CN114983944B - Preparation method of tiamulin fumarate soluble powder - Google Patents

Preparation method of tiamulin fumarate soluble powder Download PDF

Info

Publication number
CN114983944B
CN114983944B CN202210838306.9A CN202210838306A CN114983944B CN 114983944 B CN114983944 B CN 114983944B CN 202210838306 A CN202210838306 A CN 202210838306A CN 114983944 B CN114983944 B CN 114983944B
Authority
CN
China
Prior art keywords
tiamulin fumarate
soluble powder
mixture
citric acid
sieved
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN202210838306.9A
Other languages
Chinese (zh)
Other versions
CN114983944A (en
Inventor
廖仕学
曲俊腾
王文静
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guobang Pharmaceutical Group Co Ltd
Shandong Guobang Pharmaceutical Co Ltd
Original Assignee
Guobang Pharmaceutical Group Co Ltd
Shandong Guobang Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Guobang Pharmaceutical Group Co Ltd, Shandong Guobang Pharmaceutical Co Ltd filed Critical Guobang Pharmaceutical Group Co Ltd
Priority to CN202210838306.9A priority Critical patent/CN114983944B/en
Publication of CN114983944A publication Critical patent/CN114983944A/en
Application granted granted Critical
Publication of CN114983944B publication Critical patent/CN114983944B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/141Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
    • A61K9/146Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12Antidiarrhoeals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Epidemiology (AREA)
  • Communicable Diseases (AREA)
  • Medicinal Preparation (AREA)
  • Emergency Medicine (AREA)
  • Pulmonology (AREA)
  • Oncology (AREA)

Abstract

The invention discloses a preparation method of tiamulin fumarate soluble powder, belonging to the technical field of veterinary drugs, and the preparation method comprises the following steps: preparing a binder, preparing a mixture and preparing tiamulin fumarate soluble powder; the method for preparing the tiamulin fumarate soluble powder comprises the steps of taking anhydrous citric acid and sodium chloride, sieving, adding the sieved anhydrous citric acid and the sieved sodium chloride into a mixture, adding the anhydrous citric acid and the sieved sodium chloride into a mixing barrel together, and starting a hopper mixer to mix to obtain the tiamulin fumarate soluble powder; the invention can avoid the use of organic solvent, prolong the drug effect, avoid the irritant gas and paralysis of the tiamulin fumarate soluble powder, improve the content and water solubility of active substances in the tiamulin fumarate soluble powder and reduce the sensitivity of the tiamulin fumarate soluble powder to water quality.

