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58results about "Pill delivery" patented technology

Gastric retention controlled drug delivery system

ActiveUS20040180088A1Maintain physical integrityFast swellingOrganic active ingredientsNervous disorderControlled drugsControl release
The present invention provides a gastric retention controlled drug delivery system comprising: (a) a controlled release core comprising a drug, a highly swellable polymer and a gas generating agent, said core being capable of swelling and achieving floatation rapidly while maintaining its physical integrity in gastrointestinal fluids for prolonged periods, and (b) a rapidly releasing coat composition comprising the same drug as in the core and pharmaceutically acceptable excipients, wherein the coating composition surrounds the core such that the system provides a biphasic release of the drug in gastrointestinal fluids.
Owner:SUN PHARMA INDS

Medicine for trenting flooding and spotting, haematemesis and homafecia

ActiveCN1785367APowder deliveryAerosol deliveryCurative effectUterine bleeding
A Chinese medicine in the form of capsule, tablet, powder, dripping pill, or aerosol for treating uterine bleeding, hematemesis and hematochezia is prepared from 11 Chinese-medicinal materials including rhubarb, coptis root, notoginseng, donkey-hide gelatin, etc.
Owner:XIAN CHIHO PHARMA

Mucosal Bioadhesive SLow Release Carrier for Delivering Active Principles

InactiveUS20090169511A1BiocideAntibacterial agentsBioadhesiveLactose
A mucosal bioadhesive slow release carrier comprising an active principle and devoid of starch, lactose, which can release the active principal for a duration of longer than 20 hours. This bioadhesive carrier contains a diluent, an alkali metal alkylsulfate, a binding agent, at least one bioadhesive polymer and at least one sustained release polymer, as well as a method for its preparation.
Owner:ONXEO SA

Controlled release formulation for treating sleep disorders

InactiveUS20130078304A1BiocideOrganic active ingredientsZaleplonTreatment sleep
The invention relates to a controlled-release formulation for preventing and / or treating sleep disorders comprising Zaleplon or a pharmaceutically acceptable salt thereof in immediate release form and Zolpidem or a pharmaceutically acceptable salt thereof in sustained release form, wherein Zaleplon or a pharmaceutically acceptable salt thereof and Zolpidem or a pharmaceutically acceptable salt thereof are released in two phases where the first phase is a immediate release phase of Zaleplon or a pharmaceutically acceptable salt thereof and the second phase is a sustained release phase of Zolpidem or a pharmaceutically acceptable salt thereof.
Owner:TAIWAN BIOTECH

Composition and method for treatment of metabolic disorders

ActiveUS20180228863A1Safely eliminated through excretionFast dissolutionDispersion deliveryPeptide/protein ingredientsTherapeutic effectEndocrine system
The present invention provides compositions and methods for treatment of metabolic syndromes. Namely, the presently disclosed compositions and methods are provided for affecting the function of the gastrointestinal endocrine system in key regions of the gut, thereby, producing therapeutic effects on obesity, diabetes and other metabolic disorders. The compositions include components for forming luminal barriers within the gastrointestinal tract of a subject where the barrier is created in-situ via interaction of resident mucin with the mucin-interacting agent.
Owner:THE JOHN HOPKINS UNIV SCHOOL OF MEDICINE

Anti-gout novel medical preparation

InactiveCN101152262ALower uric acid levelsPowder deliverySkeletal disorderFreeze-dryingOTERACIL POTASSIUM
The invention relates to the drug technical field and concretely provides a novel drug preparation for resisting the gout. The preparation includes the raw materials of two traditional Chinese medicines of a wormwood leaf and a plantain seed, which are mixed, dipped and boiled for obtaining a water-extract to be filtered, heated, condensed, centrifugally residue removed, freeze-dried, dissolved by normal saline, filtered by a filter membrane and finally made into the novel drug preparation for resisting the gout. The animal text shows that the novel drug preparation of the invention can very effectively reduce the oteracil potassium to induce the uric acid standard in the blood of a mouse with the hyperuricemia and greatly improve and effectively cure the mice of arthrocele and difficult action, and the novel drug is further used for resisting the human gout to take particular effect.
Owner:邱日辉 +1

Traditional Chinese medicine composition, preparation thereof and preparation method of preparation

