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Journal Abstract Search
112 related items for PubMed ID: 18271300
1. Mathematical evaluation of similarity factor using various weighing approaches on aceclofenac marketed formulations by model-independent method. Soni TG, Desai JU, Nagda CD, Gandhi TR, Chotai NP. Pharmazie; 2008 Jan; 63(1):31-4. PubMed ID: 18271300 [Abstract] [Full Text] [Related]
2. Diclofenac sodium multisource prolonged release tablets--a comparative study on the dissolution profiles. Bertocchi P, Antoniella E, Valvo L, Alimonti S, Memoli A. J Pharm Biomed Anal; 2005 Apr 01; 37(4):679-85. PubMed ID: 15797788 [Abstract] [Full Text] [Related]
3. Quality surveillance of immediate release aceclofenac tablets (100 mg) available in local market. Bushra R, Shoaib MH, Ali H, Shafiq Y, Zafar F, Alam S, Aslam N. Pak J Pharm Sci; 2017 Nov 01; 30(6):2193-2201. PubMed ID: 29175789 [Abstract] [Full Text] [Related]
4. Modulating drug release profiles by lipid semi solid matrix formulations for BCS class II drug--an in vitro and an in vivo study. M K, Sistla R, Shastri NR. Drug Deliv; 2015 May 01; 22(3):418-26. PubMed ID: 24471823 [Abstract] [Full Text] [Related]
5. Irregular absorption profiles observed from diclofenac extended release tablets can be predicted using a dissolution test apparatus that mimics in vivo physical stresses. Garbacz G, Wedemeyer RS, Nagel S, Giessmann T, Mönnikes H, Wilson CG, Siegmund W, Weitschies W. Eur J Pharm Biopharm; 2008 Oct 01; 70(2):421-8. PubMed ID: 18582568 [Abstract] [Full Text] [Related]
6. In vitro determination of aceclofenac Mouth Dissolving Tablets. Shobhit S, Gupta SK. Polim Med; 2013 Oct 01; 43(4):227-9. PubMed ID: 24596037 [Abstract] [Full Text] [Related]
7. A new principal component analysis-based approach for testing "similarity" of drug dissolution profiles. Maggio RM, Castellano PM, Kaufman TS. Eur J Pharm Sci; 2008 May 10; 34(1):66-77. PubMed ID: 18394869 [Abstract] [Full Text] [Related]
8. Preparation and, in vitro, preclinical and clinical studies of aceclofenac spherical agglomerates. Usha AN, Mutalik S, Reddy MS, Ranjith AK, Kushtagi P, Udupa N. Eur J Pharm Biopharm; 2008 Oct 10; 70(2):674-83. PubMed ID: 18606224 [Abstract] [Full Text] [Related]
9. Development and evaluation of a time-specific pulsatile-release tablet of aceclofenac: a solution for morning pain in rheumatoid arthritis. Qureshi J, Ahuja A, Baboota S, Chutani K, Jain S, Ali J. Methods Find Exp Clin Pharmacol; 2009 Oct 10; 31(1):15-23. PubMed ID: 19357794 [Abstract] [Full Text] [Related]
10. Application of dynamic neural networks in the modeling of drug release from polyethylene oxide matrix tablets. Petrović J, Ibrić S, Betz G, Parojcić J, Durić Z. Eur J Pharm Sci; 2009 Sep 10; 38(2):172-80. PubMed ID: 19632323 [Abstract] [Full Text] [Related]
11. Formulation of a extended release tablet containing dexibuprofen. Yi HG, Chi MH, Kim YI, Woo JS, Park ES. Arch Pharm Res; 2008 Dec 10; 31(12):1637-43. PubMed ID: 19099235 [Abstract] [Full Text] [Related]
12. Two different approaches for the prediction of in vivo plasma concentration-time profile from in vitro release data of once daily formulations of diltiazem hydrochloride. Bendas ER. Arch Pharm Res; 2009 Sep 10; 32(9):1317-29. PubMed ID: 19784589 [Abstract] [Full Text] [Related]
13. Probability of passing dissolution acceptance criteria for an immediate release tablet. Dumont ML, Berry MR, Nickerson B. J Pharm Biomed Anal; 2007 May 09; 44(1):79-84. PubMed ID: 17379465 [Abstract] [Full Text] [Related]
15. Development of a reaction-limited model of dissolution: application to official dissolution tests experiments. Dokoumetzidis A, Papadopoulou V, Valsami G, Macheras P. Int J Pharm; 2008 May 01; 355(1-2):114-25. PubMed ID: 18206324 [Abstract] [Full Text] [Related]
16. Statistical method for evaluation of dissolution stability in the formulation development of solid dosage forms: tablets of amonafide. Gil-Alegre ME, Bernabeu JA, Camacho MA, Torres-Suarez AI. Pharmazie; 2004 Jul 01; 59(7):541-7. PubMed ID: 15296092 [Abstract] [Full Text] [Related]