Search bioRxiv⌕ Search

Biology subjects

Kurniawan, D. W.

Publications and source records attributed to Kurniawan, D. W..

2 recordsLinked to original sources

Subchronic Toxicity Study of Nitric Oxide Nano Bubbles Injection in Sprague-Dawley Rats

Following the success of hydrogen nanobubble technology, development has expanded to include similar products with other gases, such as nitric oxide (NO). In previous studies, NO donors have been frequently used for both therapeutic and diagnostic purposes. However, the use of NO in nanoformulations has received little attention thus far. Thus, 90 days of subchronic toxicity testing in Sprague-Dawley rats were used in this study to assess potential adverse effects of intravenous administration of NO nanobubbles (NONB). Hematological factors, serum biochemistry, and histology of the liver, kidney, heart, lung, and spleen were investigated. The findings of the intravenous NONB injection trial in rats, using graded doses of 0.01 mL, 0.04 mL, and 0.06 mL, demonstrated no deaths during the 90-day treatment period. Biochemical parameters for liver function, lipid profile, kidney function, and serum electrolyte levels remain within acceptable limits, with slight variations in sodium and potassium levels. This condition was also supported by histological findings in the liver, kidney, and spleen, indicating mild to moderate damage, while the heart and lungs were normal. Thus, the intravenous administration of NONB at a dose of up to 0.06 mL in this subchronic toxicity test remains safe. Further studies with adjustments to the test formulation are highly encouraged until the clinical trial stage in humans.

pharmacology and toxicology↗

Evaluating the Safety of Intravenous Injection of Nitric Oxide, Magnesium, and Hydrogen Nano Bubble Solution in Sprague Dawley Rats

Nanobubble technology exhibits outstanding stability and permeability and has been extensively developed in pharmaceuticals, dentistry, and medicine. The Hydrogen Nano Bubble (HNB) solution containing NO and magnesium is projected to have an even greater therapeutic effect than has ever been investigated. An experimental study using Sprague-Dawley rats was conducted to assess the intravenous injections safety. Each rat received a single injection into the tail vein at a dose of 2 mL. On the other hand, aquades were injected into the rats in the control group. Observations were made every 30 minutes for the first four hours, then every four hours for the first twenty-four hours, and once daily for the next fourteen days. The LD50, urea-creatinine level, SGOT/SGPT level, and organ histology, including liver, kidney, heart, lung, and spleen, were evaluated. The solution appears safe for intravenous administration, as there were no adverse side effects during the trial, and all values were still within the normal range. Additional investigation is required to assess the long-term harmful impact.

pharmacology and toxicology↗