HPLC-DAD and UV-Spectrophotometry for the determination of lychnopholide in nanocapsule dosage dorm : validation and application to release kinetic study.
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2012
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Abstract
Simple and sensitive methods using high-performance liquid chromatography–
diode array detection (HPLC–DAD) and ultraviolet
(UV)–spectrophotometry were developed and compared to quantify
lychnopholide (LYC) in poly-1-caprolactone nanocapsules and to
study its release kinetics. Both methods were validated concerning
their specificity, linearity, limits of detection and quantification, precision,
accuracy and stability. HPLC–DAD analyses were conducted
using an RP C18 column, isocratic elution with a methanol–water
(60:40 v/v) mobile phase at 0.8 mL/min flow rate and detection at
265 nm. The linear response (r2 > 0.999) was obtained within a
concentration range of 2–25 mg/mL using HPLC–DAD and 5–
40 mg/mL using spectrophotometry. Intra-day and inter-day precision
were obtained with low relative standard deviation values.
The accuracy of the methods was within the range 98–101% for
HPLC–DAD and from 96–100% for UV–spectrophotometry. Both
methods were suitable to be applied for the determination of drug
loading percentage (>96%) and encapsulation efficiency (>90%).
Furthermore, the sensitivity of HPLC–DAD method allows studies
of LYC release/dissolution in sink conditions. LYC presented 100%
dissolution after 24 h, whereas only 60% of LYC was released from
the nanocapsule dosage form, with no burst effect. The methods
fulfilled all validation parameters evaluated for LYC quantification in
the polymeric nanocapsules and have proven to be accurate, selective
and sensitive in the previously mentioned applications.
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BRANQUINHO, R. T. et al. HPLC-DAD and UV-Spectrophotometry for the determination of lychnopholide in nanocapsule dosage dorm: validation and application to release kinetic study. Journal Of Chromatographic Science, v. 52, p.19-26, 2012. Disponível em: <https://academic.oup.com/chromsci/article/52/1/19/268140/HPLC-DAD-and-UV-Spectrophotometry-for-the>. Acesso em: 10 jan. 2017.