| dc.contributor.advisor | Purwaningsih, Henny | |
| dc.contributor.author | Angraini, Dinni | |
| dc.date.accessioned | 2026-08-07T04:44:11Z | |
| dc.date.available | 2026-08-07T04:44:11Z | |
| dc.date.issued | 2026 | |
| dc.identifier.uri | http://repository.ipb.ac.id/handle/123456789/177623 | |
| dc.description.abstract | Lorazepam merupakan obat golongan benzodiazepina yang digunakan
untuk terapi gangguan kecemasan dan insomnia. Mutu sediaan tablet lorazepam
dievaluasi melalui uji disolusi untuk mengetahui kemampuan zat aktif terlepas dari
sediaan dan tersedia untuk diabsorpsi tubuh. Penelitian ini bertujuan menganalisis
pengaruh variasi suhu dan kecepatan pengadukan terhadap hasil disolusi lorazepam
menggunakan metode kromatografi cair kinerja tinggi (KCKT). Metode divalidasi
melalui pengujian kesesuaian sistem, spesifisitas, linearitas, rentang, akurasi,
presisi, dan robustness. Hasil validasi menunjukkan seluruh parameter memenuhi
batas keberterimaan sehingga metode dinyatakan valid. Pengujian disolusi
dilakukan pada suhu 25,0 °C, 37,0 °C, dan 40,0 °C serta kecepatan pengadukan 50,
75, dan 100 rpm. Kondisi optimum diperoleh pada suhu 37,0 °C dan kecepatan
pengadukan 100 rpm karena menghasilkan sistem disolusi yang paling stabil dan
reprodusibel. | |
| dc.description.abstract | Lorazepam is a benzodiazepine drug used for the treatment of anxiety
disorders and insomnia. The quality of lorazepam tablets was evaluated through
dissolution testing to determine the ability of the active ingredient to be released
from the dosage form and become available for absorption. This study aimed to
analyze the effects of temperature and stirring speed variations on the dissolution
performance of lorazepam using High-Performance Liquid Chromatography
(HPLC). The analytical method was validated through system suitability,
specificity, linearity, range, accuracy, precision, and robustness tests. The
validation results showed that all parameters met the acceptance criteria, indicating
that the method was valid for lorazepam analysis. Dissolution testing was
performed at temperatures of 25.0, 37.0, and 40.0 °C and stirring speeds of 50, 75,
and 100 rpm. The optimum condition was achieved at 37.0 °C and a stirring speed
of 100 rpm, which produced the most stable and reproducible dissolution system. | |
| dc.description.sponsorship | | |
| dc.language.iso | id | |
| dc.publisher | IPB University | id |
| dc.title | . Analisis Pengaruh Variasi Suhu dan Kecepatan Pengadukan Disolusi Bahan Aktif Lorazepam dalam Sediaan Tablet Menggunakan KCKT | id |
| dc.title.alternative | Analysis of the Effect of Temperature and Agitation Speed Variations on the Dissolution of Lorazepam Active Substance in Tablet Dosage Form Using HPLC | |
| dc.type | Tugas Akhir | |
| dc.subject.keyword | dissolution | id |
| dc.subject.keyword | KCKT | id |
| dc.subject.keyword | stirring speed | id |
| dc.subject.keyword | lorazepam | id |
| dc.subject.keyword | temperature | id |
| dc.subtype | Undergraduate Theses | |