A Pharmaceutical Composition Comprising A Liposomal Formulation Of Efavirenz, Its Preparation And Application Thereof

Authors

  • Dhanashree Balasaheb Nale
  • Shinde Nalini Sudhir
  • Malgunde Anuja Abbaso
  • Kadam Shrikant Sambhajirao
  • Bandal Rajendra Shivajirao
  • Sayyad Naziya Moulalli

DOI:

https://doi.org/10.52783/jns.v14.3546

Keywords:

antiviral, DDS, Efavirenz, ARVs, poorly soluble drug

Abstract

In many countries, Efavirenz is the primary non nucleotide reverse transcriptase inhibitor for first-line antiretroviral therapy. It is an orally active antiviral drug that is specific for human immunodeficiency virus type 1 (HIV-1). Its effectiveness is due to its lengthy half-life, which ranges from 52 to 76 hours after numerous doses. The medication is poorly soluble in water. One of the most difficult difficulties for formulation scientists in the research sector will be the oral delivery of poorly soluble drugs. We intended to investigate effective encapsulation of efavirenz (EFV, which is one of the powerful (ARVs) using varied mass ratios of crude soybean lecithin and cholesterol, since the liposome is the most clinically successful DDS and yet is often investigated for ARVs delivery

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Published

2025-04-12

How to Cite

1.
Balasaheb Nale D, Sudhir SN, Abbaso MA, Sambhajirao KS, Shivajirao BR, Moulalli SN. A Pharmaceutical Composition Comprising A Liposomal Formulation Of Efavirenz, Its Preparation And Application Thereof. J Neonatal Surg [Internet]. 2025Apr.12 [cited 2025Apr.24];14(15S):601-14. Available from: https://jneonatalsurg.com/index.php/jns/article/view/3546