtain a phase A, putting NP-700, dihydroxyaluminum and glycerol into a stainless steel large container, and stirring uniformly to obtain a phase B;
s4, adding the phase B into the phase A, placing in a vacuum stirrer, stirring to obtain paste, taking out the paste, coating the paste on a non-woven fabric bag, and placing at room temperature after coating, and naturally solidifying and forming the paste.
Preferably, the fine powder obtained in the step S1 is filtered by a 100-150-mesh filter screen, so as to obtain fine powder with a powder diameter of 100-150 mu m.
Preferably, the stirring speed of the vacuum stirrer in the step S4 is 120-160 r/min, and the stirring time is about 5 min.
Preferably, the external prescription comprises the following raw materials in parts by weight: 0.5 part of carbomer, NP-7008.0 parts, 0.3 part of aluminum glycinate, 30 parts of glycerol, 0.01 part of EDTA, 0.05 part of citric acid, 35 parts of compound fine powder and 80 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 5.0 parts of mulberry twig, 5.0 parts of wormwood, 1.0 part of coconut shell, 1.0 part of morinda officinalis and 1.0 part of prepared fleece-flower root.
Preferably, the external prescription comprises the following raw materials in parts by weight: the external prescription comprises the following raw materials in parts by weight: 1.0 part of carbomer, 9.0 parts of NP-700, 0.5 part of aluminum glycyrrhizate, 50 parts of glycerin, 0.05 part of EDTA, 0.2 part of citric acid, 40 parts of compound fine powder and 90 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 6.5 parts of mulberry twig, 5.5 parts of wormwood, 1.5 parts of coconut shell, 1.5 parts of morinda officinalis and 1.5 parts of prepared fleece-flower root.
Preferably, the external prescription comprises the following raw materials in parts by weight: 2.0 parts of carbomer, NP-70010.0 parts, 0.8 part of aluminum glycinate, 60 parts of glycerin, 0.07 part of EDTA, 0.3 part of citric acid, 50 parts of compound fine powder and 100 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 7.0 parts of mulberry twig, 6.0 parts of wormwood, 2.0 parts of coconut shell, 2.0 parts of morinda officinalis and 2.0 parts of prepared fleece-flower root.
Compared with the prior art, the invention has the following beneficial effects:
1. in the invention, the matrix is directly placed under the room temperature condition after being coated in the molding process, and is naturally cured and molded without heating, so that the water evaporation is avoided, the preparation process is simplified, the protection of effective components is facilitated, the pain is basically avoided during tearing, the comfort of a patient in use is improved, the steel ball with the weight of 5.6g can be obtained through the adhesion test result and the heat resistance test, the adhesion test is greater than 150s, the adhesion of the external prescription is good, the external prescription can be well fixed at a diseased part, and the heat resistance of the external prescription can reach 50 ℃.
2. In the invention, the existing paste refining and process needs to be heated, the matrix selected by the invention is NP-700 and carbomer high molecular polymer, which can be well dissolved at room temperature, and the paste refining and process does not need to be heated, so that the operation is simple.
3. According to the invention, the mulberry twig is used for mainly strengthening bones, the wormwood is used for mainly warming, the coconut shell is used for mainly dispelling wind, the morinda officinalis and the prepared fleece-flower root are used for mainly tonifying kidney and strengthening bones, and statistics is carried out on data after treatment on a plurality of groups of patients, so that the total effective rate of the invention can reach 83.33%, and therefore, the invention has a relatively obvious relieving effect on neck-shoulder discomfort and waist-leg ache caused by damp-cold wind evil in the neck and lumbar vertebra.
Detailed Description
The invention is further described in connection with the following detailed description, in order to make the technical means, the creation characteristics, the achievement of the purpose and the effect of the invention easy to understand.
In the description of the present invention, it should be noted that the terms "upper," "lower," "inner," "outer," "front," "rear," "both ends," "one end," "the other end," and the like indicate an orientation or a positional relationship, which are merely for convenience of describing the present invention and simplifying the description, but do not indicate or imply that the apparatus or elements to be referred to must have a specific orientation, be constructed and operated in a specific orientation, and thus should not be construed as limiting the present invention. Furthermore, the terms "first," "second," and the like, are used for descriptive purposes only and are not to be construed as indicating or implying relative importance.
In the description of the present invention, it should be noted that, unless explicitly specified and limited otherwise, the terms "mounted," "provided," "connected," and the like are to be construed broadly, and may be fixedly connected, detachably connected, or integrally connected, for example; can be mechanically or electrically connected; can be directly connected or indirectly connected through an intermediate medium, and can be communication between two elements. The specific meaning of the above terms in the present invention will be understood in specific cases by those of ordinary skill in the art.
