Evidence map›Paper›PMID 30597888›Full record

ArticleMarine drugs2018

Nano-in-Micro Delivery System Prepared by Co-Axial Air Flow for Oral Delivery of Conjugated Linoleic Acid.

Qian Li, Fangfang Xue, Junle Qu, Liwei Liu, Rui Hu, Chenguang Liu

Abstract read
In one paragraph

Article in Marine drugs, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Qian LiKey Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, China. liqian123@szu.edu.cn.
Fangfang XueCollege of Marine Life Sciences, Ocean University of China, Qingdao 266003, China. kikyoqq123@163.com.
Junle QuKey Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, China. jlqu@szu.edu.cn.ORCID 0000-0001-7833-4711
Liwei LiuKey Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, China. liulw@szu.edu.cn.
Rui HuKey Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, China. rhu@szu.edu.cn.
Chenguang LiuCollege of Marine Life Sciences, Ocean University of China, Qingdao 266003, China. liucg@ouc.edu.cn.

Funding

China Postdoctoral Science Foundation 2017M622756National Basic Research Program of China 2015CB352005National Natural Science Foundation of China 61525503/61620106016/81727804/61722508Natural Science Foundation of Guangdong Province Innovation Team 2014A030312008Science and Technology Innovation Commission of Shenzhen KQJSCX20170327151457055, JCYJ20170817094609727, JCYJ20170412105003520, JCYJ20150930104948169, JCYJ20160328144746940, GJHZ20160226202139185
6 · The paper itself

Abstract

The preparation of a nano-in-micro delivery system (NiMDS) under mild conditions without using toxic organic solvents and expensive equipment still faces challenges. In this study, we introduced the co-axial air flow method to prepare NiMDS for the oral delivery of conjugated linoleic acid (CLA). The chitosan nanoparticles were prepared using the stearic-acid-modified chitosan through self-aggregation. Then, the chitosan nanoparticles were incorporated into alginate microparticles by the co-axial air flow method. The obtained chitosan nanoparticles and NiMDS were spherical in shape with the average sizes of 221⁻243 nm and 130⁻160 μm, respectively. Compared with alginate microparticles, the hybrid particles were of fewer fragments, were bigger in size, had a higher mechanical strength, and showed a controlled release in the phosphate buffer solution (pH 1.2 or 7.4). The release kinetics study showed that encapsulating the chitosan nanoparticles into the alginate microparticles inhibited the dissolution of alginate microparticles at the initial stage. These results revealed the potential of NiMDS as an ideal oral carrier for the sustained release of CLA in the gastrointestinal environment.

Indexed as

Administration, OralAlginatesCaco-2 CellsCell Line, TumorChitosanDelayed-Action PreparationsDrug CarriersDrug Delivery SystemsHumansLinoleic Acids, ConjugatedNanoparticlesParticle SizeSolubilityAlginatesChitosanDelayed-Action PreparationsDrug CarriersLinoleic Acids, Conjugatedco-axial air flowgastrointestinal releasenano-in-micro

Identifiers

PMID30597888
PMCPMC6356465

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Registered trials

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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.