What is the difference between povidone and crospovidone
In general, crosslinked polyvinyl-pyrrolidone PVP grades show a limited swelling behavior to a certain particle volume, whereas Ac-Di-Sol and Primojel have more or less unlimited swelling and form a gel.
It is also noteworthy that neither swelling pressure nor volume expansion alone can explain the disintegration efficacy of excipients 3. Swelling of disintegrant particles is perhaps the most widely accepted mechanism for tablet disintegration, primarily because almost all disintegrants swell to some extent. To determine swelling volume in water, 10 g of polymers were weighed into a mL graduated cylinder.
The graduated cylinder was filled with water, closed, and shaken very well. The sediment volume was determined after 24 h. Kollidon CL-F has similar swelling volume to Polyplasdone.
Ac-Di-Sol and Primojel have the highest swelling volume. Because of its low bulk density 0. To determine the hydration capacity, 2 g of polymer were weighed into a centrifuge vessel with 40 mL of water. The polymer swelled for 15 min, and the suspension was centrifuged at rpm for 15 min. The supernatant was poured off, and the residual weight was determined. Crospovidone is one of the three superdisintegrants described in the literature.
The mechanism of action is a capillary action with a secondary swelling effect. The improvement of tablet disintegration also has been observed through predictable swelling without gel formation. Furthermore, swelling properties paired with particle-size distribution make the finer grades of crospovidone work efficiently in fast-disintegrating formulations.
The following formulations were tested to determine the disintegration properties:. Formulation 1. Formulation 1 consisted of Improve this answer. Sign up or log in Sign up using Google. Sign up using Facebook.
Sign up using Email and Password. Post as a guest Name. Email Required, but never shown. Featured on Meta. Now live: A fully responsive profile. Version labels for answers. Related Povidone-iodine PVP—I vs.
After the s and s contact times, PVP-I oral antiseptic rinse at all 3 concentrations of 0. The H2 O2 solutions at concentrations of 1. Povidone-Iodine 0. Isotonic saline 0. Challenges, outlook, and future perspectives In the current scrutiny, synthesis, grades, properties, and applications of PVP as a pharmaceutical excipient are discussed. Conclusion Based on the current literature survey, PVP is considered a widely used excipient for pharmaceutical, food, and cosmetic industry.
Funding None. Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. References 1. Haaf F. Polymers of n-vinylpyrrolidone: synthesis, characterization and uses. Koczkur K. Polyvinylpyrrolidone PVP in nanoparticle synthesis. Kurakula Mallesh, Koteswara Rao G. Moving polyvinyl pyrrolidone electrospun nanofibers and bioprinted scaffolds toward multidisciplinary biomedical applications.
European Polymer Journal. Panda H. Asia Pacific Business Press Inc. Jun Y. Preparation and evaluation of acetaminophen tablets, kor. Teodorescu M. Rowe R. Handbook of Pharmaceutical Excipients. Budavari S. Merck and Co. Corporation B. Soluble Polyvinylpyrrolidone for the Pharmaceutical Industry; Technical Literature: Soluble Kollidon Grades. Ziaei-Azad H. Bimetallic catalysts: requirements for stabilizing PVP removal depend on the surface composition.
Graf C. A general method for the controlled embedding of nanoparticles in silica colloids. Self-organized monolayer of nanosized ceria colloids stabilized by poly vinylpyrrolidone J. Food Chemicals Codex. Teng J. Effect of water vapor sorption on local structure of poly vinylpyrrolidone J. JRS Pharma.
Technical Literature. Vivapharm PVPP; Vivapharm PVP; Shah U. Evaluation of the functional equivalence of crospovidone NF from different sources.
Physical characterization. USP Stage 4 Harmonization. Fikentscher V. Systematics of celluloses based on their viscosity in solution. Vieweg R. Wiley, Carl-Hanser-Verlag; Miinchen: Ernst B. Auflage, Verlag Chemie; Weinheim, Band: Kauffmann H. Angew, No title, makromol. Breitenbach J. Budapest; No title, makromol. Liu Z. Studies on the free radical polymerization of N-vinylpyrrolidinone in 3-methylbutanone. Luo L. Novel amphiphilic diblock copolymer of low molecular weight poly N-vinylpyrrolidone -block-poly D,L-lactide : synthesis, characterization, and micellization.
