Lipid drug conjugate nanoparticle as a potential nanocarrier for the oral delivery of pemetrexed diacid: Formulation design, characterization, ex vivo, and in vivo assessment

International Journal of Biological Macromolecules
Kriti SoniKanchan Kohli

Abstract

The present work was to develop lipid drug conjugated (LDC) nanoparticles for the potential oral delivery of pemetrexed diacid (PTX) and evaluation of its in vitro, ex vivo and in vivo potentials. The LDC was prepared by salt formation of PTX with stearic acid and followed by cold homogenization technique to produce the LDC nanoparticles. FTIR analysis of LDC proved the presence of amide bond in LDC powder indicating the conjugation between drug and lipid. LDC nanoparticles was found to have particle size 121.9±1.85nm and zeta potential -51.6mV±1.23 and entrapment efficiency 81.0±0.89%. TEM images revealed spherical morphology and were in corroboration with particle size measurements. Ex vivo gut permeation studies revealed a very good enhancement in permeation of drug present in the LDC as compared to plain drug solution and were confirmed by CLSM. MTT assay conformed significant% toxicity at the end of 24h and 48h. Furthermore, the AUC0-24 of PTX from the optimized LDC nanoparticels was found to be 4.22 folds higher than that from PTX suspension on oral administration. Thus, LDC has high potential for the oral delivery of PTX in cancer therapy and future prospects for the industrial purpose.

Citations

May 21, 2019·Expert Opinion on Drug Metabolism & Toxicology·Subham Banerjee, Jonathan Pillai
Nov 22, 2019·Preparative Biochemistry & Biotechnology·Güliz AkŞenay Hamarat Şanlıer
Jul 25, 2019·Pharmaceutics·Ruby MaharjanYoungro Byun
Mar 29, 2021·Advanced Drug Delivery Reviews·Souhaila H El MoukhtariMaría J Blanco-Prieto

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