Camila F. Rediguieri
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Camila F. Rediguieri has a total of 23 co-authors. Here are the top co-authors by number of shared publications:
Sabine Kopp
World Health Organization, Geneva, Switzerland
3 shared publicationsVinod P. Shah
International Pharmaceutical Federation (FIP), The Hague, the Netherlands
3 shared publicationsHans E. Junginger
Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok, Thailand
2 shared publicationsJennifer B. Dressman
Institute of Pharmaceutical Technology, Goethe University, Frankfurt am Main, Germany
2 shared publicationsKamal K. Midha
University of Saskatchewan, Saskatoon, Saskatchewan, Canada
2 shared publicationsSalomon Stavchansky
Pharmaceutics Division, College of Pharmacy, University of Texas in Austin, Austin, Texas 78712
2 shared publications
Latest Publications
- 1 August 2013
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 102 (8) , 2409-2423
Biowaiver Monographs for Immediate-Release Solid Oral Dosage Forms: Zidovudine (Azidothymidine)
- 1 August 2013
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 102 (8) , 2409-2423
Biowaiver Monographs for Immediate-Release Solid Oral Dosage Forms: Zidovudine (Azidothymidine)
- 1 December 2011
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 100 (12) , 5346
Rediguieri CF, Porta V, Nunes DSG, Nunes TM, Junginger HE, Kopp S, Midha KK, Shah VP, Stavchansky S, Dressman JB, Barends DM. 2011. Biowaiver monographs for immediate‐release solid oral dosage forms: Metronidazole. J Pharm Sci 100:1618–1627.
- 1 December 2011
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 100 (12) , 5346
Rediguieri CF, Porta V, Nunes DSG, Nunes TM, Junginger HE, Kopp S, Midha KK, Shah VP, Stavchansky S, Dressman JB, Barends DM. 2011. Biowaiver monographs for immediate‐release solid oral dosage forms: Metronidazole. J Pharm Sci 100:1618–1627.
- 1 May 2011
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 100 (5) , 1618-1627
Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Metronidazole
- 1 May 2011
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 100 (5) , 1618-1627
Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Metronidazole
- 1 November 2007
- Published by American Chemical Society (ACS) in Biomacromolecules
- Vol. 8 (11) , 3345-3354
Thermodynamic Incompatibility and Complex Formation in Pectin/Caseinate Mixtures
The instability of polysaccharide/protein mixtures occurs because of either thermodynamic incompatibility or complexation. We studied which instability mechanism dominated given the external conditions. Therefore the effect of temperature, pH, and biopolymer concentration on the phase separation of pectin/caseinate mixtures was investigated. At pH > 6, thermodynamic incompatibility with spinodal decomposition was observed in pectin/caseinate mixtures resulting in the formation of water-in-water emulsions in intermediate stages of the phase separation process. The demixing rate of these emulsions and appearance of two macroscopic phases (lower phase enriched with caseinate and upper phase with pectin) was retarded when the pectin concentration increased or when the storage temperature decreased due to a higher viscosity of the mixtures at those conditions. As the pH of the mixture was lowered below 6, pectin accumulated in the caseinate-rich phase. Complexation of pectin and caseinate led to the formation of microparticles (∼3 μm), whose shape depends on the biopolymer concentration ratio and rate of acidification. These pectin/caseinate particles do not coalesce and are insensitive to salt addition.
- 1 November 2007
- Published by American Chemical Society (ACS) in Biomacromolecules
- Vol. 8 (11) , 3345-3354
Thermodynamic Incompatibility and Complex Formation in Pectin/Caseinate Mixtures
The instability of polysaccharide/protein mixtures occurs because of either thermodynamic incompatibility or complexation. We studied which instability mechanism dominated given the external conditions. Therefore the effect of temperature, pH, and biopolymer concentration on the phase separation of pectin/caseinate mixtures was investigated. At pH > 6, thermodynamic incompatibility with spinodal decomposition was observed in pectin/caseinate mixtures resulting in the formation of water-in-water emulsions in intermediate stages of the phase separation process. The demixing rate of these emulsions and appearance of two macroscopic phases (lower phase enriched with caseinate and upper phase with pectin) was retarded when the pectin concentration increased or when the storage temperature decreased due to a higher viscosity of the mixtures at those conditions. As the pH of the mixture was lowered below 6, pectin accumulated in the caseinate-rich phase. Complexation of pectin and caseinate led to the formation of microparticles (∼3 μm), whose shape depends on the biopolymer concentration ratio and rate of acidification. These pectin/caseinate particles do not coalesce and are insensitive to salt addition.