45results about How to "Take fast" patented technology

A dispersing table of amlodipine benzosulfonate for treating hypertension is proportionally prepared from amlodipine benzosulfonate, microcrystalline cellulose, anhydrous lactose, carboxymethyl starch sodium, micropowdered silica gel, and magnesium stearate.

The invention discloses a medicinal composition containing sildenafil citrate and PD-1 type pregelatinized starch and a preparation method thereof. The medicinal preparation prepared from the medicinal composition containing the sildenafil citrate and the PD-1 type pregelatinized starch and the preparation method provided by the invention can be completely disintegrated in water at a degree of 37 DEG C within 15 to 30 seconds, and can pass through a screen in a size of 600 to 710 mu m.

The invention provides a phloroglucinol oral disintegrating tablet, which takes the phloroglucinol as the active ingredient, and disintegrating agents, fillers, lubricants, flavoring agents, binding agents and effervescent agents are added for preparation. The invention further provides a preparation method of the phloroglucinol oral disintegrating tablet. The phloroglucinol oral disintegrating tablet of the invention not only has the rapid disintegration, good taste and no sense of gravel, but can also can be taken under the condition of no water and have the rapid action and more convenient taking, so the invention can improve the compliance of the patients and the efficacy of the drug and other features of the orally disintegrating tablet, at the same time, the invention has light tablet weight, small volume, no powder falling, good brittleness and better dissolution effect than the freeze-dried orally disintegrating tablet. The production cost is low, the dissolution is faster, the invention is more beneficial to the absorption, and the invention can play the effect of pain reliving faster. The invention has the advantage that the invention can carry out the preparation by only adopting the ordinary pressing equipments and the simple technique without the need of special production equipments and conditions.

The present invention discloses unhatched-egg-extract-containing senile cardiovascular disease prevention instant powder, and relates to the technical field of health food products, and the unhatched-egg-extract--containing senile cardiovascular disease prevention instant powder is made from the following raw materials in parts by weight: 5-10 parts of a live-birth unhatched-egg-extract, 8-15 parts of live-birth unhatched-egg yolk powder, 20-25 parts of ginkgo biloba leaf, 15-20 parts of black fungus, 15-20 parts of spinach root, 15-20 parts of coconut powder, 13-16 parts of cattail pollen, 10-15 parts of maltodextrin, 10-15 parts of angelica, 10-15 parts of grape seed, 8-13 parts of cinnamon leaf, 7-11 parts of myotonin rice bran oil, 6-10 parts of cortex periplocae, 6-10 parts of wine residue, 5-8 parts bitter gourd seeds and 4-6 parts of kelp. The unhatched-egg-extract-containing senile cardiovascular disease prevention instant powder has rich nutritional value and good preventive effect, has no side effects after taking, is easy to take, can be quickly dissolved in water, can be easily absorbed and metabolized by human body after taking, and is an effective senile cardiovascular disease prevention product.

The invention relates to a drug doser which is capable of dosing rapidly. An upper bottle body and a lower bottle body of the drug doser are designed independently, so that the drug doser can be assembled and disassembled conveniently, and operations such as sterilization and the like can be achieved according to different natures of substances held by the upper bottle body and the lower bottle body. By pressing a piston downwards, the piston punctures seal film, a first accommodation cavity is communicated with a second accommodation cavity through a guide groove, and accordingly, accommodation substances in the second accommodation cavity can enter the first accommodation cavity along the guide groove to be mixed with the accommodation substances in the first accommodation cavity. When mixing is completed, the lower bottle body is taken out directly, the mixed substances can be poured out from an opening end directly, drugs can be taken rapidly, and the drug doser is convenient to use.

The invention belongs to the field of food and particularly relates to lucid ganoderma effervescent tablets and a preparation method thereof. The lucid ganoderma essence effervescent tablets are prepared from ganoderma spore extract, NaHCO3, tartaric acid, lactose, tea polyphenol, cacao husk pigments, PEG6000, jasmine flower essence, green tea and absolute ethyl alcohol. According to the lucid ganoderma effervescent tablets and the preparation method thereof, the ganoderma spore extract serves as a main raw material of the lucid ganoderma healthcare products, the content of effective nutritional ingredients is increased, the bioavailability of the effective nutritional ingredients in the human body is improved, and the advantages of soothing the nerves of the human body, aiding sleep, improving immunity and the like of lucid ganoderma are enhanced. The tea polyphenol, the cacao husk pigments, the jasmine flower essence, green tea essence, lactose and other high-quality flavoring agents are added, and the taste of ganoderma spore powder is improved. The prepared lucid ganoderma essence effervescent tablets have the advantages of being rapid in disintegration, convenient to take and rapid in effect taking, high bioavailability is achieved, and healthcare benefits can be increased.

The invention discloses an ambroxol hydrochloride oally disintegrating tablet and a preparation method thereof. The orally disintegrating tablet consists of effective dose of ambroxol hydrochloride and pharmaceutical adjuvants, wherein the pharmaceutical adjuvants include a taste masking agent, a filler, a flavoring agent, a disintegrant, an adhesive and a lubricant; and the disintegrant is a combination of cross-linked povidone and other disintegrants. The ambroxol hydrochloride oally disintegrating tablet prepared by the invention has the characteristics of being convenient to take without the use of water, rapid in disintegrating, rapid in absorption, high in bioavailability and the like. The preparation method of the finished product (the ambroxol hydrochloride oally disintegrating tablet) provided by the invention is low in cost, simple in processing equipment, easy and controllable in implementation, low in operating cost, economic and convenient, and applicable to large-scale production.

