Preparation of Ivermectin

Ivermectin is a drug derived from avermectins, a group of compounds produced by the bacterium Streptomyces avermitilis. It is widely used as an antiparasitic agent in both humans and animals. Below is an overview of its preparation process:

1. Cultivation of Streptomyces avermitilis

  • Isolation: The bacterium Streptomyces avermitilis is grown in a controlled fermentation environment.
  • Fermentation medium: The growth medium typically contains nutrients like glucose, soybean meal, and essential salts to support microbial growth and metabolite production.
  • Optimal conditions: The fermentation is carried out under specific conditions of pH, temperature (25–28°C), and aeration to maximize the production of avermectins.

2. Extraction of Avermectins

  • After fermentation, the culture broth contains the avermectins, which are extracted using organic solvents such as ethyl acetate or methanol.
  • The solvents are used to separate the compounds from the microbial biomass and the fermentation medium.
Preparation of Ivermectin-Xi'an Lyphar Biotech Co., Ltd

3. Purification of Avermectins

The crude extract is subjected to:

  • Liquid-liquid extraction to separate impurities.
  • Chromatographic techniques, such as silica gel or reverse-phase chromatography, to isolate specific avermectin derivatives.

4. Chemical Modification to Ivermectin

  • The purified avermectins (specifically avermectin B1a and B1b) are chemically modified to produce ivermectin.
  • Hydrogenation: Selective hydrogenation of specific functional groups (e.g., double bonds) creates ivermectin from the parent compounds.
  • Proportioning: The final product contains about 80% of ivermectin B1a and 20% of ivermectin B1b.

5. Formulation

The synthesized ivermectin is formulated into different dosage forms depending on its intended use:

  • Tablets for oral administration (humans).
  • Injections for veterinary use.
  • Topical formulations like creams or lotions for external use.
Preparation of Ivermectin-Xi'an Lyphar Biotech Co., Ltd

6. Quality Control

Rigorous testing ensures the product meets standards for:

  • Purity (high-performance liquid chromatography, HPLC).
  • Potency (bioassays).
  • Safety (toxicity studies).

Would you like detailed steps on any specific aspect of the process?