D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Chemistry D-index 62 Citations 10,769 241 World Ranking 5821 National Ranking 50

Overview

What is she best known for?

The fields of study she is best known for:

  • Biochemistry
  • Enzyme
  • Internal medicine

Her primary areas of study are Chromatography, Solubility, Drug delivery, Bioavailability and Pharmacology. Anette Müllertz combines Chromatography and Lipolysis in her studies. She combines subjects such as Precipitation, Dissolution, Hydrolysis, Pharmacology toxicology and Aqueous solution with her study of Solubility.

Her Drug delivery research includes themes of Biochemistry and In vivo. Her research in Bioavailability intersects with topics in Oral administration, Pharmacokinetics, In vitro and Absorption. Her Pharmacology study which covers Biopharmaceutical that intersects with Biochemical engineering.

Her most cited work include:

  • A dynamic in vitro lipolysis model: I. Controlling the rate of lipolysis by continuous addition of calcium (247 citations)
  • In vitro models for the prediction of in vivo performance of oral dosage forms (229 citations)
  • New perspectives on lipid and surfactant based drug delivery systems for oral delivery of poorly soluble drugs. (202 citations)

What are the main themes of her work throughout her whole career to date?

Anette Müllertz spends much of her time researching Chromatography, Drug delivery, Pharmacology, Bioavailability and Solubility. She conducts interdisciplinary study in the fields of Chromatography and Lipolysis through her research. Her Drug delivery research incorporates elements of Oral administration, In vivo, In vitro, Biochemistry and Drug.

Many of her research projects under Pharmacology are closely connected to Delivery system and Danazol with Delivery system and Danazol, tying the diverse disciplines of science together. Anette Müllertz interconnects Absorption and Pharmacokinetics in the investigation of issues within Bioavailability. Her Solubility research is multidisciplinary, incorporating elements of Phospholipid and Supersaturation.

She most often published in these fields:

  • Chromatography (36.82%)
  • Drug delivery (33.11%)
  • Pharmacology (23.99%)

What were the highlights of her more recent work (between 2018-2021)?

  • Drug delivery (33.11%)
  • Chromatography (36.82%)
  • In vivo (16.55%)

In recent papers she was focusing on the following fields of study:

The scientist’s investigation covers issues in Drug delivery, Chromatography, In vivo, Solubility and In vitro. Her research integrates issues of Oral administration, Pharmacology, Drug, Self nanoemulsifying and Permeation in her study of Drug delivery. The Chromatography study combines topics in areas such as Pharmacokinetics, Cmax and Bioavailability.

Her study on In vivo also encompasses disciplines like

  • Insulin that connect with fields like Proteolysis, Intestinal absorption, Absorption, Glyceride and Phosphatidylcholine,
  • Gastrointestinal tract and Distribution most often made with reference to Small intestine. Anette Müllertz has included themes like Composition, Supersaturation and Excipient in her Solubility study. Her In vitro research incorporates themes from Osteopontin, Nano- and Integrin binding.

Between 2018 and 2021, her most popular works were:

  • Successful oral delivery of poorly water-soluble drugs both depends on the intraluminal behavior of drugs and of appropriate advanced drug delivery systems (82 citations)
  • In vitro models for the prediction of in vivo performance of oral dosage forms: Recent progress from partnership through the IMI OrBiTo collaboration. (38 citations)
  • In vitro digestion models to evaluate lipid based drug delivery systems; present status and current trends (31 citations)

In her most recent research, the most cited papers focused on:

  • Biochemistry
  • Enzyme
  • Internal medicine

Her primary scientific interests are in Drug delivery, Drug, Intestinal absorption, Permeation and Chromatography. Her Drug delivery study combines topics from a wide range of disciplines, such as Pharmaceutical sciences, Bioavailability, In vivo and Oral retinoid. In her work, Dosage form is strongly intertwined with Targeted drug delivery, which is a subfield of Bioavailability.

Her study in Drug is interdisciplinary in nature, drawing from both Internal medicine, Disease, Inflammatory bowel disease and Ulcerative colitis. Her studies in Chromatography integrate themes in fields like Lipase inhibitors, In vitro, Lipid digestion and Solubility. Her Solubility research includes themes of Soybean oil, Composition, Cinnarizine, Solubilization and Aqueous solution.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

A dynamic in vitro lipolysis model: I. Controlling the rate of lipolysis by continuous addition of calcium

Niels Hønberg Zangenberg;Anette Müllertz;Henning Gjelstrup Kristensen;Lars Hovgaard.
European Journal of Pharmaceutical Sciences (2001)

342 Citations

In vitro models for the prediction of in vivo performance of oral dosage forms

Edmund S. Kostewicz;Bertil Abrahamsson;Marcus Brewster;Joachim Brouwers.
European Journal of Pharmaceutical Sciences (2014)

298 Citations

Toward the establishment of standardized in vitro tests for lipid‐based formulations, part 1: Method parameterization and comparison of in vitro digestion profiles across a range of representative formulations

Hywel David Williams;Philip J Sassene;Karen Kleberg;Jean-Claude Bakala-N'Goma.
Journal of Pharmaceutical Sciences (2012)

296 Citations

Enzymes with xylanase activity from aspergillus aculeatus

Kofod Lene Venke;Kauppinen Markus Sakari;Christgau Stephan;Heldt-Hansen Hans Peter.
(1994)

292 Citations

New perspectives on lipid and surfactant based drug delivery systems for oral delivery of poorly soluble drugs.

Anette Müllertz;Anayo Ogbonna;Shan Ren;Thomas Rades.
Journal of Pharmacy and Pharmacology (2010)

289 Citations

Lipid-based formulations for oral administration of poorly water-soluble drugs.

Huiling Mu;René Holm;René Holm;Anette Müllertz.
International Journal of Pharmaceutics (2013)

281 Citations

Comparison of drug transporter gene expression and functionality in Caco-2 cells from 10 different laboratories.

Rose Hayeshi;Constanze Hilgendorf;Per Artursson;Patrick Augustijns.
European Journal of Pharmaceutical Sciences (2008)

277 Citations

A dynamic in vitro lipolysis model. II: Evaluation of the model.

Niels Hønberg Zangenberg;Anette Müllertz;Henning Gjelstrup Kristensen;Lars Hovgaard.
European Journal of Pharmaceutical Sciences (2001)

244 Citations

Solubilisation of poorly water-soluble drugs during in vitro lipolysis of medium- and long-chain triacylglycerols.

Janne Ørskov Christensen;Kirsten Schultz;Birgitte Mollgaard;Henning Gjelstrup Kristensen.
European Journal of Pharmaceutical Sciences (2004)

224 Citations

Early pharmaceutical profiling to predict oral drug absorption: current status and unmet needs

Christel A.S. Bergström;René Holm;Søren Astrup Jørgensen;Sara B.E. Andersson.
European Journal of Pharmaceutical Sciences (2014)

223 Citations

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