Effect of hydrophilic swellable polymers on dissolution enhancement of carbamazepine solid dispersions studied using response surface methodology

No abstract is available for this paper.

• Publication year

  2007

• Venue

  AAPS PharmSciTech

• Publication date

  2007-04-06

• Fields of study

  Medicine, Materials Science, Chemistry

• Identifiers
  DOI 10.1208/pt0802027PMID 17622105PMCID PMC2750367
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2004influential reference
• Physicochemical Characterization of Solid Dispersions of Indomethacin with PEG 6000, Myrj 52, Lactose, Sorbitol, Dextrin, and Eudragit® E100

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