Saccharin Extraction And Analysis Of Drug And Food Samples By Derivative Ultraviolet (UV) Spectrophotometry

Saccharin extraction and analysis of drug and food samples was investegated by spectrophotometry ultraviolet (uv) derivative method were studied. The saccharin extraction was carried out using solvent of ethanol/chloroform (2:8 v/v). The limit of detection (LOD) and limit of quantification (LOQ) of...

Full description

Bibliographic Details
Main Authors: Sarwendah Ratnawati Hermanto, Roto Roto, Agus Kuncaka
Format: Article
Language:Indonesian
Published: Universitas Islam Indonesia 2018-09-01
Series:Eksakta: Jurnal Ilmu-Ilmu MIPA
Subjects:
Online Access:https://journal.uii.ac.id/Eksakta/article/view/10523
id doaj-fa4b5ac5a9c24db6aab4d53b869acb46
record_format Article
spelling doaj-fa4b5ac5a9c24db6aab4d53b869acb462020-11-24T21:27:37ZindUniversitas Islam IndonesiaEksakta: Jurnal Ilmu-Ilmu MIPA1411-10472503-23642018-09-01182859610.20885/eksakta.vol18.iss2.art18257Saccharin Extraction And Analysis Of Drug And Food Samples By Derivative Ultraviolet (UV) SpectrophotometrySarwendah Ratnawati Hermanto0Roto Roto1Agus Kuncaka2Politeknik Negeri KetapangUniversitas Gadjah Mada, Jalan Sekip Utara Bulaksumur, Yogyakarta, telp. (0274)545188Universitas Gadjah Mada, Jalan Sekip Utara Bulaksumur, Yogyakarta, telp. (0274)545188Saccharin extraction and analysis of drug and food samples was investegated by spectrophotometry ultraviolet (uv) derivative method were studied. The saccharin extraction was carried out using solvent of ethanol/chloroform (2:8 v/v). The limit of detection (LOD) and limit of quantification (LOQ) of the proposed method were  0.50 ppm and 1.82 ppm for the second order and 0.47 ppm and 1.58 ppm for the fourth, while for the zero order were 2,75 ppm and 8,55 ppm. The calibration curve was linear in the concentration range from 20-100 ppm (R2= 0.996 for the second order and R2=0.997 for the fourth). The percent recovery of saccharin was in the range 95.20-104.40% for the second order and 97.20-102.40% for the fourth. The range of saccharin concentration (w/w) in drugs, candies and toothpaste for the fourth derivative were 1.39±0.02 mg/kg until 7.15±0.05 mg/kg, 0.21±0.01 mg/kg until 2.09±0.01 mg/kg, and 0.15±0.03 mg/kg until 0.63±0.04 mg/kg, respectively.https://journal.uii.ac.id/Eksakta/article/view/10523analysisderivative UV spectrophotometryextractionsaccharin
collection DOAJ
language Indonesian
format Article
sources DOAJ
author Sarwendah Ratnawati Hermanto
Roto Roto
Agus Kuncaka
spellingShingle Sarwendah Ratnawati Hermanto
Roto Roto
Agus Kuncaka
Saccharin Extraction And Analysis Of Drug And Food Samples By Derivative Ultraviolet (UV) Spectrophotometry
Eksakta: Jurnal Ilmu-Ilmu MIPA
analysis
derivative UV spectrophotometry
extraction
saccharin
author_facet Sarwendah Ratnawati Hermanto
Roto Roto
Agus Kuncaka
author_sort Sarwendah Ratnawati Hermanto
title Saccharin Extraction And Analysis Of Drug And Food Samples By Derivative Ultraviolet (UV) Spectrophotometry
title_short Saccharin Extraction And Analysis Of Drug And Food Samples By Derivative Ultraviolet (UV) Spectrophotometry
title_full Saccharin Extraction And Analysis Of Drug And Food Samples By Derivative Ultraviolet (UV) Spectrophotometry
title_fullStr Saccharin Extraction And Analysis Of Drug And Food Samples By Derivative Ultraviolet (UV) Spectrophotometry
title_full_unstemmed Saccharin Extraction And Analysis Of Drug And Food Samples By Derivative Ultraviolet (UV) Spectrophotometry
title_sort saccharin extraction and analysis of drug and food samples by derivative ultraviolet (uv) spectrophotometry
publisher Universitas Islam Indonesia
series Eksakta: Jurnal Ilmu-Ilmu MIPA
issn 1411-1047
2503-2364
publishDate 2018-09-01
description Saccharin extraction and analysis of drug and food samples was investegated by spectrophotometry ultraviolet (uv) derivative method were studied. The saccharin extraction was carried out using solvent of ethanol/chloroform (2:8 v/v). The limit of detection (LOD) and limit of quantification (LOQ) of the proposed method were  0.50 ppm and 1.82 ppm for the second order and 0.47 ppm and 1.58 ppm for the fourth, while for the zero order were 2,75 ppm and 8,55 ppm. The calibration curve was linear in the concentration range from 20-100 ppm (R2= 0.996 for the second order and R2=0.997 for the fourth). The percent recovery of saccharin was in the range 95.20-104.40% for the second order and 97.20-102.40% for the fourth. The range of saccharin concentration (w/w) in drugs, candies and toothpaste for the fourth derivative were 1.39±0.02 mg/kg until 7.15±0.05 mg/kg, 0.21±0.01 mg/kg until 2.09±0.01 mg/kg, and 0.15±0.03 mg/kg until 0.63±0.04 mg/kg, respectively.
topic analysis
derivative UV spectrophotometry
extraction
saccharin
url https://journal.uii.ac.id/Eksakta/article/view/10523
work_keys_str_mv AT sarwendahratnawatihermanto saccharinextractionandanalysisofdrugandfoodsamplesbyderivativeultravioletuvspectrophotometry
AT rotoroto saccharinextractionandanalysisofdrugandfoodsamplesbyderivativeultravioletuvspectrophotometry
AT aguskuncaka saccharinextractionandanalysisofdrugandfoodsamplesbyderivativeultravioletuvspectrophotometry
_version_ 1725974435335241728