TRINEUROSOL HP INJ
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Trineurosol-HP Injection is a standout product in our VETERINARY VITAMIN INJECTABLE category. Crafted with utmost pharmaceutical precision by Tridoss Laboratories Pvt. Ltd. a trusted Indian pharmaceutical manufacturer this injectable delivers Hydroxocobalamin, the most biologically superior and clinically preferred form of parenteral Vitamin B12, directly into the systemic circulation via intramuscular or subcutaneous injection bypassing the gastrointestinal absorption pathway that is frequently impaired in the very animals that need B12 supplementation most. Unlike Cyanocobalamin the cheaper and more commonly used synthetic B12 form Hydroxocobalamin is the naturally occurring, biologically active cobalamin that binds directly to plasma proteins for superior tissue retention, has a significantly longer plasma half-life that reduces injection frequency requirements, and does not require hepatic conversion before becoming biologically active. For animals with pancreatic exocrine insufficiency, chronic intestinal malabsorption, inflammatory bowel disease, or severe dietary B12 deficiency conditions where oral B12 supplementation is completely ineffective parenteral Hydroxocobalamin injection is the only reliable therapeutic option for achieving and maintaining adequate tissue B12 levels. With Trineurosol-HP, you can trust that you are offering every animal patient the very best in pharmaceutical-grade, biologically superior parenteral B12 repletion.
Composition:
Each 1ml ampoule of Trineurosol-HP Injection contains a precisely formulated, pharmaceutical-grade composition for reliable parenteral delivery:
- Hydroxocobalamin 1000mcg/ml (Active Ingredient): the naturally occurring, biologically active form of Vitamin B12 distinguished from the synthetic Cyanocobalamin form by its superior pharmacokinetic profile in three clinically important ways. First, Hydroxocobalamin binds avidly to transcobalamin transport proteins in plasma, achieving significantly higher and more sustained tissue B12 concentrations than Cyanocobalamin following injection. Second, its longer plasma half-life means effective therapeutic B12 tissue concentrations are maintained for significantly longer periods between injections reducing treatment frequency requirements and improving practical compliance in clinical practice. Third, unlike Cyanocobalamin which must first be converted to Hydroxocobalamin or Methylcobalamin by hepatic metabolism before becoming biologically active, Hydroxocobalamin enters the active coenzyme pool directly delivering faster, more complete, and more reliable therapeutic action in the two critical B12-dependent enzymatic pathways: the methylcobalamin pathway (methionine synthesis, DNA methylation, and folate metabolism) and the adenosylcobalamin pathway (propionate metabolism and the methylmalonyl-CoA to succinyl-CoA conversion essential for neurological myelin sheath maintenance)
- Sodium Chloride IP (Isotonic Vehicle): a pharmaceutical-grade isotonic saline base that maintains the osmolality of the injectable solution within the physiological range ensuring minimal tissue irritation, vascular compatibility, and patient comfort upon intramuscular or subcutaneous injection
- Glacial Acetic Acid / Sodium Acetate (pH Buffer): a pharmaceutical buffer system that maintains the solution pH at the optimal range for Hydroxocobalamin stability and parenteral bioavailability preventing chemical degradation of the active ingredient during storage and ensuring complete solubility and stability at the time of injection
- Water for Injection IP (Sterile Vehicle): sterile, pyrogen-free water meeting Indian Pharmacopoeia standards for parenteral preparations the aqueous base delivering the active ingredient in a completely clear, injectable solution free from particulate matter and microbial contamination
