Research Article
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Article title
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Abstract
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Keywords
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Introduction
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Methodology
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Experimental preparation of the mobile phase
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Preparation of 0.05% methanolic Sodium Hydroxide
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Preparation of LT4 standard solution (200 µg/mL)
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Chromatographic conditions
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Construction of calibration graph
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Pharmaceutical tablets
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Results and discussion
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Optimization of chromatographic conditions
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Detection wavelength
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Column type
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Mobile phase (composition, ratio, aqueous phase)
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Flow rate
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Method validation and statistical analysis
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System suitability
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Method validation
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Linearity and concentration range
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Limit of detection and Limit of quantification
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Accuracy
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Precision
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Specificity
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Robustness
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Pharmaceutical application
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Conclusion
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References
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