Description

Preparation method of tiamulin fumarate soluble powder
Technical Field
The invention relates to the technical field of veterinary drugs, and in particular relates to a preparation method of tiamulin fumarate soluble powder.
Background
The tiamulin fumarate is fumarate of tiamulin, white or white-like crystalline powder, odorless and tasteless, and can be used for treating chronic respiratory diseases of chicken, mycoplasma pneumonia of swine and hemophilus pleuropneumonia of Haemophilus, and dysentery caused by treponema suis; in addition, tiamulin fumarate is extremely sensitive to mycoplasma, and is one of the most effective drugs for treating mycoplasmosis at present.
However, the current use of tiamulin fumarate has the following problems: organic solvents are frequently used in preparation of the preparation, so that on one hand, the problem of organic solvent residue exists, which affects animal health, and on the other hand, the problem of safety needs to be considered when the organic solvents are used in preparation, so that the investment cost and the production complexity are increased; materials such as a filling agent, an adhesive and the like are adopted in the preparation, the prepared preparation product cannot fully cover the pungent smell of the raw materials, and after the preparation product is dissolved, the pungent smell can be further released, so that the feeding and drinking amount of animals are influenced; the tiamulin fumarate has large molecular weight, and the molecules are too large to completely enter a cavity of beta-cyclodextrin, so that the inclusion effect is poor, the stability is poor, the content of raw materials is limited, and soluble powder with high material content cannot be prepared; the tiamulin fumarate is sensitive to water quality in a drinking water administration process, underground well water or common tap water is mostly used in a culture site, the water quality is poor, effective components are separated out and wasted, and the use effect is influenced.
In order to solve the problems, the current main solution is to use an enteric coating material, but the enteric coating material is not dissolved under acidic and neutral conditions, only can be used for mixing and feeding, is not suitable for the current situation of drinking water feeding in poultry breeding, and can not solve the problems that the soluble powder with high raw material content can not be prepared and the water quality is sensitive in the drinking water feeding process.
Chinese patent CN100337622C discloses a solid dispersion containing tiamulin fumarate and a preparation method thereof, which comprises heating and melting tiamulin fumarate and a medical water-soluble carrier in the presence of an organic solvent, cooling and solidifying, pulverizing, and drying to remove the organic solvent; the patent has the following defects: the preparation process uses organic solvent, and the prepared solid dispersible tablet can generate pungent odor after being dissolved.
Chinese patent CN104146949A discloses a tiamulin fumarate premix and a preparation method thereof, which comprises the steps of crushing, mixing, granulating and screening a tiamulin fumarate raw material and gelatin to obtain a final premix; the patent has the following defects: the prepared tiamulin fumarate premix can generate pungent smell after being dissolved.
Chinese patent CN104490788B discloses tiamulin fumarate particles and a preparation method thereof, wherein a filler and an adhesive are added into a tiamulin fumarate raw material, boiling granulation is carried out, then the prepared particles are added into a coating solution for coating, the adhesive is at least one of pregelatinized starch or hydroxypropyl methyl cellulose, the filler is at least one of soluble starch, lactose and glucose, and the coating agent is HPMC, PEG, tween-80, talcum powder and ethanol; the patent has the following defects: the preparation process uses organic solvent, and the prepared tiamulin fumarate particles can generate pungent odor after being dissolved.
Chinese patent CN105878228B discloses tiamulin fumarate soluble powder and a preparation method thereof, wherein beta-cyclodextrin is adopted as an inclusion agent, tiamulin fumarate is dissolved in ethanol, a saturated aqueous solution of the beta-cyclodextrin is added, the inclusion compound is precipitated by cooling and adding excessive ethanol, and EDTA, sodium dodecyl sulfate and a filler are added to obtain the final soluble powder after filtration and drying; the patent has the following defects: the preparation process uses an organic solvent, has poor clathration effect and poor stability, limits the content of raw materials, and cannot prepare tiamulin fumarate soluble powder with high raw material content.
Chinese patent CN111419823B discloses a tiamulin fumarate enteric-coated pellet and a preparation method and application thereof, wherein tiamulin fumarate is added into PEG6000 in a molten state, and then the mixture is cooled, solidified and crushed into particles, and then enteric-coated, wherein coating liquid is HP-55, talcum powder and ethanol water; the patent has the following defects: organic solvents were used in the preparation.
Disclosure of Invention
Aiming at the defects in the prior art, the invention provides a preparation method of tiamulin fumarate soluble powder, which can avoid the use of organic solvents, prolong the drug effect, avoid irritant gas and paralytic feeling of the tiamulin fumarate soluble powder, improve the content and water solubility of active substances in the tiamulin fumarate soluble powder and reduce the sensitivity of the tiamulin fumarate soluble powder to water quality.
In order to solve the technical problems, the technical scheme adopted by the invention is as follows:
a preparation method of tiamulin fumarate soluble powder comprises the following steps: preparing a binder, preparing a mixture and preparing tiamulin fumarate soluble powder;
the method for preparing the adhesive comprises the steps of adding PVP-K30 into water, stirring and fully dissolving, then adding water-soluble acrylic resin JT-206, and stirring uniformly to obtain the adhesive;
