Evidence map›Paper›PMID 36998671›Full record

ReviewNanoscale advances2023

Lipid-based colloidal nanoparticles for applications in targeted vaccine delivery.

Muhammad Saad Khan, Sila Appak Baskoy, Celina Yang, Joohye Hong, Jayoung Chae, Heejin Ha, Sungjun Lee, Masayoshi Tanaka, Yonghyun Choi, Jonghoon Choi

Open access · goldAbstract readReview
In one paragraph

Review in Nanoscale advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

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  13. Lipid-based nanoparticles: innovations in ocular drug delivery.Frontiers in molecular biosciences · 2024
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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

10 authors at 4 institutions in 4 countries.

Muhammad Saad KhanDepartment of Physics, Toronto Metropolitan University 350 Victoria Street Toronto M5B2K3 Canada.
Sila Appak BaskoyInstitute for Biomedical Engineering, Science and Technology (iBEST), St. Michael's Hospital 209 Victoria Street Toronto M5B1W8 Canada.
Celina YangDepartment of Physics, Toronto Metropolitan University 350 Victoria Street Toronto M5B2K3 Canada.
Joohye HongSchool of Integrative Engineering, Chung-Ang University Seoul 06974 Republic of Korea dydgus5057@cau.ac.kr nanomed@cau.ac.kr.
Jayoung ChaeSchool of Integrative Engineering, Chung-Ang University Seoul 06974 Republic of Korea dydgus5057@cau.ac.kr nanomed@cau.ac.kr.
Heejin HaSchool of Integrative Engineering, Chung-Ang University Seoul 06974 Republic of Korea dydgus5057@cau.ac.kr nanomed@cau.ac.kr.
Sungjun LeeSchool of Integrative Engineering, Chung-Ang University Seoul 06974 Republic of Korea dydgus5057@cau.ac.kr nanomed@cau.ac.kr.
Masayoshi TanakaDepartment of Chemical Science and Engineering, Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku Yokohama-shi 226-8503 Kanagawa Japan.ORCID https://orcid.org/0000-0002-4701-5352
Yonghyun ChoiSchool of Integrative Engineering, Chung-Ang University Seoul 06974 Republic of Korea dydgus5057@cau.ac.kr nanomed@cau.ac.kr.
Jonghoon ChoiSchool of Integrative Engineering, Chung-Ang University Seoul 06974 Republic of Korea dydgus5057@cau.ac.kr nanomed@cau.ac.kr.ORCID https://orcid.org/0000-0003-3554-7033
Chung-Ang University · KRSt. Michael's Hospital · CATeradyne (United States) · USTokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bioactive molecules and their effects have been influenced by their solubility and administration route. In many therapeutic reagents, the performance of therapeutics is dependent on physiological barriers in the human body and delivery efficacy. Therefore, an effective and stable therapeutic delivery promotes pharmaceutical advancement and suitable biological usage of drugs. In the biological and pharmacological industries, lipid nanoparticles (LNPs) have emerged as a potential carrier to deliver therapeutics. Since studies reported doxorubicin-loaded liposomes (Doxil®), LNPs have been applied to numerous clinical trials. Lipid-based nanoparticles, including liposomes, solid lipid nanoparticles (SLNs), and nanostructured lipid nanoparticles, have also been developed to deliver active ingredients in vaccines. In this review, we present the type of LNPs used to develop vaccines with attractive advantages. We then discuss messenger RNA (mRNA) delivery for the clinical application of mRNA therapeutic-loaded LNPs and recent research trend of LNP-based vaccine development.

Identifiers

PMID36998671
PMCPMC10044484
OpenAlexW4321235251

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.