Physicochemical study of ciprofloxacin with β-cyclodextrin

K. Shrinivas Aithal, N. Udupa

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The interaction between ciprofloxacin and β-cyclodextrin leading to the formation of an inclusion complex was studied by phase-solubility, UV, X-ray diffractometry, differential scanning, calorimetry differential thermal analysis, infra red and NMR spectroscopy. Partial inclusion of the drug moiety within the β-cyclodextrin cavity along with an interaction of the carbonyl function of the carboxylic acid of ciprofloxacin with the hydroxyl function of β-cyclodextrin leaving the piperazine moiety hanging around the narrower rim of the cyclodextrin cavity was established. Change in the crystallinity coupled with improved stability of the drug was also observed on complexation. For improved stability, the complex may be used in place of the drug alone.

Original languageEnglish
Pages (from-to)451-455
Number of pages5
JournalPharmaceutical Sciences
Volume2
Issue number10
Publication statusPublished - 1996

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Cyclodextrins
Ciprofloxacin
Differential Thermal Analysis
Drug Stability
Differential Scanning Calorimetry
Carboxylic Acids
Pharmaceutical Preparations
Hydroxyl Radical
Solubility
Magnetic Resonance Spectroscopy
X-Rays

All Science Journal Classification (ASJC) codes

  • Pharmaceutical Science

Cite this

Shrinivas Aithal, K. ; Udupa, N. / Physicochemical study of ciprofloxacin with β-cyclodextrin. In: Pharmaceutical Sciences. 1996 ; Vol. 2, No. 10. pp. 451-455.
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Physicochemical study of ciprofloxacin with β-cyclodextrin. / Shrinivas Aithal, K.; Udupa, N.

In: Pharmaceutical Sciences, Vol. 2, No. 10, 1996, p. 451-455.

Research output: Contribution to journalArticle

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