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1.
J Cell Mol Med ; 11(6): 1367-76, 2007.
Article in English | MEDLINE | ID: mdl-18205706

ABSTRACT

Molecular imprinting is a technique for the synthesis of polymers capable to bind target molecules selectively. The imprinting of large proteins, such as cell adhesion proteins or cell receptors, opens the way to important and innovative biomedical applications. However, such molecules can incur into important conformational changes during the preparation of the imprinted polymer impairing the specificity of the recognition cavities. The "epitope approach" can overcome this limit by adopting, as template, a short peptide sequence representative of an accessible fragment of a larger protein. The resulting imprinted polymer can recognize both the template and the whole molecule thanks to the specific cavities for the epitope. In this work two molecularly imprinted polymer formulations (a macroporous monolith and nanospheres) were obtained using the protected peptide Z-Thr-Ala-Ala-OMe, as template, and Z-Thr-Ile-Leu-OMe, as analogue for the selectivity evaluation, methacrylic acid, as functional monomer, and trimethylolpropane trimethacrylate and pentaerythritol triacrylate (PETRA), as cross-linkers. Polymers were synthesized by precipitation polymerization and characterized by standard techniques. Polymerization and rebinding solutions were analyzed by high performance liquid chromatography. The highly cross-linked polymers retained about 70% of the total template amount, against (20% for the less cross-linked ones). The extracted template amount and the rebinding capacity decreased with the cross-linking degree, while the selectivity showed the opposite behaviour. The PETRA cross-linked polymers showed the best recognition (MIP 2-, alpha=1.71) and selectivity (MIP 2+, alpha'=5.58) capabilities. The cytotoxicity tests showed normal adhesion and proliferation of fibroblasts cultured in the medium that was put in contact with the imprinted polymers.


Subject(s)
Biomedical Technology/instrumentation , Peptides/chemistry , Polymers/chemistry , Polymers/pharmacology , Animals , Cell Death/drug effects , Cross-Linking Reagents/pharmacology , Mice , Microscopy, Electron, Scanning , NIH 3T3 Cells , Polymers/chemical synthesis , Porosity/drug effects , Spectroscopy, Fourier Transform Infrared , Temperature
2.
Minerva Cardioangiol ; 41(12): 591-5, 1993 Dec.
Article in Italian | MEDLINE | ID: mdl-8139780

ABSTRACT

Report of a case of a 54-year-old man who, during acute anterior myocardial infarction developed an apical thrombus and an embolism of the right leg. The serial echocardiographic study demonstrates how the original shape of the thrombus acutely changed at the same time of the embolic episode and how the new morphology of the thrombotic mass after embolism and thrombolytic plus anticoagulant therapy (performed for the acute ischaemic episode of the leg) was widely different from the initial one. The role of cross-sectional echocardiography is emphasized for the diagnostic value in case of intraventricular thrombi and for possible utilization also for therapeutic guidance.


Subject(s)
Echocardiography , Embolism/etiology , Heart Diseases/etiology , Myocardial Infarction/complications , Popliteal Artery , Thrombosis/etiology , Acute Disease , Drug Therapy, Combination , Embolism/diagnostic imaging , Embolism/drug therapy , Heart Diseases/complications , Heart Diseases/diagnostic imaging , Heart Diseases/drug therapy , Heart Ventricles/diagnostic imaging , Humans , Male , Middle Aged , Myocardial Infarction/diagnostic imaging , Myocardial Infarction/drug therapy , Popliteal Artery/diagnostic imaging , Thrombosis/complications , Thrombosis/diagnostic imaging , Thrombosis/drug therapy , Time Factors
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