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HRK Supply Loteprednol etabonate raw Materials powder
Product Overview:
Loteprenol is a new type of glucocorticoid that can be used to treat corticosteroid-sensitive inflammation such as eyelid and bulbar conjunctivitis, uveitis, cornea and anterior ganglia. At present, the local use of glucocorticoids in clinical practice can significantly reduce ocular surface inflammation, but there are many side effects, which cannot be used for a long time. After eye drop, this product can be rapidly metabolized into inactive products, reducing systemic toxicity, minimizing adverse reactions of glucocorticoids, and its anti-inflammatory effect is stronger than prednisolone.
HRK Supply Loteprednol etabonate raw Materials powder Attributes
CAS:82034-46-6
MF:C24H31ClO7
MW:466.95
EINECS:200-010-0
Specification: 99% min Loteprednol etabonate Powder
Sample:Loteprednol etabonate Powder
Packaging:1kg/bag, 25kg/drum
Brand: Henrikang
Appearance:white
Storage: Cool Dry Place
Shelf Life: 2 Years
Test Method: HPLC
HRK Supply Loteprednol etabonate raw Materials powder Details
Loteprednol etabonate Powder Usage and Synthesis.
1. When the use of corticosteroids can safely reduce edema and inflammation, this product can be applied to the treatment of eyelid and bulbar conjunctivitis, uveitis, cornea and anterior ganglia inflammation of corticosteroid sensitive inflammation. (such as seasonal allergic conjunctivitis, rosacea keratitis, superficial punctate keratitis, herpes zoster keratitis, iritis, cyclitis, atopic keratitis, etc.).
2. This product is also suitable for treating postoperative inflammation after various eye operations.
Uses of Loteprednol etabonate.
Because Loteprednisolone is synthesized by structural modification of prednisolone compounds, Loteprednisolone is easily hydrolyzed to inactive organic acids, and when applied to the eye, it is rapidly metabolized to inactive products, reducing systemic toxicity and having a stronger anti-inflammatory effect than prednisolone.
Pharmacological action of Loteprednol etabonate.
The high fat solubility of cloteprednol makes its corneal permeability better, and it is easy to be hydrolyzed into inactive organic acids, and can be rapidly metabolized into inactive products after eye drop, reducing systemic toxicity. Compared with other glucocorticoids, its anti-inflammatory effect is stronger, and the effect of increasing iOP is less, so it is safer and has better efficacy. The metabolic site of this product is in the cornea, which avoids the ultrastructural changes of trabecular network caused by the high concentration of hormones in aqueous humor, which obstructs the outflow of aqueous humor and causes the increase of intraocular pressure. Compared to flumilone, it showed a lower tendency to increase IOP. The mechanism of action of its combination with cyclosporine in the treatment of dry eye is to inhibit the apoptosis of lacrimal acinic cells and conjunctival goblet cells, promote the apoptosis of lymphocytes, and thus inhibit the inflammation of the eye surface, but it is easy to cause irritation symptoms such as stinging and burning sensation. It has no effect on intraocular pressure, little irritation, mild effect and strong anti-inflammatory effect, so it is used more and more widely in ophthalmic treatment.
Product method of Bulk Loteprednol etabonate Powder.