the manufacturer of the water-soluble acrylic resin JT-206 is New Material Co., ltd of Fushan City;
in the preparation of the adhesive, the weight ratio of PVP-K30, water and water-soluble acrylic resin JT-206 is 3-5;
the method for preparing the mixture comprises adding tiamulin fumarate into a fluidized bed granulator, starting the fluidized bed granulator, and controlling the air intake at 50-75m 3 H, the air inlet temperature is 50-80 ℃, the adhesive is added through the peristaltic pump, the rated rotating speed of the peristaltic pump is controlled to be 20-50%, and after the adhesive is added, the air inlet quantity is adjusted to be 60-90m 3 H, drying for 15-20min at the air inlet temperature of 70-90 ℃ to obtain a mixture;
in the prepared mixture, the weight ratio of the tiamulin fumarate to the binder is 60-80;
the method for preparing the tiamulin fumarate soluble powder comprises the steps of taking anhydrous citric acid and sodium chloride, processing the anhydrous citric acid and the sodium chloride with 30-mesh and 80-mesh sieves respectively, taking the middle part of 30-mesh to 80-mesh sieves to obtain the sieved anhydrous citric acid and the sieved sodium chloride, adding the sieved anhydrous citric acid and the sieved sodium chloride into a mixture, adding the mixture into a mixing barrel together, starting a hopper mixer to mix, controlling the rotating speed to be 50-100rpm, and mixing for 15-20min to obtain the tiamulin fumarate soluble powder;
in the preparation of the tiamulin fumarate soluble powder, the weight ratio of the sieved anhydrous citric acid to the sieved sodium chloride to the mixture is (0.5-1).
Compared with the prior art, the invention has the following beneficial effects:
(1) The preparation method of the tiamulin fumarate soluble powder can avoid the use of an organic solvent and solve the problem of organic solvent residue;
(2) The preparation method of the tiamulin fumarate soluble powder can avoid irritant gas and paralytic feeling of the tiamulin fumarate soluble powder, increase water drinking amount, dissolve the tiamulin fumarate soluble powder prepared by the invention into tap water according to 1 ten thousand ppm of tiamulin fumarate, feel with tongue tip, have no obvious paralytic feeling, dissolve the tiamulin fumarate soluble powder prepared by the invention according to 125ppm of tiamulin fumarate, carry out drinking water administration on white feather broilers, continuously use for 5 days, and daily average water drinking amount is 142-151mL;
(3) The preparation method of the tiamulin fumarate soluble powder can improve the water solubility of the tiamulin fumarate soluble powder, the tiamulin fumarate soluble powder prepared by the invention is added into tap water at room temperature according to 1 ten thousand ppm of tiamulin fumarate, and the mixture is stirred for 3min after being added, wherein the turbidity is 8.9-13.5NTU;
(4) The preparation method of the tiamulin fumarate soluble powder can improve the stability of the tiamulin fumarate soluble powder and reduce the sensitivity of the tiamulin fumarate soluble powder to water quality, the tiamulin fumarate soluble powder prepared by the method is dissolved in 20 ℃ tap water according to 1 ten thousand ppm of tiamulin fumarate, and then the solution is settled after standing for 24 hours, no sediment and no floating matter exist, and the effective content of the supernatant is 97.5-98.2%;
(5) The preparation method of the tiamulin fumarate soluble powder can prolong the drug effect of the tiamulin fumarate soluble powder, improve the blood concentration of chickens after drinking water administration, and improve the blood concentration by more than 14% compared with the existing product.
Drawings
Fig. 1 is a graph comparing the blood concentration in vivo of tiamulin fumarate soluble powders prepared in examples 1 to 4 and comparative examples 1 to 3.
Detailed Description
In order to more clearly understand the technical features, objects, and effects of the present invention, specific embodiments of the present invention will now be described.
Example 1
A preparation method of tiamulin fumarate soluble powder comprises the following steps:
1. adding PVP-K30 into water, stirring and fully dissolving, then adding water-soluble acrylic resin JT-206, and stirring uniformly to obtain an adhesive;
the manufacturer of the water-soluble acrylic resin JT-206 is New Material Co., ltd of Fushan City;
wherein the weight ratio of PVP-K30, water and water-soluble acrylic resin JT-206 is 3;
2. adding tiamulin fumarate into fluidized bed granulator, starting the fluidized bed granulator, and controlling air intake at 75m 3 The inlet air temperature is 60 ℃, the adhesive is added through the peristaltic pump, the rated rotating speed of the peristaltic pump is controlled to be 25%, and after the adhesive is added, the inlet air volume is adjusted to be 90m 3 Drying for 17min at the air inlet temperature of 70 ℃ to obtain a mixture;
the weight ratio of the tiamulin fumarate to the adhesive is 60;
3. taking anhydrous citric acid and sodium chloride, respectively processing the anhydrous citric acid and the sodium chloride by using a 30-mesh sieve and a 80-mesh sieve, taking the middle part of the mixture from 30 meshes to 80 meshes to obtain the sieved anhydrous citric acid and the sieved sodium chloride, adding the sieved anhydrous citric acid and the sieved sodium chloride into the mixture, then adding the mixture into a mixing barrel together, starting a hopper mixer to mix, controlling the rotating speed to be 50rpm, and mixing for 15min to obtain tiamulin fumarate soluble powder;
wherein the weight ratio of the sieved anhydrous citric acid to the sieved sodium chloride to the mixture is 0.6.
Example 2
A preparation method of tiamulin fumarate soluble powder comprises the following steps:
1. adding PVP-K30 into water, stirring and fully dissolving, then adding water-soluble acrylic resin JT-206, and stirring uniformly to obtain an adhesive;
the manufacturer of the water-soluble acrylic resin JT-206 is New Material Co., ltd of Fushan City;
wherein the weight ratio of PVP-K30, water and water-soluble acrylic resin JT-206 is 5;
