CN105616357A - Resveratrol dry suspension and preparation method thereof - Google Patents

Resveratrol dry suspension and preparation method thereof Download PDF

Info

Publication number
CN105616357A
CN105616357A CN201610006889.3A CN201610006889A CN105616357A CN 105616357 A CN105616357 A CN 105616357A CN 201610006889 A CN201610006889 A CN 201610006889A CN 105616357 A CN105616357 A CN 105616357A
Authority
CN
China
Prior art keywords
resveratrol
dry suspension
preparation
dry
mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201610006889.3A
Other languages
Chinese (zh)
Inventor
郭敏
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201610006889.3A priority Critical patent/CN105616357A/en
Publication of CN105616357A publication Critical patent/CN105616357A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1652Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/045Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
    • A61K31/05Phenols

Abstract

The invention discloses a resveratrol dry suspension and a preparation method thereof and belongs to the field of pharmaceutic preparations. The resveratrol dry suspension consists of a suspending aid, ethanol, corrigent and an auxiliary agent. The preparation method has the characteristics of simple preparation method, high sedimentation volume ratio, good in medicine content uniformity and the like, and is easily accepted by patients.

Description

A kind of resveratrol dry suspension and preparation method thereof
Technical field
The invention belongs to field of pharmaceutical preparations, be specifically related to a kind of resveratrol dry suspension and preparation method thereof.
Background technology
Resveratrol is a kind of phenols phytoalexin being found in Pericarpium Vitis viniferae and other plant, because resveratrol has anticancer, antioxidation, antiinflammatory, antibacterial effect and likes liking to people, plant origin mention because Frenchman often drinks in higher fatty acid thing containing resveratrol, so in other western countries at the bottom of French Incidence of CHD, resveratrol can be learnt from this information because effectively suppressing high-fat preventive and therapeutic effect. Existing Countries and area develop resveratrol using resveratrol and goods thereof as dietary supplement.
Resveratrol is insoluble in water, it is impossible to use after water-soluble, affects the absorption after it uses and convenience, brings restriction to its application.
Summary of the invention
An object of the present invention is to provide a kind of resveratrol dry suspension.
For achieving the above object, the technical scheme is that and be achieved in that:
A kind of resveratrol dry suspension, is made up of resveratrol 1-30% and adjuvant 70-99% part.
Further, resveratrol dry suspension described above, it is characterised in that described adjuvant is made up of suspending agent 1-5%, correctives 0-10%, filler 55-98%, solvent 2-30%.
Further, resveratrol dry suspension described above, it is characterized in that, described suspending agent is one or more in carbomer, gummi arabicum pulveratum, tragacanth, sodium carboxymethyl cellulose, hydroxy propyl cellulose, sodium alginate, microcrystalline Cellulose, it is preferred to sodium carboxymethyl cellulose.
Further, resveratrol dry suspension described above, it is characterized in that, described correctives is one or more compositions in sucralose, aspartame, sucrose, strawberry essence, trisodium citrate, it is preferable that the mixture of sucralose and strawberry essence.
Further, resveratrol dry suspension described above, it is characterised in that described solvent is one or more mixture in ethanol or glycerol, it is preferable that ethanol.
Further, resveratrol dry suspension described above, it is characterized in that, described filler is one or more mixture in lactose, mannitol, starch, xylitol, maltose alcohol, starch milk saccharide complex, sorbitol, it is preferable that the mixture of starch milk saccharide complex and mannitol.
The preparation method that it is a further object of the present invention to provide a kind of resveratrol dry suspension. In order to realize this purpose, the present invention is achieved by the following technical solutions:
Weigh the resveratrol of recipe quantity, add the solvent of recipe quantity, stirring, make resveratrol dissolve completely, obtain settled solution; Successively suspensoid, correctives, filler is added in solution, stirring, make soft material; By made soft material granulation, crossing 20 mesh sieves, 60 degrees Celsius dry, 20 mesh sieve granulate and get final product.
Beneficial effect of the present invention
The invention provides a kind of resveratrol dry suspension and preparation method thereof, solve resveratrol and be insoluble in water, it is impossible to by the water-soluble rear defect used, product sedimentation volume ratio is high, medicament contg homogeneity is good. Preparation method provided by the invention is simple, it is easy to accomplish.
Detailed description of the invention
Embodiment 1: resveratrol dry suspension and preparation method thereof
One, prescription: resveratrol 1g, sodium carboxymethyl cellulose 5g, ethanol 2g, starch milk saccharide complex 50g, mannitol 44g.
Two, preparation method: weigh the resveratrol of recipe quantity, adds the solvent of recipe quantity, stirring, makes resveratrol dissolve completely, obtains settled solution; Successively suspensoid, correctives, filler is added in solution, stirring, make soft material; By made soft material granulation, crossing 20 mesh sieves, 60 degrees Celsius dry, 20 mesh sieve granulate and get final product.
Embodiment 2: resveratrol dry suspension and preparation method thereof
One, prescription: resveratrol 30g, sodium carboxymethyl cellulose 1g, ethanol 30g, sucralose 9g, strawberry essence 1g, starch milk saccharide complex 35g, mannitol 24g.
Two, preparation method: weigh the resveratrol of recipe quantity, adds the solvent of recipe quantity, stirring, makes resveratrol dissolve completely, obtains settled solution; Successively suspensoid, correctives, filler is added in solution, stirring, make soft material; By made soft material granulation, crossing 20 mesh sieves, 60 degrees Celsius dry, 20 mesh sieve granulate and get final product.
Embodiment 3: resveratrol dry suspension and preparation method thereof
One, prescription: resveratrol 15g, sodium carboxymethyl cellulose 3g, ethanol 20g, sucralose 4.9g, strawberry essence 0.1g, starch milk saccharide complex 60g, mannitol 17g.
Two, preparation method: weigh the resveratrol of recipe quantity, adds the solvent of recipe quantity, stirring, makes resveratrol dissolve completely, obtains settled solution; Successively suspensoid, correctives, filler is added in solution, stirring, make soft material; By made soft material granulation, crossing 20 mesh sieves, 60 degrees Celsius dry, 20 mesh sieve granulate and get final product.
Test example: be the character of resveratrol dry suspension product, mouthfeel and sedimentation volume ratio test below
Experimental agents: the resveratrol dry suspension of embodiment 1��3 preparation.
Experimental technique: character by observing, nasil method, homogeneity and sedimentation volume ratio carry out according to " Chinese Pharmacopoeia " version two in 2010.
Experimental result: see table 1 below:
Table 1 resveratrol dry suspension character and sedimentation volume ratio result
Laboratory sample Face shaping Mouthfeel Homogeneity Sedimentation volume ratio
Embodiment 1 White or faint yellow granule Sweet, mouthfeel is good Qualified 0.91
Embodiment 2 White or faint yellow granule Sweet, mouthfeel is good Qualified 0.95
Embodiment 3 White or faint yellow granule Sweet, mouthfeel is good Qualified 0.93
The foregoing is only presently preferred embodiments of the present invention, not in order to limit the present invention, all within the spirit and principles in the present invention, any amendment of making, equivalent replacement, improvement etc., should be included within protection scope of the present invention.

