Evidence map›Paper›PMID 24590879›Full record

ArticlePharmaceutical research2014

Directed self-assembled nanoparticles of probucol improve oral delivery: fabrication, performance and correlation.

Zhiwen Zhang, Shijun Jiang, Zeying Liu, Baohua Niu, Wangwen Gu, Yaping Li, Jingbin Cui

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Article in Pharmaceutical research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Zhiwen ZhangCenter of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Haike Road, Shanghai, 201203, China.
Shijun Jiang
Zeying Liu
Baohua Niu
Wangwen Gu
Yaping Li
Jingbin Cui

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe are reporting on the development of a unique drug delivery platform by directed self-assembly technique to improve the oral delivery of hydrophobic drugs.

methodsHerein, a series of probucol directed self-assembled nanoparticles (PDN) were developed with two components of probucol and surfactant such as Tween 20, Tween 80, D-alpha-tocopheryl polyethylene glycol 1,000 succinate (TPGS) and HS-15, which was respectively named as T20-PDN, T80-PDN, TP-PDN and HS-PDN. The formation of various PDNs was determined by in vitro characterization and the physicochemical properties of these PDNs were determined. Moreover, the performance of PDN in enhancing the oral delivery and possible correlation between the in vitro properties and in vivo performances were investigated.

resultsPDN was homogenous nanometer-sized particles with negative surface charge. The cellular uptake of probucol in Caco-2 cell monolayer was respectively increased 1.15, 1.82, 1.59 and 5.31-fold by these PDN. In particular, the oral bioavailability of these PDN was significantly improved 3.0, 4.1, 5.4 and 10.4 folds compared with the free drug suspension. The enhanced cellular uptake and oral bioavailability were correlated with the characters of involved surfactants and the particle size of PDN.

conclusionsThereby, the directed self-assembled nanoparticles could provide a new strategy for enhancing the oral delivery of hydrophobic drugs.

Indexed as

Administration, OralAnimalsAnticholesteremic AgentsBiological AvailabilityCaco-2 CellsDrug CarriersHumansMaleNanoparticlesParticle SizePolyethylene GlycolsPolysorbatesProbucolRats, Sprague-DawleySurface-Active AgentsVitamin EAnticholesteremic AgentsDrug CarriersPolyethylene GlycolsPolysorbatesProbucolSurface-Active AgentstocophersolanVitamin E

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.