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pharmacology & pharmacy (44) 44
neusilin (38) 38
index medicus (30) 30
dissolution (27) 27
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Journal Article
Journal of Pharmaceutical Sciences, ISSN 0022-3549, 01/2018, Volume 107, Issue 1, pp. 170 - 182
A promising approach to increase the aqueous solubility, hence the bioavailability, of poorly water-soluble drugs is to convert them into their amorphous state... 
mesoporous Neusilin | amorphous drug | high drug-load | poorly water-soluble drug | impregnation | stability | dissolution enhancement | mesoporous Neusilin (R) | MESOPOROUS CARBON | CHEMISTRY, MEDICINAL | FENOFIBRATE | STATE | ITRACONAZOLE | CHEMISTRY, MULTIDISCIPLINARY | DELIVERY | SOLID DISPERSIONS | LIPID-BASED FORMULATIONS | DISSOLUTION | PHARMACOLOGY & PHARMACY | SILICA | PHYSICAL STABILITY
Journal Article
Powder Technology, ISSN 0032-5910, 10/2019, Volume 355, pp. 675 - 687
This article aims to compare three commercially available co-processed excipients (CPEs), namely the F-Melts® type C, M and F1. All three CPEs were subjected... 
Neusilin | Orally dispersible tablets | Direct compression | Co-processed excipients | F-melt | Fujicalin | IMMEDIATE-RELEASE | PHARMACEUTICAL POWDERS | MECHANISM | SPEED | ENGINEERING, CHEMICAL | FORCE | TABLET DISINTEGRANT | STARCH | TENSILE-STRENGTH | PARTICLE-SIZE | Viscoelasticity | Compression | Excipients | Wettability | Compression tests | Compacts | Physical properties | Melts
Journal Article
International Journal of Pharmaceutics, ISSN 0378-5173, 03/2018, Volume 539, Issue 1-2, pp. 184 - 189
[Display omitted] Achieving adequate content uniformity (CU) is a significant challenge in the development and manufacturing of low dose oral tablets. Using... 
Neusilin | Amorphous | Aeroperl | Stability | Particle engineering | NEUSILIN US2 | AMORPHIZATION | DELIVERY | Neusilin (R) | Aeroperl (R) | FLOW PROPERTIES | DISSOLUTION ENHANCEMENT | PHARMACOLOGY & PHARMACY | POWDER | MANUFACTURABILITY
Journal Article
Drug Delivery and Translational Research, ISSN 2190-393X, 01/2018, Volume 8, Issue 3, pp. 552 - 564
Journal Article
International Journal of Pharmaceutics, ISSN 0378-5173, 01/2019, Volume 555, pp. 11 - 18
[Display omitted] The aim of this study is to improve the bioavailability of ticagrelor, BCS class 4 drug, using solid dispersion technique, and to evaluate... 
Neusilin® US2 | Solid dispersion | d-α-Tocopheryl polyethylene glycol-1000 succinate | Ticagrelor | Pharmacokinetics | Caco-2 cell | d-alpha-Tocopheryl polyethylene glycol-1000 | AZD6140 | ANTAGONIST | BERBERINE | VITAMIN-E TPGS | P-GLYCOPROTEIN | CLOPIDOGREL | INHIBITION | DISSOLUTION | PHARMACOLOGY & PHARMACY | ABSORPTION | POWDER | succinate Neusilin (R) US2
Journal Article
Journal of Drug Delivery Science and Technology, ISSN 1773-2247, 06/2017, Volume 39, pp. 467 - 474
The aim was to develop immediate-release carbamazepine lipid matrix tablets by using the melt granulation technique, application of Quality by design. The... 
Neusilin® UFL2 | Melt granulation | Lipid matrix tablets | Immediate release tablets | Experimental design | Carbamazepine | Neusilin | UFL2 | DESIGN | Neusilin (R) UFL2 | FORMULATION | SEDDS | DISSOLUTION | US2 | CLASSIFICATION-SYSTEM | PHARMACOLOGY & PHARMACY | DRUG-DELIVERY SYSTEMS
Journal Article
Journal of Drug Delivery Science and Technology, ISSN 1773-2247, 10/2019, Volume 53, p. 101211
Current study explores the potential of nanostructured lipid carriers (NLCs) for bioavailability enhancement of ezetimibe on oral administration. Microemulsion... 
Neusilin® US2 | Pseudoternary phase diagram | Nanostructured lipid carrier | Hyperlipidemia | Ezetimibe | DESIGN | SELF-NANOEMULSIFYING GRANULES | DRUG-DELIVERY SYSTEM | Neusilin (R) US2 | NANOPARTICLES | DISSOLUTION | FORMULATIONS | SMEDDS | ENHANCEMENT | PHARMACOLOGY & PHARMACY | OPTIMIZATION | IN-VIVO EVALUATION
Journal Article
Drug Development and Industrial Pharmacy, ISSN 0363-9045, 03/2019, Volume 45, Issue 3, pp. 405 - 414
Background: Recrystallization of drug and incomplete drug release from liquisolid formulation are two major hurdles in the development of a supersaturated... 
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