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Editorial

How can we better realize the potential of immobilized artificial membrane chromatography in drug discovery and development?

Pages 273-276 | Received 24 Sep 2019, Accepted 15 Jan 2020, Published online: 18 Feb 2020

Figures & data

Figure 1. Schematic representation of hydrated octanol (adapted from [Citation4] with permission of the American Chemical Society), of the liposome (adapted from [Citation8] under CC BY-SA 3.0) and of the IAM stationary phase and membrane lipid bilayer. (Reproduced from [Citation9] with permission of Regis Technologies).

Figure 1. Schematic representation of hydrated octanol (adapted from [Citation4] with permission of the American Chemical Society), of the liposome (adapted from [Citation8] under CC BY-SA 3.0) and of the IAM stationary phase and membrane lipid bilayer. (Reproduced from [Citation9] with permission of Regis Technologies).

Figure 2. New generation IAM columns IAM.PC.MG and IAM.PC.DD2. In solid circles: the charged centers of phospholipids, in dashed circles: the glycerol moiety. Reproduced from [Citation10] with permission of Taylor & Francis.

Figure 2. New generation IAM columns IAM.PC.MG and IAM.PC.DD2. In solid circles: the charged centers of phospholipids, in dashed circles: the glycerol moiety. Reproduced from [Citation10] with permission of Taylor & Francis.

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