A Static Headspace Gas Chromatography Method for Quantitation of Residual Solvents in Nanoformulations

Author:

Kattel Krishna,Clogston Jeffrey D.

Publisher

Springer US

Reference3 articles.

1. Witschi C, Doelker E (1997) Residual solvents in pharmaceutical products: acceptable limits, influences on physicochemical properties, analytical methods and documented values. Eur J Pharm Biopharm 43(3):215–242

2. <467> Residual solvents. United States Pharmacopeia-National Formulary. https://www.uspnf.com/sites/default/files/usp_pdf/EN/USPNF/generalChapter467Current.pdf. Accessed 19 July 2023

3. Impurities: Guideline for Residual Solvents, Q3C(R8). International Council for Harmonisation of Technical Requirements for Pharmacueticals for Human Use. https://database.ich.org/sites/default/files/ICH_Q3C-R8_Guideline_Step4_2021_0422_1.pdf. Accessed 19 July 2023

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