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Identification And Determination of Levels the Drug Chemical Sibutramin Hydrochloride in Body Slimming Herbs Circulating in the City of Salatiga

Journal of Science and Technology Research for Pharmacy · Vol. 4 No. 2 (2025) · pp. 30–36

DOI
10.15294/jstrp.v4i2.9977
ISSN
2776-0685
Published
2025-06-24
Publisher
Universitas Negeri Semarang
Language
eng

Abstract

Background: Sibutramine hydrochloride is strictly prohibited from being present in weight loss herbal medicines according to the regulations of the Indonesian National Agency of Drug and Food Control (Badan POM RI) No.KH.00.01.43. However, due to increasing competition, many traditional medicine producers seek greater profits by adding sibutramine hydrochloride (SH) to their products. Aim: This study aimed to establish the validity of the UV-VIS spectrophotometer method for analyzing sibutramine hydrochloride and to test the levels and content of sibutramine hydrochloride in weight loss herbal medicine samples sold in Salatiga City. Materials and Methods: A total of 8 samples of weight loss capsules obtained from traditional medicine stores in Salatiga City were subjected to qualitative and quantitative tests. Validation parameters included linearity, limit of detection (LoD), limit of quantification (LoQ), precision, and accuracy. Results: The study revealed a linear regression equation of y=0.0397x + 0.046 with r=0.9975 and r^2=0.9950, with a maximum wavelength of 223 nm. The LOD was 1.01 mg/L and LOQ was 3.37 mg/L. Precision, expressed as % RSD, was 0.147%, and percent recoveries (% recovery) were 98.263%, 89.337%, and 91.703%. Qualitative tests on each sample compared spectra and maximum wavelengths with standard sibutramine hydrochloride spectra, identifying samples A, B, C, E, and F as negative for sibutramine hydrochloride, while samples D, G, and H tested positive. Quantitative analysis determined sibutramine hydrochloride concentrations in weight loss herbal medicines using linear regression equations. The concentrations in samples D, G, and H were 6.0117 mg/L, 6.7254 mg/L, and 6.0117 mg/L, respectively. The percentage content of sibutramine hydrochloride in samples D, G, and H was 3.00%, 3.36%, and 3.00%, respectively. Conclusion: The UV-VIS spectrophotometer method is validated for analyzing sibutramine hydrochloride in weight loss herbal medicines across all tested parameters. Samples A, B, C, E, and F were found negative for sibutramine hydrochloride, whereas samples D, G, and H tested positive.

Keywords

Collaboration network of the authors

15 authors · 20 co-authorship links

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  • State University of Semarang
  • Affiliation unknown
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Co-authorOrganisationJoint articles
Zalza Zalzabila Adelya PutriAffiliation unknown1
AmeliyanaAffiliation unknown1
Nurul Fajar AgustinaAffiliation unknown1
Erika WuryaningsihAffiliation unknown1
Muhammad Shidqi Naufal AthallaAffiliation unknown1
Ernessa Indah Rotua SIRAITAffiliation unknown1
Rahma Annisa IzzaniaAffiliation unknown1
Sigit PriatmokoState University of Semarang1
Senda Kartika RakainsaAffiliation unknown1
Dhatu Sekar LarasatiAffiliation unknown1
Neli Syahida Ni’maAffiliation unknown1
Sitarina WidyariniAffiliation unknown1
Nanang FakhrudinAffiliation unknown1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) https://journal.unnes.ac.id/journals/JSTRP/oai, first harvested 5 Nov 2026, last seen 5 Nov 2026.
Original metadata (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/  http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en">Identification And Determination of Levels the Drug Chemical Sibutramin Hydrochloride in Body Slimming Herbs Circulating in the City of Salatiga</dc:title>
	<dc:creator xml:lang="en">Prisma Detty Nuryana</dc:creator>
	<dc:creator xml:lang="en">Endah Widhihastuti</dc:creator>
	<dc:subject xml:lang="en">Sibutramine Hydrochloride</dc:subject>
	<dc:subject xml:lang="en">UV-VIS Spectrophotometer</dc:subject>
	<dc:subject xml:lang="en">Weight Loss Herbal Medicine</dc:subject>
	<dc:subject xml:lang="en">Analytical Method Performance</dc:subject>
	<dc:description xml:lang="en">Background: Sibutramine hydrochloride is strictly prohibited from being present in weight loss herbal medicines according to the regulations of the Indonesian National Agency of Drug and Food Control (Badan POM RI) No.KH.00.01.43. However, due to increasing competition, many traditional medicine producers seek greater profits by adding sibutramine hydrochloride (SH) to their products.
Aim: This study aimed to establish the validity of the UV-VIS spectrophotometer method for analyzing sibutramine hydrochloride and to test the levels and content of sibutramine hydrochloride in weight loss herbal medicine samples sold in Salatiga City.
Materials and Methods: A total of 8 samples of weight loss capsules obtained from traditional medicine stores in Salatiga City were subjected to qualitative and quantitative tests. Validation parameters included linearity, limit of detection (LoD), limit of quantification (LoQ), precision, and accuracy.
Results: The study revealed a linear regression equation of y=0.0397x + 0.046 with r=0.9975 and r^2=0.9950, with a maximum wavelength of 223 nm. The LOD was 1.01 mg/L and LOQ was 3.37 mg/L. Precision, expressed as % RSD, was 0.147%, and percent recoveries (% recovery) were 98.263%, 89.337%, and 91.703%. Qualitative tests on each sample compared spectra and maximum wavelengths with standard sibutramine hydrochloride spectra, identifying samples A, B, C, E, and F as negative for sibutramine hydrochloride, while samples D, G, and H tested positive. Quantitative analysis determined sibutramine hydrochloride concentrations in weight loss herbal medicines using linear regression equations. The concentrations in samples D, G, and H were 6.0117 mg/L, 6.7254 mg/L, and 6.0117 mg/L, respectively. The percentage content of sibutramine hydrochloride in samples D, G, and H was 3.00%, 3.36%, and 3.00%, respectively.
Conclusion: The UV-VIS spectrophotometer method is validated for analyzing sibutramine hydrochloride in weight loss herbal medicines across all tested parameters. Samples A, B, C, E, and F were found negative for sibutramine hydrochloride, whereas samples D, G, and H tested positive.</dc:description>
	<dc:publisher xml:lang="en">Universitas Negeri Semarang</dc:publisher>
	<dc:date>2025-06-24</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.unnes.ac.id/journals/JSTRP/article/view/9977</dc:identifier>
	<dc:identifier>10.15294/jstrp.v4i2.9977</dc:identifier>
	<dc:source xml:lang="en">Journal of Science and Technology Research for Pharmacy; Vol. 4 No. 2 (2024): Journal of Science and Technology Research for Pharmacy; 30-36</dc:source>
	<dc:source>2776-0685</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.unnes.ac.id/journals/JSTRP/article/view/9977/4541</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2025 Journal of Science and Technology Research for Pharmacy</dc:rights>
</oai_dc:dc>