About: Application of pharmaceutical QbD for enhancement of the solubility and dissolution of a class II BCS drug using polymeric surfactants and crystallization inhibitors: development of controlled-release tablets.

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About: Application of pharmaceutical QbD for enhancement of the solubility and dissolution of a class II BCS drug using polymeric surfactants and crystallization inhibitors: development of controlled-release tablets. Goto Sponge NotDistinct Permalink

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scientific article published on 24 June 2011

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description	videnskabelig artikel (da) article científic (ca) articol științific (ro) articolo scientifico (it) artigo científico (gl) artigo científico (pt) artigo científico (pt-br) artikull shkencor (sq) artículo científico (es) bilimsel makale (tr) scienca artikolo (eo) vedecký článok (sk) vetenskaplig artikel (sv) vitenskapelig artikkel (nb) vitskapeleg artikkel (nn) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научная статья (ru) научни чланак (sr) מאמר מדעי (he) artikel ilmiah (id) article scientifique (fr) বৈজ্ঞানিক নিবন্ধ (bn) artículu científicu espublizáu en 2011 (ast) 2011 nî lūn-bûn (nan) 2011年の論文 (ja) 2011年論文 (zh-hk) 2011年論文 (zh-tw) 2011年論文 (zh-hant) 2011年論文 (yue) 2011年論文 (zh-mo) 2011年论文 (zh) 2011年论文 (zh-cn) 2011年论文 (zh-sg) 2011年论文 (zh-hans) 2011年论文 (wuu) 2011年论文 (zh-my) 2011년 논문 (ko) наукова стаття, опублікована в червні 2011 (uk) scientific article published on 24 June 2011 (en) scientific article published on 24 June 2011 (en-ca) scientific article published on 24 June 2011 (en-gb) مقالة علمية نشرت في 24 يونيو 2011 (ar)
publication date	wds:Q38312135-AF3B3D22-A3E2-44C1-87F3-A93E5AF99B7D
publication date	2011-06-24 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q38312135-FB638518-18FC-4C09-BE73-7EE95AD1DFC8
language of work or name	English
exact match	wds:Q38312135-3985DBFD-57ED-458F-9C6E-4F2D658818CB
exact match	https://scigraph.springernature.com/pub.10.1208/s12249-011-9646-6
cites work	wds:Q38312135-014A69C6-F8CE-4C4B-A03B-671B0C50997B wds:Q38312135-0AF750B7-BF36-41EE-B51F-86398DE92A49 wds:Q38312135-1535564B-AF76-4867-AE71-E9188A0737EF wds:Q38312135-176738CC-9D1F-46CB-898D-FE719EF6E85A wds:Q38312135-25100044-E508-476B-8746-B9062A426728 wds:Q38312135-2BBF5907-3D34-4481-AB9A-741E1021E7A7 wds:Q38312135-425E7142-3C66-4761-9DB3-CE95DBBA5B87 wds:Q38312135-444487A4-734C-4CD1-B0C2-ED7C5CB7B16D wds:Q38312135-48DB05D6-02DA-462F-8347-9EEA2CD1576A wds:Q38312135-5A6C1CEC-863D-4A96-9432-2B6B32FB63E8 wds:Q38312135-618174A3-B5ED-4B2D-AEDB-EB10712295B5 wds:Q38312135-714444E8-0D2E-40A4-BE58-419AD4BDDE05 wds:Q38312135-7499E807-806B-4865-99EF-9DA1C13E3263 wds:Q38312135-7EC262D2-40C6-4A52-BDA8-489FE2186D04 wds:Q38312135-7F64A1A4-E512-4852-88EB-CDEDCCE236F8 wds:Q38312135-83969A08-36F1-4B9E-A615-9C243DD22FCE wds:Q38312135-93D7FD06-7678-4E90-9475-639384A38C2F wds:Q38312135-968AD0DB-739E-47CF-AA89-A309E6E7FE11 wds:Q38312135-9A3F3910-3CB5-444E-9DA3-7548795EA76A wds:Q38312135-A016BD19-0877-44D4-9D8E-ED275453B353 wds:Q38312135-A57FAC57-96E5-4084-8522-CC3A4506FAC8 wds:Q38312135-B299DAB5-AE25-4A04-A76C-E533208E6073 wds:Q38312135-C6941BFC-4B94-49AD-9394-F8DBD0E42B59 wds:Q38312135-CB41BE8F-F679-4BB0-9AC4-1637C635932C wds:Q38312135-D3C2A9F5-C60B-4A5C-9D15-85F45FBC2EF7 wds:Q38312135-ED23EE3B-B651-4F06-9551-F91F45D2E9E1 wds:Q38312135-FB080AF7-08F5-4996-BF1D-FE6E35FBA871
cites work	Physical properties of solid molecular dispersions of indomethacin with poly(vinylpyrrolidone) and poly(vinylpyrrolidone-co-vinyl-acetate) in relation to indomethacin crystallization Formulation and in vitro evaluation of ibuprofen-Carbopol 974P-NF controlled release matrix tablets. III: Influence of co-excipients on release rate of the drug Pharmaceutical quality by design: product and process development, understanding, and control Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions Crystallization of hydrocortisone acetate: influence of polymers Micronization of drugs using supercritical carbon dioxide Effect of water-soluble carriers on dissolution characteristics of nifedipine solid dispersions The concept of dissolution efficiency Preparation, characterization and in vitro evaluation of solid dispersions containing docetaxel Ability of Different Polymers to Inhibit the Crystallization of Amorphous Felodipine in the Presence of Moisture High molecular weight polyethylene oxides (PEOs) as an alternative to HPMC in controlled release dosage forms. Effect of polymer type on the dissolution profile of amorphous solid dispersions containing felodipine Chitosan-sodium alginate nanoparticles as submicroscopic reservoirs for ocular delivery: formulation, optimisation and in vitro characterisation. Miscibility behavior and formation mechanism of stabilized felodipine-polyvinylpyrrolidone amorphous solid dispersions Preparation of a solid dispersion of felodipine using a solvent wetting method Dissolution Rates of High Energy Sulfathiazole‐Povidone Coprecipitates II: Characterization of Form of Drug Controlling Its Dissolution Rate via Solubility Studies Influence of Different Polymers on the Crystallization Tendency of Molecularly Dispersed Amorphous Felodipine Dissolution improvement of four poorly water soluble drugs by cogrinding with commonly used excipients Study of formulation variables influencing the drug release rate from matrix tablets by experimental design Controlled release from solid dispersion composed of poly(ethylene oxide)â CarbopolÂ® interpolymer complex with various cross-linking degrees of CarbopolÂ® Use of surfactants as plasticizers in preparing solid dispersions of poorly soluble API: selection of polymer-surfactant combinations using solubility parameters and testing the processability Improved physicochemical characteristics of felodipine solid dispersion particles by supercritical anti-solvent precipitation process.

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