InactiveCN105641619AEffusion is curativeDefinite curative effectPowder deliveryAnthropod material medical ingredientsAngelica Sinensis RootRhizome
The invention discloses a traditional Chinese medicine composition, a preparation thereof and a preparation method of the preparation. The traditional Chinese composition is prepared from turtle shell, Morinda officinalis, dogwood, the bark of eucommia, fructus psoraleae, herba cistanche, cynomorium songaricum, glossy privet fruits, teasel roots, ginseng, radix angelica sinensis, Caulis Spatholobi, the root of red-rooted salvia, peach seeds, safflower carthamus, pseudo-ginseng, rhizoma sparganii, curcuma zedoary, leeches, the rhizome of chuanxiong, the root of bidentate achyranthes, rhizoma curcumae longae, woodlouses, processed monkshood, radix aconiti preparata, prepared kusnezoff monkshood root, herba ephedra, Asarum delavayi, cassia twigs, clove, radix angelicae dahurioae, centipedes, scorpions, rhizoma corydalis, prepared nux vomica, gastrodia elata, long-noded pit viper, lumbricus, rhizoma anemarrhenae, cortex acanthopanacis, homalomena occulta, radix rehmanniae, pawpaw, akebiaquinata, fructus amomi, amur cork-tree, radix angelicae pubescentis, drynaria rhizome, common threewingnut root, the dried root and stem of Dioscorea septemloba Thunbt and Dioscorea hypoglauca Palibin and rhizoma atractylodis. The traditional Chinese medicine composition can effectively cure bone diseases such as knee joint effusion and rheumatic arthritis.
Owner:葛小平

Drug for treating rheumatoid arthritis

ActiveCN106880789AGood curative effectShorten the timeAnthropod material medical ingredientsAntipyreticAngelica Sinensis RootClinical manifestation
The invention discloses a drug for treating rheumatoid arthritis. The drug is prepared from radix aconiti kusnezoffi preparata, radix aconiti preparata, radix angelicae, asarum, lumbricus, rhizoma arisaematis, flos carthami, yam rhizome, semen coicis, radix angelica sinensis, placenta and ants according to a proper ratio. The medicines are ground into fine powder, and the fine powder is coated with raw honey to form pellets. Due to the fact that the toxicity of the formula is high, the drug needs to be stopped for two days to observe the pharmacodynamic function after being used for one week. The drug has a remarkable curative effect for rheumatoid arthritis, especially when clinical manifestations include symmetrical pain and swelling of multiple joints in the whole body, symmetrical stiffness or tightness of joints, even deformation to different degrees, alternate chills and fever, limb joint and muscular ache, unsmooth flexion and extension, or unstable pain, and even severe pain, swelling, hardness and deformation of joints. Treatment of 200 patients confirmed through blood and modern medical equipment proves that 166 patients are cured, 11 patients are improved, the effective rate is 88.5%, and the cure rate is 83%.
Owner:SHAANXI UNIV OF CHINESE MEDICINE

Glipizide orally disintegrating tablet and preparation method thereof

InactiveCN107412175AEvenly dispersedReduce usageMetabolism disorderSulfonylurea active ingredientsFiller ExcipientIrritation
The invention discloses a glipizide orally disintegrating tablet and a preparation method of the glipizide orally disintegrating tablet. The orally disintegrating tablet comprises glipizide and pharmaceutically acceptable auxiliary materials with effective doses, wherein the pharmaceutically acceptable auxiliary materials comprise a filling agent, a flavoring agent, a disintegrating agent, a lubricant and an adhesive; the filling agent is composed of mannitol and microcrystalline cellulose; the flavoring agent is mannitol; the disintegrating agent is a composition of crospovidone, low-substituted hydroxypropyl cellulose and sodium carboxymethyl starch, and the weight ratio of the crospovidone to the low-substituted hydroxypropyl cellulose to the sodium carboxymethyl starch is (5-20): (5-30): (2-10); the lubricant is magnesium stearate; the adhesive is purified water. The product can rapidly disintegrate in the oral cavity, and is good in taste, easy to swallow, and free of irritation to the oral mucosa. The glipizide orally disintegrating tablet prepared by adopting the preparation method disclosed by the invention is uniform, meanwhile, the production cost is low, and thus large-scale production can be realized.
Owner:CHONGQING CONQUER PHARML

