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31 results about "Doxycycline Hyclate" patented technology

The hyclate salt form of doxycycline, a synthetic, broad-spectrum tetracycline antibiotic exhibiting antimicrobial activity. Doxycycline hyclate binds reversibly to the 30S ribosomal subunit, possibly to the 50S ribosomal subunit as well, thereby blocking the binding of aminoacyl-tRNA to the mRNA-ribosome complex. This leads to an inhibition of protein synthesis. In addition, this agent has exhibited inhibition of collagenase activity.

Doxycycline-hyclate-carried GTR/GBR composite membrane and preparation method thereof

The invention discloses a doxycycline-hyclate-carried GTR (Guide Tissue Regeneration)/GBR (Guide Bone Regeneration) composite membrane and a preparation method thereof and belongs to the technical field of medicines. The GTR/GBR composite membrane adopts a three-layer structure, wherein the upper surface layer, the lower surface layer and the sandwich layer are all manufactured through sequence electrospinning; the upper surface layer and the lower surface layer are prepared from a natural polymer material and a mixed solution through which the polymer material is synthesized; the sandwich layer is a membrane layer prepared from a doxycycline-hyclate-carried solution through which the polymer material is synthesized. The uniaxial sequence electrospinning method is adopted to prepare the composite membrane adopting the three-layer structure, so that the medicine entrapment efficiency of fibers is improved, the preliminary burst effect of a medicine is reduced/eliminated, and continuously slow release of the medicine is realized. The two surface layers of the three-layer medicine-carried composite membrane can not only serve as porous barriers to control the medicine release rate so as to realize continuously slow release of the medicine but also prevent direct contact between the medicine and tissues to improve the compatibility between the tissues and the membrane so as to be more conducive to tissue repair and regeneration.
Owner:FOURTH MILITARY MEDICAL UNIVERSITY

Preparation method of doxycycline hyclate freeze-dried powder injection

ActiveCN105078905ASolve technical problems that are difficult to freeze-dryImprove freeze-drying efficiencyAntibacterial agentsPowder deliveryAtrophyFreeze-drying
The invention discloses a preparation method of doxycycline hyclate freeze-dried powder injection. The method includes steps of material preparing, freeze drying and the like, wherein pre-freezing is performed in three steps, the temperature of materials is fast decreased to about minus 20 DEG C, then the temperature of the materials is decreased to about minus 30 DEG C at a constant speed, and the temperature of the materials is finally fast decreased to about minus 40 DEG C and the temperature is kept; sublimation is performed in two steps, the temperature of the materials is increased to about minus 20 DEG C and the temperature is kept for 5-10 hours, and then the temperature of the materials is increased to about minus 5 DEG C and the temperature is kept for 1-3 hours. The method has the advantages that the special freeze drying process is used to solve the technical problem that the doxycycline hyclate liquid is difficult in freeze drying, doxycycline hyclate liquid solid content can reach above 50%, freeze drying efficiency is increased, freeze drying cycle is shortened, and products are full in appearance, free of atrophy, collapse, fracture and the like, and good in re-dissolving performance and mass stability.
Owner:HAINAN GENERAL & KANGLI PHARMA

Veterinary compound florfenicol injection and preparation method thereof

The invention discloses compound florfenicol injection and a preparation method thereof. The compound florfenicol injection comprises the following components: 500g of florfenicol, 500g of doxycycline hyclate, 500g of tilmicosin phosphate, 3,000g of polyvinylpyrrolidone, 4,000g of N, N-dimethylacetylamide, 200g of magnesium chloride, 20g of sodium formaldehyde sulphoxylate and 10,000 milliliters of water for injection. The preparation method comprises the following steps of: (1) preparing; (2) adding doxycycline into the polyvinylpyrrolidone, heating to 80 DEG C, stirring until a mixture is clarified, adding the tilmicosin phosphate, and stirring until a mixture is clarified; (3) heating dimethylacetylamide to 50 DEG C, adding the florfenicol, and stirring for dissolving; (4) adding 1,000 milliliters of water for injection, adding the magnesium chloride and the sodium formaldehyde sulphoxylate in turn, and stirring for dissolving; and (5) mixing solution prepared in the step (2) and the step (3), gradually adding solution prepared in the step (4) under stirring, replenishing the water for injection until the total volume of the water for injection is 10,000 milliliters, uniformly stirring, filtering, filling nitrogen, encapsulating, and sterilizing at the temperature of between 110 and 115 DEG C for 30 minutes to prepare the compound florfenicol injection.
Owner:HUBEI WUDANG ANIMAL PHARMA

Device and method for recycling ethyl alcohol in refined mother solution of doxycycline hyclate