2. adding tiamulin fumarate into fluidized bed granulator, starting the fluidized bed granulator, and controlling air intake at 75m 3 The air inlet temperature is 70 ℃, the adhesive is added through the peristaltic pump, the rated rotating speed of the peristaltic pump is controlled to be 20%, and after the adhesive is added, the air inlet volume is adjusted to be 90m 3 Drying for 20min at 75 deg.C to obtain mixture;
the weight ratio of the tiamulin fumarate to the adhesive is 80;
3. taking anhydrous citric acid and sodium chloride, respectively processing the anhydrous citric acid and the sodium chloride by using a 30-mesh sieve and a 80-mesh sieve, respectively taking the middle part of the citric acid from 30 meshes to 80 meshes to obtain the sieved anhydrous citric acid and the sieved sodium chloride, respectively weighing the sieved anhydrous citric acid, adding the sieved sodium chloride into the mixture, then adding the mixture into a mixing barrel, starting a hopper mixer to mix, controlling the rotating speed to be 70rpm, and mixing for 20min to obtain tiamulin fumarate soluble powder;
wherein the weight ratio of the sieved anhydrous citric acid to the sieved sodium chloride to the mixture is 1.
Example 3
A preparation method of tiamulin fumarate soluble powder comprises the following steps:
1. adding PVP-K30 into water, stirring and fully dissolving, then adding water-soluble acrylic resin JT-206, and stirring uniformly to obtain an adhesive;
the manufacturer of the water-soluble acrylic resin JT-206 is New Material Co., ltd of Fushan City;
wherein the weight ratio of PVP-K30, water and water-soluble acrylic resin JT-206 is 3.5;
2. adding tiamulin fumarate into fluidized bed granulator, starting the fluidized bed granulator, and controlling air intake at 75m 3 The air inlet temperature is 50 ℃, the adhesive is added through the peristaltic pump, the rated rotating speed of the peristaltic pump is controlled to be 30%, and after the adhesive is added, the air inlet volume is adjusted to be 90m 3 Drying for 15min at 90 ℃ to obtain a mixture;
the weight ratio of the tiamulin fumarate to the adhesive is 75;
3. taking anhydrous citric acid and sodium chloride, respectively processing the anhydrous citric acid and the sodium chloride by using a 30-mesh sieve and a 80-mesh sieve, respectively taking the middle part of the citric acid from 30 meshes to 80 meshes to obtain the sieved anhydrous citric acid and the sieved sodium chloride, respectively weighing the sieved anhydrous citric acid, adding the sieved sodium chloride into the mixture, then adding the mixture into a mixing barrel, starting a hopper mixer to mix, controlling the rotating speed to be 100rpm, and mixing for 20min to obtain tiamulin fumarate soluble powder;
wherein, the weight ratio of the sieved anhydrous citric acid to the sieved sodium chloride to the mixture is 0.5.
Example 4
A preparation method of tiamulin fumarate soluble powder comprises the following steps:
1. adding PVP-K30 into water, stirring and fully dissolving, then adding water-soluble acrylic resin JT-206, and stirring uniformly to obtain an adhesive;
the manufacturer of the water-soluble acrylic resin JT-206 is New Material Co., ltd of Fushan City;
wherein the weight ratio of PVP-K30, water and water-soluble acrylic resin JT-206 is 3.2;
2. weighing tiamulin fumarate, adding into a fluidized bed granulator, starting the fluidized bed granulator, and controlling the air intake at 50m 3 H, the air inlet temperature is 80 ℃, the adhesive is added through the peristaltic pump, the rated rotating speed of the peristaltic pump is controlled to be 50%, and the air inlet volume is adjusted after the adhesive is addedIs 60m 3 Drying for 18min at the air inlet temperature of 80 ℃ to obtain a mixture;
the weight ratio of the tiamulin fumarate to the adhesive is 65.7;
3. taking anhydrous citric acid and sodium chloride, respectively processing the anhydrous citric acid and the sodium chloride by using a 30-mesh sieve and a 80-mesh sieve, respectively taking the middle part of the 30-mesh sieve to the 80-mesh sieve to obtain the sieved anhydrous citric acid and the sieved sodium chloride, respectively weighing the sieved anhydrous citric acid, adding the sieved sodium chloride into the mixture, adding the mixture into a mixing barrel, starting a hopper mixer to mix, controlling the rotating speed to be 100rpm, and mixing for 15min to obtain tiamulin fumarate soluble powder;
wherein, the weight ratio of the sieved anhydrous citric acid to the sieved sodium chloride is 0.9.
Example 5
A preparation method of tiamulin fumarate soluble powder comprises the following steps:
1. adding PVP-K30 into water, stirring and fully dissolving, then adding water-soluble acrylic resin JT-206, and stirring uniformly to obtain an adhesive;
the manufacturer of the water-soluble acrylic resin JT-206 is New Material Co., ltd of Foshan City;
wherein the weight ratio of PVP-K30, water and water-soluble acrylic resin JT-206 is 4;
2. adding tiamulin fumarate into fluidized bed granulator, starting the fluidized bed granulator, and controlling air intake at 60m 3 H, the air inlet temperature is 60 ℃, the adhesive is added through the peristaltic pump, the rated rotating speed of the peristaltic pump is controlled to be 25%, and after the adhesive is added, the air inlet volume is adjusted to be 80m 3 The air inlet temperature is 80 ℃, and after drying is carried out for 17min, a mixture is obtained;
the weight ratio of the tiamulin fumarate to the adhesive is 70;
3. taking anhydrous citric acid and sodium chloride, respectively processing the anhydrous citric acid and the sodium chloride by using a 30-mesh sieve and a 80-mesh sieve, taking the middle part of the mixture from 30 meshes to 80 meshes to obtain the sieved anhydrous citric acid and the sieved sodium chloride, adding the sieved anhydrous citric acid and the sieved sodium chloride into the mixture, then adding the mixture into a mixing barrel together, starting a hopper mixer to mix, controlling the rotating speed to be 70rpm, and mixing for 17min to obtain tiamulin fumarate soluble powder;
wherein the weight ratio of the sieved anhydrous citric acid to the sieved sodium chloride to the mixture is 0.6.
