Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Venugopala Rao Dama"'
Publikováno v:
Acta Chromatographica.
In this study, we report the systematic approach for characterization of two major degradant impurities, which are not listed in any compendia and were formed during the stability studies of Dihydroergotamine mesylate injection (DHE). An ion-pair UPL
Publikováno v:
Analytical Methods. 12:304-316
Among all chemical sameness characterization tests of Therapeutic Peptides (TPs), one of the most significant and challenging aspects is to demonstrate comparable impurity profiles (both qualitative & quantitative) between a generic product and refer
Publikováno v:
Journal of Applied Pharmaceutical Science.
Publikováno v:
Analytical Methods. 10:2481-2493
Control of the chiral purity of Nα-Fmoc/Boc amino acid derivatives (Nα-PADs) used in the manufacturing of therapeutic peptides is an important material quality attribute to reduce the risk of undesired pharmacological and toxicological effects aris
Publikováno v:
Amino acids. 51(2)
Qualitative and quantitative determination of amino acid composition using amino acid analysis (AAA) is an important quality attribute and considered an identity of therapeutic peptide drugs by the regulatory agencies. Although huge literature is ava
Autor:
Malleswara Reddy A; Analytical Research and Development, Integrated Product Development, Dr. Reddyâs Laboratories Ltd., Bachupally, Hyderabad-500 072, India. malleswarareddya@drreddys.com, Banda N, Govind Dagdu S, Venugopala Rao D, Kocherlakota CS, Krishnamurthy V
Publikováno v:
Scientia pharmaceutica [Sci Pharm] 2010 Apr-Jun; Vol. 78 (2), pp. 215-31. Date of Electronic Publication: 2010 Mar 05.