Densely packed alkyl chains with hydrophilic head groups can have both a hydrophobic interaction and a hydrophilic one with guest substrates. This specific environment provided by lipid membranes is essential for molecular recognition in biological membranes and has been studied in the areas of chemical sensing and separation [1, 2]. Proteins or other biologically active substances, especially those produced by recombinant microorganisms, are usually contaminated with lipopolysaccharide (LPS) [3]. LPS, which Selleckchem ABT737 originates from an outer membrane

of Gram-negative bacteria, consists 4EGI-1 mouse of a polysaccharide and a terminal lipid A moiety. Lipid A is composed of a diglucosamine that is highly substituted with amide- and ester-linked long-chain fatty acids and negatively charged with phosphate groups. For pharmaceutical uses of those active substances, LPS has to be removed to not higher than 0.1 ng mL-1 because of its strong pyrogenicity [4]. Intensive studies

have been done on the removal of LPS from protein solutions [5]. For example, LPS was selectively removed by ion-exchange chromatography using DEAE-Sepharose CL-6B [6] and affinity chromatography using adsorbents bearing histidine [7], polymyxin B [8], and polycation PI3K Inhibitor Library cell assay [9]. However, the removal of LPS is suggested to be extremely difficult when LPS is associated with protein to be purified [5] and has been an issue in pharmaceutical technology and science. We have reported the covalent immobilization of polymeric lipid membranes of N-octadecylchitosan consisting

of 2-deoxy-2-octadecylamino-d-glucopyranose (GlcNC18; Figure 1), 2-amino-2-deoxy-d-glucopyranose Methisazone (GlcN), and 2-acetamido-2-deoxy-d-glucopyranose (GlcNAc) to carboxylated porous supports composed of chitosan [10], and the selective removal of LPS from bovine serum albumin (BSA) solution using the resulting porous materials [11]. In this paper, we would like to report further data of a successful LPS removal to as low as 0.02 ng mL-1 from human serum albumin (HSA) solution with a quantitative recovery of protein showing the possibility of their practical use. Figure 1 Monosaccharide components of N -octadecylchitosan. Methods Materials and general methods Chitosan was purchased from Dai-ichi Kogyo Seiyaku Co., Ltd. (Kyoto, Japan). The degree of deacetylation was determined as 87 mol% by colloidal titration. Intrinsic viscosity was 1.42 dL g-1 (0.2 M CH3COOH/0.1 M CH3COONa, 30°C) which corresponded to 2.67 × 104 of molecular weight relative to poly(ethylene glycol). A cross-linked porous chitosan having a particle size of 45 to 420 μm and an average pore diameter of 2 μm, a product of Kurita Water Industries, Ltd. (Tokyo, Japan), was used as obtained. 1-Bromooctadecane, succinic anhydride (Kishida Chemical Co., Ltd.