A Chinese medicine for treating menalgia is prepared from cyperus tuber and Chinese angelica root through extracting by supercritical CO2 and dispensing. Its preparing process is also disclosed.

The invention discloses a medicament for treating seborrheic dermatitis. The medicament is prepared from the following raw material medicaments by weight: 15 to 20g of honeysuckle flower, 15 to 20g of scutellaria root, 15 to 18g of Chinese angelica, 10 to 15g of liquorice, 10 to 15g of Mongolian dandelion herb, 8 to 10g of selfheal spike, 7 to 10g of rehmannia root and 8 to 10g of folium artemisiae argyi. The medicament has the advantages of high recovery rate, simple using method, thorough treatment and no relapse after recovery.

A detection device which, when an arrhythmia occurs, can prompt rapid taking of a countermeasure against the arrhythmia, and an alarm system having the detection device are provided. A portable detection device 10 has: a measuring section which can measure an electrocardiogram in a state where the section is applied to the body surface of the user; an analyzing section which analyzes whether the electrocardiogram contains an abnormal waveform indicating an arrhythmia or not; and a transmitting section which, if the analyzing section detects the abnormal waveform, transmits a detection signal indicating that the abnormal waveform is detected, to a communication terminal 20 around the user.

The invention discloses a medicament for curing psoriasis, comprising the materials of black-tail snake, tuberfleeceflower, dendrobium, ledebouriella root, catmint, sophora flavescens ait, monkshood, scorpion, atractylodes, notopterygium, radix scrophulariae and liquorice. The invention has the advantages that firstly, 6-9g powder is taken and put into suitable boiled water to immerse for 15-20 minutes, and then can be taken orally, thereby the medicament is taken conveniently and the patient is easy to accept; secondly, the dose is small, and the medicament is only required to take three times each day after meals; thirdly, the side effect is little, and the invention doesn't have hormone and cytotoxic drugs; fourthly, the action is quick, each period of treatment is 7 to 15 days, and one period of treatment can do execution; fifthly, the curative effect is stable, and the common patient taking the medicament insistently can be cured through clinical trials for years; sixthly, the symptom is not easy to recur, the invention doesn't have toxic and side effects, the curing charge is low, and the medicament source is wide and the price is low; and seventhly, the invention for curing psoriasis has 90% effective rate and 85% cure rate.

The invention provides a medicine preparation for treating postmenopausal osteoporosis and belongs to the technical field of medicines. The medicine preparation contains alfacalcidol, tibolone and necessary pharmaceutical excipients. The medicine preparation for treating postmenopausal osteoporosis, provided by the invention, has the advantages of good disintegration, good absorbing degree, high bioavailability, quick curing effect and convenience for taking. Pharmacological actions of the alfacalcidol and the tibolone can be taken to a maximum extent, the defect of single preparation in efficacy is compensated, and the medicine preparation is an excellent medicine preparation for treating the postmenopausal osteoporosis.

The invention belongs to the field of pharmaceutical preparations, and particularly relates to effervescent tablets containing a stiripentol solid dispersion and a preparation method thereof. According to the effervescent tablets disclosed by the invention, in one aspect, an indissolvable drug is prepared into an amorphous solid dispersion, so that the defect that the permeability of gastrointestinal tracts is reduced by other solubilizing means is overcome while the water solubility and the dissolution rate are improved, and the effervescent tablets have relatively high encapsulation efficiency (16.67%-50%); in the other aspect, a common, easily available and safe enteric-coated material is selected as a solid dispersion carrier to ensure that the stiripentol is released in the small intestine in a positioned manner and cannot be dissociated in advance in a physiological solution to cause damage of gastric acid to medicine like other preparation means; and besides, compared with commercially available dosage forms (capsules and dry suspensions), the effervescent tablets overcome the problem that the content is easy to cake, and has the advantages of stable storage, convenience in taking, good taste, particular suitability for epilepsy children who cannot swallow solid preparations, and the like.

The invention discloses a traditional Chinese medicine for treating appendicitis, which is prepared from the following raw material medicaments by weight: 30 grams of mongolian dandelion herb, 20 grams of hairyvein agrimonia herb and bud, 15 grams of peach seed, 10 grams of rhubarb, 15 grams of coix seed and 10 grams of Japanese honeysuckle stem. The invention has the advantages that: the traditional Chinese medicine treats the appendicitis fundamentally and avoids arousing pains in patients in the treatment process, the effectiveness is quick, the method is simple, and toxic and side effects are prevented.

The invention discloses a medicament for treating skin diseases. The medicament is prepared from the following components by weight: 20-30 g of figwort, 10-15 g of Chinese violet, 8-10 g of gypsum, 5-8 g of China root, 6-8 g of angelica dahurica, 12-15 g of wild Chrysanthemum and 10-14 g of plantago seed. The medicament has the advantages of capability of treating a patient fundamentally without causing any pain in the treating process, quick response, simple method and no toxic or side effect.