Medicine for treating chronic pelvic inflammation and its preparation method

Aminolevulinic acid hydrochloride liniment

The invention relates to aminolevulinic acid hydrochloride liniment, which is composed of a solvent and powder, wherein the powder is prepared by mixing aminolevulinic acid hydrochloride with traditional Chinese medicine effective components according to the weight ratio of 3:2; when the aminolevulinic acid hydrochloride liniment disclosed by the invention is used, the solvent and the powder are mixed and dissolved together. The aminolevulinic acid hydrochloride liniment disclosed by the invention has the advantages of being simple and convenient for preparation, wide in medicine source, low in cost, high in acne curative rate and wide in application prospect.

Compound omeprazole capsule and preparation method thereof

The invention relates to a compound omeprazole capsule and a preparation method thereof. The capsule is prepared from omeprazole, sodium bicarbonate, crosslinked sodium carboxymethylcellulose, sodium stearyl fumarate, and traditional Chinese medicinal herbal concentrated extracts. The invention also discloses a preparation method of the compound omeprazole capsule. The compound omeprazole capsule can treat both symptoms and root causes of gastric ulcer, and has advantages of good dissolution and powder fluidity, has low toxic and adverse effects, is easily absorbed by human body, and has wide application prospects.

Method for preparing fenticonazole nitrate suppository

The invention discloses a method for preparing fenticonazole nitrate suppository, comprising the following process steps of: (1) sieving fenticonazole nitrate through a sieve with 100 meshes to obtain sieve powder; (2) proportioning: weighting 130 parts of fenticonazole nitrate powder, 90 parts of wool grease and 780 parts of mixed fatty glyceride according to the quality ratio; (3) uniformly mixing the wool grease with the mixed fatty glyceride, heating to 45 DEG C and melting and then adding the fenticonazole nitrate power, grinding and uniformly mixing; and (4) reducing the temperature to 38 DEG C, pouring into a suppository die on which a lubricating agent is coated, scratching the excessive part outside the die after the die is condensed, stripping die to obtain the suppository containing 0.2g of enticonazole nitrate in each grain, completely inspecting, packaging and warehousing. The invention solves the problems of complex preparation process and high production cost in the prior ...

Aceclofenac paracetamol tablet and preparation technique

The invention discloses an aceclofenac paracetamol tablet, which uses aceclofenac and paracetamol as basic medicines, starch as a filling agent, hyprolose as a disintegrant, 20 percent polyvinyl pyrrolidone anhydrous ethyl alcohol solution as an adhesive, and magnesium stearate as a lubricant, and is prepared through pelletizing, drying, finishing granule, tabletting and lagging cover. Because the aceclofenac and the paracetamol are prepared into compound preparation, the aceclofenac paracetamol tablet has antipyretic, anti-inflammatory and analgesic efficacies, is suitable for the treatment of pain and inflammation symptoms caused by osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, lumbago, toothache and the like, and for the treatment of gynecological inflammation, and ear, nose and throat inflammations, and can be widely applied to the clinic.

Postpartum stasis removing particles

The invention relates to postpartum stasis particles. The postpartum stasis particles are prepared from the following raw materials by weight: 936g of motherwort, 117g of angelica sinensis, 135.5g of ligusticum wallichii and 58.5 g of baked ginger; the postpartum stasis particles are prepared by a conventional granulating method. The postpartum stasis removing particles are applied dialectically on the basis of the prior art; the traditional Chinese medicament components have the advantages of compatibility of interactions, coordination performance and low cost; and clinical tests prove that the postpartum stasis removing particles have a very good treatment effect on postpartum stasis and the application prospect is wide.

Caterpillar fungus stilbene ginseng capsule

The invention relates to caterpillar fungus stilbene ginseng capsule. The caterpillar fungus stilbene ginseng capsule is prepared from the following raw materials by weight: 140g of caterpillar fungus, 1,400g of astragalus membranaceus, 560g of salviae miltiorrhizae, 560g of safflower and 280g of spina date seed. The caterpillar fungus stilbene ginseng capsule disclosed by the invention treats both principal and secondary aspects of chronic nephritis, is easy to prepare, has an exact treatment effect, is based on a rigorous formula and has a wide application prospect.

Staphylococcus albus tablet and preparation method thereof

The invention relates to a staphylococcus albus tablet, comprising the following active ingredients in parts by weight: 10 parts of powdered staphylococcus albus, 50 parts of burdock root, 40 parts of thunberg fritillary bulb, 40 parts of pericarpium granati, 35 parts of campsis grandiflora, 30 parts of curcuma zedoary, 30 parts of perilla leaf, 25 parts of radish seed, 25 parts of rhizoma corydalis, 20 parts of honeysuckle, 20 parts of mangnolia officinalis, 20 parts of ginkgo and 20 parts of almond. The staphylococcus albus tablet can take effect quickly, hardly causes toxic or side effects and has a broad application prospect.

