Applications and Future Potential of X-ray Diffraction in Pharmaceutical Polymorphism: A Literature Review

Rizki Rava Dwiputra, Departement of Pharmacy, University of Singaperbangsa Karawang, Indonesia
Jasmine Rahma Saputri, Departement of Pharmacy, University of Singaperbangsa Karawang, Indonesia
Marsah Rahmawati Utami, Departement of Pharmacy, University of Singaperbangsa Karawang, Indonesia

Abstract


Polymorphism in drug compounds is a significant phenomenon in pharmacy because it affects physicochemical properties such as solubility, stability, and bioavailability, which impact the effectiveness and safety of drugs. X-ray diffraction (XRD) is one of the methods that can be used to identify and analyze the polymorphic properties of drug compounds. This article reviews the utilization of XRD in various studies, showing that this method is effective for identifying polymorphism, detecting changes in crystal forms, monitoring crystalline phase transitions, and characterizing the formation of new crystalline phases. Although very useful, XRD has limitations in detecting amorphous phases and requires optimal sample preparation. For more comprehensive results, XRD is often combined with other techniques such as DSC and FTIR. Overall, XRD plays an important role in drug development and quality control, and this technology is expected to continue evolving, including its ability to directly monitor the crystallization process to enhance drug quality and stability.

Full Text:

PDF


DOI: https://doi.org/10.21831/ijoce.v7i2.79071

Refbacks



Our journal is indexed by:

    

Creative Commons License 

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Indonesian Journal of Chemistry and Environment (IJoCE)

e-ISSN 2599-3186
Published by: Department of Chemistry, Universitas Negeri Yogyakarta

 

View My Stats