Claims (7)

1. a resveratrol dry suspension, is made up of resveratrol 1-30% and adjuvant 70-99% part.
2. resveratrol dry suspension according to claim 1, it is characterised in that described adjuvant is made up of suspending agent 1-5%, correctives 0-10%, filler 55-98%, solvent 2-30%.
3. resveratrol dry suspension according to claim 1, it is characterized in that, described suspending agent is one or more in carbomer, gummi arabicum pulveratum, tragacanth, sodium carboxymethyl cellulose, hydroxy propyl cellulose, sodium alginate, microcrystalline Cellulose, it is preferred to sodium carboxymethyl cellulose.
4. resveratrol dry suspension according to claim 1, it is characterized in that, described correctives is one or more compositions in sucralose, aspartame, sucrose, strawberry essence, trisodium citrate, it is preferable that the mixture of sucralose and strawberry essence.
5. resveratrol dry suspension according to claim 1, it is characterised in that described solvent is one or more mixture in ethanol or glycerol, it is preferable that ethanol.
6. resveratrol dry suspension according to claim 1, it is characterized in that, described filler is one or more mixture in lactose, mannitol, starch, xylitol, maltose alcohol, starch milk saccharide complex, sorbitol, it is preferable that the mixture of starch milk saccharide complex and mannitol.
7. the preparation method of a resveratrol dry suspension, it is characterised in that weigh the resveratrol of recipe quantity, adds the solvent of recipe quantity, stirring, makes resveratrol dissolve completely, obtains settled solution; Successively suspensoid, correctives, filler is added in solution, stirring, make soft material; By made soft material granulation, crossing 20 mesh sieves, 60 degrees Celsius dry, 20 mesh sieve granulate and get final product.
CN201610006889.3A 2016-01-07 2016-01-07 Resveratrol dry suspension and preparation method thereof Pending CN105616357A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610006889.3A CN105616357A (en) 2016-01-07 2016-01-07 Resveratrol dry suspension and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610006889.3A CN105616357A (en) 2016-01-07 2016-01-07 Resveratrol dry suspension and preparation method thereof

