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Determination of related substances in the pharmaceutical excipient triacetin by gas chromatography

Published on Mar. 21, 2024Total Views: 846 times Total Downloads: 400 times Download Mobile

Author: ZHANG Yue 1, 2 SHI Rong 1, 2 ZHENG Jinfeng 1, 2 LIU Yanming 1, 2 XIE Yingying 3 LI Ying 3

Affiliation: 1. Hunan Institute for Drug Control, Changsha 410001, China 2. NMPA Key Laboratory for Pharmaceutical Excipients Engineering Technology Research, Changsha 410001, China 3. Hunan Drug Inspection Center, Changsha 410001, China

Keywords: Triacetin Gas chromatography Related substances Pharmaceutical excipients

DOI: 10.12173/j.issn.1008-049X.202312007

Reference: ZHANG Yue, SHI Rong, ZHENG Jinfeng, LIU Yanming, XIE Yingying, LI Ying.Determination of related substances in the pharmaceutical excipient triacetin by gas chromatography[J].Zhongguo Yaoshi Zazhi,2024, 27(2):227-232.DOI: 10.12173/j.issn.1008-049X.202312007.[Article in Chinese]

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Abstract

Objective To determine the related substances in the pharmaceutical excipient triacetin by gas chromatography (GC).

Methods  Rtx-1701 and DB-1701 chromatographic column (30 m×0.25 mm, 0.25 μm) was used, with nitrogen as the carrier gas, the flow rate was 1.5 mL/min, the inlet temperature was 200 ℃, the hydrogen flame ionization detector was used, the temperature of the measuring instrument was 250 ℃, and the program heating was used.

Results  Under this chromatographic condition, each substance could be effectively separated, and showed good linearity at 2-40 μg/mL (r>0.99). The recovery rates of acetic acid, glycerol, 1-monoglyceryl acetate, 1,2-diglyceryl acetate and 1,3-diglyceryl acetate were 100.7% (RSD=3.12%), 95.1% (RSD=3.66%), 99.43% (RSD=4.62%), 103.66% (RSD=5.88%) and 103.15% (RSD=4.17%) (n=6), respectively.

Conclusion  This method has high accuracy and good reproducibility, which can be used for the determination of related substances in the triacetin, and provides a reference for the quality standard of triacetin.

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References

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