TY - JOUR
T1 - The Use of Chitosan Nanoparticles for Delivery of CpG ODN in Treatment of Allergic Balb/C Mice
AU - Iswanti, Febriana Catur
AU - Putri, Qarina Hasyala
AU - Prijanti, Ani Retno
AU - Djauzi, Samsuridjal
AU - Sadikin, Mohamad
AU - Witarto, Arief Budi
AU - Yamazaki, Tomohiko
N1 - Funding Information:
The authors would like to thank to Universitas Indonesia for PUTI 2020 grant No.NKB-1903/UN2.RST/HKP.05.00/2020 for supporting part of this study.
Publisher Copyright:
© 2023,Reports of Biochemistry and Molecular Biology. All Rights Reserved.
PY - 2023
Y1 - 2023
N2 - Background: This study aims to prepare high stability chitosan nanoparticles (CNP) and examine the ability of CNP in CpG-ODN delivery when treating allergic mice model. Methods: Preparation and characterization of CNP were performed by ionic gelation, dynamic light scattering, and zeta sizer. The CNP cytotoxicity and activation ability of CpG ODN delivered with CNP were tested using a cell counting kit-8 and Quanti blue method. Allergic mice were injected intraperitoneal with 10 ug ovalbumin on day 0 and 7, and then treated with intranasal CpG ODN/CpG ODN, delivered with CNP/CNP, on the third week three times per week for three weeks. The ELISA method measured cytokine and IgE profiles in the allergic mice’s plasma and spleen. Results: CNP results have sizes 27.73 nm±3.67 dan 188.23 nm±53.47, spherical in shape and nontoxic, and did not alter the NF-κB activation of CpG ODN in RAW-blue cells. The application of CpG ODN delivered by chitosan nanoparticles shows no statistical difference between groups of IFN-γ, IL-10, and IL-13 in Balb/c mice’s plasma and spleen, in contrast with IgE level.
AB - Background: This study aims to prepare high stability chitosan nanoparticles (CNP) and examine the ability of CNP in CpG-ODN delivery when treating allergic mice model. Methods: Preparation and characterization of CNP were performed by ionic gelation, dynamic light scattering, and zeta sizer. The CNP cytotoxicity and activation ability of CpG ODN delivered with CNP were tested using a cell counting kit-8 and Quanti blue method. Allergic mice were injected intraperitoneal with 10 ug ovalbumin on day 0 and 7, and then treated with intranasal CpG ODN/CpG ODN, delivered with CNP/CNP, on the third week three times per week for three weeks. The ELISA method measured cytokine and IgE profiles in the allergic mice’s plasma and spleen. Results: CNP results have sizes 27.73 nm±3.67 dan 188.23 nm±53.47, spherical in shape and nontoxic, and did not alter the NF-κB activation of CpG ODN in RAW-blue cells. The application of CpG ODN delivered by chitosan nanoparticles shows no statistical difference between groups of IFN-γ, IL-10, and IL-13 in Balb/c mice’s plasma and spleen, in contrast with IgE level.
KW - Allergy
KW - Chitosan nanoparticle
KW - CpG ODN
KW - Immunotherapy
KW - Mice spleen
UR - http://www.scopus.com/inward/record.url?scp=85163072641&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:85163072641
SN - 2322-3480
VL - 11
SP - 600
EP - 613
JO - Reports of Biochemistry and Molecular Biology
JF - Reports of Biochemistry and Molecular Biology
IS - 4
ER -