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Published in 2019 at "International Journal of Pharmaceutics"
DOI: 10.1016/j.ijpharm.2018.11.036
Abstract: Graphical abstract Figure. No caption available. Abstract The first objective of this study was to optimize a supersaturatable self‐nanoemulsifying drug delivery system (S‐SNEDDS) containing silymarin through the investigation of the single and synergistic effect of… read more here.
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Published in 2021 at "Drug Delivery"
DOI: 10.1080/10717544.2021.1986601
Abstract: Abstract Albendazolum (ABZ) is a BCS class II drug. It has challenging biopharmaceutical properties, which include poor solubility and dissolution rate. These properties have laid the ground for developing a supersaturated self-nanoemulsifying drug delivery system… read more here.
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Published in 2022 at "Pharmaceutical Development and Technology"
DOI: 10.1080/10837450.2022.2070644
Abstract: Abstract A self-nanoemulsifying drug delivery system (SNEDDS) was developed to enhance the dissolution and oral bioavailability (BA) of revaprazan (RVP). Various SNEDDSs containing 200 mg of RVP were formulated using Capmul MCM, Tween 80, and Brij… read more here.
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Published in 2017 at "Expert Opinion on Drug Delivery"
DOI: 10.1080/17425247.2016.1218462
Abstract: ABSTRACT Introduction: Lipid-based drug delivery systems (LBDDS) are the most promising technique to formulate the poorly water soluble drugs. Nanotechnology strongly influences the therapeutic performance of hydrophobic drugs and has become an essential approach in… read more here.
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Published in 2017 at "Die Pharmazie"
DOI: 10.1691/ph.2017.6089
Abstract: Self-nanoemulsifying drug delivery systems (SNEDDS) offer an efficient choice to improve the poor dissolution and erratic bioavailability of poorly-water soluble drugs. However, liquid SNEDDS experience some manufacturing and stability limitations. To overcome these limitations, the… read more here.
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Published in 2021 at "International Journal of Nanomedicine"
DOI: 10.2147/ijn.s287665
Abstract: Purpose The purpose of this proposed research was to investigate a nano-formulation developed using self-nanoemulsifying drug delivery system (SNEDDS) to improve the pharmacodynamic potential of rosuvastatin by assisting its transportation through lymphatic circulation. Methods The… read more here.
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Published in 2019 at "Frontiers in Pharmacology"
DOI: 10.3389/fphar.2019.00459
Abstract: Objective The aim of this study was to investigate the in vitro and in vivo performance of self-nanoemulsifying drug delivery systems (SNEDDSs) of talinolol (TAL), a poorly water-soluble drug. Methods Self-nanoemulsifying drug delivery systems of… read more here.
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Published in 2021 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms22084077
Abstract: A self-nanoemulsifying drug delivery system (SNEDDS) was developed to enhance the absorption of heparin after oral administration, in which heparin was compounded with phospholipids to achieve better fat solubility in the form of heparin-phospholipid (HEP-Pc)… read more here.
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Published in 2022 at "Molecules"
DOI: 10.3390/molecules27103085
Abstract: Psoriatic arthritis is an autoimmune disease of the joints that can lead to persistent inflammation, irreversible joint damage and disability. The current treatments are of limited efficacy and inconvenient. Apremilast (APR) immediate release tablets Otezla®… read more here.
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Published in 2022 at "Pharmaceutics"
DOI: 10.3390/pharmaceutics14040772
Abstract: Cefuroxime axetil (CA) is an oral cephalosporin which hydrolyzes rapidly to the active parent compound cefuroxime. CA is known to have incomplete oral bioavailability (30–50%) due to its poor solubility and enzymatic conversion to cefuroxime… read more here.
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Published in 2018 at "Research Journal of Pharmacy and Technology"
DOI: 10.5958/0974-360x.2018.00221.4
Abstract: The aim of this work was to improve the invitro dissolution of Simvastatin through development of self nanoemulsifying capsules. Simvastatin is a poorly-water soluble drug and cholesterol lowering agent. It has poor oral bioavailability (5%)… read more here.