Functional poly(p-phenylene)s as targeting and drug carrier materials

Polymers have a substantial attention in drug delivery systems owing to the diverse intrinsic advantages. It is important to carry the drug to the target site and release to exert its effects. Herein, poly(p-phenylene)s with amino and poly(ethylene glycol) substituents (PPP-NH₂-g-PEG) were used as a carrier for doxorubicin (DOX), an anticancer drug, and haloperidol, a sigma receptor targeting ligand. Both human cervix adenocarcinoma cell line (HeLa) and human keratinocyte cell line (HaCaT) having different Sigma receptor 1 (SigmaR1) expression levels were compared. HeLa was found to express twofold SigmaR1 compared to HaCaT cells. Cell imaging studies showed that, DOX cell uptake was higher in HeLa cells when targeted with haloperidol.     

Investigation of the Performance of Silicone Rubber Modified Bitumen

Silicon - The pavement performance, which constitutes a large part of the highway costs, is directly related to the engineering properties of the bituminous binder used in asphalt pavements. Thus;...     

Molecularly imprinted hydrogels for fibrinogen recognition

Molecularly imprinted hydrogels (MIHs) composed of N-isopropylacrylamide (NIPA) and maleic acid (MA) monomers and fibrinogen (Fbg, MW: 340 kDa, pI: 5.8) imprinted molecule were fabricated in pH buffer solutions (pH_prep: 4.0, 5.8 and 8.0). The non-imprinted hydrogels were also prepared in the same conditions without Fbg imprinted molecule. The adsorption equilibrium constant and the maximum adsorption capacity of the MIH prepared in pH 4.0 were evaluated to 9.61 mL mg^?1 and 38.99 mg protein g^?1 dry gel in pH 4.0 buffer solution, respectively. The selectivity tests were also performed by using two reference molecules as bovine serum albumin (BSA, MW: 67 kDa, pI: 4.78) and urease (MW: 480 kDa, pI: 5.99). The MIHs have 2.37–4.23 times higher selectivity for the Fbg imprinted molecule than the non-imprinted hydrogels prepared in the same conditions. Easy preparation of the MIHs, their high stability and ability to recognize small and large proteins, as well as to discriminate molecules with small variations in charge, make this approach attractive and broadly applicable in biotechnology, assays and sensors.