2017
DOI: 10.22146/ijc.22640
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Design and Optimization of Self Nano-Emulsifying Drug Delivery System Containing a New Anti-inflamatory Agent Pentagamavunon-0

Abstract: Pentagamavunon-0 is a potent anti-inflammatory drug. The oral bioavailability of PGV-0 is very low due to its low solubility in water. The aim of this study is to design and optimize SNEDDS formulation to improve dissolution of ABSTRAK Pentagamavunon-0 merupakan obat anti-inflamasi yang poten. Ketersediaan hayati PGV-0 sangat rendah dikarenakan kelarutannya yang rendah dalam air. Tujuan studi ini adalah untuk mendesain dan mengoptimasi sebuah formula SNEDDS untuk meperbaiki disolusi PGV-0 dengan menggunakan Si… Show more

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Cited by 10 publications
(23 citation statements)
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“…Referring to the previous reports (Astuti, 2017), the best oil, surfactant, and cosurfactant for PGV-0 SNEDDS formulation was oleic acid, tween 20:labrasol (1:1), and PEG 400, respectively. The selected excipient showed the highest ability to dissolve PGV-0.…”
Section: Excipient Selection and Pgv-0 Snedds Preparationmentioning
confidence: 70%
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“…Referring to the previous reports (Astuti, 2017), the best oil, surfactant, and cosurfactant for PGV-0 SNEDDS formulation was oleic acid, tween 20:labrasol (1:1), and PEG 400, respectively. The selected excipient showed the highest ability to dissolve PGV-0.…”
Section: Excipient Selection and Pgv-0 Snedds Preparationmentioning
confidence: 70%
“…The excipients selection for the PGV-0 SNEDDS formulation was reported by Astuti (2017). Briefly, the excipients were selected based on the ability to dissolve PGV-0 and self-nanoemulsifying properties.…”
Section: Excipients Selection For Snedds Formulationmentioning
confidence: 99%
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