Comparative example 1
A preparation method of tiamulin fumarate soluble powder comprises the following steps:
1. weighing tiamulin fumarate and medicinal gelatin, adding into a mixing barrel, starting mixing at 100rpm for 20min, and taking out to obtain a primary mixture;
the weight ratio of the tiamulin fumarate to the medicinal gelatin is 80;
2. transferring the primary mixture into a crusher, starting the crusher, controlling the rotating speed to be 3000rpm, crushing for 3min to obtain crushed materials, sieving the crushed materials with a 80-mesh sieve, and taking undersize as a mixture;
3. adding the mixture into a wet granulator, adding purified water for wet granulation to obtain wet granules, transferring the wet granules into a fluidized bed, drying, and drying to obtain tiamulin fumarate soluble powder;
the weight ratio of the mixture to the purified water is 100.
Comparative example 2
A commercial tiamulin fumarate premix, manufacturer: loyang Henrel Biotechnology Ltd, lot number 2108033, content specification 80%;
comparative example 3
A commercial tiamulin fumarate premix, manufacturer: shanghai Shenya health products Co., ltd, batch No. 21120803, content specification 80%;
test example 1
The water solubility of tiamulin fumarate soluble powders prepared in examples 1 to 4 and comparative examples 1 to 3 was tested, and the test method and test results were as follows:
the test results of examples 1 to 4 and comparative examples 1 to 3 were as follows, in which 1 ten thousand ppm of tiamulin fumarate was added to room temperature tap water, stirred for 3min after the addition, and the turbidity after the dissolution was measured:
Figure 346519DEST_PATH_IMAGE001
from the above results, it can be seen that the water solubility of the tiamulin fumarate soluble powders prepared in examples 1-4 was better than that of the tiamulin fumarate soluble powders of comparative examples 1-3.
Test example 2
The taste masking effect of the tiamulin fumarate soluble powders prepared in examples 1 to 4 and comparative examples 1 to 3 was tested, and the test method and the test results were as follows:
dissolving tiamulin fumarate in tap water according to the proportion of 1 ten thousand ppm, and then using the tongue tip to feel whether paralysis is caused or not, wherein the results are as follows:
Figure 391836DEST_PATH_IMAGE002
in order to further compare and mask the taste effect, 800 white feather broilers of 30 days old are selected and divided into 8 groups, each group comprises 100 broilers, the tiamulin fumarate soluble powder prepared in examples 1-5 and comparative examples 1-3 is dissolved according to 125ppm of tiamulin fumarate, drinking water administration is respectively carried out on each group of white feather broilers, the white feather broilers are continuously used for 5 days, the water intake of each day is recorded at the same time, the average water intake of 5 days is calculated, and the calculation result is as follows:
Figure 488842DEST_PATH_IMAGE003
from the results, the tiamulin fumarate soluble powder prepared in the embodiments 1-5 can ensure that the daily water intake of poultry is 142-151mL, on one hand, the water intake is increased, on the other hand, the feed intake is increased, the breeding efficiency is improved, and on the other hand, when a disease outbreak occurs, the water intake is increased, enough medicine can be taken in, and the medicine effect is ensured.
Test example 3
The stability of the tiamulin fumarate soluble powders prepared in examples 1 to 5 and comparative examples 1 to 3 was tested, and the test method and test results were as follows:
dissolving 1 ten thousand ppm of tiamulin fumarate in tap water at 20 ℃, standing for 24h and 24h, observing the dissolved state, taking supernatant, and detecting the effective content, so as to compare the stability of the product after dissolution, wherein the detection result is as follows:
Figure 444160DEST_PATH_IMAGE004
the above data show that the product prepared by the scheme of the invention can maintain better stability within 24 hours, does not precipitate and float, is clear, the effective content of the upper layer is still maintained at 97.5-98.2%, and the product of the comparative example precipitates and precipitates to different degrees, so that the effective content of the upper layer is reduced and is 3.3-14.5% lower than that of the scheme of the invention.
Test example 4
The in vivo absorption effect of the tiamulin fumarate soluble powder prepared in examples 1 to 3 and comparative examples 1 to 3 was tested, and the test method and test results were as follows:
in order to further verify the difference of absorption effects in vivo, 600 white feather broilers of 30 days old are selected and equally divided into 6 groups, each group is 100, each group is administered with drinking water after the tiamulin fumarate soluble powder prepared in examples 1-3 and comparative examples 1-3 is dissolved according to 125ppm of tiamulin fumarate, blood plasma of the chickens starts to be collected 0.5h after administration to detect the blood plasma concentration, and the contrast graph of the obtained blood plasma concentration in vivo is shown in figure 1 after detection till 24h after administration;
as can be seen from the comparison of the in vivo blood concentration shown in figure 1, the bioavailability of the examples 1 and 3 in vivo is greatly improved compared with that of the comparative examples 1-3, the AUC is improved by more than 14%, the peak reaching time is close, but the effective blood concentration is maintained for a longer time, which indicates that the time for exerting the drug effect is longer.
All percentages used in the present invention are mass percentages unless otherwise indicated.
Finally, it should be noted that: although the present invention has been described in detail with reference to the foregoing embodiments, it will be apparent to those skilled in the art that changes may be made in the embodiments and/or equivalents thereof without departing from the spirit and scope of the invention. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.

