Pharmaceutical Sciences: Analytical Methods
نویسندگان
چکیده
منابع مشابه
Analytical methods for residual solvents determination in pharmaceutical products.
Residual solvents (RS) are not desirable substances in the final pharmaceutical product and their acceptable limits have been published in pharmacopoeias and ICH guidelines. The intension of this paper was to review and discuss some of the current analytical procedures including gas chromatographic (GC) and other alternative techniques which are used for residual solvents determination. GC meth...
متن کاملJournal of Pharmaceutical and Biomedical Sciences
Recently, a new class of in vitro and ex vivo radiotracers/radioprotectors, the nitroxyl–labeled agent N-[N'-(2-chloroethyl)-N’-nitrosocarbamoylglycine amide of 2,2,6,6-tetramethyl-4aminopiperidine-1-oxyl (SLCNUgly), has been discovered. Our previous investigations demonstrated that SLCNUgly is a low-molecular-weight stable free radical which is freely membrane permeable, easily crosses the blo...
متن کاملInternational Journal of Pharmaceutical and Chemical Sciences
Epilepsy is the second most common neurologic disorder after stroke. Approximately 1% of the world’s population has epilepsy, is a condition where the patient suffers from recurrent seizures. Control to seizures numerous conventional drugs came into existence. Most of the epileptic patients need polytherapy of conventional anticonvulsants and still not 100% cured. The major drawback due to thes...
متن کاملInternational Journal of Pharmaceutical and Chemical Sciences
Diabetes mellitus is one of the world’s major diseases. It currently affects an estimated143 million people worldwide and the number is growing rapidly. In the India, about 1-5% population suffer from diabetes or related complication. So there is need to cure this disease. Anti-diabetic drugs treat diabetes mellitus by lowering glucose levels in the blood. With the exceptions of insulin, exenat...
متن کاملInternational Journal of Pharmaceutical and Chemical Sciences
The control of impurities in Formulated products and Active Pharmaceutical ingredient’s were regulated by various regulatory authorities like US-FDA,ICH,MHRA,TGA etc.As per International Conference on Harmonization guidelines, the Impurity may be defined as any component of new drug product that is not the drug substance or an excipient in drug product. Nowadays apart from purity profile there ...
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ژورنال
عنوان ژورنال: Pharmaceutica Analytica Acta
سال: 2013
ISSN: 2153-2435
DOI: 10.4172/2153-2435.1000e150