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LIPO-DRIVE

LIPO-DRIVE IM is a sterile intramuscular injectable lipotropic/metabolic support blend constructed for research applications in fat metabolism, hepatic protection, and energy optimization. It includes:

  • L-Carnitine (300 mg): transports fatty acids into mitochondria for oxidation
  • Methionine (25 mg): methyl donor; supports glutathione synthesis and detox cycles
  • Inositol (50 mg) & Choline (50 mg): support lipid signaling, insulin sensitivity, and hepatic lipid export
  • B12 (1 mg) & B6 (50 mg): cofactor support for metabolism and the methyl cycle
  • NADH (50 mg): provides reducing equivalents for mitochondrial ATP production

This integrated blend is suited for preclinical studies in metabolic stress, lipid utilization, hepatic health, obesity models, and energy dynamics investigations.

Research use only — not for human or veterinary use.

PEPTIDES4ALL LIPO-DRIVE – Intramuscular Lipotropic & Energetic Metabolic Blend

LIPO-DRIVE IM is a sterile intramuscular (IM) injectable formulation designed for research use, combining a lipotropic and mitochondrial support matrix to promote fat mobilization, metabolic efficiency, hepatic function, and energy metabolism. This blend pairs classical lipid-metabolism cofactors with methyl donors and redox support agents for a multi-axis metabolic tool.

Composition (per dose):

  • L-Carnitine — 300 mg

  • Methionine — 25 mg

  • Inositol — 50 mg

  • Choline — 50 mg

  • Vitamin B12 — 1 mg

  • Vitamin B6 — 50 mg

  • NADH — 50 mg


Scientific Evidence & Research Findings

L-Carnitine (300 mg)

  • Carnitine is key to transporting long-chain fatty acids into mitochondria for β-oxidation, supporting energy production from fats. (Linus Pauling Institute)

  • Its roles are expanding beyond simple fatty acid transport — research now emphasizes its involvement in mitochondrial homeostasis, epigenetic regulation, inflammation, and inter-organ metabolic signaling. BioMed Central

  • Some meta-analyses show that supplemental L-carnitine (higher doses) can modestly improve lipid profiles (e.g. decreased LDL, improved HDL) in certain populations. PMC

Methionine & Methylation Cycle

  • Methionine is a principal methyl donor (via S-adenosylmethionine, SAM) in methylation reactions, gluathione synthesis, and detoxification pathways.

  • The methyl group donation from methionine and choline is critical in hepatic methyl-carbon metabolism. In bovine hepatocyte studies, choline and methionine differentially regulate methyl carbon pathways, with implications for VLDL export and oxidative stress mitigation. PLOS

  • Choline plays a critical role in hepatic lipid metabolism through its conversion to phosphatidylcholine via the phosphatidylethanolamine N-methyltransferase (PEMT) pathway. This process is essential for very-low-density lipoprotein (VLDL) synthesis and the export of triglycerides from the liver. The interplay between choline and methionine—both methyl donors in the S-adenosylmethionine (SAM) cycle—is fundamental to maintaining hepatic lipid balance and preventing steatosis.
    (PMC Article: “Choline Metabolism Provides Novel Insights into Nonalcoholic Fatty Liver Disease

Inositol, Choline & B-Vitamins

  • Inositol plays roles in lipid signaling, insulin sensitivity, and cellular signaling pathways relevant to metabolic health (in the literature on PCOS, insulin resistance, etc.).

  • Choline is essential for liver function, lipid metabolism, and lipotropic action. Dietary choline is necessary for VLDL export and preventing hepatic fat accumulation. PMC

  • Vitamins B6 & B12 support energy metabolism, the methyl-folate cycle, mitochondrial function, and red blood cell formation — all of which are foundational in efficient metabolism and recovery.

NADH

  • NADH is a reduced coenzyme form of vitamin B3 (niacin) and plays a direct role in mitochondrial electron transport, ATP generation, redox balance, and cellular bioenergetics.

  • By supplying reducing equivalents, NADH may help support energetic demands in metabolic stress or exercise models, and facilitate oxidative metabolism.


Key Research Benefits & Applications

  • Fat Mobilization & Mitochondrial Oxidation: Carnitine transports fatty acids into mitochondria; NADH supplies reducing equivalents for electron transport; methionine/choline/in­ositol support hepatic lipid export and methyl cycle.

  • Hepatic Protection & Lipid Homeostasis: Methyl donors (methionine, choline) and inositol support liver methylation, VLDL export, and protect against hepatic steatosis.

  • Metabolic & Energetic Efficiency: B6/B12 ensure cofactor sufficiency; NADH helps energy chain flux; the blend aims to reduce metabolic bottlenecks.

  • Integrated Lipotropic Action: This formula offers multiple angles to support fat metabolism — substrate delivery, methyl support, redox balance, and mitochondrial drive.


Formulation, Handling & Storage

  • Formulation: Sterile, preservative-free IM injectable solution
  • Administration: Intramuscular injection (e.g. deltoid, gluteal) under sterile technique
  • Storage: –20 °C, shielded from light and moisture; handle under lab protocols 

Intended Use 

For research purposes only. Must be handled in accordance with institutional protocols and ethical guidelines.

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