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| 1 | Salt formation to improve drug solubility显示文摘 | Serajuddin AT | 2007 | Adv Drug Deliv Rev2007，59，7： | 1 |
| 2 | Salt formation to improve drug solubility 显示文摘 | SERAJUDDIN A T | 2007 | Adv Drug Deliv Rev2007，59，7： | 1 |
| 3 | Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems and recent breakthroughs显示文摘 | Serajuddin AT | 1999 | J Pharm Sci1999，88，10： | 1 |
| 4 | Solid dispersion of poorly water soluble drugs: early promises, subsequent problems, and recent breakthroughs 显示文摘 | SERAJUDDIN AT | 1999 | J Pharm Sci1999，88，10： | 1 |
| 5 | Solid dispersion of poorly water-soluble drugs:early promises,subsequent problems,and recent breakthroughs显示文摘 | Abu T M Serajuddin | 1999 | J Pharm Sci1999，88，10： | 1 |
| 6 | Relative lipophilicities, solubilities, and structure pharmacological considerations of 3-hydroxy-3 -methylglutaryl-coenzyme Areduetase inhibitors pravastatin, lovastatin, mevastatin, and simvastatin显示文摘 | Serajuddin AT Ranadive SA Mahoney EM | 1991 | J Pharm Sei1991，80，9： | 1 |
| 7 | Salt formation to improve drug solubility 显示文摘 | Serajuddin AT | 2007 | Adv Drug Deliv Rev2007，59，7： | 1 |
| 8 | Solid dispersion of poorly water-soluble drugs:early promises,subsequent problems,and recent breakthroughs显示文摘 | Abu TM SERAJUDDIN | 1999 | J Pharm Sci1999，88，10： | 1 |
| 9 | Selection of solid dosage form composition through drug-excipient compatibility testing 显示文摘 | SERAJUDDIN A T THAKUR A B GHOSHAL R N | 1999 | Jour- nal of Pharmaceutical Sciences1999，88，7： | 1 |
| 10 | Moisture sorption behavior of selected bulking used in lyophilized products 显示文摘 | FAKES M G DALI M V HABY T A MORRIS K R VARIA S A SERAJUDDIN A T M | 2000 | PDA Journal of Pharmaceutical Science and Technology2000，54，2： | 1 |
| 11 | Solid dispersion of poorly water -soluble drugs: early promises, subsequent problems, and recent breakthroughs 显示文摘 | Abu T M Serajuddin | 1999 | J Pharm Sci1999，88，10： | 1 |
| 12 | Bioavailability enhancement of poorly water-soluble drugs by solid dispersion in surface-active vehicles:a recent breakthrough显示文摘 | Serajuddin A T M | 1997 | La Gazette de rAPGI(France)1997，14，1： | 1 |
| 13 | Solid dispersion of poorly water mluble drugs early promises, subsequent problems and recent breakthroughs 显示文摘 | Serajuddin AT | 1999 | J Pharm Sei1999，88，10： | 1 |
| 14 | Education in pharmaceutical sciences needs a brand new direction to meet the challenges of drug research and development 显示文摘 | | 1998 | Pharmaceutical Research1998，15，： | 1 |
| 15 | Selection of solid dosage from composition through drug-excipient compatibility testing显示文摘 | Serajuddin A T M Thakur A B Ghoshal R N | | 0，，07： | 1 |
| 16 | Bioavailability enhancement of a poorly water-soluble drug by solid dispersion in polyethylene glycol–polysorbate 80 mixture显示文摘 | Hemant N Joshi Ravindra W Tejwani Martha Davidovich Vaishali P Sahasrabudhe Mohammed Jemal Mohinder S Bathala Sailesh A Varia Abu T.M Serajuddin | 2003 | International Journal of Pharmaceutics2003，，1： | 1 |
| 17 | Salt formation to improve drug solubility显示文摘 | Serajuddin A T | 2007 | Adv Drug Deliv Rev2007，59，7： | 1 |
| 18 | Salt formation to improve drug solubility显示文摘 | Serajuddin A T M | 2007 | Adv Drug Delivery Rev2007，59，： | 1 |
| 19 | Relative lipophilicities, solubilities, and structure pharmacological considerations of 3-hydroxy-3-methylglutaryl-coenzyme-A (HMG-CoA) reductase inhibitors pravastatin,lovastatin, mevastatin, and simvastatin显示文摘 | Serajuddin ATM Ranadive SA Mahoney EM | 1991 | J Pharmacol Sci1991，80，9： | 1 |
| 20 | Selection of solid dosage form composition through drug excipient com- patibility testing 显示文摘 | Serajuddin AT Thakur AB Ghoshal RN | 1999 | Journal of Pharmaceutical Sciences 1999 American Chemical Society1999，30，7： | 1 |
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