Authors :
Ramesh Raj Seeha; Shilpi Chauhan; Preeti Mann
Volume/Issue :
Volume 10 - 2025, Issue 6 - June
Google Scholar :
https://tinyurl.com/4zcd5dn2
DOI :
https://doi.org/10.38124/ijisrt/25jun546
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Abstract :
Hydrocortisone and camphor are widely used active pharmaceutical ingredients (APIs) in topical formulations
for the treatment of various dermatological conditions such as inflammation, pruritus, and muscular pain. Accurate and
reliable estimation of these compounds is crucial for ensuring product quality, efficacy, and patient safety. High-
Performance Liquid Chromatography (HPLC) has emerged as a preferred analytical technique for the simultaneous
estimation of hydrocortisone and camphor due to its high sensitivity, specificity, and reproducibility. This review explores
the current analytical approaches for quantifying hydrocortisone and camphor in topical dosage forms, with a focus on
HPLC methodologies. It discusses the principles of HPLC and highlights key parameters including mobile phase
composition, detection wavelength, flow rate, column selection, and sample preparation techniques that impact method
efficiency and resolution. Furthermore, it evaluates the validation parameters such as linearity, precision, accuracy,
robustness, and limits of detection (LOD) and quantification (LOQ) that are essential to comply with regulatory standards.
Several studies are analysed to compare their methodological variations and outcomes. The review also emphasizes the
significance of method development and optimization for complex matrices like creams, gels, and ointments, where
excipients can interfere with accurate detection. Overall, this review provides a comprehensive understanding of HPLC-
based estimation methods for hydrocortisone and camphor, which can aid in developing standardized protocols for routine
quality control in pharmaceutical manufacturing.
Keywords :
Hplc, Hydrocortisone, Camphor, High-Performance Liquid Chromatography, Topical Formulation.
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Hydrocortisone and camphor are widely used active pharmaceutical ingredients (APIs) in topical formulations
for the treatment of various dermatological conditions such as inflammation, pruritus, and muscular pain. Accurate and
reliable estimation of these compounds is crucial for ensuring product quality, efficacy, and patient safety. High-
Performance Liquid Chromatography (HPLC) has emerged as a preferred analytical technique for the simultaneous
estimation of hydrocortisone and camphor due to its high sensitivity, specificity, and reproducibility. This review explores
the current analytical approaches for quantifying hydrocortisone and camphor in topical dosage forms, with a focus on
HPLC methodologies. It discusses the principles of HPLC and highlights key parameters including mobile phase
composition, detection wavelength, flow rate, column selection, and sample preparation techniques that impact method
efficiency and resolution. Furthermore, it evaluates the validation parameters such as linearity, precision, accuracy,
robustness, and limits of detection (LOD) and quantification (LOQ) that are essential to comply with regulatory standards.
Several studies are analysed to compare their methodological variations and outcomes. The review also emphasizes the
significance of method development and optimization for complex matrices like creams, gels, and ointments, where
excipients can interfere with accurate detection. Overall, this review provides a comprehensive understanding of HPLC-
based estimation methods for hydrocortisone and camphor, which can aid in developing standardized protocols for routine
quality control in pharmaceutical manufacturing.
Keywords :
Hplc, Hydrocortisone, Camphor, High-Performance Liquid Chromatography, Topical Formulation.