Claims (1)

1. A preparation method of tiamulin fumarate soluble powder is characterized by comprising the following steps: preparing a binder, preparing a mixture and preparing tiamulin fumarate soluble powder;
the method for preparing the adhesive comprises the steps of adding PVP-K30 into water, stirring and fully dissolving, then adding water-soluble acrylic resin JT-206, and stirring uniformly to obtain the adhesive;
in the preparation of the adhesive, the weight ratio of PVP-K30, water and water-soluble acrylic resin JT-206 is 3-5;
the method for preparing the mixture comprises adding tiamulin fumarate into a fluidized bed granulator, starting the fluidized bed granulator, and controlling the air intake at 50-75m 3 The air inlet temperature is 50-80 ℃, the adhesive is added through the peristaltic pump, the rated rotating speed of the peristaltic pump is controlled to be 20-50%, and after the adhesive is added, the air inlet quantity is adjusted to be 60-90m 3 Drying for 15-20min at air inlet temperature of 70-90 deg.C to obtain mixture;
in the prepared mixture, the weight ratio of the tiamulin fumarate to the binder is 60-80;
the method for preparing the tiamulin fumarate soluble powder comprises the steps of taking anhydrous citric acid and sodium chloride, processing the anhydrous citric acid and the sodium chloride with 30-mesh and 80-mesh sieves respectively, taking the middle part of the mixture from 30-mesh to 80-mesh sieves to obtain the sieved anhydrous citric acid and the sieved sodium chloride, adding the sieved anhydrous citric acid and the sieved sodium chloride into the mixture, adding the anhydrous citric acid and the sieved sodium chloride into a mixing barrel together, starting a hopper mixer to mix, controlling the rotation speed to be 50-100rpm, and mixing for 15-20min to obtain the tiamulin fumarate soluble powder;
in the preparation of the tiamulin fumarate soluble powder, the weight ratio of the sieved anhydrous citric acid to the sieved sodium chloride to the mixture is (0.5-1).
CN202210838306.9A 2022-07-18 2022-07-18 Preparation method of tiamulin fumarate soluble powder Active CN114983944B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202210838306.9A CN114983944B (en) 2022-07-18 2022-07-18 Preparation method of tiamulin fumarate soluble powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202210838306.9A CN114983944B (en) 2022-07-18 2022-07-18 Preparation method of tiamulin fumarate soluble powder

