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A Review on Analytical Methods for Tigecycline Estimation From Its Bulk and Dosage Form
Bansi Rakholiya1, Priyangi Shah1, Yash Patel1
1Charotar University of Science and Technology, Department of Pharmaceutical Chemistry and Analysis, Ramanbhai Patel College of Pharmacy, CHARUSAT Campus, Changa, Petlad, Anand, Gujarat 388 421, India.
Tigecycline (TIG) is a vital drug prone to degradation, necessitating robust analytical methods for quality control. This review examines various techniques for TIG analysis, highlighting the need for stability-indicating and eco-friendly approaches.
Area of Science:
- Analytical Chemistry
- Pharmaceutical Analysis
Background:
- Tigecycline (TIG), a glycylcycline antibiotic, faces stability challenges due to its complex structure, impacting its quality control.
- Its instability in solution necessitates analysis of lyophilized powder, posing challenges for accurate quantification.
Approach:
- A comprehensive literature review from 1999-2022 was conducted to identify and evaluate analytical methodologies for TIG.
- The review focuses on methods for determining TIG in bulk, lyophilized powder, and pharmacopoeial preparations.
Key Points:
- Various analytical techniques including UV-visible spectrophotometry, spectrofluorimetry, RP-HPLC, FT-IR, and electrophoresis are reported for TIG quantification and characterization.
- Reversed-phase high-performance liquid chromatography (RP-HPLC) is effective without derivatization, while fluorescence methods require it.
Conclusions:
- Existing analytical methods for tigecycline quality control vary in complexity and environmental impact.
- There is a critical need for developing simpler, faster, and more eco-friendly analytical methods for tigecycline, minimizing organic solvent use and tedious sample preparation.
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