Lindawati, Lindawati (2022) PENGARUH KOMBINASI PROPILEN GLIKOL DAN LAKTOSA DALAM PEMBUATAN TABLET LIQUISOLID NIFEDIPIN DENGAN METODE KEMPA LANGSUNG. Skripsi thesis, Universitas Setia Budi.
Text
ABSTRAK.pdf Download (90kB) |
|
Text
BAB I.pdf Download (608kB) |
|
Text
BAB II.pdf Restricted to Repository staff only Download (451kB) | Request a copy |
|
Text
BAB III.pdf Restricted to Repository staff only Download (229kB) | Request a copy |
|
Text
BAB IV.pdf Restricted to Repository staff only Download (316kB) | Request a copy |
|
Text
BAB V.pdf Restricted to Repository staff only Download (86kB) | Request a copy |
|
Text
DAFTAR PUSTAKA.pdf Download (314kB) |
|
Text
LAMPIRAN.pdf Download (1MB) |
|
Text
form pernyataan publikasi LINDA.pdf Download (160kB) |
|
Text
linda revisi suket.pdf Download (22kB) |
Abstract
Nifedipine is a water-insoluble drug, its water dissolution rate is quite low, so it requires efforts to increase its dissolution and improve its bioavailability. The purpose of this study was to determine the impact and comparison of Propylene Glycol as a non-volatile solvent and lactose as an absorbent (carrier material) on the physical properties of the Nifedipine liquisolid tablets and to determine the dissolution profile of the Nifedipine liquisolid tablets. This study used samples of Nifedipine which were formulated using propylene glycol and lactose excipients using the direct compression method with a ratio of formula 1 (5% propylene glycol : 95% lactose), formula 2 (10% propylene glycol : 95% lactose), formula 3 (15 % propylene glycol : 85% lactose). Tests performed on the manufacture of Nifedipine liquisolid tablets included physical tests of tablets and dissolution rate. Research data were analyzed using One way ANOVA. The results showed that propylene glycol had a significant effect on increasing friability, dissolution, content uniformity, and tablet disintegration time, while lactose had a significant effect on increasing tablet hardness. The interaction of the two has a significant effect on increasing the uniformity of tablet content. A good formula from all physical quality tests and dissolution tests is contained in formula 3 with a ratio of propylene glycol: lactose (15%: 85%). Keywords: Nifedipine liquisolid, propylene glycol, lactose, dissolution, tablet physical quality test
Item Type: | Thesis (Skripsi) |
---|---|
Uncontrolled Keywords: | Nifedipine liquisolid, propylene glycol, lactose, dissolution, tablet physical quality test |
Subjects: | R Medicine > RS Pharmacy and materia medica |
Divisions: | Fakultas Farmasi > Prodi S1 Farmasi |
Depositing User: | Tifany Nur Arfiana |
Date Deposited: | 05 Apr 2023 03:00 |
Last Modified: | 05 Apr 2023 03:00 |
URI: | http://repo.setiabudi.ac.id/id/eprint/5798 |
Actions (login required)
View Item |