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1.

Acid-treated yeast cell wall as a binder displaying function of disintegrant.

Ozeki T, Katsuyama H, Yasuzawa Y, Takashima Y, Kasai T, Eguchi T, Kakiuchi H, Yuasa H, Okada H.

AAPS PharmSciTech. 2003;4(3):E41.

2.

Application of acid-treated yeast cell wall (AYC) as a pharmaceutical additive. II: effects of curing on the medicine release from AYC-coated tablets.

Yuasa H, Kaneshige J, Ozeki T, Kasai T, Eguchi T, Ishiwaki N.

Int J Pharm. 2000 Nov 19;209(1-2):69-77.

PMID:
11084247
3.

Application of acid-treated yeast cell wall (AYC) as a pharmaceutical additive I. AYC as a novel coating material.

Kasai T, Eguchi T, Ishiwaki N, Kaneshige J, Ozeki T, Yuasa H.

Int J Pharm. 2000 Aug 25;204(1-2):53-9.

PMID:
11011986
4.

Application of acid-treated yeast cell wall (AYC) as a pharmaceutical additive. III. AYC aqueous coating onto granules and film formation mechanism of AYC.

Yuasa H, Kaneshige J, Ozeki T, Kasai T, Eguchi T, Ishiwaki N.

Int J Pharm. 2002 Apr 26;237(1-2):15-22.

PMID:
11955800
5.

Extrusion granulation and high shear granulation of different grades of lactose and highly dosed drugs: a comparative study.

Keleb EI, Vermeire A, Vervaet C, Remon JP.

Drug Dev Ind Pharm. 2004 Jul;30(6):679-91.

PMID:
15285342
6.

The effects of formulation factors on the moist granulation technique for controlled-release tablets.

Railkar AM, Schwartz JB.

Drug Dev Ind Pharm. 2001 Oct;27(9):893-8.

PMID:
11763466
7.

Evaluation of different fast melting disintegrants by means of a central composite design.

Di Martino P, Martelli S, Wehrlé P.

Drug Dev Ind Pharm. 2005 Jan;31(1):109-21.

PMID:
15704862
8.

Low-substituted hydroxypropylcellulose as a sustained-drug release matrix base or disintegrant depending on its particle size and loading in formulation.

Kawashima Y, Takeuchi H, Hino T, Niwa T, Lin TL, Sekigawa F, Kawahara K.

Pharm Res. 1993 Mar;10(3):351-5.

PMID:
8464806
9.

Roll compaction/dry granulation: effect of raw material particle size on granule and tablet properties.

Herting MG, Kleinebudde P.

Int J Pharm. 2007 Jun 29;338(1-2):110-8. Epub 2007 Jan 28.

PMID:
17324537
11.

Continuous twin screw granulation: influence of process variables on granule and tablet quality.

Vercruysse J, Córdoba Díaz D, Peeters E, Fonteyne M, Delaet U, Van Assche I, De Beer T, Remon JP, Vervaet C.

Eur J Pharm Biopharm. 2012 Sep;82(1):205-11. doi: 10.1016/j.ejpb.2012.05.010. Epub 2012 Jun 9.

PMID:
22687571
12.

Comparison of different dry binders for roll compaction/dry granulation.

Herting MG, Klose K, Kleinebudde P.

Pharm Dev Technol. 2007;12(5):525-32.

PMID:
17963152
13.
14.

Physical mechanical and tablet formation properties of hydroxypropylcellulose: in pure form and in mixtures.

Picker-Freyer KM, Dürig T.

AAPS PharmSciTech. 2007 Nov 9;8(4):E92. doi: 10.1208/pt0804092.

16.

Evolution of structure and properties of granules containing microcrystalline cellulose and polyvinylpyrrolidone during high-shear wet granulation.

Osei-Yeboah F, Feng Y, Sun CC.

J Pharm Sci. 2014 Jan;103(1):207-15. doi: 10.1002/jps.23776. Epub 2013 Nov 11.

PMID:
24218097
17.

Characterization of chitosan acetate as a binder for sustained release tablets.

Nunthanid J, Laungtana-Anan M, Sriamornsak P, Limmatvapirat S, Puttipipatkhachorn S, Lim LY, Khor E.

J Control Release. 2004 Sep 14;99(1):15-26.

PMID:
15342177
18.

Evaluation of a drug with wax-like properties as a melt binder.

Dhumal RS, Shimpi SL, Chauhan B, Mahadik KR, Paradkar A.

Acta Pharm. 2006 Dec;56(4):451-61.

PMID:
19839137
19.

Chitosan and sodium sulfate as excipients in the preparation of prolonged release theophylline tablets.

Alsarra IA, El-Bagory I, Bayomi MA.

Drug Dev Ind Pharm. 2005 May;31(4-5):385-95.

PMID:
16093204
20.

Formulation study for lansoprazole fast-disintegrating tablet. III. Design of rapidly disintegrating tablets.

Shimizu T, Sugaya M, Nakano Y, Izutsu D, Mizukami Y, Okochi K, Tabata T, Hamaguchi N, Igari Y.

Chem Pharm Bull (Tokyo). 2003 Oct;51(10):1121-7.

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