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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Materials and methods
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Materials
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Development of the HPLC method
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Validation of the HPLC method
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System suitability
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Linearity
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Accuracy
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Precision
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Specificity
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LOD and LOQ
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Robustness
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Stressed degradation
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Nanoparticles preparation
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Characterisation of loaded nanoparticles
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Zeta potential and particle size investigation
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Estimation of drug content and entrapment efficiency
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Fourier transform infrared spectroscopy (FTIR)
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In vitro release
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Morphology investigation
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Statistical analysis
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Results and discussion
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HPLC method and validation
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Specificity
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Characterization of loaded nanoparticles
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Zeta potential and particle size investigation
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Content and entrapment efficiency
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Fourier transform infrared spectroscopy (FTIR)
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In vitro release
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Morphology investigation
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Conclusion
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Acknowledgement
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References
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