-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
Liraglutide acetate is a medication used to treat type 2 diabetes.
It is a glucagon-like peptide-1 (GLP-1) receptor agonist, which means it helps the body produce more insulin and decrease glucose production in the liver.
Liraglutide acetate is dosed once a day and is taken by subcutaneous injection.
The chemical formula for liraglutide acetate is C66H83NO15C14O24.
It has a molecular weight of 3879.
51 g/mol.
Liraglutide acetate is a white to off-white, odorless, and hygroscopic powder.
It is soluble in water, but the solubility is dependent on the pH of the solution.
The manufacturing process of liraglutide acetate involves several steps.
The first step is the synthesis of the peptide.
This is done by using a solid-phase peptide synthesizer or by a liquid-phase synthesis method.
The synthesized peptide is then cleaved from the resin and purified by HPLC (high-performance liquid chromatography).
The purified peptide is then processed to form the acetate ester.
The final product is a white to off-white, odorless, and hygroscopic powder, which is then formulated into a solution for injection.
The pharmacokinetics of liraglutide acetate are characterized by a rapid absorption after subcutaneous injection.
The peak plasma concentration (Cmax) is reached around 1–3 hours after administration and the drug has a half-life (t1/2) of approximately 3–5 hours.
The drug is metabolized in the liver by degradation enzymes, such as dipeptidyl peptidase-4 (DPP-4) and neutral endopeptidase (NEP).
The major metabolite of liraglutide acetate is liraglutide, which has a similar pharmacological activity as the parent compound.
The metabolite is then excreted in the urine.
The efficacy and safety of liraglutide acetate have been evaluated in several clinical trials.
In type 2 diabetes patients, treatment with liraglutide acetate resulted in significantly improved glycemic control, as well as weight loss, compared to placebo.
The product labeling recommends a starting dose of 0.
6 mg/day, and the dose can be adjusted based on the patient's glycemic response and tolerability.
The most common adverse effects of liraglutide acetate are gastrointestinal symptoms, such as nausea, vomiting, and diarrhea.
These symptoms are usually mild and resolve on their own, but they can be managed with dose adjustments and supportive care.
Other adverse effects, such as pancreatitis and gallbladder problems, have been reported, but the frequency is low.
In conclusion, Liraglutide acetate is a medication used to treat type 2 diabetes.
It is a GLP-1 receptor agonist which helps the body produce more insulin and decrease glucose production in the liver.
The manufacturing process involves several steps and the pharmacokinetics of liraglutide acetate is characterized by a rapid absorption after subcutaneous injection.
The efficacy and safety of liraglutide acetate have been evaluated in several clinical trials and the most common adverse effects are gastrointestinal symptoms, but other adverse effects like pancreatitis and gallbladder problems have been reported.