Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Gaetano Capasso"'
Autor:
Francesca Maestrelli, Natascia Mennini, Paola Mura, Matteo Cecchi, Gaetano Capasso, Marzia Cirri
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 63:17-25
The complexing, solubilizing and amorphizing abilities toward oxaprozin (a poorly water-soluble anti-inflammatory agent) of some β-cyclodextrin derivatives (hydroxypropyl-βCd, heptakis-2,6-di-O-methyl-βCd (DIMEB) amorphous randomly substituted met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dfcc1a78f6aa589b783fae32437b1da
https://doi.org/10.1007/s10847-008-9484-7
https://doi.org/10.1007/s10847-008-9484-7
Autor:
M.L. González-Rodríguez, Gaetano Capasso, Carla Ghelardini, Antonio M. Rabasco, Paola Mura, Francesca Maestrelli
Publikováno v:
Journal of liposome research. 19(4)
This study aimed to investigate the influence of the preparation conditions on the performance of an ethosomal formulation for topical delivery of the local anesthetic agent, benzocaine (BZC). Ethosomes were prepared with different techniques, such a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffeb9fb179b4d89f16c4bbec4cec9d08
https://pubmed.ncbi.nlm.nih.gov/19863160
https://pubmed.ncbi.nlm.nih.gov/19863160
Publikováno v:
Journal of liposome research. 18(2)
This study aimed to optimize, by means of an experimental design multivariate strategy, a liposomal formulation for topical delivery of the local anaesthetic agent benzocaine. The formulation variables for the vesicle lipid phase uses potassium glycy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4db90e0a448b8dd05a0037823d893fd1
https://pubmed.ncbi.nlm.nih.gov/18569447
https://pubmed.ncbi.nlm.nih.gov/18569447
Publikováno v:
Journal of pharmaceutical and biomedical analysis. 45(3)
Interaction products of metformin hydrochloride (MF.HCl), an oral anti-hyperglycaemic agent highly soluble in water, with triacetyl-beta-cyclodextrin (TAbetaCyD), a hydrophobic CyD derivative practically insoluble in water, were prepared to evaluate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42a529249f4b343c828ffa89891e863a
https://pubmed.ncbi.nlm.nih.gov/17822867
https://pubmed.ncbi.nlm.nih.gov/17822867
Autor:
Francesca Maestrelli, Matteo Cecchi, Marzia Cirri, Gaetano Capasso, Natascia Mennini, Paola Mura
Publikováno v:
Journal of Inclusion Phenomena & Macrocyclic Chemistry; Feb2009, Vol. 63 Issue 1/2, p17-25, 9p