Yamago S. Highly versatile organostibine mediators for living radical polymerization. Controllable synthesis of poly N-vinylpyrrolidone and its block copolymers by atom transfer radical polymerization. Awasthi R. Drug Deliv. Beyond Polyethyl. Elsevier Inc. Poly vinylpyrrolidone pp. Chiefari J.
Gaynor S. Matyjaszewski K. Percec V. Rosen B. Single-electron transfer and single-electron transfer degenerative chain transfer living radical polymerization. Ray B. Highly controlled synthesis of poly N-vinylpyrrolidone and its block copolymers by organostibine-mediated living radical polymerization.
Yusa S. Thermo-responsive diblock copolymers of poly N-isopropylacrylamide and poly N-vinylpyrroridone synthesized via organotellurium-mediated controlled radical polymerization TERP Macromolecules.
Highly controlled living radical polymerization through dual activation of organobismuthines. De Farias M. Synthesis and applications of polystyrene-block-poly N-vinylpyrrolidone copolymers. Coessens, T. Pintauer, K. Benaglia M. Universal switchable RAFT agents. Liu Q. RAFT polymerization of N-vinylpyrrolidone mediated by cyanopropyldithionaphthalate in the presence of a fluoroalcohol: the possibility of altering monomer properties by hydrogen bonding?
Kreft K. Qualitative determination of polyvinylpyrrolidone type by near-infrared spectrometry. Acta Helv. Frauenfelder L.
Universal chromatographic-colorimetric method for the determination of trace amounts of polyvinylpyrrolidone and its copolymers in foods, beverages, laundry products, and cosmetics. AOAC Int. Ericsson I. Trace determination of high molecular weight polyvinylpyrrolidone by pyrolysis-gas chromatography. Robinson B. Lewis Publishers; Burnette L. A review of the physiological properties of PVP. Toilet Goods Assoc.
Shelanski M. Final two-year report of a chronic oral toxicity study with PVP K in rats. Unpublished report from the industrial biological research and testing laboratories, United States of America, submitt. To world heal. Hanka R. Intestinal absorption of polyvinylpyrrolidone. Nihon Univ. Scheffner D. Ravin H. Polyvinyl pyrrolidone as a plasma expander; studies on its excretion, distribution and metabolism. Pratten M. Effects of temperature, metabolic inhibitors and some other factors on fluid-phase and adsorptive pinocytosis by rat peritoneal macrophages.
Nair B. Final report on the safety assessment of polyvinylpyrrolidone PVP Int. Heinrich H. Wessel W. Polyvinylpyrrolidone PVP , its diagnostic, therapeutic and technical application and consequences thereof. IPCS Inchem; Christensen M. Acta Med. Hizawa K.
Subcutaneous pseudosarcomatous polyvinylpyrrolidone granuloma. Cameron A. Blood plasma expander-PVP. Jenkins L. Evaluation of polyvinyl pyrrolidone as a plasma expander.
A Arch. Kimaro E. Formulation development of chewable albendazole tablets with improved dissolution rate. Morin G. A comparison of granules produced by high-shear and fluidized-bed granulation methods. Wan L. Effect of polyvinylpyrrolidone solutions containing dissolved drug on characteristics of lactose fluidized bed granules. Varshosaz J. Effect of binder level and granulating liquid on phenylbutazone pellets prepared by extrusion-spheronization.
Drug Dev. Barbosa E. Acta Pharm. The effect of the physical states of binders on high-shear wet granulation and granule properties: a mechanistic approach toward understanding high-shear wet granulation process.
