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Items: 1 to 20 of 98

1.

Lignin and Cellulose Blends as Pharmaceutical Excipient for Tablet Manufacturing via Direct Compression.

Domínguez-Robles J, Stewart SA, Rendl A, González Z, Donnelly RF, Larrañeta E.

Biomolecules. 2019 Aug 28;9(9). pii: E423. doi: 10.3390/biom9090423.

2.

Novel multifunctional pharmaceutical excipients derived from microcrystalline cellulose-starch microparticulate composites prepared by compatibilized reactive polymer blending.

Builders PF, Bonaventure AM, Tiwalade A, Okpako LC, Attama AA.

Int J Pharm. 2010 Mar 30;388(1-2):159-67. doi: 10.1016/j.ijpharm.2009.12.056. Epub 2010 Jan 8.

PMID:
20060448
3.

Utility of Microcrystalline Cellulose for Improving Drug Content Uniformity in Tablet Manufacturing Using Direct Powder Compression.

Nakamura S, Tanaka C, Yuasa H, Sakamoto T.

AAPS PharmSciTech. 2019 Mar 22;20(4):151. doi: 10.1208/s12249-019-1365-4.

PMID:
30903317
4.

Direct compression of cushion-layered ethyl cellulose-coated extended release pellets into rapidly disintegrating tablets without changes in the release profile.

Hosseini A, Körber M, Bodmeier R.

Int J Pharm. 2013 Dec 5;457(2):503-9. doi: 10.1016/j.ijpharm.2013.07.042. Epub 2013 Jul 25.

PMID:
23892153
6.

Direct compression of cellulose and lignin isolated by a new catalytic treatment.

Penkina A, Antikainen O, Hakola M, Vuorinen S, Repo T, Yliruusi J, Veski P, Kogermann K, Heinämäki J.

AAPS PharmSciTech. 2013 Sep;14(3):1129-36. doi: 10.1208/s12249-013-0002-x. Epub 2013 Jul 19.

7.

Cinnamyl O-amine functionalized chitosan as a new excipient in direct compressed tablets with improved drug delivery.

Ren G, Clancy C, Tamer TM, Schaller B, Walker GM, Collins MN.

Int J Biol Macromol. 2019 Sep 2. pii: S0141-8130(19)33447-6. doi: 10.1016/j.ijbiomac.2019.08.265. [Epub ahead of print]

PMID:
31487516
8.

Pharmaceutical design of a new lactose-free coprocessed excipient: application of hydrochlorothiazide as a low solubility drug model.

Viscasillas Clerch A, Fernandez Campos F, Del Pozo A, Calpena Campmany AC.

Drug Dev Ind Pharm. 2013 Jul;39(7):961-9. doi: 10.3109/03639045.2012.686507. Epub 2012 May 21.

PMID:
22607083
9.
10.

The impact of roller compaction and tablet compression on physicomechanical properties of pharmaceutical excipients.

Iyer RM, Hegde S, Dinunzio J, Singhal D, Malick W.

Pharm Dev Technol. 2014 Aug;19(5):583-92. doi: 10.3109/10837450.2013.813541. Epub 2013 Aug 14.

PMID:
23941645
11.

Spray-dried cellulose nanofibers as novel tablet excipient.

Kolakovic R, Peltonen L, Laaksonen T, Putkisto K, Laukkanen A, Hirvonen J.

AAPS PharmSciTech. 2011 Dec;12(4):1366-73. doi: 10.1208/s12249-011-9705-z. Epub 2011 Oct 18.

12.

Evaluation of non-crystalline cellulose as a novel excipient in solid dose products.

Pawar K, Render D, Rangari V, Lee Y, Babu RJ.

Drug Dev Ind Pharm. 2018 Sep;44(9):1512-1519. doi: 10.1080/03639045.2018.1472276. Epub 2018 May 21.

PMID:
29734848
13.

Effect of disintegrants on the properties of multiparticulate tablets comprising starch pellets and excipient granules.

Mehta S, De Beer T, Remon JP, Vervaet C.

Int J Pharm. 2012 Jan 17;422(1-2):310-7. doi: 10.1016/j.ijpharm.2011.11.017. Epub 2011 Nov 11.

PMID:
22101283
14.

Cellactose a co-processed excipient: a comparison study.

Arida AI, Al-Tabakha MM.

Pharm Dev Technol. 2008;13(2):165-75. doi: 10.1080/10837450701831294 .

PMID:
18379907
15.

Continuous direct tablet compression: effects of impeller rotation rate, total feed rate and drug content on the tablet properties and drug release.

Järvinen MA, Paaso J, Paavola M, Leiviskä K, Juuti M, Muzzio F, Järvinen K.

Drug Dev Ind Pharm. 2013 Nov;39(11):1802-8. doi: 10.3109/03639045.2012.738681. Epub 2012 Nov 19.

PMID:
23163644
16.

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. doi: 10.1208/s12249-013-9968-7. Epub 2013 May 7.

17.

Design of Controlled Release System for Paracetamol Based on Modified Lignin.

Pishnamazi M, Hafizi H, Shirazian S, Culebras M, Walker GM, Collins MN.

Polymers (Basel). 2019 Jun 18;11(6). pii: E1059. doi: 10.3390/polym11061059.

18.

On the role of API in determining porosity, pore structure and bulk modulus of the skeletal material in pharmaceutical tablets formed with MCC as sole excipient.

Ridgway C, Bawuah P, Markl D, Zeitler JA, Ketolainen J, Peiponen KE, Gane P.

Int J Pharm. 2017 Jun 30;526(1-2):321-331. doi: 10.1016/j.ijpharm.2017.04.038. Epub 2017 Apr 19.

19.

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