The invention discloses a device and method for recycling ethyl alcohol in a refined mother solution of doxycycline hyclate. The specific device for recycling ethyl alcohol comprises a pressure reduction distillation kettle, a neutralization kettle, a press filter, a to-be-recycled ethyl alcohol intermediate tank, a distillation tower, a vaporization membrane separation device and a finished product tank which are connected in sequence; the distillation tower is connected with a side material solution inlet of the vaporization membrane separation device, and a side material solution outlet ofthe vaporization membrane separation device is connected with the finished product tank. According to the device and method for recycling the ethyl alcohol in the refined mother solution of the doxycycline hyclate, the rate of recycling absolute ethyl alcohol reaches 85% or above, the content of the recycled ethyl alcohol reaches 99.5% or above, the moisture content is smaller than 0.5%, the content of chloroethane is lower than 200 ppm, and the recycle device and method accord with the standard of recycle application. The technology is stable, the recycle rate is high, the production cost isgreatly lowered, low-temperature pressure reduction distillation is adopted, the energy is saved, the emission amount of the ethyl alcohol is lowered, and the environmental pollution is reduced.
Owner:CHANGZHOU PHARMA FACTORY

Ureaplasma urealyticum/mycoplasma hominis combined rapid culture and drug sensitivity detection kit

Provided is a ureaplasma urealyticum/mycoplasma hominis combined rapid culture and drug sensitivity detection kit. The kit can complete detection in 8-24 h, and meanwhile, drug-resistant detection of various antibiotics can be performed. The combined rapid culture kit is mainly composed of pork stomach digestive juice or lung digestive juice, a beef extracting solution or a beef heart extracting solution, cattle serum or horse serum or other animal serum, sodium chloride, peptone, yeast powder, urea, L-arginine, phenol red indicator or cresol red indicator, and penicillin or other antibiotics. The drug detection kit can detect doxycycline hyclate, roxithromycin, acetylspiramycin, gatifloxacin, clarithromycin, azithromycin, clindamycin, erythromycin, kitasamycin, ofloxacin, levofloxacin hydrochloride, sparfloxacin, ciprofloxacin, doxycycline, erythromycin cydocarbonate and various other antibiotics. By means of the detection kit, not only is the mycoplasma detection time shortened, but also drug-resistant detection can be performed at the same time so that clinical medication can be guided. The detection kit has the beneficial effects of being high in sensitivity, high in specificity, high in detection rate, easy and convenient to operate and the like.
Owner:姜洪波 +1

Veterinary compound florfenicol injection and preparation method thereof

The invention discloses compound florfenicol injection and a preparation method thereof. The compound florfenicol injection comprises the following components: 500g of florfenicol, 500g of doxycycline hyclate, 500g of tilmicosin phosphate, 3,000g of polyvinylpyrrolidone, 4,000g of N, N-dimethylacetylamide, 200g of magnesium chloride, 20g of sodium formaldehyde sulphoxylate and 10,000 milliliters of water for injection. The preparation method comprises the following steps of: (1) preparing; (2) adding doxycycline into the polyvinylpyrrolidone, heating to 80 DEG C, stirring until a mixture is clarified, adding the tilmicosin phosphate, and stirring until a mixture is clarified; (3) heating dimethylacetylamide to 50 DEG C, adding the florfenicol, and stirring for dissolving; (4) adding 1,000 milliliters of water for injection, adding the magnesium chloride and the sodium formaldehyde sulphoxylate in turn, and stirring for dissolving; and (5) mixing solution prepared in the step (2) and the step (3), gradually adding solution prepared in the step (4) under stirring, replenishing the water for injection until the total volume of the water for injection is 10,000 milliliters, uniformly stirring, filtering, filling nitrogen, encapsulating, and sterilizing at the temperature of between 110 and 115 DEG C for 30 minutes to prepare the compound florfenicol injection.
Owner:HUBEI WUDANG ANIMAL PHARMA

Preparation technology for improving purity of doxycycline hyclate injection

The invention relates to a preparation technology for improving the purity of a doxycycline hyclate injection. The preparation technology comprises following steps: grinding doxycycline hyclate into powder by the use of a ball mill, and dissolving the powder in water so as to form a solution A; dissolving ethyl cellulose in an organic solvent so as to form a solution B; pouring the solution A into the solution B under a stirring condition, wherein an emulsion is formed after the solution A disperses in the solution B; dissolving gelatin in distilled water under a water-bath condition at 60-80 DEG C so as to prepare a protection solution D which is standby at the constant temperature of 30 DEG C; drooping the emulsion C into the protection solution D under a stirring condition so as to form a solution E, and stirring the solution under a condition that the temperature of the water-bath is raised to 50 DEG C from 30 DEG C so that the organic solvent volatilizes; and then performing suction filtration on the solution E, washing the solution E, and drying the solution E so as to obtain the white powder doxycycline hyclate. According to the invention, problems that the dissolving speed is relatively slow in a conventional preparation process of doxycycline hyclate preparations and the doxycycline hyclate for injection contains impurities in the conventional preparation process are solved.
Owner:CHINA CHENGDU ANIMAL HUSBANDRY IND BIOPHARM
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