TY - JOUR
T1 - Cellulose nanocrystals/zeolitic imidazolate framework-L (CNCs/ZIF-L) composites for loading and diffusion-controlled release of doxorubicin hydrochloride
AU - Wijaya, Christian J.
AU - Hartono, Sandy B.
AU - Putro, Jindrayani N.
AU - Anggono, Juliana
AU - Sembiring, Tarzan
AU - Putra, Herlian E.
AU - Yuliana, Maria
AU - Lie, Jenni
AU - Santoso, Shella P.
AU - Chen, Chien Yen
AU - Soetaredjo, Felycia E.
AU - Ismadji, Suryadi
AU - Gunawan, Setiyo
N1 - Publisher Copyright:
© 2024 Taiwan Institute of Chemical Engineers
PY - 2024/12
Y1 - 2024/12
N2 - Background: Zeolitic imidazolate framework-L (ZIF-L) has great potential as a doxorubicin hydrochloride (DOX) drug carrier for oral chemotherapy applications. This medical application will greatly support the development of cancer treatment and reduce the cancer fatality rate. However, ZIF-L as a type of metal-organic framework (MOFs) faces several challenges to be implemented in biomedical applications which impact the drug loading and release mechanisms. Methods: CNCs/ZIF-L composites were fabricated via a green in-situ method using CNCs mass percentages of 2.5, 5, 7.5, and 10 % of Zn(NO3)2·6H2O. All composites were tested for the DOX loading and release mechanisms and antioxidant activity. Significant findings: Here, the addition of CNCs enhances the DOX loading capacity of CNCs/ZIF-L composite up to 1508.91 ± 7.72 mg/g due to the presence of abundant active functional groups. In addition, the DOX release profile is another interesting potential that occurs through a diffusion-controlled release mechanism. This shows the ability of CNCs/ZIF-L composite to deliver drugs orally where DOX is released consistently at a certain concentration level for prolonged treatment. Moreover, the IC50 value of DOX@CNCs/ZIF-L drug reaching 480.21 mg/L proves that the effectiveness of DOX is maintained even though it is administered orally in the form of solid material.
AB - Background: Zeolitic imidazolate framework-L (ZIF-L) has great potential as a doxorubicin hydrochloride (DOX) drug carrier for oral chemotherapy applications. This medical application will greatly support the development of cancer treatment and reduce the cancer fatality rate. However, ZIF-L as a type of metal-organic framework (MOFs) faces several challenges to be implemented in biomedical applications which impact the drug loading and release mechanisms. Methods: CNCs/ZIF-L composites were fabricated via a green in-situ method using CNCs mass percentages of 2.5, 5, 7.5, and 10 % of Zn(NO3)2·6H2O. All composites were tested for the DOX loading and release mechanisms and antioxidant activity. Significant findings: Here, the addition of CNCs enhances the DOX loading capacity of CNCs/ZIF-L composite up to 1508.91 ± 7.72 mg/g due to the presence of abundant active functional groups. In addition, the DOX release profile is another interesting potential that occurs through a diffusion-controlled release mechanism. This shows the ability of CNCs/ZIF-L composite to deliver drugs orally where DOX is released consistently at a certain concentration level for prolonged treatment. Moreover, the IC50 value of DOX@CNCs/ZIF-L drug reaching 480.21 mg/L proves that the effectiveness of DOX is maintained even though it is administered orally in the form of solid material.
KW - Cellulose nanocrystals
KW - Composite
KW - Doxorubicin hydrochloride
KW - Drug carrier
KW - Zeolitic imidazolate framework-L
UR - http://www.scopus.com/inward/record.url?scp=85209136081&partnerID=8YFLogxK
U2 - 10.1016/j.jtice.2024.105831
DO - 10.1016/j.jtice.2024.105831
M3 - Article
AN - SCOPUS:85209136081
SN - 1876-1070
VL - 165
JO - Journal of the Taiwan Institute of Chemical Engineers
JF - Journal of the Taiwan Institute of Chemical Engineers
M1 - 105831
ER -