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Journal Abstract Search
317 related items for PubMed ID: 21241802
1. Pharmaceutical acrylic beads obtained by suspension polymerization containing cellulose nanowhiskers as excipient for drug delivery. Villanova JC, Ayres E, Carvalho SM, Patrício PS, Pereira FV, Oréfice RL. Eur J Pharm Sci; 2011 Mar 18; 42(4):406-15. PubMed ID: 21241802 [Abstract] [Full Text] [Related]
2. Design of prolonged release tablets using new solid acrylic excipients for direct compression. Villanova JC, Ayres E, Oréfice RL. Eur J Pharm Biopharm; 2011 Nov 18; 79(3):664-73. PubMed ID: 21827852 [Abstract] [Full Text] [Related]
3. Graft copolymers of ethyl methacrylate on waxy maize starch derivatives as novel excipients for matrix tablets: physicochemical and technological characterisation. Marinich JA, Ferrero C, Jiménez-Castellanos MR. Eur J Pharm Biopharm; 2009 May 18; 72(1):138-47. PubMed ID: 19146956 [Abstract] [Full Text] [Related]
4. Controlled release matrix tablets of glipizide: Influence of different grades of ethocel and Co-excipient on drug release. Mehsud SU, Khan GM, Hussain A, Akram M, Akhlaq M, Khan KA, Shakoor A. Pak J Pharm Sci; 2016 May 18; 29(3):779-87. PubMed ID: 27166548 [Abstract] [Full Text] [Related]
5. DEVELOPMENT AND EVALUATION OF IVABRADINE HCI-LOADED POLYMERIC MICROSPHERES PREPARED WITH EUDRAGIT L100-55 (METHACRYLIC ACID-ETHYL ACRYLATE COPOLYMER) AND ETHYL CELLULOSE FOR CONTROLLED DRUG RELEASE. Majeed A, Ranjha NM, Hanif M, Abbas G, Khan MA. Acta Pol Pharm; 2017 Mar 18; 74(2):565-578. PubMed ID: 29624261 [Abstract] [Full Text] [Related]
6. 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. PubMed ID: 20060448 [Abstract] [Full Text] [Related]
7. Evaluating tamsulosin hydrochloride-released microparticles prepared using single-step matrix coating. Maeda A, Shinoda T, Ito N, Baba K, Oku N, Mizumoto T. Int J Pharm; 2011 Apr 15; 408(1-2):84-90. PubMed ID: 21291970 [Abstract] [Full Text] [Related]
8. Influence of excipients, drugs, and osmotic agent in the inner core on the time-controlled disintegration of compression-coated ethylcellulose tablets. Lin SY, Lin KH, Li MJ. J Pharm Sci; 2002 Sep 15; 91(9):2040-6. PubMed ID: 12210050 [Abstract] [Full Text] [Related]
9. The effect of polymer properties on direct compression and drug release from water-insoluble controlled release matrix tablets. Grund J, Koerber M, Walther M, Bodmeier R. Int J Pharm; 2014 Jul 20; 469(1):94-101. PubMed ID: 24746409 [Abstract] [Full Text] [Related]
10. 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):. PubMed ID: 31466387 [Abstract] [Full Text] [Related]
12. A study on maize proteins as a potential new tablet excipient. Georget DM, Barker SA, Belton PS. Eur J Pharm Biopharm; 2008 Jun 28; 69(2):718-26. PubMed ID: 18294824 [Abstract] [Full Text] [Related]
13. Structural modifications of polymethacrylates: impact on thermal behavior and release characteristics of glassy solid solutions. Claeys B, De Coen R, De Geest BG, de la Rosa VR, Hoogenboom R, Carleer R, Adriaensens P, Remon JP, Vervaet C. Eur J Pharm Biopharm; 2013 Nov 28; 85(3 Pt B):1206-14. PubMed ID: 23485474 [Abstract] [Full Text] [Related]