Full rhizoma gastrodiae tablet

The invention relates to a full rhizoma gastrodiae tablet for treating apoplexy sequel. The full rhizoma gastrodiae tablet is prepared by the following steps: baking 500g of rhizoma gastrodiae, crushing into fine powder; sieving by using a 100-mesh sieve; adding 20g of microcrystalline cellulose, 50g of powdered sugar and 10g of low-substituted hydroxypropyl cellulose; evenly mixing, and pelletizing by 10% ethanol; drying, and adding 5.8g of magnesium stearate; evenly mixing and pressing into 1000 pieces; packaging by using a film coating, so as to obtain the full rhizoma gastrodiae tablet. The full rhizoma gastrodiae tablet disclosed by the invention has a significant effect on the apoplexy sequel and has a broad application prospect.

Norcantharidin and production method thereof

The invention relates to norcantharidin and a production method thereof. The norcantharidin is prepared from the following raw medicinal materials in parts by weight: 2 parts of norcantharidin, 200 parts of oldenlandia diffusa, 200 parts of rhizoma sparganii, 100 parts of poria, 100 parts of spina gleditsiae, 80 parts of schizonepeta, 80 parts of sculellaria barbata, 50 parts of circium japonicum, 50 parts of trchosahthes kirilowii maxin, 50 parts of manyprickle acanthopanax root and 20 parts of nidus vespae. According to the production method, the peak-valley phenomenon occurring when conventional preparations are administrated frequently can be avoided, and the drug utilization and the compliance of patient administration can be improved, so that the aims of improving curative effects of medicines and reducing adverse response of medicines can be achieved. The norcantharidin has an excellent application prospect.

Difenidol hydrochloride and preparation method thereof

The invention relates to difenidol hydrochloride and a preparation method thereof. The difenidol hydrochloride is prepared from the following raw materials in parts by weight: 5 parts of difenidol hydrochloride, 20 parts of inula flower root, 20 parts of nux vomica, 18 parts of rhizoma alismatis, 18 parts of fingered citron, 15 parts of the root of kudzu vine, 15 parts of the root of red-rooted salvia, 15 parts of rhizoma sparganii, 12 parts of glossy privet fruit, 12 parts of caulis bambusae in taeniam, 10 parts of rhizoma arisaematis, 5 parts of polygala tenuifolia and 5 parts of dandelion. The preparation method comprises the steps of adding auxiliary materials for dietary fiber drugs such as starch according to a general pharmaceutical method, and preparing capsules, tablets, granules and other dosage forms. The compound difenidol hydrochloride medicine composition treats both symptoms and root causes of vertigo, is non-toxic and harmless to a human body, does not have a side effect ...

Gynecological hemostatic capsule

The invention relates to gynecological hemostatic capsule. The gynecological hemostatic capsule is prepared from the following raw materials in parts by weight: 138.9g of prepared rehmannia root, 69.4g of fructus schizandrae, 69.4g of eucommia ulmoides, 69.4g of teasel root, 138.9g of white peony root, 69.4g of Chinese yam, 138.9g of oyster, 111.1g of cuttlebone, 138.9g of garden burnet, 69.4g of pollen typhae and 69.4g of mistletoe. The cynecological hemostatic capsule can treat both principal and secondary aspects of chronic nephritis, has an exact treatment effect, is based on a strict formula, is easy to prepare and low in cost, has the functions of tonify Qi, nourishing blood, and activating the circulation of blood to remove stasis and has a wide application prospect.

Compound Yimu capsule and preparation method thereof

The invention relates to a compound Yimu capsule and a preparation method thereof. The capsule is prepared from the following four medicinal materials: 1,084 g of Leonurus japonicus, 544 g of Angelica sinensis, 272 g of Ligusticum chuanxiong, and 100 g of Aucklandia lappa. zlThe invention also discloses a method for preparing the compound Yimu capsule. According to the preparation method, the preparation process parameters of Yimu capsule are optimized; through controlling temperature, ethanol reflux time and the like, the efficacy of Yimu capsule is improved, the drug effects of traditional Chinese medicinal components are fully exerted, and wide application prospects are realized.

Preparation technique of compound oral liquid for tonifying blood containing red skin of peanut

The invention discloses a compound red-skin blood-enriching oral liquid, which is prepared by taking peanut red skin, medlar, dates, and edible tree fungus as main materials and honey, saccharose, and citric acid as auxiliary materials through processes such as boiling, filtration, concentration and so on. The medicine has efficacies of tonifying the blood, nourishing qi, and strengthening the spleen, is clinically used for the treatment of ischemic anemia and leukocytopenia, and has low price and simple manufacturing technology.