Example 1
The external prescription for cervical vertebra and lumbar vertebra diseases of the embodiment comprises the following raw materials in parts by weight: 0.5 part of carbomer, 0.3 part of aluminum glycyrrhizate, 30 parts of glycerol, 0.01 part of EDTA, 0.05 part of citric acid, 35 parts of compound fine powder and 80 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 5.0 parts of mulberry twig, 5.0 parts of wormwood, 1.0 part of coconut shell, 1.0 part of morinda officinalis and 1.0 part of prepared fleece-flower root.
The manufacturing steps are as follows; selecting 5.0 parts of mulberry twig, 5.0 parts of wormwood, 1.0 part of coconut shell, 1.0 part of morinda officinalis and 1.0 part of prepared fleece-flower root, placing into an ultrafine grinder, grinding into fine powder with the powder diameter of 100-150 mu m, drying and fully mixing the fine powder, placing the mixed finished product into a non-woven fabric bag with the size of about 11cm multiplied by 8cm, sealing the non-woven fabric bag into a bag, adding purified water into a container with 0.5 part of carbomer, soaking for 12 hours, adding 0.01 part of EDTA into the soaked carbomer solution, uniformly stirring to obtain a phase A, then placing 8.0 parts of NP-700, 0.3 part of aluminum glycinate and 30 parts of glycerol into a stainless steel large container, uniformly stirring to obtain a phase B, finally adding the phase B into the phase A, placing into a vacuum stirrer, stirring for 5min under the condition of 140r/min, taking out the paste, coating the paste, placing the non-woven fabric into a room temperature after coating, curing under the condition, and naturally molding the non-woven fabric.
Example 2
The difference between the present example and example 1 is that the weight parts of the components are different, wherein carbomer 1.0 part, NP-700.0 parts, aluminum glycinate 0.5 parts, glycerin 50 parts, EDTA 0.05 parts, citric acid 0.2 parts, compound fine powder 40 parts, water 90 parts, the compound fine powder is composed of the following raw materials by weight: 6.5 parts of mulberry twig, 5.5 parts of wormwood, 1.5 parts of coconut shell, 1.5 parts of morinda officinalis and 1.5 parts of prepared fleece-flower root.
Example 3
The difference between the present example and example 1 is that the weight parts of the components are different, wherein carbomer 2.0 parts, NP-700.0 parts, aluminum glycinate 0.8 parts, glycerin 60 parts, EDTA 0.07 parts, citric acid 0.3 parts, compound fine powder 50 parts, water 100 parts, the compound fine powder is composed of the following raw materials by weight: 7.0 parts of mulberry twig, 6.0 parts of wormwood, 2.0 parts of coconut shell, 2.0 parts of morinda officinalis and 2.0 parts of prepared fleece-flower root.
Comparative example
The comparative example used a black plaster on the market.
The prescription is applied to the surface of the uncomfortable skin of a patient and fixed after 30 persons suffering from cervical and lumbar discomfort are randomly selected during clinical trial, and the prescription is specifically applied once daily, used before sleeping every night, torn off after the morning, continuously applied for 8-10 hours, and used for one period every 5 days, if the prescription takes effect, the period is prolonged by 1-2 periods, and if the prescription is ineffective, the trial is terminated. The actual records show that the statistical results are shown in the following table 1:
table 1 treatment results
From the data in the table 1, the total effective rate of the invention reaches 83.33% in the treatment of 30 people, which shows that the invention can play a relatively obvious role in relieving neck and shoulder discomfort, waist and leg ache caused by damp cold wind evil in the neck and lumbar vertebra.
50 persons were randomly selected, of which women 28 persons and men 22 persons, and then each person was attached with the plaster of the example and the plaster of the comparative example on the left and right arms, respectively, with the results shown in table 2 below:
table 2 difference between examples and comparative examples
From the above table 2, it can be seen that the present invention has a low probability of feeling painful when pulled after use, whereas the conventional present invention has a probability of feeling painful when pulled of more than 50%, thus proving that the present invention has good comfort when used.
And (5) measuring primary adhesion, namely removing the anti-adhesion paper from the cataplasm, and standing at room temperature for more than 2 hours without overlapping each other. The surfaces of the inclined plate and the stainless steel ball are wiped, and the adhesive surface of the adhesive patch is upwards and flatly fixed on the inclined plate by using a double-sided adhesive tape. The steel balls with different specifications are freely rolled down from the top end of the inclined plane, and the maximum ball number which can be stuck by the paste surface is recorded. And (3) carrying out adhesion force measurement, namely scrubbing the test plate and the loading plate with absolute ethyl alcohol before an experiment, taking a sample cut into 5cm multiplied by 8cm, longitudinally sticking the sample to the middle parts of the test plate and the loading plate which are close to each other, rolling the sample back and forth for three times by using a compression roller, sticking the sample on the plate, standing for 20min at room temperature, and fixing the sample on a test frame. A 200g weight was hung and the time for the test article to fall off the test plate was recorded. The results are shown in Table 3 below.
Table 3 adhesion test results according to the above test results, the tentative initial adhesion test should be capable of adhering No. 15 steel balls (steel balls weight 5.6 g), and the holding adhesion test is more than 150s, so as to indicate that the external preparation of the present invention has good adhesion and can be well fixed at the affected part.
