| scholarly article | Q13442814 |
| P356 | DOI | 10.1081/DDC-120018203 |
| P953 | full work available at URL | http://www.tandfonline.com/doi/pdf/10.1081/DDC-120018203 |
| P698 | PubMed publication ID | 12741611 |
| P2093 | author name string | M. C. Gohel | |
| L. D. Patel | |||
| P2860 | cites work | Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards | Q33935245 |
| USE OF NONAQUEOUS SOLVENTS IN PARENTERAL PRODUCTS. | Q35408160 | ||
| Study of the influence of both cyclodextrins and L-lysine on the aqueous solubility of nimesulide; isolation and characterization of nimesulide-L-lysine-cyclodextrin complexes | Q36854787 | ||
| Pharmaceutical Applications of Solid Dispersion Systems | Q40000294 | ||
| The concept of dissolution efficiency | Q40313091 | ||
| Effect of particle size on the compaction mechanism and tensile strength of tablets | Q47268123 | ||
| Estimation of the increase in solubility of drugs as a function of bile salt concentration. | Q51583931 | ||
| In vitro release evaluation of hydrocortisone liquisolid tablets. | Q52240604 | ||
| Powdered solution technology: principles and mechanism. | Q52412639 | ||
| Selection and use of crystallization inhibitors for matrix-type transdermal drug-delivery systems containing sex steroids. | Q52980276 | ||
| Inhibitory effect of 2-hydroxypropyl-beta-cyclodextrin on crystal-growth of nifedipine during storage: superior dissolution and oral bioavailability compared with polyvinylpyrrolidone K-30 | Q67518614 | ||
| Solubilization and wetting effects of bile salts on the dissolution of steroids | Q67882536 | ||
| Dissolution Rates of Corticoid Solutions Dispersed on Silicas | Q70202581 | ||
| Effect of solubilizing excipients on permeation of poorly water-soluble compounds across Caco-2 cell monolayers | Q73174157 | ||
| Study of phase behavior of poly(ethylene glycol)-polysorbate 80 and poly(ethylene glycol)-polysorbate 80-water mixtures | Q73911561 | ||
| What is the true solubility advantage for amorphous pharmaceuticals? | Q73933448 | ||
| Gastric juice as a dissolution medium: surface tension and pH | Q77187568 | ||
| Product development studies on the tablet formulation of ibuprofen to improve bioavailability | Q77756716 | ||
| Solid state studies of drug-cyclodextrin inclusion complexes in PEG 6000 prepared by a new method | Q78056780 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | organic chemistry | Q11351 |
| pharmacology | Q128406 | ||
| pharmaceutical science | Q7180763 | ||
| P304 | page(s) | 299-310 | |
| P577 | publication date | 2003-03-01 | |
| P1433 | published in | Drug Development and Industrial Pharmacy | Q5308840 |
| P1476 | title | Processing of nimesulide-PEG 400-PG-PVP solid dispersions: preparation, characterization, and in vitro dissolution | |
| Processing of Nimesulide-PEG 400-PG-PVP Solid Dispersions: Preparation, Characterization, and In Vitro Dissolution | |||
| P478 | volume | 29 |
| Q41925228 | Characterization of olanzapine-solid dispersions |
| Q41989862 | Comparison of the effect of tromethamine and polyvinylpyrrolidone on dissolution properties and analgesic effect of nimesulide. |
| Q64072226 | Development and Evaluation of Poorly Water-Soluble Celecoxib as Solid Dispersions Containing Nonionic Surfactants Using Fluidized-Bed Granulation |
| Q37360630 | Effect of hydrophilic swellable polymers on dissolution enhancement of carbamazepine solid dispersions studied using response surface methodology |
| Q38011598 | Impact of excipient interactions on drug bioavailability from solid dosage forms |
| Q46984694 | Investigations on factors affecting chitosan for dissolution enhancement of oxcarbazepine by spray dried microcrystal formulation with an experimental design approach |
| Q33958686 | Supersaturated dissolution data and their interpretation: the TPGS-carbamazepine model case |
Search more.