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|
Deadline for Manuscript Submission
|October 31st, 2022|
Deadline for Publication
|October 15, 2022|
Special Issue Description
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.
*Aminoglycoside modifying enzymes
Manuscript Submission information
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Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page.