Preformulation Studies of Rosuvastatin

Authors

  • Pallavi Rajput Department of Pharmaceutical Technology, NIET, Greater Noida
  • Anju Gauniya Department of Pharmaceutical Technology, NIET, Greater Noida.

Abstract

Reliable experimental determination of the solubility of active pharmaceutical ingredients (APIs) in solvents and the correlation for solubility analysis is crucial for the accelerated design and optimization of procedures in the drug industry for isolation, purification and formulation. In this study, the antihypercholesterolemic drug rosuvastatin was evaluated for solubility, effect of pH, compatibity with various exepients. In this research, the rosuvastatin, an antihypercholesterolemic drug was analysed for solubility, pH effect, and compatibility with different excipients. Drug dispersion  subjected to Differential scanning calorimetry and X-ray powder diffractometry.

Keywords: Hypercholesterolaemia, HMG-CoA reductase inhibitors, DSC, XRPD

DOI

https://doi.org/10.22270/jddt.v9i3-s.2968

Author Biographies

Pallavi Rajput, Department of Pharmaceutical Technology, NIET, Greater Noida

Department of Pharmaceutical Technology, NIET, Greater Noida.

Anju Gauniya, Department of Pharmaceutical Technology, NIET, Greater Noida.

Department of Pharmaceutical Technology, NIET, Greater Noida.

Published

2019-06-22
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How to Cite

1.
Rajput P, Gauniya A. Preformulation Studies of Rosuvastatin. J. Drug Delivery Ther. [Internet]. 2019 Jun. 22 [cited 2026 Feb. 1];9(3-s):729-35. Available from: https://www.jddtonline.info/index.php/jddt/article/view/2968

How to Cite

1.
Rajput P, Gauniya A. Preformulation Studies of Rosuvastatin. J. Drug Delivery Ther. [Internet]. 2019 Jun. 22 [cited 2026 Feb. 1];9(3-s):729-35. Available from: https://www.jddtonline.info/index.php/jddt/article/view/2968