Evidence map›Paper›PMID 34138119›Full record

ArticleNano-micro letters2020

Artificial Nanoscale Erythrocytes from Clinically Relevant Compounds for Enhancing Cancer Immunotherapy.

Wenquan Ou, Kang Sik Nam, Dae Hoon Park, Jungho Hwang, Sae Kwang Ku, Chul Soon Yong, Jong Oh Kim, Jeong Hoon Byeon

Open access · diamondAbstract read
In one paragraph

Article in Nano-micro letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 3 institutions in 1 country.

Wenquan Ou *College of Pharmacy, Yeungnam University, Gyeongsan, 38541, Republic of Korea.
Kang Sik Nam *School of Mechanical Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
Dae Hoon ParkSchool of Mechanical Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
Jungho HwangSchool of Mechanical Engineering, Yonsei University, Seoul, 03722, Republic of Korea. hwangjh@yonsei.ac.kr.
Sae Kwang KuCollege of Korean Medicine, Daegu Haany University, Gyeongsan, 38610, Republic of Korea.
Chul Soon YongCollege of Pharmacy, Yeungnam University, Gyeongsan, 38541, Republic of Korea.
Jong Oh KimCollege of Pharmacy, Yeungnam University, Gyeongsan, 38541, Republic of Korea. jongohkim@yu.ac.kr.
Jeong Hoon ByeonSchool of Mechanical Engineering, Yeungnam University, Gyeongsan, 38541, Republic of Korea. postjb@yu.ac.kr.
Yeungnam University · KRYonsei University · KRDaegu Haany University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Because of enhanced efficacy and lower side effects, cancer immunotherapies have recently been extensively investigated in clinical trials to overcome the limitations of conventional cancer monotherapies. Although engineering attempts have been made to build nanosystems even including stimulus nanomaterials for the efficient delivery of antigens, adjuvants, or anticancer drugs to improve immunogenic cancer cell death, this requires huge R&D efforts and investment for clinically relevant findings to be approved for translation of the nanosystems. To this end, in this study, an air-liquid two-phase electrospray was developed for stable bubble pressing under a balance between mechanical and electrical parameters of the spray to continuously produce biomimetic nanosystems consisting of only clinically relevant compounds [paclitaxel-loaded fake blood cell Eudragit particle (Eu-FBCP/PTX)] to provide a conceptual leap for the timely development of translatable chemo-immunotherapeutic nanosystems. This was pursued as the efficacy of systems for delivering anticancer agents that has been mainly influenced by nanosystem shape because of its relevance to transporting behavior to organs, blood circulation, and cell-membrane interactions. The resulting Eu-FBCP/PTX nanosystems exhibiting phagocytic and micropinocytic uptake behaviors can confer better efficacy in chemo-immunotherapeutics in the absence and presence of anti-PD-L1 antibodies than similar sized PTX-loaded spherical Eu particles (Eu-s/PTX).

Indexed as

Air–liquid two-phase electrosprayAnti-PD-L1 antibodiesCancer immunotherapiesPaclitaxel-loaded fake blood cell Eudragit particleTranslatable chemo-immunotherapeutic nanosystems

Identifiers

PMID34138119
PMCPMC7770689
OpenAlexW3016879668

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.