Development and validation of a dissolution method using HPLC for diclofenac potassium in oral suspension
The present study describes the development and validation of an in vitro dissolution method for evaluation to release diclofenac potassium in oral suspension. The dissolution test was developed and validated according to international guidelines. Parameters like linearity, specificity, precision an...
Saved in:
Main Authors: | Alexandre Machado Rubim (Author), Jaqueline Bandeira Rubenick (Author), Luciane Varini Laporta (Author), Clarice Madalena Bueno Rolim (Author) |
---|---|
Format: | Book |
Published: |
Universidade de São Paulo,
2014-04-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A simple method for the quantification of diclofenac potassium in oral suspension by high-performance liquid chromatography with UV-detection
by: Alexandre Machado Rubim, et al.
Published: (2013) -
Inclusion complex of amiodarone hydrochloride with cyclodextrins: preparation, characterization and dissolution rate evaluation
by: Alexandre Machado Rubim, et al.
Published: (2017) -
Amiodarone hydrochloride: enhancement of solubility and dissolution rate by solid dispersion technique
by: Alexandre Machado Rubim, et al.
Published: (2015) -
Preparation of mupirocin-loaded polymeric nanocapsules using essential oil of rosemary
by: Jaqueline Bandeira Rubenick, et al.
Published: (2017) -
Validation of high performance liquid chromatography method for determination of meloxicam loaded PEGylated nanocapsules
by: Francine Rodrigues Ianiski, et al.
Published: (2015)