Publications (2)

Publication Number Publication Date
CN114983944A CN114983944A (en) 2022-09-02
CN114983944B true CN114983944B (en) 2022-10-28

Family

ID=83021689

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202210838306.9A Active CN114983944B (en) 2022-07-18 2022-07-18 Preparation method of tiamulin fumarate soluble powder

Country Status (1)

Country Link
CN (1) CN114983944B (en)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH072638B2 (en) * 1986-07-28 1995-01-18 日本化薬株式会社 Preparation for oral administration
CN102406611A (en) * 2011-09-30 2012-04-11 上海恒丰强动物药业有限公司 Tiamulin soluble powder and preparation method thereof
CN104490788A (en) * 2014-11-26 2015-04-08 上海同仁药业有限公司 Tiamulin fumarate particles and preparation method thereof
CN105878228A (en) * 2016-06-27 2016-08-24 河北天元药业有限公司 Soluble powder with tiamulin hydrogen famarate and method for preparing soluble powder
CN106822033A (en) * 2015-12-07 2017-06-13 王玉万 The capsule core material and its micro-capsule of drug containing are prepared as capsule core material with maize cob meal
CN107308115A (en) * 2017-07-05 2017-11-03 山东中牧兽药有限公司 A kind of fumaric acid tiamulin soluble powder
CN108261410A (en) * 2016-12-30 2018-07-10 武汉回盛生物科技股份有限公司 A kind of safe ten thousand rhzomorphs inclusion enteric coated preparations of tartaric acid and preparation method
CN113750049A (en) * 2021-10-08 2021-12-07 山东惠民德赛克生物科技有限公司 Soluble powder of antibacterial composition and preparation method thereof

