PENGEMBANGAN METODE ANALISIS PARASETAMOL DALAM TABLET SECARA KLT-SPEKTROFOTODENSITOMETRI UNTUK PEMERIKSAAN OBAT YANG DIDUGA PALSU
Paracetamol was used as an analgesic-antipireutic agent, sold freely and could be obtained easily in single dose or combination with other active ingredients. Counterfeit drug was often defined with identity including the presence and amount of active ingredients are not appropriate to the compen...
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Format: | Final Project |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/45425 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Paracetamol was used as an analgesic-antipireutic agent, sold freely and could be obtained
easily in single dose or combination with other active ingredients. Counterfeit drug was often
defined with identity including the presence and amount of active ingredients are not
appropriate to the compendial or spesification. This research was aimed to develop suitable
analysis methode for paracetamol in tablet by determining the presence and amount of active
ingredien for it applying to investigate a counterfeit drug. Paracetamol was extracted using
ethanol then diluted until fix concentrate. Paracetamol solution was spotted on TLC plate
then developed using a mixture of dichloromethane-methanol (8,5:1,5) as a mobile phase.
Paracetamol spot was measured using spectrophotodensitometry at wavelength 247 nm. The
analytical methods was validated. Calibration curve resulted a linear with of equation y =
7611.5x + 1604.7 and correlation coefficient (r) 0.999; limit of detection was 0.085 µg; limit
of quantitation was 0.25 µg. Accuracy test of paracetamol standard showed with recovery of
100.308% 101.198%, 99.098% at 0.4; 0.8; 1.2 µg / spot and 98,712%, 100,692%, 101,995%
for tablet formulation. Interday precision testing resulted with the coefficient variation (CV)
of 1.464%, 1.1%, 1.443% and 1.849%, 1.29%, 1.1% for intraday precision. The method was
validated and used for sample in the market. The presence of paracetamol was positive in all
samples and the level of paracetamol were in the range of 96.18% - 107.72%.
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