102 results about "Amylodextrin" patented technology

The invention discloses a maple knotweed intestine wei kang dispersible tablet and process for preparation, containing maple knotweed extract and medicinal findings. The proportioning is that maple knotweed extract is 100 parts, the usage of medicinal finding disintegrating agent is 2 to 50 parts, and the usage of medicinal finding filling agent is 5-100 parts, wherein the disintegrating agent is selected from at least one of microcrystal cellulose, cross linked polyvidon, sodium carboxymethylstarch, and low-substituted hydroxypropyl cellulose and cross linked carboxymethyl cellulose sodium. The filling agent is selected from at least one of compressibility starch, starch gum, milk sugar lactose, microcrystal cellulose, and manna sugar. The knotweed intestine wei kang dispersible tablet has the advantages of excellent dispersed state, short disintegration time, quick medicine dissolving, high biology availability, convenient intake, simple medicament arts, low producing cost, and convenient storage and transportation, and does not need vacuum refrigeration, dehumidification, and special package.

The invention belongs to the field of pharmaceutical preparations and particularly relates to a tilmicosin film-controlled enteric-coated sustained release preparation. The preparation comprises an inner core layer and a film coating layer. The inner core layer comprises raw tilmicosin powder and an inner core layer auxiliary material. The inner core layer auxiliary material comprises two or more of starch, dextrin, sucrose, microcrystalline cellulose, povidone, methylcellulose, hydroxypropyl methylcellulose, hydroxyethylcellulose, xanthan gum, chitin and sodium alginate. The preparation method has a low material loss and a high yield. The tilmicosin film-controlled enteric-coated sustained release preparation masks the bitter taste of tilmicosin, greatly improves the palatability of tilmicosin, cannot be dissolved in a stomach dissolution rate determination test, only collapses and releases in an alkaline environment in the intestine, significantly improves the drug efficacy and reduces the clinical dosage of drugs.

The invention provides a production method of an antiobesity drug and antiobesity granules. The antiobesity drug consists of Artemisia argyi, hawthorns, semen cassiae, coix seeds, wolfberry, oriental wormwood, onions, cucumbers and liquorice. The antiobesity granules are prepared by adopting the following steps of mixing and pulping the onions and the cucumbers, extracting, filtering, concentrating, drying and grinding to obtain extraction powder; mixing and grinding the residual components and then adding into water, carrying out reflux extraction twice, filtering, mixing two supernates, concentrating at reduced pressure, carrying out spray drying on the concentrated solution to obtain a mixed extract after drying; mixing the extraction powder with the dried mixed extract to obtain an another mixed extraction powder; and mixing amylodextrin, water and the mixed extraction powder, pressing cakes, pelleting, and drying to obtain the antiobesity granules. The antiobesity drug is prepared by compounding raw materials which are in homology of medicine and food according to a certain proportion, can take a weight-losing effect through promoting blood circulation to remove blood stasis and reducing triglyceride, blood sugar, beta lipoprotein and the like in the blood, and can treat obesity.

The invention relates to a method for producing high proteined feedstuff by sugar grains fermentation which comprises, utilizing saccharifying enzyme, pectolase and phytase, to degrade amylodextrin, pectine and phytic acid in the sugar draff liquid, then utilizing yeast accretion to consume sugar, ash and inorganic salts in the fermented solution. The preparing process comprises the steps of raw material selection, phytic acid degradation, pectine degradation, amylodextrin degradation, saccharomycete activating, fermentation and culture, finally separating and drying.

The invention relates to a warm reinforcing sea cucumber slice and a processing method thereof, and belongs to the field of sea cucumber finishing technology. Fresh sea cucumber is used as the main raw material of the warm reinforcing sea cucumber slice, such new food raw materials as Antarctic krill oil, chitosan oligosaccharide, xylooligosaccharide, clam meat polysaccharide, marine collagen peptide and the like are added, such medical and edible dual purpose Chinese herbal medicine components as wolfberry fruits, orange peel, fructus momordicae, raspberry, mulberry and the like are used for assisting, and such additives as starch, dextrin and the like are added to together form the warm reinforcing sea cucumber slice; and the warm reinforcing sea cucumber slice is prepared by the steps of treating raw materials, carrying out enzymolysis, mixing, tabletting and sterilizing. The warm reinforcing sea cucumber slice is relatively simple in preparation process, is comprehensive in nutrition structure and has the functions of nourishing yin and tonifying yang, tonifying Qi and relieving fatigue, improving immunity and the like, so that the warm reinforcing sea cucumber slice is an ideal warm reinforcing product.

The invention discloses eggshell calcium malate chewable tablets and a preparation method thereof, belongs to the technical field of functional foods and particularly relates to a method for preparing eggshell calcium malate by utilizing a high-voltage pulsed electric field, and the eggshell calcium malate chewable tablets capable of supplementing calcium required by a human body and a manufacturing method thereof. The method for preparing the calcium malate by utilizing eggshells comprises the following steps: naturally air-drying the eggshells, then crushing, sieving, adding acid, adding water and then performing treatment by the high-voltage pulsed electric field, and the chewable tablets comprise eggshell calcium malate powder, dextrin, starch, xylitol, malic acid, citric acid, magnesium stearate, sodium isoascorbiate and fresh milk essence. The preparation method comprise the following steps: taking the eggshell calcium malate powder as a main functional ingredient, taking the starch, the dextrin, the xylitol, the citric acid, the malic acid, the sodium isoascorbiate, the magnesium stearate and the fresh milk essence as auxiliary materials, performing pretreatment, mixing the materials, granulating, drying, stabilizing the size and tabletting for preparing products. The eggshells are taken as the main raw materials, the high-voltage pulsed electric field is used for treatment and optimization, then the yield of calcium ions in the calcium malate can be as high as 98.34%, the treatment time is short (50 mu s), and the treatment can be performed continuously, thereby being more conductive to industrial production. The eggshell calcium malate chewable tablets have the characteristics and the advantages of delicate mouthfeel, sweet, sour and delicious taste, convenience in taking, high calcium content, significant calcium supplementation effect, difficulty in moisture absorption, simpleness in storage method, long shelf life and the like.

The invention relates to an oral Chinese herba preparation for treating postpartum qi and blood deficiency of woman and a production method thereof. The oral Chinese herba preparation comprises nine traditional Chinese medicines, such as astragalus root, Chinese angelica, prepared rehmannia root, rhizoma atractylodis macrocephalae, white paeony root, szechuan lovage rhizome, euonymus fortunei, dried orange peel and liquorice. The method comprises the following steps: adding water and decocting, filtering, concentrating, depositing with alcohol, filtering, recovering the alcohol, concentrating,and the like, obtaining clear paste; adding starch, dextrin, microcrystalline cellulose, polyvinylpyrrolidone, and the like, granulating, drying, trimming and separating the particles into 5,000 particles; and packaging to obtain the oral Chinese herba preparation. The Chinese herba preparation has simple prescription, easy processing and low cost, and the product has fine compound, effective hemostasis and favorable curative effect and is particularly suitable for post-operation hemostasis.