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH072638B2 (en) * 1986-07-28 1995-01-18 日本化薬株式会社 Preparation for oral administration
CN102406611A (en) * 2011-09-30 2012-04-11 上海恒丰强动物药业有限公司 Tiamulin soluble powder and preparation method thereof
CN104490788A (en) * 2014-11-26 2015-04-08 上海同仁药业有限公司 Tiamulin fumarate particles and preparation method thereof
CN106822033A (en) * 2015-12-07 2017-06-13 王玉万 The capsule core material and its micro-capsule of drug containing are prepared as capsule core material with maize cob meal
CN105878228A (en) * 2016-06-27 2016-08-24 河北天元药业有限公司 Soluble powder with tiamulin hydrogen famarate and method for preparing soluble powder
CN108261410A (en) * 2016-12-30 2018-07-10 武汉回盛生物科技股份有限公司 A kind of safe ten thousand rhzomorphs inclusion enteric coated preparations of tartaric acid and preparation method
CN107308115A (en) * 2017-07-05 2017-11-03 山东中牧兽药有限公司 A kind of fumaric acid tiamulin soluble powder
CN113750049A (en) * 2021-10-08 2021-12-07 山东惠民德赛克生物科技有限公司 Soluble powder of antibacterial composition and preparation method thereof

Also Published As

Publication number Publication date
CN114983944A (en) 2022-09-02

Similar Documents

Publication Publication Date Title
US20160256390A1 (en) Process for producing cellulose derivatives of high bulk density and good flowability
JP2000500140A (en) Cellulose acetate phthalate visceral coating composition
CN105193763B (en) A kind of hydrobromic acid Vortioxetine piece and preparation method thereof
JP2001518083A (en) Stabilization of acid-sensitive benzimidazoles by amino acid / cyclodextrin mixtures
CN113171344B (en) Tolvaptan oral preparation and preparation method thereof
JP3368898B1 (en) Process for producing granules containing branched chain amino acids
CN105412026B (en) Acotiamide hydrochloride hydrate piece and preparation method thereof
CN108186578A (en) A kind of preparation method of Ritonavir solid dispersions
CN113648327B (en) Pharmaceutical composition and preparation method thereof
CN114983944B (en) Preparation method of tiamulin fumarate soluble powder
CN112826798B (en) Ibuprofen pharmaceutical composition, preparation method and application
CN110313618B (en) Vitamin D 2 Method for preparing microcapsule
CN110693839B (en) Solid dispersion of varlitinib mesylate and preparation method and application thereof
CN107412198A (en) Duloxetine hydrochloride enteric slow release granule and preparation method thereof
CN107519144A (en) A kind of preparation method of telmisartan amlodipine tablets
JPS5877811A (en) Preparation of stable and easily absorbable pharmaceutical preparation of nifedipine
CN104606145B (en) ibuprofen granule and preparation method thereof
JP2000086509A (en) Production of sofalcone-containing preparation
Jain et al. Improvement of the dissolution behavior of the poorly water soluble drug diacerein by solid dispersion technology and its formulation into tablet dosage form
BR112013000233A2 (en) method of controlling or adjusting the release of an active ingredient and using a diluent control in a composition
CN114681404A (en) Repaglinide granule pharmaceutical composition and preparation method thereof
CN108024963A (en) On-mechanical technique for digoxin micronizing
EP4327805A1 (en) 13c methacetin granule, and preparation method therefor and use thereof
CN106389341A (en) Penfluridol polyanhydride pellet and penfluridol long-acting controlled release tablet as well as preparation method of penfluridol long-acting controlled release tablet
CN113307734A (en) Preparation method of calcium acetate raw material and preparation

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant