| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0928-0987(98)00055-4 |
| P698 | PubMed publication ID | 10072475 |
| P2093 | author name string | Lindahl A | |
| Kristensen HG | |||
| Hovgaard L | |||
| Knutson L | |||
| Bønløkke L | |||
| Lennernäs H | |||
| P2860 | cites work | A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability | Q28293773 |
| Per Cent Absorbed Time Plots Derived from Blood Level and/or Urinary Excretion Data | Q30859110 | ||
| Clinical Pharmacokinetics of Carbamazepine | Q40877361 | ||
| Physical-chemical behavior of dietary and biliary lipids during intestinal digestion and absorption. 2. Phase analysis and aggregation states of luminal lipids during duodenal fat digestion in healthy adult human beings | Q41228115 | ||
| Physiochemical and physiological mechanisms for the effects of food on drug absorption: the role of lipids and pH. | Q41364364 | ||
| Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms | Q41714891 | ||
| Pharmacokinetics of carbamazepine in normal man | Q42102627 | ||
| Physiologic Surface-Active Agents and Drug Absorption IV: Effect of Pre-Micellar Concentrations of Surfactant on Dissolution Rate | Q47786714 | ||
| Characterization of fluids from the stomach and proximal jejunum in men and women | Q50956608 | ||
| Distribution and elimination kinetics of carbamazepine in man | Q67396517 | ||
| Plasma kinetics of carbamazepine and its epoxide metabolite in man after single and multiple doses | Q67396551 | ||
| Regional jejunal perfusion, a new in vivo approach to study oral drug absorption in man | Q67591105 | ||
| Solubilization and wetting effects of bile salts on the dissolution of steroids | Q67882536 | ||
| The bioinequivalence of carbamazepine tablets with a history of clinical failures | Q67994620 | ||
| Physical-chemical behavior of dietary and biliary lipids during intestinal digestion and absorption. 1. Phase behavior and aggregation states of model lipid systems patterned after aqueous duodenal contents of healthy adult human beings | Q68758865 | ||
| Simultaneous measurement of phenobarbital, carbamazepine, phenytoin and 5-(4-hydroxyphenyl)-5-phenylhydantoin in serum by high-performance liquid chromatography | Q68980886 | ||
| Gastrointestinal bioavailability: determination of in vivo release profiles of solid oral dosage forms by deconvolution | Q69804437 | ||
| Jejunal permeability and hepatic extraction of fluvastatin in humans | Q71828066 | ||
| Studies on Absorption and Excretion of Drug. VII. A New Estimation Method for the Release of Drugs from Dosage Forms and the Availability in vivo | Q71858518 | ||
| A Residence-Time Distribution Analysis of the Hydrodynamics within the Intestine in Man during a Regional Single-pass Perfusion with Loc-I-Gut: In-vivo Permeability Estimation | Q73584101 | ||
| A new approach for direct in vivo dissolution studies of poorly soluble drugs | Q73849620 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | deconvolution | Q1183700 |
| P304 | page(s) | 19-27 | |
| P577 | publication date | 1999-04-01 | |
| P1433 | published in | European Journal of Pharmaceutical Sciences | Q5412738 |
| P1476 | title | A comparison between direct determination of in vivo dissolution and the deconvolution technique in humans | |
| P478 | volume | 8 |
| Q51950534 | A clinical single-pass perfusion investigation of the dynamic in vivo secretory response to a dietary meal in human proximal small intestine. |
| Q37631534 | Comparative in vitro dissolution study of carbamazepine immediate-release products using the USP paddles method and the flow-through cell system |
| Q46651828 | Determination of intraluminal theophylline concentrations after oral intake of an immediate- and a slow-release dosage form. |
| Q42638823 | Direct estimation of the in vivo dissolution of spironolactone, in two particle size ranges, using the single-pass perfusion technique (Loc-I-Gut) in humans |
| Q51557252 | Dissolution of hydrocortisone in human and simulated intestinal fluids |
| Q43164713 | Effect of a single gemfibrozil dose on the pharmacokinetics of rosuvastatin in bile and plasma in healthy volunteers |
| Q42207382 | Influence of drug release properties of conventional solid dosage forms on the systemic exposure of highly soluble drugs |
| Q39846636 | Predicting intestinal precipitation--a case example for a basic BCS class II drug |
| Q52005114 | Quantitative biopharmaceutics classification system: the central role of dose/solubility ratio |
Search more.