This research is focused on the production of structures of biomedical interest using supercritical assisted processes: Supercritical freeze extraction, Supercritical gel drying and Supercritical phase separation. These processes have been selected to overcome the limitations of the traditional ones used in this field; indeed, they produce structures with a disordered microporosity, without an organization at nanometric level, with poor mechanical properties and with potential cytotoxic effect due to the residues of organic solvents and crosslinking agents. These problems reduce the efficiency of the cells culture on these structures in terms of adhesion, proliferation and differentiation in the tissue that it would to regenerate. Therefore, during the experimentation, several polymers, of natural and synthetic origin, were tested for bone, tendon and vascular applications. In particular, in this thesis:  synthetic and natural structures characterized by a micrometric porosity and wrinkled pore walls were produced by Supercritical freeze extraction process,  in the case of polymer/drug composite structures, a homogeneous distribution and controlled release of the active compound was assured,  aerogels starting from natural polymers, that mimic the tissue extracellular matrix at nanometric level were produced by Supercritical gel drying,  bioactive materials were tested; in particular, graphene oxide exfoliation and purification, during the formation of cellulose acetate nanocomposites, was obtained by Supercritical phase separation,  FEM Modeling was developed, confirming that mechanical properties of aerogels depend on how the nanofibrous network is connected in the space and that bending is the major mode of deformation of the network. [edited by Author]

Green processes based on SC-CO2: application to materials of biomedical interest

BALDINO, LUCIA
2015

Abstract

This research is focused on the production of structures of biomedical interest using supercritical assisted processes: Supercritical freeze extraction, Supercritical gel drying and Supercritical phase separation. These processes have been selected to overcome the limitations of the traditional ones used in this field; indeed, they produce structures with a disordered microporosity, without an organization at nanometric level, with poor mechanical properties and with potential cytotoxic effect due to the residues of organic solvents and crosslinking agents. These problems reduce the efficiency of the cells culture on these structures in terms of adhesion, proliferation and differentiation in the tissue that it would to regenerate. Therefore, during the experimentation, several polymers, of natural and synthetic origin, were tested for bone, tendon and vascular applications. In particular, in this thesis:  synthetic and natural structures characterized by a micrometric porosity and wrinkled pore walls were produced by Supercritical freeze extraction process,  in the case of polymer/drug composite structures, a homogeneous distribution and controlled release of the active compound was assured,  aerogels starting from natural polymers, that mimic the tissue extracellular matrix at nanometric level were produced by Supercritical gel drying,  bioactive materials were tested; in particular, graphene oxide exfoliation and purification, during the formation of cellulose acetate nanocomposites, was obtained by Supercritical phase separation,  FEM Modeling was developed, confirming that mechanical properties of aerogels depend on how the nanofibrous network is connected in the space and that bending is the major mode of deformation of the network. [edited by Author]
25-mag-2015
Inglese
Biopolymer
Scaffold
Supercritical CO2
CIAMBELLI, Paolo
REVERCHON, Ernesto
DE MARCO, Iolanda
Università degli Studi di Salerno
File in questo prodotto:
File Dimensione Formato  
abstract in inglese L. Baldino.pdf.pdf

accesso aperto

Licenza: Tutti i diritti riservati
Dimensione 19.85 kB
Formato Adobe PDF
19.85 kB Adobe PDF Visualizza/Apri
abstract in italiano L. Baldino.pdf.pdf

accesso aperto

Licenza: Tutti i diritti riservati
Dimensione 70.95 kB
Formato Adobe PDF
70.95 kB Adobe PDF Visualizza/Apri
tesi L. Baldino.pdf.pdf

accesso aperto

Licenza: Tutti i diritti riservati
Dimensione 9.21 MB
Formato Adobe PDF
9.21 MB Adobe PDF Visualizza/Apri
108986814138211460751315598205616606827.pdf

accesso solo da BNCF e BNCR

Licenza: Tutti i diritti riservati
Dimensione 5.75 MB
Formato Adobe PDF
5.75 MB Adobe PDF
154366573585169236479740290951568608113.pdf

accesso solo da BNCF e BNCR

Licenza: Tutti i diritti riservati
Dimensione 70.95 kB
Formato Adobe PDF
70.95 kB Adobe PDF
83753841627128715808109800801716049690.pdf

accesso solo da BNCF e BNCR

Licenza: Tutti i diritti riservati
Dimensione 19.85 kB
Formato Adobe PDF
19.85 kB Adobe PDF

I documenti in UNITESI sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14242/311105
Il codice NBN di questa tesi è URN:NBN:IT:UNISA-311105