Liposomal Formulation For Oral Delivery Of Sarecycline: Usefulness As A Semisolid-Dispersion System

Open Access Special Issue Topic

Liposomal Formulation for Oral Delivery of Sarecycline: Usefulness as a Semisolid-Dispersion System

This special issue belongs to	Research & Reviews: A Journal of Pharmaceutical sciences Special Issues
Related section	NA
Deadline for Manuscript Submission	October 31st, 2022
Deadline for Publication	October 15, 2022

Special Issue Description

Dear Collegues,

Liposomes are tiny, spherical artificial vesicles that can be made from cholesterol and safe, natural phospholipids. In addition to biocompatibility, liposomes' size and hydrophobic and hydrophilic properties make them ideal drug delivery platforms. A tetracycline-derived antibiotic with a limited scope is called recycling.

It was authorized by the FDA in October 2018 for the treatment of inflammatory lesions of non-nodular moderate to severe acne vulgaris in patients 9 years of age and older. It was created exclusively for the treatment of acne. The study aims to establish the efficacy of liposomal formulation for poorly soluble pharmaceuticals and to comprehend the mechanism and process of oral drug absorption from liposomes.

Keywords

*Sarecycline
*Liposome
*Semi-solid Dispersion
*Anti-bacterial combinations
*Aminoglycoside modifying enzymes

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