Evidence map›Paper›PMID 31671569›Full record

ArticlePharmaceutics2019

Development of Folate-Functionalized PEGylated Zein Nanoparticles for Ligand-Directed Delivery of Paclitaxel.

Zar Chi Soe, Wenquan Ou, Milan Gautam, Kishwor Poudel, Bo Kyun Kim, Le Minh Pham, Cao Dai Phung, Jee-Heon Jeong, Sung Giu Jin, Han-Gon Choi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 47 citations in OpenAlex.

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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

13 authors at 5 institutions in 2 countries.

Zar Chi SoeCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. zarchisoeygn96@gmail.com.
Wenquan OuCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. owqcn@foxmail.com.
Milan GautamCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. gtmmilan2@gmail.com.
Kishwor PoudelCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. poudel.kishwor99@gmail.com.
Bo Kyun KimCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. kyunsbk14@naver.com.
Le Minh PhamCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. phamleminh87@gmail.com.
Cao Dai PhungCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. phungcaodai@gmail.com.
Jee-Heon JeongCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. jeeheon@yu.ac.kr.
Sung Giu JinDepartment of Pharmaceutical Engineering, Dankook University, 119 Dandae-ro, Dongnamgu, Cheonan 31116, Korea. sklover777@gmail.com.
Han-Gon ChoiCollege of Pharmacy, Institute of Pharmaceutical Science and Technology, Hanyang University, 55 Hanyangdaehak-ro, Sangnok-gu, Ansan 426-791, Korea. hangon@hanyang.ac.kr.ORCID 0000-0002-2318-387X
Sae Kwang KuDepartment of Anatomy and Histology, College of Korean Medicine, Haany University, Gyeongsan 712-715, Korea. gucci200@hanmail.net.ORCID 0000-0003-1269-3804
Chul Soon YongCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. csyong@yu.ac.kr.
Jong Oh KimCollege of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyeongsan 712-749, Korea. jongohkim@yu.ac.kr.ORCID 0000-0002-4929-851X
Yeungnam University · KRDaegu Haany University · KRDankook University · KRHanyang University · KRUniversity of Pharmacy Mandalay · MM

Funding

National Research Foundation of Korea 2018R1A2A2A05021143, 2018R1A5A2025272
6 · The paper itself

Abstract

In this study, we investigated the active targeted delivery of a hydrophobic drug, paclitaxel (PTX), via receptor-mediated endocytosis by folate receptors expressed on cancer cells using a protein-based nanoparticle system. PTX was loaded on zein nanoparticles and conjugated with folate (PTX/Zein-FA) to estimate its chemotherapeutic efficacy in folate receptor-expressing KB cancer cells. PTX/Zein-FA nanoparticles were successfully developed, with a nanoparticle size of ~180 nm and narrow polydispersity index (~0.22). Accelerated release of PTX in an acidic environment was observed for PTX/Zein-FA. An in vitro cellular study of PTX/Zein-FAs in KB cells suggested that PTX/Zein-FA improved the cytotoxic activity of PTX on folate receptors overexpressed in cancer cells by inducing proapoptotic proteins and inhibiting anti-apoptotic proteins. In addition, PTX/Zein-FA exhibited anti-migratory properties and could alter the cell cycle profile of KB cells. A549 cells, which are folate receptor-negative cancer cells, showed no significant enhancement in the in vitro cellular activities of PTX/Zein-FA. We describe the antitumor efficacy of PTX/Zein-FA in KB tumor-bearing mice with minimum toxicity in healthy organs, and the results were confirmed in comparison with free drug and non-targeted nanoparticles.

Indexed as

folic acidnanoparticlepaclitaxelzein

Identifiers

PMID31671569
PMCPMC6920870
OpenAlexW2982483577

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.