Publications (1)

Publication Number Publication Date
CN105616357A true CN105616357A (en) 2016-06-01

Family

ID=56031988

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610006889.3A Pending CN105616357A (en) 2016-01-07 2016-01-07 Resveratrol dry suspension and preparation method thereof

Country Status (1)

Country Link
CN (1) CN105616357A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1935120A (en) * 2005-08-04 2007-03-28 昆明杉榆生物技术有限公司 Effervescent dry-mixed suspension agent
CN102307568A (en) * 2009-02-04 2012-01-04 帝斯曼知识产权资产管理有限公司 Resvertrol compositions
RU2557942C1 (en) * 2014-03-19 2015-07-27 Александр Александрович Кролевец Method for producing supramolecular nanocapsules of resveratrol in xanthan gum

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1935120A (en) * 2005-08-04 2007-03-28 昆明杉榆生物技术有限公司 Effervescent dry-mixed suspension agent
CN102307568A (en) * 2009-02-04 2012-01-04 帝斯曼知识产权资产管理有限公司 Resvertrol compositions
RU2557942C1 (en) * 2014-03-19 2015-07-27 Александр Александрович Кролевец Method for producing supramolecular nanocapsules of resveratrol in xanthan gum

Similar Documents

Publication Publication Date Title
KR102456326B1 (en) Antiviral Composition Against Influenza Virus, Composition for Treating Respiratory Disease, and Anti-Aging Composition Containing Extract of Black Ginseng
CN102406679B (en) Traditional Chinese medicine American ginseng buccal tablet
CN110248651A (en) Composition comprising sulfated polysaccharide
CN116490198A (en) Aloe-based compositions comprising polysaccharides and polyphenols for modulating immune homeostasis
CN104825570B (en) A kind of composition and application thereof inhibiting helicobacter pylori
AU620463B2 (en) A composition containing an extract obtained by a water-containing organic solvent, and a process for preparing the same
EP3572088B1 (en) A panax plant extract and pharmaceutical composition and use thereof
CN105125570B (en) A kind of pharmaceutical composition containing erythromycin thiocyanate and preparation method thereof
CN101862333B (en) Stable sodium levofolinate oral preparation and preparation method thereof
TW201900218A (en) Composition for disintegrating tablet containing microfibrous cellulose and active ingredient
CN102309442A (en) Ambroxol hydrochloride oral aqueous composition and preparation method thereof
CN103120652B (en) Phloroglucin orally disintegrating tablet and preparation method thereof
JP5969680B1 (en) Chitosan powder, method for producing the same, and preparation containing chitosan
JP2012527233A (en) Method for producing fermented ginseng concentrate or powder
CN108498626A (en) Defaecation or composition, preparation method, purposes and its preparation for adjusting intestinal flora
CN102100902B (en) Counterflow effervescent tablets
CN111803452A (en) Preparation process of effervescent granules containing phenylephrine hydrochloride composition
CN105616357A (en) Resveratrol dry suspension and preparation method thereof
KR101927404B1 (en) Liquid composition comprising compound K at high concentration and producing method thereof
CN103110587A (en) Alfacalcidol dry suspension and preparation method thereof
CN105902497B (en) A kind of preparation method of water-solubility florfenicol veterinary drug preparation
JP7029886B2 (en) Pharmaceutical composition and its manufacturing method
CN113975259B (en) Ambroxol hydrochloride compound effervescent tablet and preparation method thereof
CN115212172A (en) Berberine tannate suspension granules for children and preparation method thereof
CN101249119B (en) Compound compound paracetamol and zincgluconate dispersible tablet and method of preparing the same

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20160601