Preparation method of domperidone tablets

ActiveCN109481410AIncrease productivityHigh tablet hardnessOrganic active ingredientsDigestive systemCelluloseMagnesium stearate
The invention provides a preparation method of domperidone tablets, comprising the following steps: (1) material preparation: performing site-clearing inspection, getting a raw material domperidone, and ingredients lactose G200, pregelatinized starch, low-substituted hydroxypropyl cellulose, povidone K30, lauryl sodium sulfate, silica and magnesium stearate; (2) pelleting: sieving and uniformly mixing raw material and ingredients except povidone K30, silica and magnesium stearate, then slowly adding a povidone K30 solution, uniformly stirring, and sieving to prepare wet particles, drying, sieving and collecting to obtain dry particles; (3) generally blending: respectively adding silica and magnesium stearate into the dry particles obtained in the step (2), to obtain generally mixed particles; and (4) tabletting, and the like. The method is high in production efficiency, and can enable the prepared domperidone tablets to be high in dissolving-out speed and relatively long in expirationdate while ensuring relatively high streptomycin hardness.
Owner:WEIAO PHARM (SICHUAN) CO LTD

Traditional Chinese medicine pills for treating puerperal uterine subinvolution and preparation method thereof

The invention discloses traditional Chinese medicine pills for treating puerperal uterine subinvolution and a preparation method thereof, and belongs to the field of traditional Chinese medicines. The active ingredients of the traditional Chinese medicine pills consist of the following raw materials: Chinese date, root of sandhill tylophora, Chinese yam, dried longan pulp, rehmannia root, heterophylly faalsestarwort root, root of silverweed cinquefoil, herb of bifurcate cinquefoil, stem of noble dendrobium, mulberry fruit, manyflower solomonseal rhizome, chinese granesbill, cowpea, lalang grass rhizome, rhizoma corydalis, medicinal cyathula root, giant knotweed rhizome, motherwort herb, red rice, diverse wormwood herb, India madder root, curcuma longa, licorice root and crocus sativus. The drug properties of the medicinal materials for preparing the traditional Chinese medicine pills disclosed by the invention supplement with one another, and the traditional Chinese medicine pills are applied according to indications, has the effects of reinforcing the spleen to replenish qi, reinforcing the kidney to control bleeding, nourishing yin to tonify blood, cooling blood to stop bleeding, promoting blood circulation to remove blood stasis, breaking blood to promote the circulation of qi and inducing menstruation to stop pain, is good in absorption effect and significant in curative effect, does not have toxic or side effects and clinical adverse reactions, and is clinically verified to have a relatively high curative rate for treating the puerperal uterine subinvolution.
Owner:程志娟

Traditional Chinese medicine porous core-shell type composite particle powder as well as preparation method and application thereof

InactiveCN113081971AIncreased porous structureFlat surfacePowder deliveryDigestive systemFoaming agentSpray dried
The invention discloses traditional Chinese medicine porous core-shell type composite particle powder as well as a preparation method and application thereof. The preparation method comprises the following steps: extracting traditional Chinese medicines by adopting a solvent, then filtering and concentrating to obtain a traditional Chinese medicine extraction concentrated solution, mixing the traditional Chinese medicine extraction concentrated solution, a shell layer material and a pore-foaming agent, stirring and dissolving the mixture to be uniform, and performing spray drying on the obtained mixture to obtain the traditional Chinese medicine porous core-shell type composite particle powder. The traditional Chinese medicine porous core-shell type composite particle powder prepared by the process provided by the invention has a remarkable porous structure, is spherical or sphere-like, and has a smooth surface; besides, the co-spray drying process adopted by the invention can be used for directly preparing the porous core-shell type particle powder in the spray drying stage of the traditional Chinese medicine extraction concentrated solution, so that the method is beneficial to process amplification for actual production, and is suitable for continuous production; moreover, after the traditional Chinese medicine porous core-shell type composite particle powder provided by the invention and a pharmaceutically acceptable carrier are prepared into tablets through direct pressing, the obtained tablets disintegrate faster.
Owner:JIANGXI UNIVERSITY OF TRADITIONAL CHINESE MEDICINE
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