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Items: 1 to 20 of 211

1.

Drug carrier systems for solubility enhancement of BCS class II drugs: a critical review.

Kumar S, Bhargava D, Thakkar A, Arora S.

Crit Rev Ther Drug Carrier Syst. 2013;30(3):217-56. Review.

PMID:
23614647
2.

Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications.

Kawabata Y, Wada K, Nakatani M, Yamada S, Onoue S.

Int J Pharm. 2011 Nov 25;420(1):1-10. doi: 10.1016/j.ijpharm.2011.08.032. Epub 2011 Aug 30. Review.

PMID:
21884771
3.

Recent advances and patents in solid dispersion technology.

Iqbal B, Ali A, Ali J, Baboota S, Gupta S, Dang S, Shadab M, Sahni JK.

Recent Pat Drug Deliv Formul. 2011 Sep;5(3):244-64. Review.

PMID:
21834778
4.

Biopharmaceutical classification of poorly soluble drugs with respect to "enabling formulations".

Buckley ST, Frank KJ, Fricker G, Brandl M.

Eur J Pharm Sci. 2013 Sep 27;50(1):8-16. doi: 10.1016/j.ejps.2013.04.002. Epub 2013 Apr 11. Review.

PMID:
23583787
5.

Solid dispersions: a review.

Dhirendra K, Lewis S, Udupa N, Atin K.

Pak J Pharm Sci. 2009 Apr;22(2):234-46. Review.

PMID:
19339238
6.

Inorganic matrices: an answer to low drug solubility problem.

Perioli L, Pagano C.

Expert Opin Drug Deliv. 2012 Dec;9(12):1559-72. doi: 10.1517/17425247.2012.733693. Epub 2012 Oct 12. Review.

PMID:
23061519
7.

Pharmaceutical solid dispersion technology: a strategy to improve dissolution of poorly water-soluble drugs.

Kumar S, Gupta SK.

Recent Pat Drug Deliv Formul. 2013 Aug;7(2):111-21. Review.

PMID:
23331062
8.

[Application research of hot-melt extrusion in preparation of solid dispersion].

Chen MW, Chen WR, Chen TK, Chen RE, Wang YT.

Yao Xue Xue Bao. 2012 Feb;47(2):163-7. Review. Chinese.

PMID:
22512025
9.

Biowaiver extension potential and IVIVC for BCS Class II drugs by formulation design: Case study for cyclosporine self-microemulsifying formulation.

Yang SG.

Arch Pharm Res. 2010 Nov;33(11):1835-42. doi: 10.1007/s12272-010-1116-2. Epub 2010 Nov 30.

PMID:
21116787
10.

Current trends and future perspectives of solid dispersions containing poorly water-soluble drugs.

Vo CL, Park C, Lee BJ.

Eur J Pharm Biopharm. 2013 Nov;85(3 Pt B):799-813. doi: 10.1016/j.ejpb.2013.09.007. Epub 2013 Sep 18. Review.

PMID:
24056053
11.

Drug delivery strategies for poorly water-soluble drugs.

Fahr A, Liu X.

Expert Opin Drug Deliv. 2007 Jul;4(4):403-16. Review.

PMID:
17683253
12.

Solid dispersions, part I: recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs.

Bikiaris DN.

Expert Opin Drug Deliv. 2011 Nov;8(11):1501-19. doi: 10.1517/17425247.2011.618181. Epub 2011 Sep 16. Review.

PMID:
21919807
13.

Supercritical fluid particle design for poorly water-soluble drugs (review).

Sun Y.

Curr Pharm Des. 2014;20(3):349-68. Review.

PMID:
23651403
14.

Cyclodextrin and phospholipid complexation in solubility and dissolution enhancement: a critical and meta-analysis.

Semalty A.

Expert Opin Drug Deliv. 2014 Aug;11(8):1255-72. doi: 10.1517/17425247.2014.916271. Epub 2014 Jun 7. Review.

PMID:
24909802
15.

Improved dissolution behavior of lipophilic drugs by solid dispersions: the production process as starting point for formulation considerations.

Srinarong P, de Waard H, Frijlink HW, Hinrichs WL.

Expert Opin Drug Deliv. 2011 Sep;8(9):1121-40. doi: 10.1517/17425247.2011.598147. Epub 2011 Jul 2. Review.

PMID:
21722000
16.

Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates.

Blagden N, de Matas M, Gavan PT, York P.

Adv Drug Deliv Rev. 2007 Jul 30;59(7):617-30. Epub 2007 May 29. Review.

PMID:
17597252
17.

Evaluation of drug load and polymer by using a 96-well plate vacuum dry system for amorphous solid dispersion drug delivery.

Chiang PC, Ran Y, Chou KJ, Cui Y, Sambrone A, Chan C, Hart R.

AAPS PharmSciTech. 2012 Jun;13(2):713-22. doi: 10.1208/s12249-012-9795-2. Epub 2012 May 5.

18.

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 1;76(1):170-8. doi: 10.1016/j.colsurfb.2009.10.030. Epub 2009 Nov 11. Erratum in: Colloids Surf B Biointerfaces. 2010 Sep 1;79(2):535.

PMID:
19945828
19.

The utility of cyclodextrins for enhancing oral bioavailability.

Carrier RL, Miller LA, Ahmed I.

J Control Release. 2007 Nov 6;123(2):78-99. Epub 2007 Aug 16. Review.

PMID:
17888540
20.

Solubilization of poorly water-soluble drugs using solid dispersions.

Tran TT, Tran PH, Khanh TN, Van TV, Lee BJ.

Recent Pat Drug Deliv Formul. 2013 Aug;7(2):122-33. Review.

PMID:
23244679
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