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Journal Abstract Search
105 related items for PubMed ID: 12455473
21. A quick method for the quantitative analysis of mixtures. 1. Powder X-ray diffraction. Dong W, Gilmore C, Barr G, Dallman C, Feeder N, Terry S. J Pharm Sci; 2008 Jun; 97(6):2260-76. PubMed ID: 17876772 [Abstract] [Full Text] [Related]
22. Sensitivity of dissolution rate to location in the paddle dissolution apparatus. Healy AM, McCarthy LG, Gallagher KM, Corrigan OI. J Pharm Pharmacol; 2002 Mar; 54(3):441-4. PubMed ID: 11902812 [Abstract] [Full Text] [Related]
28. The effect of beam size on real-time determination of powder blend homogeneity by an online near infrared sensor. Li W, Johnson MC, Bruce R, Rasmussen H, Worosila GD. J Pharm Biomed Anal; 2007 Jan 17; 43(2):711-7. PubMed ID: 16908115 [Abstract] [Full Text] [Related]
30. Theophylline granule formulation prepared by the wet granulation method: comparison of in vitro dissolution profiles and estimation of in vivo plasma concentrations. Karasulu E, Apaydin S, Ince I, Tuglular I. Eur J Drug Metab Pharmacokinet; 2006 Jan 17; 31(4):291-8. PubMed ID: 17315541 [Abstract] [Full Text] [Related]
31. Evaluation of USP apparatus 3 for dissolution testing of immediate-release products. Yu LX, Wang JT, Hussain AS. AAPS PharmSci; 2002 Jan 17; 4(1):E1. PubMed ID: 12049485 [Abstract] [Full Text] [Related]
32. Improvement of flow and bulk density of pharmaceutical powders using surface modification. Jallo LJ, Ghoroi C, Gurumurthy L, Patel U, Davé RN. Int J Pharm; 2012 Feb 28; 423(2):213-25. PubMed ID: 22197769 [Abstract] [Full Text] [Related]
34. Evaluation of basket and paddle dissolution methods using different performance standards. Prasad VK, Shah VP, Hunt J, Purich E, Knight P, Cabana BE. J Pharm Sci; 1983 Jan 28; 72(1):42-4. PubMed ID: 6827462 [Abstract] [Full Text] [Related]
39. Is the use of a 200 ml vessel suitable for dissolution of low dose drug products? Crail DJ, Tunis A, Dansereau R. Int J Pharm; 2004 Jan 09; 269(1):203-9. PubMed ID: 14698592 [Abstract] [Full Text] [Related]