Method development is one of the most time-consuming tasks in today’s pharmaceutical analytical laboratories.1 Usually, condition scouting is the first step followed by fine-tuning of the best set of parameters found. A means of speeding up the entire process by utilizing Agilent Rapid Resolution HT columns in combination with the Agilent 1200 Series Rapid Resolution LC (RRLC) system is described. How separation condition scouting and method fine-tuning resulted in a robust method for the quantization of diasteromeric and regioisomeric impurities of an active pharmaceutical ingredient within one and a half days is demon-strated. The final method not only is much faster than comparable conventional methods but also saves a significant amount...
The potential of chemometrics for drug impurity profiling has been examined in this thesis. Generall...
peer reviewedThe pharmaceutical industry is highly regulated by quality policies. The concept of ris...
The potential of chemometrics for drug impurity profiling has been examined in this thesis. Generall...
Impurity profiling is the process of acquiring and evaluating data that establishes biological safet...
AbstractLiquid chromatography (LC) is considered by many as a mature technique. Nonetheless, LC tech...
LC-MS has become an important tool in all areas of drug discovery and development within pharmaceuti...
This Application Note describes: • The use of a high-throughput rapid resolution LC/MS TOF system fo...
The performance of five curve resolution methods was compared systematically for the identification ...
As the drug safety and efficacy is hampered in the presence of an impurity, the international regula...
Increasing productivity in the analysis of impurities in metoclopramide hydrochloride formulations u...
There is an ever increasing interest in impurities present in APIs. Now days, not only purity profil...
The purpose of this research is to design and validate a unique, simple, and effective RP-HPLC analy...
Impurities are always an ‘essential evil’, that will however be present with the drug products with ...
Objective: To propose a comprehensive, simple, and affordable RP-HPLC method for impurity profiling ...
The potential of chemometrics for drug impurity profiling has been examined in this thesis. Generall...
The potential of chemometrics for drug impurity profiling has been examined in this thesis. Generall...
peer reviewedThe pharmaceutical industry is highly regulated by quality policies. The concept of ris...
The potential of chemometrics for drug impurity profiling has been examined in this thesis. Generall...
Impurity profiling is the process of acquiring and evaluating data that establishes biological safet...
AbstractLiquid chromatography (LC) is considered by many as a mature technique. Nonetheless, LC tech...
LC-MS has become an important tool in all areas of drug discovery and development within pharmaceuti...
This Application Note describes: • The use of a high-throughput rapid resolution LC/MS TOF system fo...
The performance of five curve resolution methods was compared systematically for the identification ...
As the drug safety and efficacy is hampered in the presence of an impurity, the international regula...
Increasing productivity in the analysis of impurities in metoclopramide hydrochloride formulations u...
There is an ever increasing interest in impurities present in APIs. Now days, not only purity profil...
The purpose of this research is to design and validate a unique, simple, and effective RP-HPLC analy...
Impurities are always an ‘essential evil’, that will however be present with the drug products with ...
Objective: To propose a comprehensive, simple, and affordable RP-HPLC method for impurity profiling ...
The potential of chemometrics for drug impurity profiling has been examined in this thesis. Generall...
The potential of chemometrics for drug impurity profiling has been examined in this thesis. Generall...
peer reviewedThe pharmaceutical industry is highly regulated by quality policies. The concept of ris...
The potential of chemometrics for drug impurity profiling has been examined in this thesis. Generall...