Estimation of Impurity Profiles of Drugs and Related Materials. 12. Isolation and Identification of an Isomeric Impurity in Danazol

In: Pharmaceutical Research · 1995 · vol. 12(2) , pp. 295–298 · doi:10.1023/a:1016201630774 · PMID:7784348 · W313347481
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This study reports the isolation and identification of a new isomeric impurity in danazol, termed isodanazol, using chromatography and spectroscopy, and demonstrates its quantitative determination.

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This paper studied danazol by detecting, isolating, and characterizing a newly found isomeric impurity named isodanazol. Using reversed-phase HPLC and TLC for detection, preparative HPLC for separation, and mass spectrometry and NMR spectroscopy (COSY, HETCOR, NOE) for structural determination, the authors reported that isodanazol contains an isomeric isoxazole ring whose UV spectrum differs markedly from danazol; they interpreted this difference using quantum chemical calculations. The quantitative determination of the impurity was described to be possible down to the 0.05% level by HPLC, gas chromatography, and TLC densitometry, with the key caveat being that the study focuses on analytical characterization rather than any biological or clinical consequences. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

We report on a new isomeric impurity of danazol. This impurity designated as isodanazol was detected by reversed-phase high-performance liquid chromatography (HPLC) and thin-layer chromatography (TLC). Its structure was determined after separation by preparative HPLC. Mass spectrometry revealed the isomeric nature of the impurity while the UV spectrum indicated profound difference in the isoxazole moieties. The structure of the isomeric isoxazole ring in isodanazol was determined by NMR spectroscopy using COSY, HETCOR and NOE measurements. The difference between the U V spectra of danazol and isodanazol is explained on the basis of the difference between the aromaticities of their isoxazole rings supported by quantum chemical calculations. The quantitative determination of the impurity down to the 0.05% level can be performed by HPLC, gas chromatography and TLC densitometry. Similar content being viewed by others

References

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