These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
168 related articles for article (PubMed ID: 22197771)
1. Nano-sized flake carboxymethyl cassava starch as excipient for solid dispersions. Lin X; Gao W; Li C; Chen J; Yang C; Wu H Int J Pharm; 2012 Feb; 423(2):435-9. PubMed ID: 22197771 [TBL] [Abstract][Full Text] [Related]
2. Effect of the solid-dispersion method on the solubility and crystalline property of tacrolimus. Joe JH; Lee WM; Park YJ; Joe KH; Oh DH; Seo YG; Woo JS; Yong CS; Choi HG Int J Pharm; 2010 Aug; 395(1-2):161-6. PubMed ID: 20580799 [TBL] [Abstract][Full Text] [Related]
3. Dissolution behaviour of nalidixic acid solid dispersions using water soluble dispersion carriers. Mallick S; Sahu A; Pal K Acta Pol Pharm; 2004; 61(1):21-30. PubMed ID: 15259854 [TBL] [Abstract][Full Text] [Related]
4. Combining SEM, TEM, and micro-Raman techniques to differentiate between the amorphous molecular level dispersions and nanodispersions of a poorly water-soluble drug within a polymer matrix. Karavas E; Georgarakis M; Docoslis A; Bikiaris D Int J Pharm; 2007 Aug; 340(1-2):76-83. PubMed ID: 17478064 [TBL] [Abstract][Full Text] [Related]
5. Development of prednisone:polyethylene glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters. Leonardi D; Barrera MG; Lamas MC; Salomón CJ AAPS PharmSciTech; 2007 Dec; 8(4):E108. PubMed ID: 18181529 [TBL] [Abstract][Full Text] [Related]
6. Novel valsartan-loaded solid dispersion with enhanced bioavailability and no crystalline changes. Yan YD; Sung JH; Kim KK; Kim DW; Kim JO; Lee BJ; Yong CS; Choi HG Int J Pharm; 2012 Jan; 422(1-2):202-10. PubMed ID: 22085435 [TBL] [Abstract][Full Text] [Related]
7. To enhance dissolution rate of poorly water-soluble drugs: glucosamine hydrochloride as a potential carrier in solid dispersion formulations. Al-Hamidi H; Edwards AA; Mohammad MA; Nokhodchi A Colloids Surf B Biointerfaces; 2010 Mar; 76(1):170-8. PubMed ID: 19945828 [TBL] [Abstract][Full Text] [Related]
8. Influence of water uptake, gel network, and disintegration time on prednisone release from encapsulated solid dispersions. Leonardi D; Salomon CJ Pharm Dev Technol; 2010; 15(2):184-91. PubMed ID: 19621984 [TBL] [Abstract][Full Text] [Related]
9. Solid molecular dispersions of poorly water-soluble drugs in poly(2-hydroxyethyl methacrylate) hydrogels. Zahedi P; Lee PI Eur J Pharm Biopharm; 2007 Mar; 65(3):320-8. PubMed ID: 17182231 [TBL] [Abstract][Full Text] [Related]
10. Development and optimization of solid dispersion containing pellets of itraconazole prepared by high shear pelletization. Ye G; Wang S; Heng PW; Chen L; Wang C Int J Pharm; 2007 Jun; 337(1-2):80-7. PubMed ID: 17241757 [TBL] [Abstract][Full Text] [Related]
11. Effect of excipients on dissolution enhancement of aceclofenac solid dispersions studied using response surface methodology: a technical note. Kumar S; Gupta SK Arch Pharm Res; 2014 Mar; 37(3):340-51. PubMed ID: 23674128 [TBL] [Abstract][Full Text] [Related]
12. Development and in-vivo assessment of the bioavailability of oridonin solid dispersions by the gas anti-solvent technique. Li S; Liu Y; Liu T; Zhao L; Zhao J; Feng N Int J Pharm; 2011 Jun; 411(1-2):172-7. PubMed ID: 21511016 [TBL] [Abstract][Full Text] [Related]
13. Non-destructive determination of the coating film thickness by X-ray powder diffractometry and correlation with the dissolution behavior of film-coated tablets. Yamada H; Terada K; Suryanarayanan R J Pharm Biomed Anal; 2010 Mar; 51(4):952-7. PubMed ID: 19945243 [TBL] [Abstract][Full Text] [Related]
14. Comparison of different methods for preparation of a stable riccardin D formulation via nano-technology. Liu G; Zhang D; Jiao Y; Zheng D; Liu Y; Duan C; Jia L; Zhang Q; Lou H Int J Pharm; 2012 Jan; 422(1-2):516-22. PubMed ID: 22119965 [TBL] [Abstract][Full Text] [Related]
15. Development of biodegradable porous starch foam for improving oral delivery of poorly water soluble drugs. Wu C; Wang Z; Zhi Z; Jiang T; Zhang J; Wang S Int J Pharm; 2011 Jan; 403(1-2):162-9. PubMed ID: 20937370 [TBL] [Abstract][Full Text] [Related]
16. Preparation and characterization of emulsified solid dispersions containing docetaxel. Chen Y; Shi Q; Chen Z; Zheng J; Xu H; Li J; Liu H Arch Pharm Res; 2011 Nov; 34(11):1909-17. PubMed ID: 22139690 [TBL] [Abstract][Full Text] [Related]
17. Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis. Zidan AS; Rahman Z; Sayeed V; Raw A; Yu L; Khan MA Int J Pharm; 2012 Feb; 423(2):341-50. PubMed ID: 22100517 [TBL] [Abstract][Full Text] [Related]
18. Formation of nano/micro-dispersions with improved dissolution properties upon dispersion of ritonavir melt extrudate in aqueous media. Tho I; Liepold B; Rosenberg J; Maegerlein M; Brandl M; Fricker G Eur J Pharm Sci; 2010 Apr; 40(1):25-32. PubMed ID: 20172027 [TBL] [Abstract][Full Text] [Related]
19. New direct compression excipient from tigernut starch: physicochemical and functional properties. Builders PF; Anwunobi PA; Mbah CC; Adikwu MU AAPS PharmSciTech; 2013 Jun; 14(2):818-27. PubMed ID: 23649994 [TBL] [Abstract][Full Text] [Related]
20. Preparation of a solid dispersion of felodipine using a solvent wetting method. Kim EJ; Chun MK; Jang JS; Lee IH; Lee KR; Choi HK Eur J Pharm Biopharm; 2006 Oct; 64(2):200-5. PubMed ID: 16750355 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]