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https://www.researchgate.net/publication/6746232_Drug_Solubilization_and_Delivery_from_Cyclodextrin-Pluronic_Aggregates
Request PDF Drug Solubilization and Delivery from Cyclodextrin-Pluronic Aggregates Colloidal systems based on Pluronic F127 (PF127) and hydroxypropyl-beta-cyclodextrin (HPbetaCD) have been ...
https://www.ncbi.nlm.nih.gov/pubmed/17048534
Drug solubilization and delivery from cyclodextrin-Pluronic aggregates. Rodriguez-Perez AI(1), Rodriguez-Tenreiro C, Alvarez-Lorenzo C, Concheiro A, Torres-Labandeira JJ. Author information: (1)Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia, Universidad de Santiago de Compostela, 15782-Santiago de Compostela, Spain.Author: Rodriguez-Perez Ai, Rodriguez-Tenreiro C, Alvarez-Lorenzo C, Concheiro A, Torres-Labandeira Jj
https://www.ingentaconnect.com/content/asp/jnn/2006/00000006/f0020009/art00067
Drug Solubilization and Delivery from Cyclodextrin-Pluronic Aggregates Buy Article: $106.38 + tax ... able to increase up to 100 times the SN solubility in pH5.8 phosphate buffer, showed temperature-dependent drug diffusion coefficients, able to control the release for one week at 37 °C.
https://www.sciencedirect.com/science/article/pii/S1773224710500467
Cyclodextrins in drug delivery systems F.J. Otero-Espinar, â Ž [email protected] ... A. Concheiro, J.J. Torres-Labandeira, Drug solubilization and delivery from cyclodextrin-pluronic aggregates J. Nanosci. Nanotechnol. 6: (2006) 3179-3186 164.Author: F.J. Otero-Espinar, J.J. Torres-Labandeira, C. Alvarez-Lorenzo, J. Blanco-Méndez
https://link.springer.com/article/10.1023%2FA%3A1012136608249
May 01, 1997 · Since their discovery, cyclodextrins and their ability to form inclusion complexes have fascinated chemists, formulators and recently, entrepreneurs. This mini-review has as its objective, a critical assessment of the current status of cyclodextrins in the formulation and delivery of pharmaceuticals and commentary on their potential future uses.Author: Valentine J. Stella, Roger A. Rajewski
https://www.sciencedirect.com/science/article/pii/S0378517305004400
Evaluation of cyclodextrin solubilization of drugs. ... in pharmaceutical formulations. Lipophilic drug molecules, as well as drug/cyclodextrin complexes, are known to form aggregates in aqueous solutions, and common pharmaceutical ... M. MássonRole of cyclodextrins in improving oral drug delivery. Am. J. Drug Deliv., 2 (2004), pp. 261-275.Author: Thorsteinn Loftsson, Dagný Hreinsdóttir, Már Másson
https://www.researchgate.net/publication/51900858_Competitive_displacement_of_drugs_from_cyclodextrin_inclusion_complex_by_polypseudorotaxane_formation_with_poloxamer_Implications_in_drug_solubilization_and_delivery
Competitive displacement of drugs from cyclodextrin inclusion complex by polypseudorotaxane formation with poloxamer: Implications in drug solubilization and delivery
https://www.ncbi.nlm.nih.gov/pubmed/27951706
Dec 13, 2016 · These results combined together give new insights into the mechanisms of protection of the drugs against CD-induced micellar breakup. The outcomes are practical guidelines to improve the design of drug delivery systems as well as a better understanding of competitive assembly mechanisms leading to shape and function modulation. PMID: 27951706Author: Margarita Valero, Franca Castiglione, Andrea Mele, Marcelo A. da Silva, Isabelle Grillo, Gustavo Gon...
https://link.springer.com/article/10.1007%2Fs10847-010-9779-3
Apr 04, 2010 · The purpose of this study was to investigate the physicochemical properties of drug-saturated aqueous cyclodextrin (CD) solutions. Phase solubility profiles of different drugs were determined in aqueous solutions containing γ-cyclodextrin (γCD) and/or hydroxypropyl-γ-cyclodextrin (HPγCD) in absence or presence of water-soluble polymers.Author: Phatsawee Jansook, Maria D. Moya-Ortega, Thorsteinn Loftsson
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