Enzyme-Loaded Gel Core Nanostructured Lipid Carriers to Improve Treatment of Lysosomal Storage Diseases: Formulation and In Vitro Cellular Studies of Elosulfase Alfa-Loaded Systems

Mucopolysaccharidosis IVA (Morquio A) is a rare inherited metabolic disease caused by deficiency of the lysosomal enzyme N-acetylgalatosamine-6-sulfate-sulfatase (GALNS). Until now, treatments employed included hematopoietic stem cell transplantation and enzyme replacement therapy (ERT); the latter...

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Main Authors: J. Víctor Álvarez (Author), Carolina Herrero Filgueira (Author), Alexandre de la Fuente González (Author), Cristóbal Colón Mejeras (Author), Andrés Beiras Iglesias (Author), Shunji Tomatsu (Author), José Blanco Méndez (Author), Asteria Luzardo Álvarez (Author), María Luz Couce (Author), Francisco J. Otero Espinar (Author)
Format: Book
Published: MDPI AG, 2019-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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