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Development and Evaluation of a Multi-Modal Hyaluronic Acid Hydrogel for Anti-Inflammatory Drug Delivery for Multiple Sclerosis Therapy

Current treatments for multiple sclerosis (MS) are hindered by adherence challenges linked to frequent systemic dosing regimens, which demand active patient participation and often lead to suboptimal therapeutic outcomes. Conventional disease-modifying therapies (DMTs) administered orally or via injection, struggle to balance efficacy with patient quality of life, compounded by risks of systemic toxicity and rapid drug clearance. Recent surveys underscore a growing demand for implantable drug delivery systems (DDS) that minimize dosing frequency, reduce patient burden, and enhance long-term compliance. This dissertation addresses these unmet needs by developing an injectable hydrogel platform based on aldehyde-functionalized hyaluronic acid (HAOX) and chondroitin sulfate (CSOX), designed for localized, sustained delivery of antiinflammatory therapeutics. Central to this innovation is the immobilization of polyelectrolyte complexes (PECs) within the covalently crosslinked hydrogel matrix. Unlike conventional nanoparticle-based DDS, which rely on freely diffusing carriers prone to burst release and instability, immobilized PECs exploit electrostatic interactions between therapeutic agents (minocycline, MN; Fluorescein isothiocyanate-modified synthetic Preimplantation Factor, FITCSPIF) and the anionic sulfate groups of CSOX. This strategy enhances drug retention, reduces manufacturing complexity, and eliminates the need for costly encapsulation processes.
ISBN:978-80-7678-351-5
EAN:9788076783515
Počet stran 42 stran
Datum vydání 11. 09. 2025
Pořadí vydání První
Jazyk anglický
Autor: Habibah Tutut Ummul
Nakladatelství Univerzita Tomáše Bati ve Zlíně
Tématická skupina 999 - nezařazeno
Neprodejná publikace. Publikaci je možné poptávat zde: Volně dostupné na http://hdl.handle.net/10563/56897
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