• Nenhum resultado encontrado

Quím. Nova vol.32 número4

N/A
N/A
Protected

Academic year: 2018

Share "Quím. Nova vol.32 número4"

Copied!
3
0
0

Texto

Loading

Imagem

Table 2. Results from accuracy of the method Sample  (µg mL -1 ) Standard added (µg mL-1) Found  (µg mL-1 ) Accuracy (%) 16.90 ± 0.11 2 19.25 ± 0.56 102.07320.36 ± 0.24102.72 4 21.24 ± 0.14 102.01 Mean recovery (%) 102.27 ± 0.39
Table 4. Results from the drug assay in the dissolution test

Referências

Documentos relacionados

Comparative evaluation of the nitrate reduction assay, the MTT test, and the resazurin microtitre assay for drug susceptibility testing of clinical isolates of

selected treatment [ 17 , 19 ]. In the present study, we performed this assay, providing a simple, accessible and accurate method of assessing alveolar bone loss during

A simple, rapid and reproducible HPLC method was developed for the simultaneous determination of amlodipine and valsartan in their combined dosage forms, and for drug

The aim of the present work is to develop a simple and reliable low injection method with spectrophotometric detection for the quantitative analysis of ketoconazole in tablets

The aim of the present work was the development of a new disso- lution test for ornidazole coated tablets using a new high performance liquid chromatography (HPLC) method, to assay

So, the aim of the present work was to develop and validate a reliable method using LC-UV to assay mometasone furoate in creams as well as in nasal sprays, using simple conditions,

A novel stability-indicating high-performance liquid chromatographic assay method was developed and validated for quantitative determination of pramipexole dihydrochloride

In this study, a dissolution test and a simple HPLC method were developed and validated to evaluate the dissolution performance of tablets containing ALB and PRA for veterinary