Part II. Granulation and granule properties. Kasperek R. The application of povidone in the preparation of modified release tablets. Issues Pharm. Rotteglia E. Zhou Y. Preparation of 5-aminosalicylic acid enteric time-controlled released tablets and study on their dissolution. Buehler V. Preparation of Ascorbic Acid Granules. Sanaboina J. Preparation and evaluation of valsartan liquid filling formulations for soft gels.
Javadzadeh Y. Liquisolid technique for dissolution rate enhancement of a high dose water-insoluble drug carbamazepine Int. Molaei M. Enhancement of ketoconazole dissolution rate by the liquisolid technique. Zhang W. Factors affecting the dissolution of indomethacin solid dispersions.
Jachowicz R. Dissolution rates of partially water-soluble drugs from solid dispersion systems. Corrigan O. Drug membrane transport enhancement using high energy drug polyvinylpyrrolidone PVP co-precipitates. Nabekura T. Preparation and in vivo ocular absorption studies of disulfiram solid dispersion.
Verma U. Barmpalexis P. Frizon F. Dissolution rate enhancement of loratadine in polyvinylpyrrolidone K solid dispersions by solvent methods. Powder Technol. Doreth M. Amorphization within the tablet: using microwave irradiation to form a glass solution in situ.
Prosapio V. Uzun I. Coprecipitation of Cefuroxime Axetil-PVP composite microparticles by batch supercritical antisolvent process. Elagamy H. Development and evaluation of rapidly dissolving buccal films of naftopidil: in vitro and in vivo evaluation. Khalil E. Aqueous solubility of diclofenac diethylamine in the presence of pharmaceutical additives: a comparative study with diclofenac sodium. Samprasit W. Yasir M. Insights into polymers: film formers in mouth dissolving films.
Drug Invent. Ziller K. Conteol of crystal growth in drug suspensions: 1 design of a conteol unit and application to acetaminophen suspensions Drug Dev. Asada K. Acrylic emulsion pressure-sensitive adhesives using polyvinyl alcohol as a protective colloid. Preparation of microscopic catalysts and colloids for catalytic nitrate and nitrite reduction and their use in a hollow fibre dialyser loop reactor. Stability of dispersions of iron oxide in mixed solutions of polyvinylpyrrolidone and sodium alkyl sulfate.
Rushil S. Freeze dried injectable drug product development: selection of non functional additivies. Pramanick S. Excipient selection in parenteral formulation development. Reed K. Patel Dipti H. Formulation and evaluation of drug-free ophthalmic films prepared by using various synthetic polymers. Young Pharm. Wang H. Nanocomplexes based polyvinylpyrrolidone KPF for ocular drug delivery of naringenin.
Patel J. Factorial designs in ophthalmic formulation development of Enalkiren. Liang Bo, Capriotti Joseph A. USA1; Malet F. Preservative-free ocular hydrating agents in symptomatic contact lens wearers: saline versus PVP solution.
Eye Contact Lens. Yanai R. Evaluation of povidone-iodine as a disinfectant solution for contact lenses: antimicrobial activity and cytotoxicity for corneal epithelial cells. Contact Lens Anterior Eye. Hoteling A. Characterization and quantitation of PVP content in a silicone hydrogel contact lens produced by dual-phase polymerization processing. B Appl. Zakhlebnaia O. The use of polyvinylpyrrolidone as a stabilizer in the lyophilization of Brucella.
Taylor L. Sugar-polymer hydrogen bond interactions in lyophilized amorphous mixtures. Van Steirteghem A. High fertilization and implantation rates after intracytoplasmic sperm injection. Chun M. Arch Pharm. Seoul ; 36 — Suksaeree J. Formulation, characterization, and in vitro evaluation of transdermal patches for inhibiting crystallization of mefenamic acid.
Giuliano E. Mucosal applications of poloxamer based hydrogels: an overview. Rac V. PVA Cryogel as model hydrogel for iontophoretic transdermal drug delivery investigations. Colloids Surf. Soluble polyvinylpyrrolidone Povidone. Insoluble polyvinylpyrrolidone Crospovidone. Vinylpyrrolidone-vinyl acetate copolymer Copovidone. Registration and toxicological data.
0コメント