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X-ray powder diffraction patterns for certain fluoroquinolone antibiotic drugs
Subbiah Thangadurai1, Sudhir Kumar Shukla, Asim Kumar Srivastava
1Department of Geology & Mining, Guindy, Chennai-600 032, India. kalankathanga@hotmail.com
Acta Pharmaceutica (Zagreb, Croatia)
|February 11, 2004
Summary
X-ray powder diffraction (XRD) data were collected for six fluoroquinolone antibiotics. This new crystallographic data provides useful information for identifying these important antibacterial drugs.
Area of Science:
- Analytical Chemistry
- Crystallography
- Pharmaceutical Sciences
Background:
- Fluoroquinolone antibiotics are crucial antibacterial agents.
- Accurate identification of these drugs is essential for quality control and clinical use.
- Characterization of drug substances aids in understanding their physical properties.
Purpose of the Study:
- To obtain and present X-ray powder diffraction (XRD) data for six pure fluoroquinolone antibiotic drugs.
- To provide reference crystallographic information for ciprofloxacin, norfloxacin, enrofloxacin, ofloxacin, pefloxacin, and sparfloxacin.
- To facilitate the identification of these pharmaceutical compounds.
Main Methods:
- X-ray powder diffraction (XRD) was performed on pure samples of six fluoroquinolone antibiotics.
- Data acquisition covered a Bragg angle (2theta) range from 10 to 70 degrees.
- Lattice spacing (A) and relative line intensities (I/I(I)) were tabulated.
Main Results:
- XRD patterns were successfully generated for ciprofloxacin, norfloxacin, enrofloxacin, ofloxacin, pefloxacin, and sparfloxacin.
- Tabulated data include specific lattice spacing and relative line intensities for each drug.
- The generated data represent unique crystallographic fingerprints for these fluoroquinolones.
Conclusions:
- The obtained XRD data provide valuable new information for the identification of the studied fluoroquinolone antibiotics.
- This crystallographic dataset can serve as a reference for pharmaceutical analysis and quality assurance.
- The findings contribute to the characterization of important antibacterial drug substances.