801-2, Jindong Mansion, No. 536 Xueshi Road, Yinzhou, Ningbo 315100, P.R.China | info@newlystar-medtech.com |
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Place of Origin: | China |
Brand Name: | Newlystar |
Certification: | ISO |
Model Number: | 250mg/bag |
Minimum Order Quantity: | 50000 bags |
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Price: | Negotiation |
Packaging Details: | 10 bags per box |
Delivery Time: | 30days |
Payment Terms: | L/C, T/T |
Supply Ability: | 100, 000 boxes |
Product: | L-Carnitine Milk Shake For Meal Replacement | Standard: | Food Grade Product |
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Specification: | 250mg/bag | Flavor: | Strawberry, Vanilla, Matcha |
Highlight: | meal supplements,health food supplements |
Gastric Nutritional Dietary Supplement L Carnitine Milk Shake for Meal Replacement
Product : L-Carnitine Milk Shake for Meal Replacement
Standard : Food Grade Product
Specification : 250mg/bag
Flavor : Strawberry, vanilla, matcha
Description
Constituent of striated muscle and liver. It is used therapeutically to stimulate gastric and pancreatic secretions and in the treatment of hyperlipoproteinemias.
Indication
For treatment of primary systemic carnitine deficiency, a genetic impairment of normal biosynthesis or utilization of levocarnitine from dietary sources, or for the treatment of secondary carnitine deficiency resulting from an inborn error of metabolism such as glutaric aciduria II, methyl malonic aciduria, propionic acidemia, and medium chain fatty acylCoA dehydrogenase deficiency. Used therapeutically to stimulate gastric and pancreatic secretions and in the treatment of hyperlipoproteinemias. Parenteral levocarnitine is indicated for the prevention and treatment of carnitine deficiency in patients with end-stage renal disease.
Pharmacodynamics
Levocarnitine is a carrier molecule in the transport of long chain fatty acids across the inner mitochondrial membrane. It also exports acyl groups from subcellular organelles and from cells to urine before they accumulate to toxic concentrations. Lack of carnitine can lead to liver, heart, and muscle problems. Carnitine deficiency is defined biochemically as abnormally low plasma concentrations of free carnitine, less than 20 µmol/L at one week post term and may be associated with low tissue and/or urine concentrations. Further, this condition may be associated with a plasma concentration ratio of acylcarnitine/levocarnitine greater than 0.4 or abnormally elevated concentrations of acylcarnitine in the urine. Only the L isomer of carnitine (sometimes called vitamin BT) affects lipid metabolism. The "vitamin BT" form actually contains D,L-carnitine, which competitively inhibits levocarnitine and can cause deficiency. Levocarnitine can be used therapeutically to stimulate gastric and pancreatic secretions and in the treatment of hyperlipoproteinemias.
Mechanism of action
Levocarnitine can be synthesised within the body from the amino acids lysine or methionine. Vitamin C (ascorbic acid) is essential to the synthesis of carnitine. Levocarnitine is a carrier molecule in the transport of long chain fatty acids across the inner mitochondrial membrane. It also exports acyl groups from subcellular organelles and from cells to urine before they accumulate to toxic concentrations. Only the L isomer of carnitine (sometimes called vitamin BT) affects lipid metabolism. Levocarnitine is handled by several proteins in different pathways including carnitine transporters, carnitine translocases, carnitine acetyltransferases and carnitine palmitoyltransferases.
Contact Person: Mr. Luke Liu
Tel: 86--57487019333
Fax: 86-574-8701-9298
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