177 related articles for article (PubMed ID: 29588588)
1. Tri-block polymer with interfacial layer formation ability and its use in maintaining supersaturated drug solution after dissolution of solid dispersions.
Fu JJ; Liu CC
Int J Nanomedicine; 2018; 13():1611-1619. PubMed ID: 29588588
[TBL] [Abstract][Full Text] [Related]
2. Solubility and bioavailability enhancement study of lopinavir solid dispersion matrixed with a polymeric surfactant - Soluplus.
Zi P; Zhang C; Ju C; Su Z; Bao Y; Gao J; Sun J; Lu J; Zhang C
Eur J Pharm Sci; 2019 Jun; 134():233-245. PubMed ID: 31028820
[TBL] [Abstract][Full Text] [Related]
3. Physicochemical characterisation, drug polymer dissolution and in vitro evaluation of phenacetin and phenylbutazone solid dispersions with polyethylene glycol 8000.
Khan S; Batchelor H; Hanson P; Perrie Y; Mohammed AR
J Pharm Sci; 2011 Oct; 100(10):4281-94. PubMed ID: 21560130
[TBL] [Abstract][Full Text] [Related]
4. Solution behavior of PVP-VA and HPMC-AS-based amorphous solid dispersions and their bioavailability implications.
Qian F; Wang J; Hartley R; Tao J; Haddadin R; Mathias N; Hussain M
Pharm Res; 2012 Oct; 29(10):2765-76. PubMed ID: 22315020
[TBL] [Abstract][Full Text] [Related]
5. [Study on the properties of felodipine solid dispersions prepared by different technologies].
Shi NQ; Zhang H; Zhang Y; Feng B; Li ZQ; Qi XR
Beijing Da Xue Xue Bao Yi Xue Ban; 2016 Dec; 48(6):1067-1073. PubMed ID: 27987515
[TBL] [Abstract][Full Text] [Related]
6. Development of solid dispersions of β-lapachone in PEG and PVP by solvent evaporation method.
Dos Santos KM; Barbosa RM; Vargas FGA; de Azevedo EP; Lins ACDS; Camara CA; Aragão CFS; Moura TFLE; Raffin FN
Drug Dev Ind Pharm; 2018 May; 44(5):750-756. PubMed ID: 29206496
[TBL] [Abstract][Full Text] [Related]
7. The use of amphiphilic copolymer in the solid dispersion formulation of nimodipine to inhibit drug crystallization in the release media: Combining nano-drug delivery system with solid preparations.
Wei MY; Lei XP; Fu JJ; Chen MY; Li JX; Yu XY; Lin YL; Liu JP; Du LR; Li X; Zhang Y; Miao YL; Huang YG; Liang L; Fu JJ
Mater Sci Eng C Mater Biol Appl; 2020 Jun; 111():110836. PubMed ID: 32279765
[TBL] [Abstract][Full Text] [Related]
8. Determination of drug-polymer solubility from supersaturated spray-dried amorphous solid dispersions: A case study with Efavirenz and Soluplus®.
Costa BLA; Sauceau M; Del Confetto S; Sescousse R; Ré MI
Eur J Pharm Biopharm; 2019 Sep; 142():300-306. PubMed ID: 31247317
[TBL] [Abstract][Full Text] [Related]
9. Novel supercritical carbon dioxide impregnation technique for the production of amorphous solid drug dispersions: a comparison to hot melt extrusion.
Potter C; Tian Y; Walker G; McCoy C; Hornsby P; Donnelly C; Jones DS; Andrews GP
Mol Pharm; 2015 May; 12(5):1377-90. PubMed ID: 25730138
[TBL] [Abstract][Full Text] [Related]
10. A comparative study on the effects of amphiphilic and hydrophilic polymers on the release profiles of a poorly water-soluble drug.
Irwan AW; Berania JE; Liu X
Pharm Dev Technol; 2016 Mar; 21(2):231-8. PubMed ID: 25496001
[TBL] [Abstract][Full Text] [Related]
11. Application and functional characterization of POVACOAT, a hydrophilic co-polymer poly(vinyl alcohol/acrylic acid/methyl methacrylate) as a hot-melt extrusion carrier.
Xu M; Zhang C; Luo Y; Xu L; Tao X; Wang Y; He H; Tang X
Drug Dev Ind Pharm; 2014 Jan; 40(1):126-35. PubMed ID: 23336809
[TBL] [Abstract][Full Text] [Related]
12. Investigation of the interactions of enteric and hydrophilic polymers to enhance dissolution of griseofulvin following hot melt extrusion processing.
Bennett RC; Keen JM; Bi YV; Porter S; Dürig T; McGinity JW
J Pharm Pharmacol; 2015 Jul; 67(7):918-38. PubMed ID: 25645386
[TBL] [Abstract][Full Text] [Related]
13. An investigation into the use of polymer blends to improve the printability of and regulate drug release from pharmaceutical solid dispersions prepared via fused deposition modeling (FDM) 3D printing.
Alhijjaj M; Belton P; Qi S
Eur J Pharm Biopharm; 2016 Nov; 108():111-125. PubMed ID: 27594210
[TBL] [Abstract][Full Text] [Related]
14. Non-invasive insight into the release mechanisms of a poorly soluble drug from amorphous solid dispersions by confocal Raman microscopy.
Punčochová K; Vukosavljevic B; Hanuš J; Beránek J; Windbergs M; Štěpánek F
Eur J Pharm Biopharm; 2016 Apr; 101():119-25. PubMed ID: 26861928
[TBL] [Abstract][Full Text] [Related]
15. The influence of drug physical state on the dissolution enhancement of solid dispersions prepared via hot-melt extrusion: a case study using olanzapine.
Pina MF; Zhao M; Pinto JF; Sousa JJ; Craig DQ
J Pharm Sci; 2014 Apr; 103(4):1214-23. PubMed ID: 24765654
[TBL] [Abstract][Full Text] [Related]
16. An investigation into the dissolution properties of celecoxib melt extrudates: understanding the role of polymer type and concentration in stabilizing supersaturated drug concentrations.
Abu-Diak OA; Jones DS; Andrews GP
Mol Pharm; 2011 Aug; 8(4):1362-71. PubMed ID: 21696180
[TBL] [Abstract][Full Text] [Related]
17. Rational design of block copolymer micelles to control burst drug release at a nanoscale dimension.
Soleymani Abyaneh H; Vakili MR; Zhang F; Choi P; Lavasanifar A
Acta Biomater; 2015 Sep; 24():127-39. PubMed ID: 26093068
[TBL] [Abstract][Full Text] [Related]
18. Self-Association of Rafoxanide in Aqueous Media and Its Application in Preparing Amorphous Solid Dispersions.
Meng F; Liu T; Schneider E; Alzobaidi S; Gil M; Zhang F
Mol Pharm; 2017 May; 14(5):1790-1799. PubMed ID: 28375620
[TBL] [Abstract][Full Text] [Related]
19. Enhanced solubility of piperine using hydrophilic carrier-based potent solid dispersion systems.
Thenmozhi K; Yoo YJ
Drug Dev Ind Pharm; 2017 Sep; 43(9):1501-1509. PubMed ID: 28425323
[TBL] [Abstract][Full Text] [Related]
20. Stabilization of solid dispersions of nimodipine and polyethylene glycol 2000.
Urbanetz NA
Eur J Pharm Sci; 2006 May; 28(1-2):67-76. PubMed ID: 16472995
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
