Evidence map›Paper›PMID 33652827›Full record

ArticleMolecules (Basel, Switzerland)2021

Simulation of the In Vivo Fate of Polymeric Nanoparticles Traced by Environment-Responsive Near-Infrared Dye: A Physiologically Based Pharmacokinetic Modelling Approach.

Lei Li, Haisheng He, Sifang Jiang, Jianping Qi, Yi Lu, Ning Ding, Hai-Shu Lin, Wei Wu, Xiaoqiang Xiang

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  5. Rational nanoparticle design: Optimization using insights from experiments and mathematical models.Journal of controlled release : official journal of the Controlled Release Society · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Lei LiDepartment of Clinical Pharmacy and Pharmacy Administration, School of Pharmacy, Fudan University, Shanghai 201203, China.
Haisheng HeKey Laboratory of Smart Drug Delivery of MOE and PLA, School of Pharmacy, Fudan University, Shanghai 201203, China.
Sifang JiangWest China School of Pharmacy, Sichuan University, Chengdu 610041, China.
Jianping QiKey Laboratory of Smart Drug Delivery of MOE and PLA, School of Pharmacy, Fudan University, Shanghai 201203, China.
Yi LuKey Laboratory of Smart Drug Delivery of MOE and PLA, School of Pharmacy, Fudan University, Shanghai 201203, China.ORCID 0000-0002-9655-7510
Ning DingDepartment of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai 201203, China.
Hai-Shu LinCollege of Pharmacy, Shenzhen Technology University, Shenzhen 518118, China.ORCID 0000-0002-6034-1363
Wei WuKey Laboratory of Smart Drug Delivery of MOE and PLA, School of Pharmacy, Fudan University, Shanghai 201203, China.ORCID 0000-0002-0164-0814
Xiaoqiang XiangDepartment of Clinical Pharmacy and Pharmacy Administration, School of Pharmacy, Fudan University, Shanghai 201203, China.ORCID 0000-0002-8683-2603
Fudan University · CNShenzhen Technology University · CNSichuan University · CN

Funding

Foundation of Shanghai Municipal Commission of Health and Family Planning 201840057National Natural Science Foundation of China 81473409National Science & Technology Major Project"Key New Drug Creation and Manufacturing Program",China 2018ZX09711002-006-008Shanghai Science and Technology Innovation Fund 18140900900
6 · The paper itself

Abstract

The application of physiologically based pharmacokinetic models to nanoparticles is still very restricted and challenging, owing to the complicated in vivo transport mechanisms involving nanoparticles, including phagocytosis, enhanced permeability and retention effects, cellular recognition, and internalisation, enzymatic degradation, lymphatic transport, and changes in physical properties. In our study, five nanoparticle formulations were synthesised using polycaprolactone as a framework material and methoxy poly (ethylene glycol)-poly(ε-caprolactone) as a long-circulating decorating material, as well as types of environmentally responsive near-infrared aza-boron-dipyrromethene dyes. According to quantification data and direct visualisation involving specific organs, a phagocytosis physiologically based pharmacokinetic model was developed to describe the dynamics of nanoparticles within and between organs in mice, considering cellular mechanisms involving phagocytosis and enhanced permeability and retention effects. Our results offer a better understanding of the in vivo fate of polymeric nanoparticles.

Indexed as

Drug Delivery SystemsPharmacokineticsAnimalsColoring AgentsComputer SimulationHumansMiceNanoparticlesPolyestersPolyethylene GlycolsPolymersColoring AgentspolycaprolactonePolyestersPolyethylene GlycolsPolymersbiodistributionmethoxy poly (ethylene glycol)-poly (ε-caprolactone)nanoparticlesphagocytosisphysiologically based pharmacokinetic model

Identifiers

PMID33652827
PMCPMC7956253
OpenAlexW3134618276

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.