Flufenamic acid-loaded self-nanoemulsifying drug delivery system for oral delivery: from formulation statistical optimization to preclinical anti-inflammatory assessment
S Alshehri, SS Imam, A Hussain, AM Alyousef… - Journal of Oleo …, 2020 - jstage.jst.go.jp
This research work aimed to prepare and optimize “self-nanoemulsifying drug delivery
system (SNEDDS)” by applying full factorial design (FFD) to improve solubilization and …
system (SNEDDS)” by applying full factorial design (FFD) to improve solubilization and …
Current Status of Potential Antiviral Drugs Derived from Plant, Marine, and Microbial Sources
R Saini, MI Ali, M Pant, A Warghane - Anti-Infective Agents, 2024 - ingentaconnect.com
Natural substances have been the principal source of medications since antiquity. Natural
goods are gaining popularity as a source of novel medications. This article investigates a …
goods are gaining popularity as a source of novel medications. This article investigates a …
A Comprehensive Insight on Self Emulsifying Drug Delivery Systems
R Kadian, A Nanda - Recent Advances in Drug Delivery and …, 2022 - ingentaconnect.com
Background: The oral route is a highly recommended route for the delivery of a drug. But
most lipophilic drugs are difficult to deliver via this route due to their low aqueous solubility …
most lipophilic drugs are difficult to deliver via this route due to their low aqueous solubility …
In vitro release test of nano-drug delivery systems based on analytical and technological perspectives
E Nemutlu, İ Eroğlu, H Eroğlu… - Current Analytical …, 2019 - ingentaconnect.com
Background: Nanotech products are gaining more attention depending on their advantages
for improving drug solubility, maintenance of drug targeting, and attenuation of drug toxicity …
for improving drug solubility, maintenance of drug targeting, and attenuation of drug toxicity …
[PDF][PDF] Lipid based drug delivery system for enhancing oral bioavailability-a contemporary review
N Tejeswari, CV Harini, T Hyndavi, Y Jyotsna… - J Glob Trends Pharm …, 2014 - jgtps.com
Lipid based formulations such as self emulsifying drug delivery system (SEDDS) and self
microemulsifying drug delivery systems (SMEDDS) are designed to improve the oral …
microemulsifying drug delivery systems (SMEDDS) are designed to improve the oral …
[PDF][PDF] 齐墩果酸线粒体靶向脂质体的制备及抗胰腺癌研究
谭晓柯, 武香香, 曾华辉, 朱鑫 - 中南药学, 2022 - genizer.com
目的制备齐墩果酸(OA) 线粒体靶向脂质体(α-TOS-TPP-OA), 以实现药物的靶向性并提高其抗
胰腺癌的活性. 方法通过两步反应, 合成三苯基膦(TPP) 修饰的生育酚琥珀酸酯(α-TOS) …
胰腺癌的活性. 方法通过两步反应, 合成三苯基膦(TPP) 修饰的生育酚琥珀酸酯(α-TOS) …
[HTML][HTML] Formulation and in vitro Characterization of a novel Solid lipid-based drug delivery system
H Ma, M Chu, K Itagaki, P Xin, X Zhou… - Chemical and …, 2014 - jstage.jst.go.jp
The liquid self-emulsifying drug delivery system (L-SEDDS), commonly used to deliver
effective but poorly water-soluble oleanolic acid (OA), has many limitations such as high …
effective but poorly water-soluble oleanolic acid (OA), has many limitations such as high …
Pharmacokinetics and Metabolism of Phytochemicals Having Anti-obesity and Antidiabetic Activity
B Dinda, A Chakraborty - Natural Products in Obesity and Diabetes …, 2022 - Springer
The pharmacokinetics and metabolic knowledge of natural medicine (phytochemicals and
herbal formulations) are highly beneficial for clinical dose adjustment and in the …
herbal formulations) are highly beneficial for clinical dose adjustment and in the …
[PDF][PDF] 冬凌草甲素植烷三醇立方液晶纳米粒的制备和体外研究
史璇, 彭婷婷, 吴传斌 - 中国药学杂志, 2018 - journal11.magtechjournal.com
目的冬凌草甲素水溶性差, 生物半衰期短, 生物利用度低, 制备冬凌草甲素立方液晶纳米粒,
提高其溶解度, 延长药物作用时间. 方法以新型液晶材料植烷三醇, 结合丙二醇-泊洛沙姆407 …
提高其溶解度, 延长药物作用时间. 方法以新型液晶材料植烷三醇, 结合丙二醇-泊洛沙姆407 …