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Results: 1 to 20 of 107

1.

Dissolution improvement of poorly water-soluble drug by cogrinding method using jar mill.

Xu Y, Mao L, Li X, Wang Y, Wei P.

Pak J Pharm Sci. 2013 May;26(3):495-502.

PMID:
23625422
[PubMed - indexed for MEDLINE]
2.

Dissolution improvement of four poorly water soluble drugs by cogrinding with commonly used excipients.

Vogt M, Kunath K, Dressman JB.

Eur J Pharm Biopharm. 2008 Feb;68(2):330-7. Epub 2007 May 21.

PMID:
17574401
[PubMed - indexed for MEDLINE]
3.

A nifedipine coground mixture with sodium deoxycholate. II. Dissolution characteristics and stability.

Suzuki H, Ogawa M, Hironaka K, Ito K, Sunada H.

Drug Dev Ind Pharm. 2001 Oct;27(9):951-8.

PMID:
11763473
[PubMed - indexed for MEDLINE]
4.

Solid dispersion prepared by continuous cogrinding in an air jet mill.

Muehlenfeld C, Kann B, Windbergs M, Thommes M.

J Pharm Sci. 2013 Nov;102(11):4132-9. doi: 10.1002/jps.23731. Epub 2013 Sep 16.

PMID:
24105729
[PubMed - indexed for MEDLINE]
5.

Amino acids as co-amorphous stabilizers for poorly water soluble drugs--Part 1: preparation, stability and dissolution enhancement.

Löbmann K, Grohganz H, Laitinen R, Strachan C, Rades T.

Eur J Pharm Biopharm. 2013 Nov;85(3 Pt B):873-81. doi: 10.1016/j.ejpb.2013.03.014. Epub 2013 Mar 26.

PMID:
23537574
[PubMed - indexed for MEDLINE]
6.

Evaluation of in vitro-in vivo correlation and anticonvulsive effect of carbamazepine after cogrinding with microcrystalline cellulose.

Barzegar-Jalali M, Nayebi AM, Valizadeh H, Hanaee J, Barzegar-Jalali A, Adibkia K, Anoush M, Sistanizad M.

J Pharm Pharm Sci. 2006;9(3):307-16.

PMID:
17207414
[PubMed - indexed for MEDLINE]
Free Article
7.

In vivo evaluation of modified gum karaya as a carrier for improving the oral bioavailability of a poorly water-soluble drug, nimodipine.

Murali Mohan Babu GV, Kumar NR, Sankar KH, Ram BJ, Kumar NK, Murthy KV.

AAPS PharmSciTech. 2002;3(2):E12.

PMID:
12916949
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Dissolution and solid-state characterization of poorly water-soluble drugs in the presence of a hydrophilic carrier.

Talukder R, Reed C, Dürig T, Hussain M.

AAPS PharmSciTech. 2011 Dec;12(4):1227-33. doi: 10.1208/s12249-011-9697-8. Epub 2011 Sep 20.

PMID:
21932161
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Cogrinding as a tool to produce sustained release behavior for theophylline particles containing magnesium stearate.

Nokhodchi A, Okwudarue ON, Valizadeh H, Momin MN.

AAPS PharmSciTech. 2009;10(4):1243-51. doi: 10.1208/s12249-009-9326-y. Epub 2009 Oct 28.

PMID:
19862623
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Formation of fine drug particle by cogrinding with cyclodextrins. Part II. The influence of moisture condition during cogrinding process on fine particle formation.

Wongmekiat A, Tozuka Y, Oguchi T, Yamamoto K.

Int J Pharm. 2003 Oct 20;265(1-2):85-93.

PMID:
14522121
[PubMed - indexed for MEDLINE]
11.

Improvement of dissolution and bioavailability of Ginsenosides by hot melt extrusion and cogrinding.

Luo Y, Xu L, Xu M, Tao X, Ai R, Tang X.

Drug Dev Ind Pharm. 2013 Jan;39(1):109-16. doi: 10.3109/03639045.2012.659189. Epub 2012 Feb 18.

PMID:
22339205
[PubMed - indexed for MEDLINE]
12.

In-vitro and in-vivo evaluation of enteric-coated starch-based pellets prepared via extrusion/spheronisation.

Dukić-Ott A, De Beer T, Remon JP, Baeyens W, Foreman P, Vervaet C.

Eur J Pharm Biopharm. 2008 Sep;70(1):302-12. doi: 10.1016/j.ejpb.2008.04.019. Epub 2008 Apr 29.

PMID:
18579353
[PubMed - indexed for MEDLINE]
13.

Liquisolid technique for dissolution rate enhancement of a high dose water-insoluble drug (carbamazepine).

Javadzadeh Y, Jafari-Navimipour B, Nokhodchi A.

Int J Pharm. 2007 Aug 16;341(1-2):26-34. Epub 2007 Mar 30.

PMID:
17498898
[PubMed - indexed for MEDLINE]
14.

A nifedipine coground mixture with sodium deoxycholate. I. Colloidal particle formation and solid-state analysis.

Suzuki H, Ogawa M, Hironaka K, Ito K, Sunada H.

Drug Dev Ind Pharm. 2001 Oct;27(9):943-9.

PMID:
11763472
[PubMed - indexed for MEDLINE]
15.

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.

PMID:
22315020
[PubMed - indexed for MEDLINE]
16.

Development and characterization of naproxen-chitosan solid systems with improved drug dissolution properties.

Mura P, Zerrouk N, Mennini N, Maestrelli F, Chemtob C.

Eur J Pharm Sci. 2003 May;19(1):67-75.

PMID:
12729863
[PubMed - indexed for MEDLINE]
17.

Monoglyceride-based self-assembling copolymers as carriers for poorly water-soluble drugs.

Rouxhet L, Dinguizli M, Latere Dwan'isa JP, Ould-Ouali L, Twaddle P, Nathan A, Brewster ME, Rosenblatt J, Ariën A, Préat V.

Int J Pharm. 2009 Dec 1;382(1-2):244-53. doi: 10.1016/j.ijpharm.2009.07.036. Epub 2009 Aug 8.

PMID:
19666096
[PubMed - indexed for MEDLINE]
18.

Characterization and stability of solid dispersions based on PEG/polymer blends.

Bley H, Fussnegger B, Bodmeier R.

Int J Pharm. 2010 May 10;390(2):165-73. doi: 10.1016/j.ijpharm.2010.01.039. Epub 2010 Feb 10.

PMID:
20132875
[PubMed - indexed for MEDLINE]
19.

Enhancement of the dissolution rate and oral absorption of a poorly water soluble drug by formation of surfactant-containing microparticles.

Wong SM, Kellaway IW, Murdan S.

Int J Pharm. 2006 Jul 6;317(1):61-8. Epub 2006 May 2.

PMID:
16647232
[PubMed - indexed for MEDLINE]
20.

Characterization of ibuproxam binary and ternary dispersions with hydrophilic carriers.

Cirri M, Mura P, Rabasco AM, Ginés JM, Moyano JR, Gònzalez-Rodrìguez ML.

Drug Dev Ind Pharm. 2004 Jan;30(1):65-74.

PMID:
15000431
[PubMed - indexed for MEDLINE]

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