I am a physical chemist with expertise in the field of colloidal science, skilled in experiments, theory and simulations to solve pharmaceutical problems – from small molecules to macromolecules like mRNA.
I have been working at AstraZeneca for over 25 years on gastrointestinal absorption, oral vaccines, molecular simulations, nanoparticle systems of poorly soluble drugs and more recently, on lipid nanoparticles and exosomes incorporating nucleic acids.
I received my PhD at Chalmers University of Technology in 1993. In 2007, I became an adjunct Professor at the Department of Chemistry and Molecular Biology, University of Gothenburg, which enhances my interaction with the academic community.
I enjoy collaboration and solving problems with scientific rigor and believe that the solutions we deliver make a real impact to innovation and product development, and ultimately patients.
CURRENT ROLE
2018
2017
2016
Featured publications
Promoting intestinal lymphatic transport targets a liver-X receptor (LXR) agonist (WAY-252,623) to lymphocytes and enhances immunomodulation.
Cao E, Lindgren A, Martinsson S, Hu LJ, Lindfors L, Sigfridsson K, Skantze U, Michaelsson E, Trevaskis NL, Porter CJH. Journal of Controlled Release, (2019), 296: 29. Publication link
Successful reprogramming of cellular protein production through mRNA delivered by functionalized lipid nanoparticles.
Arteta MY, Kjellman T, Bartesaghi S, Wallin S, Wu X, Kvistc AJ, Dabkowska A, Székely N, Radulescu A, Bergenholtz J, Lindfors L. Proceedings of the National Academy of Sciences (2018), 115: E3351. Publication link.
Nanocrystal formulations of a poorly soluble drug. 1. In vitro characterization of stability, stabilizer adsorption and uptake in liver cells.
Sigfridsson K, Skantze U, Skantze P, Johansson S, Grant I, Smedsrød B, Fuglesteg B, Elvevold K, Lindfors L. International Journal of Pharmaceutics (2017), 518: 29. Publication link.
Nanocrystal formulations of a poorly soluble drug. 2. Evaluation of nanocrystal liver uptake and distribution after intravenous administration to mice.
Sigfridsson K, Skantze P, Skantze U, Svensson L, Löfgren L, Nordell P, Michaelsson E, Smedsrød B, Fuglesteg B, Elvevold K, Lindfors L. International Journal of Pharmaceutics (2017), 524: 248. Publication link.
Development of target-specific liposomes for delivering small molecule drugs after reperfused myocardial infarction.
Krishna Dasa SS, Suzuki R, Gutknecht M, Brinton LT, Tian Y, Michaelsson E, Lindfors L, Klibanov AL, French BA, Kelly KA. Journal of Controlled Release (2015), 220: 556. Publication link.
Secondary Crystal Nucleation: Nuclei Breeding Factory Uncovered.
Anwar J, Khan S, Lindfors L. Angewandte Chemie (2014), 127: 14894. Publication link.
Nucleation and crystal growth in supersaturated solutions of a model drug
Lindfors L, Forssén S, Westergren J, Olsson U. Journal of Colloid and Interface Science (2008), 325: 404. Publication link.
Amorphous drug nanosuspensions.1.Inhibition of Ostwald ripening
Lindfors L, Skantze P, Skantze U, Rasmusson M, Zackrisson A, Olsson U. Langmuir (2007), 22: 906. Publication link.
Amorphous drug nanosuspensions.2. Experimental determination of bulk monomer concentrations
Lindfors L, Forssén S, Skantze P, Skantze U, Zackrisson A, Olsson U. Langmuir (2007), 22: 911. Publication link.
Amorphous drug nanosuspensions.3. Particle dissolution and crystal growth
Lindfors L, Skantze P, Skantze U, Westergren J, Olsson U. Langmuir (2007), 23: 9866. Publication link.