A Review on Pharmacosomes as Novel Drug Delivery Systems

Authors

  • Kaveri Bhaurao Borse
  • Sneha Dayanand Ade
  • Monika Ambadas Boddhul
  • Gayatri Balaji Charate
  • Dipali Bolde

DOI:

https://doi.org/10.5281/zenodo.11214620

Keywords:

pharmacosomes, covalently, phospholipid, amphiphilic, vesicular

Abstract

Pharmacosomes are drug-lipid complexes that can form ultrafine vesicular, micellar, or hexagonal aggregates based on their chemical structure. It is based on the concept that a drug binds covalently to a lipid, with the resulting molecule being the carrier and the active chemical are present at the same time. The physicochemical qualities vary depending on both the medication and the lipid. Pharmacosomes: As offer advantages over conventional vesicles, making them a promising alternative. Encapsulating drugs in small amphiphilic vesicles prolongs their circulation, decreases toxicity, and increases efficacy. Cell wall transfer and the solubility of a poorly water-soluble chemical. This review covers Pharmacosomes' composition, synthesis, characterization, and therapeutic applications. Drug pharmacosomes are an effective method of delivering the medication directly to the infection site, which contributes a decrease in drug toxicity without harmful effects. They also reduce the cost of therapy by increasing the drug's bioavailability, especially for poorly soluble drugs. Pharmacosomes are suitable for incorporating both hydrophilic and lipophilic medication. Pharmacosomes have been developed for a variety of anti-inflammatory drugs, including nonsteroidal, neurological drugs.

Downloads

Download data is not yet available.

Downloads

Published

18-05-2024

Issue

Section

Articles

How to Cite

[1]
K. B. Borse, S. D. Ade, M. A. Boddhul, G. B. Charate, and D. Bolde, “A Review on Pharmacosomes as Novel Drug Delivery Systems”, IJRESM, vol. 7, no. 5, pp. 97–100, May 2024, doi: 10.5281/zenodo.11214620.