Pharmaceutical preparation for removing blood stasis after delivery as well as detection and detection method for pharmaceutical preparation

The invention relates to a pharmaceutical preparation for removing blood static after delivery as well as an application and a detection method for the pharmaceutical preparation. The pharmaceutical preparation is prepared from the following raw materials in parts by weight: 1248 parts of leonurus, 156 parts of Chinese angelica, 178 parts of ligusticum wallichii and 78 parts of baked gingers. The pharmaceutical preparation is prepared by pelletizing according to a normal method. The granule for removing blood static after delivery disclosed by the invention is applied dialectically based on the prior art, and various traditional Chinese medicine components cooperate with each other to coordinate effects, so that the pharmaceutical preparation is low in cost, good in treatment effect in removing blood static after delivery according to the clinical verifications, and is very wide in application prospect.

Preparation method of norcantharidin

The invention provides a preparation method of norcantharidin, and relates to the technical field of organic synthesis. The preparation method comprises the following steps: mixing dehydrogenated norcantharidin, 2, 6-dimethyl-1, 4-dihydro-3, 5-dipyridinedicarboxylic acid diethyl ester, an organic solvent and a palladium carbon catalyst, and carrying out hydrogenation reduction reaction in a protective atmosphere to obtain the norcantharidin, the hydrogenation reduction reaction is carried out under a normal pressure condition. According to the method, 2, 6-dimethyl-1, 4-dihydro-3, 5-dipicolinic acid diethyl ester is used as a hydrogen source for catalytic hydrogenation reduction of the dehydrogenated norcantharidin, and the norcantharidin can be prepared through normal-pressure hydrogenation reduction. According to the invention, 2, 6-dimethyl-1, 4-dihydro-3, 5-dipicolinic acid diethyl ester is adopted to replace hydrogen, a more stable hydrogen source is adopted, the reaction is carried ...

Capsule for clearing away turbid and tonifying kidneys

The invention relates to a capsule for clearing away turbid and tonifying kidneys. The capsule is prepared from the following raw materials by weight: 100g of cordyceps sinensis, 1400g of astragalus membranaceus, 280g of root of red-rooted salvia, 280g of flowers carthami, 280g of spina date seeds, 500g of semen cuscutae and 100g of rheum officinale. The applied capsule for clearing away turbid and tonifying the kidneys is used for treating both deficiency and excess and treating both symptoms and root causes, is accurate in curative effect, rigorous in formula, and simple and convenient to prepare, and has a broad application prospect.

Deep-buried large chamber supporting device and method

The invention relates to the technical field of chamber supporting, in particular to a deep-buried large chamber supporting device and method. The deep-buried large chamber supporting device comprises an E-shaped steel belt, a two-way tray and a supporting device; spherical structures are arranged at the two ends of the E-shaped steel belt, and at least three sets of steel belt ribs are arranged at the upper end of the E-shaped steel belt. The two-way tray comprises an upper tray and a lower tray, the upper tray and the lower tray are connected through steel plates, and anchor holes are formed in the connecting positions of the steel plates; the spherical structures at the two ends of the E-shaped steel belt are inserted into connecting gaps of the upper tray body and the lower tray body of the two-way tray respectively, anchor rods or anchor cables penetrate into anchor holes of the two-way tray to be fixed to an upper rock body of a chamber, and the E-shaped steel belt is supported through ...

Preparation process of drug particles used for after-delivery blood stasis removal

The invention relates to a preparation process of drug particles used for after-delivery blood stasis removal. The drug particles are prepared by 1248 parts of leonurus, 156 parts of angelica sinensis, 178 parts of ligusticum wallichii and 78 parts of baked ginger and pelleted according to conventional methods. On the basis of the prior art, the drug particles for after-delivery blood stasis removal are applied dialectically, and various components of traditional Chinese medicine are matched to coordinate effect, so that the preparation process is low in cost and has excellent treatment effect for the after-delivery blood stasis removal via clinical test and wide application prospect.

Compound oral liquid for tonifying blood containing red skin of peanut and preparation technique

The invention discloses a compound red-skin blood-enriching oral liquid, which is prepared by taking peanut red skin, medlar, dates, and edible tree fungus as main materials and honey, saccharose, and citric acid as auxiliary materials through processes such as boiling, filtration, concentration and so on. The medicine has efficacies of tonifying the blood, nourishing qi, and strengthening the spleen, is clinically used for the treatment of ischemic anemia and leukocytopenia, and has low price and simple manufacturing technology.