2014
DOI: 10.1016/j.carbpol.2014.03.099
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Modified pullulan nanoparticles for oral delivery of lopinavir: Formulation and pharmacokinetic evaluation

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Cited by 53 publications
(22 citation statements)
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“…By comparing different classes of dendrimers differing in their surface coating, including dendrimers coated with sialic acid (sialic acid conjugated polypropylenimine (PPI) dendrimers (SPPI)), with mannose (mannose conjugated PPI dendrimers (MPPI)) or with both sialic acid and mannose (sialic acid conjugated-mannosylated PPI dendrimers (SMPPI)), they concluded that both sialic acid and mannose receptors cooperate in macrophagic uptake of these nanoparticles with additive effects. Macrophagic accumulation and high disposition in the spleen have been demonstrated also for the protease inhibitors lopinavir loaded in modified pullulan nanoparticles [151] and for nanoformulated atazanavir [152]. …”
Section: Role Of the Spleen In The Pharmacokinetics Of Nanoparticlmentioning
confidence: 99%
“…By comparing different classes of dendrimers differing in their surface coating, including dendrimers coated with sialic acid (sialic acid conjugated polypropylenimine (PPI) dendrimers (SPPI)), with mannose (mannose conjugated PPI dendrimers (MPPI)) or with both sialic acid and mannose (sialic acid conjugated-mannosylated PPI dendrimers (SMPPI)), they concluded that both sialic acid and mannose receptors cooperate in macrophagic uptake of these nanoparticles with additive effects. Macrophagic accumulation and high disposition in the spleen have been demonstrated also for the protease inhibitors lopinavir loaded in modified pullulan nanoparticles [151] and for nanoformulated atazanavir [152]. …”
Section: Role Of the Spleen In The Pharmacokinetics Of Nanoparticlmentioning
confidence: 99%
“…This is because, in the drug‐loaded nanocarrier system, the drug is not available in free form. The plasma drug exposure of drug‐loaded nanocarrier system administered through any extravascular route is dependent on the absorption and disposition properties of the carrier system and how the loaded drug releases from the carrier system in the blood …”
Section: Introductionmentioning
confidence: 99%
“…The plasma drug exposure of drug-loaded nanocarrier system administered through any extravascular route is dependent on the absorption and disposition properties of the carrier system and how the loaded drug releases from the carrier system in the blood. [13,[17][18][19] It is anticipated that in patients with HIV/TB co-infection, where there are chances of drug-induced hepatotoxicity, dose adjustment (reduction) of LPV (conventional formulations) can lead to a further decrease in distribution of drug to viral reservoirs. On contrary to this, in hepatotoxic condition, nanocarrier delivery systems like SLNs would be more efficient in preventing undue plasma exposure compared with conventional formulations of LPV.…”
Section: Introductionmentioning
confidence: 99%
“…[28] This polysaccharide is especially used as a coating material in the food and pharmaceutical industries due to its non-toxic, water-soluble, colorless, tasteless, odorless, and heat-stable characteristics. [29] Ravi and Vats [30] developed pullulan nanoparticles for the delivery of human immunodeficiency virus (HIV) protease inhibitor Laponivar. According to the results of this study, it was observed that high microencapsulation efficiency values were obtained.…”
Section: Introductionmentioning
confidence: 99%