Zobrazeno 1 - 6
of 6
pro vyhledávání: '"N. M. VOLPATO"'
Publikováno v:
Revista de Ciências Farmacêuticas Básica e Aplicada, Vol 29, Iss 3, Pp 285-289 (2009)
O objetivo deste estudo foi comparar a liberação do p-metoxicinamato de octila (MCO) a partir de três formulações em gel. A primeira contendo o MCO livre, a segunda contendo o MCO incluso em β-ciclodextrina (β-CD/MCO) e a terceira contendo o M
Externí odkaz:
https://doaj.org/article/07ff421496db4058b6733c3ba5434931
Publikováno v:
Die Pharmazie. 69(2)
A stability-indicating capillary zone electrophoresis (CZE) method was validated for the determination of vildagliptin (VLG) in pharmaceutical dosage forms using ranitidine hydrochloride (RH) as internal standard. The CZE method was carried out in a
Publikováno v:
Revista de Ciências Farmacêuticas Básica e Aplicada, Vol 29, Iss 3 (2008)
Revista de Ciências Farmacêuticas Básica e Aplicada, Vol 29, Iss 3, Pp 285-289 (2009)
Revista de Ciências Farmacêuticas Básica e Aplicada, Vol 29, Iss 3, Pp 285-289 (2009)
O objetivo deste estudo foi comparar a liberação do p-metoxicinamato de octila (MCO) a partir de três formulações em gel. A primeira contendo o MCO livre, a segunda contendo o MCO incluso em β-ciclodextrina (β-CD/MCO) e a terceira contendo o M
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 52(6-7)
Salmon calcitonin (sCt) was administered by transdermal iontophoresis in rabbits, using a new drug reservoir assembled directly on the skin, based on a dry disc containing sCt to be dissolved at the application site. The hypocalcemic effect was taken
Publikováno v:
Pharmaceutical research. 14(1)
The aim of the work was to study iontophoretic transdermal administration of salmon calcitonin (sCt) in rabbits, with particular attention to drug reservoir composition. A dry sCt disc, to be dissolved on the application site, was used for preparing
Publikováno v:
Pharmaceutical research. 12(11)
Iontophoresis was employed for enhancing the transdermal delivery of acyclovir through nude mouse skin in vitro, with the aim of understanding the mechanisms responsible for drug transport, in order to properly set the conditions of therapeutical app