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Monitoring of Simvastatin impurities by HPLC with microemulsion eluents

Authorized Users Only
2006
Authors
Malenović, Anđelija
Medenica, Mirjana
Ivanović, D.
Jančić, Biljana
Article (Published version)
Metadata
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Abstract
The use of microemulsions as eluents in HPLC has shown excellent potential. We have developed a novel approach for the analysis of Simvastatin and its six impurities, applying microemulsions as mobile phase. The method was validated and applied to the analysis of commercially available tablets in order to confirm that the proposed approach is useful for the application of this technique to drug analysis. A microemulsion eluent containing 0.9% w/w of diisopropylether, 1.7% w/w of sodium dodecyl-sulphate (SDS), 7.0% w/w of co-surfactant such as n-butanol and 90.4% w/w of aqueous 25 mM di-sodium phosphate pH 7.0 was used for the analysis. Separations were performed on a 3.5 mu m X Terra(TM) 50 x 4.6 mm column at 30 degrees C. Detection was performed at 238 nm with an eluent flow rate of 0.3 mL min(-1). The optimized and validated method can be used for the identification and simultaneous determination of Simvastatin and its six impurities in bulk drug and in pharmaceutical dosage forms.
Keywords:
column liquid chromatography / microemulsion eluents / Simvastatin impurities / pharmaceutical formulations
Source:
Chromatographia, 2006, 63
Publisher:
  • Springer Heidelberg, Heidelberg

DOI: 10.1365/s10337-006-0747-4

ISSN: 0009-5893

WoS: 000239016200015

Scopus: 2-s2.0-33745150015
[ Google Scholar ]
30
26
URI
https://farfar.pharmacy.bg.ac.rs/handle/123456789/818
Collections
  • Radovi istraživača / Researchers’ publications
Institution/Community
Pharmacy
TY  - JOUR
AU  - Malenović, Anđelija
AU  - Medenica, Mirjana
AU  - Ivanović, D.
AU  - Jančić, Biljana
PY  - 2006
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/818
AB  - The use of microemulsions as eluents in HPLC has shown excellent potential. We have developed a novel approach for the analysis of Simvastatin and its six impurities, applying microemulsions as mobile phase. The method was validated and applied to the analysis of commercially available tablets in order to confirm that the proposed approach is useful for the application of this technique to drug analysis. A microemulsion eluent containing 0.9% w/w of diisopropylether, 1.7% w/w of sodium dodecyl-sulphate (SDS), 7.0% w/w of co-surfactant such as n-butanol and 90.4% w/w of aqueous 25 mM di-sodium phosphate pH 7.0 was used for the analysis. Separations were performed on a 3.5 mu m X Terra(TM) 50 x 4.6 mm column at 30 degrees C. Detection was performed at 238 nm with an eluent flow rate of 0.3 mL min(-1). The optimized and validated method can be used for the identification and simultaneous determination of Simvastatin and its six impurities in bulk drug and in pharmaceutical dosage forms.
PB  - Springer Heidelberg, Heidelberg
T2  - Chromatographia
T1  - Monitoring of Simvastatin impurities by HPLC with microemulsion eluents
VL  - 63
DO  - 10.1365/s10337-006-0747-4
ER  - 
@article{
author = "Malenović, Anđelija and Medenica, Mirjana and Ivanović, D. and Jančić, Biljana",
year = "2006",
abstract = "The use of microemulsions as eluents in HPLC has shown excellent potential. We have developed a novel approach for the analysis of Simvastatin and its six impurities, applying microemulsions as mobile phase. The method was validated and applied to the analysis of commercially available tablets in order to confirm that the proposed approach is useful for the application of this technique to drug analysis. A microemulsion eluent containing 0.9% w/w of diisopropylether, 1.7% w/w of sodium dodecyl-sulphate (SDS), 7.0% w/w of co-surfactant such as n-butanol and 90.4% w/w of aqueous 25 mM di-sodium phosphate pH 7.0 was used for the analysis. Separations were performed on a 3.5 mu m X Terra(TM) 50 x 4.6 mm column at 30 degrees C. Detection was performed at 238 nm with an eluent flow rate of 0.3 mL min(-1). The optimized and validated method can be used for the identification and simultaneous determination of Simvastatin and its six impurities in bulk drug and in pharmaceutical dosage forms.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Chromatographia",
title = "Monitoring of Simvastatin impurities by HPLC with microemulsion eluents",
volume = "63",
doi = "10.1365/s10337-006-0747-4"
}
Malenović, A., Medenica, M., Ivanović, D.,& Jančić, B.. (2006). Monitoring of Simvastatin impurities by HPLC with microemulsion eluents. in Chromatographia
Springer Heidelberg, Heidelberg., 63.
https://doi.org/10.1365/s10337-006-0747-4
Malenović A, Medenica M, Ivanović D, Jančić B. Monitoring of Simvastatin impurities by HPLC with microemulsion eluents. in Chromatographia. 2006;63.
doi:10.1365/s10337-006-0747-4 .
Malenović, Anđelija, Medenica, Mirjana, Ivanović, D., Jančić, Biljana, "Monitoring of Simvastatin impurities by HPLC with microemulsion eluents" in Chromatographia, 63 (2006),
https://doi.org/10.1365/s10337-006-0747-4 . .

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