Taking 2 pieces of three samples of the external prescription of the invention, removing the cover lining, heating at 50 ℃ for 3 hours, and observing after the external prescription is naturally cooled, wherein the back of the ointment has no turbidity, the ointment has smooth surface and still has viscosity after finger touch test, thus the external prescription of the invention has good heat resistance.
The foregoing has shown and described the basic principles and main features of the present invention and the advantages of the present invention. It will be understood by those skilled in the art that the present invention is not limited to the embodiments described above, and that the above embodiments and descriptions are merely illustrative of the principles of the present invention, and various changes and modifications may be made without departing from the spirit and scope of the invention, which is defined in the appended claims. The scope of the invention is defined by the appended claims and equivalents thereof.

Claims (6)

1. An external prescription for cervical vertebra and lumbar vertebra diseases is characterized in that: the material consists of the following raw materials in parts by weight: 0.5 to 2.0 parts of carbomer, 8.0 to 10.0 parts of NP-700, 0.3 to 0.8 part of aluminum glycyrrhizate, 30 to 60 parts of glycerin, 0.01 to 0.07 part of EDTA, 0.05 to 0.3 part of citric acid, 35 to 50 parts of compound fine powder and 80 to 100 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 5.0 to 7.0 parts of mulberry twig, 5.0 to 6.0 parts of wormwood, 1.0 to 2.0 parts of coconut shell, 1.0 to 2.0 parts of morinda officinalis and 1.0 to 2.0 parts of prepared fleece-flower root;
the method comprises the following steps:
s1, weighing certain parts by weight of mulberry twig, wormwood, coconut shell, morinda officinalis and prepared fleece-flower root according to the formula, respectively processing the mulberry twig, wormwood, coconut shell, morinda officinalis and prepared fleece-flower root into powder by a superfine pulverizer, screening the powder by a filter screen, drying the powder, and fully mixing the powder;
s2, placing the mixed finished product into a non-woven fabric bag with the size of about 11cm multiplied by 8cm, and sealing the bag;
s3, adding purified water into a carbomer container with a certain amount, soaking for 12 hours, adding EDTA into the soaked carbomer solution, stirring uniformly to obtain a phase A, putting NP-700, dihydroxyaluminum and glycerol into a stainless steel large container, and stirring uniformly to obtain a phase B;
s4, adding the phase B into the phase A, placing in a vacuum stirrer, stirring to obtain paste, taking out the paste, coating the paste on a non-woven fabric bag, and placing at room temperature after coating, and naturally solidifying and forming the paste.
2. The external prescription for cervical and lumbar diseases according to claim 1, wherein: and (3) filtering the fine powder obtained in the step (S1) through a 100-150-mesh filter screen to obtain fine powder with a powder diameter of 100-150 mu m.
3. The external prescription for cervical and lumbar diseases according to claim 2, wherein: the stirring speed of the vacuum stirrer in the step S4 is 120-160 r/min, and the stirring time is about 5 min.
4. A cervical and lumbar vertebra disease external prescription according to claim 3, wherein: the external prescription comprises the following raw materials in parts by weight: 0.5 part of carbomer, 0.3 part of aluminum glycyrrhizate, 30 parts of glycerol, 0.01 part of EDTA, 0.05 part of citric acid, 35 parts of compound fine powder and 80 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 5.0 parts of mulberry twig, 5.0 parts of wormwood, 1.0 part of coconut shell, 1.0 part of morinda officinalis and 1.0 part of prepared fleece-flower root.
5. A cervical and lumbar vertebra disease external prescription according to claim 3, wherein: the external prescription comprises the following raw materials in parts by weight: 1.0 part of carbomer, 9.0 parts of NP-700, 0.5 part of aluminum glycyrrhizate, 50 parts of glycerin, 0.05 part of EDTA, 0.2 part of citric acid, 40 parts of compound fine powder and 90 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 6.5 parts of mulberry twig, 5.5 parts of wormwood, 1.5 parts of coconut shell, 1.5 parts of morinda officinalis and 1.5 parts of prepared fleece-flower root.
6. A cervical and lumbar vertebra disease external prescription according to claim 3, wherein: the external prescription comprises the following raw materials in parts by weight: 2.0 parts of carbomer, 10.0 parts of NP-700, 0.8 part of aluminum glycyrrhizate, 60 parts of glycerin, 0.07 part of EDTA, 0.3 part of citric acid, 50 parts of compound fine powder and 100 parts of water, wherein the compound fine powder comprises the following raw materials in parts by weight: 7.0 parts of mulberry twig, 6.0 parts of wormwood, 2.0 parts of coconut shell, 2.0 parts of morinda officinalis and 2.0 parts of prepared fleece-flower root.
CN202210271512.6A 2022-03-18 2022-03-18 External prescription for cervical vertebra and lumbar vertebra diseases Active CN114533805B (en)

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