Designed Functional Dispersion for Insulin Protection from Pepsin Degradation and Skeletal Muscle Cell Proliferation: In Silico and In Vitro Study.
Veera Chandra Sekhar Reddy ChittepuPoonam KalhotraTzayhri Gallardo-VelázquezRaúl René Robles-de la TorreGuillermo Osorio-RevillaPublished in: Nanomaterials (Basel, Switzerland) (2018)
Functionalized single-walled carbon nanotubes with polyethylene glycol (PEGylated SWCNTs) are a promising nanomaterial that recently has emerged as the most attractive "cargo" to deliver chemicals, peptides, DNA and RNAs into cells. Insulin therapy is a recommended therapy to treat diabetes mellitus despite its side effects. Recently, functional dispersion made up of bioactive peptides, bioactive compounds and functionalized carbon nanomaterials such as PEGylated SWCNTs have proved to possess promising applications in nanomedicine. In the present study, molecular modeling simulations are utilized to assist in designing insulin hormone-PEGylated SWCNT composites, also called functional dispersion; to achieve this experimentally, an ultrasonication tool was utilized. Enzymatic degradation assay revealed that the designed functional dispersion protects about 70% of free insulin from pepsin. In addition, sulforhodamine B (SRB) assay, the quantification of insulin and glucose levels in differentiated skeletal muscle cell supernatants, reveals that functional dispersion regulates glucose and insulin levels to promote skeletal muscle cell proliferation. These findings offer new perspectives for designed functional dispersion, as potential pharmaceutical preparations to improve insulin therapy and promote skeletal muscle cell health.
Keyphrases
- skeletal muscle
- type diabetes
- glycemic control
- cell proliferation
- insulin resistance
- healthcare
- mental health
- induced apoptosis
- quantum dots
- oxidative stress
- nitric oxide
- mass spectrometry
- health information
- signaling pathway
- gold nanoparticles
- hydrogen peroxide
- molecular dynamics
- circulating tumor
- high resolution
- nucleic acid