In this work, novel smart surfaces for in situ cell staining were realized by covalent attachment of pH-responsive microgels on platforms dedicated to microfluidics for lab-on-chip. The poly(methacrylic acid) microgels were firstly synthesized in solution and then covalently immobilized on a glass surface. As they preserve their pH-sensitive nature after the covalent immobilization, microgels were loaded with an oligothiophene-conjugated anti-human CD4 monoclonal antibody, and finally incubated with a Jurkat T-cell suspension. The physiological pH of the extracellular environment induced the pH-triggered release of the labeled antiCD4 antibodies and the selective staining of the CD4-positive subpopulations within the Jurkat cell suspension. The realization of this type of smart surface for the encapsulation of specific monoclonal antibodies and their release in an on-demand way should have an enormous potential in developing fully integrated platforms for cell analysis.

Smart surfaces for pH controlled cell staining

Laura Blasi;Giuseppe Ciccarella;
2009

Abstract

In this work, novel smart surfaces for in situ cell staining were realized by covalent attachment of pH-responsive microgels on platforms dedicated to microfluidics for lab-on-chip. The poly(methacrylic acid) microgels were firstly synthesized in solution and then covalently immobilized on a glass surface. As they preserve their pH-sensitive nature after the covalent immobilization, microgels were loaded with an oligothiophene-conjugated anti-human CD4 monoclonal antibody, and finally incubated with a Jurkat T-cell suspension. The physiological pH of the extracellular environment induced the pH-triggered release of the labeled antiCD4 antibodies and the selective staining of the CD4-positive subpopulations within the Jurkat cell suspension. The realization of this type of smart surface for the encapsulation of specific monoclonal antibodies and their release in an on-demand way should have an enormous potential in developing fully integrated platforms for cell analysis.
2009
Istituto di Nanotecnologia - NANOTEC
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
Istituto Nanoscienze - NANO
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/918
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