Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ahmed E. El-Gendy"'
Publikováno v:
Pharmaceutical Chemistry Journal. 55:206-212
A sensitive, simple and rapid RP-HPLC method with fluorescence detection has been developed to simultaneously quantify amlodipine besylate (AML) and olmesartan medoxomil (OLM) in their combined pharmaceutical preparation. The method development was d
Publikováno v:
Research Journal of Pharmacy and Technology. :1880-1886
Green chemistry is an emerging field concerned with safe practices in chemical method development. The purpose of the study is to develop a sensitive, environmentally friendly spectrofluorimetric method by studying and optimizing variables affecting
Publikováno v:
Acta Chromatographica. 33:234-244
Chloroquine phosphate (CQ) the antimalarial drug and suggested to treat the pandemic disease coronavirus (COVID-19) is often adulterated with some of the non-steroidal anti-inflammatory drugs (NSAIDs) such as paracetamol, aspirin (ASP), or both. The
Animal products are a major source of human exposure to steroids, this resulted in a critical request for applicable methods for the determination of these steroid hormones in pure form and in different matrices such as hen eggs, chicken liver and wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d354f9b45f74850d9c1cc3f8a89eae3
Publikováno v:
Analytical Chemistry Letters. 8:813-828
This study describes a rapid and sensitive HPLC method using fluorescence detection, which enables the determination of Sitagliptin mono phosphate (SIT) and Itopride Hydrochloride (ITP) as internal standard with good accuracy and precision to allow i
Publikováno v:
Records of Pharmaceutical and Biomedical Sciences. 2:34-46
A Quality by Design approach was used to develop a sensitive spectrophotometric method for determination of glucosamine Sulphate in pharmaceutical dosage forms and optimize a derivatization reaction of glucosamine with o-phthalaldhyde. This strategy
Publikováno v:
European Journal of Chemistry. 6:422-429
Two stability-indicating methods were developed and validated for the quantitative determination of acemetacin (ACM) in presence of its degradation products and impurities. The first method was based on separation of ACM from its degradation products