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Intact Fibrillated 3D-Printed Cellulose Macrofibrils/CaCO(3) for Controlled Drug Delivery

The tendency to use cellulose fibrils for direct ink writing (DIW) of three-dimensional (3D) printing has been growing extensively due to their advantageous mechanical properties. However, retaining cellulose in its fibrillated forms after the printing process has always been a challenge. In this st...

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Detalles Bibliográficos
Autores principales: Mohan, Denesh, Teong, Zee Khai, Sajab, Mohd Shaiful, Kamarudin, Nur Hidayatul Nazirah, Kaco, Hatika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227662/
https://www.ncbi.nlm.nih.gov/pubmed/34201366
http://dx.doi.org/10.3390/polym13121912
Descripción
Sumario:The tendency to use cellulose fibrils for direct ink writing (DIW) of three-dimensional (3D) printing has been growing extensively due to their advantageous mechanical properties. However, retaining cellulose in its fibrillated forms after the printing process has always been a challenge. In this study, cellulose macrofibrils (CMFs) from oil palm empty fruit bunch (OPEFB) fibers were partially dissolved for consistent viscosity needed for DIW 3D printing. The printed CMF structure obtained from optimized printing profiles (volumetric flow rate, Q(v) = 9.58 mm/s; print speed, v = 20 mm/s), exhibited excellent mechanical properties (tensile strength of 66 MPa, Young’s modulus of 2.16 GPa, and elongation of 8.76%). The remarkable structural and morphological effects of the intact cellulose fibrils show a homogeneous distribution with synthesized precipitated calcium carbonate (CaCO(3)) nanoparticles. The shear-aligned CMF/CaCO(3) printed composite exhibited a sustained therapeutic drug release profile that can reduce rapid release that has adverse effects on healthy cells. In comparison with the initial burst release of 5-fluorouracil (5-FU) by CaCO(3), the controlled release of 5-fluorouracil can be varied (48 to 75%) with the composition of CMF/CaCO(3) allowing efficient release over time.