Hydroxychloroquine - Isotope Labelled Standards
References
FAQ's
References
- Morris, Raymond G., Estimation of plasma hydroxychloroquine by high-performance liquid chromatography with ultraviolet detection, Journal of Chromatography, Biomedical Applications, Volume: 338, Issue: 2, Pages: 422-7, 1985
- Tett, S. E.; Cutler, D. J.; Brown, K. F., High-performance liquid chromatographic assay for hydroxychloroquine and metabolites in blood and plasma, using a stationary phase of poly(styrene divinylbenzene) and a mobile phase at pH 11, with fluorimetric detection, Journal of Chromatography, Biomedical Applications, Volume: 344, Pages: 241-8, 1985
Frequently Asked Questions
Are there any specific impurity testing requirements for Hydroxychloroquine in pharmacopeial standards?
Pharmacopeial standards, such as the United States Pharmacopeia (USP) or the European Pharmacopoeia (EP), outline specific impurity testing requirements for Hydroxychloroquine to ensure its quality and safety.
Can Hydroxychloroquine impurities impact its stability under different storage conditions?
Impurities in Hydroxychloroquine can influence its stability under specific storage conditions, such as temperature and humidity. Proper storage guidelines help maintain drug integrity.
Which solvent helps in analyzing Hydroxychloroquine impurities?
When analyzing many impurities in Hydroxychloroquine, Methanol is the common solvent.
How should Hydroxychloroquine impurities be stored in terms of temperature?
The recommendation is to store Hydroxychloroquine impurities at a controlled room temperature, within 2-8 °C.
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