Jamaledin, Rezvan (2021) Controlled release of bacteriophage from PLGA microparticles included in fully implantable bicompartmental polymeric microneedles to induce the innate and adaptive immune system response. [Tesi di dottorato]

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Item Type: Tesi di dottorato
Resource language: English
Title: Controlled release of bacteriophage from PLGA microparticles included in fully implantable bicompartmental polymeric microneedles to induce the innate and adaptive immune system response
Creators:
Creators
Email
Jamaledin, Rezvan
jamaledinrezvan@gmail.com
Date: 12 July 2021
Number of Pages: 106
Institution: Università degli Studi di Napoli Federico II
Department: Ingegneria Chimica, dei Materiali e della Produzione Industriale
Dottorato: Ingegneria dei prodotti e dei processi industriali
Ciclo di dottorato: 33
Coordinatore del Corso di dottorato:
nome
email
D'Anna, Andrea
UNSPECIFIED
Tutor:
nome
email
Raffaele, Vecchione
UNSPECIFIED
Antonio Netti, Paolo
UNSPECIFIED
Date: 12 July 2021
Number of Pages: 106
Keywords: PLGA microparticles, polymeric microneedles
Settori scientifico-disciplinari del MIUR: Area 03 - Scienze chimiche > CHIM/05 - Scienza e tecnologia dei materiali polimerici
Date Deposited: 29 Jul 2021 20:30
Last Modified: 07 Jun 2023 10:41
URI: http://www.fedoa.unina.it/id/eprint/13689

Collection description

The increasing demand for patient-compliance therapies in recent years has led to the development of intradermal and transdermal drug/vaccine delivery, which has several superiorities as compared to conventional methods. This research project endeavored to successfully encapsulate filamentous bacteriophage (Fd) into a Poly(lactic-co-glycolic acid)-based microparticulate system (PLGA MPs). The release profile of these microparticles suggests that they could be used to successfully induce immune and adaptive system. It was the first time that filamentous bacteriophages have been encapsulated in PLGA. The present study also devised a microneedle (MNs) system. A multi compartment microneedles (MNs) system was validated for a number of actives encapsulation (ex. laccase, collagenase) during the PhD activity and upon this optimization the system has been coupled with pillars as a strong mechanical pedestal to increase insertion ability. At the moment, in vivo intradermal delivery from MPs and MNs encapsulated bacteriophages are under investigation. Aside from the development of bacteriophage delivery systems, novel work in the application of fd-bacteriophage was completed with extremely successful results.

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