Biomedical subjects

M Ulbricht

Publications and source records attributed to M Ulbricht.

4 recordsLinked to original sources

PubMed2001

Molecularly imprinted polymer membranes for substance-selective solid-phase extraction from water by surface photo-grafting polymerization.

Hydrophilized polyvinylidene fluoride microfiltration membranes were surface-modified in the presence of a template (terbumeton) in methanol with a graft copolymer of a functional monomer (2-acrylamido-2-methyl-1-propane sulfonic acid, AMPS, methacrylic acid, MAA, or acrylic acid, AA) and a cross-linker (N,N'-methylene-bis-acrylamide) using UV irradiation and benzophenone as photoinitiator. As result, membranes covered with a thin layer of imprinted polymer selective to terbumeton were obtained. Blank membranes were prepared with the same monomer composition, but in the absence of the template. The membranes' capacity to adsorb terbumetone from aqueous solution was evaluated yielding information regarding the effect of polymer synthesis (type and concentration of functional monomer, concentration of cross-linker) on the resulting membranes' recognition properties. UV spectroscopic studies of the interactions with terbumetone revealed that AMPS forms a stronger complex than MAA and AA. In agreement with that finding, imprinting with AMPS gave higher affinities than with MAA and AA. The terbumeton-imprinted membranes showed significantly higher sorption capability to this herbicide than to similar compounds (atrazine, desmetryn, metribuzine). With the novel surface modification technology, the low non-specific binding properties of the hydrophilized microfiltration membrane could successfully be combined with the receptor properties of molecular imprints, yielding substance-specific molecularly imprinted polymer composite membranes. The high affinity of these synthetic affinity membranes to triazine herbicides together with their straightforward and inexpensive preparation provides a good basis for the development of applications of imprinted polymers in separation processes such as solid-phase extraction.

Membranes, Artificial↗

PubMed2001

Thin layer molecularly imprinted microfiltration membranes by photofunctionalization using a coated alpha-cleavage photoinitiator.

A novel approach towards thin-layer molecularly imprinted polymer (MIP) composite membranes was developed based on using benzoin ethyl ether (BEE), a very efficient alpha-scission photoinitiator. The triazine herbicide desmetryn was used as the template, and a mixture of the functional monomer 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS) and the cross-linker N,N'-methylene-bis-acrylamide (MBAA) in methanol was copolymerised via photoinitiation followed by deposition on the surface of either hydrophobic or hydrophilically precoated polyvinylidene fluoride (PVDF) microfiltration membranes. Blanks were prepared under identical conditions, but without the template. Especially, the degree of functionalization (DF) of the PVDF membranes with poly(AMPS-co-MBAA), the membrane permeabilities and non-specific vs. MIP-specific template binding from aqueous solutions during fast filtration were studied in detail to evaluate the effects of the preparation conditions, in particular the coating of the membrane surface with the photoinitiator prior to UV irradiation and the influence of the precoated hydrophilic layer on PVDF. Significant template specificities of the MIP membranes compared with the blanks were only achieved for the preparations including coating the two types of PVDF membranes with BEE. In contrast, a homogeneous photoinitiation of the copolymerisation in the membrane pore volume yielded functional layers with similar DF but with only non-specific desmetryn binding. All data clearly indicate the significant contribution of MIP stabilization by the support material in layers of optimum thickness to the MIP specificity. Main advantages of the novel approach are the potential to synthesize MIP composite membranes by controlled deposition onto any kind of polymer support, and the very fast MIP preparations due to a very efficient photoinitiator and small MIP layer thickness. Due to the mechanical and chemical stability in combination with high permeabilities, thin-layer MIP composite membranes have a large application potential, e.g., in solid phase extraction.

Journal Article↗

PubMed2000

Modulating the biocompatibility of polymer surfaces with poly(ethylene glycol): effect of fibronectin.

A novel approach described earlier for improving polymer substratum biocompatibility(1) is further elucidated. Polysulfone (PSf) spin-coating films were modified by covalent end-on grafting of hydrophilic and sterically demanding photo-reactive poly(ethylene glycol) (PEG) conjugates (ABMPEG; 10 kDa). The degree of grafting density was varied systematically, yielding a wide spectrum of attained surface characteristics monitored by air-water contact angles (captive bubble method). Fibronectin (FN) adsorption was studied by in situ ellipsometry and found to decrease monotonically as ABMPEG grafting density increased. The adhesive interaction of human skin fibroblasts with these substrata and, in particular, the effect of FN precoating were investigated in detail. A clear optimum of cell-substratum interactions was found for mildly modified substrata, employing well established microscopic and immunofluorescence techniques, namely the monitoring of cell adhesion and spreading, overall cell morphology, organization of FN receptors, and focal adhesions as well as FN matrix formation. The results suggest that cell interactions with hydrophobic polymer substrata are enhanced considerably when modified with hydrophilic and sterically demanding PEG moieties at a low surface coverage due to enhanced biologic activity of adsorbed and intercalated adhesive proteins such as FN.

Biocompatible Materials↗

PubMed1998

Ultrafiltration membrane surfaces with grafted polymer 'tentacles': preparation, characterization and application for covalent protein binding.

Ultrafiltration (UF) membranes from polysulfone (PSf) were functionalized by heterogeneous photo-initiated graft copolymerization of acrylic acid (AA). With radiation susceptible PSf, only proper selection of the UV energy (lambda > 350 nm; for selective excitation of the photoinitiator) yielded membranes with preserved UF barrier layer. Possibilities for adjusting structure and morphology of the graft polymer (g-PAA) layer by variation of functionalization parameters such as AA concentration and UV irradiation time were investigated. Very long grafted chains (Mw > 10(5) g mol(-1)) at varied grafting density (GD = 0.01 ... 1.2 nmol cm(-2), relative to the outer surface area) were obtained. Partial penetration of the UF barrier layer by g-PAA was verified. Covalent immobilization of bovine serum albumin (BSA), gamma-globulin (gamma-Gl) and alkaline phosphatase (APh) was achieved by coupling with a water soluble carbodiimide. Bound BSA and gamma-Gl amounts were up to gamma = 10 microg cm(-2), for membranes accessible only from the outer surface thus not using the entire pore volume. Locally addressed covalent protein immobilization after photo-patterning the PSf surface could be visualized with a fluorescent FITC-BSA conjugate. A strong salt effect onto immobilized APh activity (increase with NaCl concentration) was observed, indicating internal transport/accessibility limitations in the g-PAA layer. Correlations between PAA structure (Mw, GD) and accessibility (from BSA or gamma-G1 binding and APh activity) could be established. The 'tentacle' g-PAA functionalized PSf UF membranes having preserved UF barrier and, e.g., with surface-bound receptors will find application in cell cultures under diffusion or perfusion conditions.

Acrylic Resins↗