To evaluate the reliability of the BIACORE method as a useful method for measuring the mucoadhesive interaction between chitosan and mucin, the mucin-particle method was used for comparison. In this study, the adhesivities of different-molecular-weight chitosans (chitosan Mw. 150,000, CS; low-molecular-weight chitosan, LCS) and hydrophobically modified chitosans (dodecylated CS, d-CS; dodecylated LCS, d-LCS) to mucin were determined. The BIACORE method showed that CS, LCS and d-CS could interact with mucin based on the increased resonance unit (RU) response after mucin was passed over the chitosans-immobilized sensor chip surface. Sensorgrams obtained from the interaction between these polymers and mucin also indicated the rate and strength of binding reaction. The rate and strength were higher for unmodified chitosans than hydrophobically modified chitosans. The simple in vitro mucoadhesive test or mucin-particle method revealed that the turbidity of unmodified chitosan/mucin mixtures was higher than that of dodecylated chitosans for all concentration of chitosans and mucin. The results from both BIACORE and the mucin-particle method implied that hydrophobic modification of chitosan reduced its adhesivity to mucin. The results from these two methods corresponded well. Therefore, the BIACORE method has promised as an alternative method for evaluating the adhesivity of adhesive polymers to mucin.
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http://dx.doi.org/10.1016/j.ijpharm.2007.12.001 | DOI Listing |
Comput Struct Biotechnol J
December 2024
Production and R&D Center I of LSS (Life Science Service), GenScript Biotech Corporation, No. 28, Yongxi Rd., Nanjing, 211100, Jiangsu, China.
The application of antibody therapeutics is promising in the field of immunotherapy. While, heterologization should be done in most cases before applying the therapeutic antibodies into bodies, e.g.
View Article and Find Full Text PDFJ Pept Sci
January 2025
Graduate School of Bioscience, Nagahama Institute of Bio-Science and Technology, Nagahama, Shiga, Japan.
Guanylate cyclase C (GC-C), a receptor expressed on the apical membrane of intestinal mucosal cells, is activated by heat-stable enterotoxin (STa) produced by enterotoxigenic Escherichia coli, as well as the endogenous ligands guanylin and uroguanylin. In this study, novel peptides that interact with GC-C were generated using the cDNA display method, and their binding affinity and biological activity were evaluated. While the linear peptide library did not yield peptides with sufficient affinity for GC-C, three cyclic peptides (GCC-P1, GCC-P2, and GCC-P3), each containing two cysteine residues within a 15-residue sequence, were obtained from a cyclic peptide library containing nine-residue random sequences.
View Article and Find Full Text PDFNeuro Oncol
October 2024
Division of Stem Cell Biology, Institute for Genetic Medicine, Hokkaido University, Sapporo 060-0815, Japan.
Background: The discovery of glioblastoma (GBM)-initiating cells (GICs) has impacted GBM research. These cells are not only tumorigenic, but also exhibit resistance to radiotherapy and chemotherapy. Therefore, it is crucial to characterize GICs thoroughly and identify new therapeutic targets.
View Article and Find Full Text PDFAAPS J
September 2024
Clinical Pharmacology, Pharmacometrics, & Bioanalysis, Bristol Myers Squibb Company, Princeton, New Jersey, 08543, USA.
Pre-existing anti-AAV antibodies can be detected using ligand binding-based assay formats. One such format is the MSD-based bridging assay, which uses sulfo-tag-labeled AAV vectors as detection reagents. However, no method has been developed to accurately measure the degree of sulfo-tag labeling on AAV vectors.
View Article and Find Full Text PDFJ Immunol Methods
November 2024
Unidad de Inmunología Microbiana, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, 28220 Madrid, Spain.
We present a time-course saturation ELISA for measuring the equilibrium constant of the monoclonal antibody (mAb) SIM 28 against horse radish peroxidase (HRP). The curves of HRP binding to a series of fixed mAb dilutions were plotted to completion, and the K (= K) value (time to occupy 50 % of the mAb paratopes) was determined for each mAb dilution and HRP concentration. Analysis of the kinetic mechanism of the reaction by Lineweaver-Burk and Hanes plots showed that the slope and y-intercept were affected, indicating that mAb ligand saturation follows non-competitive inhibition kinetics in this assay format.
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